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| Concurrent BRAFV600E and BRCA Mutations in MSS Metastatic Colorectal Cancer: Prevalence and Case Series of mCRC patients with prolonged OS. Cancer treatment and research communications 2022 Apr 32 100569. Cannon Timothy Lewis, Randall Jamie N, Sokol Ethan S, Alexander Sonja M, Wadlow Raymond C, Winer Arthur A, Barnett Daniel M, Rayes Danny L, Nimeiri Halla S, McGregor Kimberly |
| 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 |
| 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 |
| Mutations in DNA Repair Genes and Clinical Outcomes of Patients With Metastatic Colorectal Cancer Receiving Oxaliplatin or Irinotecan-containing Regimens. American journal of clinical oncology 2020 Dec . Marks Eric I, Matera Robert, Olszewski Adam J, Yakirevich Evgeny, El-Deiry Wafik S, Safran Howard, Carneiro Benedito |
| 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 |
| A Comprehensive Analysis of Alterations in DNA Damage Repair Pathways Reveals a Potential Way to Enhance the Radio-Sensitivity of Esophageal Squamous Cell Cancer. Frontiers in oncology 2020 10 575711. Wang Guangchao, Guo Shichao, Zhang Weimin, Li Zhangfu, Xu Jiancheng, Li Dan, Wang Yan, Zhan Qim |
| 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 |
| DNA repair and cancer in colon and rectum: Novel players in genetic susceptibility. International journal of cancer 2019 Jun . Pardini Barbara, Corrado Alda, Paolicchi Elisa, Cugliari Giovanni, Berndt Sonja I, Bezieau Stephane, Bien Stephanie A, Brenner Hermann, Caan Bette J, Campbell Peter T, Casey Graham, Chan Andrew T, Chang-Claude Jenny, Cotterchio Michelle, Gala Manish, Gallinger Steven J, Haile Robert W, Harrison Tabitha A, Hayes Richard B, Hoffmeister Michael, Hopper John L, Hsu Li, Huyghe Jeroen, Jenkins Mark A, Le Marchand Loic, Lin Yi, Lindor Noralane M, Nan Hongmei, Newcomb Polly A, Ogino Shuji, Potter John D, Schoen Robert E, Slattery Martha L, White Emily, Vodickova Ludmila, Vymetalkova Veronika, Vodicka Pavel, Gemignani Federica, Peters Ulrike, Naccarati Alessio, Landi Stefa |
| Genetic interaction analysis among oncogenesis-related genes revealed novel genes and networks in lung cancer development. Oncotarget 2019 Mar 10 (19): 1760-1774. Li Yafang, Xiao Xiangjun, Bossé Yohan, Gorlova Olga, Gorlov Ivan, Han Younghun, Byun Jinyoung, Leighl Natasha, Johansen Jakob S, Barnett Matt, Chen Chu, Goodman Gary, Cox Angela, Taylor Fiona, Woll Penella, Wichmann H Erich, Manz Judith, Muley Thomas, Risch Angela, Rosenberger Albert, Han Jiali, Siminovitch Katherine, Arnold Susanne M, Haura Eric B, Bolca Ciprian, Holcatova Ivana, Janout Vladimir, Kontic Milica, Lissowska Jolanta, Mukeria Anush, Ognjanovic Simona, Orlowski Tadeusz M, Scelo Ghislaine, Swiatkowska Beata, Zaridze David, Bakke Per, Skaug Vidar, Zienolddiny Shanbeh, Duell Eric J, Butler Lesley M, Houlston Richard, Artigas María Soler, Grankvist Kjell, Johansson Mikael, Shepherd Frances A, Marcus Michael W, Brunnström Hans, Manjer Jonas, Melander Olle, Muller David C, Overvad Kim, Trichopoulou Antonia, Tumino Rosario, Liu Geoffrey, Bojesen Stig E, Wu Xifeng, Le Marchand Loic, Albanes Demetrios, Bickeböller Heike, Aldrich Melinda C, Bush William S, Tardon Adonina, Rennert Gad, Teare M Dawn, Field John K, Kiemeney Lambertus A, Lazarus Philip, Haugen Aage, Lam Stephen, Schabath Matthew B, Andrew Angeline S, Bertazzi Pier Alberto, Pesatori Angela C, Christiani David C, Caporaso Neil, Johansson Mattias, McKay James D, Brennan Paul, Hung Rayjean J, Amos Christopher |
Genome-wide association analyses identify 139 loci associated with macular thickness in the UK Biobank cohort.
