Whole-exome Sequencing of Nigerian Prostate Tumors from the Prostate Cancer Transatlantic Consortium (CaPTC) Reveals DNA Repair Genes Associated with African Ancestry.
Cancer Research Communications
White, Jason A JA; Kaninjing, Ernest T ET; Adeniji, Kayode A KA; Jibrin, Paul P; Obafunwa, John O JO; Ogo, Chidiebere N CN; Mohammed, Faruk F; Popoola, Ademola A; Fatiregun, Omolara A OA; Oluwole, Olabode P OP; Karanam, Balasubramanyam B; Elhussin, Isra I; Ambs, Stefan S; Tang, Wei W; Davis, Melissa M; Polak, Paz P; Campbell, Moray J MJ; Brignole, Kathryn R KR; Rotimi, Solomon O SO; Dean-Colomb, Windy W; Odedina, Folake T FT; Martin, Damali N DN; Yates, Clayton C
Publication Date: 2022-09
Variant appearance in text: BRCA1: 5339T>C; L1780P; rs80357474
Effect of BRCA1/2 Mutational Status on Survival Outcomes According to Secondary Cytoreductive Surgery and Maintenance Therapy in Platinum-Sensitive Relapsed Ovarian Cancer: A Real-World Evidence Study.
Cancer Research And Treatment
Kim, Se Ik SI; Lim, Hyunji H; Kim, Hee Seung HS; Chung, Hyun Hoon HH; Kim, Jae-Weon JW; Park, Noh Hyun NH; Song, Yong-Sang YS; Lee, Maria M
Publication Date: 2022-07-19
Variant appearance in text: BRCA1: 5339T>C; Leu1780Pro
An integrative model for the comprehensive classification of BRCA1 and BRCA2 variants of uncertain clinical significance.
Npj Genomic Medicine
Iversen, Edwin S ES; Lipton, Gary G; Hart, Steven N SN; Lee, Kun Y KY; Hu, Chunling C; Polley, Eric C EC; Pesaran, Tina T; Yussuf, Amal A; LaDuca, Holly H; Chao, Elizabeth E; Karam, Rachid R; Goldgar, David E DE; Couch, Fergus J FJ; Monteiro, Alvaro N A ANA
Feasibility of targeted cascade genetic testing in the family members of BRCA1/2 gene pathogenic variant/likely pathogenic variant carriers.
Scientific Reports
Lee, Jeeyeon J; Ham, Ji Yeon JY; Park, Ho Yong HY; Jung, Jin Hyang JH; Kim, Wan Wook WW; Kang, Byeongju B; Chae, Yee Soo YS; Lee, Soo Jung SJ; Lee, In Hee IH; Lee, Nan Young NY
Publication Date: 2022-02-03
Variant appearance in text: BRCA1: 5339T>C; Leu1780Pro
Quantifying prediction of pathogenicity for within-codon concordance (PM5) using 7541 functional classifications of BRCA1 and MSH2 missense variants.
Genetics In Medicine : Official Journal Of The American College Of Medical Genetics
Loong, Lucy L; Cubuk, Cankut C; Choi, Subin S; Allen, Sophie S; Torr, Beth B; Garrett, Alice A; Loveday, Chey C; Durkie, Miranda M; Callaway, Alison A; Burghel, George J GJ; Drummond, James J; Robinson, Rachel R; Berry, Ian R IR; Wallace, Andrew A; Eccles, Diana M DM; Tischkowitz, Marc M; Ellard, Sian S; Ware, James S JS; Hanson, Helen H; Turnbull, Clare C; ,
Publication Date: 2022-03
Variant appearance in text: BRCA1: 5339T>C; L1780P
Prevalence and clinical characterization of BRCA1 and BRCA2 mutations in Korean patients with epithelial ovarian cancer.
Cancer Science
Paik, E Sun ES; Heo, Eun Jin EJ; Choi, Chel Hun CH; Kim, Jae-Hoon JH; Kim, Jae-Weon JW; Kim, Yong-Man YM; Park, Sang-Yoon SY; Lee, Jeong-Won JW; Kim, Jong-Won JW; Kim, Byoung-Gie BG
Publication Date: 2021-12
Variant appearance in text: BRCA1: 5339T>C; L1780P
Prevalence and clinical characterization of BRCA1 and BRCA2 mutations in Korean patients with epithelial ovarian cancer.
