HuGE Literature Finder
Records 1-17
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Two truncating variants in FANCC and breast cancer risk.
Scientific reports 2019 Aug 9 (1): 12524. Dörk Thilo, Peterlongo Paolo, Mannermaa Arto, Bolla Manjeet K, Wang Qin, Dennis Joe, Ahearn Thomas, Andrulis Irene L, Anton-Culver Hoda, Arndt Volker, Aronson Kristan J, Augustinsson Annelie, Freeman Laura E Beane, Beckmann Matthias W, Beeghly-Fadiel Alicia, Behrens Sabine, Bermisheva Marina, Blomqvist Carl, Bogdanova Natalia V, Bojesen Stig E, Brauch Hiltrud, Brenner Hermann, Burwinkel Barbara, Canzian Federico, Chan Tsun L, Chang-Claude Jenny, Chanock Stephen J, Choi Ji-Yeob, Christiansen Hans, Clarke Christine L, Couch Fergus J, Czene Kamila, Daly Mary B, Dos-Santos-Silva Isabel, Dwek Miriam, Eccles Diana M, Ekici Arif B, Eriksson Mikael, Evans D Gareth, Fasching Peter A, Figueroa Jonine, Flyger Henrik, Fritschi Lin, Gabrielson Marike, Gago-Dominguez Manuela, Gao Chi, Gapstur Susan M, García-Closas Montserrat, García-Sáenz José A, Gaudet Mia M, Giles Graham G, Goldberg Mark S, Goldgar David E, Guénel Pascal, Haeberle Lothar, Haiman Christopher A, Håkansson Niclas, Hall Per, Hamann Ute, Hartman Mikael, Hauke Jan, Hein Alexander, Hillemanns Peter, Hogervorst Frans B L, Hooning Maartje J, Hopper John L, Howell Tony, Huo Dezheng, Ito Hidemi, Iwasaki Motoki, Jakubowska Anna, Janni Wolfgang, John Esther M, Jung Audrey, Kaaks Rudolf, Kang Daehee, Kapoor Pooja Middha, Khusnutdinova Elza, Kim Sung-Won, Kitahara Cari M, Koutros Stella, Kraft Peter, Kristensen Vessela N, Kwong Ava, Lambrechts Diether, Marchand Loic Le, Li Jingmei, Lindström Sara, Linet Martha, Lo Wing-Yee, Long Jirong, Lophatananon Artitaya, Lubinski Jan, Manoochehri Mehdi, Manoukian Siranoush, Margolin Sara, Martinez Elena, Matsuo Keitaro, Mavroudis Dimitris, Meindl Alfons, Menon Usha, Milne Roger L, Mohd Taib Nur Aishah, Muir Kenneth, Mulligan Anna Marie, Neuhausen Susan L, Nevanlinna Heli, Neven Patrick, Newman William G, Offit Kenneth, Olopade Olufunmilayo I, Olshan Andrew F, Olson Janet E, Olsson Håkan, Park Sue K, Park-Simon Tjoung-Won, Peto Julian, Plaseska-Karanfilska Dijana, Pohl-Rescigno Esther, Presneau Nadege, Rack Brigitte, Radice Paolo, Rashid Muhammad U, Rennert Gad, Rennert Hedy S, Romero Atocha, Ruebner Matthias, Saloustros Emmanouil, Schmidt Marjanka K, Schmutzler Rita K, Schneider Michael O, Schoemaker Minouk J, Scott Christopher, Shen Chen-Yang, Shu Xiao-Ou, Simard Jacques, Slager Susan, Smichkoska Snezhana, Southey Melissa C, Spinelli John J, Stone Jennifer, Surowy Harald, Swerdlow Anthony J, Tamimi Rulla M, Tapper William J, Teo Soo H, Terry Mary Beth, Toland Amanda E, Tollenaar Rob A E M, Torres Diana, Torres-Mejía Gabriela, Troester Melissa A, Truong Thérèse, Tsugane Shoichiro, Untch Michael, Vachon Celine M, Ouweland Ans M W van den, Veen Elke M van, Vijai Joseph, Wendt Camilla, Wolk Alicja, Yu Jyh-Cherng, Zheng Wei, Ziogas Argyrios, Ziv Elad, , , Dunning Alison M, Pharoah Paul D P, Schindler Detlev, Devilee Peter, Easton Douglas |
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Distinct homologous recombination gene expression profiles after neoadjuvant chemotherapy associated with clinical outcome in patients with ovarian cancer.
Gynecologic oncology 2018 03 148 (3): 553-558. Kessous Roy, Octeau David, Klein Kathleen, Tonin Patricia N, Greenwood Celia M T, Pelmus Manuela, Laskov Ido, Kogan Liron, Salvador Shannon, Lau Susie, Yasmeen Amber, Gotlieb Walter |
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Prevalence of pathogenic germline variants detected by multigene sequencing in unselected Japanese patients with ovarian cancer.
Oncotarget 2017 Dec 8 (68): 112258-112267. Hirasawa Akira, Imoto Issei, Naruto Takuya, Akahane Tomoko, Yamagami Wataru, Nomura Hiroyuki, Masuda Kiyoshi, Susumu Nobuyuki, Tsuda Hitoshi, Aoki Daisu |
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The association of genetic variations in DNA repair pathways with severe toxicities in NSCLC patients undergoing platinum-based chemotherapy.
