Stefan Mundlos
Humboldt-Universität zu Berlin
Affiliation Humboldt-Universität zu Berlin Top Publications The single-cell transcriptional landscape of mammalian organogenesis (2019) – 5,024 citations Cbfa1, a Candidate Gene for Cleidocranial Dysplasia Syndrome, Is Essential for Osteoblast Differentiation and Bone Development (1997) – 2,838 citations Disruptions of Topological Chromatin Domains Cause Pathogenic Rewiring of Gene-Enhancer Interactions (2015) – 2,372 citations Mutations Involving the ... <a title="Stefan Mundlos" class="read-more" href="https://journalsworld.com/researchers/stefan-mundlos/" aria-label="Read more about Stefan Mundlos">Read more</a>
Read biography ↓Biography, research & contributions
Affiliation
Humboldt-Universität zu Berlin
Top Publications
- The single-cell transcriptional landscape of mammalian organogenesis (2019) - 5,024 citations
- Cbfa1, a Candidate Gene for Cleidocranial Dysplasia Syndrome, Is Essential for Osteoblast Differentiation and Bone Development (1997) - 2,838 citations
- Disruptions of Topological Chromatin Domains Cause Pathogenic Rewiring of Gene-Enhancer Interactions (2015) - 2,372 citations
- Mutations Involving the Transcription Factor CBFA1 Cause Cleidocranial Dysplasia (1997) - 1,508 citations
- The Human Phenotype Ontology: A Tool for Annotating and Analyzing Human Hereditary Disease (2008) - 1,085 citations
At a glance
- Full name
- Stefan Mundlos
- ORCID
- 0000-0002-9788-3166
- OpenAlex ID
- https://openalex.org/A5023743496
Research interests
- Genomics and Rare Diseases, Congenital limb and hand anomalies, Connective tissue disorders research, Genomic variations and chromosomal abnormalities, Genomics and Chromatin Dynamics
Research topics
Education
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Selected research & further reading
A curated reading list, not a ranking by citation count. References use DOI metadata, matching public scholarly records or authoritative lecture sources.
See the source-linked reading and original works in the research guide above.
Citation & publication trends
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Source: OpenAlex · Retrieved 2026-10-08. Metrics are database-specific and are not a scientific ranking.
Most-cited linked publications
Publications matched across ORCID and OpenAlex. Citation counts are source-specific.
- 5,024OpenAlex citations
- 2,838OpenAlex citations
- 2,372OpenAlex citations
- 1,508OpenAlex citations
- The Human Phenotype Ontology: A Tool for Annotating and Analyzing Human Hereditary Disease ↗2008 · The American Journal of Human Genetics1,085OpenAlex citations
Recent linked publications
Publications matched across ORCID and OpenAlex. Citation counts are source-specific.
- The Human Phenotype Ontology: A Tool for Annotating and Analyzing Human Hereditary Disease ↗2008 · The American Journal of Human Genetics
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Institutions
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Awards & honors
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Career timeline
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Co-authors
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Education & career institution links
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Sign in to claim this profileSources & data information
Editorial review: 2026-10-08 · Last data update: 2026-10-08 00:17:59
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