Stefan Mundlos
Humboldt-Universität zu Berlin(DE)Berlin-Brandenburger Centrum für Regenerative Therapien(DE)Berlin Institute of Health at Charité - Universitätsmedizin Berlin(DE)Max Planck Institute for Molecular Genetics(DE)Charité - Universitätsmedizin Berlin(DE)Charité - Universitätsmedizin Berlin(DE)
Publications by Year
Research Areas
Connective tissue disorders research, Congenital limb and hand anomalies, Genomic variations and chromosomal abnormalities, Genomics and Chromatin Dynamics, Hedgehog Signaling Pathway Studies
Most-Cited Works
- → The single-cell transcriptional landscape of mammalian organogenesis(2019)4,546 cited
- → Cbfa1, a Candidate Gene for Cleidocranial Dysplasia Syndrome, Is Essential for Osteoblast Differentiation and Bone Development(1997)2,806 cited
- → Disruptions of Topological Chromatin Domains Cause Pathogenic Rewiring of Gene-Enhancer Interactions(2015)2,236 cited
- → Mutations Involving the Transcription Factor CBFA1 Cause Cleidocranial Dysplasia(1997)1,491 cited
- → The Human Phenotype Ontology: A Tool for Annotating and Analyzing Human Hereditary Disease(2008)1,043 cited
- → The receptor tyrosine kinase Ror2 is involved in non‐canonical Wnt5a/JNK signalling pathway(2003)791 cited