International journal of cancer 2017 Aug . Zheng Yi, Deng Zheng, Yin Jiye, Wang Shiming, Lu Daru, Wen Xiaoke, Li Xiangping, Xiao Di, Hu Chengping, Chen Xiang, Zhang Wei, Zhou Honghao, Liu Zhaoqi |
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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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Fanconi anemia genes in lung adenocarcinoma- a pathway-wide study on cancer susceptibility.
Journal of biomedical science 2016 Feb 23 23. Yang Shi-Yi, Hsiung Chia-Ni, Li Yao-Jen, Chang Gee-Chen, Tsai Ying-Huang, Chen Kuan-Yu, Huang Ming-Shyan, Su Wu-Chou, Chen Yuh-Min, Hsiung Chao A, Yang Pan-Chyr, Chen Chien-Jen, Wu Pei-Ei, Yu Jyh-Cherng, Shen Chen-Yang, Hsu Huan-Mi |
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The risk for developing cancer in Israeli ATM, BLM, and FANCC heterozygous mutation carriers.
Cancer genetics 2015 Dec . Laitman Yael, Boker-Keinan Lital, Berkenstadt Michal, Liphsitz Irena, Weissglas-Volkov Daphna, Ries-Levavi Liat, Sarouk Ifat, Pras Elon, Friedman Eit |
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Genetic variants associated with risk of atrial fibrillation regulate expression of PITX2, CAV1, MYOZ1, C9orf3 and FANCC.
Journal of molecular and cellular cardiology 2015 Aug 85 207-14. Martin Ruairidh I R, Babaei Mahsa Sheikhali, Choy Mun-Kit, Owens W Andrew, Chico Timothy J A, Keenan Daniel, Yonan Nizar, Koref Mauro Santibáñez, Keavney Bernard |
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Candidate gene analysis of BRCA1/2 mutation-negative high-risk Russian breast cancer patients.
Cancer letters 2015 Apr 359 (2): 259-61. Sokolenko Anna P, Preobrazhenskaya Elena V, Aleksakhina Svetlana N, Iyevleva Aglaya G, Mitiushkina Natalia V, Zaitseva Olga A, Yatsuk Olga S, Tiurin Vladislav I, Strelkova Tatiana N, Togo Alexandr V, Imyanitov Evgeny |
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FANCA and FANCG are the major Fanconi anemia genes in the Korean population.
Clinical genetics 2013 Sep 84 (3): 271-5. Park J, Chung N-G, Chae H, Kim M, Lee S, Kim Y, Lee J-W, Cho B, Jeong D C, Park I |
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Exome Sequencing Identifies Rare Deleterious Mutations in DNA Repair Genes FANCC and BLM as Potential Breast Cancer Susceptibility Alleles.
PLoS genetics 2012 Sep 8 (9): 9. Thompson ER, Doyle MA, Ryland GL, Rowley SM, Choong DY, Tothill RW, Thorne H, Barnes DR, Li J, Ellul J, Philip GK, Antill YC, James PA, Trainer AH, Mitchell G, Campbell IG |
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Association of FANCC and PTCH1 with the development of early dysplastic lesions of the head and neck.
Annals of surgical oncology 2012 Jul 19 Suppl 3 S528-38. Ghosh Amlan, Ghosh Susmita, Maiti Guru Prasad, Mukherjee Sudeshna, Mukherjee Nupur, Chakraborty Jayanta, Roy Anup, Roychoudhury Susanta, Panda C |
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Association of FANCC polymorphisms with FEV1 decline in aspirin exacerbated respiratory disease.
Molecular biology reports 2012 Mar 39 (3): 2385-94. Kim Jeong-Hyun, Park Byung-Lae, Pasaje Charisse Flerida A, Bae Joon Seol, Park Jong Sook, Park Sung Woo, Uh Soo-Taek, Choi Jae-Sung, Kim Yong-Hoon, Kim Mi-Kyeong, Choi Inseon S, Cho Sang Heon, Choi Byoung Whui, Park Choon-Sik, Shin Hyoung D |
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Evaluation of Fanconi anaemia genes FANCA, FANCC and FANCL in cervical cancer susceptibility.
Gynecologic oncology 2011 May . Juko-Pecirep I, Ivansson EL, Gyllensten UB |
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The Fanconi anemia family of genes and its correlation with breast cancer susceptibility and breast cancer features.
Breast cancer research and treatment 2009 Jun . Barroso E, Pita G, Arias JI, Menendez P, Zamora P, Blanco M, Benitez J, Ribas G |
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Germ line Fanconi anemia complementation group C mutations and pancreatic cancer.
Cancer research 2005 Jan 65 (2): 383-6. Couch Fergus J, Johnson Michele R, Rabe Kari, Boardman Lisa, McWilliams Robert, de Andrade Mariza, Petersen Glor |
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Transcriptional silencing of Fanconi anaemia genes and clinical outcome in head and neck cancer.
Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2004 Jul 22 (14_suppl): 9546. Gasco M, Sullivan A, Smith P, Farrell P, Numico G, Colantonio I, Merlano M, Crook |
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- Page last updated:Apr 08, 2021
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