HuGE Literature Finder
Records 1-100
|
Clinical Impact of Somatic Variants in Homologous Recombination Repair-Related Genes in Ovarian High-Grade Serous Carcinoma.
Cancer research and treatment : official journal of Korean Cancer Association 2020 Jan . Choi Min Chul, Hwang Sohyun, Kim Sewha, Jung Sang Geun, Park Hyun, Joo Won Duk, Song Seung Hun, Lee Chan, Kim Tae-Heon, Kang Haeyoun, An Hee Ju |
|
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 |
|
Germline DNA Sequencing Reveals Novel Mutations Predictive of Overall Survival in a Cohort of Pancreatic Cancer Patients.
Clinical cancer research : an official journal of the American Association for Cancer Research 2019 Dec . Goldstein Jennifer B, Zhao Li, Wang Xuemei, Ghelman Yael, Overman Michael J, Javle Milind, Shroff Rachna T, Varadhachary Gauri R, Wolf Robert A, McAllister Florencia, Futreal P Andrew, Fogelman David |
|
Prevalence of pathogenic germline cancer risk variants in high-risk urothelial carcinoma.
Genetics in medicine : official journal of the American College of Medical Genetics 2019 Dec . Nassar Amin H, Abou Alaiwi Sarah, AlDubayan Saud H, Moore Nicholas, Mouw Kent W, Kwiatkowski David J, Choueiri Toni K, Curran Catherine, Berchuck Jacob E, Harshman Lauren C, Nuzzo Pier V, Chanza Nieves Martinez, Van Allen Eliezer, Esplin Edward D, Yang Shan, Callis Thomas, Garber Judy E, Rana Huma Q, Sonpavde Gu |
|
Identification of germline pathogenic variants in DNA damage repair genes by a next-generation sequencing multigene panel in BRCAX patients.
Clinical biochemistry 2019 Nov . Rodríguez-Balada Marta, Roig Bàrbara, Melé Mireia, Albacar Cinta, Serrano Sara, Salvat Mònica, Querol Montserrat, Borràs Joan, Martorell Lourdes, Gumà Jos |
|
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 |
|
A Novel Mutation-BRCA1 Associated Hereditary Haplotype of Intragenic Markers of BRCA1 Gene in a Family with History of Breast Cancer
Asian Pacific journal of cancer prevention : APJCP 2019 Feb 20 (2): 611-614. Miresmaeili Seyed Mohsen, Jafari Fatem |
|
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 |
|
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 |
|
Whole exome sequencing of breast cancer (TNBC) cases from India: association of MSH6 and BRIP1 variants with TNBC risk and oxidative DNA damage.
Molecular biology reports 2018 Aug . Aravind Kumar M, Naushad Shaik Mohammad, Narasimgu Narasimhulu, Nagaraju Naik S, Kadali Srilatha, Shanker Uday, Lakshmi Narasu |
|
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 |
|
Prospective Evaluation of Germline Alterations in Patients With Exocrine Pancreatic Neoplasms.
Journal of the National Cancer Institute 2018 Feb . Lowery Maeve A, Wong Winston, Jordan Emmet J, Lee Jonathan W, Kemel Yelena, Vijai Joseph, Mandelker Diana, Zehir Ahmet, Capanu Marinela, Salo-Mullen Erin, Arnold Angela G, Yu Kenneth H, Varghese Anna M, Kelsen David P, Brenner Robin, Kaufmann Erica, Ravichandran Vignesh, Mukherjee Semanti, Berger Michael F, Hyman David M, Klimstra David S, Abou-Alfa Ghassan K, Tjan Catherine, Covington Christina, Maynard Hannah, Allen Peter J, Askan Gokce, Leach Steven D, Iacobuzio-Donahue Christine A, Robson Mark E, Offit Kenneth, Stadler Zsofia K, O'Reilly Eileen |
|
The Landscape of Somatic Genetic Alterations in Breast Cancers From ATM Germline Mutation Carriers.
