Publikationen von Daniel M. Ibrahim
Alle Typen
Zeitschriftenartikel (14)
1.
Zeitschriftenartikel
623 (7988), S. 772 - 781 (2023)
Single-cell, whole-embryo phenotyping of mammalian developmental disorders. Nature 2.
Zeitschriftenartikel
185 (20), S. 3689 - 3704 (2022)
Repression and 3D-restructuring resolves regulatory conflicts in evolutionarily rearranged genomes. Cell 3.
Zeitschriftenartikel
181 (5), e30, S. 1062 - 1079 (2020)
Unblending of Transcriptional Condensates in Human Repeat Expansion Disease. Cell 4.
Zeitschriftenartikel
61, 61:1-8 (2020)
The role of 3D chromatin domains in gene regulation: a multi-facetted view on genome organization. Current Opinion in Genetics & Development 5.
Zeitschriftenartikel
51 (8), S. 1263 - 1271 (2019)
Functional dissection of the Sox9-Kcnj2 locus identifies nonessential and instructive roles of TAD architecture. Nature Genetics 6.
Zeitschriftenartikel
21 (3), S. 305 - 310 (2019)
Serial genomic inversions induce tissue-specific architectural stripes, gene misexpression and congenital malformations. Nature Cell Biology 7.
Zeitschriftenartikel
115 (51), S. 13021 - 13026 (2018)
Mutation in LBX1/Lbx1 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 8.
Zeitschriftenartikel
8 (1), 1218 (2017)
Odd skipped-related 1 identifies a population of embryonic fibro-adipogenic progenitors regulating myogenesis during limb development. Nature Communications 9.
Zeitschriftenartikel
27 (2), S. 223 - 233 (2017)
Characterization of hundreds of regulatory landscapes in developing limbs reveals two regimes of chromatin folding. Genome Research 10.
Zeitschriftenartikel
13 (1), e1006567 (2017)
Genome-Wide Binding of Posterior HOXA/D Transcription Factors Reveals Subgrouping and Association with CTCF. PLoS Genetics 11.
Zeitschriftenartikel
538 (7624), S. 265 - 269 (2016)
Formation of novel chromatin domains determines pathogenicity of genomic duplications. Nature 12.
Zeitschriftenartikel
170 (3), S. 615 - 621 (2016)
A homozygous HOXD13 missense mutation causes a severe form of synpolydactyly with metacarpal to carpal transformation. American Journal of Medical Genetics Part A 13.
Zeitschriftenartikel
10 (5), S. 833 - 839 (2015)
Deletions, Inversions, Duplications: Engineering of Structural Variants using CRISPR/Cas in Mice. Cell Reports 14.
Zeitschriftenartikel
23 (12), S. 2091 - 2102 (2013)
Distinct global shifts in genomic binding profiles of limb malformation associated HOXD13 mutations. Genome Research Konferenzbeitrag (1)
15.
Konferenzbeitrag
Identification of potential regulatory elements in Capture-C interaction profiles. In: Genome Regulation in 3D. Genome Regulation in 3D, Rehovot, Israel, 28. Juni 2015 - 30. Juni 2015. Weizmann Institute, Rehovot, Israel (2015)
Hochschulschrift - Doktorarbeit (1)
16.
Hochschulschrift - Doktorarbeit
ChIP-seq Reveals Mutation-Specific Pathomechanismus of HOXD13 Missense Mutations. Dissertation, Humboldt University, FB Mathemathik, Berlin (2014)
Sonstige (2)
17.
Sonstige
Functional dissection of TADs reveals non-essential and instructive roles in regulating gene expression, bioRxiv (Preprint Server) 2019, (2019)
18.
Sonstige
Crowdfunded whole-genome sequencing of the celebrity cat Lil BUB identifies causal mutations for her osteopetrosis and polydactyly, bioRxiv (Preprint Server), (2019)
Preprint (1)
19.
Preprint
Promoter repression and 3D-restructuring resolves divergent developmental gene expression in TADs. (2021)