Stavit A. Shalev

Ha'Emek Med. Ctr
Afula, Z 18101, Israel

Last Updated: 09/26/2026

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Found 102 publications

Early-Onset Calcium Pyrophosphate Disease Associated With Genetic Hypomagnesemia: Beyond Gitelman Syndrome.

Early-Onset Calcium Pyrophosphate Disease Associated With Genetic Hypomagnesemia: Beyond Gitelman Syndrome.

Journal: The Journal of rheumatology

Published: June 15, 2026

Exome sequencing and large-scale analysis of electronic medical record-linked biobank data identify candidate deafness genes.

Exome sequencing and large-scale analysis of electronic medical record-linked biobank data identify candidate deafness genes.

Journal: Journal of medical genetics

Published: June 07, 2026

Phenotypic and Genotypic Characterization of 171 Patients with Syndromic Inherited Retinal Diseases Highlights the Importance of Genetic Testing for Accurate Clinical Diagnosis.

Phenotypic and Genotypic Characterization of 171 Patients with Syndromic Inherited Retinal Diseases Highlights the Importance of Genetic Testing for Accurate Clinical Diagnosis.

Journal: Genes

Published: May 25, 2025

Exploring the unique characteristics of genes with dual autosomal dominant and recessive inheritance: mechanisms, phenotypes and candidate identification.

Exploring the unique characteristics of genes with dual autosomal dominant and recessive inheritance: mechanisms, phenotypes and candidate identification.

Journal: Journal of medical genetics

Published: April 21, 2025

Correction: The genetic landscape of Lynch syndrome in the Israeli population.

Correction: The genetic landscape of Lynch syndrome in the Israeli population.

Journal: Familial cancer

Published: March 21, 2025

The genetic landscape of Lynch syndrome in the Israeli population.

The genetic landscape of Lynch syndrome in the Israeli population.

Journal: Familial cancer

Published: September 07, 2024

The distribution of regions of homozygosity (ROH) among consanguineous populations-implications for a routine genetic counseling service.

The distribution of regions of homozygosity (ROH) among consanguineous populations-implications for a routine genetic counseling service.

Journal: Journal of human genetics

Published: August 15, 2024

Personal journeys to and in human genetics and dysmorphology.

Personal journeys to and in human genetics and dysmorphology.

Journal: American journal of medical genetics. Part A

Published: November 05, 2023

Erratum to "A randomized trial to investigate needle redirections/re-insertions using a handheld ultrasound device versus traditional palpation for spinal anesthesia in obese women undergoing cesarean delivery" [Int. J. Obstetric Anesth. 49 (2022) 103229].

Erratum to "A randomized trial to investigate needle redirections/re-insertions using a handheld ultrasound device versus traditional palpation for spinal anesthesia in obese women undergoing cesarean delivery" [Int. J. Obstetric Anesth. 49 (2022) 103229].

Journal: International journal of obstetric anesthesia

Published: July 29, 2023

Genomic analyses in Cornelia de Lange Syndrome and related diagnoses: Novel candidate genes, genotype-phenotype correlations and common mechanisms.

Genomic analyses in Cornelia de Lange Syndrome and related diagnoses: Novel candidate genes, genotype-phenotype correlations and common mechanisms.

Journal: American journal of medical genetics. Part A

Published: March 23, 2023

Genetic variant in complement receptor 1 (CR1, CD35) is associated with a cluster of severe fatal COVID-19 in a family.

Genetic variant in complement receptor 1 (CR1, CD35) is associated with a cluster of severe fatal COVID-19 in a family.

Journal: The Journal of infection

Published: March 11, 2023

Educational tools support informed decision-making for genetic carrier screening in a heterogenic Israeli population.

Educational tools support informed decision-making for genetic carrier screening in a heterogenic Israeli population.

Journal: Journal of community genetics

Published: February 28, 2023

Showing 1-12 of 102

Last Updated: 09/26/2026