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: BRIP1: 890A>G; K297R; rs28997570
REVEL and BayesDel outperform other in silico meta-predictors for clinical variant classification.
Scientific Reports
Tian, Yuan Y; Pesaran, Tina T; Chamberlin, Adam A; Fenwick, R Bryn RB; Li, Shuwei S; Gau, Chia-Ling CL; Chao, Elizabeth C EC; Lu, Hsiao-Mei HM; Black, Mary Helen MH; Qian, Dajun D
Whole-exon sequencing of human myeloma cell lines shows mutations related to myeloma patients at relapse with major hits in the DNA regulation and repair pathways.
Journal Of Hematology & Oncology
Tessoulin, Benoît B; Moreau-Aubry, Agnès A; Descamps, Géraldine G; Gomez-Bougie, Patricia P; Maïga, Sophie S; Gaignard, Alban A; Chiron, David D; Ménoret, Emmanuelle E; Le Gouill, Steven S; Moreau, Philippe P; Amiot, Martine M; Pellat-Deceunynck, Catherine C
Identification of genetic variants for clinical management of familial colorectal tumors.
Bmc Medical Genetics
Dominguez-Valentin, Mev M; Nakken, Sigve S; Tubeuf, Hélène H; Vodak, Daniel D; Ekstrøm, Per Olaf PO; Nissen, Anke M AM; Morak, Monika M; Holinski-Feder, Elke E; Martins, Alexandra A; Møller, Pål P; Hovig, Eivind E
Publication Date: 2018-02-20
Variant appearance in text: BRIP1: K297R; rs28997570
No evidence that protein truncating variants in BRIP1 are associated with breast cancer risk: implications for gene panel testing.
Journal Of Medical Genetics
Easton, Douglas F DF; Lesueur, Fabienne F; Decker, Brennan B; Michailidou, Kyriaki K; Li, Jun J; Allen, Jamie J; Luccarini, Craig C; Pooley, Karen A KA; Shah, Mitul M; Bolla, Manjeet K MK; Wang, Qin Q; Dennis, Joe J; Ahmad, Jamil J; Thompson, Ella R ER; Damiola, Francesca F; Pertesi, Maroulio M; Voegele, Catherine C; Mebirouk, Noura N; Robinot, Nivonirina N; Durand, Geoffroy G; Forey, Nathalie N; Luben, Robert N RN; Ahmed, Shahana S; Aittomäki, Kristiina K; Anton-Culver, Hoda H; Arndt, Volker V; , ; Baynes, Caroline C; Beckman, Matthias W MW; Benitez, Javier J; Van Den Berg, David D; Blot, William J WJ; Bogdanova, Natalia V NV; Bojesen, Stig E SE; Brenner, Hermann H; Chang-Claude, Jenny J; Chia, Kee Seng KS; Choi, Ji-Yeob JY; Conroy, Don M DM; Cox, Angela A; Cross, Simon S SS; Czene, Kamila K; Darabi, Hatef H; Devilee, Peter P; Eriksson, Mikael M; Fasching, Peter A PA; Figueroa, Jonine J; Flyger, Henrik H; Fostira, Florentia F; García-Closas, Montserrat M; Giles, Graham G GG; Glendon, Gord G; González-Neira, Anna A; Guénel, Pascal P; Haiman, Christopher A CA; Hall, Per P; Hart, Steven N SN; Hartman, Mikael M; Hooning, Maartje J MJ; Hsiung, Chia-Ni CN; Ito, Hidemi H; Jakubowska, Anna A; James, Paul A PA; John, Esther M EM; Johnson, Nichola N; Jones, Michael M; Kabisch, Maria M; Kang, Daehee D; , ; Kosma, Veli-Matti VM; Kristensen, Vessela V; Lambrechts, Diether D; Li, Na N; , ; Lindblom, Annika A; Long, Jirong J; Lophatananon, Artitaya A; Lubinski, Jan J; Mannermaa, Arto A; Manoukian, Siranoush S; Margolin, Sara S; Matsuo, Keitaro K; Meindl, Alfons A; Mitchell, Gillian G; Muir, Kenneth K; , ; Nevelsteen, Ines I; van den Ouweland, Ans A; Peterlongo, Paolo P; Phuah, Sze Yee SY; Pylkäs, Katri K; Rowley, Simone M SM; Sangrajrang, Suleeporn S; Schmutzler, Rita K RK; Shen, Chen-Yang CY; Shu, Xiao-Ou XO; Southey, Melissa C MC; Surowy, Harald H; Swerdlow, Anthony A; Teo, Soo H SH; Tollenaar, Rob A E M RA; Tomlinson, Ian I; Torres, Diana D; Truong, Thérèse T; Vachon, Celine C; Verhoef, Senno S; Wong-Brown, Michelle M; Zheng, Wei W; Zheng, Ying Y; Nevanlinna, Heli H; Scott, Rodney J RJ; Andrulis, Irene L IL; Wu, Anna H AH; Hopper, John L JL; Couch, Fergus J FJ; Winqvist, Robert R; Burwinkel, Barbara B; Sawyer, Elinor J EJ; Schmidt, Marjanka K MK; Rudolph, Anja A; Dörk, Thilo T; Brauch, Hiltrud H; Hamann, Ute U; Neuhausen, Susan L SL; Milne, Roger L RL; Fletcher, Olivia O; Pharoah, Paul D P PD; Campbell, Ian G IG; Dunning, Alison M AM; Le Calvez-Kelm, Florence F; Goldgar, David E DE; Tavtigian, Sean V SV; Chenevix-Trench, Georgia G
Publication Date: 2016-05
Variant appearance in text: BRIP1: 890A>G; Lys297Arg; rs28997570
Germline variation in cancer-susceptibility genes in a healthy, ancestrally diverse cohort: implications for individual genome sequencing.
Plos One
Bodian, Dale L DL; McCutcheon, Justine N JN; Kothiyal, Prachi P; Huddleston, Kathi C KC; Iyer, Ramaswamy K RK; Vockley, Joseph G JG; Niederhuber, John E JE
Publication Date: 2014
Variant appearance in text: BRIP1: K297R; rs28997570
Genome-wide testing of putative functional exonic variants in relationship with breast and prostate cancer risk in a multiethnic population.
Plos Genetics
Haiman, Christopher A CA; Han, Ying Y; Feng, Ye Y; Xia, Lucy L; Hsu, Chris C; Sheng, Xin X; Pooler, Loreall C LC; Patel, Yesha Y; Kolonel, Laurence N LN; Carter, Erin E; Park, Karen K; Le Marchand, Loic L; Van Den Berg, David D; Henderson, Brian E BE; Stram, Daniel O DO
Publication Date: 2013-03
Variant appearance in text: BRIP1: K297R; rs28997570
A recurrent truncating germline mutation in the BRIP1/FANCJ gene and susceptibility to prostate cancer.
British Journal Of Cancer
Kote-Jarai, Z Z; Jugurnauth, S S; Mulholland, S S; Leongamornlert, D A DA; Guy, M M; Edwards, S S; Tymrakiewitcz, M M; O'Brien, L L; Hall, A A; Wilkinson, R R; Al Olama, A A AA; Morrison, J J; Muir, K K; Neal, D D; Donovan, J J; Hamdy, F F; Easton, D F DF; Eeles, R R; , ; ,