Resultados de procura

Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations por Jimmy Z. Liu, Suzanne van Sommeren, Hailiang Huang, Siew C. Ng, Rudi Alberts, Atsushi Takahashi, Stephan Ripke, James Lee, Luke Jostins-Dean, Tejas Shah, Shifteh Abedian, Jae Hee Cheon, Judy H. Cho, Naser Ebrahim Daryani, Lude Franke, Yuta Fuyuno, Ailsa Hart, Ramesh C. Juyal, Garima Juyal, Won Ho Kim, Andrew P. Morris, Hossein Poustchi, William G. Newman, Vandana Midha, Timothy R. Orchard, Homayon Vahedi, Ajit Sood, Joseph J.�Y. Sung, Reza Malekzadeh, Harm-Jan Westra, Keiko Yamazaki, Suk-Kyun Yang, Jeffrey C. Barrett, Andre Franke, Behrooz Z Alizadeh, Miles Parkes, B.K. Thelma, Mark Daly, Michiaki Kubo, Carl A. Anderson, Rinse K. Weersma

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Genetics in schizophrenia: where are we and what next? por Arun K. Tiwari, Clement C. Zai, Daniel J. Müller, James L. Kennedy

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Molecular neurobiological clues to the pathogenesis of bipolar disorder por Paul J. Harrison

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Association of STAT4 with Rheumatoid Arthritis in the Korean Population por Hye‐Soon Lee, Elaine F. Remmers, Julie Le, Daniel L. Kastner, Sang‐Cheol Bae, Peter K. Gregersen

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Network-Based Analysis of Schizophrenia Genome-Wide Association Data to Detect the Joint Functional Association Signals por Suhua Chang, Kechi Fang, Kunlin Zhang, Jing Wang

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Erratum: Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease por Denise Harold, Richard Abraham, Paul Hollingworth, Rebecca Sims, Amy Gerrish, Marian L. Hamshere, Jaspreet Singh Pahwa, Valentina Moskvina, Kimberley Dowzell, Amy L. Williams, Nicola Jones, Charlene Thomas, Alexandra Stretton, Angharad R. Morgan, Simon Lovestone, John Powell, Petroula Proitsi, Michelle K. Lupton, Carol Brayne, David C. Rubinsztein, Michael Gill, Brian Lawlor, Aoibhinn Lynch, Kevin Morgan, Kristelle Brown, Peter Passmore, David Craig, Bernadette McGuinness, Stephen Todd, Clive Holmes, David Mann, A. David Smith, Seth Love, Patrick G. Kehoe, John Hardy, Simon Mead, Nick C. Fox, Martin N. Rossor, John Collinge, Wolfgang Maier, Frank Jessen, Britta Schürmann, Hendrik van den Bussche, Isabella Heuser, Johannes Kornhuber, Jens Wiltfang, Martin Dichgans, Lutz Frölich, Harald Hampel, Michael Hüll, Dan Rujescu, Alison Goate, John Kauwe, Carlos Cruchaga, Petra Nowotny, John C. Morris, Kevin H. Mayo, Kristel Sleegers, Karolien Bettens, Sebastiaan Engelborghs, Peter Paul De Deyn, Christine Van Broeckhoven, Gill Livingston, Nicholas Bass, Hugh Gurling, Andrew McQuillin, Rhian Gwilliam, Panos Deloukas, Ammar Al‐Chalabi, Christopher E. Shaw, Magda Tsolaki, Andrew B. Singleton, Rita Guerreiro, Thomas W. Mühleisen, Markus M. Nöthen, Susanne Moebus, Karl‐Heinz Jöckel, Norman Klopp, H‐Erich Wichmann, Minerva M. Carrasquillo, V. Shane Pankratz, Steven G. Younkin, Peter Holmans, Michael O’Donovan, Michael J. Owen, Julie Williams

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Genomic risk prediction of complex human disease and its clinical application por Gad Abraham, Michael Inouye

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From Pharmacogenetics to Pharmacogenomics: The Way toward the Personalization of Antidepressant Treatment por Chiara Fabbri, Stefano Porcelli, Alessandro Serretti

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Genetics of Eating Disorders por Cynthia M. Bulik, Lauren E. Blake, Jehannine Austin

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Association Mapping for Fruit, Plant and Leaf Morphology Traits in Eggplant por Ezio Portis, Fabio Cericola, Lorenzo Barchi, Laura Toppino, N. Acciarri, Laura Pulcini, T. Sala, Sergio Lanteri, Giuseppe Leonardo Rotino

