Cochava Klein

Petah Tiqwa, M, Israel

Last Updated: 09/26/2026

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Found 11 publications

The Value of ROH Metrics for Predicting Morbidity: Insights From a Large Cohort Analysis of Chromosomal Microarray.

The Value of ROH Metrics for Predicting Morbidity: Insights From a Large Cohort Analysis of Chromosomal Microarray.

Journal: Clinical genetics

Published: October 15, 2024

Is There an Alternative "Advanced Maternal Age" Threshold for Recommendation of Invasive Prenatal Testing?

Is There an Alternative "Advanced Maternal Age" Threshold for Recommendation of Invasive Prenatal Testing?

Journal: Journal of obstetrics and gynaecology Canada : JOGC = Journal d'obstetrique et gynecologie du Canada : JOGC

Published: July 22, 2024

Regions of Homozygocity size patterns among diverse ethnic groups in Israel: Toward tailored diagnostic reporting thresholds.

Regions of Homozygocity size patterns among diverse ethnic groups in Israel: Toward tailored diagnostic reporting thresholds.

Journal: American journal of medical genetics. Part A

Published: April 24, 2024

Exploring the human genomic landscape: patterns of common homozygosity regions in a large middle eastern cohort.

Exploring the human genomic landscape: patterns of common homozygosity regions in a large middle eastern cohort.

Journal: Human molecular genetics

Published: April 18, 2024

Prevalence of high-penetrant copy number variants in 7734 low-risk pregnancies.

Prevalence of high-penetrant copy number variants in 7734 low-risk pregnancies.

Journal: American journal of obstetrics & gynecology MFM

Published: September 01, 2023

Chromosomal Microarray Analysis Compared With Noninvasive Prenatal Testing in Pregnancies With Abnormal Maternal Serum Screening.

Chromosomal Microarray Analysis Compared With Noninvasive Prenatal Testing in Pregnancies With Abnormal Maternal Serum Screening.

Journal: Obstetrics and gynecology

Published: November 02, 2021

Residual risk for clinically significant copy number variants in low-risk pregnancies, following exclusion of noninvasive prenatal screening-detectable findings.

Residual risk for clinically significant copy number variants in low-risk pregnancies, following exclusion of noninvasive prenatal screening-detectable findings.

Journal: American journal of obstetrics and gynecology

Published: July 20, 2021

Prenatal and postnatal chromosomal microarray analysis in 885 cases of various congenital heart defects.

Prenatal and postnatal chromosomal microarray analysis in 885 cases of various congenital heart defects.

Journal: Archives of gynecology and obstetrics

Published: July 16, 2021

The phenotype of 15 cases with rare 8q24.13-q24.3 deletions-A new syndrome or still an enigma?

The phenotype of 15 cases with rare 8q24.13-q24.3 deletions-A new syndrome or still an enigma?

Journal: American journal of medical genetics. Part A

Published: November 01, 2020

Based on a cohort of 52,879 microarrays, recurrent intragenic FBN2 deletion encompassing exons 1-8 does not cause Beals syndrome.

Based on a cohort of 52,879 microarrays, recurrent intragenic FBN2 deletion encompassing exons 1-8 does not cause Beals syndrome.

Journal: European journal of medical genetics

Published: February 18, 2020

Chromosomal microarray vs. NIPS: analysis of 5541 low-risk pregnancies.

Chromosomal microarray vs. NIPS: analysis of 5541 low-risk pregnancies.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: December 28, 2018

Showing 1-11 of 11

Last Updated: 09/26/2026