Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk
Manjeet K. Bolla(University of Cambridge), Thibaud Boutin(University of Minnesota), Ilja M. Nolte(University Medical Center Groningen), Katherine S. Ruth(University of Exeter), Sarah E. Medland(QIMR Berghofer Medical Research Institute), Daniel I. Chasman(Brigham and Women's Hospital), Raymond Noordam(Leiden University Medical Center), Ivana Kolčić(Boston University), Hilary K. Finucane(Broad Institute), Chunyan He(Indiana University Health), Ayellet V. Segrè(Broad Institute), Hannes Helgason(deCODE Genetics (Iceland)), Jouke‐Jan Hottenga(Vrije Universiteit Amsterdam), Natalia Perjakova(Brigham and Women's Hospital), Archie Campbell(Vanderbilt University), Robert Karlsson(Harvard University), Ayush Giri(Vanderbilt Health), Sean Whalen(Gladstone Institutes), Massimo Mangino(King's College London), Eric Boerwinkle(Training Programs in Epidemiology and Public Health Interventions Network), Po‐Ru Loh(Broad Institute), Irene L. Andrulis(University of Toronto), Javier Benı́tez(Spanish National Cancer Research Centre), Elisabeth Altmaier(Vita-Salute San Raffaele University), Felix R. Day(University of Cambridge), Sven Bergmann(SIB Swiss Institute of Bioinformatics), Patrick Sulem(deCODE Genetics (Iceland)), Teresa Nutile(Institute of Genetics and Biophysics), Marzyeh Amini(University Medical Center Groningen), Lavinia Paternoster(University of Bristol), Murielle Bochud(Centre universitaire de médecine générale et santé publique, Lausanne), Stig E. Bojesen(University of Copenhagen), Ellen W. Demerath(University of Minnesota), Marco Brumat(University of Trieste), Caterina Barbieri(Vita-Salute San Raffaele University), Alexander Teumer(Medical University of Białystok), Abhishek Sarkar(Broad Institute), Kathryn L. Lunetta(Boston University), Stefania Bandinelli(Spanish National Cancer Research Centre), Albert V. Smith(University of Iceland), Matthias W. Beckmann, Deborah J. Thompson, Lynda M. Rose(Broad Institute), George McMahon(University Medical Center Groningen), Eleonora Porcu(Edinburgh Royal Infirmary), Lisette Stolk(Mount Sinai Hospital), Eva Albrecht(University Medical Center Groningen), Katharina E. Schraut(University of Iceland)
Cited by 642
Related Papers
A global reference for human genetic variation
|Nature|2015|19.9k
A second generation human haplotype map of over 3.1 million SNPs
|Nature|2007|4.6k
Detecting Novel Associations in Large Data Sets
|Science|2011|3.4k