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Allgemeine Inhalte

Molekulare Gynäkologie

Relevanz: 6%
 

AG Molekulare Gynäkologie Frauenklinik im Forschungszentrum, Klinik für Frauenheilkunde und Geburtshilfe Medizinische Hochschule Hannover, Carl-Neuberg-Str. 1, D-30625 Hannover Wissenschaftliche Schwerpunkte: - Molekulare Ursachen gynäkologischer Erkrankungen - Genetische Störungen der Replikation und DNA-Reparatur Ort: Forschungslabore der Frauenklinik, Gebäude I11, Ebene SO Kontakt: Dr. rer. nat. Thilo Dörk-Bousset Dipl.-Biochemiker, Fachhumangenetiker Tel.: 0511-532-6075 (Büro) Tel.: 0511-532-6077 (Labor) Fax: 0511-532-6081 E-Mail: doerk.thilo@mh-hannover.de Mitarbeiterinnen und Mitarbeiter: Dr. rer. nat. Kristine Bousset (wiss. Mitarbeiterin) Dr. rer. nat. Dhanya Ramachandran (wiss. Mitarbeiterin) Dr. rer. nat. Lisa-Marie Speith (wiss. Mitarbeiterin) Iulia Folcut (M.Sc., naturwiss. Doktorandin) Maria del Mar Haro Hereu (M.Sc., naturwiss. Doktorandin) Lara Thomys (M.Sc., naturwiss. Doktorandin) Luisa Hölzl (M.Sc., naturwiss. Doktorandin) Anna Zvarych (M.Sc., naturwiss. Doktorandin) Mengying Li (Doktorandin der Humanmedizin) Yu-zhen Xiao (Doktorandin der Humanmedizin) Louisa Lenfort (Doktorandin der Humanmedizin) Emilia Kaufmann (Doktorandin der Humanmedizin) Manya Jain (M.Sc., wissenschaftl. Hilfskraft) Valeriia Obrizan (M.Sc., techn. Assistentin) Susanne Iordanidis (BTA) Britta Wieland (BTA) Peter Schürmann (MTA) Laufende Forschungsprojekte: Molekularbiologie des Mammakarzinoms Molekulare Genetik des Ovarialkarzinoms Molekulare Genetik des Endometriumkarzinoms Genetische Epidemiologie des Zervixkarzinoms Erbliche DNA-Reparaturstörungen Molekulare Ursachen von Schwangerschaftskomplikationen Weiterbildungsangebote: Doktorarbeiten in naturwissenschaftlichen Promotionsstudiengängen (Dr. rer. nat., MD/PhD "Molecular Medicine") Doktorarbeiten im Studiengang Humanmedizin Master- und Bachelorarbeiten in den Studiengängen Biochemie, Biologie und Life Sciences Laborpraktika im Rahmen der Studiengänge Biochemie, Biologie und Life Sciences Unterstützung von Advanced Clinician Scientists (6 Jahre mit 50% geschützter Forschungszeit) Enge Kooperationspartner an der MHH: Klinik für Strahlentherapie und spezielle Onkologie Institut für Experimentelle Hämatologie Drittmittelgeber in den letzten zehn Jahren: Bruno und Helene Jöster Stiftung Bundesministerium für Forschung, Technologie und Raumfahrt Claudia von Schilling Stiftung Deutsche Forschungsgemeinschaft Hans-Werner & Josephine Hector Stiftung Monika Kutzner Stiftung Rudolf Bartling Stiftung Wilhelm Sander Stiftung Wissenschaftliche Publikationen der letzten Jahre: siehe hier Stand: 31. Juli 2026

Allgemeine Inhalte

Forschung und Lehre an der Frauenklinik

Relevanz: 6%
 

Forschung | Lehre | Studien Gesamtüberblick über Aktivitäten in Forschung, Lehre und Studien aus allen Fachbereichen der Klinik für Frauenheilkunde und Geburtshilfe.

Allgemeine Inhalte

Forschung

Relevanz: 6%
 

Forschung in der Frauenklinik Die Frauenklinik ist mit drei Arbeitsgruppen im Forschungszentrum vertreten und führt darüber hinaus weitere Forschungsprojekte durch. Frauenklinik im Forschungszentrum Dr. rer. nat. Thilo Dörk-Bousset Tel.: 0511/532-6075 (Büro) Tel.: 0511/532-6077 (Labor) Fax: -6081 E-Mail: doerk.thilo @ mh-hannover.de MHH - OE 6411 - Gebäude I11, Ebene S0. Die Frauenklinik unterhält im TPFZ einen Laborbereich, in dem gynäkologisch-onkologische und geburtshilfliche Forschungsthemen experimentell bearbeitet werden. Weitere Forschungsprojekte in der Frauenklinik AG HPV-induzierte Neoplasien Univ.-Prof. Dr. med. Peter Hillemanns Wissenschaftliche Schwerpunkte: • Evaluation verschiedener Testmethoden zur Diagnostik der genitalen HPV-Infektion • Photodynamische Diagnostik und Therapie HPV-assoziierter Dysplasien der Zervix und Vulva • Prävention der HPV-Infektion durch Impfung • Gesundheitsökonomische Untersuchungen zu HPV-assoziierten Dysplasien / Karzinomen Kontakt: Klinik für Frauenheilkunde und Geburtshilfe Univ.-Prof. Dr. med. Peter Hillemanns Tel.: 0511-532-6144 Fax.: 0511-532-6145 Mitwirkende: Frauenklinik im Forschungszentrum MHH Prof. Dr. rer. nat. Ralf Hass Dr. rer. nat. Thilo Dörk-Bousset Laufende Forschungsprojekte: • HPV-Impfstudien [HPV 070] • Selbstuntersuchungsmethoden zum HPV Abstrich im Rahmen der Zervixkarzinomprävention [HaSCo] • Genetische Disposition für Dysplasien und Karzinome der Cervix [ZerviGen] (siehe AG Molekulare Gynäkologie des Forschungszentrums ) • Vergleich verschiedener HPV-Testsysteme • Photodynamische Therapie der CIN 2 – 3 [Cevira] • HPV-Nachweis aus Urin • Therapeutische HPV 16 Impfung bei CIN 2/3 [VB C-01] • Therapeutische HPV 16 Impfung und Checkpoint-Inhibition bei rezidiviertem Zervixkarzinom [VB C-02] (siehe clinicaltrails und Company Announcement inkl. Grafik ) • Zervixkarzinom und Sentinel. Internationale Phase 3 Studie [SENTICOL III] (siehe PubMed ) • Studiengruppe Kolposkopie Drittmittel der letzten fünf Jahre: • Deutsche Krebsgesellschaft (DKH) • Deutsche Forschungsgemeinschaft (DFG) • Bundesministerium für Bildung und Forschung (BMBF) • Land Niedersachsen • Volkswagenstiftung • Wilhelm Sander-, Jöster-, Bartling Stiftung • Novartis Institute of Biomedical Research • German Alliance for Global Health Research Wissenschaftliche Publikationen der letzten fünf Jahre: Items 1-15 of 15 ( Display the 15 citations in PubMed ) 1. A therapeutic antigen-presenting cell-targeting DNA vaccine VB10.16 in HPV16-positive high-grade cervical intraepithelial neoplasia: results from a phase 1/2a trial. Hillemanns P, Denecke A, Woelber L, Böhmer G, Jentschke M, Schjetne KW, Bruins Slot KMH, Fredriksen AB. Clin Cancer Res. 2022 Sep 21:CCR-22-1927. doi: 10.1158/1078-0432.CCR-22-1927. Online ahead of print. PMID: 36129459 2. FAM19A4/miR124-2 methylation testing and HPV16/18 genotyping in HPV-positive women under the age of 30 years. Vink FJ, Meijer CJLM, Hesselink AT, Floore AN, Lissenberg-Witte BI, Bonde JH, Pedersen H, Cuschieri K, Bhatia R, Poljak M, Oštrbenk Valenčak A, Hillemanns P, Quint WGV, Del Pino M, Kenter GG, Steenbergen RDM, Heideman DAM, Bleeker MCG. Clin Infect Dis. 2022 Jun 10:ciac433. doi: 10.1093/cid/ciac433. Online ahead of print. PMID: 35686306 3. Multicentre, prospective, randomised controlled trial to evaluate hexaminolevulinate photodynamic therapy (Cevira) as a novel treatment in patients with high-grade squamous intraepithelial lesion: APRICITY phase 3 study protocol. Chen F, Novák Z, Dannecker C, Mokráš C, Sui L, Zhang Y, You Z, Han L, Lang J, Hillemanns P. BMJ Open. 2022 Jun 6;12(6):e061740. doi: 10.1136/bmjopen-2022-061740. PMID: 35667715 Free PMC article. 4. Evaluation of FAM19A4/miR124-2 methylation performance in the management of CIN3 diagnosed pregnant women. Hampl M, Hesselink AT, Meijer CJLM, Denecke A, Einhorn I, Reinecke-Luethge A, Geppert CI, Jentschke M; Members of the German Study Group of Colposcopy (SGK), Petry KU, Hillemanns P. Int J Cancer. 2022 Nov 1;151(9):1578-1585. doi: 10.1002/ijc.34153. Epub 2022 Jun 20. PMID: 35666529 5. Diagnosis, Therapy and Follow-up of Cervical Cancer. Guideline of the DGGG, DKG and DKH (S3-Level, AWMF Registry No. 032/033OL, May 2021) - Part 1 with Recommendations on Epidemiology, Screening, Diagnostics and Therapy. Beckmann MW, Stübs FA, Koch MC, Mallmann P, Dannecker C, Dietl A, Sevnina A, Mergel F, Lotz L, Hack CC, Ehret A, Gantert D, Martignoni F, Cieslik JP, Menke J, Ortmann O, Stromberger C, Oechsle K, Hornemann B, Mumm F, Grimm C, Sturdza A, Wight E, Loessl K, Golatta M, Hagen V, Dauelsberg T, Diel I, Münstedt K, Merz E, Vordermark D, Lindel K, Wittekind C, Küppers V, Lellé R, Neis K, Griesser H, Pöschel B, Steiner M, Freitag U, Gilster T, Schmittel A, Friedrich M, Haase H, Gebhardt M, Kiesel L, Reinhardt M, Kreißl M, Kloke M, Horn LC, Wiedemann R, Marnitz S, Letsch A, Zraik I, Mangold B, Möckel J, Alt C, Wimberger P, Hillemanns P, Paradies K, Mustea A, Denschlag D, Henscher U, Tholen R, Wesselmann S, Fehm T. Geburtshilfe Frauenheilkd. 2022 Feb 11;82(2):139-180. doi: 10.1055/a-1671-2158. eCollection 2022 Feb. PMID: 35169387 Free PMC article. 6. Genome-wide association study and functional follow-up identify 14q12 as a candidate risk locus for cervical cancer. Ramachandran D, Dennis J, Fachal L, Schürmann P, Bousset K, Hülse F, Mao Q, Wang Y, Jentschke M, Böhmer G, Strauß HG, Hirchenhain C, Schmidmayr M, Müller F, Runnebaum I, Hein A, Stübs F, Koch M, Ruebner M, Beckmann MW, Fasching PA, Luyten A, Dürst M, Hillemanns P, Easton DF, Dörk T. Hum Mol Genet. 2022 Aug 17;31(15):2483-2497. doi: 10.1093/hmg/ddac031. PMID: 35157032 Free PMC article. 7. CoCoss-Trial: Concurrent Comparison of Self-Sampling Devices for HPV-Detection. Ertik FC, Kampers J, Hülse F, Stolte C, Böhmer G, Hillemanns P, Jentschke M. Int J Environ Res Public Health. 2021 Oct 2;18(19):10388. doi: 10.3390/ijerph181910388. PMID: 34639688 Free PMC article. 8. Association of preoperative cone biopsy with recurrences after radical hysterectomy. Klapdor R, Hertel H, Delebinski L, Hillemanns P. Arch Gynecol Obstet. 2022 Jan;305(1):215-222. doi: 10.1007/s00404-021-06145-0. Epub 2021 Jul 21. PMID: 34291339 Free PMC article. 9. Protective operative techniques in radical hysterectomy in early cervical carcinoma and their influence on disease-free and overall survival: a systematic review and meta-analysis of risk groups. Kampers J, Gerhardt E, Sibbertsen P, Flock T, Klapdor R, Hertel H, Jentschke M, Hillemanns P. Arch Gynecol Obstet. 2021 Sep;304(3):577-587. doi: 10.1007/s00404-021-06082-y. Epub 2021 May 22. PMID: 34021804 Free PMC article. Review. 10. Prophylactic HPV vaccination after conization: A systematic review and meta-analysis. Jentschke M, Kampers J, Becker J, Sibbertsen P, Hillemanns P. Vaccine. 2020 Sep 22;38(41):6402-6409. doi: 10.1016/j.vaccine.2020.07.055. Epub 2020 Aug 4. PMID: 32762871 Review. 11. Statement of the AGO and AG-CPC on the Aftercare/Follow-up for Surgical Procedures of the Lower Genital Tract after the Introduction of a New Cancer Screening Guideline. Hillemanns P, Tempfer C, Beckmann MW, Küppers V, Quaas J. Geburtshilfe Frauenheilkd. 2020 Aug;80(8):809-812. doi: 10.1055/a-1193-5136. Epub 2020 Aug 14. PMID: 32817987 Free PMC article. 12. Association of genomic variants at PAX8 and PBX2 with cervical cancer risk. Ramachandran D, Wang Y, Schürmann P, Hülse F, Mao Q, Jentschke M, Böhmer G, Strauß HG, Hirchenhain C, Schmidmayr M, Müller F, Runnebaum I, Hein A, Koch M, Ruebner M, Beckmann MW, Fasching PA, Luyten A, Dürst M, Hillemanns P, Dörk T. Int J Cancer. 2021 Apr 27. doi: 10.1002/ijc.33614. Online ahead of print. PMID: 33905146 Free article. 13. Performance of a six-methylation-marker assay on self-collected cervical samples - A feasibility study. Klischke L, von Ehr J, Kohls F, Kampers J, Hülse F, Schmitz M, Hennig A, Dörk T, Hillemanns P, Jentschke M. J Virol Methods. 2021 Sep;295:114219. doi: 10.1016/j.jviromet.2021.114219. Epub 2021 Jun 24. PMID: 34175345 14. Completion of radical hysterectomy does not improve survival of patients with cervical cancer and intraoperatively detected lymph node involvement: ABRAX international retrospective cohort study. Cibula D, Dostalek L, Hillemanns P, Scambia G, Jarkovsky J, Persson J, Raspagliesi F, Novak Z, Jaeger A, Capilna ME, Weinberger V, Klat J, Schmidt RL, Lopez A, Scibilia G, Pareja R, Kucukmetin A, Kreitner L, El-Balat A, Pereira GJR, Laufhütte S, Isla-Ortiz D, Toptas T, Gil-Ibanez B, Vergote I, Runnenbaum I. Eur J Cancer. 2021 Jan;143:88-100. doi: 10.1016/j.ejca.2020.10.037. Epub 2020 Dec 5. PMID: 33290995 15. Psychological distress in cervical cancer screening: results from a German online survey. Jentschke M, Lehmann R, Drews N, Hansel A, Schmitz M, Hillemanns P. Arch Gynecol Obstet. 2020 Sep;302(3):699-705. doi: 10.1007/s00404-020-05661-9. Epub 2020 Jun 27. PMID: 32594298 Free PMC article. AG Translationale Gynäkologische Immunonkologie Prof. Dr. med. Rüdiger Klapdor, Dr. med. Jens Hachenberg, Dr. med. Jan Lennart Stalp Forschungsschwerpunkte: • Chimäre Antigen Rezeptoren gegen gynäkologische Karzinome • NK-Zell-Therapie • Adoptive Immuntherapie gegen Ovarialkarzinom • Adoptive Immuntherapie gegen Zervixkarzinom • Adoptive Immuntherapie gegen Mammakarzinom Beschreibung: Das Immunsystem schützt uns nicht nur vor fremden Infektionen sondern auch vor eigenen bösartigen Zellen und verhindert so täglich die Entstehung von Krebs. In einigen Fällen reicht diese Wächterfunktion aber nicht aus und es kann sich zum Beispiel Eierstockkrebs entwickeln. Bisherige Therapieverfahren wie ausgedehnte Operationen und Chemotherapie sind leider nicht in allen Fällen erfolgreich und gehen mit teils starken Nebenwirkungen einher. Ideal wäre es, das eigene Immunsystem so neuauszurichten, dass es die Krebszellen erkennt und eigenständig eliminiert. Eine mögliche Strategie hierfür ist es Immunzellen, wie T- oder natürliche Killerzellen (NK), mit speziellen Rezeptoren auszustatten, die gezielt die Tumorzellen erkennen können. Die speziellen Rezeptoren, die wir benutzen, nennen sich chimäre Antigenrezeptoren (CAR). Wir haben bereits verschiedene Rezeptoren hergestellt, die unspezifische Immunzellen (NK-Zellen) gegen die Tumorzellen sensibilisieren. Auf dem Foto ist ein Experiment gezeigt, bei dem Eierstockkrebszellen (grün) mit von uns spezifizierten NK-Zellen (rot) kombiniert wurden. Bild A zeigt den Zustand am Anfang. Bild B nach einigen Stunden. Hier zeigt sich, dass praktisch alle grünen Krebszellen zerstört worden sind. In unseren Experimenten konnten wir zeigen, dass wir nicht nur verschiedene Eierstockkrebszellen zielgerichtet eliminieren können, sondern auch ganz spezifisch Krebsstammzellen angreifen können, die sich dadurch auszeichnen, dass sie weniger empfindlich gegen Chemotherapie sind. Gerade dieser Ansatz kann eine zukünftige Therapie für Eierstockkrebs sein, der sich nicht gut über Chemotherapie behandeln lässt. Diese Strategien werden aktuell in weiteren Versuchen getestet, um sie idealerweise in einigen Jahren auch als Therapie bei Patientinnen verwenden zu können. Kontakt: Prof. Dr. med. Rüdiger Klapdor klapdor.ruediger @ mh-hannover.de Dr. med. Jens Hachenberg hachenberg.jens @ mh-hannover.de Dr. med. Jan Lennart Stalp stalp.jan @ mh-hannover.de Kooperationen: • Frauenklinik im Forschungszentrum, MHH • Institut für Experimentelle Hämatologie, MHH • Institut für Pathologie, MHH • Fraunhofer-Institut für Toxikologie und Experimentelle Medizin Förderungen: • Dr. med. Lennart Stalp und Dr. rer. nat. Ivana Kutle sind Fellows des nationalen Translationalen Tandem Programms für Gen- und Zelltherapie (nTTP-GCT) koordiniert von der Biomedical Innovation Academy des Berlin Institute of Health (BIH) und gefördert vom Bundesministerium für Forschung, Technologie und Raumfahrt (BMFTR). Jahrgang 2025 - GCT ; nTTP-GCT_Stalp_Kutle_dt.pdf • Förderung durch die Bruno und Helene Jöster Stiftung Wissenschaftliche Publikationen: Anti-FAP CAR-NK cells as a novel targeted therapy against cervical cancer and cancer-associated fibroblasts. Polten R, Kutle I, Stalp JL, Hachenberg J, Seyda AK, Neubert L, Kamp JC, von Kaisenberg C, Schaudien D, Hillemanns P, Klapdor R, Morgan M, Schambach A. Oncoimmunology. 2025 Dec;14(1):2556714. doi: 10.1080/2162402X.2025.2556714. Epub 2025 Sep 17. PMID: 40960024; PMCID: PMC12716053. Anti-Mesothelin CAR-NK cells as a novel targeted therapy against cervical cancer. Kutle I, Polten R, Stalp JL, Hachenberg J, Todzey F, Hass R, Zimmermann K, von der Ohe J, von Kaisenberg C, Neubert L, Kamp JC, Schaudien D, Seyda AK, Hillemanns P, Klapdor R, Morgan MA, Schambach A. Front Immunol. 2024 Dec 16;15:1485461. doi: 10.3389/fimmu.2024.1485461. Erratum in: Front Immunol. 2025 Feb 21;16:1571555. doi: 10.3389/fimmu.2025.1571555. PMID: 39781381; PMCID: PMC11707549. Tumor Organoid and Spheroid Models for Cervical Cancer. Kutle I, Polten R, Hachenberg J, Klapdor R, Morgan M, Schambach A. Cancers (Basel). 2023 Apr 27;15(9):2518. doi: 10.3390/cancers15092518. PMID: 37173984; PMCID: PMC10177622. Towards Novel Gene and Cell Therapy Approaches for Cervical Cancer. Polten R, Kutle I, Hachenberg J, Klapdor R, Morgan M, Schambach A. Cancers (Basel). 2022 Dec 30;15(1):263. doi: 10.3390/cancers15010263. PMID: 36612258; PMCID: PMC9818159. NK Cell-Mediated Eradication of Ovarian Cancer Cells with a Novel Chimeric Antigen Receptor Directed against CD44. Klapdor R, Wang S, Morgan MA, Zimmermann K, Hachenberg J, Büning H, Dörk T, Hillemanns P, Schambach A. Biomedicines. 2021 Sep 28;9(10):1339. doi: 10.3390/biomedicines9101339. PMID: 34680456 Free PMC article. Characterization of a Novel Third-Generation Anti-CD24-CAR against Ovarian Cancer. Klapdor R, Wang S, Morgan M, Dörk T, Hacker U, Hillemanns P, Büning H, Schambach A. Int J Mol Sci. 2019 Feb 3;20(3):660. doi: 10.3390/ijms20030660. PMID: 30717444 Free PMC article. Improved Killing of Ovarian Cancer Stem Cells by Combining a Novel Chimeric Antigen Receptor-Based Immunotherapy and Chemotherapy. Klapdor R, Wang S, Hacker U, Büning H, Morgan M, Dörk T, Hillemanns P, Schambach A. Hum Gene Ther. 2017 Oct;28(10):886-896. doi: 10.1089/hum.2017.168. Epub 2017 Aug 24. PMID: 288364693. Research Obstetric Biobank Univ.-Prof. Dr. med. Constantin von Kaisenberg Die Research Obstetric Biobank der Geburtshilfe & Pränatalmedizin hat das Ziel, Schwangerschaftsprodukte für wissenschaftliche Fragestellungen in geeigneter Form zu asservieren und ist Teil der Biobank der MHH. Vordringliches Ziel ist es, individuelle Forschungskooperationen innerhalb und außerhalb der Frauenklinik einzugehen sowie wissenschaftlich interessierten Mitarbeitern der Frauenklinik den Zugang zu interdisziplinären Kooperationen zu ermöglichen. Verantwortlicher für die Research Obstetric Biobank: Univ.-Prof. Dr. med C.S. von Kaisenberg Leiter des Bereiches Geburtshilfe und Pränatalmedizin DEGUM III, Diploma in Fetal Medicine (FMF UK) Klinik für Gynäkologie, Geburtshilfe und Reproduktionsmedizin Medizinische Hochschule Hannover Carl-Neuberg-Str. 1 D-30625 Hannover fon: +49 (0) 511 532-0, +49 (0) 176 1532 3454 fax: +49 (0) 511 532 8004 e-mail: vonkaisenberg.constantin @ mh-hannover.de Wissenschaftliche Kooperationen Kooperationen innerhalb der Frauenklinik Arbeitsgruppe Prof. Hass, AG Biochemie und Tumorbiologie: • Expansion of umbilical cord derived mesenchymal stem cells with regards to GMP-conform production process. Prof. Hass, PD Dr. Kasper. • Charakterisierung von subpopulationen mesenchymaler Stammzellen der Nabelschnur unter normoxischen und hypoxischen Bedingungen. PhD student Niendorf. Arbeitsgruppe Frau Prof. Dr. von Versen-Höynck, AG Experimentelle Geburtshilfe: • Die Rolle von Adenosin in der plazentaren Entwicklung und im plazentaren Aminosäuretransport. Prof. Dr. von Versen-Höynck / Natallia Darashchonak • Die Rolle von Vitamin D bei plazentaren Entwicklungsvorgängen (Pilotstudie). Prof. Dr. von Versen-Höynck • MicroRNA’s bei Präeklampsie und HELLP (Pilotstudie). Prof. Dr. von Versen-Höynck • Maternale PKU’: In-vitro-Untersuchungen zum plazentaren Aminosäuretransport und –metabolismus (Kooperation Pädiatrie). Prof. Das, Klinik für Pädiatrie, Doktorandin Kristin Goedecke • Untersuchungen zur Rolle von Vitamin D bei endothelialen Reparaturprozessen (Kooperation Pädiatrie). Prof. Das, Klinik für Pädiatrie, StrucMed Programm • Chronische Hypoxie der Nabelschnur: Auswirkung auf die aerobe Energiebereitstellung, insbesondere Regulation der mitochondrialen ATPsynthase in HUVEC (Kooperation Pädiatrie). Prof. Das, Klinik für Pädiatrie, StrucMed Programm Kooperationen MHH-intern Arbeitsgruppe Prof. Schambach, Experimentelle Hämatologie, Hans-Borst-Zentrum für Herz- und Stammzellforschung: • Entwicklung eines Standardprotokolls zur ex vivo Expansion von hämatopoietischen Stammzellen (HSCs) aus Nabelschnurblut, fünf Unterprojekte in CB-HERMES (Cord Blood-Hematopoietic stem cells: Reliable Methods for ex-vivo ExpanSion). Dr. Schiedlmeier, Dr. Lachmann • Generation of human hematopoietic malignancies with CRISPR/cas9. Dr. Dr. Schwarzer • Klonalität mesenchymaler Stammzellkulturen aus Nabelschnur. Dr. Rothe Arbeitsgruppe Prof. Martin, Rebirth II: • Induction of pluripotent stem cells from young versus aged somatic cells: differences in reprogramming rates, karyotypic abnormalities and frequency of accumulated mutations. PhD student: Katarzyna Osetek • Development of a biohybrid lung: endothelialization of polymeric gas exchange membranes. Dr. Michael Pflaum, LEBAO Arbeitsgruppe Frau Prof. Hansen, Klinik für Pädiatrische Pneumologie, Allergologie und Neonatologie: • Neonatal B cells: functional and developmental characterization of human B cell subpopulations, Frau Dr. Meyer-Bahlburg • Charakterisierung immunologischer Toleranzzustände im neonatalen Immunsystem. Prof. Dorothee Viemann, Frau Dr. Sabine Pirr, Frau Dr. Judith Friesenhagen, Andrea Weitz Arbeitsgruppe Dr. Kirsch: • Analysis of Intercellular Contacts in Primary Endothelial Cells. Svjetlana Lovric, Michaela Beese, Kristin Wyss, Johanna Kegel Arbeitsgruppe Prof. Reinhardt: • Akute myeloische Leukämie und Trisomie 21. Herr Dr. Klusmann Arbeitsgruppe Frau Prof. Melk: • Endotheliale zelluläre Seneszenz- ein neues Target für vaskuläre Protektion? Untersuchung der INK4a/ARF Expression bei SNP-Varianten des Genlokus CDNK2A/B, die mit cardiovaskulärem Risiko einhergehen. Frau Dr. Hömme Arbeitsgruppe Frau Prof. Petri, Neurologie: • Therapeutisches Potenzial humaner Nabelschnurblutzellen bei der Amyotrophen Lateralsklerose (ALS). Susanne Petri • Untersuchungen zur Regeneration von Immunzellen nach hämatopoietischer Stammzelltransplantation Erwachsener. Prof. Krueger, Regenerative Immunologie, Jonas Blume Kooperationen international Arbeitsgruppe Geburtshilfe und Pränatalmedizin, Prof. C. S. v. Kaisenberg: • Prognosis Trial (Roche) zur Prädiktion der Präeklampsie. Prof. Dr. C.S. v. Kaisenberg, Dr. Jentschke

