Prof. Dr. med. Bernd Wollnik
human genetics
human genetics
Overview
Country, City
Germany, Gottingen
Health facility
University Hospital Gottingen
Medical unit
Department of human genetics
About the doctor
Skills & Expertise
mutation
gene
genetics
hearing
hearing loss
phenotype
microcephaly
osteogenesis
osteogenesis imperfecta
kabuki syndrome
nonsyndromic hearing loss
heart
dysplasia
cancer
microphthalmia
craniosynostosis
deficiency
cardiomyopathy
hearing impairment
head
ladd syndrome
cenanilenz syndrome
epilepsy
lossoffunction mutations
bone fragility
nicolaidesbaraitser syndromes
kidney
bloom syndrome
cadasil syndrome
gene mutations
motor apraxia
usher syndrome
oculodentodigital dysplasia
coffinsiris syndrome
bone
limb
malformations
lipoma
long qt syndrome
nonsyndromic hearing impairment
bosma arhinia microphthalmia
colorectal cancer
heart failure
hypertrophic cardiomyopathy
smithlemliopitz syndrome
microcephaly syndrome
progeroid syndromes
muscle fibrosis
hand anomalies
21qter mutations
Resume
CV (Curriculum Vitae)
Education
- 1988-1995 Studied human medicine at the Rheinische Friedrich-Wilhelms University Bonn
- 1990-1992 Defense of the dissertation at the Rheinische Friedrich-Wilhelms University Bonn
- 1995 Obtaining a license for medical practice
- 1997 Medical Fellow and Postdoc at the center for molecular neurobiology at the University of Hamburg
- 1997 Fellow from the German Academic Exchange Service for a young scientist to continue scientific work at the Child Health Institute at the University of Istanbul
- Obtaining specialization in human genetics
- Habilitation and a teaching license
Experience
- 1995-1997 Doctor in an internship at the Department of neurology and center for molecular neurobiology of the University Hamburg
- 1998-2004 Head of molecular genetics unit of the division of medical genetics at the Istanbul University
- 1999 Foreign lecturer position and Head of the division of molecular genetics of the Child Health Institute at the Istanbul University
- Head of the Institute of Human Genetics at the University of Cologne
- 2013-2015 Director of center for rare diseases at the University Hospital of Cologne
- 2015 Professor and Director of the Department of human genetics at the University Hospital Gottingen
Awards & Memberships
- 2001 International Scientific Award from Istanbul University
- 2002 Young Scientist Award from the Turkish Academy of Science
- 2004-2012 Junior Research Group Leader at the Center for Molecular Medicine Cologne, Institute of Human Genetics of the University of Cologne
- Head of a research group at the Center for Molecular Medicine Cologne
- Member of the national rare disease consortia SKELNET and FACE
- Actively Funded Member of the Cologne excellence cluster on cellular stress responses in aging-associated diseases
- Co-Ordinator of the network CRANIRARE
Languages
English
German
Publications
B3GALT6-linkeropathy: Three illustrative patients spanning the disease spectrum.
October, 2023
N4-hydroxycytidine, the active compound of Molnupiravir, promotes SARS-CoV-2 mutagenesis and escape from a neutralizing nanobody.
30 August, 2023
Null and missense mutations of ERI1 cause a recessive phenotypic dichotomy in humans.
6 July, 2023
Location
Robert-Koch-Straße, 40, 37075 Gottingen, Germany
FAQ
Where does the doctor practice?
What is the specialization of Prof. Dr. med. Bernd Wollnik?
The primary specialization of the doctor is human genetics.
What is the experience of the specialist?
Prof. Dr. med. Bernd Wollnik has been practicing for more than 29 years.
Prof. Dr. med. Bernd Wollnik
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© Prof. Dr. med. Bernd Wollnik
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