Journal of the National Cancer Institute 2018 Feb . Weigelt Britta, Bi Rui, Kumar Rahul, Blecua Pedro, Mandelker Diana L, Geyer Felipe C, Pareja Fresia, James Paul A, , Couch Fergus J, Eccles Diana M, Blows Fiona, Pharoah Paul, Li Anqi, Selenica Pier, Lim Raymond S, Jayakumaran Gowtham, Waddell Nic, Shen Ronglai, Norton Larry, Wen Hannah Y, Powell Simon N, Riaz Nadeem, Robson Mark E, Reis-Filho Jorge S, Chenevix-Trench Georg |
|
Association of Single-Nucleotide Polymorphisms in Monoubiquitinated FANCD2-DNA Damage Repair Pathway Genes With Breast Cancer in the Chinese Population.
Technology in cancer research & treatment 2018 Jan 17 1533033818819841. Chen Fei-Yu, Wang Hao, Li Hui, Hu Xue-Li, Dai Xu, Wang Shou-Man, Yan Guo-Jiao, Jiang Ping-Lan, Hu Yuan-Ping, Huang Juan, Tang Li- |
|
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 |
|
Prevalence of Aflatoxin-associated TP53R249S mutation in Hepatocellular Carcinoma in Hispanics in South Texas.
Cancer prevention research (Philadelphia, Pa.) 2017 Oct . Jiao Jingjing, Niu Weibo, Wang Ying, Baggerly Keith A, Ye Yuanqing, Wu Xifeng, Davenport Dewitt, Almeda Jose Luis, Betancourt-Garcia Monica M, Forse R Armour, Stevenson Heather L, Watt Gordon P, McCormick Joseph B, Fisher-Hoch Susan P, Beretta Lau |
|
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 |
|
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 |
|
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 |
|
Novel BRCA1 splice-site mutation in ovarian cancer patients of Slavic origin.
Familial cancer 2017 Jul . Krivokuca Ana, Dragos Vita Setrajcic, Stamatovic Ljiljana, Blatnik Ana, Boljevic Ivana, Stegel Vida, Rakobradovic Jelena, Skerl Petra, Jovandic Stevo, Krajc Mateja, Magic Mirjana Brankovic, Novakovic Srdj |
|
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 |
|
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 |
|
Clinical Significance of DNA Damage Response Factors and Chromosomal Instability in Primary Lung Adenocarcinoma.
Anticancer research 2017 04 37 (4): 1729-1735. Okamoto Tatsuro, Kohno Mikihiro, Ito Kensaku, Takada Kazuki, Katsura Masakazu, Morodomi Yosuke, Toyokawa Gouji, Shoji Fumihiro, Maehara Yoshihi |
|
Association of breast cancer risk with genetic variants showing differential allelic expression: Identification of a novel breast cancer susceptibility locus at 4q21.
Oncotarget 2016 Dec 7 (49): 80140-80163. Hamdi Yosr, Soucy Penny, Adoue Véronique, Michailidou Kyriaki, Canisius Sander, Lemaçon Audrey, Droit Arnaud, Andrulis Irene L, Anton-Culver Hoda, Arndt Volker, Baynes Caroline, Blomqvist Carl, Bogdanova Natalia V, Bojesen Stig E, Bolla Manjeet K, Bonanni Bernardo, Borresen-Dale Anne-Lise, Brand Judith S, Brauch Hiltrud, Brenner Hermann, Broeks Annegien, Burwinkel Barbara, Chang-Claude Jenny, , Couch Fergus J, Cox Angela, Cross Simon S, Czene Kamila, Darabi Hatef, Dennis Joe, Devilee Peter, Dörk Thilo, Dos-Santos-Silva Isabel, Eriksson Mikael, Fasching Peter A, Figueroa Jonine, Flyger Henrik, García-Closas Montserrat, Giles Graham G, Goldberg Mark S, González-Neira Anna, Grenaker-Alnæs Grethe, Guénel Pascal, Haeberle Lothar, Haiman Christopher A, Hamann Ute, Hallberg Emily, Hooning Maartje J, Hopper John L, Jakubowska Anna, Jones Michael, Kabisch Maria, Kataja Vesa, Lambrechts Diether, Le Marchand Loic, Lindblom Annika, Lubinski Jan, Mannermaa Arto, Maranian Mel, Margolin Sara, Marme Frederik, Milne Roger L, Neuhausen Susan L, Nevanlinna Heli, Neven Patrick, Olswold Curtis, Peto Julian, Plaseska-Karanfilska Dijana, Pylkäs Katri, Radice Paolo, Rudolph Anja, Sawyer Elinor J, Schmidt Marjanka K, Shu Xiao-Ou, Southey Melissa C, Swerdlow Anthony, Tollenaar Rob A E M, Tomlinson Ian, Torres Diana, Truong Thérèse, Vachon Celine, Van Den Ouweland Ans M W, Wang Qin, Winqvist Robert, , Zheng Wei, Benitez Javier, Chenevix-Trench Georgia, Dunning Alison M, Pharoah Paul D P, Kristensen Vessela, Hall Per, Easton Douglas F, Pastinen Tomi, Nord Silje, Simard Jacqu |
|
Whole-exome sequencing of Finnish hereditary breast cancer families.
