Launch week offerEnds in00h00m00s

annual Promonthly Pro

Stefan Mundlos

Group leader

Max Planck Institute for Molecular Genetics

Germany

Research Interests

ApplyKite TwinLearns as you apply

Make your next move.

Prepare your application

Review drafts before you send them.

Explore related searches

Professors in Germany Professors in Cell Biology Cell Biology professors in Germany

Articles (20)

Year:

2026

Year:

2026

Year:

2026

Year:

2026

Year:

2025

Year:

2025

Year:

2025

Year:

2025

Year:

2025

Year:

2025

Year:

2025

Year:

2024

Year:

2024

Year:

2024

Year:

2024

Year:

2024

Year:

2024

Year:

2024

Year:

2024

Year:

2022

Collaborators (27)

Monika Piwecka

Principal Investigator

Institute of Bioorganic Chemistry Polish Academy of Sciences

POLAND

View details

Paul Waters

Associate Professor

UNSW Sydney

AUSTRALIA

View details

Meghna Ahuja Bhasin

University Hospital Bonn

GERMANY

View details

Ludger Schöls

Section head

Eberhard Karls Universität Tübingen

GERMANY

View details

Sugirthan Sivalingam

GERMANY

View details

Simon McGowan

University of Oxford

UNITED KINGDOM

View details

Francisco J. Barrionuevo

Universidad de Granada

SPAIN

View details

Felix Boschann

GERMANY

View details

Prof. Dr. Andreas Mayer

Professor of RNA Biology and Genomics

Medical University of Innsbruck

AUSTRIA

View details

Petra Knaus

Freie Universität Berlin

GERMANY

View details

Ernest Turro

Associate Professor

Icahn School of Medicine at Mount Sinai

UNITED STATES

View details

Jessica Gardner

University College London

UNITED KINGDOM

View details

Theresa Brunet

Klinikum rechts der Isar der Technischen Universität München

GERMANY

View details

Dominik Seelow

Professor

Berlin Institute of Health at Charité - Universitätsmedizin Berlin

GERMANY

View details

Miguel Burgos

Professor

Universidad de Granada

SPAIN

View details

Björn Fischer-Zirnsak

Head of Laboratory Human Genetics

Charité - Universitätsmedizin Berlin

GERMANY

View details

Guillaume Andrey

Associate Professor

University of Geneva

SWITZERLAND

View details

Catharina Schütz

Academic Staff, full professor

TUD Dresden University of Technology

GERMANY

View details

Vassilis Roukos

Assistant Professor

University of Patras

GREECE

View details

Andranik Ivanov

Charité - Universitätsmedizin Berlin

GERMANY

View details

Guido Bommer

Full Professor

Université catholique de Louvain

BELGIUM

View details

Samantha Knight

Head of Clinical Academic Development

University of Oxford

UNITED KINGDOM

View details

Michael Cheetham

University College London

UNITED KINGDOM

View details

Eduardo Calpena

University of Oxford

UNITED KINGDOM

View details

Alison Hardcastle

University College London

UNITED KINGDOM

View details

Knut Mai

Charité - Universitätsmedizin Berlin

GERMANY

View details

Juan M Vaquerizas

Chair in Developmental and Regulatory Genomics

Imperial College London

UNITED KINGDOM

View details

ApplyKite TwinLearns as you apply

Make your next move.

Prepare your application

Review drafts before you send them.

Stefan Mundlos

Research Interests

Make your next move.

Explore related searches

Articles (20)

A biallelic MRPL42 variant causes a combined oxidative phosphorylation deficiency syndrome revealed by multi-omics.

50 Jahre (und mehr) Humangenetik/Medizinische Genetik in Berlin.

Identification of biallelic loss-of-function PREP variants in three individuals with syndromic intellectual disability.

Temporal loss of En1 during limb development causes distinct phenotypes.

Enhancer adoption by an LTR retrotransposon generates viral-like particles, causing developmental limb phenotypes

A transcription coupling model for how enhancers communicate with their target genes

Inter-chromosomal insertions at Xq27.1 associated with retinal dystrophy induce dysregulation of LINC00632 and CDR1as/ciRS-7

Comparative single-cell analyses reveal evolutionary repurposing of a conserved gene programme in bat wing development

Genome-Wide Demographic Analyses of Balaenid Whales Revealed Complex History of Gene Flow Associated with Past Climate Oscillation

A missing enzyme-rescue metabolite as cause of a rare skeletal dysplasia.

Multi-tool copy number detection highlights common body size-associated variants in miniature pig breeds from different geographical regions.

Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings.

REEV: review, evaluate and explain variants.

Type II topoisomerases shape multi-scale 3D chromatin folding in regions of positive supercoils.

Loss-of-function variants affecting the STAGA complex component SUPT7L cause a developmental disorder with generalized lipodystrophy.

Familial severe skeletal Class II malocclusion with gingival hyperplasia caused by a complex structural rearrangement at the KCNJ2-KCNJ16 locus

Protocol for chromatin accessibility profiling of human endothelial cells cultured under fluid shear stress using ATAC-seq

Incomplete transcriptional dosage compensation of chicken and platypus sex chromosomes is balanced by post-transcriptional compensation.

A Novel Variant in the WRN Gene Detected in a Case of Early-Onset Severe Insulin Resistance Displaying Some but Not All Hallmarks of Progeroid Werner Syndrome.

Cell adhesion and immune response, two main functions altered in the transcriptome of seasonally regressed testes of two mammalian species

Collaborators (27)

Monika Piwecka

Paul Waters

Meghna Ahuja Bhasin

Ludger Schöls

Sugirthan Sivalingam

Simon McGowan

Francisco J. Barrionuevo

Felix Boschann

Prof. Dr. Andreas Mayer

Petra Knaus

Ernest Turro

Jessica Gardner

Theresa Brunet

Dominik Seelow

Miguel Burgos

Björn Fischer-Zirnsak

Guillaume Andrey

Catharina Schütz

Vassilis Roukos

Andranik Ivanov

Guido Bommer

Samantha Knight

Michael Cheetham

Eduardo Calpena

Alison Hardcastle

Knut Mai

Juan M Vaquerizas

Make your next move.