Two truncating variants in FANCC and breast cancer risk
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Published:2019-08-29
Issue:1
Volume:9
Page:
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ISSN:2045-2322
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Container-title:Scientific Reports
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language:en
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Short-container-title:Sci Rep
Author:
Dörk Thilo, , Peterlongo Paolo, Mannermaa Arto, Bolla Manjeet K., Wang Qin, Dennis Joe, Ahearn Thomas, Andrulis Irene L.ORCID, Anton-Culver Hoda, Arndt VolkerORCID, 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 HiltrudORCID, 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 MiriamORCID, Eccles Diana M., Ekici Arif B.ORCID, Eriksson Mikael, Evans D. Gareth, Fasching Peter A.ORCID, Figueroa JonineORCID, 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 AlexanderORCID, Hillemanns Peter, Hogervorst Frans B. L., Hooning Maartje J., Hopper John L., Howell Tony, Huo Dezheng, Ito HidemiORCID, 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, Lubiński Jan, Manoochehri Mehdi, Manoukian Siranoush, Margolin Sara, Martinez Elena, Matsuo KeitaroORCID, Mavroudis Dimitris, Meindl Alfons, Menon UshaORCID, Milne Roger L.ORCID, Mohd Taib Nur Aishah, Muir KennethORCID, Mulligan Anna Marie, Neuhausen Susan L., Nevanlinna HeliORCID, Neven Patrick, Newman William G.ORCID, Offit Kenneth, Olopade Olufunmilayo I., Olshan Andrew F., Olson Janet E., Olsson Håkan, Park Sue K., Park-Simon Tjoung-Won, Peto JulianORCID, Plaseska-Karanfilska Dijana, Pohl-Rescigno Esther, Presneau Nadege, Rack Brigitte, Radice Paolo, Rashid Muhammad U., Rennert GadORCID, Rennert Hedy S., Romero AtochaORCID, Ruebner Matthias, Saloustros Emmanouil, Schmidt Marjanka K.ORCID, Schmutzler Rita K., Schneider Michael O., Schoemaker Minouk J., Scott ChristopherORCID, Shen Chen-Yang, Shu Xiao-Ou, Simard Jacques, Slager Susan, Smichkoska Snezhana, Southey Melissa C., Spinelli John J., Stone JenniferORCID, 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 ThérèseORCID, Tsugane ShoichiroORCID, 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 ArgyriosORCID, Ziv Elad, Dunning Alison M.ORCID, Pharoah Paul D. P.ORCID, Schindler Detlev, Devilee PeterORCID, Easton Douglas F.ORCID,
Funder
Cancer Research UK
Publisher
Springer Science and Business Media LLC
Subject
Multidisciplinary
Reference37 articles.
1. Ceccaldi, R., Sarangi, P. & D’Andrea, A. D. The Fanconi anaemia pathway: new players and new functions. Nat. Rev. Mol. Cell Biol. 17, 337–349 (2016). 2. Knies, K. et al. Biallelic mutations in the ubiquitin ligase RFWD3 cause Fanconi anemia. J. Clin. Invest. 127, 3013–3027 (2017). 3. Nalepa, G. & Clapp, D. W. Fanconi anaemia and cancer: an intricate relationship. Nat. Rev. Cancer 18, 168–185 (2018). 4. Ramus, S. J. et al. Germline Mutations in the BRIP1, BARD1, PALB2, and NBN Genes in Women With Ovarian Cancer. J. Natl. Cancer Inst. 107, 11 (2015). 5. Easton, D. F. et al. No evidence that protein truncating variants in BRIP1 are associated with breast cancer risk: implications for gene panel testing. J. Med. Genet. 53, 298–309 (2016).
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