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Noam Hadar

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NPJ Genomic Medicine|October 10, 2025
A ciliopathy combining Joubert syndrome and Oro-Facial-Digital syndrome caused by bi-allelic 5'-UTR loss-of-function CEP83 variantMatan M Jean, Anan Yunis, Tzofit Elbaz-Biton, et al.
Human Genetics|April 12, 2024
VARista: a free web platform for streamlined whole-genome variant analysis across T2T, hg38, and hg19Noam Hadar, Vadim Dolgin, Katya Oustinov, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 10, 2025
Early-Onset Movement Disorder Syndrome Caused by Biallelic Variants in PDE1B Encoding Phosphodiesterase 1BTomer Poleg, Noam Hadar, Eyal Kristal, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|August 15, 2025
Intronic and Coding Genetic Variants in Autosomal Recessive Polycystic Kidney Disease Among Israeli Bedouins of Arabian Peninsula AncestryNadav Agam, Ohad Wormser, Ari Biller, et al.
Kidney International Reports|April 30, 2025
Genetic Terminal Complement Deficiency in Israeli Bedouins With Kidney FailureGuy Chowers, Dror Ben-Ruby, Danit Atias-Varon, et al.
Clinical Kidney Journal|February 10, 2025
Multiethnic prevalence of the <i>APOL1</i> G1 and G2 variants among the Israeli dialysis populationDror Ben-Ruby, Danit Atias-Varon, Maayan Kagan, et al.
Pageof 3

Showing results (21-30 of 26) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 26 results.
NPJ Genomic Medicine|October 10, 2025
A ciliopathy combining Joubert syndrome and Oro-Facial-Digital syndrome caused by bi-allelic 5'-UTR loss-of-function CEP83 variantMatan M Jean, Anan Yunis, Tzofit Elbaz-Biton, et al.
Human Genetics|April 12, 2024
VARista: a free web platform for streamlined whole-genome variant analysis across T2T, hg38, and hg19Noam Hadar, Vadim Dolgin, Katya Oustinov, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 10, 2025
Early-Onset Movement Disorder Syndrome Caused by Biallelic Variants in PDE1B Encoding Phosphodiesterase 1BTomer Poleg, Noam Hadar, Eyal Kristal, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|August 15, 2025
Intronic and Coding Genetic Variants in Autosomal Recessive Polycystic Kidney Disease Among Israeli Bedouins of Arabian Peninsula AncestryNadav Agam, Ohad Wormser, Ari Biller, et al.
Kidney International Reports|April 30, 2025
Genetic Terminal Complement Deficiency in Israeli Bedouins With Kidney FailureGuy Chowers, Dror Ben-Ruby, Danit Atias-Varon, et al.
Clinical Kidney Journal|February 10, 2025
Multiethnic prevalence of the <i>APOL1</i> G1 and G2 variants among the Israeli dialysis populationDror Ben-Ruby, Danit Atias-Varon, Maayan Kagan, et al.
Pageof 3