HuGE Literature Finder
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Records 1-73
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Analysis of polymorphisms in genes associated with the FA/BRCA pathway in three patients with multiple primary malignant neoplasms.
Artificial cells, nanomedicine, and biotechnology 2019 Dec 47 (1): 1101-1112. Wang Le, Wang Hao, Wang Ting, Liu Jinhui, Chen Wei, Wang Yamin, Chen Chao, Zhu Hongli, Dai Pengg |
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A common SNP in the uracil-DNA glycosylase gene UNG decreases ovarian cancer risk in BRCA2 mutation carriers.
Molecular oncology 2019 Feb . Baquero Juan Miguel, Benítez-Buelga Carlos, Fernández Victoria, Urioste Miguel, García-Giménez Jose Luis, Perona Rosario, , Benítez Javier, Osorio A |
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Modulation of homologous recombination repair gene polymorphisms on genetic damage in chromate exposed workers.
Environmental toxicology and pharmacology 2019 Jan 66 126-132. Long Changmao, Liu Jiaxing, Hu Guiping, Feng Huimin, Zhou Di, Wang Jing, Zhai Xinxia, Zhao Zuchang, Yu Shanfa, Wang Tiancheng, Jia Gua |
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RAD50 germline mutations are associated with poor survival in BRCA1/2-negative breast cancer patients.
International journal of cancer 2018 Oct 143 (8): 1935-1942. Fan Cong, Zhang Juan, Ouyang Tao, Li Jinfeng, Wang Tianfeng, Fan Zhaoqing, Fan Tie, Lin Benyao, Xie Yunt |
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Addition of triple negativity of breast cancer as an indicator for germline mutations in predisposing genes increases sensitivity of clinical selection criteria.
BMC cancer 2018 Sep 18 (1): 926. Hoyer Juliane, Vasileiou Georgia, Uebe Steffen, Wunderle Marius, Kraus Cornelia, Fasching Peter A, Thiel Christian T, Hartmann Arndt, Beckmann Matthias W, Lux Michael P, Reis And |
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Frequency of Germline Mutations in Cancer Susceptibility Genes in Malignant Mesothelioma.
Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2018 Aug JCO2018785204. Panou Vasiliki, Gadiraju Meghana, Wolin Arthur, Weipert Caroline M, Skarda Emily, Husain Aliya N, Patel Jyoti D, Rose Buerkley, Zhang Shannon R, Weatherly Madison, Nelakuditi Viswateja, Knight Johnson Amy, Helgeson Maria, Fischer David, Desai Arpita, Sulai Nanna, Ritterhouse Lauren, Røe Oluf D, Turaga Kiran K, Huo Dezheng, Segal Jeremy, Kadri Sabah, Li Zejuan, Kindler Hedy L, Churpek Jane |
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Germline cancer susceptibility gene variants, somatic second hits, and survival outcomes in patients with resected pancreatic cancer.
Genetics in medicine : official journal of the American College of Medical Genetics 2018 Jul . Yurgelun Matthew B, Chittenden Anu B, Morales-Oyarvide Vicente, Rubinson Douglas A, Dunne Richard F, Kozak Margaret M, Qian Zhi Rong, Welch Marisa W, Brais Lauren K, Da Silva Annacarolina, Bui Justin L, Yuan Chen, Li Tingting, Li Wanwan, Masuda Atsuhiro, Gu Mancang, Bullock Andrea J, Chang Daniel T, Clancy Thomas E, Linehan David C, Findeis-Hosey Jennifer J, Doyle Leona A, Thorner Aaron R, Ducar Matthew D, Wollison Bruce M, Khalaf Natalia, Perez Kimberly, Syngal Sapna, Aguirre Andrew J, Hahn William C, Meyerson Matthew L, Fuchs Charles S, Ogino Shuji, Hornick Jason L, Hezel Aram F, Koong Albert C, Nowak Jonathan A, Wolpin Brian |
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Genetic variation in the NEIL2 DNA glycosylase gene is associated with oxidative DNA damage in BRCA2 mutation carriers.
