| | Other Issues: previous | next | latest | archiveEditors' Corner This Month in The Journal Robin E. Williamson PMCID: PMC2561940 This Month in Genetics Kathryn B. Garber PMCID: PMC2561941 Perspectives in Human Genetics Civilian and Military Genetics: Nondiscrimination Policy in a Post-GINA World Susannah Baruch and Kathy Hudson PMCID: PMC2561935 Articles Japanese Population Structure, Based on SNP Genotypes from 7003 Individuals Compared to Other Ethnic Groups: Effects on Population-Based Association Studies Yumi Yamaguchi-Kabata, Kazuyuki Nakazono, Atsushi Takahashi, Susumu Saito, Naoya Hosono, Michiaki Kubo, Yusuke Nakamura, and Naoyuki Kamatani PMCID: PMC2561928 A Combinatorial Approach to Detecting Gene-Gene and Gene-Environment Interactions in Family Studies Xiang-Yang Lou, Guo-Bo Chen, Lei Yan, Jennie Z. Ma, Jamie E. Mangold, Jun Zhu, Robert C. Elston, and Ming D. Li PMCID: PMC2561932 Mutation of C20orf7 Disrupts Complex I Assembly and Causes Lethal Neonatal Mitochondrial Disease Canny Sugiana, David J. Pagliarini, Matthew McKenzie, Denise M. Kirby, Renato Salemi, Khaled K. Abu-Amero, Hans-Henrik M. Dahl, Wendy M. Hutchison, Katherine A. Vascotto, Stacey M. Smith, Robert F. Newbold, John Christodoulou, Sarah Calvo, Vamsi K. Mootha, Michael T. Ryan, and David R. Thorburn PMCID: PMC2561934 Targeting Dyrk1A with AAVshRNA Attenuates Motor Alterations in TgDyrk1A, a Mouse Model of Down Syndrome Jon Ortiz-Abalia, Ignasi Sahún, Xavier Altafaj, Núria Andreu, Xavier Estivill, Mara Dierssen, and Cristina Fillat PMCID: PMC2561933 Reports Mutations in LPIN1 Cause Recurrent Acute Myoglobinuria in Childhood Avraham Zeharia, Avraham Shaag, Riekelt H. Houtkooper, Tareq Hindi, Pascale de Lonlay, Gilli Erez, Laurence Hubert, Ann Saada, Yves de Keyzer, Gideon Eshel, Frédéric M. Vaz, Ophry Pines, and Orly Elpeleg PMCID: PMC2561931 A Connective Tissue Disorder Caused by Mutations of the Lysyl Hydroxylase 3 Gene Antti M. Salo, Helen Cox, Peter Farndon, Celia Moss, Helen Grindulis, Maija Risteli, Simon P. Robins, and Raili Myllylä PMCID: PMC2561927 Recurrent CNVs Disrupt Three Candidate Genes in Schizophrenia Patients Terry Vrijenhoek, Jacobine E. Buizer-Voskamp, Inge van der Stelt, Eric Strengman, Genetic Risk and Outcome in Psychosis (GROUP) Consortium, Chiara Sabatti, Ad Geurts van Kessel, Han G. Brunner, Roel A. Ophoff, and Joris A. Veltman PMCID: PMC2561936 Mutations in CHD7, Encoding a Chromatin-Remodeling Protein, Cause Idiopathic Hypogonadotropic Hypogonadism and Kallmann Syndrome Hyung-Goo Kim, Ingo Kurth, Fei Lan, Irene Meliciani, Wolfgang Wenzel, Soo Hyun Eom, Gil Bu Kang, Georg Rosenberger, Mustafa Tekin, Metin Ozata, David P. Bick, Richard J. Sherins, Steven L. Walker, Yang Shi, James F. Gusella, and Lawrence C. Layman PMCID: PMC2561938 Population-Based Genome-wide Association Studies Reveal Six Loci Influencing Plasma Levels of Liver Enzymes Xin Yuan, Dawn Waterworth, John R.B. Perry, Noha Lim, Kijoung Song, John C. Chambers, Weihua Zhang, Peter Vollenweider, Heide Stirnadel, Toby Johnson, Sven Bergmann, Noam D. Beckmann, Yun Li, Luigi Ferrucci, David Melzer, Dena Hernandez, Andrew Singleton, James Scott, Paul Elliott, Gerard Waeber, Lon Cardon, Timothy M. Frayling, Jaspal S. Kooner, and Vincent Mooser PMCID: PMC2561937 The H Syndrome Is Caused by Mutations in the Nucleoside Transporter hENT3 Vered Molho-Pessach, Israela Lerer, Dvorah Abeliovich, Ziad Agha, Abdulasalam Abu Libdeh, Valentina Broshtilova, Orly Elpeleg, and Abraham Zlotogorski PMCID: PMC2561939 Letters to the Editor Comparing Algorithms for Genotype Imputation Jonathan Marchini and Bryan Howie PMCID: PMC2561929 Reply to Marchini and Howie D.Y. Lin and Y. Hu PMCID: PMC2561930 Announcement Am J Hum Genet. 2008 October 10; 83(4): 542. Published online 2008 October 3. doi: 10.1016/j.ajhg.2008.09.014.PMCID: PMC2665718 Erratum HLA-DRB1![[low asterisk]](corehtml/pmc/pmcents/lowast.gif) 0401 and HLA-DRB10408 Are Strongly Associated with the Development of Antibodies against Interferon-β Therapy in Multiple Sclerosis Steve Hoffmann, Sabine Cepok, Verena Grummel, Klaus Lehmann-Horn, Jörg Hackermüller, Peter F. Stadler, Hans-Peter Hartung, Achim Berthele, Florian Deisenhammer, Ralf Wassmuth, and Bernhard Hemmer PMCID: PMC2665717 Corrects: Steve Hoffmann, et al. HLA-DRB10401 and HLA-DRB10408 Are Strongly Associated with the Development of Antibodies against Interferon-β Therapy in Multiple Sclerosis. Am J Hum Genet. 2008 August 8; 83(2): 219–227. |
