Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects
- Creator: Marshall, Christian R. , Howrigan, Daniel P. , Gujral, Madhusudan , Brandler, William M. , Malhotra, Dheeraj , Wang, Zhouzhi , Fuentes Fajarado, Karin V. , Maile, Michelle S. , Ripke, Stephan , Agartz, Ingrud , Albus, Margot , Alexander, Madeline , Merico, Daniele , Atkins, Joshua , Cairns, Murray J. , Carr, Vaughan J. , Henskens, Frans A. , Kelly, Brian J. , Loughland, Carmel L. , Michie, Patricia T. , Schall, Ulrich , Scott, Rodney J. , Tooney, Paul A. , Thiruvahindrapuram, Bhooma , Wu, Jing Qin , Wu, Wenting , Greer, Douglas S. , Antaki, Douglas , Shetty, Aniket , Holmans, Peter A. , Pinto, Dalila
- Resource Type: journal article
- Date: 2017
Rare germline copy number deletions of likely functional importance are implicated in endometrial cancer predisposition
- Creator: Moir-Meyer, Gemma L. , Pearson, John F. , Pharoah, Paul D. , Dunning, Alison M. , Thompson, Deborah J. , Easton, Douglas F. , Spurdle, Amanda B. , Walker, Logan C. , Lose, Felicity , The Australian National Endometrial Cancer Study Group, , Scott, Rodney J. , McEvoy, Mark , Attia, John , Holliday, Elizabeth G. , The Hunter Community Study, , Studies of Epidemiology and Risk Factors in Cancer Heredity,
- Resource Type: journal article
- Date: 2015