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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: May 28, 2023. (Total: 217323Documents)
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Records 1 - 4 (of 4 Records)

Query Trace: Fanconi Anemia and CHEK2[original query]
BRCA1, TP53, and CHEK2 germline mutations in uterine serous carcinoma.
Cancer 2013 Jan 119 (2): 332-8.
Pennington Kathryn P, Walsh Tom, Lee Ming, Pennil Christopher, Novetsky Akiva P, Agnew Kathy J, Thornton Anne, Garcia Rochelle, Mutch David, King Mary-Claire, Goodfellow Paul, Swisher Elizabeth
Exome sequencing identifies FANCM as a susceptibility gene for triple-negative breast cancer.
Proceedings of the National Academy of Sciences of the United States of America 2014 Oct 111 (42): 15172-7.
Kiiski Johanna I, Pelttari Liisa M, Khan Sofia, Freysteinsdottir Edda S, Reynisdottir Inga, Hart Steven N, Shimelis Hermela, Vilske Sara, Kallioniemi Anne, Schleutker Johanna, Leminen Arto, Bützow Ralf, Blomqvist Carl, Barkardottir Rosa B, Couch Fergus J, Aittomäki Kristiina, Nevanlinna He
Germline mutations in a DNA repair pathway are associated with familial colorectal cancer.
JCI insight 2021 9 6 (18): .
Xu Pingping, Sun Danfeng, Gao Yaqi, Jiang Yi, Zhong Ming, Zhao Gang, Chen Jinxian, Wang Zheng, Liu Qiang, Hong Jie, Chen Haoyan, Chen Ying-Xuan, Fang Jing-Yu
Genomic Analyses of Germline and Somatic Variation in High-Grade Serous Ovarian Cancer.
Research square 2023 3 .
Adamson Aaron W, Ding Yuan Chun, Steele Linda, Leong Lucile A, Morgan Robert, Wakabayashi Mark T, Han Ernest S, Dellinger Thanh H, Lin Paul S, Hakim Amy A, Wilczynski Sharon, Warden Charles D, Tao Shu, Bedell Victoria, Cristea Mihaela C, Neuhausen Susan
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