Daniel Murad Ibrahim, PhD
Affiliations: | Max Planck Institute for Molecular Genetics, Berlin, Berlin, Germany |
Google:
"Daniel Ibrahim"Parents
Sign in to add mentor| Ansgar Klebes | research assistant | 2007-2009 | Humboldt University Berlin |
| Stefan Mundlos | grad student | (DevTree) |
BETA: Related publications
See more...
Publications
|
You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect. |
| Huang X, Henck J, Qiu C, et al. (2023) Single-cell, whole-embryo phenotyping of mammalian developmental disorders. Nature |
| Weischenfeldt J, Ibrahim DM. (2023) When 3D genome changes cause disease: the impact of structural variations in congenital disease and cancer. Current Opinion in Genetics & Development. 80: 102048 |
| 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 |
| Basu S, Mackowiak SD, Niskanen H, et al. (2020) Unblending of Transcriptional Condensates in Human Repeat Expansion Disease. Cell |
| Ibrahim DM, Mundlos S. (2020) The role of 3D chromatin domains in gene regulation: a multi-facetted view on genome organization. Current Opinion in Genetics & Development. 61: 1-8 |
| Ibrahim DM, Mundlos S. (2020) Three-dimensional chromatin in disease: What holds us together and what drives us apart? Current Opinion in Cell Biology. 64: 1-9 |
| Despang A, Schöpflin R, Franke M, et al. (2019) Functional dissection of the Sox9-Kcnj2 locus identifies nonessential and instructive roles of TAD architecture. Nature Genetics |
| Cao J, Spielmann M, Qiu X, et al. (2019) The single-cell transcriptional landscape of mammalian organogenesis. Nature |
| Kraft K, Magg A, Heinrich V, et al. (2019) Serial genomic inversions induce tissue-specific architectural stripes, gene misexpression and congenital malformations. Nature Cell Biology |
| Hernandez-Miranda LR, Ibrahim DM, Ruffault PL, et al. (2018) Mutation in precludes transcription factor cooperativity and causes congenital hypoventilation in humans and mice. Proceedings of the National Academy of Sciences of the United States of America |