Oncotarget 2017 Dec 8 (70): 114626-114636. Benítez-Buelga Carlos, Baquero Juan Miguel, Vaclova Tereza, Fernández Victoria, Martín Paloma, Inglada-Perez Lucia, Urioste Miguel, Osorio Ana, Benítez Javi |
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BRCA locus-specific loss of heterozygosity in germline BRCA1 and BRCA2 carriers.
Nature communications 2017 Aug 8 (1): 319. Maxwell Kara N, Wubbenhorst Bradley, Wenz Brandon M, De Sloover Daniel, Pluta John, Emery Lyndsey, Barrett Amanda, Kraya Adam A, Anastopoulos Ioannis N, Yu Shun, Jiang Yuchao, Chen Hao, Zhang Nancy R, Hackman Nicole, D'Andrea Kurt, Daber Robert, Morrissette Jennifer J D, Mitra Nandita, Feldman Michael, Domchek Susan M, Nathanson Katherine |
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Germline BRCA mutations in Asian patients with pancreatic adenocarcinoma: a prospective study evaluating risk category for genetic testing.
Investigational new drugs 2017 Aug . Lee Kyoungmin, Yoo Changhoon, Kim Kyu-Pyo, Park Kyoung-Jin, Chang Heung-Moon, Kim Tae Won, Lee Jae-Lyun, Lee Woochang, Lee Sang Soo, Park Do Hyun, Song Tae Jun, Seo Dong Wan, Lee Sung Koo, Kim Myung-Hwan, Shin Sang Hyun, Hwang Dae Wook, Song Ki Byung, Lee Jae Hoon, Kim Song Cheol, Ryoo Baek-Ye |
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Germline EMSY sequence alterations in hereditary breast cancer and ovarian cancer families.
BMC cancer 2017 Jul 17 (1): 496. Määttä Kirsi M, Nurminen Riikka, Kankuri-Tammilehto Minna, Kallioniemi Anne, Laasanen Satu-Leena, Schleutker Johan |
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Network Meta-Analysis on the Effects of DNA Damage Response-Related Gene Mutations on Overall Survival of Breast Cancer Based on TCGA Database.
Journal of cellular biochemistry 2017 May . Liu Chang, Chang Hong, Li Xiao-Han, Qi Ya-Fei, Wang Jin-Ou, Zhang Ying, Yang Xiang-Ho |
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Analysis of chromosomal radiosensitivity of healthy BRCA2 mutation carriers and non-carriers in BRCA families with the G2 micronucleus assay.
Oncology reports 2017 Mar 37 (3): 1379-1386. Baert Annelot, Depuydt Julie, Van Maerken Tom, Poppe Bruce, Malfait Fransiska, Van Damme Tim, De Nobele Sylvia, Perletti Gianpaolo, De Leeneer Kim, Claes Kathleen B M, Vral An |
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Association of PALB2 sequence variants with the risk of early-onset breast cancer in patients from Turkey.
Molecular biology reports 2016 Aug . Cecener G, Guney Eskiler G, Egeli U, Tunca B, Alemdar A, Gokgoz S, Tasdelen |
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Ovarian cancer: Status of homologous recombination pathway as a predictor of drug response.
Critical reviews in oncology/hematology 2016 May 101 50-9. De Picciotto Nicolas, Cacheux Wulfran, Roth Arnaud, Chappuis Pierre O, Labidi-Galy S Intidh |
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The Fanconi anemia DNA damage repair pathway in the spotlight for germline predisposition to colorectal cancer.
European journal of human genetics : EJHG 2016 May . Esteban-Jurado Clara, Franch-Expósito Sebastià, Muñoz Jenifer, Ocaña Teresa, Carballal Sabela, López-Cerón Maria, Cuatrecasas Miriam, Vila-Casadesús Maria, Lozano Juan José, Serra Enric, Beltran Sergi, Brea-Fernández Alejandro, Ruiz-Ponte Clara, Castells Antoni, Bujanda Luis, Garre Pilar, Caldés Trinidad, Cubiella Joaquín, Balaguer Francesc, Castellví-Bel Ser |
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The role of germline alterations in the DNA damage response genes BRIP1 and BRCA2 in melanoma susceptibility.
