HuGE Literature Finder
Records 1-30
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Investigation into the origins of an ancient BRCA1 founder mutation identified among Chinese families in Singapore.
International journal of cancer 2020 Aug . Shaw Tarryn, Chan Sock Hoai, Teo Jing Xian, Chong Siao Ting, Li Shao-Tzu, Courtney Eliza, Ishak Diana, Sankar Haresh, Ang Zoe Li Ting, Chiang Jianbang, Loh Marie, Zhou Li, Lee Soo Chin, Yeh Hui-Yuan, Kolinjivadi Arun Mouli, Lim Weng Khong, Ngeow Joan |
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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 |
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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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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 |
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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 |
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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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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 |
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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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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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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 |
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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 |
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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- |
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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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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 |
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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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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 |
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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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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 |
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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 |
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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 |
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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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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 |
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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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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 |
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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 |
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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 |
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- Page last updated:Nov 27, 2020
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