European journal of human genetics : EJHG 2016 Oct . Määttä Kirsi, Rantapero Tommi, Lindström Anna, Nykter Matti, Kankuri-Tammilehto Minna, Laasanen Satu-Leena, Schleutker Johan |
|
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 |
|
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 |
|
Haplotype analysis of BRCA1 intragenic markers in Iranian patients with familial breast and ovarian cancer.
International journal of reproductive biomedicine (Yazd, Iran) 2016 Apr 14 (4): 271-4. Miresmaeili Seyed Mohsen, Kordi Tamandani Dor Mohammad, Kalantar Seyed Mehdi, Moshtaghioun Seyed Mohamm |
|
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 |
|
Common variation in BRCA1 may have a role in progression to lethal prostate cancer after radiation treatment.
Prostate cancer and prostatic diseases 2016 Mar . Sanchez A, Schoenfeld J D, Nguyen P L, Fiorentino M, Chowdhury D, Stampfer M J, Sesso H D, Giovannucci E, Mucci L A, Shui I |
|
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 |
|
Genetic evaluation of BRCA1 associated a complex genes with triple-negative breast cancer susceptibility in chinese women.
Oncotarget 2016 Feb . Ling Hong, Li Shan, Wu Yang, Zheng Yi-Zi, Qiao Feng, Yao Ling, Cao Zhi-Gang, Ye Fu-Gui, Wu Jiong, Hu Xin, Wang Bin, Shao Zhi-Mi |
|
ABRAXAS (FAM175A) and Breast Cancer Susceptibility: No Evidence of Association in the Breast Cancer Family Registry.
PloS one 2016 11 (6): e0156820. Renault Anne-Laure, Lesueur Fabienne, Coulombe Yan, Gobeil Stéphane, Soucy Penny, Hamdi Yosr, Desjardins Sylvie, Le Calvez-Kelm Florence, Vallée Maxime, Voegele Catherine, , Hopper John L, Andrulis Irene L, Southey Melissa C, John Esther M, Masson Jean-Yves, Tavtigian Sean V, Simard Jacqu |
|
Increased chromosomal radiosensitivity in asymptomatic carriers of a heterozygous BRCA1 mutation.
Breast cancer research : BCR 2016 18 (1): 52. Baert Annelot, Depuydt Julie, Van Maerken Tom, Poppe Bruce, Malfait Fransiska, Storm Katrien, van den Ende Jenneke, Van Damme Tim, De Nobele Sylvia, Perletti Gianpaolo, De Leeneer Kim, Claes Kathleen B M, Vral An |
|
Mutational landscape of MCPyV-positive and MCPyV-negative merkel cell carcinomas with implications for immunotherapy.
Oncotarget 2015 Dec . Goh Gerald, Walradt Trent, Markarov Vladimir, Blom Astrid, Riaz Nadeem, Doumani Ryan, Stafstrom Krista, Moshiri Ata, Yelistratova Lola, Levinsohn Jonathan, Chan Timothy A, Nghiem Paul, Lifton Richard P, Choi Jaehy |
|
Relationship between Caffeine and Levels of DNA Repair and Oxidative Stress in Women with and without a BRCA1 Mutation.
Journal of nutrigenetics and nutrigenomics 2015 Dec 8 (4-6): 174-184. Nikitina Dina, Chen Zhou, Vallis Katherine, Poll Aletta, Ainsworth Peter, Narod Steven A, Kotsopoulos Joan |
Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair.
