%0 Journal Article
%A Dörk, Thilo
%A Peterlongo, Paolo
%A Mannermaa, Arto
%A Bolla, Manjeet K
%A Wang, Qin
%A Dennis, Joe
%A Ahearn, Thomas
%A Andrulis, Irene L
%A Anton-Culver, Hoda
%A Arndt, Volker
%A Aronson, Kristan J
%A Augustinsson, Annelie
%A Freeman, Laura E Beane
%A Beckmann, Matthias W
%A Beeghly-Fadiel, Alicia
%A Behrens, Sabine
%A Bermisheva, Marina
%A Blomqvist, Carl
%A Bogdanova, Natalia V
%A Bojesen, Stig E
%A Brauch, Hiltrud
%A Brenner, Hermann
%A Burwinkel, Barbara
%A Canzian, Federico
%A Chan, Tsun L
%A Chang-Claude, Jenny
%A Chanock, Stephen J
%A Choi, Ji-Yeob
%A Christiansen, Hans
%A Clarke, Christine L
%A Couch, Fergus J
%A Czene, Kamila
%A Daly, Mary B
%A Dos-Santos-Silva, Isabel
%A Dwek, Miriam
%A Eccles, Diana M
%A Ekici, Arif B
%A Eriksson, Mikael
%A Evans, D Gareth
%A Fasching, Peter A
%A Figueroa, Jonine
%A Flyger, Henrik
%A Fritschi, Lin
%A Gabrielson, Marike
%A Gago-Dominguez, Manuela
%A Gao, Chi
%A Gapstur, Susan M
%A García-Closas, Montserrat
%A García-Sáenz, José A
%A Gaudet, Mia M
%A Giles, Graham G
%A Goldberg, Mark S
%A Goldgar, David E
%A Guénel, Pascal
%A Haeberle, Lothar
%A Haiman, Christopher A
%A Håkansson, Niclas
%A Hall, Per
%A Hamann, Ute
%A Hartman, Mikael
%A Hauke, Jan
%A Hein, Alexander
%A Hillemanns, Peter
%A Hogervorst, Frans B L
%A Hooning, Maartje J
%A Hopper, John L
%A Howell, Tony
%A Huo, Dezheng
%A Ito, Hidemi
%A Iwasaki, Motoki
%A Jakubowska, Anna
%A Janni, Wolfgang
%A John, Esther M
%A Jung, Audrey
%A Kaaks, Rudolf
%A Kang, Daehee
%A Kapoor, Pooja Middha
%A Khusnutdinova, Elza
%A Kim, Sung-Won
%A Kitahara, Cari M
%A Koutros, Stella
%A Kraft, Peter
%A Kristensen, Vessela N
%A Kwong, Ava
%A Lambrechts, Diether
%A Marchand, Loic Le
%A Li, Jingmei
%A Lindström, Sara
%A Linet, Martha
%A Lo, Wing-Yee
%A Long, Jirong
%A Lophatananon, Artitaya
%A Lubiński, Jan
%A Manoochehri, Mehdi
%A Manoukian, Siranoush
%A Margolin, Sara
%A Martinez, Elena
%A Matsuo, Keitaro
%A Mavroudis, Dimitris
%A Meindl, Alfons
%A Menon, Usha
%A Milne, Roger L
%A Mohd Taib, Nur Aishah
%A Muir, Kenneth
%A Mulligan, Anna Marie
%A Neuhausen, Susan L
%A Nevanlinna, Heli
%A Neven, Patrick
%A Newman, William G
%A Offit, Kenneth
%A Olopade, Olufunmilayo I
%A Olshan, Andrew F
%A Olson, Janet E
%A Olsson, Håkan
%A Park, Sue K
%A Park-Simon, Tjoung-Won
%A Peto, Julian
%A Plaseska-Karanfilska, Dijana
%A Pohl-Rescigno, Esther
%A Presneau, Nadege
%A Rack, Brigitte
%A Radice, Paolo
%A Rashid, Muhammad U
%A Rennert, Gad
%A Rennert, Hedy S
%A Romero, Atocha
%A Ruebner, Matthias
%A Saloustros, Emmanouil
%A Schmidt, Marjanka K
%A Schmutzler, Rita K