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A Kernel of Truth por John Blangero, Vincent P. Diego, Thomas D. Dyer, Marcio Almeida, Juan M. Peralta, Jack W. Kent, Jeff T. Williams, Laura Almasy, Harald H.H. Göring

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Genome-wide association study on antipsychotic-induced weight gain in the CATIE sample por Eva J. Brandl, Arun K. Tiwari, Clement C. Zai, Erika L. Nurmi, Nabilah I. Chowdhury, Tamara Arenovich, Marcos Sanches, Vanessa F. Gonçalves, Jinjin Shen, Jeffrey A. Lieberman, Herbert Y. Meltzer, James L. Kennedy, D Müller

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Phenotypic extremes in rare variant study designs por Gina M. Peloso, Daniel J. Rader, Stacey Gabriel, Sekar Kathiresan, Mark J. Daly, Benjamin M. Neale

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The immunogenetics of primary biliary cirrhosis: A comprehensive review por Gwilym J. Webb, K A Siminovitch, Gideon M. Hirschfield

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A Powerful Pathway-Based Adaptive Test for Genetic Association with Common or Rare Variants por Wei Pan, Il‐Youp Kwak, Peng Wei

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Genetics of Anorexia Nervosa por Jessica H. Baker, Katherine Schaumberg, Melissa A. Munn‐Chernoff

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A Two-Stage Meta-Analysis Identifies Several New Loci for Parkinson's Disease por Vincent Plagnol, Michael A. Nalls, José Brás, D.G. Hernandez, Manu Sharma, Una‐Marie Sheerin, Mohamad Saad, Javier Simón‐Sánchez, Claudia Schulte, Suzanne Lesage, Sigurlaug Sveinbjörnsdóttir, Philippe Amouyel, Sampath Arepalli, Roger A. Barker, C. Bellinguez, Yoav Ben‐Shlomo, Henk W. Berendse, Daniela Berg, Kailash P. Bhatia, Rob M.A. de Bie, Alessandro Biffi, B.R. Bloem, Zoltán Bochdanovits, Marina de Nadai Bonin Gomes, Kathrin Brockmann, Janet Brooks, David J. Burn, Gavin Charlesworth, Honglei Chen, Patrick F. Chinnery, S. A. Chong, Carl E Clarke, Mark Cookson, Jonathan M. Cooper, Jean‐Christophe Corvol, Carl Counsell, Philippe Damier, J.F. Dartigues, Panos Deloukas, Günther Deuschl, David T. Dexter, Karin D. van Dijk, Allissa Dillman, F. Durif, Alexandra Dürr, Sarah Edkins, Jonathan Evans, Thomas Foltynie, Colin L. Freeman, Jingping Gao, Michelle Gardner, J. Raphael Gibbs, Alison Goate, Emma Gray, Rita Guerreiro, Ómar Gústafsson, Curtis C. Harris, Garrett Hellenthal, Jacobus J. van Hilten, Albert Hofman, A. R. Hollenbeck, Janice L. Holton, Joshua Shulman, Xia Huang, H Huber, Gavin Hudson, Sarah Hunt, Johanna Huttenlocher, Thomas Illig, Pálmi V. Jónsson, Cordelia Langford, Andrew J. Lees, Peter Lichtner, Patricia Limousin, Grisel Lopez, D. Lorenz, A. McNeill, Catriona Moorby, Matthew Moore, Huw R. Morris, Karen Morrison, Ese Mudanohwo, Sean S. O’Sullivan, John F. Pearson, Richard D. Pearson, Joel S. Perlmutter, Hannes Pétursson, M. Pirinen, Pierre Pollak, Bart Post, Sally Potter, Bernard Ravina, Tamás Révész, Olaf Rieß, Fernando Rivadeneira, Patrizia Rizzu, Mina Ryten, Stephen Sawcer, Peter Heutink, Nicholas Wood

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Test for Rare Variants by Environment Interactions in Sequencing Association Studies por Xinyi Lin, Seunggeun Lee, Michael C. Wu, Chaolong Wang, Han Chen, Zilin Li, Xihong Lin

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Candidate gene case‐control association studies: advantages and potential pitfalls por Ann K. Daly, Christopher P. Day

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Contemporary Considerations for Constructing a Genetic Risk Score: An Empirical Approach por Benjamin A. Goldstein, Lingyao Yang, Elias Salfati, Themistocles L. Assimes

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