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Forschungszentrum

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Frauenklinik im Forschungszentrum Dr. rer. nat. Thilo Dörk-Bousset Tel.: 0511/532-6075 (Büro) Tel.: 0511/532-6077 (Labor) Fax: 0511/532-6081 E-Mail: doerk.thilo@mh-hannover.de MHH - OE 6411 - Gebäude I11, Ebene S0. Die Frauenklinik unterhält im TPFZ einen Laborbereich, in dem gynäkologisch-onkologische und geburtshilfliche Forschungsthemen experimentell bearbeitet werden. Für weitere Informationen siehe < hier >.

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AG Reproduktionsmedizin und Molekulare Perinatologie

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AG Reproduktionsmedizin und Molekulare Perinatologie Prof. Dr. med. Frauke von Versen, M.Sc. Prof. Dr. med. Frauke von Versen, M.Sc. Tel.: 0511 532-6080 (Büro) Tel.: 0511 532-6084 (Labor) Fax: 0511 532-6081 E-Mail: vonversen-hoeynck.frauke @ mh-hannover.de Lageplan: So finden Sie zu uns Forschungsschwerpunkte: Die ursprünglichen Projekte der Arbeitsgruppe Reproduktionsmedizin und Molekulare Perinatologie befassten sich zunächst mit geburtshilflichen und perinatalen Themen. Seit einigen Jahren legen wir unseren Fokus nun v.a. auf reproduktionsmedizinische Aspekte und bearbeiten interdisziplinär grundlagenwissenschaftliche, translationale und klinische Fragestellungen. Ein Schwerpunkt unserer Grundlagenforschung liegt aktuell in der Untersuchung von Gründen und Mechanismen, die zu Unterschieden im mütterlichen und kindlichen Outcome nach Anwendung von Verfahren der assistierten Reproduktion, führen. Hier interessiert uns u.a. das erhöhte Risiko für hypertensive Schwangerschaftserkrankungen und Makrosomie bei Schwangerschaften, die nach der Übertragung eines zuvor eingefrorenen und wieder aufgetauten Embryos entstanden sind (Kryo-Embryotransfer). Außerdem untersuchen wir Faktoren, welche zur reproduktiven Alterung aber auch vorzeitigen Gefäßalterung und damit möglicherweise zu einem erhöhten kardiovaskulären Risiko im späteren Leben beitragen. Ein neuer Forschungsschwerpunkt widmet sich den Pathomechanismen der Endometriose, die eine beeinträchtigte Fertilität verursachen können. Projekte, die derzeit bearbeitet werden: Gynäkologische Endokrinologie und Reproduktionsmedizin: ► Aufbau einer harmonisierten Daten- und Biobank zur Erforschung der Zusammenhänge zwischen Endometriose und Infertilität sowie Schwangerschaftskomplikationen (EndoFERT) ► Erforschung der Pathomechanismen der Endometriose im Zusammenhang mit Infertilität unter Nutzung eines 3D organ-on-a-chip Modells (EndoFERT) ► Altersbedingte Dezidualisierungsdefekte endometrialer Stromazellen bei Frauen mit fortgeschrittenem maternalen Alter (Endo-Age) ► Einfluss verschiedener Protokolle für Auftauzyklen auf klinische, maternale und kindliche Outcomes ► Einfluss von Corpus luteum Produkten auf die Dezidualisierung, die Plazentaentwicklung und die mütterliche Gesundheit ► Einfluss von Kinderwunschbehandlung auf die mütterliche Gesundheit und Komplikationen in der Schwangerschaft ► Einfluss der Pandemie und Akzeptanz der Impfung gegen SARS-Cov2 bei Frauen mit Kinderwunsch ► Kinderwunsch und Familienplanung bei Organtransplantierten Molekulare Perinatologie: ► Endotheliale Genregulationsmechanismen bei Gefäßerkrankungen und präeklamptischen Schwangerschaften ► Epigenetische Unterschiede mütterlicher und fetaler endothelialer Vorläuferzellen in gesunden und komplizierten Schwangerschaften ► Einfluss immunsuppressiver Therapien bei weiblichen Nierentransplantierten auf die Gesundheit und Funktion endothelialer Vorläuferzellen ► Die Bedeutung von Vitamin D und Proteinen der DNA-Schadensantwort für die Regulation von oxidativem Stress in der Präeklampsie ► Die Rolle von Vitamin D in der Pathophysiologie der Präeklampsie Kooperationen Prof. Dr. med. Anibh Das, Pädiatrische Nieren- und Stoffwechselerkrankungen, MHH Carl A. Hubel, PhD, Magee-Womens Research Institute, University of Pittsburgh, USA PD Dr. med. Ralf Dechend, Charite Berlin und Max Delbrück Center for Molecular Medicine, Berlin Prof Dr. med Tanja Groten, Frauenklinik, Friedrich-Schiller-University Jena, Germany Valerie L. Baker, MD, Division of Reproductive Medicine, Stanford University, USA Virginia D. Winn, MD, PhD, Perinatal Biology Laboratory, Stanford University, USA Prof. Dr. med. Alexandra Bielfeld, UNIKID, Department of Obstetrics and Gynecology, University Hospital Düsseldorf Prof. Dr. Udo Markert, Placenta Lab, Department of Obstetrics, University Hospital Jena, Germany Prof. Dr. Martin Götte, Department of Obstetrics and Gynecology, University Hospital Münster Fördermittel ► Deutsche Forschungsgemeinschaft ► Boehringer Ingelheim Stiftung- Exploration Grant Program ► IFB-Tx. (Integrated Research and Treatment Center Transplantation) Start-up Förderung durch BMBF ► Deutsche Diabetes Gesellschaft ► Preeclampsia Foundation ► Europäische Union ► Bundesministerium für Bildung und Forschung (BMBF) ► außerdem: HiLF Programm der MHH, Gesellschaft der Freunde der MHH Doktoranden/-innen der AG und Gastwissenschaftlerinnen cand. Bsc. Fiona Sieber (Betreuung seit 03/2026) cand. med. Eva Scheer (Betreuung seit 04/2025) cand. rer. nat. Cara Juli (Betreuung seit 09/2024) cand. med. Amelie Gonder (Betreuung seit 03/2024) cand. med. Jasmin Neuhold (Betreuung seit 03/2024) cand. rer. nat. Julia Beckmann (Betreuung seit 02/2024) Alumni Abschlussarbeiten in der Finalisierung: cand. med. Johanna Neubohn (Betreuung seit 11/2024) cand. med. Marlene Böhm (Betreuung seit 10/2023) cand. med. Nele Breuste (Betreuung seit 06/2023) cand. med. Sara Meier (Betreuung seit 08/2022) cand. med. Nina Schirm (Betreuung seit 03/2020) cand. med. Lea Böhm (Betreuung seit 03/2020) cand. med. Cara Schmidt (Betreuung seit 10/2019) cand. med. Svenja Arifi-Ziemek (Zweitbetreuung seit 08/2017) cand. med. Nadia Meyer (Betreuung seit 08/2017) cand. med. Berina Kipke (Betreuung seit 2015) Alumni 2025 Jessica Kern: Fear of fertility side effects is a major cause for COVID-19 vaccine hesitance in infertile patients- eine multizentrische Befragung von Patientinnen in Kinderwunschbehandlung. (Dr. med., Hannover, 2025) Klara Leuckefeld: Altersbedingte Dezidualisierungsdefekte in humanen endometrialen Stromazellen (B.Sc. Biochemie) Eva Scheer: Inwiefern beeinflusst das Wetter die Ergebnisse von In-vitro-Fertilisation und Intrazytoplasmatischer Spermieninjektion (Wissenschaftsmodul) Shona Wedner-Ross: The impact of the COVID-19 pandemic on women seeking fertility treatment in Germany: the patient´s perspective (Dr. med., Hannover, 2025) 2024 Johanna Neubohn: Clinical outcomes of stimulated cycle versus hormone replacement therapy cycle frozen embryo transfer in women with polycystic ovary syndrome (Wissenschaftsmodul) Jasmin Neuhold: Exploration of gender equality in Gynecology and Obstetrics (Wissenschaftsmodul) Amelie Gonder: Knowledge about fertility and perspectives on family planning among female physicians at Hannover Medical School (Wissenschaftsmodul) Clara Springer: Investigations on in vitro decidualization and relaxin effects in human endometrial stromal cells to elucidate mechanisms in the pathophysiology of preeclampsia (Dr. med., Hannover, 2024) Tim Büder: Vitamin D3, Proteine der DNA-Schadensantwort und die Regulation von oxidativem Stress in der Präeklampsie (Dr. med., Hannover, 2024) 2023 Julia Beckmann: Untersuchungen zur funktionellen Bedeutung der alternativen Spleißvariante CADM1 endothelialer Vorläuferzellen aus Nabelschnurblut (MSc Biomedizin, Hannover, November 2023) Luka Kroning: Einfluss der Gelbkörperanzahl in Kryoembryotransferzyklen zum Konzeptionszeitpunkt auf die neonatale Gesundheit (Dr. med., Hannover, 2023) Freya Waschkies: Pregnancy Outcomes After Frozen-Thawed Embryo Transfer in the Absence of a Corpus Luteum (Dr. med., Hannover, 2023) Ina Sejko, Bsc: Human endometrial stromal cell decidualization (Universität Göttingen, Gastwissenschaftlerin 12/2022 bis 01/2023) 2022 cand. PhD Maja Gajic, MSc: Hydroxychloroquin - a potential candidate for the treatment of preeclampsia (Universität Graz, Gastwissenschaftlerin 10/2021 bis 07/2022) 2021 Franka Kausch: Untersuchung des Einflusses von Vitamin D3 auf die plazentare Angiogenese in vitro (Dr. med., Hannover, 2021) 2020 Simone Warnecke: Hypoxie am Modell kultivierter HUVECs - Die Rolle von Sirtuinen als Regulatoren des aeroben Energiestoffwechsels (Dr. med., Hannover, 2020, Zweitbetreuung) 2019 Catharina Meissner: Awareness, knowledge and perceptions of infertility, fertility assessment and assisted reproductive technologies in the era of oocyte freezing among female and male university students (Dr. med., Hannover, 2019) Mareike Sandvoß: HELLP Syndrom - Veränderte Konzentrationen des Fettsäureoxidation- Regulators Sirtuin 4 bei Hypoxie (Dr. med., Hannover, 2019, Zweitbetreuung) 2018 Sophie Schmitz: Gestational diabetes mellitus: an evaluation of gynecologists’ knowledge of guidelines and counseling behavior (Dr. med., Hannover, 2018) Akin Sarisin: Der Einfluß Adenosins und des A2B-Adenosinrezeptors auf trophoblastäre und endotheliale Funktionen während der Plazentaentwicklung (Dr. med., Hannover, 2018) 2017 Lea Völkening: Funktionelle Charakterisierung von RAD50 in der Mitose (Dr. rer. nat., Hannover, 2017, Zweitbetreuung) Nina Dressler: BMI and season are associated with vitamin D deficiency in women with impaired fertility – a two centre analysis (Dr. med., Hannover, 2017) 2016 Sonja Helbig: Functional Consequences of CHEK2 and TERT Breast Cancer Risk Variants (Dr. rer. nat., Hannover, 2016, Zweitbetreuung) 2015 Lars Brodowski: Untersuchungen zum Effekt von Vitamin D auf endotheliale Vorläuferzellen unter präeklamptischen Bedingungen (Dr. med., Hannover, 2015) Juan Gui: Impact of gestational diabetes mellitus on endothelial colony-forming cell characteristics (PhD, China, 2015) 2014 Sarah Hass: Der Einfluss von Vitamin D₃ auf endotheliale Reparaturprozesse im Zusammenhang mit der Präeklampsie (Dr. med., Hannover, 2014) Vera Kreuzer: Der Einfluss des durch Hypoxie induzierbaren Moleküls Adenosin und seiner Rezeptoren A2A und A2B auf plazentare Prozesse (Dr. med., Hannover, 2014) May-Britt Heidrich: Präeklampsie und kardiovaskuläre Langzeitrisiken - Was wissen niedergelassene Gynäkologen? (Dr. med., Hannover, 2014) Mary Doreen Meusel: Die Rolle des Adenosinrezeptors A2A in plazentaren Entwicklungsprozessen (Dr. med., Hannover, 2014) 2013 Mariam Haidar: Vitamin D improves the angiogenic properties of endothelial progenitor cells (Dr. med., Hannover, 2013) Natallia Darashchonak: Die Rolle des Adenosinrezeptors A2B in plazentaren Entwicklungsprozessen (Dr. rer. nat., Hannover, 2013)

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EKFS-Promotionskolleg "DigiStrucMed": Digitale Transformation in der Medizin