%A Schneider, Michael O
%A Schoemaker, Minouk J
%A Scott, Christopher
%A Shen, Chen-Yang
%A Shu, Xiao-Ou
%A Simard, Jacques
%A Slager, Susan
%A Smichkoska, Snezhana
%A Southey, Melissa C
%A Spinelli, John J
%A Stone, Jennifer
%A Surowy, Harald
%A Swerdlow, Anthony J
%A Tamimi, Rulla M
%A Tapper, William J
%A Teo, Soo H
%A Terry, Mary Beth
%A Toland, Amanda E
%A Tollenaar, Rob A E M
%A Torres, Diana
%A Torres-Mejía, Gabriela
%A Troester, Melissa A
%A Truong, Thérèse
%A Tsugane, Shoichiro
%A Untch, Michael
%A Vachon, Celine M
%A Ouweland, Ans M W van den
%A Veen, Elke M van
%A Vijai, Joseph
%A Wendt, Camilla
%A Wolk, Alicja
%A Yu, Jyh-Cherng
%A Zheng, Wei
%A Ziogas, Argyrios
%A Ziv, Elad
%A Dunning, Alison M
%A Pharoah, Paul D P
%A Schindler, Detlev
%A Devilee, Peter
%A Easton, Douglas F
%A Balleine, Rosemary
%A Baxter, Robert
%A Braye, Stephen
%A Carpenter, Jane
%A Dahlstrom, Jane
%A Forbes, John
%A Lee, C Soon
%A Marsh, Deborah
%A Morey, Adrienne
%A Pathmanathan, Nirmala
%A Scott, Rodney
%A Simpson, Peter
%A Spigelman, Allan
%A Wilcken, Nicholas
%A Yip, Desmond
%A Zeps, Nikolajs
%A Børresen-Dale, Anne-Lise
%A Grenaker Alnæs, Grethe I
%A Sahlberg, Kristine K
%A Ottestad, Lars
%A Kåresen, Rolf
%A Schlichting, Ellen
%A Holmen, Marit Muri
%A Sauer, Toril
%A Haakensen, Vilde
%A Engebråten, Olav
%A Naume, Bjørn
%A Fosså, Alexander
%A Kiserud, Cecile E
%A Reinertsen, Kristin V
%A Helland, Åslaug
%A Riis, Margit
%A Geisler, Jürgen
%T Two truncating variants in FANCC and breast cancer risk.
%J Scientific reports
%V 9
%N 1
%@ 2045-2322
%C [London]
%I Macmillan Publishers Limited, part of Springer Nature
%M DKFZ-2019-02125
%P 12524
%D 2019
%X Fanconi anemia (FA) is a genetically heterogeneous disorder with 22 disease-causing genes reported to date. In some FA genes, monoallelic mutations have been found to be associated with breast cancer risk, while the risk associations of others remain unknown. The gene for FA type C, FANCC, has been proposed as a breast cancer susceptibility gene based on epidemiological and sequencing studies. We used the Oncoarray project to genotype two truncating FANCC variants (p.R185X and p.R548X) in 64,760 breast cancer cases and 49,793 controls of European descent. FANCC mutations were observed in 25 cases (14 with p.R185X, 11 with p.R548X) and 26 controls (18 with p.R185X, 8 with p.R548X). There was no evidence of an association with the risk of breast cancer, neither overall (odds ratio 0.77, 95
%F PUB:(DE-HGF)16
%9 Journal Article
%$ pmid:31467304
%R 10.1038/s41598-019-48804-y
%U https://inrepo02.dkfz.de/record/144683