HuGE Literature Finder
Records 1-30
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Pathogenic Germline Mutations in Chinese Patients with Gastric Cancer Identified by Next-Generation Sequencing.
Oncology 2020 Jun 1-6. Zhou Jing, Zhao Zhengyi, Zhang Yuzi, Bao Celimuge, Cui Longgang, Cai Shangli, Bai Yuezong, Shen Lin, Zhang Xiaoti |
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FANCL gene mutations in premature ovarian insufficiency.
Human mutation 2020 Feb . Yang Yajuan, Guo Ting, Liu Ran, Ke Hanni, Xu Weiwei, Zhao Shidou, Qin Yingyi |
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Polymorphisms and rare variants identified by next-generation sequencing confer risk for lung cancer in han Chinese population.
Pathology, research and practice 2020 Feb 152873. Li Xiaoqi, Liu Jinsheng, Wang Ke, Zhou Juan, Zhang Hang, Zhang Mancang, Shi Yongyo |
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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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Brief Report: Novel Germline Mutations in DNA Damage Repair in Patients with Malignant Pleural Mesotheliomas.
Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer 2019 Dec . Guo Robin, DuBoff Mariel, Jayakumaran Gowtham, Kris Mark G, Ladanyi Marc, Robson Mark E, Mandelker Diana, Zauderer Marjorie |
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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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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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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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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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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 |
- Page last reviewed:Oct 1, 2020
- Page last updated:Nov 24, 2020
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