Genes, chromosomes & cancer 2016 Apr . Tuominen Rainer, Engström Pär G, Helgadottir Hildur, Eriksson Hanna, Unneberg Per, Kjellqvist Sanela, Yang Muyi, Lindén Diana, Edsgärd Daniel, Hansson Johan, Höiom Veroni |
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Toxicity of (neo)adjuvant chemotherapy for BRCA1- and BRCA2-associated breast cancer.
Breast cancer research and treatment 2016 Apr . Drooger Jan C, Heemskerk-Gerritsen Bernadette A M, Smallenbroek Nyrée, Epskamp Cynthia, Seynaeve Caroline M, Jager Agn |
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Molecular insights into the OGG1 gene, a cancer risk modifier in BRCA1 and BRCA2 mutations carriers.
Oncotarget 2016 Mar . Benitez-Buelga Carlos, Vaclová Tereza, Ferreira Sofia, Urioste Miguel, Inglada-Perez Lucia, Soberón Nora, Blasco Maria A, Osorio Ana, Benitez Javi |
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A variant at a potentially functional microRNA-binding site in BRIP1 was associated with risk of squamous cell carcinoma of the head and neck.
Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine 2015 Dec . Liu Hongliang, Gao Fengqin, Dahlstrom Kristina R, Li Guojun, Sturgis Erich M, Zevallos Jose P, Wei Qingyi, Liu Zhenshe |
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Loss of heterozygosity for chromosomal regions 15q14-21.1, 17q21.31, and 13q12.3-13.1 and its relevance for prostate cancer.
Medical oncology (Northwood, London, England) 2015 Nov 32 (11): 246. Nowacka-Zawisza Maria, Forma Ewa, Walczak Maciej, Ró?a?ski Waldemar, Bry? Magdalena, Krajewska Wanda |
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The RAD51 135G>C polymorphism is related to the effect of adjuvant therapy in early breast cancer.
Journal of cancer research and clinical oncology 2015 May 141 (5): 797-804. Söderlund Leifler K, Asklid A, Fornander T, Stenmark Askmalm |
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Two PALB2 germline mutations found in both BRCA1+ and BRCAx familial breast cancer.
Breast cancer research and treatment 2015 May 151 (1): 219-24. Downs Bradley, Kim Yeong C, Xiao Fengxia, Snyder Carrie, Chen Peixian, Fleissner Elizabeth A, Becirovic Dina, Wen Hongxiu, Sherman Simon, Cowan Kenneth H, Lynch Henry T, Wang San Mi |
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DNA repair gene polymorphisms and clinical outcome of patients with primary small cell carcinoma of the esophagus.
Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine 2015 Mar 36 (3): 1539-48. Zhou Qiang, Zou Bing-Wen, Xu Yong, Xue Jian-Xin, Meng Mao-Bin, Liu Fang-Jiu, Deng Lei, Ma Dai-Yuan, Ao Rui, Lu Y |
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Whole genomes redefine the mutational landscape of pancreatic cancer.