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Navigation [Startseite ►] [Über das Programm ►] [Bewerbungsprozess für Studierende ►] [ Bewerbungsprozess für Projektleitungen ►] [Projekte ►] [ Aktuelles ►] [ Downloads ►] Über das Programm DigiStrucMed: Digitale Transformation in der Medizin Das Else Kröner-Graduiertenkolleg „Digitale Transformation in der Medizin“ (DigiStrucMed) ist ein strukturiertes Ausbildungsprogramm für Medizinpromovierende und Masterstudierende der Informatik, das in Kooperation zwischen der Medizinischen Hochschule Hannover und dem Peter L. Reichertz Institut (PLRI) der TU Braunschweig, dem Forschungsinstitut L3S der Leibniz Universität Hannover sowie der Hochschule Hannover durchgeführt wird. Das Programm ermöglicht es Studierenden der Medizin (Promovierende) und der Informatik (Masterstudierende im Rahmen ihrer Abschlussarbeit), gemeinsam Forschungsarbeiten im Themengebiet „Digitale Transformation in der Medizin“ durchzuführen. Das Vorliegen oder der Erwerb von informatischen Kenntnissen im Rahmen des Programms ist hierbei für Studierende der Medizin nicht zwingend notwendig. ► Für Studierende Warum DigiStrucMed? Promotionsarbeiten in der Medizin, Masterarbeiten im Bereich Informatik Rahmen : Ein strukturiertes Ausbildungsprogramm mit einem formalen Rahmen für Projektbetreuung, wissenschaftliche Weiterbildung und interdisziplinäre Kommunikation. Betreuung : Kontinuierliche und enge wissenschaftliche Betreuung mit 2 Betreuern aus der eigenen und einem Co-Betreuer aus der jeweils anderen Disziplin. Kompetenzerwerb : Medizinpromovierende (optional für Informatiker): 50 Stunden Lehrveranstaltungen in Form von Vorlesungen und Seminaren zu relevanten Themen (z.B. gute wissenschaftliche Praxis, Datenschutz und Datensicherheit, Datenstrukturen, Deep Learning, statistischer Auswertung, Konzeption einer klinischen Studie, wissenschaftliches Schreiben und Präsentationstechniken). Präsentationen und Austausch : Vernetzung der Studierenden und intensiver interdisziplinärer wissenschaftlicher Austausch und Feedback durch Einführungsveranstaltung und mehrere eigene Projektpräsentationen. Finanzielle Förderung : Monatliches Stipendium von 1000 € für Medizinpromovierende bzw. finanzielle Unterstützung für Masterand:innen (Beschäftigung als studentische Hilfskraft, ca. 450 € monatlich) Kongresse & Kooperationen : Möglichkeit zur Teilnahme an Kongressen und Besuch von Kooperationspartnern Zeitlicher Ablauf Medizinpromovierende Die Medizinstudierenden, die am DigiStrucMed Programm teilnehmen, unterbrechen ihr Medizinstudium für insgesamt ein Jahr: 10 Monate widmen sie sich der praktischen Arbeit im Projekt und 2 Monate dienen dazu, die Daten zu analysieren und schriftlich zusammenzufassen. Die Promovierenden bleiben an der MHH als Studierende eingeschrieben und erhalten während der Forschungszeit ein Entgelt in Form des Stipendiums für insgesamt 12 Monate. Sie nehmen während der Förderperiode (verpflichtend) zwei Freisemester. Die Dissertation wird anschließend studienbegleitend in den darauffolgenden 12 Monaten abgeschlossen. Der Projektbeginn erfolgt zum 01. August eines Jahres. Informatikstudierende Die Masterstudierenden, die am DigiStrucMed-Programm teilnehmen, können regulär dem Curriculum ihrer Hochschule folgen. Der Projektbeginn erfolgt zwischen dem 01. August und dem 1. Februar des darauffolgenden Jahres. Hier geht es weiter zum Bewerbungsverfahren für Studierende ► ► Für Projektverantwortliche Finanzielle Unterstützung Finanzielle Unterstützung im Rahmen von Stipendien für bis zu 10 Promovierende der Medizin durch die Else-Kröner Fresenius Stiftung Finanzielle Unterstützung im Rahmen von Einstellungen von bis zu 10 Masterstudierenden der Informatik als studentische Hilfskraft Sachmittelunterstützung in Höhe von bis zu 9.500 Euro pro Projekt (Verbrauchsmaterialien) Kongress- und Reisekostenunterstützung für die Medizinpromovierende Interdisziplinäre Projektentwicklung Vermittlung von Projektpartner:innen aus den Bereichen Medizin und Informatik im Rahmen einer Speed-Dating-Konferenz Bildung von Projektteams mit jeweils einem Promovierenden aus der Medizin sowie einem Masterstudierenden aus dem Bereich der Informatik. Projektübergreifender interdisziplinärer Austausch und Vernetzung der Teilnehmer:innen im Rahmen von mehreren Veranstaltungen zur Projektpräsentation pro Jahrgang. Zeitlicher Ablauf Projektleiter und Projektverantwortliche, die am DigiStrucMed-Programm teilnehmen, betreuen für 12 Monate Medizinpromovierende der Medizin bzw. für 6 Monate Masterstudierende der Informatik im Rahmen ihrer Abschlussarbeit. Der Projektbeginn erfolgt für Medizinstudierende zum 01. August eines Jahres. Ein späterer Beginn für Studierende der Informatik ist möglich. Hier geht es weiter zum Bewerbungsverfahren für Projektleiter:innen ► Navigation [Startseite ►] [Über das Programm ►] [Bewerbungsverfahren für Studierende ►] [ Bewerbungsverfahren für Projektleiter:innen ►] [Projekte ►] [ Aktuelles ►] [ Downloads ►]

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EKFS-Graduiertenkolleg "DigiStrucMed": Digitale Transformation in der Medizin

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EKFS-Graduiertenkolleg DigiStrucMed Digitale Transformation in der Medizin: Interdisziplinäre Promotionsarbeiten in Medizin (Dr. med.) und Masterarbeiten in Informatik (M.Sc.) Navigation [Startseite ►] [Über das Programm ►] [Bewerbungsverfahren für Studierende ►] [ Bewerbungsverfahren für Projektleiter:innen ►] [Projekte ►] [ Aktuelles ►] [ Downloads ►] Herzlich willkommen beim Else Kröner-Graduiertenkolleg „Digitale Transformation in der Medizin" Das Else Kröner-Graduiertenkolleg „Digitale Transformation in der Medizin“ ist ein strukturiertes Ausbildungsprogramm für Promovierende und Masterstudierende, das in Kooperation zwischen der Medizinischen Hochschule Hannover und dem Peter L. Reichertz Institut (PLRI) der TU Braunschweig, dem Forschungsinstitut L3S der Leibniz Universität Hannover sowie der Hochschule Hannover durchgeführt wird. Das Programm ermöglicht es Studierenden der Medizin (Promovierende) und der Informatik (Masterstudierende im Rahmen ihrer Abschlussarbeit), gemeinsam Forschungsarbeiten im Themengebiet „Digitale Transformation in der Medizin“ durchzuführen. Das Vorliegen oder der Erwerb von informatischen Kenntnissen im Rahmen des Programms ist hierbei für Studierende der Medizin nicht zwingend notwendig. Mehr über das Programm erfahren ►

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Promotionsprogramm ChEG

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Promotionsprogramm 2020 - 2024 Chronische Erkrankungen und Gesundheitskompetenz (ChEG) Im Rahmen des von der Robert Bosch Stiftung geförderten Promotionsprogramms „Chronische Erkrankungen und Gesundheitskompetenz (ChEG)“ sind zum 01.04.2020 an der Medizinischen Hochschule Hannover am Institut für Epidemiologie, Sozialmedizin und Gesundheitssystemforschung 12 Promotionsstipendien an exzellente Nachwuchswissenschaftlerinnen und -wissenschaftler aus folgenden Disziplinen vergeben worden: Public Health, Sozialwissenschaften, Pflegewissenschaften, Medizin, Psychologie, Gesundheitskommunikation, Gesundheitspädagogik, Sprach- oder Übersetzungswissenschaft etc. Ziel des Programms ist die wissenschaftliche Entwicklung von theoretischen Konzepten und empirischen Grundlagen im Bereich der Gesundheitskompetenz, bezogen auf Individuen, Versorgungseinrichtungen und das Gesundheitssystem. ChEG bietet eine ausgezeichnete wissenschaftliche Ausbildung im Rahmen eines innovativen Studienprogramms, eine individuelle Betreuung sowie inner- und transdisziplinäre Diskussionsforen. Das Promotionsprogramm wird von der Medizinischen Hochschule Hannover in Kooperation mit der Universität Bielefeld, der Pädagogischen Hochschule Freiburg, der Universität Hildesheim und der Hochschule für Musik, Theater und Medien Hannover, durchgeführt. Ansprechpartnerinnen: Prof. Dr. Marie-Luise Dierks / Dr. Gabriele Seidel Institut für Epidemiologie, Sozialmedizin und Gesundheitssystemforschung Forschungsschwerpunkt Patientenorientierung und Gesundheitsbildung OE 5410 Medizinische Hochschule Hannover 30623 Hannover Tel. 0511 532 8425 Dierks.Marie-Luise @ mh-hannover.de

