Investigation of genes important in neurodevelopment disorders in adult human brain Gilles MaussionAlpha B. DialloCarl Ernst Original Investigation 21 July 2015 Pages: 1037 - 1053
Whole exome sequencing in extended families with autism spectrum disorder implicates four candidate genes Nicola H. ChapmanAlejandro Q. Nato Jr.Ellen M. Wijsman Original Investigation 24 July 2015 Pages: 1055 - 1068
Mutations in human IFT140 cause non-syndromic retinal degeneration Mingchu XuLizhu YangRui Chen Original Investigation 28 July 2015 Pages: 1069 - 1078
Common polygenic variation contributes to risk of migraine in the Norfolk Island population A. J. Rodriguez-AcevedoM. A. FerreiraL. R. Griffiths Original Investigation 29 July 2015 Pages: 1079 - 1087
‘Splitting versus lumping’: Temple–Baraitser and Zimmermann–Laband Syndromes Nuria C. BramswigC. W. OckeloenH.-J. Lüdecke Original Investigation 12 August 2015 Pages: 1089 - 1097
The nuclear localization pattern and interaction partners of GTF2IRD1 demonstrate a role in chromatin regulation Paulina Carmona-MoraJocelyn WidagdoStephen J. Palmer Original Investigation 15 August 2015 Pages: 1099 - 1115
Allowing for population stratification in case-only studies of gene–environment interaction, using genomic control Pankaj YadavSandra Freitag-WolfMichael Krawczak Original Investigation 22 August 2015 Pages: 1117 - 1125
Sequencing of candidate genes in Dominican families implicates both rare exonic and common non-exonic variants for carotid intima-media thickness at bifurcation Liyong WangAshley BeechamRalph L. Sacco Original Investigation 30 August 2015 Pages: 1127 - 1138
T (brachyury) is linked to a Mendelian form of neural tube defects in humans Ranad ShaheenEssam AlshailFowzan S. Alkuraya Letter to the Editor 26 July 2015 Pages: 1139 - 1141