Nature 2015 Feb 518 (7540): 495-501. Waddell Nicola, Pajic Marina, Patch Ann-Marie, Chang David K, Kassahn Karin S, Bailey Peter, Johns Amber L, Miller David, Nones Katia, Quek Kelly, Quinn Michael C J, Robertson Alan J, Fadlullah Muhammad Z H, Bruxner Tim J C, Christ Angelika N, Harliwong Ivon, Idrisoglu Senel, Manning Suzanne, Nourse Craig, Nourbakhsh Ehsan, Wani Shivangi, Wilson Peter J, Markham Emma, Cloonan Nicole, Anderson Matthew J, Fink J Lynn, Holmes Oliver, Kazakoff Stephen H, Leonard Conrad, Newell Felicity, Poudel Barsha, Song Sarah, Taylor Darrin, Waddell Nick, Wood Scott, Xu Qinying, Wu Jianmin, Pinese Mark, Cowley Mark J, Lee Hong C, Jones Marc D, Nagrial Adnan M, Humphris Jeremy, Chantrill Lorraine A, Chin Venessa, Steinmann Angela M, Mawson Amanda, Humphrey Emily S, Colvin Emily K, Chou Angela, Scarlett Christopher J, Pinho Andreia V, Giry-Laterriere Marc, Rooman Ilse, Samra Jaswinder S, Kench James G, Pettitt Jessica A, Merrett Neil D, Toon Christopher, Epari Krishna, Nguyen Nam Q, Barbour Andrew, Zeps Nikolajs, Jamieson Nigel B, Graham Janet S, Niclou Simone P, Bjerkvig Rolf, Grützmann Robert, Aust Daniela, Hruban Ralph H, Maitra Anirban, Iacobuzio-Donahue Christine A, Wolfgang Christopher L, Morgan Richard A, Lawlor Rita T, Corbo Vincenzo, Bassi Claudio, Falconi Massimo, Zamboni Giuseppe, Tortora Giampaolo, Tempero Margaret A, , Gill Anthony J, Eshleman James R, Pilarsky Christian, Scarpa Aldo, Musgrove Elizabeth A, Pearson John V, Biankin Andrew V, Grimmond Sean |
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Prevalence of Germline Mutations in Genes Engaged in DNA Damage Repair by Homologous Recombination in Patients with Triple-Negative and Hereditary Non-Triple-Negative Breast Cancers.
PloS one 2015 10 (6): e0130393. Domagala Pawel, Jakubowska Anna, Jaworska-Bieniek Katarzyna, Kaczmarek Katarzyna, Durda Katarzyna, Kurlapska Agnieszka, Cybulski Cezary, Lubinski J |
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The CHEK2 1100delC allelic variant is not present in familial and sporadic breast cancer cases from Moroccan population.
SpringerPlus 2015 4 38. Marouf Chaymaa, Hajji Omar, Diakité Brehima, Tazzite Amal, Jouhadi Hassan, Benider Abdellatif, Nadifi Sella |
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A recessive variant of XRCC4 predisposes to non- BRCA1/2 breast cancer in chinese women and impairs the DNA damage response via dysregulated nuclear localization.
Oncotarget 2014 Dec 5 (23): 12218-32. He Min, Hu Xin, Chen Li, Cao A-Yong, Yu Ke-Da, Shi Ting-Yan, Kuang Xia-Ying, Shi Wen-Biao, Ling Hong, Li Shan, Qiao Feng, Yao Ling, Wei Qingyi, Di Gen-Hong, Shao Zhi-Mi |
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Overall survival and clinical characteristics of pancreatic cancer in BRCA mutation carriers.
British journal of cancer 2014 Sep 111 (6): 1132-8. Golan T, Kanji Z S, Epelbaum R, Devaud N, Dagan E, Holter S, Aderka D, Paluch-Shimon S, Kaufman B, Gershoni-Baruch R, Hedley D, Moore M J, Friedman E, Gallinger |
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Association of DNA repair and cell cycle gene variations with breast cancer risk in Northeast Indian population: a multiple interaction analysis.
Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine 2014 Jun 35 (6): 5885-94. Wasson Mishi Kaushal, Chauhan Pradeep Singh, Singh L C, Katara Dheeraj, Dev Sharma Jagannath, Zomawia Eric, Kataki Amal, Kapur Sujala, Saxena Suni |
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Lymphocyte telomere length is long in BRCA1 and BRCA2 mutation carriers regardless of cancer-affected status.
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2014 Jun 23 (6): 1018-24. Pooley Karen A, McGuffog Lesley, Barrowdale Daniel, Frost Debra, Ellis Steve D, Fineberg Elena, Platte Radka, Izatt Louise, Adlard Julian, Bardwell Julian, Brewer Carole, Cole Trevor, Cook Jackie, Davidson Rosemarie, Donaldson Alan, Dorkins Huw, Douglas Fiona, Eason Jacqueline, Houghton Catherine, Kennedy M John, McCann Emma, Miedzybrodzka Zosia, Murray Alex, Porteous Mary E, Rogers Mark T, Side Lucy E, Tischkowitz Marc, Walker Lisa, Hodgson Shirley, Eccles Diana M, Morrison Patrick J, Evans D Gareth, Eeles Rosalind A, Antoniou Antonis C, Easton Douglas F, Dunning Alison M, |
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Low prevalence of germline PALB2 mutations in Australian triple-negative breast cancer.
