Chana Vinkler

Holon, TA, Israel

Last Updated: 09/26/2026

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Found 15 publications

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 Diagnostic Yield and Implications of Targeted Founder Pathogenic Variant Testing in an Israeli Cohort.

The Diagnostic Yield and Implications of Targeted Founder Pathogenic Variant Testing in an Israeli Cohort.

Journal: Cancers

Published: November 10, 2023

Autosomal dominant non-syndromic hearing loss maps to DFNA33 (13q34) and co-segregates with splice and frameshift variants in ATP11A, a phospholipid flippase gene.

Autosomal dominant non-syndromic hearing loss maps to DFNA33 (13q34) and co-segregates with splice and frameshift variants in ATP11A, a phospholipid flippase gene.

Journal: Human genetics

Published: May 24, 2021

Re-evaluating the pathogenicity of the c.783+2T>C BAP1 germline variant.

Re-evaluating the pathogenicity of the c.783+2T>C BAP1 germline variant.

Journal: Human mutation

Published: December 07, 2020

Spectrum of genes for inherited hearing loss in the Israeli Jewish population, including the novel human deafness gene ATOH1.

Spectrum of genes for inherited hearing loss in the Israeli Jewish population, including the novel human deafness gene ATOH1.

Journal: Clinical genetics

Published: May 04, 2020

Prenatal clubfoot increases the risk for clinically significant chromosomal microarray results - Analysis of 269 singleton pregnancies.

Prenatal clubfoot increases the risk for clinically significant chromosomal microarray results - Analysis of 269 singleton pregnancies.

Journal: Early human development

Published: February 12, 2020

Diagnostic yield of multigene panel testing in an Israeli cohort: enrichment of low-penetrance variants.

Diagnostic yield of multigene panel testing in an Israeli cohort: enrichment of low-penetrance variants.

Journal: Breast cancer research and treatment

Published: January 08, 2020

The yield of full BRCA1/2 genotyping in Israeli Arab high-risk breast/ovarian cancer patients.

The yield of full BRCA1/2 genotyping in Israeli Arab high-risk breast/ovarian cancer patients.

Journal: Breast cancer research and treatment

Published: May 22, 2019

The rare 13q33-q34 microdeletions: eight new patients and review of the literature.

The rare 13q33-q34 microdeletions: eight new patients and review of the literature.

Journal: Human genetics

Published: April 16, 2019

Non-visualization of fetal gallbladder in microarray era - a retrospective cohort study and review of the literature.

Non-visualization of fetal gallbladder in microarray era - a retrospective cohort study and review of the literature.

Journal: The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians

Published: February 20, 2018

Severe growth deficiency, microcephaly, intellectual disability, and characteristic facial features are due to a homozygous QARS mutation.

Severe growth deficiency, microcephaly, intellectual disability, and characteristic facial features are due to a homozygous QARS mutation.

Journal: Neurogenetics

Published: January 11, 2017

Showing 1-12 of 15

Last Updated: 09/26/2026