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Neuroonkologisches Zentrum

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Neuroonkologisches Zentrum Das Neuroonkologische Zentrum der MHH beschäftigt sich mit der diagnostischen Klärung und der chirurgischen, der medikamentösen und, in Zusammenarbeit mit der Strahlentherapie, der strahlentherapeutischen Behandlung von Erkrankungen des Gehirns, der Wirbelsäule und der Schädelbasis auf höchstem Niveau. Das Motto der Patientenfürsorge ist das integrierte patientenzentrierte Vorgehen. Das Zentrum erfüllt die von der Deutschen Krebsgesellschaft festgelegten Qualitätskriterien und führt die Auszeichnung "Neuroonkologisches Zentrum mit Empfehlung der Deutschen Krebsgesellschaft e.V." . Spezialisten der N eurochirurgie, der Neurologie/ medikamentöse Tumortherapie, der Strahlentherapie, Neuroradiologie, Pathologie/ Histologie und bei Bedarf der Kinderonkologie arbeiten dafür fachübergreifend zusammen und können bei der individuellen Therapieplanung auf modernste diagnostische und therapeutische Verfahren zurückgreifen. Wir setzen neueste Behandlungsmethoden nach dem Stand der Wissenschaft ein. Das erwartet Sie bei uns: Diagnostik Moderne diagnostische Bildgebung und minimal invasive bildgestützte interventionelle Therapie Behandlung Das individuelle Behandlungskonzept wird im interdisziplinären Tumorboard festgelegt und koordiniert. Dabei wird das Ziel verfolgt, das bestmögliche Therapieergebnis für die Patientinnen und Patienten zu erreichen. Dazu gehört häufig eine medikamentöse Behandlung , die für die Gliome in der transsektoral eingebundenen Sprechstunde in der Neurologie des DIAKOVERE Henriettenstift angeboten wird. Mikrochirurgische Hirntumorentfernung durch minimal-invasive Operationsverfahren sowie Neuroendoskopie, Stereotaxie, fluorezenzgesteuerte Tumorsektion und neuronavigierte Biopsie zur Sicherung des Tumorgewebes Moderne technische Hilfsmittel zur Erhöhung der Operationssicherheit wie Monitoring Computergestützte Operation mit intraoperativen Überwachungsverfahren Funktionelle Operation im Wachzustand um Sprache, Bewegung und andere Gehirnfunktionen während des Eingriffs überwachsen zu können Interdisziplinäre Besprechung der einzelnen Patienten zur Planung eines individuellen Therapiekonzeptes Medikamentöse Tumortherapie Therapie mit alternierenden elektrischen Feldern, sog. TTF Erste Klinik in Niedersachsen mit der Institutszertifizierung „Spezielle Neurochirurgische Onkologie“. Rehabilitation und Nachsorge In der Phase der Nachsorge kooperieren wir mit unseren Rehabilitations- und Sportmedizinern wie auch mit einer Vielzahl von Rehabilitationskliniken. Teams der Psychoonkologie, Logopädie, Physiotherapie und spezialisierte Pflegekräfte schulen unsere Patientinnen und Patienten sowie deren Angehörige bereits während des Aufenthaltes, um eine bestmögliche Vorbereitung auf den Alltag zu Hause zu erreichen. Auf Wunsch stellen wir den Kontakt zu Vertretern der Selbsthilfegruppen her, um unseren Patienten Erfahrungsberichte „aus erster Hand“ zu ermöglichen. Weitergehendes Leistungsspektrum in der medikamentösen und strahlentherapeutischen Behandlung SPECT, PET, MR-Spektroskopie, minimal-invasive bildgestützte interventionelle Therapie Medikamentöse Tumortherapie Gesamtes Spektrum der modernen Hochpräzisionsbestrahlung (inkl. sämtlicher Methoden der Elektronen- sowie Photonenbestrahlung, Kopf- und Körperstereotaxie sowie der Brachytherapie) Onkologische Pflegeberatung Neue Therapeutika in klinischen Studien Therapie mit alternierenden elektrischen Feldern Publikationen Klinik für Neurochirurgie Sortiert nach Jahr (aktuellstes zuerst) und dann alphabetisch nach Erstautor FOERSTER A, BRAND F, BANAN R, HUENEBURG R, WEBER CAM, EWERT W, KRONENBERG J, PREVITI C, ELYAN N, BEYER U, MARTENS H, HONG B, BRAESEN JH, ERBERSDOBLER A, KRAUSS JK, STANGEL M, SAMII A, WOLF S, PRELLER M, ARETZ S, WIESE B, HARTMANN C, WEBER RG: Rare germline variants in the E-cadherin gene CDH1 are associated with the risk of brain tumors of neuroepithelial and epithelial origin. Acta Neuropathologica 2021 Apr 30. doi: 10.1007/s00401-021-02307-1. Online ahead of print HONG B, LALK M, WIESE B, MERTEN R, HEISSLER HE, RAAB P, HARTMANN C, KRAUSS JK: Primary and secondary gliosarcoma: differences in treatment outcome. British Journal of Neurosurgery in press, 2021. AL-KRINAWE Y, ESMAEILZADEH M, HARTMANN C, KRAUSS JK, HERMANN EJ: Pediatric rosette-forming glioneuronal tumor of the septum pellucidum. Childs Nervous System 36:2867-2870, 2020. BANAN R, ABBETMEIER-BASSE M, HONG B, DUMITRU CA, SAHM F, NAKAMURA M, KRAUSS JK, HARTMANN C: The prognostic significance of clinicopathological features in meningiomas: microscopic brain invasion can predict patient outcome in otherwise benign meningiomas. Neuropathology and Applied Neurobiology in press, 2021. Jan 28. doi: 10.1111/nan.12700. Online ahead of print BANAN R, STICHEL D, BLECK A, HONG B, LEHMANN U, SUWALA A, REINHARDT A, SCHRIMPF D, BUSLEI R, STADELMANN C, EHLERT K, PRINZ M, ACKER T, SCHITTENHELM J, KAUL D, SCHWEIZER L, CAPPER D, HARTER PN, ETMINAN N, JONES DTW, PFISTER SM, HEROLD-MENDE C, WICK W, SAHM F, VON DEIMLING A, HARTMANN C, REUSS DE. Infratentorial IDH-mutant astrocytoma is a distinct subtype. Acta Neuropathol. 2020 Oct;140(4):569-581. ESMAEILZADEH M, HONG B, POLEMIKOS M, AL-AFIF S, HERMANN EJ, SCHEINICHEN D, VON KAISENBERG C, HILLEMANNS P, KRAUSS JK: Spinal emergency surgery during pregnancy: contemporary strategies and outcome. World Neurosurgery 139:e421-e427, 2020. ESMAEILZADEH M, UKSUL N, HONG B, VON KAISENBERG C, SCHEINICHEN D, LANG JM, HERMANN EJ, HILLEMANNS P, KRAUSS JK: Intracranial emergencies during pregnancy requiring urgent neurosurgical treatment. Clinical Neurology and Neurosurgery 195:105905. doi: 10.1016/j.clineuro.2020.105905, 2020. AKÇAKAYA MO, SARYYEVA A, HEISSLER HE, KRAUSS JK: Glial tumors and deep brain stimulation: an increasingly recognized association? Journal of Clinical Neuroscience 64:1-3, 2019. BERKELMANN L, BADER A, MESHKSAR S, HATIPOGLU MAJERNIK G, KRAUSS JK, SCHWABE K, MANTEUFFEL D, NGEZAHAYO A: Tumour-treating fields (TTFields): investigations on the mechanism of action by electromagnetical exposure of cells in telophase/ cytokinesis. Scientific Reports 14;9(1):7362. doi: 10.1038/s41598-019-43621-9, 2019. HONG B, HERMANN EJ, FEUERHAKE F, KRAUSS JK: Secondary extradural spinal manifestation of esthesioneuroblastoma. British Journal of Neurosurgery 33:594-596, 2019. AL MAHDI MM, KRAUSS JK, NAKAMURA M, BRANDIS A, HONG B: Early ectopic recurrence of craniopharyngioma in the cerebellopontine angle. Turkish Neurosurgery 28:313-316, 2018. AL-AFIF S, HATIPOGLU MAJERNIK G, HERMANN EJ, ESMAEILZADEH M, HARTMANN C, KRAUSS JK: Intracranial foreign material granulomas after cranial surgery. Acta Neurochirurgica 160:2069-2075, 2018. AL-AFIF, HATIPOGLU MAJERNIK G, AL-KRINAWE Y, ESMAEILZADEH M, HARTMANN C, KRAUSS JK: The role of neurosurgery in the treatment of intracranial tumor-like inflammatory lesions. World Neurosurgery Dec 13:S1878-8750(18)32803-1. doi: 10.1016/j.wneu.2018.12.003, 2018. HONG B, BANAN R, CHRISTIANS A, NAKAMURA M, LALK M, LEHMANN U, HARTMANN C, KRAUSS JK: Cerebellar glioblastoma: a clinical series with contemporary molecular analysis. Acta Neurochirurgica 160:2237-2248, 2018. HONG B, POLEMIKOS M, HEISSLER HE, HARTMANN C, NAKAMURA M, KRAUSS JK: Challenges in cerebrospinal fluid shunting in patients with glioblastoma. Fluids and Barriers of the CSN 15(1):16. doi: 10.1186/s12987-018-0101-x, 2018. WILD F, HARTMANN C, HEISSLER HE, HONG B, KRAUSS JK, NAKAMURA M: Surgical treatment of spinal ependymomas: experience in 49 patients. World Neurosurgery 111:703-709, 2018. WU Z, NAKAMURA M, KRAUSS JK, SCHWABE K, JOHN N: Intracranial rat glioma model for tumor resection and local treatment. Journal of Neuroscience Methods 299:1-7, 2018. BEYER U, BRAND F, MARTENS H, WEDER J, CHRISTIANS A, ELYAN N, HENTSCHEL B, WESTPHAL M, SCHACKERT G, PIETSCH T, HONG B, KRAUSS JK, SAMII A, RAAB P, DAS A, DUMITRU CA, SANDALCIOGLU IE, HAKENBERG OW, ERBERSDOBLER A, LEHMANN U, REIFENBERGER G, WELLER M, REIJNS MAM, PRELLER M, WIESE B, HARTMANN C, WEBER RG: Rare ADAR and RNASEH2B variants and a type I interferon signature in glioma and prostate carcinoma risk and tumorigenesis. Acta Neuropathologica 134:905-922, 2017. BEYER U, BRAND F, MARTENS H, WEDER J, CHRISTIANS A, ELYAN N, HENTSCHEL B, WESTPHAL M, SCHACKERT G, PIETSCH T, HONG B, KRAUSS JK, SAMII A, RAAB P, DAS A, DUMITRU CA, SANDALCIOGLU IE, HAKENBERG OW, ERBERSDOBLER A, LEHMANN U, REIFENBERGER G, WELLER M, REIJNS MAM, PRELLER M, WIESE B, HARTMANN C, WEBER RG, RARE ADAR and RNASEH2B variants and a type I interferon signature in glioma and prostate carcinoma risk and tumorigenesis. Acta Neuropathol. 2017 Dec;134(6):905-922. GUENTHER F, FRANK P, NAKAMURA M, HERMANN EJ, PALMAERS T. Venous air embolism in the sitting position in cranial neurosurgery: incidence and severity according to the used monitoring. Acta Neurochir (Wien). 2017 Feb;159(2):339-346. VOGT PM, METT TR, BROELSCH GF, RADTKE C, GELLRICH NC, KRAUSS JK, SAMII M, IPAKTCHI R: Interdisciplinary reconstruction of oncological resections at the skull base, scalp and facial region. Surgical Oncology 26:318-323, 2017. AL-AFIF S, NAKAMURA M, LENARZ T, KRAUSS JK: Transclival injury after routine transnasal rhinological surgery. Clinical Neurology and Neurosurgery 145:1-5, 2016. HERMANN E. Kalottentumoren bei Kindern (Kapitel 44), Sektion V: Neuroonkologie. Paediatrische Neurochirurgie. Baechli, Luetschg, Messing-Juenger (Hrsg.), Springer, 471-475 (2016) in press PETRAKAKIS I, PIRAYESH A, KRAUSS JK, RAAB P, HARTMANN C, NAKAMURA M: The sellar and suprasellar region: A "hideaway" of rare lesions. Clinical aspects, imaging findings, surgical outcome and comparative analysis. Clinical Neurology and Neurosurgery 149:154-165, 2016. PIRAYESH A, PETRAKAKIS I, RAAB P, POLEMIKOS M, KRAUSS JK, NAKAMURA M: Petroclival meningiomas: magnetic resonance imaging factors predict tumor resectability and clinical outcome. Clinical Neurology and Neurosurgery 147:90-97, 2016. WICK W, ROTH P, HARTMANN C, HAU P, NAKAMURA M, STOCKHAMMER F, SABEL MC, WICK A, KOEPPEN S, KETTER R, VAJKOCZY P, EYUPOGLU I, KALFF R, PIETSCH T, HAPPOLD C, GALLDIKS N, SCHMIDT-GRAF F, BAMBERG M, REIFENBERGER G, PLATTEN M, VON DEIMLING A, MEISNER C, WIESTLER B, WELLER M; Neurooncology Working Group (NOA) of the German Cancer Society. Long-term analysis of the NOA-04 randomized phase III trial of sequential radiochemotherapy of anaplastic glioma with PCV or temozolomide. Neuro Oncol. 2016 Nov;18(11):1529-1537. ABUHARBID G, ESMAEILZADEH M, HARTMANN C, HERMANN EJ, KRAUSS JK: Desmoplastic infantile astrocytoma with multiple intracranial and intraspinal localizations at presentation. Child's Nervous System 31:959-964, 2015. ESMAEILZADEH M, YILDIZ OE, LANG JM, WEGNER F, HAUBITZ B, FEUERHAKE F, WREDE A, BRUECK W, DENGLER R, KRAUSS JK: CLIPPERS syndrome: an entity to be faced in neurosurgery. World Neurosurgery 84:2077.e1-3, 2015. HERMANN EJ, ESMAEILZADEH M, ERTL P, POLEMIKOS M, RAAB P, KRAUSS JK: Endoscopic intracranial surgery enhanced by electromagnetic-guided neuronavigation in children. Child's Nervous System 31:1327-1333, 2015. HERMANN EJ, PETRAKAKIS I, POLEMIKOS M, RAAB P, CINIBULAK Z, NAKAMURA M, KRAUSS JK: Electromagnetic navigation-guided surgery in the semi-sitting position for posterior fossa tumours: a safety and feasibility study. Acta Neurochirurgica 157:1229-1237, 2015. HONG B, BIERTZ F, RAAB P, SCHEINICHEN D, ERTL P, GROSSHENNIG A, NAKAMURA M, HERMANN EJ, LANG JM, LANFERMANN H, KRAUSS JK: Normobaric hyperoxia for treatment of pneumocephalus afer posterior fossa surgery in the semisitting position: a prospective randomized controlled trial. Plos One 10(5):e0125710, 2015. VOGT PM, IPAKTCHI R, WEYAND B, RADTKE C, KRAUSS JK, LENARZ T: Weichteilplastische Maßnahmen bei Komplikationen im Schaedelbereich. Chirurg 86:223-237, 2015. ESMAEILZADEH M, MAJLESARA A, FARIDAR A, HAFEZI M, HONG B, ESMAEILNIA-SHIRVANI H, NEYAZI B, MEHRABI A, NAKAMURA M. Brain metastasis from gastrointestinal cancers: a systematic review. Int J Clin Pract. 2014 Jul;68(7):890-9. HONG B, KRAUSS JK, BREMER M, KARSTENS JH, HEISSLER HE, NAKAMURA M: Vestibular schwannoma microsurgery for recurrent tumors after radiation therapy or previous surgical resection. Otology and Neurotology 35:171-181, 2014. BORRMANN N, FRIEDRICH S, SCHWABE K, HEDRICH HJ, KRAUSS JK, KNAPP WH, NAKAMURA M, MEYER GJ, WALTE A: Systemic treatment with 4-211 Atphenylalanine enhances survival of rats with intracranial glioblastoma. Nuklearmedizin 52:212-221, 2013. CINIBULAK Z, KRAUSS JK, NAKAMURA M: Navigated minimally invasive presigmoidal suprabulbar infralabyrinthine approach to the jugular foramen without rerouting of the facial nerve. Neurosurgery 73 (1 Suppl Operative):ons3-ons15, 2013. FRIEDRICH S, SCHWABE K, GROTE M, KRAUSS JK, NAKAMURA M: Effect of systemic celecoxib on human meningioma after intracranial transplantation into nude mice. Acta Neurochirurgica 155:173-182, 2013. HERMANN E. AND KRAUSS J.K. Giant Pediatric Midline Tumors of the Posterior Fossa: The Combined Transventricular and Supracerebellar Technique and other Approaches. M.A. Hayat (ed.), Pediatric Cancer, Volume 4, Chapter 26: Diagnosis, Therapy, and Prognosis. Cancer 4.DOI 10.1007/978-007-6591-7 26 Springer Science+Business Media Dordrecht, 265-273 (2013) HONG B, HERMANN EJ, REUTER C, BRANDIS A, KRAUSS JK: Outcome of surgical decompression of spinal mass lesions in non Hodgkin´ s lymphoma and plasmocytoma. Clinical Neurology and Neurosurgery 115:2476-2481, 2013. HONG B, NAKAMURA M, HARTMANN C, BRANDIS A, GANSER A, KRAUSS JK: Delayed distal spinal metastasis in thymomas. Spine 15:E1709-1713, 2013. HONG B, WIESE B, BREMER M, HEISSLER HE, HEIDENREICH F, KRAUSS JK, NAKAMURA M: Multiple microsurgical resections for repeated recurrence of glioblastoma multiforme. American Journal of Clinical Oncology 36:261-268, 2013. FRIEDRICH S, SCHWABE K, KLEIN R, KRUSCHE CA, KRAUSS JK, NAKAMURA M: Comparative morphological and immunohistochemical study of human meningioma after intracranial transplantation into nude mice. Journal of Neuroscience Methods 205:1-9, 2012. STEINMANN D, MAERTENS B, JANSSEN S, WERNER M, FRUEHAUF J, NAKAMURA M, CHRISTIANSEN H, BREMER M. Hypofractionated stereotactic radiotherapy (hfSRT) after tumour resection of a single brain metastasis: report of a single-centre individualized treatment approach. J Cancer Res Clin Oncol. 2012 Sep;138(9):1523-9. WEHMING FM, WIESE B, NAKAMURA M, BREMER M, KARSTENS JH, MEYER A. Malignant glioma grade 3 and 4: how relevant is timing of radiotherapy?. Clin Neurol Neurosurg. 2012 Jul;114(6):617-21 WICK W, PLATTEN M, MEISNER C, FELSBERG J, TABATABAI G, SIMON M, NIKKHAH G, PAPSDORF K, STEINBACH JP, SABEL M, COMBS SE, VESPER J, BRAUN C, MEIXENSBERGER J, KETTER R, MAYER-STEINACKER R, REIFENBERGER G, WELLER M; NOA-08 STUDY GROUP OF NEURO-ONCOLOGY WORKING GROUP (NOA) OF GERMAN CANCER SOCIETY, PELS H, SCHLEGEL U, HERRLINGER U, PIETSCH T, SCHRAMM J, KREX D, SCHACKERT G, RAPP M, WILLE C, BLUEMCKE I, DIENER HC, BAEHR O, RIEGER J, FRANZ K, SEIFER V, PLATE KH, WILLE C, WESTPHAL M, HEIDENREICH F, WIESE B, BREMER M, NAKAMURA M, V DEIMLING A, KLEIN AC, PFENNING P, SCHEMMER D, WICK A, OERTEL J, KORTMANN R, CONRAD J, WIEWRODT D, SCHMIEDER K, WENZ F, BOGDAHN U, HAU P, BAMBERG M, MELMS A, DOEHNER H, HAPPOLD C, ZAUGG K. Temozolomide chemotherapy alone versus radiotherapy alone for malignant astrocytoma in the elderly: the NOA-08 randomised, phase 3 trial. Lancet Oncol. 2012 Jul;13(7):707-15. YOUNES WM, HERMANN EJ, KRAUSS JK: Cisternal trochlear nerve schwannoma: improvement of diplopia after subtotal tumour excision. British Journal of Neurosurgery 26:107-109, 2012. CAPELLE HH, KINFE T, KRAUSS JK: Deep brain stimulation for treatment of hemichorea-hemiballism after craniopharyngioma resection: long-term follow-up. Journal of Neurosurgery 115:966-970, 2011. GUTENBERG A, BRANDIS A, HONG B, GUNAWAN B, ENDERS C, SCHAEFER IM, BURGER R, OSTERTAG H, GAAB M, KRAUSS JK, FUEZESI L: Common molecular cytogenetic pathway in papillary tumors of the pineal region. Brain Pathology 21:672-677, 2011. HONG B, KRUSCHE CA, SCHWABE K, FRIEDRICH S, KLEIN R, KRAUSS JK, NAKAMURA M: Cyclooxygenase-2 supports tumor proliferation in vestibular schwannomas. Neurosurgery 68:1112-1117, 2011. HONG B, NAKAMURA M, BRANDIS A, BECKER K, KRAUSS JK: Spinal metastasis of papillary tumor of the pineal region. Clinical Neurology and Neurosurgery 113:235-238, 2011. KINFE T, CAPELLE HH, MIRZAYAN MJ, BOSCHERT J, WEIGEL R, KRAUSS JK: Brain tumors and neuronavigation: stereotactic versus endoscopic surgery in periventricular lesions. Acta Neurochirurgica 153:517-526, 2011. KUPSCH A, TAGLIATI M, VIDAILHET M, AZIZ T, KRACK P, MORO E, KRAUSS JK: Early postoperative management of DBS in dystonia: programming, response to stimulation, adverse events, medication changes, evaluations, and troubleshooting. Movement Disorders 26 (S1) :S37-S53, 2011. LUETJENS G, KRAUSS JK, BRANDIS A, NAKAMURA M: Bilateral sphenoorbital hyperostotic meningiomas with proptosis and visual impairment. a therapeutic challenge. Clinical Neurology and Neurosurgery 113:859-863, 2011. GHAEMI K, MIRZAYAN MJ, KRAUSS JK: Interdural epidermoid tumor of the cavernous sinus. Central European Neurosurgery 71:155-156, 2010. HONG B, HERMANN EJ, HOLLWITZ B, KLEIN R, AGARONJAN A, KRAUSS JK: Primary meningeal sarcoma with leiomyoblastic differentiation complicating pregnancy. Clinical Neurology and Neurosurgery 112:516-519, 2010. HONG B, HERMANN EJ, KLEIN R, KRAUSS JK, NAKAMURA M: Surgical resection of osteolytic calvarial lesions: clinicopathological features. Clinical Neurology and Neurosurgery 112:865-869, 2010. NAKAMURA M, KRAUSS JK: Image-guided resection of small lesions in the cavernous sinus and Meckel's cave. European Journal of Surgical Oncology 36:208-213, 2010. LUETJENS G, MIRZAYAN JM, BRANDIS A, KRAUSS JK: Exophytic giant cell glioblastoma of the medulla oblongata. Journal of Neurosurgery 110:589-593, 2009. MIRZAYAN MJ, GHARABAGHI A, SAMII M, FROEMKE C, TATAGIBA M, KRAUSS JK, ROSAHL SK: The diagnostic value of erythrocyte sedimentation rate in management of brain tumors. Neurological Research 31:514-517, 2009. MONTIBELLER GR, STAN AC, KRAUSS JK, NAKAMURA M: Calcifying pseudoneoplasm of the inferior colliculus: an unusual loaction for a rare tumor. Neurosurgery 65:E1005-1006, 2009. NAKAMURA M, STOEVER T, RODT T, MAJDANI O, LORENZ M, LENARZ T, KRAUSS JK: Neuronavigational guidance in craniofacial approaches for large paranasal tumors involving the anterior skull base and upper clival lesions. European Journal of Surgical Oncology 35:666-672, 2009. TSCHAN CA, MIRZAYAN MJ, STAN AC, PICHLMAIER MA, KRAUSS JK: Concomitant cardiac and cerebral leiomyosarcoma: a challenge for surgical and adjuvant therapy. The Journal of Thoracic and Cardiovascular Surgery 137:e12-14, 2009. BECKER H, KRAUSS JK: MRT der HWS: Nicht-erkanntes Ependymom des 4. Ventrikels. Clinical Neuroradiology 17:239-244, 2008. HERMANN EJ, HATTINGEN E, KRAUSS JK, MARQUARDT G, PILATUS U, TEWS DS, FRANZ K, SETZER M, GASSER T, ZANELLA FE, SEIFERT V, LANFERMANN H: Stereotactic biopsy in gluiomas guided by 3 Tesla 1H-chemical shift imaging of choline. Stereotactic and Functional Neurosurgery 86:300-307, 2008. HERMANN EJ, RITTIERODT M, KRAUSS JK: Combined transventricular and supracerebellar infratentorial approach preserving the vermis in giant pediatric posterior fossa midline tumors. Neurosurgery 63: ONS Suppl 1: 30-37, 2008. KINFE TM, CAPELLE HH, KRAUSS JK: Impact of surgical treatment on tremor due to posterior fossa tumors. Journal of Neurosurgery 108:692-697, 2008. KINFE TM, TSCHAN CA, STAN AC, KRAUSS JK: Solitary fibrous tumor of the foramen of Monro. Clinical Neurology and Neurosurgery 110:404-407, 2008. NAKAMURA M, STRUCK M, ROSER F, VORKAPIC P, SAMII M. Olfactory groove meningiomas: clinical outcome and recurrence rates after tumor removal through the frontolateral and bifrontal approach. Neurosurgery. 