Idan Cohen
8PUBLICATIONS
17CO-AUTHORS

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Publications (8)
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|Mar 03, 2024
Heterozygous THBS2 pathogenic variant causes Ehlers-Danlos syndrome with prominent vascular features in humans and mice.Noam Hadar, Omri Porgador, Idan Cohen
|Jan 04, 2023
X-linked C1GALT1C1 mutation causes atypical hemolytic uremic syndrome.Noam Hadar, Ruth Schreiber, Marina Eskin-Schwartz
|Aug 12, 2022
Histone Mono-Ubiquitination in Transcriptional Regulation and Its Mark on Life: Emerging Roles in Tissue Development and Disease.Liat Oss-Ronen, Tzlil Sarusi, Idan Cohen
|Jun 21, 2021
Epigenetic regulation and signalling pathways in Merkel cell development.Liat Oss-Ronen, Idan Cohen
|Dec 21, 2018
PRC1 preserves epidermal tissue integrity independently of PRC2.Idan Cohen, Dejian Zhao, Gopinathan Menon
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Frequent Collaborators
2 joint publications
Ophir D Klein
2 joint publications
Noam Hadar
2 joint publications
Yuval Yogev
2 joint publications
Ohad S Birk
1 joint publications
Omri Porgador
1 joint publications
Hilla Levi
1 joint publications
Sufa Sued-Hendrickson
1 joint publications
Marina Eskin-Schwartz
1 joint publications
Aubrey Houser
1 joint publications
Pradeep Cheema