Omer Shlomovitz

Tel Aviv, TA, Israel

Last Updated: 09/26/2026

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Found 15 publications

A Retrospective Cross-Sectional Study of 142 Patients in a Multidisciplinary Tuberous Sclerosis Clinic.

A Retrospective Cross-Sectional Study of 142 Patients in a Multidisciplinary Tuberous Sclerosis Clinic.

Journal: Clinical genetics

Published: June 23, 2025

Elucidating Mechanisms of Hypomorphic WDR19-Related Kidney Failure.

Elucidating Mechanisms of Hypomorphic WDR19-Related Kidney Failure.

Journal: Kidney international reports

Published: January 17, 2025

Intronic and Coding Genetic Variants in Autosomal Recessive Polycystic Kidney Disease Among Israeli Bedouins of Arabian Peninsula Ancestry.

Intronic and Coding Genetic Variants in Autosomal Recessive Polycystic Kidney Disease Among Israeli Bedouins of Arabian Peninsula Ancestry.

Journal: American journal of kidney diseases : the official journal of the National Kidney Foundation

Published: December 31, 2024

Genetic Terminal Complement Deficiency in Israeli Bedouins With Kidney Failure.

Genetic Terminal Complement Deficiency in Israeli Bedouins With Kidney Failure.

Journal: Kidney international reports

Published: October 09, 2024

Multiethnic prevalence of the APOL1 G1 and G2 variants among the Israeli dialysis population.

Multiethnic prevalence of the APOL1 G1 and G2 variants among the Israeli dialysis population.

Journal: Clinical kidney journal

Published: October 08, 2024

Diagnostic Utility of Exome Sequencing Among Israeli Children With Kidney Failure.

Diagnostic Utility of Exome Sequencing Among Israeli Children With Kidney Failure.

Journal: Kidney international reports

Published: May 14, 2023

Genetic Markers Among the Israeli Druze Minority Population With End-Stage Kidney Disease.

Genetic Markers Among the Israeli Druze Minority Population With End-Stage Kidney Disease.

Journal: American journal of kidney diseases : the official journal of the National Kidney Foundation

Published: December 31, 2022

Clinical impact of exome sequencing in the setting of a general pediatric ward for hospitalized children with suspected genetic disorders.

Clinical impact of exome sequencing in the setting of a general pediatric ward for hospitalized children with suspected genetic disorders.

Journal: Frontiers in genetics

Published: August 12, 2022

Genetic Variants in ARHGEF6 Cause Congenital Anomalies of the Kidneys and Urinary Tract in Humans, Mice, and Frogs.

Genetic Variants in ARHGEF6 Cause Congenital Anomalies of the Kidneys and Urinary Tract in Humans, Mice, and Frogs.

Journal: Journal of the American Society of Nephrology : JASN

Published: January 27, 2022

Poststreptococcal Myalgia and Protracted Febrile Myalgia Syndrome: Similar Yet Different.

Poststreptococcal Myalgia and Protracted Febrile Myalgia Syndrome: Similar Yet Different.

Journal: The Journal of pediatrics

Published: October 13, 2021

A multidisciplinary nephrogenetic referral clinic for children and adults-diagnostic achievements and insights.

A multidisciplinary nephrogenetic referral clinic for children and adults-diagnostic achievements and insights.

Journal: Pediatric nephrology (Berlin, Germany)

Published: August 23, 2021

Mammalian target of rapamycin inhibitors for the treatment of astrocytic hamartoma in tuberous sclerosis complex (TSC).

Mammalian target of rapamycin inhibitors for the treatment of astrocytic hamartoma in tuberous sclerosis complex (TSC).

Journal: Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie

Published: August 14, 2021

Showing 1-12 of 15

Last Updated: 09/26/2026