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Rare variant discovery by deep whole-genome sequencing of 1,070 Japanese individuals de réir Masao Nagasaki, Jun Yasuda, Fumiki Katsuoka, Naoki Nariai, Kaname Kojima, Yosuke Kawai, Yumi Yamaguchi‐Kabata, Junji Yokozawa, Inaho Danjoh, Sakae Saito, Yukuto Sato, Takahiro Mimori, Kaoru Tsuda, Rumiko Saito, Xiaoqing Pan, Satoshi Nishikawa, Shin Ito, Yoko Kuroki, Osamu Tanabe, Nobuo Fuse, Shinichi Kuriyama, Hideyasu Kiyomoto, Atsushi Hozawa, Naoko Minegishi, James Douglas Engel, Kengo Kinoshita, Shigeo Kure, Nobuo Yaegashi, Akito Tsuboi, Fuji Nagami, Hiroshi Kawame, Hiroaki Tomita, Ichiro Tsuji, Jun Nakaya, Junichi Sugawara, Kichiya Suzuki, Masahiro Kikuya, Michiaki Abe, Naoki Nakaya, Noriko Osumi, Riu Yamashita, Soichi Ogishima, Takako Takai, Teiji Tominaga, Yasuyuki Taki, Yoichi Suzuki, Masayuki Yamamoto

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A comparison of cataloged variation between International HapMap Consortium and 1000 Genomes Project data de réir Carrie C Buchanan, Eric S. Torstenson, William S. Bush, Marylyn D. Ritchie

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Frequency of CHEK2*1100delC in New York breast cancer cases and controls de réir Kenneth Offit, Heather Pierce, Tomas Kirchhoff, Prema Kolachana, Beth Rapaport, Peter K. Gregersen, Steven B. Johnson, Orit Yossepowitch, Helen J. Huang, Jaya M. Satagopan, Mark E. Robson, Lauren Scheuer, Khédoudja Nafa, Nathan A. Ellis

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

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Common genetic variations in<i>CLOCK</i>transcription factor are associated with nonalcoholic fatty liver disease de réir Silvia Sookoian

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<i>GABRA2</i> markers moderate the subjective effects of alcohol de réir Magdalena Uhart, Elise M. Weerts, Mary E. McCaul, Xiuqing Guo, Xiaofei Yan, Henry R. Kranzler, Ning Li, Gary S. Wand

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CTNNA3 and SEMA3D: Promising loci for asthma exacerbation identified through multiple genome-wide association studies de réir Michael J. McGeachie, Ann Chen Wu, Sze Man Tse, George L. Clemmer, Joanne E. Sordillo, Blanca E. Himes, Jessica Lasky‐Su, Robert Chase, Fernando D. Martínez, Peter Weeke, Christian M. Shaffer, Hua Xu, Joshua C. Denny, Dan M. Roden, Reynold A. Panettieri, Benjamin A. Raby, Scott T. Weiss, Kelan G. Tantisira

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Genome-wide association study with 1000 genomes imputation identifies signals for nine sex hormone-related phenotypes de réir Katherine S. Ruth, Purdey J. Campbell, Shelby Chew, Ee Mun Lim, Narelle Hadlow, Bronwyn Stuckey, Suzanne J. Brown, Bjarke Feenstra, John Joseph, Gabriela Surdulescu, Hou Feng Zheng, J. Brent Richards, Anna Murray, Tim D. Spector, Scott G. Wilson, John R.B. Perry

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Associação de polimorfismos em um único nucleotídeo nos genes GPX4,CYBB, CYBA, CAT e SLC2A2 e a susceptibilidade à doença renal crônica em coortes brasileira e francesas de portado... de réir Thiago A. Patente

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Targeted deep sequencing identifies rare loss-of-function variants in IFNGR1 for risk of atopic dermatitis complicated by eczema herpeticum de réir Li Gao, Lianghua Bin, Nicholas Rafaels, Lili Huang, Joseph Potee, Ingo Ruczinski, Terri H. Beaty, Amy S. Paller, Lynda C. Schneider, Richard L. Gallo, Jon M. Hanifin, Lisa A. Beck, Raif S. Geha, Rasika A. Mathias, Kathleen C. Barnes, Donald Y.M. Leung

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Human adaptations to diet, subsistence, and ecoregion are due to subtle shifts in allele frequency de réir Angela M. Hancock, David Witonsky, Edvard Ehler, Gorka Alkorta‐Aranburu, Cynthia M. Beall, Amha Gebremedhin, R. I. Sukernik, Gerd Utermann, Jonathan K. Pritchard, Graham Coop, Anna Di Rienzo

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Association of SNP rs17465637 on Chromosome 1q41 and rs599839 on 1p13.3 with Myocardial Infarction in an American Caucasian Population de réir Annabel Z. Wang, Lin Li, Bin Zhang, Gong-Qing Shen, Qing K. Wang

