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ESR1 polymorphisms and statin therapy: a sex-specific approach por 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 por Steve Davis, James Pettengill, Yan Luo, Justin L. Payne, Al Shpuntoff, Hugh Rand, Errol Strain

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Human Papillomavirus and Epstein-Barr Virus in Sinonasal Schneiderian Papillomas:<i>An In Situ Hybridization and Polymerase Chain Reaction Study</i> por M. J. Gaffey, Henry F. Frierson, Lawrence M. Weiss, Cynthia M. Barber, Gwen Baber, Mark H. Stoler

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MSTN , CKM , and DMRT3 Gene Variants in Different Lines of Quarter Horses por Guilherme Luís Pereira, Rafael de Matteis, Luciana Correia de Almeida Regitano, Luis Artur Loyola Chardulo, Rogério Abdallah Curi

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Frequency of SNP -336A/G in the promoter region of CD209 in a population from northeastern Brazil por Pietro Costa, Hygor Ferreira-Fernandes, Jefferson Soares de Oliveira, A.C.T.C. Pereira, Giovanny R. Pinto, Gustavo Portela Ferreira

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Determinação do perfil do polimorfismo da IL28B em indivíduos coinfectados pelo vírus da Hepatite C Crônica (HCV) e pelo vírus linfotrópico de células T humanas tipo 1 (HTLV-1)... por Tatiane Assone dos Santos

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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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Genetic polymorphisms in the vitamin D pathway in relation to lung cancer risk and survival por Jinyu Kong, Fangxiu Xu, Jinli Qu, Yu Wang, Ming Gao, Herbert Yu, Biyun Qian

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An Improved Opposition-Based Learning Particle Swarm Optimization for the Detection of SNP-SNP Interactions por Junliang Shang, Yan Sun, Shengjun Li, Jin‐Xing Liu, Chun-Hou Zheng, Junying Zhang

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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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Japonica array: improved genotype imputation by designing a population-specific SNP array with 1070 Japanese individuals por Yosuke Kawai, Takahiro Mimori, Kaname Kojima, Naoki Nariai, Inaho Danjoh, Rumiko Saito, Jun Yasuda, Masayuki Yamamoto, Masao Nagasaki

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Detecting genetic risk factors for Alzheimer's disease in whole genome sequence data via Lasso screening por Tao Yang, Jie Wang, Qian Sun, Derrek P. Hibar, Neda Jahanshad, Li Liu, Yalin Wang, Liang Zhan, Paul M. Thompson, Jieping Ye

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SNP-SNP interactions in breast cancer susceptibility por Venus Onay, Laurent Briollais, Julia A. Knight, Ellen Shi, Yuanyuan Wang, Sean Wells, Hong Li, Isaac Rajendram, Irene L. Andrulis, Hilmi Özçelik

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<i>MTHFR</i> and <i>MSX1</i> contribute to the risk of nonsyndromic cleft lip/palate por Triin Jagomägi, Tiit Nikopensius, Kaarel Krjutškov, Veronika Tammekivi, Triin Viltrop, Mare Saag, Andres Metspalu

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Association analysis for udder health based on SNP-panel and sequence data in Danish Holsteins por Xiaoping Wu, Mogens Sandø Lund, Goutam Sahana, Bernt Guldbrandtsen, Dongxiao Sun, Qin Zhang, Guosheng Su

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<i>NCAM1‐TTC12‐ANKK1‐DRD2</i> gene cluster and the clinical and genetic heterogeneity of adults with ADHD por Nina Roth Mota, Diego Luiz Rovaris, Djenifer B. Kappel, Felipe Almeida Picon, Eduardo S. Vitola, Carlos Alberto Iglesias Salgado, Rafael G. Karam, Luís Augusto Rohde, Eugênio H. Grevet, Claiton Henrique Dotto Bau

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Biomarkers of Adiponectin: Plasma Protein Variation and Genomic DNA Polymorphisms por Harvest F. Gu

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Association of PNPLA3 with non-alcoholic fatty liver disease in a minority cohort: the Insulin Resistance Atherosclerosis Family Study por Lynne E. Wagenknecht, Colin N. A. Palmer, Donald W. Bowden, Jerome I. Rotter, Jill M. Norris, Julie Ziegler, Yii‐Der I. Chen, Steven M. Haffner, Ann Scherzinger, Carl D. Langefeld

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Construction of High Density Sweet Cherry (Prunus avium L.) Linkage Maps Using Microsatellite Markers and SNPs Detected by Genotyping-by-Sequencing (GBS) por Verónica Guajardo, Simón Solís, Boris Sagredo, Felipe Gaínza‐Cortés, Carlos Muñoz, Ksenija Gašić, Patricio Hinrichsen

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Meta-Analysis of miR-146a Polymorphisms Association with Coronary Artery Diseases and Ischemic Stroke por Meihua Bao, Yanping Xiao, Qingsong Zhang, Huaiqing Luo, Ji Luo, Juan Zhao, Guangyi Li, Jie Zeng, Jianming Li

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