Noam Hadar

13PUBLICATIONS
34CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)African languagesProcedural content generationCardiology (incl. cardiovascular diseases)Developmental genetics (incl. sex determination)
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Publications (13)

|Sep 21, 2026
NSMCE2 / MMS21 structural variant causes chromosome breakage syndrome with primordial dwarfism and severe lung disease.

|Mar 14, 2025
Unraveling MECP2 structural variants in previously elusive Rett syndrome cases through IGV interpretation.

Tomer Poleg, Noam Hadar, Gali Heimer

|Feb 10, 2025
Multiethnic prevalence of the APOL1 G1 and G2 variants among the Israeli dialysis population.

Dror Ben-Ruby, Danit Atias-Varon, Maayan Kagan

|Dec 27, 2024
GeniePool 2.0: advancing variant analysis through CHM13-T2T, AlphaMissense, gnomAD V4 integration, and variant co-occurrence queries.

Grisha Weintraub, Noam Hadar, Ehud Gudes

|Jul 25, 2024
Developmental dysplasia of the hip caused by homozygous TRIM33 pathogenic variant affecting downstream BMP pathway.

Maya Gombosh, Regina Proskorovski-Ohayon, Yuval Yogev

|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

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Frequent Collaborators

11 joint publications

Ohad S Birk

5 joint publications

Yuval Yogev

4 joint publications

Marina Eskin-Schwartz

3 joint publications

Max Drabkin