COMPLEXO: identifying the missing heritability of breast cancer via next generation collaboration
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Peter Kraft | Mads Thomassen | Daniel J. Park | Ella Thompson | Vijai Joseph | Peter Devilee | Alfons Meindl | Paolo Peterlongo | Kenneth Offit | Ava Kwong | Douglas Easton | Heli Nevanlinna | Georgia Chenevix-Trench | Javier Benitez | Jirong Long | Jacques Simard | Paolo Radice | Fergus J Couch | Carrie Snyder | Kasmintan Schrader | Mark Robson | Penny Soucy | Melissa C Southey | Daniel J Park | Olga Sinilnikova | Tu Nguyen-Dumont | Rita Schmutzler | Sara Lindstrom | Katherine Nathanson | Eric Hahnen | Wei Zheng | F. Couch | J. Benítez | Sofia Khan | M. Southey | D. Easton | P. Kraft | K. Offit | J. Long | W. Zheng | R. Barkardottir | G. Chenevix-Trench | H. Nevanlinna | P. Devilee | S. Tavtigian | K. Nathanson | A. Meindl | R. Schmutzler | M. Dumont | P. Radice | P. Peterlongo | J. Simard | S. Lindstrom | S. Neuhausen | M. Robson | M. Dufault | O. Sinilnikova | S. Mazoyer | F. Damiola | E. Thompson | I. Campbell | S. Wang | H. Lynch | E. Hahnen | T. Hansen | D. Goldgar | B. Feng | M. Thomassen | J. Weitzel | C. Snyder | F. Lesueur | K. Schrader | P. Soucy | S. Ramus | A. Kwong | I. Pedersen | L. Jønson | D. Hunter | A. Trainer | V. Joseph | T. Törngren | A. Kvist | Martine Dumont | David E Goldgar | Henry Lynch | Yu-Tang Gao | San Ming Wang | Francesca Damiola | Ian Campbell | Sean Tavtigian | Sofia Khan | Bing-Jian Feng | Susan Neuhausen | Jeffrey N Weitzel | Fabienne Lesueur | Sylvie Mazoyer | Therese Törngren | Anders Kvist | F. Hilbers | David Hunter | Lars Jønson | Thomas VO Hansen | Yeong C Kim | Alison H Trainer | Inge S Pedersen | Michael R Dufault | TL Chris Chan | Rosa Barkardóttir | Florentine Hilbers | Susan Ramus | Yeong C. Kim | T. Nguyen-Dumont | Yu-Tang Gao | TL Chris Chan | Therese Törngren | Yu-Tang Gao
[1] R. Tothill,et al. Exome Sequencing Identifies Rare Deleterious Mutations in DNA Repair Genes FANCC and BLM as Potential Breast Cancer Susceptibility Alleles , 2012, PLoS genetics.
[2] Daniel J. Park,et al. Rare mutations in XRCC2 increase the risk of breast cancer. , 2012, American journal of human genetics.
[3] A. Uitterlinden,et al. Kathleen Cuningham Foundation Consortium For Research Into Familial Breast Cancer , 2008 .
[4] J. Benítez,et al. Rare Mutations in XRCC 2 Increase the Risk of Breast Cancer , 2022 .