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Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations Autor 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? Autor 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 Autor Paul J. Harrison

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Association of STAT4 with Rheumatoid Arthritis in the Korean Population Autor 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 Autor Suhua Chang, Kechi Fang, Kunlin Zhang, Jing Wang

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Effect of maize processing on diet selection by bovine Autor Paulo Henrique Mazza Rodrigues, Fernando F. Ferreira, Roberta Passini, Laura Maria Oliveira Borgatti, Paula Marques Meyer

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Erratum: Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease Autor 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 Autor Gad Abraham, Michael Inouye

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

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

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Understanding inflammatory bowel disease via immunogenetics Autor Katrina M. de Lange, Jeffrey C. Barrett

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Determination of the TLR4 Genotype Using Allele-Specific PCR Autor Eva Lorenz, Kathy L. Frees, David A. Schwartz

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Genome-wide association of polycystic ovary syndrome implicates alterations in gonadotropin secretion in European ancestry populations Autor M. Geoffrey Hayes, Margrit Urbanek, David A. Ehrmann, Loren L. Armstrong, Ji Young Lee, Ryan Sisk, Tugce Karaderi, Thomas M. Barber, Mark I. McCarthy, Stephen Franks, Cecilia M. Lindgren, Corrine K. Welt, Evanthia Diamanti‐Kandarakis, Dimitrios Panidis, Mark O. Goodarzi, Ricardo Azziz, Yi Zhang, Roland James, Michael Olivier, Ahmed H. Kissebah, Ruben Alvero, Huiman X. Barnhart, Valerie L. Baker, Kurt T. Barnhart, G. Wright Bates, Robert G. Brzyski, Bruce R. Carr, Sandra Ann Carson, Peter R. Casson, Nicholas A. Cataldo, Gregory M. Christman, Christos Coutifaris, Michael P. Diamond, Esther Eisenberg, Gabriella G. Gosman, Linda C. Giudice, Daniel J. Haisenleder, Hao Huang, Stephen A. Krawetz, Scott Lucidi, Peter G. McGovern, Evan R. Myers, John E. Nestler, Dana A. Ohl, Nanette Santoro, William D. Schlaff, Peter J. Snyder, Michael P. Steinkampf, J.C. Trussell, Rebecca Usadi, Qingshang Yan, Heping Zhang, Elisabet Stener‐Victorin, Richard S. Legro, Andrea Dunaif

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Comparison of Sequence Variants in the PDK4 and COX4I2 Genes Between Racing and Cutting Lines of Quarter Horses and Associations With the Speed Index Autor Guilherme Luís Pereira, Rafael de Matteis, Camila Tângari Meira, Luciana Correia de Almeida Regitano, Josineudson Augusto II de Vasconcelos Silva, Luis Artur Loyola Chardulo, Rogério Abdallah Curi

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A High-Density Screen for Linkage in Multiple Sclerosis Autor Stephen Sawcer, Maria Ban, Mel Maranian, Tai Wai Yeo, Alastair Compston, Andrew Kirby, Mark Daly, Philip L. De Jager, Emily Walsh, Eric S. Lander, John D. Rioux, David A. Hafler, Adrian J. Ivinson, Jacqueline Rimmler, Simon G. Gregory, Silke Schmidt, Margaret A Pericak‐Vance, Eva Åkesson, Jan Hillert, Pameli Datta, Annette Oturai, Lars P. Ryder, Hanne F. Harbo, Anne Spurkland, Kjell‐Morten Myhr, Mikko Laaksonen, David R. Booth, Robert Heard, Graeme J. Stewart, Robin Lincoln, Lisa F. Barcellos, Stephen L. Hauser, Jorge R. Oksenberg, S J Kenealy, Jonathan L. Haines

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

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Common and rare variants associated with kidney stones and biochemical traits Autor Ásmundur Oddsson, Patrick Sulem, Hannes Helgason, Viðar Ö. Eðvarðsson, Guðmar Þorleifsson, Garðar Sveinbjörnsson, Eik Haraldsdottir, Guðmundur I. Eyjólfsson, Ólöf Sigurðardóttir, Ísleifur Ólafsson, Gísli Másson, Hilma Hólm, Daníel F. Guðbjartsson, Unnur Þorsteinsdóttir, Ólafur S. Indridason, Runólfur Pálsson, Kāri Stefánsson

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ESR1 polymorphisms and statin therapy: a sex-specific approach Autor Lisiane Smiderle, Marilu Fiegenbaum, Mara Helena Hutz, Cézar Roberto Van Der Sand, Luis C. Van der Sand, Maria Elvira Wagner Ferreira, Renan Canibal Pires, Silvana Almeida

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CFSAN SNP Pipeline: an automated method for constructing SNP matrices from next-generation sequence data Autor Steve Davis, James Pettengill, Yan Luo, Justin L. Payne, Al Shpuntoff, Hugh Rand, Errol Strain

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Molecular Basis of Gene-Gene Interaction: Cyclic Cross-Regulation of Gene Expression and Post-GWAS Gene-Gene Interaction Involved in Atrial Fibrillation Autor Yufeng Huang, Chuchu Wang, Yufeng Yao, Xiaoyu Zuo, Shanshan Chen, Chengqi Xu, Hongfu Zhang, Qiulun Lu, Le Chang, Fan Wang, Pengxia Wang, Rongfeng Zhang, Zhenkun Hu, Qixue Song, Xiaowei Yang, Cong Li, Sisi Li, Yuanyuan Zhao, Qin Yang, Dan Yin, Xiaojing Wang, Wenxia Si, Xiuchun Li, Xin Xiong, Dan Wang, Yuan Huang, Chunyan Luo, Jia Li, Jingjing Wang, Jing Chen, Longfei Wang, Li Wang, Meng Han, Jian Ye, Feifei Chen, Jingqiu Liu, Ying Liu, Gang Wu, Bo Yang, Xiang Cheng, Yuhua Liao, Yanxia Wu, Tie Ke, Qiuyun Chen, Xin Tu, Robert C. Elston, Shaoqi Rao, Yanzong Yang, Yunlong Xia, Qing K. Wang

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