Human molecular genetics 2019 04 28 (7): 1162-1172. Gao X Raymond, Huang Hua, Kim Heej |
| 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 |
| 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 |
| 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- |
| 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 |
| 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 |
| Genetic variants within microRNA-binding site of RAD51B are associated with risk of cervical cancer in Chinese women. Cancer medicine 2016 Sep 5 (9): 2596-601. Hang Dong, Zhou Wen, Jia Meiqun, Wang Lihua, Zhou Jing, Yin Yin, Ma Hongxia, Hu Zhibin, Li Ni, Shen Hongb |
| Gene and pathway level analyses of germline DNA-repair gene variants and prostate cancer susceptibility using the iCOGS-genotyping array. British journal of cancer 2016 Mar . Saunders Edward J, Dadaev Tokhir, Leongamornlert Daniel A, Olama Ali Amin Al, Benlloch Sara, Giles Graham G, Wiklund Fredrik, Grönberg Henrik, Haiman Christopher A, Schleutker Johanna, Nordestgaard Børge G, Travis Ruth C, Neal David, Pasayan Nora, Khaw Kay-Tee, Stanford Janet L, Blot William J, Thibodeau Stephen N, Maier Christiane, Kibel Adam S, Cybulski Cezary, Cannon-Albright Lisa, Brenner Hermann, Park Jong Y, Kaneva Radka, Batra Jyotsna, Teixeira Manuel R, Pandha Hardev, Govindasami Koveela, Muir Ken, , , , Easton Douglas F, Eeles Rosalind A, Kote-Jarai Zsof |
| Prioritizing Variants in Complete Hereditary Breast and Ovarian Cancer Genes in Patients Lacking Known BRCA Mutations. Human mutation 2016 Feb . Caminsky Natasha G, Mucaki Eliseos J, Perri Ami M, Lu Ruipeng, Knoll Joan H M, Rogan Peter |
| 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 |
| 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 |
| 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 |
| Polymorphisms of homologous recombination RAD51, RAD51B, XRCC2, and XRCC3 genes and the risk of prostate cancer. Analytical cellular pathology (Amsterdam) 2015 2015 828646. Nowacka-Zawisza Maria, Wi?nik Ewelina, Wasilewski Andrzej, Skowro?ska Milena, Forma Ewa, Bry? Magdalena, Ró?a?ski Waldemar, Krajewska Wanda |
| 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 |
| Genome-wide association study of subtype-specific epithelial ovarian cancer risk alleles using pooled DNA. Human genetics 2014 May 133 (5): 481-97. Earp Madalene A, Kelemen Linda E, Magliocco Anthony M, Swenerton Kenneth D, Chenevix-Trench Georgia, , , Lu Yi, Hein Alexander, Ekici Arif B, Beckmann Matthias W, Fasching Peter A, Lambrechts Diether, Despierre Evelyn, Vergote Ignace, Lambrechts Sandrina, Doherty Jennifer A, Rossing Mary Anne, Chang-Claude Jenny, Rudolph Anja, Friel Grace, Moysich Kirsten B, Odunsi Kunle, Sucheston-Campbell Lara, Lurie Galina, Goodman Marc T, Carney Michael E, Thompson Pamela J, Runnebaum Ingo B, Dürst Matthias, Hillemanns Peter, Dörk Thilo, Antonenkova Natalia, Bogdanova Natalia, Leminen Arto, Nevanlinna Heli, Pelttari Liisa M, Butzow Ralf, Bunker Clareann H, Modugno Francesmary, Edwards Robert P, Ness Roberta B, du Bois Andreas, Heitz Florian, Schwaab Ira, Harter Philipp, Karlan Beth Y, Walsh Christine, Lester Jenny, Jensen Allan, Kjær Susanne K, Høgdall Claus K, Høgdall Estrid, Lundvall Lene, Sellers Thomas A, Fridley Brooke L, Goode Ellen L, Cunningham Julie M, Vierkant Robert A, Giles Graham G, Baglietto Laura, Severi Gianluca, Southey Melissa C, Liang Dong, Wu Xifeng, Lu Karen, Hildebrandt Michelle A T, Levine Douglas A, Bisogna Maria, Schildkraut Joellen M, Iversen Edwin S, Weber Rachel Palmieri, Berchuck Andrew, Cramer Daniel W, Terry Kathryn L, Poole Elizabeth M, Tworoger Shelley S, Bandera Elisa V, Chandran Urmila, Orlow Irene, Olson Sara H, Wik Elisabeth, Salvesen Helga B, Bjorge Line, Halle Mari K, van Altena Anne M, Aben Katja K H, Kiemeney Lambertus A, Massuger Leon F A G, Pejovic Tanja, Bean Yukie T, Cybulski Cezary, Gronwald Jacek, Lubinski Jan, Wentzensen Nicolas, Brinton Louise A, Lissowska Jolanta, Garcia-Closas Montserrat, Dicks Ed, Dennis Joe, Easton Douglas F, Song Honglin, Tyrer Jonathan P, Pharoah Paul D P, Eccles Diana, Campbell Ian G, Whittemore Alice S, McGuire Valerie, Sieh Weiva, Rothstein Joseph H, Flanagan James M, Paul James, Brown Robert, Phelan Catherine M, Risch Harvey A, McLaughlin John R, Narod Steven A, Ziogas Argyrios, Anton-Culver Hoda, Gentry-Maharaj Aleksandra, Menon Usha, Gayther Simon A, Ramus Susan J, Wu Anna H, Pearce Celeste L, Pike Malcolm C, Dansonka-Mieszkowska Agnieszka, Rzepecka Iwona K, Szafron Lukasz M, Kupryjanczyk Jolanta, Cook Linda S, Le Nhu D, Brooks-Wilson Angela, |
| 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 |
| Characterization of uterine leiomyomas by whole-genome sequencing. The New England journal of medicine 2013 Jul 369 (1): 43-53. Mehine Miika, Kaasinen Eevi, Mäkinen Netta, Katainen Riku, Kämpjärvi Kati, Pitkänen Esa, Heinonen Hanna-Riikka, Bützow Ralf, Kilpivaara Outi, Kuosmanen Anna, Ristolainen Heikki, Gentile Massimiliano, Sjöberg Jari, Vahteristo Pia, Aaltonen Lauri |
| 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 |
| 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 |
| 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 |
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- Page last updated:Aug 18, 2022
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