2008 Jun;62(6 Suppl 3):1224-32. MIRZAYAN MJ, GHARABAGHI A, SAMII M, TATAGIBA M, KRAUSS JK, ROSAHL SK: Response of C-reactive protein after craniotomy for microsurgery of intracranial tumors. Neurosurgery 60:621-625, 2007. ROSER F, NAKAMURA M, MARTINI-THOMAS R, SAMII M, TATAGIBA M. The role of surgery in meningiomas involving the optic nerve sheath. Clin Neurol Neurosurg. 2006 Jul;108(5):470-6. THOME C, ZEVGARIDIS D, MATEJIC D, SOMMER C, KRAUSS JK: Juxtaposition of an epidural intraforaminal cavernous hemangioma and an intradural schwannoma. Spine 29:524-527, 2004. WEIGEL R, SENN P, WEIS J, KRAUSS JK: Severe complications after intrathecal methotrexate for treatment of primary central nervous system lymphoma. Clinical Neurology and Neurosurgery 106:82-87, 2004. WOITZIK J, SOMMER C, KRAUSS JK: Delayed manifestation of spinal metastasis: a special feature of hemangiopericytoma. Clinical Neurology and Neurosurgery 105:159-166, 2003. POHLE T, KRAUSS JK, BURGUNDER JM: Petroclival meningioma as a cause of ipsilateral cervicofacial dyskinesias. Journal of Neurology, Neurosurgery and Psychiatry 68:113-114, 2000. KALBARCZYK A, KRAUSS JK, SEILER RW: Endoscopic stereotactic surgery for intraventricular loculated empyema. Surgical Neurology 52:412-417, 1999. PADUCH T, BABORIE A, KRAUSS JK: Bifocal temporal ganglioglioma. Neurosurgical Review 22:112-116, 1999. GLOCKER FX, KRAUSS JK, DEUSCHL G, SEEGER W, LUECKING CH: Hemifacial spasm due to posterior fossa tumors: the impact of tumor location on electrophysiological findings. Clinical Neurology and Neurosurgery 100:104-111, 1998. BORREMANS JJ, KRAUSS JK, FANARDJIAN RV, SEEGER W: Hemichorea-hemiballism associated with an ipsilateral intraventricular cyst after resection of a meningioma. Parkinsonism & Related Disorders 2:155-159, 1996. KRAUSS JK, BERTALANFFY H, SCHWECHHEIMER K, MUELLER A, SEEGER W: Ventral brain stem schwannoma at the entry zone of the hypoglossal nerve. Neurochirurgia 36:66-69, 1993. KRAUSS JK, BRAUS DF, MOHADJER M, NOBBE F, MUNDINGER F: Evaluation of the effect of treatment on movement disorders in astrocytomas of the basal ganglia and the thalamus. Journal of Neurology, Neurosurgery and Psychiatry 56:1113-1118, 1993. KRAUSS JK, WAKHLOO AK, SCHEREMET R, SEEGER W: Facial myokymia and spastic paretic facial contracture due to anaplastic pontocerebellar glioma. Neurosurgery 32:1031-1034, 1993. KRAUSS JK, NOBBE F, WAKHLOO AK, MOHADJER M, VACH W, MUNDINGER F: Movement disorders in astrocytomas of the basal ganglia and the thalamus. Journal of Neurology, Neurosurgery and Psychiatry 22:1162-1167, 1992. MUNDINGER F, BRAUS DF, KRAUSS JK, BIRG W: Long-term outcome of 89 low-grade brain-stem gliomas after interstitial radiation therapy. Journal of Neurosurgery 75:740-746, 1991. Klinik für Neurologie Sortiert nach Jahr (aktuellstes zuerst) und dann alphabetisch nach Erstautor DERLIN T, SCHULTZE-FLOREY C, WERNER RA, MOEHN N, SKRIPULETZ T, DAVID S, BEUTEL G, EDER M, ROSS TL, BENGEL FM, GANSER A, KOENECKE C. 18F-FDG PET/CT of off-target lymphoid organs in CD19-targeting chimeric antigen receptor T-cell therapy for relapsed or refractory diffuse large B-cell lymphoma. Ann Nucl Med. 2021;35:132-138. HUEMMERT MW, STADLER M, HAMBACH L, GINGELE S, BREDT M, WATTJES MP, GOEHRING G, VENTURINI L, MOEHN N, STANGEL M, TREBST C, GANSER A, WEGNER F, SKRIPULETZ T. Severe allo-immune antibody-associated peripheral and central nervous system diseases after allogeneic hematopoietic stem cell transplantation. Sci Rep. 2021;11:8527. MOEHN N, SUEHS KW, ANGELA Y, STANGEL M, IVANYI P, BEUTEL G, GUTZMER R, SKRIPULETZ T, GRIMMELMANN I. Checkpoint inhibitor induced autoimmune central nervous system disorder in patients with metastatic melanoma and Hodgkin lymphoma. Clin Exp Neuroimmunol. (in press) *equal contribution MOEHN N, WATTJES MP, ADAMS O, NAY S, TKACHENKO D, SALGE F, HEINE J, PARS K, HOEGLINGER G, RESPONDEK G, STANGEL M, SKRIPULETZ T, JACOBS R, SUEHS KW. PD-1-Inhibitor pembrolizumab for treatment of progressive multifocal leukoencephalopathy. Ther Adv Neurol Disord 2021;14:1–13 MOEHN N, KOENECKE C, SKRIPULETZ T. Neurotoxizitaet unter CAR-T-Zell-Therapie (CAR: chimaerer Antigenrezeptor). DGNeurologie. 2020;3:doi.org/10.1007/s42451-020-00172-y MOEHN N, MAHJOUB S, GUTZMER R, SATZGER I, BEUTEL G, IVANYI P, GOLPON H, WATTJES MP, STANGEL M, SKRIPULETZ T. Diagnosis and Differential Diagnosis of Neurological Adverse Events during Immune Checkpoint Inhibitor Therapy. J Oncol. 2020:8865054. STAHL K, SCHMIDT BMW, HOEPER MM, SKRIPULETZ T, MOEHN N, BEUTEL G, EDER M, WELTE T, GANSER A, FALK CS, KOENECKE C, DAVID S. Extracorporeal cytokine removal in severe CAR-T cell associated cytokine release syndrome. J Crit Care. 2020;57:124-129. BOENIG L, MOEHN N, AHLBRECHT J, WURSTER U, RAAB P, PUPPE W, SUEHS KW, STANGEL M, SKRIPULETZ T, SCHWENKENBECHER P. Leptomeningeal Metastasis: The Role of Cerebrospinal Fluid Diagnostics. Front Neurol. 2019;10:839. MOEHN N, BEUTEL G, GUTZMER R, IVANYI P, SATZGER I, SKRIPULETZ T. Neurological Immune Related Adverse Events Associated with Nivolumab, Ipilimumab, and Pembrolizumab Therapy-Review of the Literature and Future Outlook. J Clin Med. 2019;8, E1777. MOEHN N, SUEHS KW, GINGELE S, ANGELA Y, STANGEL M, GUTZMER R, SATZGER I, SKRIPULETZ T. Acute progressive neuropathy-myositis-myasthenia-like syndrome associated with immune-checkpoint inhibitor therapy in patients with metastatic melanoma. Melanoma Res. 2019;29:435-440. SCHWENKENBECHER P, CHACKO L, PUL R, SUEHS KW, WEGNER F, WURSTER U, STANGEL M, SKRIPULETZ T. Paraneoplastic cerebellar syndromes associated with antibodies against Purkinje cells. Int J Neurosci. 2018;128:721-728. SCHWENKENBECHER P, CHACKO LP, WURSTER U, PARS K, PUL R, SUEHS KW, STANGEL M, SKRIPULETZ T. Intrathecal synthesis of anti-Hu antibodies distinguishes patients with paraneoplastic peripheral neuropathy and encephalitis. BMC Neurol. 2016;16:136. KRUSCHINSKI C, HAMA Y, SKRIPULETZ T, VASKE B, KNAPP WH, SCHMIDT RE, PABST R, VON HOERSTEN S, HOFMANN M. In vivo monitoring of natural killer cell dependent clearance of lung metastasis using dynamic positron emission tomography. In Vivo 2012;26:191-5 SKRIPULETZ T, PUL R, WURSTER U, PEEST D, DENGLER R, STANGEL M. B-cell lymphoma infiltration of cerebrospinal fluid with minimal symptoms and benign course. J Clin Neurosci 2011;18:978-80. SKRIPULETZ T, PUL R, HERRMANN J, BUELTMANN E, WURSTER U, STANGEL M, TREBST C. Meningeal carcinomatosis from penile squamous cell carcinoma. J Neuro-Oncol 2010;98:417-9. Klinik für Neuroradiologie Sortiert nach Jahr (aktuellstes zuerst) und dann alphabetisch nach Erstautor HONG B, LALK M, WIESE B, MERTEN R, HEISSLER HE, RAAB P, HARTMANN C, KRAUSS JK (2021). "Primary and secondary gliosarcoma: differences in treatment and outcome." Br J Neurosurg: 1-8. BONIG L, MOHN N, AHLBRECHT J, WURSTER U, RAAB P, PUPPE W, SUHS KW, STANGEL M, SKRIPULETZ T, SCHWENKENBECHER P (2019). "Leptomeningeal Metastasis: The Role of Cerebrospinal Fluid Diagnostics." Front Neurol 10: 839. ABRAHAM L, KREIPE H, RAAB P, HUSSEIN K (2018). "[Clinical and pathological characteristics of intravascular lymphomas]." Pathologe 39(3): 242-248. BEYER U, BRAND F, MARTENS F, WEDER J, CHRISTIANS J, ELYAN N, HENTSCHEL B, WESTPHAL M, SCHACKERT G, PIETSCH T, HONG B, KRAUSS JK, SAMII A, RAAB P, DAS A, DUMITRU CA, SANDALCIOGLU IE, HAKENBERG OW, ERBERSDOBLER A, LEHMANN U, REIFENBERGER G, WELLER M, REIJNS MAM, PRELLER M, WIESE B, HARTMANN C, WEBER RG (2017). "Rare ADAR and RNASEH2B variants and a type I interferon signature in glioma and prostate carcinoma risk and tumorigenesis." Acta Neuropathol 134(6): 905-922. PIRAYESH A, PETRAKAKIS I, RAAB P, POLEMIKOS M, KRAUSS JK, NAKAMURA M (2016). "Petroclival meningiomas: Magnetic resonance imaging factors predict tumor resectability and clinical outcome." Clin Neurol Neurosurg 147: 90-97. RAAB P, PILATUS U, HATTINGEN E, FRANZ K, HERMANN EJ, ZANELLA FE, LANFERMANN H (2016). "Spectroscopic Characterization of Gliosarcomas-Do They Differ From Glioblastomas and Metastases?" J Comput Assist Tomogr 40(5): 815-819. HERMANN EJ, PETRAKAKIS I, POLEMIKOS M, RAAB P, CINIBULAK Z, NAKAMURA M, KRAUSS JK (2015). "Electromagnetic navigation-guided surgery in the semi-sitting position for posterior fossa tumours: a safety and feasibility study." Acta Neurochir (Wien). HERMANN EJ, ESMAEILZADEH M, ERTL P, POLEMIKOS M, RAAB P, KRAUSS JK (2015). "Endoscopic intracranial surgery enhanced by electromagnetic-guided neuronavigation in children." Childs Nerv Syst. HENKENBERENS C, FRANZKE A, RAAB P, OSCHLIES I, KLAPPER W, CHRISTIANSEN H (2014). "Primary EBV-positive Hodgkin's lymphoma of the CNS under azathioprine treatment : Case report and review of the literature." Strahlenther Onkol 190(9): 847-852. HEISS, WD, RAAB P, LANFERMANN H (2011). "Multimodality Assessment of Brain Tumors and Tumor Recurrence." Journal of nuclear medicine : official publication, Society of Nuclear Medicine. KORNER S, RAAB P, BRANDIS A, WEISSENBORN K (2011). "Spontaneous regression of an intracerebral lymphoma (ghost tumor) in a liver-engrafted patient." The neurologist 17(4): 218-221. HATTINGEN E, DELIC O, FRANZ K, PILATUS U, RAAB P, LANFERMANN H, GERLACH R (2010). "(1)H MRSI and progression-free survival in patients with WHO grades II and III gliomas." Neurol Res 32(6): 593-602. RAAB P, HATTINGEN E, FRANZ K, ZANELLA FE, LANFERMANN H (2010). "Cerebral gliomas: diffusional kurtosis imaging analysis of microstructural differences." Radiology 254(3): 876-881. HATTINGEN E, RAAB P, FRANZ K, ZANELLA FE, LANFERMANN H, PILATUS U (2008). "Myo-Inositol: a marker of reactive astrogliosis in glial tumors?" NMR Biomed 21(3): 233-241. HATTINGEN E, RAAB P, FRANZ K, LANFERMANN H, SETZER M, GERLACH R, ZANELLA FE, PILATUS U (2008). "Prognostic value of choline and creatine in WHO grade II gliomas." Neuroradiology 50(9): 759-767. RAAB P, PILATUS U, LANFERMANN H (2008). "Spectroscopy of brain tumors." Rad up2date(3): 239-255. Schwerpunktprofessur Neuropathologie am Institut für Pathologie Sortiert nach Jahr (aktuellstes zuerst) und dann alphabetisch nach Erstautor BANAN R, ABBETMEIER BASSE, HONG B, DUMITRU CA, SAHM F, NAKAMURA M, KRAUSS JK, HARTMANN C. The prognostic significance of clinicopathological features in meningiomas: microscopic brain invasion can predict patient outcome in otherwise benign meningiomas. Neuropathology and Applied Neurobiology. 2021. Accepted BANAN R, AKBARIAN A, SAMII M, SAMII A, BERTALANFFY H, LEHMANN U, HARTMANN C, BRÜNING R. Diffuse midline gliomas, H3 K27M-mutant are associated with less peritumoral edema and contrast enhancement in comparison to glioblastomas, H3 K27M-wildtype of midline structures. PLOS ONE. 2021. Accepted. HONG B, LALK M, WIESE B, MERTEN R, HEISSLER HE, RAAB P, HARTMANN C, KRAUSS JK. Primary and secondary gliosarcoma: differences in treatment and outcome. Br J Neurosurg. 2021 Feb 4;1-8. doi: 10.1080/02688697.2021.1872773. KOELSCHE C, SCHRIMPF D, STICHEL D, SILL M, SAHM F, REUSS DE, BLATTNER M, WORST B, HEILIG CE, BECK K, HORAK P, KREUTZFELDT S, PAFF E, STARK S, JOHANN P, SELT F, ECKER J, STURM D, PAJTLER KW, REINHARDT A, WEFERS AK, SIEVERS P, EBRAHIMI A, SUWALA A, FERNÁNDEZ-KLETT F, CASALINI B, KORSHUNOV A, HOVESTADT V, KOMMOSS FKF, KRIEGSMANN M, SCHICK M, BEWERUNGE-HUDLER M, MILDE T, WITT O, KULOZIK AE, KOOL M, ROMERO-PÉREZ L, GRÜNEWALD TGP, KIRCHNER T, WICK W, PLATTEN M, UNTERBERG A, UHL M, ABDOLLAHI A, DEBUS J, LEHNER B, THOMAS C, HASSELBLATT M, PAULUS W, HARTMANN C, STASZEWSKI O, PRINZ M, HENCH J, FRANK S, VERSLEIJEN-JONKERS YMH, WEIDEMA ME, MENTZEL T, GRIEWANK K, DE ÁLAVA E, MARTÍN JD, GASTEARENA MAI, CHANG KT, LOW SYY, CUEVAS-BOURDIER A, MITTELBRONN M, MYNAREK M, RUTKOWSKI S, SCHÜLLER U, MAUTNER VF, SCHITTENHELM J, SERRANO J, SNUDERL M, BÜTTNER R, KLINGEBIEL T, BUSLEI R, GESSLER M, WESSELING P, DINJENS WNM, BRANDNER S, JAUNMUKTANE Z, LYSKJÆR I, SCHIRMACHER P, STENZINGER A, BRORS B, GLIMM H, HEINING C, TIRADO OM, SÁINZ-JASPEADO M, MORA J, ALONSO J, DEL MURO XG, MORAN S, ESTELLER M, BENHAMIDA JK, LADANYI M, WARDELMANN E, ANTONESCU C, FLANAGAN A, DIRKSEN U, HOHENBERGER P, BAUMHOER D, HARTMANN W, VOKUHL C, FLUCKE U, PETERSEN I, MECHTERSHEIMER G, CAPPER D, JONES DTW, FRÖHLING S, PFISTER SM, VON DEIMLING A. Sarcoma classification by DNA methylation profiling. Nat Commun. 2021 Jan 21;12(1):498. doi: 10.1038/s41467-020-20603-4. THOMAS C, FEDERICO A, SILL S, BENS S, OYEN F, NEME K, JOHANN PD, HARTMANN C, HARTMANN W, SUMERAUER D, PATERNO V, SAMII A, CORDES U, SIEBERT R, FRÜHWALD MC, PAULUS W, KOOL M, HASSELBLATT M. Atypical teratoid/rhabdoid tumor (AT/RT) with molecular features of pleomorphic xanthoastrocytoma. American Journal of Surgical Pathology. 2021. Accepted. AL KRINAWE Y, ESMAEILZADEH M, HARTMANN C, KRAUSS JK, HERMANN EJ. Pediatric rosette-forming glioneuronal tumor of the septum pellucidum. Childs Nerv Syst. 2020 Mar 26. doi: 10.1007/s00381-020-04575-w. BANAN R, STICHEL D, BLECK A, HONG B, LEHMANN U, SUWALA A, REINHARDT A, SCHRIMPF D, BUSLEI R, STADELMANN C, EHLERT K, PRINZ M, ACKER T, SCHITTENHELM J, KAUL D, SCHWEIZER L, CAPPER D, HARTER P, ETMINAN N, JONES DTW, PFISTER SM, HEROLD-MENDE C, WICK W, SAHM F, DEIMLING A, HARTMANN C, REUSS DE. Infratentorial IDH- mutant astrocytoma is a distinct subtype. Acta Neuropathol. 2020 Aug 10. doi: 10.1007/s00401-020-02194-y. BEHLING F, BARRANTES-FREER A, BEHNES CL, STOCKHAMMER F, ROHDE V, RODRÍGUEZ-VILLAGRA O, BARBOZA MA, BRÜCK W, LEHMANN U, STADELMANN C, HARTMANN C. Expression of Olig2, Nestin, NogoA and AQP4 have no impact on overall survival in IDH-wildtype glioblastoma. PLoS One. 2020 Mar 11;15(3):e0229274. KIM E, SOROKIN M, KANTELHARDT S, KALASAUSKAS D, SPRANG B, FAUSS F, RINGEL F, GARAZHA A, ALBERT E, GAIFULLIN N, HARTMANN C, NAUMANN N, BIKAR S-E, GIESE A, BUZDIN A. Intratumoral heterogeneity and longitudinal changes in gene expression predict differential drug sensitivity in newly diagnosed and recurrent glioblastoma. Cancers (Basel). 2020 Feb 24;12(2). MYNAREK M, VON HOFF K, PIETSCH T, OTTENSMEIER H, WARMUTH-METZ M, BISON B, PFISTER S, KORSHUNOV A, SHARMA T, JAEGER N, RYZHOVA M, ZHELUDKOVA O, GOLANOV A, RUSHING EJ, HASSELBLATT M, KOCH A, SCHÜLLER U, VON DEIMLING A, SAHM F, SILL M, RIEMENSCHNEIDER MJ, DOHMEN H, MONORANU C-M, SOMMER C-M, STASZEWSKI O, MAWRIN C-M, SCHITTENHELM J, BRÜCK W, FILIPSKI K, HARTMANN C, MEINHARDT M, PIETSCHMANN K, HABERLER C, SLAVC I, GERBER NU, GROTZER NU, BENESCH M, SCHLEGEL P-G, DEINLEIN F, VON BUEREN AO, FRIEDRICH C, OBRECHT D, FLEISCHHACK G, KWIECIEN R, FALDUM A, KORTMANN R-D, KOOL M, RUTKOWSKI S. Nonmetastatic Medulloblastoma of Early Childhood: Results From the Prospective Clinical Trial HIT-2000 and An Extended Validation Cohort. J Clin Oncol. 2020 Apr 24:JCO1903057. doi: 10.1200/JCO.19.03057. SCHWEIZER L, THIERFELDER F, THOMAS C, SOSCHINSKI P, SUWALA A, STICHEL D, WEFERS AK, WESSELS L, MISCH M, KIM HY, JÖDICKE R, TEICHMANN D, KAUL D, KAHN J, BOCKMAYR M, HASSELBLATT M, YOUNSI A, UNTERBERG A, KNIE B, WALTER J, AL SAFATLI D, MAY SA, JÖDICKE A, NTOULIAS G, MOSKOPP D, VAJKOCZY P, HEPPNER FL, CAPPER D, HARTMANN W, HARTMANN C, VON DEIMLING A, REUSS DE, SCHÖLER A, KOCH A. Molecular characterization of CNS paragangliomas identifies cauda equina paragangliomas as a distinct tumor entity. Acta Neuropathol. 2020 Sep 14. doi: 10.1007/s00401-020-02218-7. SIEVERS P, SILL M, BLUME C, TAUZIEDE-ESPARIAT A, SCHRIMPF D, STICHEL D, REUSS DE, DOGAN H, HARTMANN C, MAWRIN C, HASSELBLATT M, STUMMER W, SCHICK U, HENCH J, FRANK S, KETTER R, SCHWEIZER L, SCHITTENHELM J, PUGET S, BRANDNER S, JAUNMUKTANE Z, KÜSTERS B, ABDULLAEV Z, PEKMEZCI M, SNUDERL M, RATLIFF M, HEROLD-MENDE C, UNTERBERG A, ALDAPE K, ELLISON DW, WESSELING P, REIFENBERGER G, WICK W, PERRY A, VARLET P, PFISTER SM, JONES DTW, VON DEIMLING A, SAHM F. Clear cell meningiomas are defined by a highly distinct DNA methylation profile and mutations in SMARCE1. German Consortium “Aggressive Meningiomas”. Acta Neuropathol. 2020 Dec 14. doi: 10.1007/s00401-020-02247-2. SUWALA AK, STICHEL D, SCHRIMPF D, KLOOR M, WEFERS AK, REINHARDT A, MAAS SLN, KRATZ CP, SCHWEIZER L, HASSELBLATT M, SNUDERL M, ABEDALTHAGAFI MSJ, ABDULLAEV Z, MONORANU CM, BERGMANN M, PEKRUN A, FREYSCHLAG C, ARONICA E, KRAMM CM, HINZ F, SIEVERS P, KORSHUNOV A, KOOL M, PFISTER SM, STURM D, JONES DTW, WICK W, UNTERBERG A, HARTMANN C, DODGSHUN A, TABORI U, WESSELING P, SAHM F, VON DEIMLING A, REUSS DE. Primary mismatch repair deficient IDH-mutant astrocytoma (PMMRDIA) is a distinct type with a poor prognosis. Acta Neuropathol. 2020 Nov 20. doi: 10.1007/s00401-020-02243-6. BERGNER CG, VAN DER MEER F, WINKLER A, WRZOS C, TÜRKMEN M, VALIZADA E, FITZNER D, HAMETNER S, HARTMANN, C, PFEIFENBRING S, STOLTENBURG‐DIDINGER G, BRÜCK W, NESSLER S, STADELMANN C. Microglia damage precedes major myelin breakdown in X-linked adrenoleukodystrophy and metachromatic leukodystrophy. Glia. 2019;1–14. doi.org/10.1002/glia.23598 CHRISTIANS A, ADEL-HOROWSKI A, BANAN R, LEHMANN U, BARTELS S, BEHLING F, BARRANTES-FREER A, STADELMANN C, ROHDE V, STOCKHAMMER F, HARTMANN C. The prognostic role of IDH mutations in homogeneously treated patients with anaplastic astrocytomas and glioblastomas. Acta Neuropathol Commun. 2019 Oct 17;7(1):156. CHRISTIANS A, POISEL E, HARTMANN C, VON DEIMLING A, PUSCH S. Characterization of the Epithelial Membrane Protein 3 interaction network reveals a potential functional link to mitogenic signal transduction regulation. Int J Cancer. 2019 Jan 7. doi: 10.1002/ijc.32107. DENG MY, SILL M, STURM D, STICHEL D, WITT H, ECKER J, WITTMANN A, SCHITTENHELM J, EBINGER M, SCHUHMANN MU, FIGARELLA-BRANGER D, ARONICA E, STASZEWSKI O, PREUSSER M, HABERLER C, LAUTEN M, SCHÜLLER U, HARTMANN C, SNUDERL M, DUNHAM C, JABADO N, WESSELING P, DECKERT M, KEYVANI K, GOTTARDO N, GIANGASPERO F, VON HOFF K, ELLISON DW, PIETSCH T, HEROLD MENDE C, MILDE T, WITT O, KOOL M, KORSHUNOV A, WICK W, VON DEIMLING A, PFISTER SM, JONES DTW, SAHM F. Diffuse Glioneuronal tumour with Oligodendroglioma-like features and Nuclear Clusters (DGONC) - a molecularly-defined glioneuronal CNS tumour class displaying recurrent monosomy 14. Neuropathol Appl Neurobiol. 2019 Dec 23. doi: 10.1111/nan.12590. GALLI R, UCKERMANN O, SEHM T, LEIPNITZ E, HARTMANN C, SAHM F, KOCH E, SCHACKERT G, STEINER G, KIRSCH M. Identification of distinctive features in human intracranial tumors by label-free nonlinear multimodal microscopy. J Biophotonics. 2019 Jun 13:e201800465. doi: 10.1002/jbio.201800465. GHASEMI DR, SILL M, OKONECHNIKOV K, KORSHUNOV A, YIP S, SCHUTZ PW, SCHEIE D, KRUSE A, HARTER PN, KASTELAN M, WAGNER M, HARTMANN C, BENZEL J, MAASS KK, KHASRAW M, STRÄTER R, THOMAS C, PAULUS W, KRATZ CP, WITT H, KAWAUCHI D, HEROLD-MENDE C, SAHM F, BRANDNER S, KOOL M, JONES DTW, VON DEIMLING A, PFISTER SM, REUSS DE, PAJTLER KW. MYCN amplification drives an aggressive form of spinal ependymoma. Acta Neuropathol. 