Julia Cohen-Grinshpun

Jerusalem, JM, Israel

Last Updated: 09/26/2026

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Found 14 publications

Letters to Editor: The risk for clinically significant copy number variants in pregnancies with two soft markers, Geriatriophobia - a new concept in the medical world in Israel

Letters to Editor: The risk for clinically significant copy number variants in pregnancies with two soft markers, Geriatriophobia - a new concept in the medical world in Israel

Journal: Harefuah

Published: December 18, 2024

Dystrophinopathy patient data as a guide to interpretation of pregestational female population screening for DMD gene variants.

Dystrophinopathy patient data as a guide to interpretation of pregestational female population screening for DMD gene variants.

Journal: Neurogenetics

Published: August 06, 2024

THE RISK FOR CLINICALLY SIGNIFICANT COPY NUMBER VARIANTS IN PREGNANCIES WITH TWO SOFT MARKERS

THE RISK FOR CLINICALLY SIGNIFICANT COPY NUMBER VARIANTS IN PREGNANCIES WITH TWO SOFT MARKERS

Journal: Harefuah

Published: June 17, 2024

MOH SCREENING FOR TBCD IN COCHIN JEWS: COLLABORATION BETWEEN MEDICAL, RESEARCH AND COMMUNITY MEMBERS IN ACHIEVING PUBLIC HEALTH GOALS

MOH SCREENING FOR TBCD IN COCHIN JEWS: COLLABORATION BETWEEN MEDICAL, RESEARCH AND COMMUNITY MEMBERS IN ACHIEVING PUBLIC HEALTH GOALS

Journal: Harefuah

Published: July 02, 2023

SUMMARY AND UPDATES IN THE FIELD OF GENETIC TESTING IN ISRAEL - AS OF 2022

SUMMARY AND UPDATES IN THE FIELD OF GENETIC TESTING IN ISRAEL - AS OF 2022

Journal: Harefuah

Published: July 02, 2023

Lessons learned from the first national population-based genetic carrier-screening program for Duchenne muscular dystrophy.

Lessons learned from the first national population-based genetic carrier-screening program for Duchenne muscular dystrophy.

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

Published: January 20, 2023

Community data-driven approach to identify pathogenic founder variants for pan-ethnic carrier screening panels.

Community data-driven approach to identify pathogenic founder variants for pan-ethnic carrier screening panels.

Journal: Human genomics

Published: August 21, 2022

A single center experience with publicly funded clinical exome sequencing for neurodevelopmental disorders or multiple congenital anomalies.

A single center experience with publicly funded clinical exome sequencing for neurodevelopmental disorders or multiple congenital anomalies.

Journal: Scientific reports

Published: April 15, 2021

Colchicine treatment increases the risk for fetal chromosomal aberrations-an observational study and systematic literature review.

Colchicine treatment increases the risk for fetal chromosomal aberrations-an observational study and systematic literature review.

Journal: Rheumatology (Oxford, England)

Published: May 30, 2020

Chromosomal Microarray Analysis Results From Pregnancies With Various Ultrasonographic Anomalies.

Chromosomal Microarray Analysis Results From Pregnancies With Various Ultrasonographic Anomalies.

Journal: Obstetrics and gynecology

Published: November 07, 2018

The limited effect of information on Israeli pregnant women at advanced maternal age who decide to undergo amniocentesis.

The limited effect of information on Israeli pregnant women at advanced maternal age who decide to undergo amniocentesis.

Journal: Israel journal of health policy research

Published: October 15, 2014

Population-based screening for breast and ovarian cancer risk due to BRCA1 and BRCA2.

Population-based screening for breast and ovarian cancer risk due to BRCA1 and BRCA2.

Journal: Proceedings of the National Academy of Sciences of the United States of America

Published: September 07, 2014

Showing 1-12 of 14

Last Updated: 09/26/2026