International journal of cancer. Journal international du cancer 2014 Jan 134 (2): 301-5. Wong-Brown Michelle W, Avery-Kiejda Kelly A, Bowden Nikola A, Scott Rodney |
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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 |
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A clinical trial of lovastatin for modification of biomarkers associated with breast cancer risk.
Breast cancer research and treatment 2013 Nov 142 (2): 389-98. Vinayak Shaveta, Schwartz Erich J, Jensen Kristin, Lipson Jafi, Alli Elizabeth, McPherson Lisa, Fernandez Adrian M, Sharma Vandana B, Staton Ashley, Mills Meredith A, Schackmann Elizabeth A, Telli Melinda L, Kardashian Ani, Ford James M, Kurian Allison |
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Pyrimidine base damage is increased in women with BRCA mutations.
Cancer letters 2013 Sep 338 (2): 267-70. Budzinski Edwin E, Patrzyc Helen B, Dawidzik Jean B, Freund Harold G, Frederick Peter, Godoy Heidi E, Voian Nicoleta C, Odunsi Kunle, Box Harold |
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Polymorphisms in double-strand breaks repair genes are associated with impaired fertility in Chinese population.
Reproduction (Cambridge, England) 2013 May 145 (5): 463-70. Ji Guixiang, Yan Lifeng, Liu Wei, Huang Cong, Gu Aihua, Wang Xin |
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Determination of Molecular Markers for BRCA1 and BRCA2 Heterozygosity Using Gene Expression Profiling.
Cancer prevention research (Philadelphia, Pa.) 2013 Jan . Salmon AY, Salmon-Divon M, Zahavi T, Barash Y, Levy-Drummer RS, Jacob-Hirsch J, Peretz T |
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Comprehensive analysis of BRCA1, BRCA2 and TP53 germline mutation and tumor characterization: a portrait of early-onset breast cancer in Brazil.
PloS one 2013 8 (3): e57581. Carraro Dirce Maria, Koike Folgueira Maria Aparecida Azevedo, Garcia Lisboa Bianca Cristina, Ribeiro Olivieri Eloisa Helena, Vitorino Krepischi Ana Cristina, de Carvalho Alex Fiorini, de Carvalho Mota Louise Danielle, Puga Renato David, do Socorro Maciel Maria, Michelli Rodrigo Augusto Depieri, de Lyra Eduardo Carneiro, Grosso Stana Helena Giorgi, Soares Fernando Augusto, Achatz Maria Isabel Alves de Souza Waddington, Brentani Helena, Moreira-Filho Carlos Alberto, Brentani Maria Mit |
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Constitutional CHEK2 mutations are infrequent in early-onset and familial breast/ovarian cancer patients from Pakistan.
BMC cancer 2013 13 312. Rashid Muhammad U, Muhammad Noor, Faisal Saima, Amin Asim, Hamann U |
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53BP1 expression in sporadic and inherited ovarian carcinoma: Relationship to genetic status and clinical outcomes.
Gynecologic oncology 2012 Dec . Pennington KP, Wickramanayake A, Norquist BM, Pennil CC, Garcia RL, Agnew KJ, Taniguchi T, Welcsh P, Swisher EM |
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Breast cancer-associated Abraxas mutation disrupts nuclear localization and DNA damage response functions.
Science translational medicine 2012 Feb 4 (122): 122ra23. Solyom Szilvia, Aressy Bernadette, Pylkäs Katri, Patterson-Fortin Jeffrey, Hartikainen Jaana M, Kallioniemi Anne, Kauppila Saila, Nikkilä Jenni, Kosma Veli-Matti, Mannermaa Arto, Greenberg Roger A, Winqvist Robe |
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Analysis of SLX4/FANCP in non-BRCA1/2-mutated breast cancer families.
