Rinat Bernstein-Molho
7PUBLICATIONS
38CO-AUTHORS
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Publications (7)
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|Mar 05, 2026
Pseudohypoxia and family history are key predictors of severe outcomes in hereditary pheochromocytoma and paraganglioma syndromes.Reut Halperin, Gili Reznick-Levi, Ayat Khalaileh
|Jun 21, 2025
Transmission ratio distortion of germline TP53 variants in Li-Fraumeni syndrome families.Naama Halpern, Iris Kventsel, Gal Strauss
|Mar 05, 2025
The impact of loco-regional treatment on ipsilateral breast cancer recurrence and outcomes in carriers of BRCA1/2 pathogenic variants.Rinat Bernstein-Molho, Ory Haisraely, Shira Galper
|Apr 17, 2024
Targeted genotyping for recurring variants in cancer susceptibility genes in non-Ashkenazi Jewish patients with breast cancer diagnosed ≥50 years.Rinat Bernstein-Molho, Narmeen Abu Shhada, Yael Laitman
|Oct 14, 2022
Controversies and Open Questions in Management of Cancer-Free Carriers of Germline Pathogenic Variants in BRCA1/BRCA2.Rinat Bernstein-Molho, Eitan Friedman, Ella Evron
|Jun 22, 2021
Yield of targeted genotyping for the recurring pathogenic variants in cancer susceptibility genes in a healthy, multiethnic Israeli population.Rinat Bernstein-Molho, Lee Galmor, Yael Laitman
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Frequent Collaborators
2 joint publications
Eitan Friedman
1 joint publications
Yael Laitman
1 joint publications
Tara M Friebel
1 joint publications
Drakoulis Yannoukakos
1 joint publications
Florentia Fostira
1 joint publications
Irene Konstantopoulou
1 joint publications
Gisella Figlioli
1 joint publications
Bernardo Bonanni
1 joint publications
Carlo Tondini
1 joint publications
Barbara Pasini
