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Public Health Genomics and Precision Health Knowledge Base (v7.1)

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HuGE Literature Finder

Records 1-15

Query Trace: Breast Neoplasms and PMS2[original query]

Germline copy number variations in BRCA1/2 negative families: Role in the molecular etiology of hereditary breast cancer in Tunisia. PloS one 2021 16 (1): e0245362. Boujemaa Maroua, Hamdi Yosr, Mejri Nesrine, Romdhane Lilia, Ghedira Kais, Bouaziz Hanen, El Benna Houda, Labidi Soumaya, Dallali Hamza, Jaidane Olfa, Ben Nasr Sonia, Haddaoui Abderrazek, Rahal Khaled, Abdelhak Sonia, Boussen Hamouda, Boubaker Mohamed Sam Similar articles in PubMed
Multigene panel testing results in patients with multiple breast cancer primaries. The breast journal 2020 Jan . Corredor Jessica, Woodson Ashley H, Gutierrez Barrera Angelica, Arun Ba Similar articles in PubMed
Germline investigation in male breast cancer of DNA repair genes by next-generation sequencing. Breast cancer research and treatment 2019 Sep . Scarpitta R, Zanna I, Aretini P, Gambino G, Scatena C, Mei B, Ghilli M, Rossetti E, Roncella M, Congregati C, Bonci F, Naccarato A G, Palli D, Caligo M Similar articles in PubMed
The rate of the recurrent MSH6 mutations in Ashkenazi Jewish breast cancer patients. Cancer causes & control : CCC 2019 Jan 30 (1): 97-101. Bernstein-Molho Rinat, Laitman Yael, Schayek Hagit, Iomdin Sarah, Friedman Eit Similar articles in PubMed
Association of Breast and Ovarian Cancers With Predisposition Genes Identified by Large-Scale Sequencing. JAMA oncology 2018 Aug . Lu Hsiao-Mei, Li Shuwei, Black Mary Helen, Lee Shela, Hoiness Robert, Wu Sitao, Mu Wenbo, Huether Robert, Chen Jefferey, Sridhar Srijani, Tian Yuan, McFarland Rachel, Dolinsky Jill, Tippin Davis Brigette, Mexal Sharon, Dunlop Charles, Elliott Aar Similar articles in PubMed
Detection of novel germline mutations in six breast cancer predisposition genes by targeted next-generation sequencing. Human mutation 2018 Jul . Dong Li, Wu Nan, Wang Shaojing, Cheng Yanan, Han Lei, Zhao Jing, Long Xinxin, Mu Kun, Li Menghui, Wei Lijuan, Wang Wanheng, Zhang Weijia, Cao Yandong, Liu Juntian, Yu Jinpu, Hao Xish Similar articles in PubMed
High frequency of pathogenic non-founder germline mutations in BRCA1 and BRCA2 in families with breast and ovarian cancer in a founder population. Hereditary cancer in clinical practice 2018 16 12. Maksimenko J, Irmejs A, Trofimovi?s G, B?rzi?a D, Skuja E, Purkalne G, Miklaševi?s E, Gardovskis Similar articles in PubMed
Associations Between Cancer Predisposition Testing Panel Genes and Breast Cancer. JAMA oncology 2017 Sep 3 (9): 1190-1196. Couch Fergus J, Shimelis Hermela, Hu Chunling, Hart Steven N, Polley Eric C, Na Jie, Hallberg Emily, Moore Raymond, Thomas Abigail, Lilyquist Jenna, Feng Bingjian, McFarland Rachel, Pesaran Tina, Huether Robert, LaDuca Holly, Chao Elizabeth C, Goldgar David E, Dolinsky Jill Similar articles in PubMed
Frequency of Germline Mutations in 25 Cancer Susceptibility Genes in a Sequential Series of Patients With Breast Cancer. Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2016 Mar . Tung Nadine, Lin Nancy U, Kidd John, Allen Brian A, Singh Nanda, Wenstrup Richard J, Hartman Anne-Renee, Winer Eric P, Garber Judy Similar articles in PubMed
Prevalence of germline mutations in cancer predisposition genes in patients with pancreatic cancer. Gastroenterology 2015 Mar 148 (3): 556-64. Grant Robert C, Selander Iris, Connor Ashton A, Selvarajah Shamini, Borgida Ayelet, Briollais Laurent, Petersen Gloria M, Lerner-Ellis Jordan, Holter Spring, Gallinger Stev Similar articles in PubMed
Risk of secondary malignancy (including breast) in patients with mismatch-repair protein deficiency. The American journal of surgical pathology 2014 Nov 38 (11): 1494-500. Clay Michael R, Allison Kimberly H, Folkins Ann K, Longacre Teri Similar articles in PubMed
Risks of Colorectal and Other Cancers After Endometrial Cancer for Women With Lynch Syndrome. Journal of the National Cancer Institute 2013 Feb . Win AK, Lindor NM, Winship I, Tucker KM, Buchanan DD, Young JP, Rosty C, Leggett B, Giles GG, Goldblatt J, Macrae FA, Parry S, Kalady MF, Baron JA, Ahnen DJ, Marchand LL, Gallinger S, Haile RW, Newcomb PA, Hopper JL, Jenkins MA Similar articles in PubMed
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 Similar articles in PubMed
Colorectal and other cancer risks for carriers and noncarriers from families with a DNA mismatch repair gene mutation: a prospective cohort study. Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2012 Mar 30 (9): 958-64. Win Aung Ko, Young Joanne P, Lindor Noralane M, Tucker Katherine M, Ahnen Dennis J, Young Graeme P, Buchanan Daniel D, Clendenning Mark, Giles Graham G, Winship Ingrid, Macrae Finlay A, Goldblatt Jack, Southey Melissa C, Arnold Julie, Thibodeau Stephen N, Gunawardena Shanaka R, Bapat Bharati, Baron John A, Casey Graham, Gallinger Steven, Le Marchand Loïc, Newcomb Polly A, Haile Robert W, Hopper John L, Jenkins Mark Similar articles in PubMed
Association of rare MSH6 variants with familial breast cancer. Breast cancer research and treatment 2010 Sep 123 (2): 315-20. Wasielewski Marijke, Riaz Muhammad, Vermeulen Joyce, van den Ouweland Ans, Labrijn-Marks Ineke, Olmer Renske, van der Spaa Linda, Klijn Jan G M, Meijers-Heijboer Hanne, Dooijes Dennis, Schutte Mie Similar articles in PubMed

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