Orit Reish
Tel Aviv, TA, Israel
Last Updated: 09/26/2026
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Found 16 publications
Pseudohypoxia and family history are key predictors of severe outcomes in hereditary pheochromocytoma and paraganglioma syndromes.
Journal: European journal of endocrinology
Published: June 27, 2025
National Rapid Genome Sequencing in Neonatal Intensive Care.
Journal: JAMA network open
Published: February 22, 2024
Intellectual disability syndrome associated with a homozygous founder variant in SGSM3 in Ashkenazi Jews.
Journal: Journal of medical genetics
Published: July 10, 2023
GENOTYPE-PHENOTYPE CORRELATIONS BY SPECIFIC FOUNDER VARIANTS IN BRCA IN ISRAELI WOMEN
Journal: Harefuah
Published: July 02, 2023
Age at diagnosis of cancer in 185delAG BRCA1 mutation carriers of diverse ethnicities: tentative evidence for modifier factors.
Journal: Familial cancer
Published: July 10, 2020
SCN3A-Related Neurodevelopmental Disorder: A Spectrum of Epilepsy and Brain Malformation.
Journal: Annals of neurology
Published: December 13, 2019
Lacosamide for SCN2A-related intractable neonatal and infantile seizures.
Journal: Epileptic disorders : international epilepsy journal with videotape
Published: October 27, 2018
Uterine cancer in Jewish Israeli BRCA1/2 mutation carriers.
Journal: Cancer
Published: August 05, 2018
The yield of targeted genotyping for the recurring mutations in BRCA1/2 in Israel.
Journal: Breast cancer research and treatment
Published: October 16, 2017
Mutations in the NEB gene cause fetal akinesia/arthrogryposis multiplex congenita.
Journal: Prenatal diagnosis
Published: September 28, 2016
Screening for germline mutations in breast/ovarian cancer susceptibility genes in high-risk families in Israel.
Journal: Breast cancer research and treatment
Published: December 10, 2015
A Homozygous Nme7 Mutation Is Associated with Situs Inversus Totalis.
Journal: Human mutation
Published: September 10, 2015
Last Updated: 09/26/2026