BMC cancer 2012 12 (1): 84. Fernández-Rodríguez Juana, Quiles Francisco, Blanco Ignacio, Teulé Alex, Feliubadaló Lídia, Valle Jesús Del, Salinas Mónica, Izquierdo Angel, Darder Esther, Schindler Detlev, Capellá Gabriel, Brunet Joan, Lázaro Conxi, Pujana Miguel Ang |
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Evaluation of single nucleotide polymorphisms (SNPs) in the p53 binding protein 1 (TP53BP1) gene in breast cancer patients treated with breast-conserving surgery and whole-breast irradiation (BCS + RT).
International journal of radiation oncology, biology, physics 2011 Jun 80 (2): 385-91. Haffty Bruce G, Goyal Sharad, Kulkarni Diptee, Green Camille, Vazquez Alexi, Schiff Devora, Moran Meena S, Yang Qifeng, Ganesan Shridar, Hirsfield Kim |
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Germline mutational analysis of the C19orf62 gene in African-American women with breast cancer.
Breast cancer research and treatment 2011 Jun 127 (3): 871-7. Zheng Yonglan, Zhang Jing, Niu Qun, Olopade Olufunmilayo I, Huo Dezhe |
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Ionizing radiation or mitomycin-induced micronuclei in lymphocytes of BRCA1 or BRCA2 mutation carriers.
Breast cancer research and treatment 2011 Jun 127 (3): 611-22. Gutiérrez-Enríquez Sara, Ramón Y Cajal Teresa, Alonso Carmen, Corral Anna, Carrasco Pablo, Cornet Mónica, Sanz Judith, Ribas Montserrat, Baiget Montserrat, Diez Orla |
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Functional implication of TRAIL -716 C/T promoter polymorphism on its in vitro and in vivo expression and the susceptibility to sporadic breast tumor.
Breast cancer research and treatment 2011 Apr 126 (2): 333-43. Pal Ranjana, Gochhait Sailesh, Chattopadhyay Shilpi, Gupta Pawan, Prakash Neeraj, Agarwal Gaurav, Chaturvedi Arun, Husain Nuzhat, Husain Syed Akhtar, Bamezai Rameshwar N |
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Rare variants in the ATM gene and risk of breast cancer.
Breast cancer research : BCR 2011 13 (4): R73. Goldgar David E, Healey Sue, Dowty James G, Da Silva Leonard, Chen Xiaoqing, Spurdle Amanda B, Terry Mary Beth, Daly Mary J, Buys Saundra M, Southey Melissa C, Andrulis Irene, John Esther M, , , Khanna Kum Kum, Hopper John L, Oefner Peter J, Lakhani Sunil, Chenevix-Trench Georg |
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Gamma-radiation sensitivity and polymorphisms in RAD51L1 modulate glioma risk.
Carcinogenesis 2010 Oct 31 (10): 1762-9. Liu Yanhong, Shete Sanjay, Wang Li-E, El-Zein Randa, Etzel Carol J, Liang Fu-Wen, Armstrong Georgina, Tsavachidis Spyros, Gilbert Mark R, Aldape Kenneth D, Xing Jinliang, Wu Xifeng, Wei Qingyi, Bondy Melissa |
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Single-nucleotide polymorphisms in the p53 pathway genes modify cancer risk in BRCA1 and BRCA2 carriers of Jewish-Ashkenazi descent.
Molecular carcinogenesis 2010 Jun 49 (6): 545-55. Yarden Ronit I, Friedman Eitan, Metsuyanim Sally, Olender Tzvia, Ben-Asher Edna, Papa Moshe |
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Elevated lung cancer risk is associated with deficiencies in cell cycle checkpoints: genotype and phenotype analyses from a case-control study.
International journal of cancer. Journal international du cancer 2010 May 126 (9): 2199-210. Zheng Yun-Ling, Kosti Ourania, Loffredo Christopher A, Bowman Elise, Mechanic Leah, Perlmutter Donna, Jones Raymond, Shields Peter G, Harris Curtis |
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Increased chromosomal radiosensitivity in women carrying BRCA1/BRCA2 mutations assessed with the G2 assay.
International journal of radiation oncology, biology, physics 2010 Mar 76 (4): 1199-205. Ernestos Beroukas, Nikolaos Pandis, Koulis Giannoukakos, Eleni Rizou, Konstantinos Beroukas, Alexandra Giatromanolaki, Michael Koukourak |
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Genetic variation in DNA repair genes and prostate cancer risk: results from a population-based study.