2019 Dec;138(6):1075-1089. HOU Y, PINHEIRO J, SAHM F, REUSS DE, SCHRIMPF D, STICHEL D, CASALINI B, KOELSCHE C, SIEVERS P, WEFERS AK, REINHARDT A, EBRAHIMI A, FERNÁNDEZ-KLETT F, PUSCH S, MEIER J, SCHWEIZER L, PAULUS W, PRINZ M, HARTMANN C, PLATE KH, REIFENBERGER G, PIETSCH T, VARLET P, PAGÈS M, SCHÜLLER U, SCHEIE D, DE STRICKER K, FRANK S, HENCH J, POLLO B, BRANDNER S, UNTERBERG A, PFISTER SM, JONES DTW, KORSHUNOV A, WICK W, CAPPER D, BLÜMCKE I, VON DEIMLING A, BERTERO L. Papillary glioneuronal tumor (PGNT) exhibits a characteristic methylation profile and fusions involving PRKCA. Acta Neuropathol. 2019 Feb 13. doi: 10.1007/s00401-019-01969-2. ZEINER PS, PREUSSE C, GOLEBIEWSKA A, ZINKE J, IRIONDO A, MULLER A, KAOMA T, FILIPSKI K, MÜLLER-ESCHNER M, BERNATZ S, BLANK AE, BAUMGARTEN P, ILINA E, GROTE A, HANSMANN ML, VERHOFF MA, FRANZ K, FEUERHAKE F, STEINBACH JP, WISCHHUSEN J, STENZEL W, NICLOU SP, HARTER PN, MITTELBRONN M. Distribution and prognostic impact of microglia/macrophage subpopulations in gliomas. Brain Pathol 2019 Jul;29(4):513-529. doi: 10.1111/bpa.12690. Epub 2019 Jan 15. REINHARDT A, STICHEL D, SCHRIMPF D, KOELSCHE C, WEFERS A, EBRAHIMI A, SIEVERS P, HUANG K, CASALINI MB, FERNÁNDEZ-KLETT F, ABIGAIL S, WELLER M, GRAMATZKI D, FELSBERG J, REIFENBERGER G, BECKER A, HANS VH, PRINZ M, STASZEWSKI O, ACKER T, DOHMEN H, HARTMANN C, PAULUS W, HESS K, BROKINKEL B, SCHITTENHELM J, BUSLEI R, DECKERT M, MAWRIN C, HEWER E, POHL U, JAUNMUKTANE Z, BRANDNER S, UNTERBERG A, HÄNGGI D, PLATTEN M, PFISTER S, WICK W, HEROLD-MENDE C, KORSHUNOV A, REUSS D, SAHM F, JONES DTW, CAPPER D, VON DEIMLING A. Tumors diagnosed as cerebellar glioblastoma comprise distinct molecular entities. Acta Neuropathol Commun. 2019 Oct 28;7(1):163. doi: 10.1186/s40478-019-0801-8. AL-AFIF S, HATIPOGLU MAJERNIK G, HERMANN EJ, ESMAEILZADEH M, HARTMANN C, KRAUSS JK. Intracranial foreign material granulomas after cranial surgery. Acta Neurochir (Wien). 2018 Sep 6. doi: 10.1007/s00701-018-3663-0. AL-AFIF S, MAJERNIK GH, AL KRINAWE Y, ESMAEILZADEH M, HARTMANN C, KRAUSS JK. 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Epub 2017 May 22. PMID: 28529312. KRATZ CP, ACHATZ MI, BRUGIÈRES L, FREBOURG T, GARBER JE, GREER MC, HANSFORD JR, JANEWAY KA, KOHLMANN WK, MCGEE R, MULLIGHAN CG, ONEL K, PAJTLER KW, PFISTER SM, SAVAGE SA, SCHIFFMAN JD, SCHNEIDER KA, STRONG LC, EVANS DGR, WASSERMAN JD, VILLANI A, MALKIN D. Cancer Screening Recommendations for Individuals with Li- Fraumeni Syndrome. Clin Cancer Res. 2017 Jun 1;23(11):e38-e45. doi:10.1158/1078-0432.CCR-17-0408. PMID: 28572266. KRATZ CP, IZRAELI S. Down syndrome, RASopathies, and other rare syndromes. Semin Hematol. 2017 Apr;54(2):123-128. doi: 10.1053/j.seminhematol.2017.04.008. Epub 2017 Apr 28. PMID: 28637616. TABORI U, HANSFORD JR, ACHATZ MI, KRATZ CP, PLON SE, FREBOURG T, BRUGIÈRES L. Clinical Management and Tumor Surveillance Recommendations of Inherited Mismatch Repair Deficiency in Childhood. Clin Cancer Res. 2017 Jun 1;23(11):e32-e37. doi: 10.1158/1078-0432.CCR-17-0574. PMID: 28572265. VILLANI A, GREER MC, KALISH JM, NAKAGAWARA A, NATHANSON KL, PAJTLER KW, PFISTER SM, WALSH MF, WASSERMAN JD, ZELLEY K, KRATZ CP. Recommendations for Cancer Surveillance in Individuals with RASopathies and Other Rare Genetic Conditions with Increased Cancer Risk. Clin Cancer Res. 2017 Jun 15;23(12):e83-e90. doi: 10.1158/1078-0432.CCR-17-0631. PMID: 28620009. WASSERMAN JD, TOMLINSON GE, DRUKER H, KAMIHARA J, KOHLMANN WK, KRATZ CP, NATHANSON KL, PAJTLER KW, PARAREDA A, REDNAM SP, STATES LJ, VILLANI A, WALSH MF, ZELLEY K, SCHIFFMAN JD. Multiple Endocrine Neoplasia and Hyperparathyroid-Jaw Tumor Syndromes: Clinical Features, Genetics, and Surveillance Recommendations in Childhood. Clin Cancer Res. 2017 Jul 1;23(13):e123-e132. doi: 10.1158/1078-0432.CCR-17-0548. PMID: 28674121; PMCID: PMC5547889. WIMMER K, BEILKEN A, NUSTEDE R, RIPPERGER T, LAMOTTKE B, URE B, STEINMANN D, REINEKE-PLAASS T, LEHMANN U, ZSCHOCKE J, VALLE L, FAUTH C, KRATZ CP. A novel germline POLE mutation causes an early onset cancer prone syndrome mimicking constitutional mismatch repair deficiency. Fam Cancer. 2017 Jan;16(1):67-71. doi: 10.1007/s10689-016-9925-1. PMID: 27573199; PMCID: PMC5243902. BEIER R, SYKORA KW, WOESSMANN W, MAECKER-KOLHOFF B, SAUER M, KREIPE HH, DÖRK-BOUSSET T, KRATZ C, LAUTEN M. Allogeneic-matched sibling stem cell transplantation in a 13-year-old boy with ataxia telangiectasia and EBV-positive non-Hodgkin lymphoma. Bone Marrow Transplant. 2016 Sep;51(9):1271-4. doi: 10.1038/bmt.2016.93. Epub 2016 May 9. PMID: 27159176. CAVÉ H, CAYE A, STRULLU M, ALADJIDI N, VIGNAL C, FERSTER A, MÉCHINAUD F, DOMENECH C, PIERRI F, CONTET A, CACHEUX V, IRVING J, KRATZ C, CLAVEL J, VERLOES A. Acute lymphoblastic leukemia in the context of RASopathies. Eur J Med Genet. 2016 Mar;59(3):173-8. doi: 10.1016/j.ejmg.2016.01.003. Epub 2016 Feb 5. PMID: 26855057. KONTNY U, FRANZEN S, BEHRENDS U, BÜHRLEN M, CHRISTIANSEN H, DELECLUSE H, EBLE M, FEUCHTINGER T, GADEMANN G, GRANZEN B, KRATZ CP, LASSAY L, LEUSCHNER I, MOTTAGHY FM, SCHMITT C, STAATZ G, TIMMERMANN B, VORWERK P, WILOP S, WOLFF HA, MERTENS R. Diagnosis and Treatment of Nasopharyngeal Carcinoma in Children and Adolescents - Recommendations of the GPOH-NPC Study Group. Klin Padiatr. 2016 Apr;228(3):105-12. English. doi: 10.1055/s-0041-111180. Epub 2016 May 2. PMID: 27135270. KRATZ CP, STANULLA M, CAVÉ H. Genetic predisposition to acute lymphoblastic leukemia: Overview on behalf of the I-BFM ALL Host Genetic Variation Working Group. Eur J Med Genet. 2016 Mar;59(3):111-5. doi: 10.1016/j.ejmg.2015.10.003. Epub 2015 Dec 15. PMID: 26699264. PAUSTIAN L, CHAO MM, HANENBERG H, SCHINDLER D, NEITZEL H, KRATZ CP, EBELL W. Androgen therapy in Fanconi anemia: A retrospective analysis of 30 years in Germany. Pediatr Hematol Oncol. 2016 Feb;33(1):5-12. doi: 10.3109/08880018.2015.1129567. Epub 2016 Feb 22. PMID: 26900943. RIPPERGER T, TAWANA K, KRATZ C, SCHLEGELBERGER B, FITZGIBBON J, STEINEMANN D. Clinical utility gene card for: Familial platelet disorder with associated myeloid malignancies. Eur J Hum Genet. 2016 Aug;24(8). doi: 10.1038/ejhg.2015.278. Epub 2016 Jan 27. PMID: 26813945; PMCID: PMC4970691. SCHEER C, KRATZ C, WITT O, CREUTZIG U, REINHARDT D, KLUSMANN JH. Hematologic Response to Vorinostat Treatment in Relapsed Myeloid Leukemia of Down Syndrome. Pediatr Blood Cancer. 2016 Sep;63(9):1677-9. doi: 10.1002/pbc.26062. Epub 2016 May 18. PMID: 27191354. SCHÜTTE P, MÖRICKE A, ZIMMERMANN M, BLECKMANN K, REISMÜLLER B, ATTARBASCHI A, MANN G, BODMER N, NIGGLI F, SCHRAPPE M, STANULLA M, KRATZ CP. Preexisting conditions in pediatric ALL patients: Spectrum, frequency and clinical impact. Eur J Med Genet. 2016 Mar;59(3):143-51. doi: 10.1016/j.ejmg.2015.12.008. Epub 2015 Dec 28. PMID: 26732628. VOGT J, WERNSTEDT A, RIPPERGER T, PABST B, ZSCHOCKE J, KRATZ C, WIMMER K. PMS2 inactivation by a complex rearrangement involving an HERV retroelement and the inverted 100-kb duplicon on 7p22.1. Eur J Hum Genet. 2016 Nov;24(11):1598-1604. doi: 10.1038/ejhg.2016.75. Epub 2016 Jun 22. PMID: 27329736; PMCID: PMC5110070. WEBER ML, SCHNEIDER DT, OFFENMÜLLER S, KAATSCH P, EINSIEDEL HG, BENESCH M, CLAVIEZ A, EBINGER M, KRAMM C, KRATZ C, LAWLOR J, LEUSCHNER I, MERKEL S, METZLER M, NUSTEDE R, PETSCH S, SEEGER KH, SCHLEGEL PG, SUTTORP M, ZOLK O, BRECHT IB. Pediatric Colorectal Carcinoma is Associated With Excellent Outcome in the Context of Cancer Predisposition Syndromes. Pediatr Blood Cancer. 2016 Apr;63(4):611-7. doi: 10.1002/pbc.25839. Epub 2015 Nov 17. PMID: 26575411. WIMMER K, BRUGIÈRES L, DUVAL A, MULERIS M, KRATZ CP, VASEN HF. Constitutional or biallelic? Settling on a name for a recessively inherited cancer susceptibility syndrome. J Med Genet. 2016 Apr;53(4):226. doi: 10.1136/jmedgenet-2015-103249. Epub 2015 Jun 3. PMID: 26041761. BEIER R, MAECKER-KOLHOFF B, SYKORA KW, CHAO M, KRATZ C, SAUER MG. Minimal antileukaemic treatment followed by reduced-intensity conditioning in three consecutive children with Fanconi anaemia and AML. Bone Marrow Transplant. 2015 Mar;50(3):463-4. doi: 10.1038/bmt.2014.283. Epub 2014 Dec 22. PMID: 25531282. CHAO MM, KUEHL JS, STRAUSS G, HANENBERG H, SCHINDLER D, NEITZEL H, NIEMEYER C, BAUMANN I, VON BERNUTH H, RASCON J, NAGY M, ZIMMERMANN M, KRATZ CP, EBELL W. Outcomes of mismatched and unrelated donor hematopoietic stem cell transplantation in Fanconi anemia conditioned with chemotherapy only. Ann Hematol. 2015 Aug;94(8):1311-8. doi: 10.1007/s00277-015-2370-7. Epub 2015 Apr 12. PMID: 25862235. CHAO MM, EBELL W, BADER P, BEIER R, BURKHARDT B, FEUCHTINGER T, HANDGRETINGER R, HANENBERG H, KOEHL U, KRATZ C, KREMENS B, LANG P, MEISEL R, MUELLER I, ROESSIG C, SAUER M, SCHLEGEL PG, SCHULZ A, STRAHM B, THOL F, SYKORA KW. Consensus of German transplant centers on hematopoietic stem cell transplantation in Fanconi anemia. Klin Padiatr. 2015 May;227(3):157-65. doi: 10.1055/s-0035-1548841. Epub 2015 May 18. PMID: 25985449. FISCHER U, FORSTER M, RINALDI A, RISCH T, SUNGALEE S, WARNATZ HJ, BORNHAUSER B, GOMBERT M, KRATSCH C, STÜTZ AM, SULTAN M, TCHINDA J, WORTH CL, AMSTISLAVSKIY V, BADARINARAYAN N, BARUCHEL A, BARTRAM T, BASSO G, CANPOLAT C, CARIO G, CAVÉ H, DAKAJ D, DELORENZI M, DOBAY MP, ECKERT C, ELLINGHAUS E, EUGSTER S, FRISMANTAS V, GINZEL S, HAAS OA, HEIDENREICH O, HEMMRICH-STANISAK G, HEZAVEH K, HÖLL JI, HORNHARDT S, HUSEMANN P, KACHROO P, KRATZ CP, TE KRONNIE G, MAROVCA B, NIGGLI F, MCHARDY AC, MOORMAN AV, PANZER-GRÜMAYER R, PETERSEN BS, RAEDER B, RALSER M, ROSENSTIEL P, SCHÄFER D, SCHRAPPE M, SCHREIBER S, SCHÜTTE M, STADE B, THIELE R, VON DER WEID N, VORA A, ZALIOVA M, ZHANG L, ZICHNER T, ZIMMERMANN M, LEHRACH H, BORKHARDT A, BOURQUIN JP, FRANKE A, KORBEL JO, STANULLA M, YASPO ML. Genomics and drug profiling of fatal TCF3-HLF-positive acute lymphoblastic leukemia identifies recurrent mutation patterns and therapeutic options. Nat Genet. 2015 Sep;47(9):1020-1029. doi: 10.1038/ng.3362. Epub 2015 Jul 27. PMID: 26214592; PMCID: PMC4603357. KRATZ CP, FRANKE L, PETERS H, KOHLSCHMIDT N, KAZMIERCZAK B, FINCKH U, BIER A, EICHHORN B, BLANK C, KRAUS C, KOHLHASE J, PAULI S, WILDHARDT G, KUTSCHE K, AUBER B, CHRISTMANN A, BACHMANN N, MITTER D, CREMER FW, MAYER K, DAUMER-HAAS C, NEVINNY-STICKEL-HINZPETER C, OEFFNER F, SCHLÜTER G, GENCIK M, ÜBERLACKER B, LISSEWSKI C, SCHANZE I, GREENE MH, SPIX C, ZENKER M. Cancer spectrum and frequency among children with Noonan, Costello, and cardio-facio-cutaneous syndromes. Br J Cancer. 2015 Apr 14;112(8):1392-7. doi: 10.1038/bjc.2015.75. Epub 2015 Mar 5. PMID: 25742478; PMCID: PMC4402457. KRATZ CP, EDELMAN DC, WANG Y, MELTZER PS, GREENE MH. Genetic and epigenetic analysis of monozygotic twins discordant for testicular cancer. Int J Mol Epidemiol Genet. 2014 Oct 22;5(3):135-9. PMID: 25379132; PMCID: PMC4214260. MUELLER CM, KORDE LA, MCMASTER ML, PETERS JA, BRATSLAVSKY G, WATKINS RJ, LING A, KRATZ CP, WULFSBERG EA, ROSENBERG PS, GREENE MH. Familial testicular germ cell tumor: no associated syndromic pattern identified. Hered Cancer Clin Pract. 2014 Feb 21;12(1):3. doi: 10.1186/1897-4287-12-3. PMID: 24559313; PMCID: PMC3937045. VASEN HF, GHORBANOGHLI Z, BOURDEAUT F, CABARET O, CARON O, DUVAL A, ENTZ-WERLE N, GOLDBERG Y, ILENCIKOVA D, KRATZ CP, LAVOINE N, LOEFFEN J, MENKO FH, MULERIS M, SEBILLE G, COLAS C, BURKHARDT B, BRUGIERES L, WIMMER K; EU-CONSORTIUM CARE FOR CMMR-D (C4CMMR-D). Guidelines for surveillance of individuals with constitutional mismatch repair-deficiency proposed by the European Consortium "Care for CMMR-D" (C4CMMR-D). J Med Genet. 2014 May;51(5):283-93. doi: 10.1136/jmedgenet-2013-102238. Epub 2014 Feb 20. PMID: 24556086. WIMMER K, KRATZ CP, VASEN HF, CARON O, COLAS C, ENTZ-WERLE N, GERDES AM, GOLDBERG Y, ILENCIKOVA D, MULERIS M, DUVAL A, LAVOINE N, RUIZ-PONTE C, SLAVC I, BURKHARDT B, BRUGIERES L; EU-CONSORTIUM CARE FOR CMMRD (C4CMMRD). Diagnostic criteria for constitutional mismatch repair deficiency syndrome: suggestions of the European consortium 'care for CMMRD' (C4CMMRD). J Med Genet. 2014 Jun;51(6):355-65. doi: 10.1136/jmedgenet-2014-102284. Epub 2014 Apr 15. PMID: 24737826. AZEVEDO MF, HORVATH A, BORNSTEIN ER, ALMEIDA MQ, XEKOUKI P, FAUCZ FR, GOURGARI E, NADELLA K, REMMERS EF, QUEZADO M, DE ALEXANDRE RB, KRATZ CP, NESTEROVA M, GREENE MH, STRATAKIS CA. Cyclic AMP and c-KIT signaling in familial testicular germ cell tumor predisposition. J Clin Endocrinol Metab. 2013 Aug;98(8):E1393-400. doi: 10.1210/jc.2012-2838. Epub 2013 Jun 14. PMID: 23771924; PMCID: PMC3733859. CHUNG CC, KANETSKY PA, WANG Z, HILDEBRANDT MA, KOSTER R, SKOTHEIM RI, KRATZ CP, TURNBULL C, CORTESSIS VK, BAKKEN AC, BISHOP DT, COOK MB, ERICKSON RL, FOSSÅ SD, JACOBS KB, KORDE LA, KRAGGERUD SM, LOTHE RA, LOUD JT, RAHMAN N, SKINNER EC, THOMAS DC, WU X, YEAGER M, SCHUMACHER FR, GREENE MH, SCHWARTZ SM, MCGLYNN KA, CHANOCK SJ, NATHANSON KL. Meta-analysis identifies four new loci associated with testicular germ cell tumor. Nat Genet. 2013 Jun;45(6):680-5. doi: 10.1038/ng.2634. Epub 2013 May 12. PMID: 23666239; PMCID: PMC3723930. FARGO JH, KRATZ CP, GIRI N, SAVAGE SA, WONG C, BACKER K, ALTER BP, GLADER B. Erythrocyte adenosine deaminase: diagnostic value for Diamond-Blackfan anaemia. Br J Haematol. 2013 Feb;160(4):547-54. doi: 10.1111/bjh.12167. Epub 2012 Dec 17. PMID: 23252420; PMCID: PMC3609920. GERMESHAUSEN M, DEERBERG S, PETER Y, REIMER C, KRATZ CP, BALLMAIER M. The spectrum of ELANE mutations and their implications in severe congenital and cyclic neutropenia. 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PMID: 20949621; PMCID: PMC3117284. KRATZ CP, BRATSLAVSKY G, SHI J. The clinical utility of testicular cancer risk loci. Genome Med. 2011 Jan 21;3(1):1. doi: 10.1186/gm215. PMID: 21255381; PMCID: PMC3092086. KRATZ CP, GREENE MH, BRATSLAVSKY G, SHI J. A stratified genetic risk assessment for testicular cancer. Int J Androl. 2011 Aug;34(4 Pt 2):e98-102. doi: 10.1111/j.1365-2605.2011.01156.x. Epub 2011 May 12. PMID: 21564132; PMCID: PMC3145032. KRATZ CP, HAN SS, ROSENBERG PS, BERNDT SI, BURDETT L, YEAGER M, KORDE LA, MAI PL, PFEIFFER R, GREENE MH. Variants in or near KITLG, BAK1, DMRT1, and TERT-CLPTM1L predispose to familial testicular germ cell tumour. J Med Genet. 2011 Jul;48(7):473-6. doi: 10.1136/jmedgenet-2011-100001. Epub 2011 May 26. PMID: 21617256; PMCID: PMC3131696. KRATZ CP, RAPISUWON S, REED H, HASLE H, ROSENBERG PS. Cancer in Noonan, Costello, cardiofaciocutaneous and LEOPARD syndromes. Am J Med Genet C Semin Med Genet. 2011 May 15;157C(2):83-9. doi: 10.1002/ajmg.c.30300. 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Best Pract Res Clin Endocrinol Metab. 2010 Jun;24(3):503-13. doi: 10.1016/j.beem.2010.01.005. PMID: 20833340; PMCID: PMC2939736. SAVOIA A, GERMESHAUSEN M, DE ROCCO D, HENSCHEL B, KRATZ CP, KUHLEN M, RATH B, STEUHL KP, WERMES C, BALLMAIER M. MYH9-related disease: Report on five German families and description of a novel mutation. Ann Hematol. 2010 Oct;89(10):1057-9. doi: 10.1007/s00277-010-0928-y. Epub 2010 Mar 10. PMID: 20221761. WIMMER K, KRATZ CP. Constitutional mismatch repair-deficiency syndrome. Haematologica. 2010 May;95(5):699-701. doi: 10.3324/haematol.2009.021626. PMID: 20442441; PMCID: PMC2864372. BOZTUG K, APPASWAMY G, ASHIKOV A, SCHÄFFER AA, SALZER U, DIESTELHORST J, GERMESHAUSEN M, BRANDES G, LEE-GOSSLER J, NOYAN F, GATZKE AK, MINKOV M, GREIL J, KRATZ C, PETROPOULOU T, PELLIER I, BELLANNÉ-CHANTELOT C, REZAEI N, MÖNKEMÖLLER K, IRANI-HAKIMEH N, BAKKER H, GERARDY-SCHAHN R, ZEIDLER C, GRIMBACHER B, WELTE K, KLEIN C. A syndrome with congenital neutropenia and mutations in G6PC3. N Engl J Med. 2009 Jan 1;360(1):32-43. doi: 10.1056/NEJMoa0805051. Erratum in: N Engl J Med. 2011 Apr 28;364(17):1682. PMID: 19118303; PMCID: PMC2778311. GERMESHAUSEN M, KRATZ CP, BALLMAIER M, WELTE K. RAS and CSF3R mutations in severe congenital neutropenia. Blood. 2009 Oct 15;114(16):3504-5. doi: 10.1182/blood-2009-07-232512. PMID: 19833857. KRATZ CP, HOLTER S, ETZLER J, LAUTEN M, POLLETT A, NIEMEYER CM, GALLINGER S, WIMMER K. Rhabdomyosarcoma in patients with constitutional mismatch-repair-deficiency syndrome. J Med Genet. 2009 Jun;46(6):418-20. doi: 10.1136/jmg.2008.064212. Epub 2009 Mar 16. PMID: 19293170. KRATZ CP, ZAMPINO G, KRIEK M, KANT SG, LEONI C, PANTALEONI F, OUDESLUYS-MURPHY AM, DI ROCCO C, KLOSKA SP, TARTAGLIA M, ZENKER M. Craniosynostosis in patients with Noonan syndrome caused by germline KRAS mutations. Am J Med Genet A. 2009 May;149A(5):1036-40. doi: 10.1002/ajmg.a.32786. PMID: 19396835. YANG Z, KONDO T, VOORHORST CS, NABINGER SC, NDONG L, YIN F, CHAN EM, YU M, WÜRSTLIN O, KRATZ CP, NIEMEYER CM, FLOTHO C, HASHINO E, CHAN RJ. Increased c-Jun expression and reduced GATA2 expression promote aberrant monocytic differentiation induced by activating PTPN11 mutants. Mol Cell Biol. 2009 Aug;29(16):4376-93. doi: 10.1128/MCB.01330-08. Epub 2009 Jun 15. PMID: 19528235; PMCID: PMC2725726. ARCHAMBEAULT S, FLORES NJ, YOSHIMI A, KRATZ CP, REISING M, FISCHER A, NOELLKE P, LOCATELLI F, SEDLACEK P, FLOTHO C, ZECCA M, EMANUEL PD, CASTLEBERRY RP, NIEMEYER CM, BADER P, LOH ML. Development of an allele-specific minimal residual disease assay for patients with juvenile myelomonocytic leukemia. Blood. 2008 Feb 1;111(3):1124-7. doi: 10.1182/blood-2007-06-093302. Epub 2007 Nov 13. PMID: 18000165; PMCID: PMC2214753. CHAN RJ, COOPER T, KRATZ CP, WEISS B, LOH ML. Juvenile myelomonocytic leukemia: a report from the 2nd International JMML Symposium. Leuk Res. 2009 Mar;33(3):355-62. doi: 10.1016/j.leukres.2008.08.022. Epub 2008 Oct 26. PMID: 18954903; PMCID: PMC2692866. ETZLER J, PEYRL A, ZATKOVA A, SCHILDHAUS HU, FICEK A, MERKELBACH-BRUSE S, KRATZ CP, ATTARBASCHI A, HAINFELLNER JA, YAO S, MESSIAEN L, SLAVC I, WIMMER K. RNA-based mutation analysis identifies an unusual MSH6 splicing defect and circumvents PMS2 pseudogene interference. Hum Mutat. 2008 Feb;29(2):299-305. doi: 10.1002/humu.20657. PMID: 18030674. FLOTHO C, KRATZ CP, BERGSTRÄSSER E, HASLE H, STARÝ J, TREBO M, VAN DEN HEUVEL-EIBRINK MM, WÓJCIK D, ZECCA M, LOCATELLI F, NIEMEYER CM; EUROPEAN WORKING GROUP OF MYELODYSPLASTIC SYNDROMES IN CHILDHOOD. Genotype-phenotype correlation in cases of juvenile myelomonocytic leukemia with clonal RAS mutations. Blood. 2008 Jan 15;111(2):966-7; author reply 967-8. doi: 10.1182/blood-2007-09-111831. PMID: 18182584. KAROW A, WALLER C, REIMANN C, NIEMEYER CM, KRATZ CP. JAK2 mutations other than V617F: a novel mutation and mini review. Leuk Res. 2008 Feb;32(2):365-6. doi: 10.1016/j.leukres.2007.02.018. Epub 2007 Apr 26. PMID: 17466371. KRATZ CP, NIEMEYER CM, KAROW A, VOLZ-FLECKENSTEIN M, SCHMITT-GRÄFF A, STRAHM B. Congenital transfusion-dependent anemia and thrombocytopenia with myelodysplasia due to a recurrent GATA1(G208R) germline mutation. Leukemia. 2008 Feb;22(2):432-4. doi: 10.1038/sj.leu.2404904. Epub 2007 Aug 23. PMID: 17713552. LAUX D, KRATZ C, SAUERBREY A. Common acute lymphoblastic leukemia in a girl with genetically confirmed LEOPARD syndrome. J Pediatr Hematol Oncol. 2008 Aug;30(8):602-4. doi: 10.1097/MPH.0b013e31817588fb. PMID: 18799937. NIEMEYER CM, KRATZ CP. Paediatric myelodysplastic syndromes and juvenile myelomonocytic leukaemia: molecular classification and treatment options. Br J Haematol. 