Yuval Yogev (Y Yogev)

ORCID

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 34

Top Venues

European journal of human genetics : EJHG

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

Clinical genetics

Journal of inherited metabolic disease

Ben-Gurion University of the Negev

Ben-Gurion University of the Negev (PHD)

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

Affiliation History

Ben-Gurion University of the Negev

Israel

Coordinator, Instructor and TA :: Emergency Medicene

Education History

Ben-Gurion University of the Negev

Israel

PHD :: The Shraga Segal Department of Microbiology, Immunology and Genetics

Publications

Marina Michelson, Keren Yosovich, Sarit Bahar, Yuval Yogev, Ohad S Birk, Mira Ginzberg, Dorit Lev
Novel phenotype associated with homozygous likely pathogenic variant in the POP1 gene. Clinical genetics 105 (6) (2024)
Noam Hadar, Omri Porgador, Elena Ezhkova, Hilla Levi, Vadim Dolgin, Yuval Yogev, Sufa Sued-Hendrickson, Ilan Shelef, Elena Didkovsky, Marina Eskin-Schwartz, Ohad S Birk
Heterozygous THBS2 pathogenic variant causes Ehlers-Danlos syndrome with prominent vascular features in humans and mice. European journal of human genetics : EJHG (2024)
Noam Hadar, Omri Porgador, Elena Ezhkova, Hilla Levi, Vadim Dolgin, Yuval Yogev, Sufa Sued-Hendrickson, Ilan Shelef, Elena Didkovsky, Marina Eskin-Schwartz, Ohad S Birk
Heterozygous THBS2 pathogenic variant causes Ehlers-Danlos syndrome with prominent vascular features in humans and mice. European journal of human genetics : EJHG (2024)
Marina Michelson, Keren Yosovich, Sarit Bahar, Yuval Yogev, Ohad S Birk, Mira Ginzberg, Dorit Lev
Novel phenotype associated with homozygous likely pathogenic variant in the POP1 gene. Clinical genetics (2024)
Chanan M Argov, Ariel Shneyour, Juman Jubran, Eric Sabag, Avigdor Mansbach, Yair Sepunaru, Emmi Filtzer, Gil Gruber, Miri Volozhinsky, Yuval Yogev, Ohad Birk, Vered Chalifa-Caspi, Lior Rokach, Esti Yeger-Lotem
Tissue-aware interpretation of genetic variants advances the etiology of rare diseases. Molecular systems biology (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, 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)
Noam Hadar, Omri Porgador, Elena Ezhkova, Hilla Levi, Vadim Dolgin, Yuval Yogev, Sufa Sued-Hendrickson, Ilan Shelef, Elena Didkovsky, Marina Eskin-Schwartz, Ohad S Birk
Heterozygous THBS2 pathogenic variant causes Ehlers-Danlos syndrome with prominent vascular features in humans and mice. European journal of human genetics : EJHG 32 (5) (2024)
Marina Michelson, Keren Yosovich, Sarit Bahar, Yuval Yogev, Ohad S Birk, Mira Ginzberg, Dorit Lev
Novel phenotype associated with homozygous likely pathogenic variant in the POP1 gene. Clinical genetics 105 (6) (2024)
Marina Michelson, Keren Yosovich, Sarit Bahar, Yuval Yogev, Ohad S Birk, Mira Ginzberg, Dorit Lev
Novel phenotype associated with homozygous likely pathogenic variant in the POP1 gene. Clinical genetics (2024)
Noam Hadar, Omri Porgador, Elena Ezhkova, Hilla Levi, Vadim Dolgin, Yuval Yogev, Sufa Sued-Hendrickson, Ilan Shelef, Elena Didkovsky, Marina Eskin-Schwartz, Ohad S Birk
Heterozygous THBS2 pathogenic variant causes Ehlers-Danlos syndrome with prominent vascular features in humans and mice. European journal of human genetics : EJHG 32 (5) (2024)
Noam Hadar, Omri Porgador, Elena Ezhkova, Hilla Levi, Vadim Dolgin, Yuval Yogev, Sufa Sued-Hendrickson, Ilan Shelef, Elena Didkovsky, Marina Eskin-Schwartz, Ohad S Birk
Heterozygous THBS2 pathogenic variant causes Ehlers-Danlos syndrome with prominent vascular features in humans and mice. European journal of human genetics : EJHG 32 (5) (2024)
Noam Hadar, Omri Porgador, Elena Ezhkova, Hilla Levi, Vadim Dolgin, Yuval Yogev, Sufa Sued-Hendrickson, Ilan Shelef, Elena Didkovsky, Marina Eskin-Schwartz, Ohad S Birk
Heterozygous THBS2 pathogenic variant causes Ehlers-Danlos syndrome with prominent vascular features in humans and mice. European journal of human genetics : EJHG 32 (5) (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)