Cancer causes & control : CCC 2010 Feb 21 (2): 289-300. Agalliu Ilir, Kwon Erika M, Salinas Claudia A, Koopmeiners Joseph S, Ostrander Elaine A, Stanford Janet |
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Association of common PALB2 polymorphisms with breast cancer risk: a case-control study.
Clinical cancer research : an official journal of the American Association for Cancer Research 2008 Sep 14 (18): 5931-7. Chen Peizhan, Liang Jie, Wang Zhanwei, Zhou Xiaoyi, Chen Lu, Li Mian, Xie Dong, Hu Zhibin, Shen Hongbing, Wang H |
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Analysis of GADD45A sequence variations in French Canadian families with high risk of breast cancer.
Journal of human genetics 2008 53 (6): 490-8. Desjardins Sylvie, Ouellette Geneviève, Labrie Yvan, Simard Jacques, , Durocher Franci |
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Identification of a novel CHEK2 variant and assessment of its contribution to the risk of breast cancer in French Canadian women.
BMC cancer 2008 8 (1): 239. Novak David J, Chen Long Qi, Ghadirian Parviz, Hamel Nancy, Zhang Phil, Rossiny Vanessa, Cardinal Guy, Robidoux André, Tonin Patricia N, Rousseau Francois, Narod Steven A, Foulkes William |
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Lymphocyte radiosensitivity in BRCA1 and BRCA2 mutation carriers and implications for breast cancer susceptibility.
International journal of cancer. Journal international du cancer 2007 Oct 121 (7): 1631-6. Barwell Julian, Pangon Laurent, Georgiou Anne, Kesterton Ian, Langman Caroline, Arden-Jones Audrey, Bancroft Elizabeth, Salmon Ashi, Locke Imogen, Kote-Jarai Zsofia, Morris Joanna R, Solomon Ellen, Berg Jonathan, Docherty Zoe, Camplejohn Richard, Eeles Rosalind, Hodgson Shirley |
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Identification of women with an increased risk of developing radiation-induced breast cancer: a case only study.
Breast cancer research : BCR 2007 9 (2): R26. Broeks Annegien, Braaf Linde M, Huseinovic Angelina, Nooijen Anke, Urbanus Jos, Hogervorst Frans B L, Schmidt Marjanka K, Klijn Jan G M, Russell Nicola S, Van Leeuwen Flora E, Van 't Veer Laura |
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Identification of a common polymorphism in the TopBP1 gene associated with hereditary susceptibility to breast and ovarian cancer.
European journal of cancer (Oxford, England : 1990) 2006 Oct 42 (15): 2647-52. Karppinen Sanna-Maria, Erkko Hannele, Reini Kaarina, Pospiech Helmut, Heikkinen Katri, Rapakko Katrin, Syväoja Juhani E, Winqvist Robe |
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Variants in the ATM-BRCA2-CHEK2 axis predispose to chronic lymphocytic leukemia.
Blood 2006 Jul 108 (2): 638-44. Rudd Matthew F, Sellick Gabrielle S, Webb Emily L, Catovsky Daniel, Houlston Richard |
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Variants in the GH-IGF axis confer susceptibility to lung cancer.
Genome research 2006 Jun 16 (6): 693-701. Rudd Matthew F, Webb Emily L, Matakidou Athena, Sellick Gabrielle S, Williams Richard D, Bridle Helen, Eisen Tim, Houlston Richard S, |
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Polymorphisms in DNA double-strand break repair genes and risk of breast cancer: two population-based studies in USA and Poland, and meta-analyses.
Human genetics 2006 May 119 (4): 376-88. García-Closas Montserrat, Egan Kathleen M, Newcomb Polly A, Brinton Louise A, Titus-Ernstoff Linda, Chanock Stephen, Welch Robert, Lissowska Jolanta, Peplonska Beata, Szeszenia-Dabrowska Neonila, Zatonski Witold, Bardin-Mikolajczak Alicja, Struewing Jeffery |
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Association of DNA repair and steroid metabolism gene polymorphisms with clinical late toxicity in patients treated with conformal radiotherapy for prostate cancer.