2008 Mar;140(6):610-24. doi: 10.1111/j.1365-2141.2007.06958.x. PMID: 18302710. PÉRON S, METIN A, GARDÈS P, ALYANAKIAN MA, SHERIDAN E, KRATZ CP, FISCHER A, DURANDY A. Human PMS2 deficiency is associated with impaired immunoglobulin class switch recombination. J Exp Med. 2008 Oct 27;205(11):2465-72. doi: 10.1084/jem.20080789. Epub 2008 Sep 29. PMID: 18824584; PMCID: PMC2571921. PFISTER S, JANZARIK WG, REMKE M, ERNST A, WERFT W, BECKER N, TOEDT G, WITTMANN A, KRATZ C, OLBRICH H, AHMADI R, THIEME B, JOOS S, RADLWIMMER B, KULOZIK A, PIETSCH T, HEROLD-MENDE C, GNEKOW A, REIFENBERGER G, KORSHUNOV A, SCHEURLEN W, OMRAN H, LICHTER P. BRAF gene duplication constitutes a mechanism of MAPK pathway activation in low-grade astrocytomas. J Clin Invest. 2008 May;118(5):1739-49. doi: 10.1172/JCI33656. PMID: 18398503; PMCID: PMC2289793. SCHUBBERT S, BOLLAG G, LYUBYNSKA N, NGUYEN H, KRATZ CP, ZENKER M, NIEMEYER CM, MOLVEN A, SHANNON K. Biochemical and functional characterization of germ line KRAS mutations. Mol Cell Biol. 2007 Nov;27(22):7765-70. doi: 10.1128/MCB.00965-07. Epub 2007 Sep 17. PMID: 17875937; PMCID: PMC2169154. DE VRIES AC, STAM RW, KRATZ CP, ZENKER M, NIEMEYER CM, VAN DEN HEUVEL-EIBRINK MM; EUROPEAN WORKING GROUP ON CHILDHOOD MDS (EWOG-MDS). Mutation analysis of the BRAF oncogene in juvenile myelomonocytic leukemia. Haematologica. 2007 Nov;92(11):1574-5. doi: 10.3324/haematol.11493. PMID: 18024410. DE VRIES AC, STAM RW, SCHNEIDER P, NIEMEYER CM, VAN WERING ER, HAAS OA, KRATZ CP, DEN BOER ML, PIETERS R, VAN DEN HEUVEL-EIBRINK MM. Role of mutation independent constitutive activation of FLT3 in juvenile myelomonocytic leukemia. Haematologica. 2007 Nov;92(11):1557-60. doi: 10.3324/haematol.11201. PMID: 18024405. EL-MONEIM AA, KRATZ CP, BÖLL S, RISTER M, PAHL HL, NIEMEYER CM. Essential versus reactive thrombocythemia in children: retrospective analyses of 12 cases. Pediatr Blood Cancer. 2007 Jul;49(1):52-5. doi: 10.1002/pbc.21128. PMID: 17171694. FLOTHO C, KRATZ C, NIEMEYER CM. Targeting RAS signaling pathways in juvenile myelomonocytic leukemia. Curr Drug Targets. 2007 Jun;8(6):715-25. doi: 10.2174/138945007780830773. PMID: 17584027. FLOTHO C, KRATZ CP, NIEMEYER CM. How a rare pediatric neoplasia can give important insights into biological concepts: a perspective on juvenile myelomonocytic leukemia. Haematologica. 2007 Nov;92(11):1441-6. doi: 10.3324/haematol.11280. PMID: 18024390. FLOTHO C, STEINEMANN D, MULLIGHAN CG, NEALE G, MAYER K, KRATZ CP, SCHLEGELBERGER B, DOWNING JR, NIEMEYER CM. Genome-wide single-nucleotide polymorphism analysis in juvenile myelomonocytic leukemia identifies uniparental disomy surrounding the NF1 locus in cases associated with neurofibromatosis but not in cases with mutant RAS or PTPN11. Oncogene. 2007 Aug 23;26(39):5816-21. doi: 10.1038/sj.onc.1210361. Epub 2007 Mar 12. PMID: 17353900. HINDERSIN S, NIEMEYER CM, GERMING U, GÖBEL U, KRATZ CP. Mutation analysis of CUTL1 in childhood myeloid neoplasias with monosomy 7. Leuk Res. 2007 Sep;31(9):1323-4. doi: 10.1016/j.leukres.2006.10.021. Epub 2006 Nov 30. PMID: 17140660. JANZARIK WG, KRATZ CP, LOGES NT, OLBRICH H, KLEIN C, SCHÄFER T, SCHEURLEN W, ROGGENDORF W, WEILLER C, NIEMEYER C, KORINTHENBERG R, PFISTER S, OMRAN H. Further evidence for a somatic KRAS mutation in a pilocytic astrocytoma. Neuropediatrics. 2007 Apr;38(2):61-3. doi: 10.1055/s-2007-984451. PMID: 17712732. KAROW A, STEINEMANN D, GÖHRING G, HASLE H, GREINER J, HARILA-SAARI A, FLOTHO C, ZENKER M, SCHLEGELBERGER B, NIEMEYER CM, KRATZ CP. Clonal duplication of a germline PTPN11 mutation due to acquired uniparental disomy in acute lymphoblastic leukemia blasts from a patient with Noonan syndrome. Leukemia. 2007 Jun;21(6):1303-5. doi: 10.1038/sj.leu.2404651. Epub 2007 Mar 15. PMID: 17361219. KRATZ CP, NIEMEYER CM, JÜTTNER E, KARTAL M, WENINGER A, SCHMITT-GRAEFF A, KONTNY U, LAUTEN M, UTZOLINO S, RÄDECKE J, FONATSCH C, WIMMER K. Childhood T-cell non-Hodgkin's lymphoma, colorectal carcinoma and brain tumor in association with café-au-lait spots caused by a novel homozygous PMS2 mutation. Leukemia. 2008 May;22(5):1078-80. doi: 10.1038/sj.leu.2405008. Epub 2007 Nov 15. PMID: 18007577. KRATZ CP, NIEMEYER CM, THOMAS C, BAUHUBER S, MATEJAS V, BERGSTRÄSSER E, FLOTHO C, FLORES NJ, HAAS O, HASLE H, VAN DEN HEUVEL-EIBRINK MM, KUCHERLAPATI RS, LANG P, ROBERTS AE, STARÝ J, STRAHM B, SWANSON KD, TREBO M, ZECCA M, NEEL B, LOCATELLI F, LOH ML, ZENKER M. Mutation analysis of Son of Sevenless in juvenile myelomonocytic leukemia. Leukemia. 2007 May;21(5):1108-9. doi: 10.1038/sj.leu.2404620. Epub 2007 Feb 22. PMID: 17315019. KRATZ CP, NIEMEYER CM, ZENKER M. An unexpected new role of mutant Ras: perturbation of human embryonic development. J Mol Med (Berl). 2007 Mar;85(3):227-35. doi: 10.1007/s00109-006-0135-4. Epub 2007 Jan 9. PMID: 17211612; PMCID: PMC1820751. KRATZ CP, STEINEMANN D, NIEMEYER CM, SCHLEGELBERGER B, KOSCIELNIAK E, KONTNY U, ZENKER M. Uniparental disomy at chromosome 11p15.5 followed by HRAS mutations in embryonal rhabdomyosarcoma: lessons from Costello syndrome. Hum Mol Genet. 2007 Feb 15;16(4):374-9. doi: 10.1093/hmg/ddl458. Epub 2006 Dec 12. Erratum in: Hum Mol Genet. 2007 Nov 15;16(22):2781. PMID: 17164262. PEIXOTO NC, KRATZ CP, ROZA T, MORSCH VM, PEREIRA ME. Effects of HgCl2 on porphobilinogen-synthase (E.C. 4.2.1.24) activity and on mercury levels in rats exposed during different precocious periods of postnatal life. Cell Biol Int. 2007 Sep;31(9):1057-62. doi: 10.1016/j.cellbi.2007.03.026. Epub 2007 Mar 28. PMID: 17490898. VAN DER BURGT I, KUPSKY W, STASSOU S, NADROO A, BARROSO C, DIEM A, KRATZ CP, DVORSKY R, AHMADIAN MR, ZENKER M. Myopathy caused by HRAS germline mutations: implications for disturbed myogenic differentiation in the presence of constitutive HRas activation. J Med Genet. 2007 Jul;44(7):459-62. doi: 10.1136/jmg.2007.049270. Epub 2007 Apr 5. PMID: 17412879; PMCID: PMC2598013. YETGIN S, AYTAC S, KALKANOGLU S, COSKUN T, ORTMANN C, KRATZ C, NIEMEYER C. Biotinidase deficiency and juvenile myelomonocytic leukemia in a Turkish infant of consanguineous parents. Pediatr Hematol Oncol. 2007 Sep;24(6):453-5. doi: 10.1080/08880010701451293. PMID: 17710663. ZENKER M, HORN D, WIECZOREK D, ALLANSON J, PAULI S, VAN DER BURGT I, DOERR HG, GASPAR H, HOFBECK M, GILLESSEN-KAESBACH G, KOCH A, MEINECKE P, MUNDLOS S, NOWKA A, RAUCH A, REIF S, VON SCHNAKENBURG C, SEIDEL H, WEHNER LE, ZWEIER C, BAUHUBER S, MATEJAS V, KRATZ CP, THOMAS C, KUTSCHE K. SOS1 is the second most common Noonan gene but plays no major role in cardio-facio-cutaneous syndrome. J Med Genet. 2007 Oct;44(10):651-6. doi: 10.1136/jmg.2007.051276. Epub 2007 Jun 23. PMID: 17586837; PMCID: PMC2597961. ZENKER M, LEHMANN K, SCHULZ AL, BARTH H, HANSMANN D, KOENIG R, KORINTHENBERG R, KREISS-NACHTSHEIM M, MEINECKE P, MORLOT S, MUNDLOS S, QUANTE AS, RASKIN S, SCHNABEL D, WEHNER LE, KRATZ CP, HORN D, KUTSCHE K. Expansion of the genotypic and phenotypic spectrum in patients with KRAS germline mutations. J Med Genet. 2007 Feb;44(2):131-5. doi: 10.1136/jmg.2006.046300. Epub 2006 Oct 20. PMID: 17056636; PMCID: PMC2598066. KRATZ CP, BÖLL S, KONTNY U, SCHRAPPE M, NIEMEYER CM, STANULLA M. Mutational screen reveals a novel JAK2 mutation, L611S, in a child with acute lymphoblastic leukemia. Leukemia. 2006 Feb;20(2):381-3. doi: 10.1038/sj.leu.2404060. PMID: 16341038. KRATZ CP, NATHRATH M, FREISINGER P, DRESSEL P, ASSMUSS HP, KLEIN C, YOSHIMI A, BURDACH S, NIEMEYER CM. Lethal proliferation of erythroid precursors in a neonate with a germline PTPN11 mutation. Eur J Pediatr. 2006 Mar;165(3):182-5. doi: 10.1007/s00431-005-0031-x. Epub 2005 Dec 21. PMID: 16369799. KRATZ CP, SCHUBBERT S, BOLLAG G, NIEMEYER CM, SHANNON KM, ZENKER M. Germline mutations in components of the Ras signaling pathway in Noonan syndrome and related disorders. Cell Cycle. 2006 Aug;5(15):1607-11. doi: 10.4161/cc.5.15.3128. Epub 2006 Aug 1. PMID: 16921267. ORTMANN CA, NIEMEYER CM, WAWER A, EBELL W, BAUMANN I, KRATZ CP. TERC mutations in children with refractory cytopenia. Haematologica. 2006 May;91(5):707-8. PMID: 16670076. REIMANN C, AROLA M, BIERINGS M, KAROW A, VAN DEN HEUVEL-EIBRINK MM, HASLE H, NIEMEYER CM, KRATZ CP. A novel somatic K-Ras mutation in juvenile myelomonocytic leukemia. Leukemia. 2006 Sep;20(9):1637-8. doi: 10.1038/sj.leu.2404303. Epub 2006 Jul 6. PMID: 16826224. SCHUBBERT S, ZENKER M, ROWE SL, BÖLL S, KLEIN C, BOLLAG G, VAN DER BURGT I, MUSANTE L, KALSCHEUER V, WEHNER LE, NGUYEN H, WEST B, ZHANG KY, SISTERMANS E, RAUCH A, NIEMEYER CM, SHANNON K, KRATZ CP. Germline KRAS mutations cause Noonan syndrome. Nat Genet. 2006 Mar;38(3):331-6. doi: 10.1038/ng1748. Epub 2006 Feb 12. Erratum in: Nat Genet. 2006 May;38(5):598. PMID: 16474405. CURTISS NP, BONIFAS JM, LAUCHLE JO, BALKMAN JD, KRATZ CP, EMERLING BM, GREEN ED, LE BEAU MM, SHANNON KM. Isolation and analysis of candidate myeloid tumor suppressor genes from a commonly deleted segment of 7q22. Genomics. 2005 May;85(5):600-7. doi: 10.1016/j.ygeno.2005.01.013. PMID: 15820312. GERMESHAUSEN M, SCHULZE H, KRATZ C, WILKENS L, REPP R, SHANNON K, WELTE K, BALLMAIER M. An acquired G-CSF receptor mutation results in increased proliferation of CMML cells from a patient with severe congenital neutropenia. Leukemia. 2005 Apr;19(4):611-7. doi: 10.1038/sj.leu.2403663. PMID: 15729385. KRATZ CP, NIEMEYER CM, CASTLEBERRY RP, CETIN M, BERGSTRÄSSER E, EMANUEL PD, HASLE H, KARDOS G, KLEIN C, KOJIMA S, STARY J, TREBO M, ZECCA M, GELB BD, TARTAGLIA M, LOH ML. The mutational spectrum of PTPN11 in juvenile myelomonocytic leukemia and Noonan syndrome/myeloproliferative disease. Blood. 2005 Sep 15;106(6):2183-5. doi: 10.1182/blood-2005-02-0531. Epub 2005 May 31. PMID: 15928039; PMCID: PMC1895140. KRATZ CP, NIEMEYER CM. Juvenile myelomonocytic leukemia. Hematology. 2005;10 Suppl 1:100-3. doi: 10.1080/10245330512331390078. PMID: 16188648. KRATZ CP, ROGGE T, KOPP M, BAUMANN I, NIEMEYER CM. Myelodysplastic features in an infant with cystic fibrosis presenting with anaemia, oedema and failure to thrive. Eur J Pediatr. 2005 Jan;164(1):56-7. doi: 10.1007/s00431-004-1548-0. Epub 2004 Oct 23. PMID: 15517378. NIEMEYER CM, KRATZ CP, HASLE H. Pediatric myelodysplastic syndromes. Curr Treat Options Oncol. 2005 May;6(3):209-14. doi: 10.1007/s11864-005-0004-3. PMID: 15869732. NIEMEYER CM, KRATZ CP. Is granulocyte colony-stimulating factor therapy a risk factor for myelodysplasia/leukemia in patients with congenital neutropenia? Haematologica. 2005 Jan;90(1):2-3. PMID: 15644298. KRATZ CP, ABD EL-MONHEIM A, MANKE EM, RISTER M, ROGGE T, NIEMEYER CM. Retrospektive Analyse des klinischen Verlaufs bei 12 Kindern mit der Verdachtsdiagnose einer essenziellen Thrombozythämie [Retrospective analysis of the clinical course of 12 children given the diagnosis essential thrombocythemia]. Klin Padiatr. 2004 Nov-Dec;216(6):349-55. German. doi: 10.1055/s-2004-832356. PMID: 15565550. KRATZ CP, ANTONIETTI L, SHANNON KM, DOLE MG, FRIEBERT SE. Acute myeloid leukemia associated with t(8;21) or trisomy 8 in children with neurofibromatosis, type 1. J Pediatr Hematol Oncol. 2003 Apr;25(4):343. doi: 10.1097/00043426-200304000-00018. PMID: 12679655. KRATZ CP, NIEHUES T, LYDING S, HEUSCH A, JANSSEN G, GÖBEL U. Evans syndrome in a patient with chromosome 22q11.2 deletion syndrome: a case report. Pediatr Hematol Oncol. 2003 Mar;20(2):167-72. doi: 10.1080/0880010390158685. PMID: 12554529. KRATZ CP, SCHWEIGER B, KEMPERDICK H, GÖBEL U. Childhood multifocal skeletal non-Hodgkin lymphoma is a differential diagnosis of battered child syndrome. Pediatr Hematol Oncol. 2003 Dec;20(8):575-7. PMID: 14578025. NIEMEYER CM, KRATZ C. Juvenile myelomonocytic leukemia. Curr Oncol Rep. 2003 Nov;5(6):510-5. doi: 10.1007/s11912-003-0013-y. PMID: 14521811. NIEMEYER CM, KRATZ C. Juvenile myelomonocytic leukemia. Curr Treat Options Oncol. 2003 Jun;4(3):203-10. doi: 10.1007/s11864-003-0021-z. PMID: 12718797. EMERLING BM, BONIFAS J, KRATZ CP, DONOVAN S, TAYLOR BR, GREEN ED, LE BEAU MM, SHANNON KM. MLL5, a homolog of Drosophila trithorax located within a segment of chromosome band 7q22 implicated in myeloid leukemia. Oncogene. 2002 Jul 18;21(31):4849-54. doi: 10.1038/sj.onc.1205615. PMID: 12101424. KRATZ CP, EMERLING BM, BONIFAS J, WANG W, GREEN ED, LE BEAU MM, SHANNON KM. Genomic structure of the PIK3CG gene on chromosome band 7q22 and evaluation as a candidate myeloid tumor suppressor. Blood. 2002 Jan 1;99(1):372-4. doi: 10.1182/blood.v99.1.372. PMID: 11756194. KRATZ CP, EMERLING BM, DONOVAN S, LAIG-WEBSTER M, TAYLOR BR, THOMPSON P, JENSEN S, BANERJEE A, BONIFAS J, MAKALOWSKI W, GREEN ED, LE BEAU MM, SHANNON KM. Candidate gene isolation and comparative analysis of a commonly deleted segment of 7q22 implicated in myeloid malignancies. Genomics. 2001 Oct;77(3):171-80. doi: 10.1006/geno.2001.6636. PMID: 11597142. KRATZ C, MAUZ-KÖRHOLZ C, KRUCK H, KÖRHOLZ D, GÖBEL U. Detection of antiphospholipid antibodies in children and adolescents. Pediatr Hematol Oncol. 1998 Jul-Aug;15(4):325-32. doi: 10.3109/08880019809014016. PMID: 9658433. GRÖBNER SN, WORST BC, WEISCHENFELDT J, BUCHHALTER I, KLEINHEINZ K, RUDNEVA VA, JOHANN PD, BALASUBRAMANIAN GP, SEGURA-WANG M, BRABETZ S, BENDER S, HUTTER B, STURM D, PFAFF E, HÜBSCHMANN D, ZIPPRICH G, HEINOLD M, EILS J, LAWERENZ C, ERKEK S, LAMBO S, WASZAK S, BLATTMANN C, BORKHARDT A, KUHLEN M, EGGERT A, FULDA S, GESSLER M, WEGERT J, KAPPLER R, BAUMHOER D, BURDACH S, KIRSCHNER-SCHWABE R, KONTNY U, KULOZIK AE, LOHMANN D, HETTMER S, ECKERT C, BIELACK S, NATHRATH M, NIEMEYER C, RICHTER GH, SCHULTE J, SIEBERT R, WESTERMANN F, MOLENAAR JJ, VASSAL G, WITT H; ICGC PEDBRAIN-SEQ PROJECT; ICGC MMML-SEQ PROJECT, BURKHARDT B, KRATZ CP, WITT O, VAN TILBURG CM, KRAMM CM, FLEISCHHACK G, DIRKSEN U, RUTKOWSKI S, FRÜHWALD M, VON HOFF K, WOLF S, KLINGEBIEL T, KOSCIELNIAK E, LANDGRAF P, KOSTER J, RESNICK AC, ZHANG J, LIU Y, ZHOU X, WAANDERS AJ, ZWIJNENBURG DA, RAMAN P, BRORS B, WEBER UD, NORTHCOTT PA, PAJTLER KW, KOOL M, PIRO RM, KORBEL JO, SCHLESNER M, EILS R, JONES DTW, LICHTER P, CHAVEZ L, ZAPATKA M, PFISTER SM. The landscape of genomic alterations across childhood cancers. Nature. 2018 Mar 15;555(7696):321-327. doi: 10.1038/nature25480. Epub 2018 Feb 28. Erratum in: Nature. 2018 Jul;559(7714):E10. PMID: 29489754. RIPPERGER T, BIELACK SS, BORKHARDT A, BRECHT IB, BURKHARDT B, CALAMINUS G, DEBATIN KM, DEUBZER H, DIRKSEN U, ECKERT C, EGGERT A, ERLACHER M, FLEISCHHACK G, FRÜHWALD MC, GNEKOW A, GOEHRING G, GRAF N, HANENBERG H, HAUER J, HERO B, HETTMER S, VON HOFF K, HORSTMANN M, HOYER J, ILLIG T, KAATSCH P, KAPPLER R, KERL K, KLINGEBIEL T, KONTNY U, KORDES U, KÖRHOLZ D, KOSCIELNIAK E, KRAMM CM, KUHLEN M, KULOZIK AE, LAMOTTKE B, LEUSCHNER I, LOHMANN DR, MEINHARDT A, METZLER M, MEYER LH, MOSER O, NATHRATH M, NIEMEYER CM, NUSTEDE R, PAJTLER KW, PARET C, RASCHE M, REINHARDT D, RIESS O, RUSSO A, RUTKOWSKI S, SCHLEGELBERGER B, SCHNEIDER D, SCHNEPPENHEIM R, SCHRAPPE M, SCHROEDER C, VON SCHWEINITZ D, SIMON T, SPARBER-SAUER M, SPIX C, STANULLA M, STEINEMANN D, STRAHM B, TEMMING P, THOMAY K, VON BUEREN AO, VORWERK P, WITT O, WLODARSKI M, WÖSSMANN W, ZENKER M, ZIMMERMANN S, PFISTER SM, KRATZ CP. Childhood cancer predisposition syndromes-A concise review and recommendations by the Cancer Predisposition Working Group of the Society for Pediatric Oncology and Hematology. Am J Med Genet A. 2017 Apr;173(4):1017-1037. doi: 10.1002/ajmg.a.38142. Epub 2017 Feb 7. PMID: 28168833. WANG Z, ZHU B, ZHANG M, PARIKH H, JIA J, CHUNG CC, SAMPSON JN, HOSKINS JW, HUTCHINSON A, BURDETTE L, IBRAHIM A, HAUTMAN C, RAJ PS, ABNET CC, ADJEI AA, AHLBOM A, ALBANES D, ALLEN NE, AMBROSONE CB, ALDRICH M, AMIANO P, AMOS C, ANDERSSON U, ANDRIOLE G JR, ANDRULIS IL, ARICI C, ARSLAN AA, AUSTIN MA, BARIS D, BARKAUSKAS DA, BASSIG BA, BEANE FREEMAN LE, BERG CD, BERNDT SI, BERTAZZI PA, BIRITWUM RB, BLACK A, BLOT W, BOEING H, BOFFETTA P, BOLTON K, BOUTRON-RUAULT MC, BRACCI PM, BRENNAN P, BRINTON LA, BROTZMAN M, BUENO-DE-MESQUITA HB, BURING JE, BUTLER MA, CAI Q, CANCEL-TASSIN G, CANZIAN F, CAO G, CAPORASO NE, CARRATO A, CARREON T, CARTA A, CHANG GC, CHANG IS, CHANG-CLAUDE J, CHE X, CHEN CJ, CHEN CY, CHEN CH, CHEN C, CHEN KY, CHEN YM, CHOKKALINGAM AP, CHU LW, CLAVEL-CHAPELON F, COLDITZ GA, COLT JS, CONTI D, COOK MB, CORTESSIS VK, CRAWFORD ED, CUSSENOT O, DAVIS FG, DE VIVO I, DENG X, DING T, DINNEY CP, DI STEFANO AL, DIVER WR, DUELL EJ, ELENA JW, FAN JH, FEIGELSON HS, FEYCHTING M, FIGUEROA JD, FLANAGAN AM, FRAUMENI JF JR, FREEDMAN ND, FRIDLEY BL, FUCHS CS, GAGO-DOMINGUEZ M, GALLINGER S, GAO YT, GAPSTUR SM, GARCIA-CLOSAS M, GARCIA-CLOSAS R, GASTIER-FOSTER JM, GAZIANO JM, GERHARD DS, GIFFEN CA, GILES GG, GILLANDERS EM, GIOVANNUCCI EL, GOGGINS M, GOKGOZ N, GOLDSTEIN AM, GONZALEZ C, GORLICK R, GREENE MH, GROSS M, GROSSMAN HB, GRUBB R 3RD, GU J, GUAN P, HAIMAN CA, HALLMANS G, HANKINSON SE, HARRIS CC, HARTGE P, HATTINGER C, HAYES RB, HE Q, HELMAN L, HENDERSON BE, HENRIKSSON R, HOFFMAN-BOLTON J, HOHENSEE C, HOLLY EA, HONG YC, HOOVER RN, HOSGOOD HD 3RD, HSIAO CF, HSING AW, HSIUNG CA, HU N, HU W, HU Z, HUANG MS, HUNTER DJ, INSKIP PD, ITO H, JACOBS EJ, JACOBS KB, JENAB M, JI BT, JOHANSEN C, JOHANSSON M, JOHNSON A, KAAKS R, KAMAT AM, KAMINENI A, KARAGAS M, KHANNA C, KHAW KT, KIM C, KIM IS, KIM JH, KIM YH, KIM YC, KIM YT, KANG CH, JUNG YJ, KITAHARA CM, KLEIN AP, KLEIN R, KOGEVINAS M, KOH WP, KOHNO T, KOLONEL LN, KOOPERBERG C, KRATZ CP, KROGH V, KUNITOH H, KURTZ RC, KURUCU N, LAN Q, LATHROP M, LAU CC, LECANDA F, LEE KM, LEE MP, LE MARCHAND L, LERNER SP, LI D, LIAO LM, LIM WY, LIN D, LIN J, LINDSTROM S, LINET MS, LISSOWSKA J, LIU J, LJUNGBERG B, LLORETA J, LU D, MA J, MALATS N, MANNISTO S, MARINA N, MASTRANGELO G, MATSUO K, MCGLYNN KA, MCKEAN-COWDIN R, MCNEILL LH, MCWILLIAMS RR, MELIN BS, MELTZER PS, MENSAH JE, MIAO X, MICHAUD DS, MONDUL AM, MOORE LE, MUIR K, NIWA S, OLSON SH, ORR N, PANICO S, PARK JY, PATEL AV, PATINO-GARCIA A, PAVANELLO S, PEETERS PH, PEPLONSKA B, PETERS U, PETERSEN GM, PICCI P, PIKE MC, PORRU S, PRESCOTT J, PU X, PURDUE MP, QIAO YL, RAJARAMAN P, RIBOLI E, RISCH HA, RODABOUGH RJ, ROTHMAN N, RUDER AM, RYU JS, SANSON M, SCHNED A, SCHUMACHER FR, SCHWARTZ AG, SCHWARTZ KL, SCHWENN M, SCOTLANDI K, SEOW A, SERRA C, SERRA M, SESSO HD, SEVERI G, SHEN H, SHEN M, SHETE S, SHIRAISHI K, SHU XO, SIDDIQ A, SIERRASESUMAGA L, SIERRI S, LOON SIHOE AD, SILVERMAN DT, SIMON M, SOUTHEY MC, SPECTOR L, SPITZ M, STAMPFER M, STATTIN P, STERN MC, STEVENS VL, STOLZENBERG-SOLOMON RZ, STRAM DO, STROM SS, SU WC, SUND M, SUNG SW, SWERDLOW A, TAN W, TANAKA H, TANG W, TANG ZZ, TARDON A, TAY E, TAYLOR PR, TETTEY Y, THOMAS DM, TIRABOSCO R, TJONNELAND A, TOBIAS GS, TORO JR, TRAVIS RC, TRICHOPOULOS D, TROISI R, TRUELOVE A, TSAI YH, TUCKER MA, TUMINO R, VAN DEN BERG D, VAN DEN EEDEN SK, VERMEULEN R, VINEIS P, VISVANATHAN K, VOGEL U, WANG C, WANG C, WANG J, WANG SS, WEIDERPASS E, WEINSTEIN SJ, WENTZENSEN N, WHEELER W, WHITE E, WIENCKE JK, WOLK A, WOLPIN BM, WONG MP, WRENSCH M, WU C, WU T, WU X, WU YL, WUNDER JS, XIANG YB, XU J, YANG HP, YANG PC, YATABE Y, YE Y, YEBOAH ED, YIN Z, YING C, YU CJ, YU K, YUAN JM, ZANETTI KA, ZELENIUCH-JACQUOTTE A, ZHENG W, ZHOU B, MIRABELLO L, SAVAGE SA, KRAFT P, CHANOCK SJ, YEAGER M, LANDI MT, SHI J, CHATTERJEE N, AMUNDADOTTIR LT. Imputation and subset-based association analysis across different cancer types identifies multiple independent risk loci in the TERT-CLPTM1L region on chromosome 5p15.33. Hum Mol Genet. 2014 Dec 15;23(24):6616-33. doi: 10.1093/hmg/ddu363. Epub 2014 Jul 15. PMID: 25027329; PMCID: PMC4240198. Geprüfte Qualität Das Neuroonkologische Zentrum erfüllt die von der Deutschen Krebsgesellschaft festgelegten Qualitätskriterien und erhält die Auszeichnung "Neuroonkologisches Zentrum mit Empfehlung der Deutschen Krebsgesellschaft e.V." ♦ das Zertifikat als pdf

