Ohad Wormser (O Wormser)

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 5

Top Topics

High Fat Diet Induced

Autism Spectrum Disorder

Endothelial Cells

Top Venues

Journal of medical virology

NPJ genomic medicine

European journal of human genetics : EJHG

Nature communications

This page only lists publications with an associated author ORCID identifier.

Publications

Yuval Yogev, Moshe Schaffer, Mark Shlapobersky, Matan M Jean, Ohad Wormser, Max Drabkin, Daniel Halperin, Riad Kassem, Alejandro Livoff, Alexandra A Tsitrina, Noam Asna, Ohad S Birk
A role of BPTF in viral oncogenicity delineated through studies of heritable Kaposi sarcoma. Journal of medical virology 96 (2) (2024)
Yuval Yogev, Moshe Schaffer, Mark Shlapobersky, Matan M Jean, Ohad Wormser, Max Drabkin, Daniel Halperin, Riad Kassem, Alejandro Livoff, Alexandra A Tsitrina, Noam Asna, Ohad S Birk
A role of BPTF in viral oncogenicity delineated through studies of heritable Kaposi sarcoma. Journal of medical virology 96 (2) (2024)
Ohad Wormser, Yonatan Perez, Vadim Dolgin, Bahman Kamali, Jared A Tangeman, Libe Gradstein, Yuval Yogev, Noam Hadar, Ofek Freund, Max Drabkin, Daniel Halperin, Inbar Irron, Erika Grajales-Esquivel, Katia Del Rio-Tsonis, Ramon Y Birnbaum, Gidon Akler, Ohad S Birk
IHH enhancer variant within neighboring NHEJ1 intron causes microphthalmia anophthalmia and coloboma. NPJ genomic medicine 8 (1) (2023)
Daniel Halperin, Alexandra Stavsky, R Kadir, Max Drabkin, Ohad Wormser, Yuval Yogev, V Dolgin, Regina Proskorovski-Ohayon, Yonatan Perez, H Nudelman, O Stoler, Barak Rotblat, T Lifschytz, Amit Lotan, G Meiri, Daniel Gitler, Ohad S Birk
CDH2 mutation affecting N-cadherin function causes attention-deficit hyperactivity disorder in humans and mice. Nature communications 12 (1) (2021)
Ohad Wormser, Libe Gradstein, Yuval Yogev, Yonatan Perez, Rotem Kadir, Inna Goliand, Yair Sadka, Saad El Riati, Hagit Flusser, Dikla Nachmias, Ruth Birk, Muhamad Iraqi, Einat Kadar, Roni Gat, Max Drabkin, Daniel Halperin, Amir Horev, Sara Sivan, Uri Abdu, Natalie Elia, Ohad S Birk
SCAPER localizes to primary cilia and its mutation affects cilia length, causing Bardet-Biedl syndrome. European journal of human genetics : EJHG 27 (6) (2019)