Frequency of germline pathogenic variants in breast cancer predisposition genes among young Turkish breast cancer patients

AD Isiklar, L Aliyeva, A Yesilyurt, A Soyder… - Breast Cancer Research …, 2023 - Springer
Purpose One of the most important risk factors for hereditary breast and ovarian cancer is
young age. We aim to report the frequency of pathogenic/likely pathogenic variants in breast …

Evaluation of hereditary/familial breast cancer patients with multigene targeted next generation sequencing panel and MLPA analysis in Turkey

E Bora, AO Caglayan, A Koc, T Cankaya, H Ozkalayci… - Cancer Genetics, 2022 - Elsevier
Breast cancer, a worldwide leading cause of cancer in women, may occur in familial cases.
Germline mutations in BRCA1/2 genes are responsible for 15% of the familial cases. With …

Risk of late-onset breast cancer in genetically predisposed women

NJ Boddicker, C Hu, JN Weitzel, P Kraft… - Journal of Clinical …, 2021 - ascopubs.org
PURPOSE The prevalence of germline pathogenic variants (PVs) in established breast
cancer predisposition genes in women in the general population over age 65 years is not …

Contribution of germline mutations in cancer predisposition genes to tumor etiology in young women diagnosed with invasive breast cancer

SK Rummel, L Lovejoy, CD Shriver… - Breast cancer research …, 2017 - Springer
Purpose Although breast cancer in young women accounts for< 10% of diagnoses annually,
tumors in young patients exhibit more aggressive characteristics and higher mortality rates …

Abstract P5-03-07: prevalence of pathogenic variants in cancer predisposition genes in women with young onset breast cancer

K Metcalfe, ML Quan, S Narod, E Warner… - Cancer Research, 2023 - AACR
Introduction: Approximately 5% of breast cancers are diagnosed in women 40 years of age
or younger. Known risk factors for young-onset breast cancer are few and can only account …

Clinical contribution of next-generation sequencing multigene panel testing for BRCA negative high-risk patients with breast cancer

AE Solmaz, L Yeniay, E Gökmen, O Zekioğlu… - Clinical Breast …, 2021 - Elsevier
Background Breast cancer is the most common malignancy in women and thought to be
hereditary in 10% of patients. Recent next-generation sequencing studies have increased …

[HTML][HTML] Inherited breast cancer predisposition in Asians: multigene panel testing outcomes from Singapore

ESY Wong, S Shekar, M Met-Domestici, C Chan… - NPJ genomic …, 2016 - nature.com
Genetic testing for germline mutations in breast cancer predisposition genes can potentially
identify individuals at a high risk of developing breast and/or ovarian cancer. There is a …

[HTML][HTML] Comprehensive germline profiling of patients with breast cancer: initial experience from a Familial Cancer Clinic

R Pramanik, S Chitikela, SVS Deo, A Gogia… - …, 2024 - ncbi.nlm.nih.gov
Objective The objective of the current study was to analyse the frequency and spectrum of
germline variant profiles and clinicopathological characteristics of breast cancer patients …

The NCCN criterion “young age at onset” alone is not an indicator of hereditary breast cancer in Iranian population

E Ebrahimi, E Sellars, R Shirkoohi, I Harirchi… - Cancer Prevention …, 2019 - AACR
Because the contribution of genetic factors to the burden of breast cancer is not well
investigated in Iran, we aimed to examine the prevalence of mutations in breast cancer …

[HTML][HTML] Prevalence of pathogenic germline variants in women with non-familial unilateral triple-negative breast cancer

K Rhiem, S Zachariae, A Waha, S Grill, A Hester… - Breast Care, 2023 - karger.com
Introduction: International guidelines recommend genetic testing for women with familial
breast cancer at an expected prevalence of pathogenic germline variants (PVs) of at least …