Stefan Mundlos
Affiliations: | RG development and disease | Max Planck Institute for Molecular Genetics, Berlin, Berlin, Germany |
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"Stefan Mundlos"Children
Sign in to add trainee| Daniel Murad Ibrahim | grad student | (Evolution Tree) | |
| Ivana Jerković | grad student | ||
| Katerina Kraft | grad student | ||
| Sigmar Stricker | grad student | ||
| Lila Allou | post-doc | (Evolution Tree) | |
| Michael Robson | post-doc | 2016- | (Evolution Tree) |
| Guillaume Andrey | post-doc | 2014-2018 | Max Planck Institute for Molecular Genetics |
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Publications
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| Melo US, Jatzlau J, Prada-Medina CA, et al. (2023) Author Correction: Enhancer hijacking at the ARHGAP36 locus is associated with connective tissue to bone transformation. Nature Communications. 14: 6301 |
| Allou L, Mundlos S. (2023) Disruption of regulatory domains and novel transcripts as disease-causing mechanisms. Bioessays : News and Reviews in Molecular, Cellular and Developmental Biology. e2300010 |
| Chamorro González R, Conrad T, Stöber MC, et al. (2023) Parallel sequencing of extrachromosomal circular DNAs and transcriptomes in single cancer cells. Nature Genetics. 55: 880-890 |
| Okonechnikov K, Camgöz A, Chapman O, et al. (2023) 3D genome mapping identifies subgroup-specific chromosome conformations and tumor-dependency genes in ependymoma. Nature Communications. 14: 2300 |
| Melo US, Jatzlau J, Prada-Medina CA, et al. (2023) Enhancer hijacking at the ARHGAP36 locus is associated with connective tissue to bone transformation. Nature Communications. 14: 2034 |
| Cova G, Glaser J, Schöpflin R, et al. (2023) Combinatorial effects on gene expression at the Lbx1/Fgf8 locus resolve split-hand/foot malformation type 3. Nature Communications. 14: 1475 |
| Castilla-Ibeas A, Zdral S, Galán L, et al. (2023) Failure of digit tip regeneration in the absence of Lmx1b suggests Lmx1b functions disparate from dorsoventral polarity. Cell Reports. 42: 111975 |
| Ringel AR, Szabo Q, Chiariello AM, et al. (2022) Repression and 3D-restructuring resolves regulatory conflicts in evolutionarily rearranged genomes. Cell. 185: 3689-3704.e21 |
| Kraft K, Yost KE, Murphy SE, et al. (2022) Polycomb-mediated genome architecture enables long-range spreading of H3K27 methylation. Proceedings of the National Academy of Sciences of the United States of America. 119: e2201883119 |
| Lybaek H, Robson M, de Leeuw N, et al. (2022) LRFN5 locus structure is associated with autism and influenced by the sex of the individual and locus conversions. Autism Research : Official Journal of the International Society For Autism Research |