Clinical cancer research : an official journal of the American Association for Cancer Research 2006 Apr 12 (8): 2545-54. Damaraju Sambasivarao, Murray David, Dufour Jennifer, Carandang Diana, Myrehaug Sten, Fallone Gino, Field Colin, Greiner Russell, Hanson John, Cass Carol E, Parliament Matth |
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Mutation analysis of the ATR gene in breast and ovarian cancer families.
Breast cancer research : BCR 2005 7 (4): R495-501. Heikkinen Katri, Mansikka Virpi, Karppinen Sanna-Maria, Rapakko Katrin, Winqvist Robe |
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ATM polymorphisms as risk factors for prostate cancer development.
British journal of cancer 2004 Aug 91 (4): 783-7. Angèle S, Falconer A, Edwards S M, Dörk T, Bremer M, Moullan N, Chapot B, Muir K, Houlston R, Norman A R, Bullock S, Hope Q, Meitz J, Dearnaley D, Dowe A, Southgate C, Ardern-Jones A, Easton D F, Eeles R A, Hall |
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A single-nucleotide polymorphism in the RAD51 gene modifies breast cancer risk in BRCA2 carriers, but not in BRCA1 carriers or noncarriers.
British journal of cancer 2004 May 90 (10): 2002-5. Kadouri L, Kote-Jarai Z, Hubert A, Durocher F, Abeliovich D, Glaser B, Hamburger T, Eeles R A, Peretz |
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Study design: evaluating gene-environment interactions in the etiology of breast cancer - the WECARE study.
Breast cancer research : BCR 2004 6 (3): R199-214. Bernstein JL, Langholz B, Haile RW, Bernstein L, Thomas DC, Stovall M, Malone KE, Lynch CF, Olsen JH, Anton-Culver H, Shore RE, Boice JD, Berkowitz GS, Gatti RA, Teitelbaum SL, Smith SA, Rosenstein BS, Børresen-Dale AL, Concannon P, Thompson WD |
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The breast cancer low-penetrance allele 1100delC in the CHEK2 gene is not present in Spanish familial breast cancer population.
International journal of cancer. Journal international du cancer 2004 Jan 108 (1): 54-6. Osorio Ana, Rodríguez-López Raquel, Díez Orland, de la Hoya Miguel, Ignacio Martínez José, Vega Ana, Esteban-Cardeñosa Eva, Alonso Carmen, Caldés Trinidad, Benítez Javi |
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TP53, BRCA1, and BRCA2 tumor suppressor genes are not commonly mutated in survivors of Hodgkin's disease with second primary neoplasms.
Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2003 Dec 21 (24): 4505-9. Nichols Kim E, Heath John A, Friedman Debra, Biegel Jaclyn A, Ganguly Arupa, Mauch Peter, Diller Li |
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Screening of homologous recombination gene polymorphisms in lung cancer patients reveals an association of the NBS1-185Gln variant and p53 gene mutations.
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2003 Aug 12 (8): 699-704. Medina Pedro P, Ahrendt Steven A, Pollan Marina, Fernandez Paloma, Sidransky David, Sanchez-Cespedes Montserr |
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A potential role for the XRCC2 R188H polymorphic site in DNA-damage repair and breast cancer.
Human molecular genetics 2002 Jun 11 (12): 1433-8. Rafii Saeed, O'Regan Paul, Xinarianos George, Azmy Iman, Stephenson Tim, Reed Malcolm, Meuth Mark, Thacker John, Cox Ange |
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BRCA1 and BRCA2 heterozygosity and repair of X-ray-induced DNA damage.
International journal of radiation biology 2002 Apr 78 (4): 285-95. Nieuwenhuis B, Van Assen-Bolt A J, Van Waarde-Verhagen M A W H, Sijmons R H, Van der Hout A H, Bauch T, Streffer C, Kampinga H |
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Mutagen sensitivity of peripheral blood from women carrying a BRCA1 or BRCA2 mutation.
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- Page last updated:Aug 15, 2019
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