Molecular genetic studies of gene identification for sarcopenia Li-Jun TanShan-Lin LiuHong-Wen Deng Review Paper 26 June 2011 Pages: 1 - 31
Common variants for atrial fibrillation: results from genome-wide association studies Xinyuan LiuFei WangJunjie Xiao Review Paper 07 July 2011 Pages: 33 - 39
Attitudes on DNA ancestry tests Jennifer K. WagnerKenneth M. Weiss Original Investigation 23 June 2011 Pages: 41 - 56
A polymorphism of the interferon-gamma-inducible protein 30 gene is associated with hyperglycemia in severely obese individuals V. TurcotL. BouchardMarie-Claude Vohl Original Investigation 24 June 2011 Pages: 57 - 66
Mutations in the NRG1 gene are associated with Hirschsprung disease Clara Sze-Man TangElly Sau-Wai NganMaria-Mercè Garcia-Barcelo Original Investigation 25 June 2011 Pages: 67 - 76
A unique genome-wide association analysis in extended Utah high-risk pedigrees identifies a novel melanoma risk variant on chromosome arm 10q Craig TeerlinkJames FarnhamLisa Cannon-Albright Original Investigation 26 June 2011 Pages: 77 - 85
Identification of a new susceptibility variant for multiple sclerosis in OAS1 by population genetics analysis Rachele CaglianiMatteo FumagalliManuela Sironi Original Investigation 07 July 2011 Pages: 87 - 97
Novel intragenic duplications and mutations of CASK in patients with mental retardation and microcephaly with pontine and cerebellar hypoplasia (MICPCH) Shin HayashiNobuhiko OkamotoJohji Inazawa Original Investigation 07 July 2011 Pages: 99 - 110
Artifact due to differential error when cases and controls are imputed from different platforms Jennifer A. SinnottPeter Kraft Original Investigation 07 July 2011 Pages: 111 - 119
Spread of X-chromosome inactivation into chromosome 15 is associated with Prader–Willi syndrome phenotype in a boy with a t(X;15)(p21.1;q11.2) translocation Satoru SakazumeHirofumi OhashiTakeo Kubota Original Investigation 07 July 2011 Pages: 121 - 130
Spectrum of large copy number variations in 26 diverse Indian populations: potential involvement in phenotypic diversity Pramod GautamPankaj JhaMitali Mukerji Original Investigation 09 July 2011 Pages: 131 - 143
High-resolution array CGH defines critical regions and candidate genes for microcephaly, abnormalities of the corpus callosum, and seizure phenotypes in patients with microdeletions of 1q43q44 Blake C. BallifJill A. RosenfeldLisa G. Shaffer Original Investigation 29 July 2011 Pages: 145 - 156
Elof Axel Carlson: Mutation: the history of an idea from Darwin to genomics Peter S. Harper Book Review 20 July 2011 Pages: 157 - 158
Alan E. H. Emery, Marcia L. H. Emery: The History of a Genetic Disease. Duchenne Muscular Dystrophy or Meryon’s Disease Reinhardt Rüdel Book Review 15 September 2011 Pages: 159 - 160