Nature genetics 2015 Nov 47 (11): 1294-1303. Day Felix R, Ruth Katherine S, Thompson Deborah J, Lunetta Kathryn L, Pervjakova Natalia, Chasman Daniel I, Stolk Lisette, Finucane Hilary K, Sulem Patrick, Bulik-Sullivan Brendan, Esko Tõnu, Johnson Andrew D, Elks Cathy E, Franceschini Nora, He Chunyan, Altmaier Elisabeth, Brody Jennifer A, Franke Lude L, Huffman Jennifer E, Keller Margaux F, McArdle Patrick F, Nutile Teresa, Porcu Eleonora, Robino Antonietta, Rose Lynda M, Schick Ursula M, Smith Jennifer A, Teumer Alexander, Traglia Michela, Vuckovic Dragana, Yao Jie, Zhao Wei, Albrecht Eva, Amin Najaf, Corre Tanguy, Hottenga Jouke-Jan, Mangino Massimo, Smith Albert V, Tanaka Toshiko, Abecasis Goncalo, Andrulis Irene L, Anton-Culver Hoda, Antoniou Antonis C, Arndt Volker, Arnold Alice M, Barbieri Caterina, Beckmann Matthias W, Beeghly-Fadiel Alicia, Benitez Javier, Bernstein Leslie, Bielinski Suzette J, Blomqvist Carl, Boerwinkle Eric, Bogdanova Natalia V, Bojesen Stig E, Bolla Manjeet K, Borresen-Dale Anne-Lise, Boutin Thibaud S, Brauch Hiltrud, Brenner Hermann, Brüning Thomas, Burwinkel Barbara, Campbell Archie, Campbell Harry, Chanock Stephen J, Chapman J Ross, Chen Yii-Der Ida, Chenevix-Trench Georgia, Couch Fergus J, Coviello Andrea D, Cox Angela, Czene Kamila, Darabi Hatef, De Vivo Immaculata, Demerath Ellen W, Dennis Joe, Devilee Peter, Dörk Thilo, Dos-Santos-Silva Isabel, Dunning Alison M, Eicher John D, Fasching Peter A, Faul Jessica D, Figueroa Jonine, Flesch-Janys Dieter, Gandin Ilaria, Garcia Melissa E, García-Closas Montserrat, Giles Graham G, Girotto Giorgia G, Goldberg Mark S, González-Neira Anna, Goodarzi Mark O, Grove Megan L, Gudbjartsson Daniel F, Guénel Pascal, Guo Xiuqing, Haiman Christopher A, Hall Per, Hamann Ute, Henderson Brian E, Hocking Lynne J, Hofman Albert, Homuth Georg, Hooning Maartje J, Hopper John L, Hu Frank B, Huang Jinyan, Humphreys Keith, Hunter David J, Jakubowska Anna, Jones Samuel E, Kabisch Maria, Karasik David, Knight Julia A, Kolcic Ivana, Kooperberg Charles, Kosma Veli-Matti, Kriebel Jennifer, Kristensen Vessela, Lambrechts Diether, Langenberg Claudia, Li Jingmei, Li Xin, Lindström Sara, Liu Yongmei, Luan Jian'an, Lubinski Jan, Mägi Reedik, Mannermaa Arto, Manz Judith, Margolin Sara, Marten Jonathan, Martin Nicholas G, Masciullo Corrado, Meindl Alfons, Michailidou Kyriaki, Mihailov Evelin, Milani Lili, Milne Roger L, Müller-Nurasyid Martina, Nalls Michael, Neale Ben M, Nevanlinna Heli, Neven Patrick, Newman Anne B, Nordestgaard Børge G, Olson Janet E, Padmanabhan Sandosh, Peterlongo Paolo, Peters Ulrike, Petersmann Astrid, Peto Julian, Pharoah Paul D P, Pirastu Nicola N, Pirie Ailith, Pistis Giorgio, Polasek Ozren, Porteous David, Psaty Bruce M, Pylkäs Katri, Radice Paolo, Raffel Leslie J, Rivadeneira Fernando, Rudan Igor, Rudolph Anja, Ruggiero Daniela, Sala Cinzia F, Sanna Serena, Sawyer Elinor J, Schlessinger David, Schmidt Marjanka K, Schmidt Frank, Schmutzler Rita K, Schoemaker Minouk J, Scott Robert A, Seynaeve Caroline M, Simard Jacques, Sorice Rossella, Southey Melissa C, Stöckl Doris, Strauch Konstantin, Swerdlow Anthony, Taylor Kent D, Thorsteinsdottir Unnur, Toland Amanda E, Tomlinson Ian, Truong Thérèse, Tryggvadottir Laufey, Turner Stephen T, Vozzi Diego, Wang Qin, Wellons Melissa, Willemsen Gonneke, Wilson James F, Winqvist Robert, Wolffenbuttel Bruce B H R, Wright Alan F, Yannoukakos Drakoulis, Zemunik Tatijana, Zheng Wei, Zygmunt