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Prof. Dr. med. Stefan Mundlos working place, University Hospital Charite Berlin
Prof. Dr. med. Stefan Mundlos
Excellent
AiroScore
10.00

Prof. Dr. med. Stefan Mundlos

molecular and human genetics, cell biology
molecular and human genetics, cell biology
User ScoreExperienceRatingPrice RangePublicationsOnline Consultations
99%27 years10/10$$$$659No

Overview

Country, City
Germany, Berlin
Health facility
University Hospital Charite Berlin
Medical unit
Institute of medical and human genetics

About the doctor

Prof. Dr. med. Stefan Mundlos is a highly experienced doctor specializing in molecular and human genetics, as well as cell biology. With over 26 years of experience, he has made significant contributions to the field through his extensive research and numerous scientific publications (668 in total). Prof. Mundlos completed his medical studies at prestigious institutions such as the University of Gottingen, the University of California San Diego, the University of Marburg, the Walter and Eliza Hall Institute in Melbourne, and the University of Heidelberg. Currently working at the Institute of Medical and Human Genetics at the University Hospital Charite in Berlin, Prof. Mundlos is widely recognized for his expertise in rare diseases. He has been involved in research for the National Action Alliance for people living with rare diseases. His research focuses on understanding the genetic basis of various disorders and developing novel treatments. In addition to his clinical and research work, Prof. Mundlos has played a significant role in various scientific organizations. He has served as a council member for the Human Genome Organization and as a panel member for European Research Council consolidator grants. His contributions to the field have been recognized internationally, and he has been a member of the Editorial Board for PLOS Genetics. Prof. Dr. med. Stefan Mundlos is highly regarded in the medical community for his expertise in molecular and human genetics. His extensive experience, research contributions, and involvement in scientific organizations make him an exceptional doctor in his field.

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 flag
English
German flag
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.

What is the rating of the doctor?

What topics does Prof. Dr. med. Stefan Mundlos expert at?

The doctor has excellent knowledge in mutations, gene, dysplasia, development, genome.

Is the specialist involved in the research?

Does the specialist offer online consultations?

No, Prof. Dr. med. Stefan Mundlos doesn’t perform virtual appointments.

Prof. Dr. med. Stefan Mundlos
Prof. Dr. med. Stefan Mundlos

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