COMPLEXO: Identifying the missing heritability of breast cancer via next generation collaboration

Breast Cancer Research

Volumn 15, Issue 3, 2013, Pages

  Southey, Melissa C ^a   Park, Daniel J ^a   Nguyen Dumont, Tu ^a   Campbell, Ian ^a,b   Thompson, Ella ^a,b   Trainer, Alison H ^b,c   Chenevix Trench, Georgia ^d   Simard, Jacques ^e   Dumont, Martine ^e   Soucy, Penny ^e   Thomassen, Mads ^f   Jønson, Lars ^g   Pedersen, Inge S ^h   Hansen, Thomas V O ^g   Nevanlinna, Heli ⁱ   Khan, Sofia ⁱ   Sinilnikova, Olga ^j,k   Mazoyer, Sylvie ^j   Lesueur, Fabienne ^l   Damiola, Francesca ^j   Schmutzler, Rita ^m,n   Meindl, Alfons ^o   Hahnen, Eric ^m,n   Dufault, Michael R ^o   Chris Chan, T L ^p,q,r   Kwong, Ava ^p,r,s   Barkardóttir, Rosa ^t,u   Radice, Paolo ^v   Peterlongo, Paolo ^w   Devilee, Peter ^x   Hilbers, Florentine ^x   Benitez, Javier ^y,z   Kvist, Anders ^aa   Törngren, Therese ^aa   Easton, Douglas ^ab   Hunter, David ^ac   Lindstrom, Sara ^ad   Kraft, Peter ^ac   Zheng, Wei ^ad   Gao, Yu Tang ^ae   Long, Jirong ^ad   Ramus, Susan ^af   Feng, Bing Jian ^ag   Weitzel, Jeffrey N ^ah   Nathanson, Katherine ^ai   Offit, Kenneth ^aj   Joseph, Vijai ^aj   Robson, Mark ^aj   Schrader, Kasmintan ^aj   Wang, San Ming ^ak   Kim, Yeong C ^ak   Lynch, Henry ^al   Snyder, Carrie ^al   Tavtigian, Sean ^am   Neuhausen, Susan ^ah   Couch, Fergus J ^an   Goldgar, David E ^am   more..

^a UNIVERSITY OF MELBOURNE   (Australia)

^b PETER MACCALLUM CANCER CENTRE   (Australia)

^c ROYAL MELBOURNE HOSPITAL   (Australia)

^d ROYAL BRISBANE AND WOMEN'S HOSPITAL   (Australia)

^e UNIVERSITÉ LAVAL   (Canada)

^f ODENSE UNIVERSITY HOSPITAL   (Denmark)

^g UNIVERSITY OF COPENHAGEN   (Denmark)

^h AALBORG UNIVERSITY HOSPITAL   (Denmark)

ⁱ UNIVERSITY OF HELSINKI   (Finland)

^j UNIVERSITÉ LYON 1   (France)

^k HOSPICES CIVILS DE LYON   (France)

^l INSERM U900   (France)

^m UNIVERSITY HOSPITAL OF COLOGNE   (Germany)

ⁿ UNIVERSITY OF COLOGNE   (Germany)

^o TECHNICAL UNIVERSITY OF MUNICH   (Germany)

^p Hong Kong Hereditary Breast Cancer Family Registry   (Hong Kong)

^q HONG KONG SANATORIUM AND HOSPITAL   (Hong Kong)

^r UNIVERSITY OF HONG KONG   (Hong Kong)

^s Hong Kong Sanatorium and Hospital   (United States)

^t LANDSPITALI UNIVERSITY HOSPITAL   (Iceland)

^u UNIVERSITY OF ICELAND   (Iceland)

^v NATIONAL CANCER INSTITUTE   (Italy)

^w FIRC INSTITUTE OF MOLECULAR ONCOLOGY   (Italy)

^x LEIDEN UNIVERSITY MEDICAL CENTER   (Netherlands)

^y Centro Nacional de Investigaciones Oncológicas   (Spain)

^z CENTRO DE INVESTIGACIÓN BIOMÉDICA EN RED DE ENFERMEDADES RARAS CIBERER   (Spain)

^aa LUND UNIVERSITY HOSPITAL   (Sweden)

^ab UNIVERSITY OF CAMBRIDGE   (United Kingdom)

^ac HARVARD SCHOOL OF PUBLIC HEALTH   (United States)

^ad VANDERBILT UNIVERSITY SCHOOL OF MEDICINE   (United States)

^ae SHANGHAI CANCER INSTITUTE   (China)

^af UNIVERSITY OF SOUTHERN CALIFORNIA   (United States)

^ag UNIVERSITY OF UTAH SCHOOL OF MEDICINE   (United States)

^ah CITY OF HOPE NATIONAL MEDICAL CENTER   (United States)

^ai UNIVERSITY OF PENNSYLVANIA   (United States)

^aj MEMORIAL SLOAN KETTERING CANCER CENTER   (United States)

^ak CREIGHTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

^al UNIVERSITY OF NEBRASKA MEDICAL CENTER   (United States)

^am UNIVERSITY OF UTAH   (United States)

^an MAYO CLINIC   (United States)

more..

Author keywords

[No Author keywords available]

Indexed keywords

BIOINFORMATICS; BREAST CANCER; CANCER RISK; CANCER SUSCEPTIBILITY; EXOME; GENETIC ASSOCIATION; GENETIC VARIABILITY; GENOME; HERITABILITY; HUMAN; LETTER; OVARY CANCER; PIPELINE; BREAST TUMOR; FEMALE; GENETIC LINKAGE; GENETIC PREDISPOSITION; GENETICS; MUTATION;

BREAST NEOPLASMS; FEMALE; GENETIC LINKAGE; GENETIC PREDISPOSITION TO DISEASE; GENOME-WIDE ASSOCIATION STUDY; HUMANS; MUTATION;

EID: 84879780529     PISSN: 14655411     EISSN: 1465542X     Source Type: Journal    
DOI: 10.1186/bcr3434     Document Type: Letter

References (5)

1. 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. kConFab Exome sequencing identifies rare deleterious mutations in DNA repair genes FANCC and BLM as potential breast cancer susceptibility alleles. PLoS Genet 2012, 8:e1002894. 10.1371/journal.pgen.1002894, 3459953, 23028338, kConFab.
2. Park DJ, Lesueur F, Nguyen-Dumont T, Pertesi M, Odefrey F, Hammet F, Neuhausen SL, John EM, Andrulis IL, Terry MB, Daly M, Buys S, Le Calvez-Kelm F, Lonie A, Pope BJ, Tsimiklis H, Voegele C, Hilbers FM, Hoogerbrugge N, Barroso A, Osorio A, , , Giles GG, Devilee P, Benitez J, Hopper JL, Tavtigian SV, Goldgar DE, Southey MC. Breast Cancer Family Registry, Kathleen Cuningham Foundation Consortium for Research into Familial Breast Cancer Rare mutations in XRCC2 increase the risk of breast cancer. Am J Hum Genet 2012, 90:734-739. 10.1016/j.ajhg.2012.02.027, 3322233, 22464251, Breast Cancer Family Registry, Kathleen Cuningham Foundation Consortium for Research into Familial Breast Cancer.
3. http://ccge.medschl.cam.ac.uk/consortia/bcac/index.html
4. CIMBA (The Consortium of Investigators of Modifiers of BRCA1/2). , http://ccge.medschl.cam.ac.uk/consortia/cimba/index.html
5. Collaborative Oncological Gene-environment Study. , http://www.cogseu.org