Daniel Halperin (Ohad S Birk, D Halperin)

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 15

Top Topics

Low Density Lipoprotein

Induced Pluripotent Stem Cells

Top Venues

Proceedings of the National Academy of Sciences of the United States of America

Journal of medical virology

American journal of medical genetics. Part A

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)
Yuval Yogev, Zamir Shorer, Arie Koifman, Ohad Wormser, Max Drabkin, Daniel Halperin, Vadim Dolgin, Regina Proskorovski-Ohayon, Noam Hadar, Geula Davidov, Hila Nudelman, Raz Zarivach, Ilan Shelef, Yonatan Perez, Ohad S Birk
Limb girdle muscular disease caused by HMGCR mutation and statin myopathy treatable with mevalonolactone. Proceedings of the National Academy of Sciences of the United States of America 120 (7) (2023)
Yuval Yogev, Zamir Shorer, Arie Koifman, Ohad Wormser, Max Drabkin, Daniel Halperin, Vadim Dolgin, Regina Proskorovski-Ohayon, Noam Hadar, Geula Davidov, Hila Nudelman, Raz Zarivach, Ilan Shelef, Yonatan Perez, Ohad S Birk
Limb girdle muscular disease caused by HMGCR mutation and statin myopathy treatable with mevalonolactone. Proceedings of the National Academy of Sciences of the United States of America 120 (7) (2023)
Yuval Yogev, Zamir Shorer, Arie Koifman, Ohad Wormser, Max Drabkin, Daniel Halperin, Vadim Dolgin, Regina Proskorovski-Ohayon, Noam Hadar, Geula Davidov, Hila Nudelman, Raz Zarivach, Ilan Shelef, Yonatan Perez, Ohad S Birk
Limb girdle muscular disease caused by HMGCR mutation and statin myopathy treatable with mevalonolactone. Proceedings of the National Academy of Sciences of the United States of America 120 (7) (2023)
Yuval Yogev, Zamir Shorer, Arie Koifman, Ohad Wormser, Max Drabkin, Daniel Halperin, Vadim Dolgin, Regina Proskorovski-Ohayon, Noam Hadar, Geula Davidov, Hila Nudelman, Raz Zarivach, Ilan Shelef, Yonatan Perez, Ohad S Birk
Limb girdle muscular disease caused by HMGCR mutation and statin myopathy treatable with mevalonolactone. Proceedings of the National Academy of Sciences of the United States of America 120 (7) (2023)
Yuval Yogev, Zamir Shorer, Arie Koifman, Ohad Wormser, Max Drabkin, Daniel Halperin, Vadim Dolgin, Regina Proskorovski-Ohayon, Noam Hadar, Geula Davidov, Hila Nudelman, Raz Zarivach, Ilan Shelef, Yonatan Perez, Ohad S Birk
Limb girdle muscular disease caused by HMGCR mutation and statin myopathy treatable with mevalonolactone. Proceedings of the National Academy of Sciences of the United States of America 120 (7) (2023)
Yuval Yogev, Zamir Shorer, Arie Koifman, Ohad Wormser, Max Drabkin, Daniel Halperin, Vadim Dolgin, Regina Proskorovski-Ohayon, Noam Hadar, Geula Davidov, Hila Nudelman, Raz Zarivach, Ilan Shelef, Yonatan Perez, Ohad S Birk
Limb girdle muscular disease caused by HMGCR mutation and statin myopathy treatable with mevalonolactone. Proceedings of the National Academy of Sciences of the United States of America 120 (7) (2023)
Yuval Yogev, Zamir Shorer, Arie Koifman, Ohad Wormser, Max Drabkin, Daniel Halperin, Vadim Dolgin, Regina Proskorovski-Ohayon, Noam Hadar, Geula Davidov, Hila Nudelman, Raz Zarivach, Ilan Shelef, Yonatan Perez, Ohad S Birk
Limb girdle muscular disease caused by HMGCR mutation and statin myopathy treatable with mevalonolactone. Proceedings of the National Academy of Sciences of the United States of America 120 (7) (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)
Daniel Halperin, Max Drabkin, Ohad Wormser, Yuval Yogev, Vadim Dolgin, Zamir Shorer, Libe Gradstein, Ilan Shelef, Hagit Flusser, Ohad S Birk
Phenotypic variability and mutation hotspot in COX15-related Leigh syndrome. American journal of medical genetics. Part A 182 (6) (2020)
Daniel Halperin, Aviad Sapir, Ohad Wormser, Max Drabkin, Yuval Yogev, Vadim Dolgin, Hagit Flusser, Daniel Halperin
Novel MTMR2 mutation causing severe Charcot-Marie-Tooth type 4B1 disease: a case report. Neurogenetics 21 (4) (2020)
Daniel Halperin, Vadim Dolgin, Michael Geylis, Max Drabkin, Yuval Yogev, Ohad Wormser, Ruth Schreiber, Hanna Shalev, Daniel Landau, Ohad S Birk
A novel SLC12A1 mutation in Bedouin kindred with antenatal Bartter syndrome type I. Annals of human genetics 83 (5) (2019)
Daniel Halperin, Rotem Kadir, Yonatan Perez, Max Drabkin, Yuval Yogev, Ohad Wormser, Erez M Berman, Ekaterina Eremenko, Barak Rotblat, Zamir Shorer, Libe Gradstein, Ilan Shelef, Ruth Birk, Uri Abdu, Hagit Flusser, Ohad S Birk
SEC31A mutation affects ER homeostasis, causing a neurological syndrome. Journal of medical genetics 56 (3) (2018)
H Flusser, Daniel Halperin, R Kadir, Z Shorer, I Shelef, O S Birk
Novel SBF1 splice-site null mutation broadens the clinical spectrum of Charcot-Marie-Tooth type 4B3 disease. Clinical genetics 94 (5) (2018)