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The Role of Local Ancestry Adjustment in Association Studies Using Admixed Populations de réir Jianqi Zhang, Daniel O. Stram

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Mendelian randomization of serum urate and parkinson disease progression de réir Kelly Claire Simon, Shirley Eberly, Xiang Gao, David Oakes, Caroline M. Tanner, Ira Shoulson, Stanley Fahn, Michael A. Schwarzschild, Alberto Ascherio

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The dual and opposite role of the TM6SF2‐rs58542926 variant in protecting against cardiovascular disease and conferring risk for nonalcoholic fatty liver: A meta‐analysis de réir Carlos J. Pirola, Silvia Sookoian

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Discovery and Fine-Mapping of Glycaemic and Obesity-Related Trait Loci Using High-Density Imputation de réir Momoko Horikoshi, Reedik Mägi, Martijn van de Bunt, Ida Surakka, Antti‐Pekka Sarin, Anubha Mahajan, Letizia Marullo, Guðmar Þorleifsson, Sara Hägg, Jouke‐Jan Hottenga, Claes Ladenvall, Janina S. Ried, Thomas W. Winkler, Sara M. Willems, Natalia Pervjakova, Tõnu Esko, Marian Beekman, Christopher P. Nelson, Christina Willenborg, Steven Wiltshire, Teresa Ferreira, Juan Fernandez, Kyle J. Gaulton, Valgerður Steinthórsdóttir, Anders Hamsten, Patrik K. E. Magnusson, Gonneke Willemsen, Yuri Milaneschi, Neil R. Robertson, Christopher J. Groves, Amanda J. Bennett, Terho Lehtimäki, Jorma Viikari, Johan Rung, Valeriya Lyssenko, Markus Perola, Iris M. Heid, Christian Herder, Harald Grallert, Martina Müller‐Nurasyid, Michael Roden, Elina Hyppönen, Aaron Isaacs, Jin‐Moo Lee, Lennart C. Karssen, Evelin Mihailov, Jeanine J. Houwing‐Duistermaat, Anton J. M. de Craen, Joris Deelen, Aki S. Havulinna, Matthew Blades, Christian Hengstenberg, Jeanette Erdmann, Heribert Schunkert, Jaakko Kaprio, Martin D. Tobin, Nilesh J. Samani, Lars Lind, Veikko Salomaa, Cecilia M. Lindgren, P. Eline Slagboom, Andres Metspalu, Cornelia M. van Duijn, Johan G. Eriksson, Annette Peters, Christian Gieger, Antti Jula, Leif Groop, Olli T. Raitakari, Chris Power, Brenda W.J.H. Penninx, Eco J. C. de Geus, Johannes H. Smit, Dorret I. Boomsma, Nancy L. Pedersen, Erik Ingelsson, Unnur Þorsteinsdóttir, Kāri Stefánsson, Samuli Ripatti, Inga Prokopenko, Mark I. McCarthy, Andrew P. Morris

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Polymorphisms in the<i>CD3Z</i>Gene Influence TCRζ Expression in Systemic Lupus Erythematosus Patients and Healthy Controls de réir Claire Gorman, Andrew I. Russell, Zhuoli Zhang, Deborah Cunninghame Graham, Andrew P. Cope, Timothy J. Vyse

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Height-reducing variants and selection for short stature in Sardinia de réir Magdalena Żołędziewska, Carlo Sidore, Charleston W. K. Chiang, Serena Sanna, Antonella Mulas, Maristella Steri, Fabio Busonero, Joseph Marcus, Michele Marongiu, Andrea Maschio, Diego Ortega‐Del Vecchyo, Matteo Floris, Antonella Meloni, Alessandro Delitala, Maria Pina Concas, Federico Murgia, Ginevra Biino, Simona Vaccargiu, Ramaiah Nagaraja, Kirk E. Lohmueller, Nicholas J. Timpson, Nicole Soranzo, Ioanna Tachmazidou, George Dedoussis, Eleftheria Zeggini, Sergio Uzzau, Chris Jones, Robert Lyons, Andrea Angius, Gonçalo R. Abecasis, John Novembre, David Schlessinger, Francesco Cucca

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Accuracy of Genomic Selection in a Rice Synthetic Population Developed for Recurrent Selection Breeding de réir Cécile Grenier, Tuong‐Vi Cao, Yolima Ospina, Constanza Quintero, Marc Châtel, Joe Tohmé, Brigitte Courtois, Nourollah Ahmadi

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Role of TM6SF2 rs58542926 in the pathogenesis of nonalcoholic pediatric fatty liver disease: A multiethnic study de réir Martina Goffredo, Sonia Caprio, Ariel E. Feldstein, Ebe D’Adamo, Melissa Shaw, Bridget Pierpont, Mary Savoye, Hongyu Zhao, A. Bale, Nicola Santoro

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