Cancer Science
Paik, E Sun ES; Heo, Eun Jin EJ; Choi, Chel Hun CH; Kim, Jae-Hoon JH; Kim, Jae-Weon JW; Kim, Yong-Man YM; Park, Sang-Yoon SY; Lee, Jeong-Won JW; Kim, Jong-Won JW; Kim, Byoung-Gie BG
Publication Date: 2021-12
Variant appearance in text: BRCA1: 5339T>C; L1780P
Clinicopathological Characterization of Double Heterozygosity for BRCA1 and BRCA2 Variants in Korean Breast Cancer Patients.
Cancer Research And Treatment
Bang, Yoon Ju YJ; Kwon, Won Kyung WK; Nam, Seok Jin SJ; Kim, Seok Won SW; Chae, Byung-Joo BJ; Lee, Se Kyung SK; Ryu, Jai Min JM; Kim, Jong-Won JW; Yu, Jonghan J; Lee, Jeong Eon JE
Publication Date: 2022-07
Variant appearance in text: BRCA1: 5339T>C; Leu1780Pro
Targeted Therapy of Papillary Thyroid Cancer: A Comprehensive Genomic Analysis.
Frontiers In Endocrinology
Hescheler, Daniel A DA; Riemann, Burkhard B; Hartmann, Milan J M MJM; Michel, Maximilian M; Faust, Michael M; Bruns, Christiane J CJ; Alakus, Hakan H; Chiapponi, Costanza C
Mutational landscape of marginal zone B-cell lymphomas of various origin: organotypic alterations and diagnostic potential for assignment of organ origin.
Virchows Archiv : An International Journal Of Pathology
Vela, Visar V; Juskevicius, Darius D; Dirnhofer, Stefan S; Menter, Thomas T; Tzankov, Alexandar A
Analysis of BRCA1/2 variants of unknown significance in the prospective Korean Hereditary Breast Cancer study.
Scientific Reports
Kim, Joo Heung JH; Park, Sunggyun S; Park, Hyung Seok HS; Park, Ji Soo JS; Lee, Seung-Tae ST; Kim, Sung-Won SW; Lee, Jong Won JW; Lee, Min Hyuk MH; Park, Sue K SK; Noh, Woo-Chul WC; Choi, Doo Ho DH; Han, Wonshik W; Jung, Sung Hoo SH
Publication Date: 2021-04-19
Variant appearance in text: BRCA1: 5339T>C; Leu1780Pro; rs80357474
Identification of targeted therapy options for gastric adenocarcinoma by comprehensive analysis of genomic data.
Gastric Cancer : Official Journal Of The International Gastric Cancer Association And The Japanese Gastric Cancer Association
Hescheler, Daniel A DA; Plum, Patrick S PS; Zander, Thomas T; Quaas, Alexander A; Korenkov, Michael M; Gassa, Asmae A; Michel, Maximilian M; Bruns, Christiane J CJ; Alakus, Hakan H
Clinicopathological Features of Patients with the BRCA1 c.5339T>C (p.Leu1780Pro) Variant.
Cancer Research And Treatment
Park, Hyung Seok HS; Ryu, Jai Min JM; Park, Ji Soo JS; Im, Seock-Ah SA; Jung, So-Youn SY; Kim, Eun-Kyu EK; Park, Woo-Chan WC; Min, Jun Won JW; Lee, Jeeyeon J; You, Ji Young JY; Lee, Jeong Eon JE; Kim, Sung-Won SW
Publication Date: 2020-07
Variant appearance in text: BRCA1: 5339T>C; Leu1780Pro
Classification of variants of uncertain significance in BRCA1 and BRCA2 using personal and family history of cancer from individuals in a large hereditary cancer multigene panel testing cohort.
Genetics In Medicine : Official Journal Of The American College Of Medical Genetics
Li, Hongyan H; LaDuca, Holly H; Pesaran, Tina T; Chao, Elizabeth C EC; Dolinsky, Jill S JS; Parsons, Michael M; Spurdle, Amanda B AB; Polley, Eric C EC; Shimelis, Hermela H; Hart, Steven N SN; Hu, Chunling C; Couch, Fergus J FJ; Goldgar, David E DE
Establishment of chemosensitivity tests in triple-negative and BRCA-mutated breast cancer patient-derived xenograft models.
