Noam Hadar

12PUBLICATIONS
33CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)African languagesProcedural content generationCardiology (incl. cardiovascular diseases)Developmental genetics (incl. sex determination)
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Publications (12)

|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

|Jan 31, 2024
ZNF142 mutation causes sex-dependent neurologic disorder.

Regina Proskorovski-Ohayon, Marina Eskin-Schwartz, Zamir Shorer

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