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)
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)
Noam Hadar, Ruth Schreiber, Marina Eskin-Schwartz, Eyal Kristal, George Shubinsky, Galina Ling, Elena Ezhkova, Michael Geylis, Amit Nahum, Yuval Yogev, Ohad S Birk
X-linked C1GALT1C1 mutation causes atypical hemolytic uremic syndrome. European journal of human genetics : EJHG (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)
Eyal Simonovsky, Moran Sharon, Maya Ziv, Omry Mauer, Idan Hekselman, Juman Jubran, Ekaterina Vinogradov, Chanan M Argov, Omer Basha, Lior Kerber, Yuval Yogev, Ayellet V Segrè, Hae Kyung Im, null null, Ohad Birk, Lior Rokach, Esti Yeger-Lotem
Predicting molecular mechanisms of hereditary diseases by using their tissue-selective manifestation. Molecular systems biology (2023)
Amit Safran, Regina Proskorovski-Ohayon, Marina Eskin-Schwartz, Yuval Yogev, Max Drabkin, Ekaterina Eremenko, Sarit Aharoni, Ofek Freund, Matan M Jean, Nadav Agam, Noam Hadar, Neta Loewenthal, Orna Staretz-Chacham, Ohad S Birk
Hyperinsulinism/hyperammonemia syndrome caused by biallelic SLC25A36 mutation. Journal of inherited metabolic disease (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)
Amit Safran, Regina Proskorovski-Ohayon, Marina Eskin-Schwartz, Yuval Yogev, Max Drabkin, Ekaterina Eremenko, Sarit Aharoni, Ofek Freund, Matan M Jean, Nadav Agam, Noam Hadar, Neta Loewenthal, Orna Staretz-Chacham, Ohad S Birk
Hyperinsulinism/hyperammonemia syndrome caused by biallelic SLC25A36 mutation. Journal of inherited metabolic disease (2023)
Noam Hadar, Ruth Schreiber, Marina Eskin-Schwartz, Eyal Kristal, George Shubinsky, Galina Ling, Elena Ezhkova, Michael Geylis, Amit Nahum, Yuval Yogev, Ohad S Birk
X-linked C1GALT1C1 mutation causes atypical hemolytic uremic syndrome. European journal of human genetics : EJHG (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)
Amit Safran, Regina Proskorovski-Ohayon, Marina Eskin-Schwartz, Yuval Yogev, Max Drabkin, Ekaterina Eremenko, Sarit Aharoni, Ofek Freund, Matan M Jean, Nadav Agam, Noam Hadar, Neta Loewenthal, Orna Staretz-Chacham, Ohad S Birk
Hyperinsulinism / hyperammonemia syndrome caused by biallelic SLC25A36 mutation. Journal of inherited metabolic disease (2023)
Maya Gombosh, Yuval Yogev, Noam Hadar, Regina Proskorovski-Ohayon, Sarit Aharoni, Libe Gradstein, Ohad S Birk
De-novo "germline second hit" loss-of-heterozygosity RBP3 deletion mutation causing recessive high myopia. Clinical genetics (2023)
Yuval Yogev, Jacob Bistritzer, Yair Sadaka, Analia Michaelovsky, Yuval Cavari, Yael Feinstein, Munir Abu-Madegem, Yakov Fellig, Ohad Wormser, Max Drabkin, Daniel Halperin, Ohad S Birk
Transcript-Based Diagnosis and Expanded Phenotype of an Intronic Mutation in TPM3 Myopathy. Molecular diagnosis & therapy 26 (5) (2022)
Sarit Aharoni, Regina Proskorovski-Ohayon, Ramesh Kumar Krishnan, Yuval Yogev, Ohad Wormser, Noam Hadar, Anna Bakhrat, Ismael Alshafee, Maya Gombosh, Nadav Agam, Libe Gradstein, Zamir Shorer, Raz Zarivach, Marina Eskin-Schwartz, Uri Abdu, Ohad S Birk
PSMC1 variant causes a novel neurological syndrome. Clinical genetics 102 (4) (2022)
Daniel Halperin, Nadav Agam, Maher Hallak, Miora Feinstein, Max Drabkin, Yuval Yogev, Ohad Wormser, Eitan Shavit, Libe Gradstein, Ilan Shelef, Aanalia Mijalovsky, Hagit Flusser, Ohad S Birk
A syndrome of severe intellectual disability, hypotonia, failure to thrive, dysmorphism, and thinning of corpus callosum maps to chromosome 7q21.13-q21.3. Clinical genetics 102 (2) (2022)
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)
Vadim Dolgin, Rachel Straussberg, Ruijuan Xu, Izolda Mileva, Yuval Yogev, Raed Khoury, Osnat Konen, Yael Barhum, Alex Zvulunov, Cungui Mao, Ohad S Birk
DEGS1 variant causes neurological disorder. European journal of human genetics : EJHG 27 (11) (2019)

Yuval Yogev.css-eqlu8i{font-size:small;padding-left:4px;} (Y Yogev)

Publication Activity (10 Years)

Top Topics

Top Venues

Yuval Yogev (Y Yogev)