Marek, Bergmann Sven, Boomsma Dorret I, Buring Julie E, Ferrucci Luigi, Montgomery Grant W, Gudnason Vilmundur, Spector Tim D, van Duijn Cornelia M, Alizadeh Behrooz Z, Ciullo Marina, Crisponi Laura, Easton Douglas F, Gasparini Paolo P, Gieger Christian, Harris Tamara B, Hayward Caroline, Kardia Sharon L R, Kraft Peter, McKnight Barbara, Metspalu Andres, Morrison Alanna C, Reiner Alex P, Ridker Paul M, Rotter Jerome I, Toniolo Daniela, Uitterlinden André G, Ulivi Sheila, Völzke Henry, Wareham Nicholas J, Weir David R, Yerges-Armstrong Laura M, , , , , , , Price Alkes L, Stefansson Kari, Visser Jenny A, Ong Ken K, Chang-Claude Jenny, Murabito Joanne M, Perry John R B, Murray An |
|
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 |
|
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 |
|
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 |
|
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 |
|
A novel recurrent CHEK2 Y390C mutation identified in high-risk Chinese breast cancer patients impairs its activity and is associated with increased breast cancer risk.
Oncogene 2015 Jan . Wang N, Ding H, Liu C, Li X, Wei L, Yu J, Liu M, Ying M, Gao W, Jiang H, Wang |
|
Low prevalence of CHEK2 gene mutations in multiethnic cohorts of breast cancer patients in Malaysia.
PloS one 2015 10 (1): e0117104. Mohamad Suriati, Isa Nurismah Md, Muhammad Rohaizak, Emran Nor Aina, Kitan Nor Mayah, Kang Peter, Kang In Nee, Taib Nur Aishah Mohd, Teo Soo Hwang, Akmal Sharifah No |
|
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 |
|
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 |
|
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 |
|
Genetic variants in BRIP1 (BACH1) contribute to risk of nonsyndromic cleft lip with or without cleft palate.
Birth defects research. Part A, Clinical and molecular teratology 2014 Sep 100 (9): 670-8. Mostowska Adrianna, Hozyasz Kamil K, Wójcicki Piotr, Galas-Filipowicz Daria, Lasota Agnieszka, Dunin-Wilczy?ska Izabella, Lianeri Margarita, Jagodzi?ski Pawe? |
|
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 |
|
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, |
|
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 |
|
Association of BRCA1/2 defects with genomic scores predictive of DNA damage repair deficiency among breast cancer subtypes.
Breast cancer research : BCR 2014 16 (6): 475. Timms Kirsten M, Abkevich Victor, Hughes Elisha, Neff Chris, Reid Julia, Morris Brian, Kalva Saritha, Potter Jennifer, Tran Thanh V, Chen Jian, Iliev Diana, Sangale Zaina, Tikishvili Eliso, Perry Michael, Zharkikh Andrey, Gutin Alexander, Lanchbury Jerry |
|
Identification of two poorly prognosed ovarian carcinoma subtypes associated with CHEK2 germ-line mutation and non-CHEK2 somatic mutation gene signatures.
Cell cycle (Georgetown, Tex.) 2014 13 (14): 2262-80. Ow Ghim Siong, Ivshina Anna V, Fuentes Gloria, Kuznetsov Vladimir |
|
Polymorphisms in DNA repair genes and MDR1 and the risk for non-Hodgkin lymphoma.
International journal of molecular sciences 2014 15 (4): 6703-16. Kim Hee Nam, Kim Nan Young, Yu Li, Kim Yeo-Kyeoung, Lee Il-Kwon, Yang Deok-Hwan, Lee Je-Jung, Shin Min-Ho, Park Kyeong-Soo, Choi Jin-Su, Kim Hyeoung-Jo |
|
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 |
|
DNA double-strand break repair genotype and phenotype and breast cancer risk within sisters from the New York site of the Breast Cancer Family Registry (BCFR).
