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Material Type: Artigo
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The Genetic Basis of Mendelian Phenotypes: Discoveries, Challenges, and OpportunitiesChong, Jessica X. ; Buckingham, Kati J. ; Jhangiani, Shalini N. ; Boehm, Corinne ; Sobreira, Nara ; Smith, Joshua D. ; Harrell, Tanya M. ; McMillin, Margaret J. ; Wiszniewski, Wojciech ; Gambin, Tomasz ; Coban Akdemir, Zeynep H. ; Doheny, Kimberly ; Scott, Alan F. ; Avramopoulos, Dimitri ; Chakravarti, Aravinda ; Hoover-Fong, Julie ; Mathews, Debra ; Witmer, P. Dane ; Ling, Hua ; Hetrick, Kurt ; Watkins, Lee ; Patterson, Karynne E. ; Reinier, Frederic ; Blue, Elizabeth ; Muzny, Donna ; Kircher, Martin ; Bilguvar, Kaya ; López-Giráldez, Francesc ; Sutton, V. Reid ; Tabor, Holly K. ; Leal, Suzanne M. ; Gunel, Murat ; Mane, Shrikant ; Gibbs, Richard A. ; Boerwinkle, Eric ; Hamosh, Ada ; Shendure, Jay ; Lupski, James R. ; Lifton, Richard P. ; Valle, David ; Nickerson, Deborah A. ; Bamshad, Michael J.American journal of human genetics, 2015-08, Vol.97 (2), p.199-215 [Periódico revisado por pares]United States: Elsevier IncTexto completo disponível |
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Material Type: Artigo
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A Method to Exploit the Structure of Genetic Ancestry Space to Enhance Case-Control StudiesColombel, Jean-Frederick ; Hugot, Jean-Pierre ; Massey, Dunecan ; Montgomery, Grant W. ; Oikonomou, Ioannis ; Peeters, Harald ; Proctor, Deborah D. ; Seibold, Frank ; Törkvist, Leif ; Andrews, Jane M. ; Bampton, Peter A. ; Florin, Timothy H. ; Krishnaprasad, Krupa ; Radford-Smith, Graham ; Simms, Lisa A. ; Laukens, Debby ; Deslandres, Colette ; Duerr, Richard H. ; Goyette, Philippe ; Haritunians, Talin ; Lahaie, Raymond G. ; Ng, Sok Meng ; Rioux, John D. ; Aerts, Jan ; Attwood, Anthony ; Ball, Stephen G. ; Brown, Morris J. ; Burton, John ; Byrnes, Jake ; Cardin, Niall ; Clee, Chris M. ; Coffey, Alison J. ; Dominiczak, Anna F. ; Evans, David M. ; Farmer, Anne ; Ferrier, Nicol ; Flynn, Edward ; Franklyn, Jayne A. ; Frayling, Timothy M. ; Freathy, Rachel M. ; Gibbs, Polly ; Gray, Emma ; Howard, Philip ; Hughes, Debbie ; Hunt, Sarah ; Jolley, Jennifer D. ; Jones, Lisa A. ; Kirov, George ; Maller, Julian ; Mansfield, John ; McGuffin, Peter ; McLay, Kirsten E. ; Mentzer, Alex ; Munroe, Patricia B. ; Newman, William ; Palotie, Aarno ; Plagnol, Vincent ; Prescott, Natalie J. ; Quail, Michael A. ; Reid, David M. ; Renwick, Anthony ; Russell, Ellie ; St Clair, David ; Scott, Richard ; Somaskantharajah, Elilan ; Steer, Sophia ; Symmons, Deborah P.M. ; Tobin, Martin D. ; Wain, Louise V. ; Walker, Mark ; Wallace, Chris ; Weedon, Michael N. ; Wilson, Anthony G. ; Yau, Chris ; Young, Allan H. ; Brown, Matthew A. ; Gough, Stephen C.L. ; Satsangi, Jack ; Ouwehand, Willem H. ; Parkes, Miles ; Rahman, Nazneen ; Samani, Nilesh J. ; Kwiatkowski, Dominic P. ; Donnelly, Peter ; Bramon, Elvira ; Casas, Juan P. ; Corvin, Aiden ; Jankowski, Janusz ; Markus, Hugh S. ; Palmer, Colin N.A. ; Plomin, Robert ; Viswanathan, Ananth C. ; Spencer, Chris C.A. ; Blackburn, Hannah ; Gillman, Matthew ; McCann, Owen T. ; Waller, Matthew ; Weston, Paul ; Whittaker, Pamela ; Roeder, KathrynAmerican journal of human genetics, 2016-05, Vol.98 (5), p.857-868 [Periódico revisado por pares]United States: Elsevier IncTexto completo disponível |
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Material Type: Artigo
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Significant Linkage of Parkinson Disease to Chromosome 2q36-37Pankratz, Nathan ; Nichols, William C. ; Uniacke, Sean K. ; Halter, Cheryl ; Rudolph, Alice ; Shults, Cliff ; Conneally, P. Michael ; Foroud, TatianaAmerican journal of human genetics, 2003-04, Vol.72 (4), p.1053-1057 [Periódico revisado por pares]Chicago, IL: Elsevier IncTexto completo disponível |