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Targeted genotyping for recurring variants in cancer susceptibility genes in non‐Ashkenazi Jewish patients with breast cancer diagnosed ≥50 years

Cancer, 2024-08, Vol.130 (16), p.2763-2769

2024

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Yield of targeted genotyping for the recurring pathogenic variants in cancer susceptibility genes in a healthy, multiethnic Israeli population

Cancer, 2021-10, Vol.127 (19), p.3599-3604

2021

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The benefit of pancreatic cancer surveillance in carriers of germline BRCA1/2 pathogenic variants

Cancer, 2024-01, Vol.130 (2), p.256-266

2024

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The spectrum of BRCA1 and BRCA2 pathogenic sequence variants in Middle Eastern, North African, and South European countries

Human mutation, 2019-11, Vol.40 (11), p.e1-e23

2019

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Uterine cancer in Jewish Israeli BRCA1/2 mutation carriers

Cancer, 2019-03, Vol.125 (5), p.698-703

2019

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Re‐evaluating the pathogenicity of the c.783+2T>C BAP1 germline variant

Human mutation, 2021-05, Vol.42 (5), p.592-599

2021

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Double heterozygosity for TP53 and BRCA1 mutations: clinical implications in populations with founder mutations

Breast cancer research and treatment, 2021-02, Vol.186 (1), p.259-263

2021

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De novo pathogenic germline variant in PALB2 in a patient with pancreatic cancer

Familial cancer, 2020-04, Vol.19 (2), p.193-196

2020

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Time trends in uptake rates of risk-reducing mastectomy in Israeli asymptomatic BRCA1 and BRCA2 mutation carriers

Breast cancer research and treatment, 2021, Vol.185 (2), p.391-399

2021

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Breast cancer surveillance for BRCA1/2 mutation carriers – is “early detection” early enough?

Breast (Edinburgh), 2020-02, Vol.49, p.81-86

2020

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Diagnostic yield of multigene panel testing in an Israeli cohort: enrichment of low-penetrance variants

Breast cancer research and treatment, 2020-06, Vol.181 (2), p.445-453

2020

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Age at diagnosis of cancer in 185delAG BRCA1 mutation carriers of diverse ethnicities: tentative evidence for modifier factors

Familial cancer, 2021-07, Vol.20 (3), p.189-194

2021

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Cranial irradiation in childhood mimicking neurofibromatosis type II

American journal of medical genetics. Part A, 2017-06, Vol.173 (6), p.1635-1639

2017

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3345: Hereditary cancer syndromes and genetic susceptibility affecting radiation decisions

Radiotherapy and oncology, 2024-05, Vol.194, p.S40-S40

Bernstein-Molho, Rinat

2024

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The complexity of management of pregnancy-associated malignant soft tissue and bone tumors

Gynecologic and obstetric investigation, 2008-01, Vol.65 (2), p.89-95

2008

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Combined weekly carboplatin and paclitaxel as primary treatment of advanced epithelial ovarian carcinoma

Gynecologic oncology, 2009-08, Vol.114 (2), p.215-218

2009

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Controversies and Open Questions in Management of Cancer-Free Carriers of Germline Pathogenic Variants in BRCA1/BRCA2

Cancers, 2022-09, Vol.14 (19), p.4592

2022

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Genetic testing in patients with triple-negative or hereditary breast cancer

Current opinion in oncology, 2021-11, Vol.33 (6), p.584-590

2021

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Controversies and Open Questions in Management of Cancer-Free Carriers of Germline Pathogenic Variants in IBRCA1/BRCA2/I

Cancers, 2022-09, Vol.14 (19)

2022

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Loss of Function RET Gene Variant and Cancer: Co-occurrence or an Association?

The Israel Medical Association journal, 2023-06, Vol.25 (6), p.445-446

2023

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Germline CDKN1B variant type and site are associated with phenotype in MEN4

Endocrine-related cancer, 2023-01, Vol.30 (1), p.1

2023

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A retrospective, single-center study comparing two neoadjuvant protocols for patients with HER2-positive breast cancer

Journal of clinical oncology, 2024-06, Vol.42 (16_suppl), p.e12623-e12623

2024

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A BRILLIANT-BRCA study: residual breast tissue after mastectomy and reconstruction

Breast cancer research and treatment, 2024-11, Vol.208 (2), p.359-367

2024

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Clinical breast exam contribution to breast cancer diagnosis in BRCA mutation carriers vs. average to intermediate risk women

Breast cancer research and treatment, 2024-08, Vol.207 (1), p.111-118

2024

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Cancer risks associated with heterozygous ATM loss of function and missense pathogenic variants based on multigene panel analysis

Breast cancer research and treatment, 2022-11, Vol.196 (2), p.355-361

2022

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Targeted genotyping for recurring variants in cancer susceptibility genes in non‐Ashkenazi Jewish patients with breast cancer diagnosed ≥50 years

Yield of targeted genotyping for the recurring pathogenic variants in cancer susceptibility genes in a healthy, multiethnic Israeli population

The benefit of pancreatic cancer surveillance in carriers of germline BRCA1/2 pathogenic variants

The spectrum of BRCA1 and BRCA2 pathogenic sequence variants in Middle Eastern, North African, and South European countries

Uterine cancer in Jewish Israeli BRCA1/2 mutation carriers

Re‐evaluating the pathogenicity of the c.783+2T>C BAP1 germline variant

Double heterozygosity for TP53 and BRCA1 mutations: clinical implications in populations with founder mutations

De novo pathogenic germline variant in PALB2 in a patient with pancreatic cancer

Time trends in uptake rates of risk-reducing mastectomy in Israeli asymptomatic BRCA1 and BRCA2 mutation carriers

Breast cancer surveillance for BRCA1/2 mutation carriers – is “early detection” early enough?

Diagnostic yield of multigene panel testing in an Israeli cohort: enrichment of low-penetrance variants

Age at diagnosis of cancer in 185delAG BRCA1 mutation carriers of diverse ethnicities: tentative evidence for modifier factors

Cranial irradiation in childhood mimicking neurofibromatosis type II

3345: Hereditary cancer syndromes and genetic susceptibility affecting radiation decisions

The complexity of management of pregnancy-associated malignant soft tissue and bone tumors

Combined weekly carboplatin and paclitaxel as primary treatment of advanced epithelial ovarian carcinoma

Controversies and Open Questions in Management of Cancer-Free Carriers of Germline Pathogenic Variants in BRCA1/BRCA2

Genetic testing in patients with triple-negative or hereditary breast cancer

Controversies and Open Questions in Management of Cancer-Free Carriers of Germline Pathogenic Variants in IBRCA1/BRCA2/I

Loss of Function RET Gene Variant and Cancer: Co-occurrence or an Association?

Germline CDKN1B variant type and site are associated with phenotype in MEN4

A retrospective, single-center study comparing two neoadjuvant protocols for patients with HER2-positive breast cancer

A BRILLIANT-BRCA study: residual breast tissue after mastectomy and reconstruction

Clinical breast exam contribution to breast cancer diagnosis in BRCA mutation carriers vs. average to intermediate risk women

Cancer risks associated with heterozygous ATM loss of function and missense pathogenic variants based on multigene panel analysis

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