Cancer causes & control : CCC 2013 Dec 24 (12): 2157-68. Wu Hui-Chen, Delgado-Cruzata Lissette, Machella Nicola, Wang Qiao, Santella Regina M, Terry Mary Be |
|
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 |
|
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 |
|
First evidence for the contribution of the genetic variations of BRCA1-interacting protein 1 (BRIP1) to the genetic susceptibility of cervical cancer.
Gene 2013 Jul 524 (2): 208-13. Ma X D, Cai G Q, Zou W, Huang Y H, Zhang J R, Wang D T, Chen B |
|
Analysis of Single Nucleotide Polymorphisms and Radiation Sensitivity of the Lung Assessed With an Objective Radiologic Endpoint.
Clinical lung cancer 2013 Jan . Kelsey CR, Jackson IL, Langdon S, Owzar K, Hubbs J, Vujaskovic Z, Das S, Marks LB |
|
Association between the c.*229C>T polymorphism of the topoisomerase II? binding protein 1 (TopBP1) gene and breast cancer.
Molecular biology reports 2013 Jan . Forma E, Brzezia?ska E, Krze?lak A, Chwatko G, Jó?wiak P, Szymczyk A, Smolarz B, Romanowicz-Makowska H, Ró?a?ski W, Bry? M |
|
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 |
|
Inactivating Mutations in GT198 in Familial and Early-Onset Breast and Ovarian Cancers.
Genes & cancer 2013 Jan 4 (1-2): 15-25. Peng Min, Bakker Janine L, Dicioccio Richard A, Gille Johan J P, Zhao Hua, Odunsi Kunle, Sucheston Lara, Jaafar Lahcen, Mivechi Nahid F, Waisfisz Quinten, Ko L |
|
MCPH1 polymorphisms are associated with risk of breast cancer.
Gene 2013 Jan . Jo YH, Kim HO, Lee J, Lee SS, Cho CH, Kang IS, Choe WJ, Baik HH, Yoon KS |
|
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 |
|
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 |
|
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 |
|
An inherited NBN mutation is associated with poor prognosis prostate cancer.
British journal of cancer 2012 Nov . Cybulski C, Woko?orczyk D, Klu?niak W, Jakubowska A, Górski B, Gronwald J, Huzarski T, Kashyap A, Byrski T, D?bniak T, Go??b A, Gliniewicz B, Sikorski A, Swita?a J, Borkowski T, Borkowski A, Antczak A, Wojnar L, Przyby?a J, Sosnowski M, Ma?kiewicz B, Zdrojowy R, Sikorska-Radek P, Matych J, Wilkosz J, Ró?a?ski W, Ki? J, Bar K, Bryniarski P, Paradysz A, Jersak K, Niemirowicz J, S?upski P, Jarzemski P, Skrzypczyk M, Dobruch J, Domaga?a P, Narod SA, Lubi?ski J |
|
Analysis of ZNF350/ZBRK1 promoter variants and breast cancer susceptibility in non-BRCA1/2 French Canadian breast cancer families.
Journal of human genetics 2012 Nov . Plourde KV, Labrie Y, Desjardins S, Belleau P, Ouellette G, Durocher F |
|
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 |
|
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 |
|
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 |
|
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 |
|
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 |
|
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 |
|
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 |
|
Genetic contribution of GADD45A to susceptibility to sporadic and non-BRCA1/2 familial breast cancers: a systematic evaluation in Chinese populations.
Breast cancer research and treatment 2010 May 121 (1): 157-67. Yu Ke-Da, Di Gen-Hong, Li Wen-Feng, Rao Nan-Yan, Fan Lei, Yuan Wen-Tao, Hu Zhen, Wu Jiong, Shen Zhen-Zhou, Huang Wei, Shao Zhi-Mi |
|
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 |
|
Elevated level of 8-oxo-7,8-dihydro-2'-deoxyguanosine in leukocytes of BRCA1 mutation carriers compared to healthy controls.
International journal of cancer. Journal international du cancer 2009 Nov 125 (9): 2209-13. Dziaman Tomasz, Huzarski Tomasz, Gackowski Daniel, Rozalski Rafal, Siomek Agnieszka, Szpila Anna, Guz Jolanta, Lubinski Jan, Olinski Rysza |
|
Analysis of the genes coding for the BRCA1-interacting proteins, RAP80 and Abraxas (CCDC98), in high-risk, non-BRCA1/2, multiethnic breast cancer cases.