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COVID-19 / SARS-CoV-2 Forschung an der MHH Auf diesen Seiten stellen wir die Forschungsvorhaben und Forschungsleistungen an der MHH zu COVID-19 vor. COVID-19 / SARS-CoV-2 Forschung Das MHH-Forschungsteam um Herr Prof. Dr. Christian Könecke (rechts) veröffentlicht erste europäische Studie dieser Art im Lancet-Journal… COVID-19 / SARS-CoV-2 Forschung Die AG Förster entwickelt einen einfachen Test zum Nachweis schützender neutralisierender Antikörper. COVID-19 / SARS-CoV-2 Forschung an der MHH Von der Grundlagenforschung bis zur Supramaximalversorgung Neben Transplantation und Regeneration bzw. Biomedizintechnik und Implantaten ist die Medizinische Hochschule Hannover (MHH) ein ausgewiesener Standort der Infektionsforschung . Sowohl durch Partnerschaften mit dem Helmholtz-Zentrum für Infektionsforschung (HZI) und Mitgliedschaften in Deutschen Zentren der Gesundheitsforschung als auch durch verschiedene Sonderforschungsbereiche, das Exzellenzcluster RESIST und das HiGHmed-Konsortium ist die MHH bestens aufgestellt. Die MHH ist dabei vom Campus bis auf die internationale Ebene hervorragend vernetzt. Dies wird durch die breite Aufstellung unserer Fördermittel nur verdeutlicht. Zu den Projekten Kontakt Koordination Lokale Stabsstelle des Netzwerk Universitätsmedizin (NUM LokS) an der MHH Patrick Kaufhold, Projektmanagement E-Mail: num-loks @ mh-hannover.de Tel.: +49 (0) 511 532 83764 Dr. Tetyana Yevsa, Leitung E-Mail: num-loks @ mh-hannover.de Tel.: +49 (0) 511 532 83164 Publikationen zur COVID-19 / SARS-CoV-2 Forschung an der MHH sortiert nach PubMed-ID (PMID) Publikationen mit PMID: 32143123 - 33368589 Cordes AK, Heim A. Rapid random access detection of the novel SARS-coronavirus-2 (SARS-CoV-2, previously 2019-nCoV) using an open access protocol for the Panther Fusion. J Clin Virol 2020;125:104305 DOI: S1386-6532(20)30047-0 Zhang L, Lin D, Sun X, Curth U, Drosten C, Sauerhering L, Becker S, Rox K, Hilgenfeld R. Crystal structure of SARS-CoV-2 main protease provides a basis for design of improved alpha-ketoamide inhibitors. Science 2020;368(6489):409-412 DOI: 10.1126/science.abb3405 Wollenberg A, Flohr C, Simon D, Cork MJ, Thyssen JP, Bieber T, de Bruin-Weller MS, Weidinger S, Deleuran M, Taieb A, Paul C, Trzeciak M, Werfel T, Seneschal J, Barbarot S, Darsow U, Torrelo A, Stalder JF, Svensson A, Hijnen D, Gelmetti C, Szalai Z, Gieler U, De Raeve L, Kunz B, Spuls P, von Kobyletzki LB, Folster-Holst R, Chernyshov PV, Christen-Zaech S, Heratizadeh A, Ring J, Vestergaard C. European Task Force on Atopic Dermatitis statement on severe acute respiratory syndrome coronavirus 2 (SARS-Cov-2) infection and atopic dermatitis. J Eur Acad Dermatol Venereol 2020;34(6):e241-e242 DOI: 10.1111/jdv.16411 Albano D, Bertagna F, Bertoli M, Bosio G, Lucchini S, Motta F, Panarotto MB, Peli A, Camoni L, Bengel FM, Giubbini R. Incidental Findings Suggestive of COVID-19 in Asymptomatic Patients Undergoing Nuclear Medicine Procedures in a High-Prevalence Region. J Nucl Med 2020;61(5):632-636 DOI: 10.2967/jnumed.120.246256 Angus DC, Berry S, Lewis RJ, Al-Beidh F, Arabi Y, van Bentum-Puijk W, Bhimani Z, Bonten M, Broglio K, Brunkhorst F, Cheng AC, Chiche JD, De Jong M, Detry M, Goossens H, Gordon A, Green C, Higgins AM, Hullegie SJ, Kruger P, Lamontagne F, Litton E, Marshall J, McGlothlin A, McGuinness S, Mouncey P, Murthy S, Nichol A, O'Neill GK, Parke R, Parker J, Rohde G, Rowan K, Turner A, Young P, Derde L, McArthur C, Webb SA. The REMAP-CAP (Randomized Embedded Multifactorial Adaptive Platform for Community-acquired Pneumonia) Study. Rationale and Design. Ann Am Thorac Soc 2020;17(7):879-891 DOI: 10.1513/AnnalsATS.202003-192SD Boettler T, Newsome PN, Mondelli MU, Maticic M, Cordero E, Cornberg M, Berg T. Care of patients with liver disease during the COVID-19 pandemic: EASL-ESCMID position paper. JHEP Rep 2020;2(3):100113 DOI: 10.1016/j.jhepr.2020.100113 Nicin L, Abplanalp WT, Mellentin H, Kattih B, Tombor L, John D, Schmitto JD, Heineke J, Emrich F, Arsalan M, Holubec T, Walther T, Zeiher AM, Dimmeler S. Cell type-specific expression of the putative SARS-CoV-2 receptor ACE2 in human hearts. Eur Heart J 2020;41(19):1804-1806 DOI: 10.1093/eurheartj/ehaa311 Hrusak O, Kalina T, Wolf J, Balduzzi A, Provenzi M, Rizzari C, Rives S, Del Pozo Carlavilla M, Alonso MEV, Dominguez-Pinilla N, Bourquin JP, Schmiegelow K, Attarbaschi A, Grillner P, Mellgren K, van der Werff Ten Bosch,J., Pieters R, Brozou T, Borkhardt A, Escherich G, Lauten M, Stanulla M, Smith O, Yeoh AEJ, Elitzur S, Vora A, Li CK, Ariffin H, Kolenova A, Dallapozza L, Farah R, Lazic J, Manabe A, Styczynski J, Kovacs G, Ottoffy G, Felice MS, Buldini B, Conter V, Stary J, Schrappe M. Flash survey on severe acute respiratory syndrome coronavirus-2 infections in paediatric patients on anticancer treatment. Eur J Cancer 2020;132:11-16 DOI: S0959-8049(20)30162-3 Gaborit BJ, Bergmann JF, Mussini C, Arribas JR, Behrens G, Walmsley S, Pozniak A, Raffi F. Plea for multitargeted interventions for severe COVID-19. Lancet Infect Dis 2020;20(10):1122-1123 DOI: S1473-3099(20)30312-1 Koch T, Dahlke C, Fathi A, Kupke A, Krahling V, Okba NMA, Halwe S, Rohde C, Eickmann M, Volz A, Hesterkamp T, Jambrecina A, Borregaard S, Ly ML, Zinser ME, Bartels E, Poetsch JSH, Neumann R, Fux R, Schmiedel S, Lohse AW, Haagmans BL, Sutter G, Becker S, Addo MM. Safety and immunogenicity of a modified vaccinia virus Ankara vector vaccine candidate for Middle East respiratory syndrome: an open-label, phase 1 trial. Lancet Infect Dis 2020;20(7):827-838 DOI: S1473-3099(20)30248-6 Teoh JYC, Roupret M, Shariat SF, Herrmann T. Intravesical therapy for bladder cancer in the pandemic of Covid-19. World J Urol 2020 DOI: 10.1007/s00345-020-03218-8 Gross S, Jahn C, Cushman S, Bar C, Thum T. SARS-CoV-2 receptor ACE2-dependent implications on the cardiovascular system: From basic science to clinical implications. 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