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Welcome to the MHH
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News

DKG certifies MHH Centre for Familial Breast and Ovarian Cancer

Relevance: 89%
 

nary team from Human Genetics, the Breast Centre, the Gynaecological Cancer Centre, Radiology and Pathology. After a comprehensive assessment by the independent certification institute OnkoZert of the [...] affected directly," says Professor Brigitte Schlegelberger, head of the FBREK Centre and the Institute of Human Genetics at the MHH. Professor Dr. Peter Hillemanns, Director of the Comprehensive Cancer Center [...] Centre range from specialised genetic counselling and genetic analysis to the possibility of an intensified early detection programme, which is supervised by the Institute for Diagnostic and Interventional

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OnkoRiskNET

Relevance: 89%
 

is the case in human genetics. This makes it all the more important to develop care concepts such as OnkoRiskNET that keep pace with this development and ensure comprehensive human genetic care in the future [...] interpreting findings and telemedical genetic counseling are intended to ensure access to genetic counseling, diagnostics and risk-adapted prevention for genetic tumor risk syndromes in structurally weak [...] future." Prof. Dr. med. Brigitte Schlegelberger, former Director of the Institute of Human Genetics at the MHH. --

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Intensified early detection

Relevance: 89%
 

screening begins, the patient must present herself at the Institute of Human Genetics to have her individual risk determined. The human genetic findings are discussed in detail with the patient and an expert [...] early detection As one of the 15 centers of the Breast and Ovarian Cancer Consortium , we at the Institute of Diagnostic and Interventional Radiology at the MHH are responsible for intensive early detection

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B Centre for Rare Diseases

Relevance: 88%
 

for Rare Syndromic Diseases The Centre for Rare Syndromic Diseases, which is part of the Institute of Human Genetics (Director: Prof. Dr. med. Nataliya Di Donato), deals with the diagnosis of syndromic diseases [...] childhood and adulthood. Competencies of the specialist center Genetic counseling Creation of a family tree Clinical-genetic examination Molecular genetic testing Molecular cytogenetic examinations Cytogenetic [...] for patients Further links You can find further information under the following links: Institute of Human Genetics Patient organizations and self-help groups You can find more information under the following

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Physicians

Relevance: 88%
 

Auber, MBA Senior consultant, deputy head of institute 0511 532 8719 auber.bernd @ mh-hannover.de Prof. Dr. med. Anke Katharina Bergmann Specialist in human genetics 0511 532 4526 bergmann.anke @ mh-hannover [...] mh-hannover.de Dr. med. Ann-Cathrine Berking Specialist in human genetics Berking.Ann-Cathrine @ mh-hannover.de Prof. Dr. Nataliya Di Donato Institute management +49(0) 511 532-36580 Didonato.Nataliya @ mh-hannover [...] mh-hannover.de Dr. med. Chen Du Specialist in human genetics Du.Chen @ mh-hannover.de Dr. med. Marina Gingele assistant physician Gingele.Marina @ mh-hannover.de Dr. med. Uni Sem Vinzenz Paul Graf assistant

News

Professor Di Donato heads the Department of Human Genetics

Relevance: 88%
 

the beginning of the month. The 43-year-old specialist in human genetics previously worked as deputy director of the Institute of Clinical Genetics at the University Hospital of the Technical University of [...] 05/04/2023 The Department of Human Genetics of Hannover Medical School (MHH) has a new director: Professor Dr. Nataliya Di Donato took over the management of Professor Dr. Brigitte Schlegelberger at the [...] Children's Research Institute in the USA for one year as part of a DFG research scholarship. Most recently, she worked in Dresden as a research group leader, deputy head of the institute and deputy speaker

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Commissioning of genetic diagnostics at the Institute of Human Genetics at the MHH

Relevance: 87%
 

Information for your test order Billing for genetic laboratory tests Your laboratory budget will not be affected by molecular genetic diagnostics! The human genetics section in Chapter 11 of the standardized [...] scale (EBM) was fundamentally revised in 2016. Human genetic services are now divided into constitutional genetic examinations (Chapter 11) and tumor genetic examinations (Chapter 19) in the EBM. Due to [...] standards. They are international standards and guarantee the quality and competence of the Institute of Human Genetics. If you have any questions, please contact Christine Blumenstein, MBA, Pharmacist, Quality

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MHH | Application for the model project Genome Sequencing, Rare Diseases

Relevance: 86%
 

protection regulations, in particular the GDPR. Colleagues of the Human Genetics outpatient clinic of the Institute of Human Genetics at MHH have access to the data. The processing of the personal data [...] country or an international organization. After collection, my data will be stored by the Institute of Human Genetics of the MHH for as long as necessary to fulfill the purpose. As a rule, this means that [...] the Hannover Medical School's data protection information . Back to the homepage of the Institute of Human Genetics | MHH

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Selective contract NAMSE

Relevance: 85%
 

reviewed as part of an interdisciplinary case conference at the ZSE. After genetic analysis at the Institute of Human Genetics, the results are discussed and interpreted in the context of the clinical phenotype [...] specialist conference Instructions for admission IV Contact person Dr. med. Tim Ripperger, PhD Institute of Human Genetics, MHH ripperger.tim @ mh-hannover.de Tel: 0511 - 532 1984 2 [...] Clinical Genomedicine. At the ZSE of the MHH, patients can also be offered such a comprehensive genetic examination as part of clinical genomic medicine. After informing and obtaining the consent of o

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Clinical genomic medicine

Relevance: 84%
 

the cooperation between the Institute of Human Genetics and the ZSE, the MHH is currently able to offer patients with rare diseases the additional option of detailed genetic testing: the "Model project [...] are caused by a genetic change in an inherited trait. However, it is not always possible to identify these causative gene variants in standard outpatient care as part of diagnostic genetic examinations.

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