Eyal M. Reinstein

Medical Genetics
8700 Beverly Blvd
Cedars Sinai Medical Center, Pact, Suite 400
Los Angeles, CA 90048

Last Updated: 09/26/2026

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Found 38 publications

Hyper IgE Syndrome in an Isolated Population in Israel.

Hyper IgE Syndrome in an Isolated Population in Israel.

Journal: Frontiers in immunology
Published: December 05, 2021

Frequent aneuploidy in primary human T cells after CRISPR-Cas9 cleavage.

Frequent aneuploidy in primary human T cells after CRISPR-Cas9 cleavage.

Journal: Nature biotechnology
Published: August 18, 2021

Prenatal diagnosis of a likely pathogenic variant in ZBTB18: Natural evolution of fetal phenotype including the long bones and corpus callosum.

Prenatal diagnosis of a likely pathogenic variant in ZBTB18: Natural evolution of fetal phenotype including the long bones and corpus callosum.

Journal: American journal of medical genetics. Part A
Published: February 03, 2021

Bi-allelic variants in IPO8 cause a connective tissue disorder associated with cardiovascular defects, skeletal abnormalities, and immune dysregulation.

Bi-allelic variants in IPO8 cause a connective tissue disorder associated with cardiovascular defects, skeletal abnormalities, and immune dysregulation.

Journal: American journal of human genetics
Published: January 24, 2021

Recurring pathogenic variants in the BRCA2 gene in the Ethiopian Jewish population. Founder mutations?

Recurring pathogenic variants in the BRCA2 gene in the Ethiopian Jewish population. Founder mutations?

Journal: Familial cancer
Published: December 09, 2020

A founder mutation in TCTN2 causes Meckel-Gruber syndrome type 8 among Jews of Ethiopian and Yemenite origin.

A founder mutation in TCTN2 causes Meckel-Gruber syndrome type 8 among Jews of Ethiopian and Yemenite origin.

Journal: American journal of medical genetics. Part A
Published: October 14, 2020

The yield of chromosomal microarray analysis among pregnancies terminated due to fetal malformations.

The yield of chromosomal microarray analysis among pregnancies terminated due to fetal malformations.

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: January 25, 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

Schizophrenia and Nail Patella Syndrome: The Dopamine Connection.

Schizophrenia and Nail Patella Syndrome: The Dopamine Connection.

Journal: The Israel Medical Association journal : IMAJ
Published: August 08, 2018

NFIB Haploinsufficiency Is Associated with Intellectual Disability and Macrocephaly.

NFIB Haploinsufficiency Is Associated with Intellectual Disability and Macrocephaly.

Journal: American journal of human genetics
Published: July 04, 2018

The association between maternal serum first trimester free βhCG, second trimester intact hCG levels and foetal growth restriction and preeclampsia.

The association between maternal serum first trimester free βhCG, second trimester intact hCG levels and foetal growth restriction and preeclampsia.

Journal: Journal of obstetrics and gynaecology : the journal of the Institute of Obstetrics and Gynaecology
Published: February 02, 2018

UTILIZATION OF WHOLE EXOME SEQUENCING IN DIAGNOSTICS OF GENETIC DISEASE: RABIN MEDICAL CENTER'S EXPERIENCE

UTILIZATION OF WHOLE EXOME SEQUENCING IN DIAGNOSTICS OF GENETIC DISEASE: RABIN MEDICAL CENTER'S EXPERIENCE

Journal: Harefuah
Published: May 29, 2017
Showing 1-12 of 38

Last Updated: 09/26/2026