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Yuval Yogev

17PUBLICATIONS

43CO-AUTHORS

Computational physiologyEpigenetics (incl. genome methylation and epigenomics)Disease surveillanceAnthropological geneticsOphthalmology and optometry not elsewhere classified

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Publications (17)

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|Sep 16, 2024

Tissue-aware interpretation of genetic variants advances the etiology of rare diseases.

Chanan M Argov, Ariel Shneyour, Juman Jubran

|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

|Feb 21, 2024

A role of BPTF in viral oncogenicity delineated through studies of heritable Kaposi sarcoma.

Yuval Yogev, Moshe Schaffer, Mark Shlapobersky

|Feb 14, 2024

Novel phenotype associated with homozygous likely pathogenic variant in the POP1 gene.

Marina Michelson, Keren Yosovich, Sarit Bahar

|Aug 14, 2023

IHH enhancer variant within neighboring NHEJ1 intron causes microphthalmia anophthalmia and coloboma.

Ohad Wormser, Yonatan Perez, Vadim Dolgin

|Jul 03, 2023

<i>SMARCA4</i> mutation causes human otosclerosis and a similar phenotype in mice.

Max Drabkin, Matan M Jean, Yael Noy

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Frequent Collaborators

12 joint publications

Ohad S Birk

7 joint publications

Max Drabkin

5 joint publications

Daniel Halperin

5 joint publications

Noam Hadar

4 joint publications

Ohad Wormser

3 joint publications

Marina Eskin-Schwartz

2 joint publications

Regina Proskorovski-Ohayon

2 joint publications

Yonatan Perez

2 joint publications

Matan M Jean

2 joint publications

Idan Cohen

Frequent Collaborators

12 joint publications

Ohad S Birk

7 joint publications

Max Drabkin

5 joint publications

Daniel Halperin

5 joint publications

Noam Hadar

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