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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 5 (of 5 Records)

Query Trace: Neoplasms and RINT1[original query]
Rare mutations in RINT1 predispose carriers to breast and Lynch syndrome-spectrum cancers.
Cancer discovery 2014 Jul 4 (7): 804-15.
Park Daniel J, Tao Kayoko, Le Calvez-Kelm Florence, Nguyen-Dumont Tu, Robinot Nivonirina, Hammet Fleur, Odefrey Fabrice, Tsimiklis Helen, Teo Zhi L, Thingholm Louise B, Young Erin L, Voegele Catherine, Lonie Andrew, Pope Bernard J, Roane Terrell C, Bell Russell, Hu Hao, Shankaracharya , Huff Chad D, Ellis Jonathan, Li Jun, Makunin Igor V, John Esther M, Andrulis Irene L, Terry Mary B, Daly Mary, Buys Saundra S, Snyder Carrie, Lynch Henry T, Devilee Peter, Giles Graham G, Hopper John L, Feng Bing-Jian, Lesueur Fabienne, Tavtigian Sean V, Southey Melissa C, Goldgar David
Reevaluation of RINT1 as a breast cancer predisposition gene.
Breast cancer research and treatment 2016 Sep 159 (2): 385-92.
Li Na, Thompson Ella R, Rowley Simone M, McInerny Simone, Devereux Lisa, Goode David, Investigators LifePool, Wong-Brown Michelle W, Scott Rodney J, Trainer Alison H, Gorringe Kylie L, James Paul A, Campbell Ian
Multigene testing of moderate-risk genes: be mindful of the missense.
Journal of medical genetics 2016 06 53 (6): 366-76.
Young E L, Feng B J, Stark A W, Damiola F, Durand G, Forey N, Francy T C, Gammon A, Kohlmann W K, Kaphingst K A, McKay-Chopin S, Nguyen-Dumont T, Oliver J, Paquette A M, Pertesi M, Robinot N, Rosenthal J S, Vallee M, Voegele C, Hopper J L, Southey M C, Andrulis I L, John E M, Hashibe M, Gertz J, , Le Calvez-Kelm F, Lesueur F, Goldgar D E, Tavtigian S
Identification of candidate cancer predisposing variants by performing whole-exome sequencing on index patients from BRCA1 and BRCA2-negative breast cancer families.
BMC cancer 2019 Apr 19 (1): 313.
Shahi Rajendra Bahadur, De Brakeleer Sylvia, Caljon Ben, Pauwels Ingrid, Bonduelle Maryse, Joris Sofie, Fontaine Christel, Vanhoeij Marian, Van Dooren Sonia, Teugels Erik, De Grève Jacqu
Analysis of 11 candidate genes in 849 adult patients with suspected hereditary cancer predisposition.
Genes, chromosomes & cancer 2020 Oct .
Cavaillé Mathias, Uhrhammer Nancy, Privat Maud, Ponelle-Chachuat Flora, Gay-Bellile Mathilde, Lepage Mathis, Molnar Ioana, Viala Sandrine, Bidet Yannick, Bignon Yves-Je
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