Human Genome Epidemiology Literature Finder
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Records 1 - 20 (of 20 Records) |
| Query Trace: Breast Neoplasms and MRE11A[original query] |
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| DNA-repair genetic polymorphisms and risk of breast cancer in Cyprus. Breast cancer research and treatment 2008 Jun . Loizidou MA, Michael T, Neuhausen SL, Newbold RF, Marcou Y, Kakouri E, Daniel M, Papadopoulos P, Malas S, Hadjisavvas A, Kyriacou K |
| Genetic variation in genes interacting with BRCA1/2 and risk of breast cancer in the Cypriot population. Breast cancer research and treatment 2010 May 121 (1): 147-56. Loizidou Maria A, Cariolou Marios A, Neuhausen Susan L, Newbold Robert F, Bashiardes Evy, Marcou Yiola, Michael Thalia, Daniel Maria, Kakouri Eleni, Papadopoulos Panayiotis, Malas Simon, Hadjisavvas Andreas, Kyriacou Kyriac |
| Variants in activators and downstream targets of ATM, radiation exposure, and contralateral breast cancer risk in the WECARE study. Human mutation 2012 Jan 33 (1): 158-64. Brooks Jennifer D, Teraoka Sharon N, Reiner Anne S, Satagopan Jaya M, Bernstein Leslie, Thomas Duncan C, Capanu Marinela, Stovall Marilyn, Smith Susan A, Wei Shan, Shore Roy E, Boice John D, Lynch Charles F, Mellemkjaer Lene, Malone Kathleen E, Liang Xiaolin, , Haile Robert W, Concannon Patrick, Bernstein Jonine |
| Modification of BRCA1-Associated Breast and Ovarian Cancer Risk by BRCA1-Interacting Genes. Cancer research 2011 Sep 71 (17): 5792-805. Rebbeck Timothy R, Mitra Nandita, Domchek Susan M, Wan Fei, Friebel Tara M, Tran Teo V, Singer Christian F, Tea Muy-Kheng Maria, Blum Joanne L, Tung Nadine, Olopade Olufunmilayo I, Weitzel Jeffrey N, Lynch Henry T, Snyder Carrie L, Garber Judy E, Antoniou Antonis C, Peock Susan, Evans D Gareth, Paterson Joan, Kennedy M John, Donaldson Alan, Dorkins Huw, Easton Douglas F, , Rubinstein Wendy S, Daly Mary B, Isaacs Claudine, Nevanlinna Heli, Couch Fergus J, Andrulis Irene L, Freidman Eitan, Laitman Yael, Ganz Patricia A, Tomlinson Gail E, Neuhausen Susan L, Narod Steven A, Phelan Catherine M, Greenberg Roger, Nathanson Katherine |
| Telomere length, telomere-related genes, and breast cancer risk: the breast cancer health disparities study. Genes, chromosomes & cancer 2013 Jul 52 (7): 595-609. Pellatt Andrew J, Wolff Roger K, Torres-Mejia Gabriela, John Esther M, Herrick Jennifer S, Lundgreen Abbie, Baumgartner Kathy B, Giuliano Anna R, Hines Lisa M, Fejerman Laura, Cawthon Richard, Slattery Martha |
| Rare key functional domain missense substitutions in MRE11A, RAD50, and NBN contribute to breast cancer susceptibility: results from a Breast Cancer Family Registry case-control mutation-screening study. Breast cancer research : BCR 2014 16 (3): R58. Damiola Francesca, Pertesi Maroulio, Oliver Javier, Le Calvez-Kelm Florence, Voegele Catherine, Young Erin L, Robinot Nivonirina, Forey Nathalie, Durand Geoffroy, Vallée Maxime P, Tao Kayoko, Roane Terrell C, Williams Gareth J, Hopper John L, Southey Melissa C, Andrulis Irene L, John Esther M, Goldgar David E, Lesueur Fabienne, Tavtigian Sean |
| Expanding the genetic basis of copy number variation in familial breast cancer. Hereditary cancer in clinical practice 2014 12 (1): 15. Masson Amy L, Talseth-Palmer Bente A, Evans Tiffany-Jane, Grice Desma M, Hannan Garry N, Scott Rodney |
| Detection of novel germline mutations for breast cancer in non-BRCA1/2 families. The FEBS journal 2015 Sep 282 (17): 3424-37. Aloraifi Fatima, McDevitt Trudi, Martiniano Rui, McGreevy Jonah, McLaughlin Russell, Egan Chris M, Cody Nuala, Meany Marie, Kenny Elaine, Green Andrew J, Bradley Daniel G, Geraghty James G, Bracken Adrian |
| Evaluation of miRNA-binding-site SNPs of MRE11A, NBS1, RAD51 and RAD52 involved in HRR pathway genes and risk of breast cancer in China. Molecular genetics and genomics : MGG 2015 Jun 290 (3): 1141-53. Wu Zhenzhen, Wang Peng, Song Chunhua, Wang Kaijuan, Yan Rui, Li Jingruo, Dai Lipi |
| 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 |
| Breast cancer risk and germline genomic profiling of women with neurofibromatosis type 1 who developed breast cancer. Genes, chromosomes & cancer 2017 9 57 (1): 19-27. Wang Xia, Teer Jamie K, Tousignant Renee N, Levin Albert M, Boulware David, Chitale Dhananjay A, Shaw Brandon M, Chen Zhihua, Zhang Yonghong, Blakeley Jaishri O, Acosta Maria T, Messiaen Ludwine M, Korf Bruce R, Tainsky Michael |
| Next-Generation Sequencing Reveals a Nonsense Mutation (p.Arg364Ter) in MRE11A Gene in an Indian Patient with Familial Breast Cancer. Breast care (Basel, Switzerland) 2017 May 12 (2): 114-116. Sharma Bhai Pratibha, Sharma Deepak, Saxena Renu, Verma Ishwar |
| Genomic analysis of inherited breast cancer among Palestinian women: Genetic heterogeneity and a founder mutation in TP53. International journal of cancer 2017 08 141 (4): 750-756. Lolas Hamameh Suhair, Renbaum Paul, Kamal Lara, Dweik Dima, Salahat Mohammad, Jaraysa Tamara, Abu Rayyan Amal, Casadei Silvia, Mandell Jessica B, Gulsuner Suleyman, Lee Ming K, Walsh Tom, King Mary-Claire, Levy-Lahad Ephrat, Kanaan Moe |
| 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 |
| 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 |
| Variants of cancer susceptibility genes in Korean BRCA1/2 mutation-negative patients with high risk for hereditary breast cancer. BMC cancer 2018 01 18 (1): 83. Park Ji Soo, Lee Seung-Tae, Nam Eun Ji, Han Jung Woo, Lee Jung-Yun, Kim Jieun, Kim Tae Il, Park Hyung Se |
| New germline BRCA2 gene variant in the Tuvinian Mongol breast cancer patients. Molecular biology reports 2019 7 46 (5): 5537-5541. Gervas Polina, Klyuch Boris, Denisov Evgeny, Kiselev Artem, Molokov Alexey, Pisareva Lubov, Malinovskaya Elena, Choynzonov Evgeny, Cherdyntseva Nadez |
| Multi-gene panel testing increases germline predisposing mutations' detection in a cohort of breast/ovarian cancer patients from Southern Italy. Frontiers in medicine 2022 9 894358. Nunziato Marcella, Di Maggio Federica, Pensabene Matilde, Esposito Maria Valeria, Starnone Flavio, De Angelis Carmine, Calabrese Alessandra, D'Aiuto Massimiliano, Botti Gerardo, De Placido Sabino, D'Argenio Valeria, Salvatore Frances |
| Pathogenicity Reclassification of Genetic Variants Related to Early-Onset Breast Cancer among Women of Mongoloid Origin. Asian Pacific journal of cancer prevention : APJCP 2022 6 23 (6): 2027-2033. Gervas Polina, Molokov Aleksey, Babyshkina Nataliya, Kiselev Artem, Zarubin Aleksei, Yumov Evgeny, Pisareva Lubov, Choynzonov Evgeny, Cherdyntseva Nadez |
| Germline Variants in 32 Cancer-Related Genes among 700 Chinese Breast Cancer Patients by Next-Generation Sequencing: A Clinic-Based, Observational Study. International journal of molecular sciences 2022 Sep 23 (19): . Yang Liu, Xie Fei, Liu Chang, Zhao Jin, Hu Taobo, Wu Jinbo, Zhao Xiaotao, Wang S |
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