A review of genome-wide association studies for multiple sclerosis: classical and hypothesis-driven approaches V. V. BashinskayaO. G. KulakovaO. O. Favorova Review Paper 25 September 2015 Pages: 1143 - 1162
Copy number variants in patients with intellectual disability affect the regulation of ARX transcription factor gene Minaka IshibashiElizabeth ManningSilke Rinkwitz Original Investigation 04 September 2015 Pages: 1163 - 1182
Scrutinizing the FTO locus: compelling evidence for a complex, long-range regulatory context Mathias Rask-AndersenMarkus Sällman AlménHelgi B. Schiöth Original Investigation 04 September 2015 Pages: 1183 - 1193
Pervasive pleiotropy between psychiatric disorders and immune disorders revealed by integrative analysis of multiple GWAS Qian WangCan YangHongyu Zhao Original Investigation 04 September 2015 Pages: 1195 - 1209
Heritabilities, proportions of heritabilities explained by GWAS findings, and implications of cross-phenotype effects on PR interval Claudia Tamar SilvaJan A. KorsAaron Isaacs Original Investigation Open access 18 September 2015 Pages: 1211 - 1219
Computational functional genomics based analysis of pain-relevant micro-RNAs Jörn LötschEllen NiederbergerAlfred Ultsch Original Investigation 18 September 2015 Pages: 1221 - 1238
Mutation in CEP63 co-segregating with developmental dyslexia in a Swedish family Elisabet EinarsdottirIdor SvenssonHans Matsson Original Investigation Open access 23 September 2015 Pages: 1239 - 1248
A genome-wide association study for colorectal cancer identifies a risk locus in 14q23.1 Mathieu LemireConghui QuThomas J. Hudson Original Investigation 24 September 2015 Pages: 1249 - 1262
Association between telomere length and chromosome 21 nondisjunction in the oocyte I. AlbizuaB. L. Rambo-MartinS. L. Sherman Original Investigation 25 September 2015 Pages: 1263 - 1270
Ghazi M Rayan and Joseph Upton III: Congenital Hand Anomalies and Associated Syndromes Ruth Newbury-Ecob Book Review 04 September 2015 Pages: 1271 - 1271