Breast cancer research and treatment 2009 Sep 117 (2): 453-9. Novak David J, Sabbaghian Nelly, Maillet Philippe, Chappuis Pierre O, Foulkes William D, Tischkowitz Ma |
|
Sequence variant discovery in DNA repair genes from radiosensitive and radiotolerant prostate brachytherapy patients.
Clinical cancer research : an official journal of the American Association for Cancer Research 2009 Aug 15 (15): 5008-16. Pugh Trevor J, Keyes Mira, Barclay Lorena, Delaney Allen, Krzywinski Martin, Thomas Dallas, Novik Karen, Yang Cindy, Agranovich Alexander, McKenzie Michael, Morris W Jim, Olive Peggy L, Marra Marco A, Moore Richard |
|
Absence of the CHEK2*1100delC mutation in non-BRCA1/2 families with multiple cancer types in a high-risk clinic population of Caucasian ancestry.
Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2009 May 27 (15_suppl): 11040. Gorin M A, Iniesta M D, Douglas J A, Milliron K J, Merajver S |
|
Germline alterations in the CLSPN gene in breast cancer families.
Cancer letters 2008 Mar 261 (1): 93-7. Erkko Hannele, Pylkäs Katri, Karppinen Sanna-Maria, Winqvist Robe |
|
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 |
|
Association of common ATM variants with familial breast cancer in a South American population.
BMC cancer 2008 8 (1): 117. González-Hormazábal Patricio, Bravo Teresa, Blanco Rafael, Valenzuela Carlos Y, Gómez Fernando, Waugh Enrique, Peralta Octavio, Ortuzar Waldo, Reyes Jose M, Jara Lili |
|
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 |
|
Breast cancer risk is associated with the genes encoding the DNA double-strand break repair Mre11/Rad50/Nbs1 complex.
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2007 Oct 16 (10): 2024-32. Hsu Huan-Ming, Wang Hui-Chun, Chen Sou-Tong, Hsu Giu-Cheng, Shen Chen-Yang, Yu Jyh-Cher |
|
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 |
|
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 |
|
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 |
|
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 |
|
Joint effects of single nucleotide polymorphisms in P53BP1 and p53 on breast cancer risk in a Chinese population.
Carcinogenesis 2006 Apr 27 (4): 766-71. Ma Hongxia, Hu Zhibin, Zhai Xiangjun, Wang Shui, Wang Xuechen, Qin Jianwei, Chen Wenseng, Jin Guangfu, Liu Jiyong, Gao Jun, Wang Xinru, Wei Qingyi, Shen Hongbi |
|
Increased rates of chromosome breakage in BRCA1 carriers are normalized by oral selenium supplementation.
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2005 May 14 (5): 1302-6. Kowalska Elzbieta, Narod Steven A, Huzarski Tomasz, Zajaczek Stanislaw, Huzarska Jowita, Gorski Bohdan, Lubinski J |
|
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 |
|
A gene-environment interaction between occupation and BRCA1/BRCA2 mutations in male breast cancer?
European journal of cancer (Oxford, England : 1990) 2004 Nov 40 (16): 2474-9. Palli Domenico, Masala Giovanna, Mariani-Costantini Renato, Zanna Ines, Saieva Calogero, Sera Francesco, Decarli Adriano, Ottini Lau |
|
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 |
|
Breast cancer risk and the DNA double-strand break end-joining capacity of nonhomologous end-joining genes are affected by BRCA1.
Cancer research 2004 Jul 64 (14): 5013-9. Bau Da-Tian, Fu Yi-Ping, Chen Shou-Tung, Cheng Ting-Chih, Yu Jyh-Cherng, Wu Pei-Ei, Shen Chen-Ya |
|
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 |
|
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 |
|
The CHEK2(*)1100delC mutation has no major contribution in oesophageal carcinogenesis.
British journal of cancer 2004 Feb 90 (4): 888-91. Koppert L B, Schutte M, Abbou M, Tilanus H W, Dinjens W N |
|
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 |
- Page last reviewed:Jul 30, 2019
- Page last updated:Feb 13, 2020
- Content source: