Human Genome Epidemiology Literature Finder
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Records 1 - 23 (of 23 Records) |
| Query Trace: Breast Neoplasms and RAD51B[original query] |
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| Mutation analysis of RAD51L1 (RAD51B/REC2) in multiple-case, non-BRCA1/2 breast cancer families. Breast cancer research and treatment 2011 Aug 129 (1): 255-63. Johnson Julie, Healey Sue, Khanna Kum Kum, , Chenevix-Trench Georg |
Genome-wide association study identifies a common variant in RAD51B associated with male breast cancer risk.
Nature genetics 2012 Nov 44 (11): 1182-4. Orr Nick, Lemnrau Alina, Cooke Rosie, Fletcher Olivia, Tomczyk Katarzyna, Jones Michael, Johnson Nichola, Lord Christopher J, Mitsopoulos Costas, Zvelebil Marketa, McDade Simon S, Buck Gemma, Blancher Christine, , Trainer Alison H, James Paul A, Bojesen Stig E, Bokmand Susanne, Nevanlinna Heli, Mattson Johanna, Friedman Eitan, Laitman Yael, Palli Domenico, Masala Giovanna, Zanna Ines, Ottini Laura, Giannini Giuseppe, Hollestelle Antoinette, Ouweland Ans M W van den, Novakovi? Srdjan, Krajc Mateja, Gago-Dominguez Manuela, Castelao Jose Esteban, Olsson Håkan, Hedenfalk Ingrid, Easton Douglas F, Pharoah Paul D P, Dunning Alison M, Bishop D Timothy, Neuhausen Susan L, Steele Linda, Houlston Richard S, Garcia-Closas Montserrat, Ashworth Alan, Swerdlow Anthony |
| Germline mutation in the RAD51B gene confers predisposition to breast cancer. BMC cancer 2013 13 (1): 484. Golmard Lisa, Caux-Moncoutier Virginie, Davy Grégoire, Al Ageeli Essam, Poirot Brigitte, Tirapo Carole, Michaux Dorothée, Barbaroux Catherine, d'Enghien Catherine Dubois, Nicolas André, Castéra Laurent, Sastre-Garau Xavier, Stern Marc-Henri, Houdayer Claude, Stoppa-Lyonnet Dominiq |
| Reproductive windows, genetic loci, and breast cancer risk. Annals of epidemiology 2014 May 24 (5): 376-82. Warren Andersen Shaneda, Trentham-Dietz Amy, Gangnon Ronald E, Hampton John M, Figueroa Jonine D, Skinner Halcyon G, Engelman Corinne D, Klein Barbara E, Titus Linda J, Egan Kathleen M, Newcomb Polly |
| Screening of HELQ in breast and ovarian cancer families. Familial cancer 2015 Sep . Pelttari Liisa M, Kinnunen Laura, Kiiski Johanna I, Khan Sofia, Blomqvist Carl, Aittomäki Kristiina, Nevanlinna He |
| 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 |
| RAD51, XRCC3, and XRCC2 mutation screening in Finnish breast cancer families. SpringerPlus 2015 4 92. Pelttari Liisa M, Kiiski Johanna I, Ranta Salla, Vilske Sara, Blomqvist Carl, Aittomäki Kristiina, Nevanlinna He |
| Germline RAD51B truncating mutation in a family with cutaneous melanoma. Familial cancer 2015 1 14 (2): 337-40. Wadt Karin A W, Aoude Lauren G, Golmard Lisa, Hansen Thomas V O, Sastre-Garau Xavier, Hayward Nicholas K, Gerdes Anne-Mar |
| An investigation of the association of genetic susceptibility risk with somatic mutation burden in breast cancer. British journal of cancer 2016 Sep 115 (6): 752-60. Zhu Bin, Mukherjee Anwesha, Machiela Mitchell J, Song Lei, Hua Xing, Shi Jianxin, Garcia-Closas Montserrat, Chanock Stephen J, Chatterjee Nilanj |
| RAD51B in Familial Breast Cancer. PloS one 2016 11 (5): e0153788. Pelttari Liisa M, Khan Sofia, Vuorela Mikko, Kiiski Johanna I, Vilske Sara, Nevanlinna Viivi, Ranta Salla, Schleutker Johanna, Winqvist Robert, Kallioniemi Anne, Dörk Thilo, Bogdanova Natalia V, Figueroa Jonine, Pharoah Paul D P, Schmidt Marjanka K, Dunning Alison M, García-Closas Montserrat, Bolla Manjeet K, Dennis Joe, Michailidou Kyriaki, Wang Qin, Hopper John L, Southey Melissa C, Rosenberg Efraim H, Fasching Peter A, Beckmann Matthias W, Peto Julian, Dos-Santos-Silva Isabel, Sawyer Elinor J, Tomlinson Ian, Burwinkel Barbara, Surowy Harald, Guénel Pascal, Truong Thérèse, Bojesen Stig E, Nordestgaard Børge G, Benitez Javier, González-Neira Anna, Neuhausen Susan L, Anton-Culver Hoda, Brenner Hermann, Arndt Volker, Meindl Alfons, Schmutzler Rita K, Brauch Hiltrud, Brüning Thomas, Lindblom Annika, Margolin Sara, Mannermaa Arto, Hartikainen Jaana M, Chenevix-Trench Georgia, , Van Dyck Laurien, Janssen Hilde, Chang-Claude Jenny, Rudolph Anja, Radice Paolo, Peterlongo Paolo, Hallberg Emily, Olson Janet E, Giles Graham G, Milne Roger L, Haiman Christopher A, Schumacher Fredrick, Simard Jacques, Dumont Martine, Kristensen Vessela, Borresen-Dale Anne-Lise, Zheng Wei, Beeghly-Fadiel Alicia, Grip Mervi, Andrulis Irene L, Glendon Gord, Devilee Peter, Seynaeve Caroline, Hooning Maartje J, Collée Margriet, Cox Angela, Cross Simon S, Shah Mitul, Luben Robert N, Hamann Ute, Torres Diana, Jakubowska Anna, Lubinski Jan, Couch Fergus J, Yannoukakos Drakoulis, Orr Nick, Swerdlow Anthony, Darabi Hatef, Li Jingmei, Czene Kamila, Hall Per, Easton Douglas F, Mattson Johanna, Blomqvist Carl, Aittomäki Kristiina, Nevanlinna He |
| Previous GWAS hits in relation to young-onset breast cancer. Breast cancer research and treatment 2016 Nov . Shi Min, O'Brien Katie M, Sandler Dale P, Taylor Jack A, Zaykin Dmitri V, Weinberg Clarice |
| Predicting Triple-Negative Breast Cancer Subtype Using Multiple Single Nucleotide Polymorphisms for Breast Cancer Risk and Several Variable Selection Methods. Geburtshilfe und Frauenheilkunde 2017 8 77 (6): 667-678. Häberle Lothar, Hein Alexander, Rübner Matthias, Schneider Michael, Ekici Arif B, Gass Paul, Hartmann Arndt, Schulz-Wendtland Rüdiger, Beckmann Matthias W, Lo Wing-Yee, Schroth Werner, Brauch Hiltrud, Fasching Peter A, Wunderle Mari |
| A polygenic risk score for breast cancer risk in a Taiwanese population. Breast cancer research and treatment 2017 Feb . Hsieh Yi-Chen, Tu Shih-Hsin, Su Chien-Tien, Cho Er-Chieh, Wu Chih-Hsiung, Hsieh Mao-Chih, Lin Shiyng-Yu, Liu Yun-Ru, Hung Chin-Sheng, Chiou Hung- |
| Contribution of germline deleterious variants in the RAD51 paralogs to breast and ovarian cancers. European journal of human genetics : EJHG 2017 Dec 25 (12): 1345-1353. Golmard Lisa, Castéra Laurent, Krieger Sophie, Moncoutier Virginie, Abidallah Khadija, Tenreiro Henrique, Laugé Anthony, Tarabeux Julien, Millot Gael A, Nicolas André, Laé Marick, Abadie Caroline, Berthet Pascaline, Polycarpe Florence, Frébourg Thierry, Elan Camille, de Pauw Antoine, Gauthier-Villars Marion, Buecher Bruno, Stern Marc-Henri, Stoppa-Lyonnet Dominique, Vaur Dominique, Houdayer Clau |
| Genetic Variations of DNA Repair Genes in Breast Cancer. Pathology oncology research : POR 2017 Oct . Özgöz Asuman, Hekimler Öztürk Kuya?, Yükseltürk Ay?egül, ?aml? Hale, Ba?kan Zuhal, Mutlu ?çduygu Fadime, Bacaks?z Mehm |
| Evaluating the breast cancer predisposition role of rare variants in genes associated with low-penetrance breast cancer risk SNPs. Breast cancer research : BCR 2018 01 20 (1): 3. Li Na, Rowley Simone M, Thompson Ella R, McInerny Simone, Devereux Lisa, Amarasinghe Kaushalya C, Zethoven Magnus, Lupat Richard, Goode David, Li Jason, Trainer Alison H, Gorringe Kylie L, James Paul A, Campbell Ian |
| Recommendations for Preventive Care for Women with Rare Genetic Cause of Breast and Ovarian Cancer. Klinicka onkologie : casopis Ceske a Slovenske onkologicke spolecnosti 2019 8 32 (Supplementum2): 6-13. Foretová Lenka, Navrátilová Marie, Svoboda Marek, Vaší?ková Petra, S?ahlová Eva Hrabincová, Házová Jana, Kleiblová Petra, Kleibl Zden?k, Machá?ková Eva, Palácová Markéta, Petráková Katarí |
| Germline variants in cancer genes in high-risk non-BRCA patients from Puerto Rico. Scientific reports 2019 Nov 9 (1): 17769. Dutil Julie, Teer Jamie K, Golubeva Volha, Yoder Sean, Tong Wei Lue, Arroyo Nelly, Karam Rachid, Echenique Miguel, Matta Jaime L, Monteiro Alvaro |
| Germline RAD51B variants confer susceptibility to breast and ovarian cancers deficient in homologous recombination. NPJ breast cancer 2021 Oct 7 (1): 135. Setton Jeremy, Selenica Pier, Mukherjee Semanti, Shah Rachna, Pecorari Isabella, McMillan Biko, Pei Isaac X, Kemel Yelena, Ceyhan-Birsoy Ozge, Sheehan Margaret, Tkachuk Kaitlyn, Brown David N, Zhang Liying, Cadoo Karen, Powell Simon, Weigelt Britta, Robson Mark, Riaz Nadeem, Offit Kenneth, Reis-Filho Jorge S, Mandelker Dia |
| Major Response to Carboplatin in a Patient With Metastatic Triple-Negative Breast Cancer With Somatic Mutation of BRCA1 and Loss of RAD51B. JCO precision oncology 2022 2 3 1-9. Seguin Lorène, Chaffanet Max, Garnier Séverine, Adélaïde José, Carbuccia Nadine, Guille Arnaud, Pakradouni Jihane, Sabatier Renaud, Popovici Cornel, Birnbaum Daniel, Bertucci François, Goncalves Antho |
| Genetic Predisposition to Male Breast Cancer: A Case Series. Anticancer research 2022 12 42 (12): 5795-5801. Apessos Angela, Agiannitopoulos Konstantinos, Pepe Georgia, Tsaousis Georgios N, Pitta Panagiota, Bili Chrysanthi, Florentin Lina, Saloustros Emmanouel, Kampletsas Eleftherios, Tryfonopoulos Dimitrios, Tsoukalas Nikolaos, Bournakis Evangelos, Zagouri Flora, Kotsakis Athanassios, Koumarianou Anna, Korantzis Ippokratis, Boukovinas Ioannis, Lypas George, Fountzilas Georgios, Michalaki Vasiliki, Xynogalos Spyridon, Linardou Helena, Papadopoulou Eirini, Nasioulas George, Georgoulias Vassil |
| Comprehensive Analysis of the Expression and Prognosis for RAD51 Family in Human Breast Cancer. International journal of general medicine 2022 15 4925-4936. Shi Yaqin, Shen Meng, Xu Mengdan, Tao Min, Chen Kai, Zhu Qingqi |
| Genetic variants in African-American and Hispanic patients with breast cancer. Oncology letters 2023 1 25 (2): 51. Dutta Pranabananda, Keung Man Y, Wu Yanyuan, Vadgama Jaydutt |
- Page last reviewed:Feb 1, 2024
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