Prevalence and clinical implications of germline mutations among Jordanian patients with ovarian cancer. The Jordanian exploratory cancer genetics (Jo‐ECAG) …

H Abdel‐Razeq, K Al‐Azzam, S Elemian… - … Genetics & Genomic …, 2023 - Wiley Online Library
Background Ovarian cancer is one of the most common gynecological malignancies. Due to
the absence of effective screening methods, ovarian cancer is usually diagnosed at late …

Comprehensive germline genomic profiling of patients with ovarian cancer: A cross-sectional study

R Pramanik, A Upadhyay, S Khurana… - Indian Journal of …, 2022 - thieme-connect.com
Introduction Ovarian cancer is the third most common cancer among Indian women. The
data on the hereditary predisposition of these cancers and the clinical outcomes of those …

Prevalence of germline mutations in women with breast and/or ovarian cancer in a tertiary care center in Pune, India

SS Kulkarni, S Nag, A Patra, HB Pant, V Agiwal… - International Journal of …, 2023 - ijmio.com
In India, the incidence of breast cancer accounted for 1, 78,361 cases, whereas ovarian
cancer accounts for 45,701 cases, according to Globocan Report 2020. These cancers are …

[HTML][HTML] Prevalence of germline BRCA1 and BRCA2 mutations and variants among ovarian, primary peritoneal and fallopian tube cancer patients: A multicentre Indian …

S Gupta, S Rajappa, SH Advani, A Agarwal… - Annals of …, 2019 - Elsevier
Background The worldwide reported prevalence of germline pathogenic BRCA1 and
BRCA2 mutations in ovarian cancer patients is 17%(3-27%) and that of variants of uncertain …

Abstract P6-02-17: A Real-World Study of BRCA1 and BRCA2 Germline Mutations among High Hereditary Risk Subjects and Patients with Breast and Ovarian Cancer …

NE Saghir, N Safi, A Masri, F Kreidieh, D Mukherji… - Cancer Research, 2023 - AACR
Background: The prevalence of pathogenic BRCA mutations in high hereditary risk breast
cancer patients (pts) in ethnic Lebanese Arab women was 5.6% in a study published in …

143P Prevalence of BRCA1/2 mutations in patients with ovarian cancer in the Gulf region: The PREDICT study

F Azribi, E Abdou, E Dawoud, M Ashour… - Annals of …, 2020 - annalsofoncology.org
Background Patients with germline mutations in BRCA1/2 are at high risk of developing
ovarian cancer (OC). However, genetic testing for BRCA1/2 mutations is still not a routine …

Germline mutations in cancer susceptibility genes in high grade serous ovarian cancer in Serbia

A Krivokuca, I Boljevic, S Jovandic, Z Magic… - Journal of human …, 2019 - nature.com
Clinical criteria for genetic testing of genes other than BRCA1/2 in epithelial ovarian cancer
(EOC) still do not exist. We assessed the frequency and predictors of deleterious mutations …

Mainstreamed genetic testing for women with ovarian cancer: first-year experience

B Rahman, A Lanceley, RS Kristeleit… - Journal of medical …, 2019 - jmg.bmj.com
Background Ovarian cancer is the fifth most common cause of cancer death for women in
the UK. Up to 18% of cases can be attributed to germline mutations in BRCA1 and BRCA2 …

Germline mutations in Black patients with ovarian, fallopian tube and primary peritoneal carcinomas

S Somasegar, AS Weiss, BM Norquist, N Khasnavis… - Gynecologic …, 2021 - Elsevier
Objective Routine genetic testing for ovarian cancer and identification of germline mutations
can help improve early detection of cancer as well as guide treatment. Knowledge of genetic …

[HTML][HTML] Germline mutations in Thai patients with nonmucinous epithelial ovarian cancer

T Manchana, P Phowthongkum… - World Journal of …, 2019 - ncbi.nlm.nih.gov
BACKGROUND Genetic testing is widely recommended for all epithelial ovarian cancer
(EOC) patients. However, an increased probability of identifying germline mutations has …