Plos One
Park, Hyung Seok HS; Lee, Jeong Dong JD; Kim, Jee Ye JY; Park, Seho S; Kim, Joo Heung JH; Han, Hyun Ju HJ; Choi, Yeon A YA; Choi, Ae Ran AR; Sohn, Joo Hyuk JH; Kim, Seung Il SI
Publication Date: 2019
Variant appearance in text: BRCA1: 5339T>C; L1780P; rs80357474
Accurate classification of BRCA1 variants with saturation genome editing.
Nature
Findlay, Gregory M GM; Daza, Riza M RM; Martin, Beth B; Zhang, Melissa D MD; Leith, Anh P AP; Gasperini, Molly M; Janizek, Joseph D JD; Huang, Xingfan X; Starita, Lea M LM; Shendure, Jay J
Publication Date: 2018-10
Variant appearance in text: BRCA1: 5339T>C; Leu1780Pro
Erratum: Prevalence of germline BRCA mutations among women with carcinoma of the peritoneum or fallopian tube.
Journal Of Gynecologic Oncology
Choi, Min Chul MC; Bae, Jin Sik JS; Jung, Sang Geun SG; Park, Hyun H; Joo, Won Duk WD; Song, Seung Hun SH; Lee, Chan C; Kim, Ji Ho JH; Lee, Ki Chan KC; Lee, Sunghoon S; Lee, Je Ho JH
Publication Date: 2018-09
Variant appearance in text: BRCA1: 5339T>C; Leu1780Pro
Comprehensive annotation of BRCA1 and BRCA2 missense variants by functionally validated sequence-based computational prediction models.
Genetics In Medicine : Official Journal Of The American College Of Medical Genetics
Hart, Steven N SN; Hoskin, Tanya T; Shimelis, Hermela H; Moore, Raymond M RM; Feng, Bingjian B; Thomas, Abigail A; Lindor, Noralane M NM; Polley, Eric C EC; Goldgar, David E DE; Iversen, Edwin E; Monteiro, Alvaro N A ANA; Suman, Vera J VJ; Couch, Fergus J FJ
Prevalence of germline BRCA mutations among women with carcinoma of the peritoneum or fallopian tube.
Journal Of Gynecologic Oncology
Choi, Min Chul MC; Bae, Jin Sik JS; Jung, Sang Geun SG; Park, Hyun H; Joo, Won Duk WD; Song, Seung Hun SH; Lee, Chan C; Kim, Ji Ho JH; Lee, Ki Chan KC; Lee, Sunghoon S; Lee, Je Ho JH
Publication Date: 2018-07
Variant appearance in text: BRCA1: 5339T>C; L1780P
HRDetect is a predictor of BRCA1 and BRCA2 deficiency based on mutational signatures.
Nature Medicine
Davies, Helen H; Glodzik, Dominik D; Morganella, Sandro S; Yates, Lucy R LR; Staaf, Johan J; Zou, Xueqing X; Ramakrishna, Manasa M; Martin, Sancha S; Boyault, Sandrine S; Sieuwerts, Anieta M AM; Simpson, Peter T PT; King, Tari A TA; Raine, Keiran K; Eyfjord, Jorunn E JE; Kong, Gu G; Borg, Åke Å; Birney, Ewan E; Stunnenberg, Hendrik G HG; van de Vijver, Marc J MJ; Børresen-Dale, Anne-Lise AL; Martens, John W M JW; Span, Paul N PN; Lakhani, Sunil R SR; Vincent-Salomon, Anne A; Sotiriou, Christos C; Tutt, Andrew A; Thompson, Alastair M AM; Van Laere, Steven S; Richardson, Andrea L AL; Viari, Alain A; Campbell, Peter J PJ; Stratton, Michael R MR; Nik-Zainal, Serena S
Identification of a Novel BRCA1 Pathogenic Mutation in Korean Patients Following Reclassification of BRCA1 and BRCA2 Variants According to the ACMG Standards and Guidelines Using Relevant Ethnic Controls.
Cancer Research And Treatment
Park, Ji Soo JS; Nam, Eun Ji EJ; Park, Hyung Seok HS; Han, Jung Woo JW; Lee, Jung-Yun JY; Kim, Jieun J; Kim, Tae Il TI; Lee, Seung-Tae ST
Publication Date: 2017-10
Variant appearance in text: BRCA1: Leu1780Pro; rs80357474