Prof. Dr. med. Stefan Mundlos
molecular and human genetics, cell biology
molecular and human genetics, cell biology
Overview
Country, City
Germany, Berlin
Health facility
University Hospital Charite Berlin
Medical unit
Institute of medical and human genetics
About the doctor
Skills & Expertise
mutations
gene
dysplasia
development
genome
brachydactyly
phenotype
chromosome
cleidocranial dysplasia
autosomal
cutis laxa
deletions
congenital
mental retardation
homozygous
neurofibromatosis
human genetics
spondyloepiphyseal dysplasia
skeletal development
robinow syndrome
retardation syndrome
mesomelic dysplasia
exome sequencing
genetic disorders
split handfoot
handfoot malformation
limb malformations
limb development
Resume
CV (Curriculum Vitae)
Education
- Studied Medicine at the University of Gottingen
- Studied Medicine at the University of California San Diego
- Studied Medicine at the University of Marburg
- Studied Medicine at the Walter and Eliza Hall Institute in Melbourne
- Studied Medicine at the University of Heidelberg
Experience
- Completed clinical training in Pediatrics and Human Genetics at the University Hospital of Mainz, Germany
- Research fellow at the Murdoch Institute for Research into Birth Defects in Melbourne, Australia
- The postdoctoral period at the Department of Cell Biology in Harvard, Boston, USA
- 1997 Habilitation in Mainz
- 1999 Nominated for a Professorship in Human Genetics at Heidelberg
- Director of the Institute for Medical and Human Genetics at the Charite
- Group leader of the Research Group Development & Disease at the Max Planck Institute for Molecular Genetics
- 2012-2015 Management, Scientific Advice to the Ministry of Health on the subject
Awards & Memberships
- 2014 Member of Editorial Board, PloS Genetics, UK
- 2015-2019 Council Member, Human Genome Organization
- 2017 Panel Member, European Research Council consolidator grants
- 2019 Member, Review Board Section 4, German Research Foundation
- Research for rare diseases as part of the National Action Alliance for people living with rare diseases
Languages
English
German
Publications
AML with complex karyotype: extreme genomic complexity revealed by combined long-read sequencing and Hi-C technology
August, 2023
Doxorubicin Changes the Spatial Organization of the Genome around Active Promoters
August, 2023
HOXD13-associated synpolydactyly: Extending and validating the genotypic and phenotypic spectrum with 38 new and 49 published families
July, 2023
Location
Charitépl., 1, 10117 Berlin, Germany
FAQ
Where does the doctor practice?
What is the specialization of Prof. Dr. med. Stefan Mundlos?
The primary specialization of the doctor is molecular and human genetics, cell biology.
What is the experience of the specialist?
Prof. Dr. med. Stefan Mundlos has been practicing for more than 27 years.
Prof. Dr. med. Stefan Mundlos
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© Prof. Dr. med. Stefan Mundlos