Unraveling the genetic component of systemic sclerosis José Ezequiel MartínLara Bossini-CastilloJavier Martín Review Paper 05 January 2012 Pages: 1023 - 1037
Altered patterns of multiple recombinant events are associated with nondisjunction of chromosome 21 Tiffany Renee OliverStuart W. TinkerStephanie L. Sherman Original Investigation 09 December 2011 Pages: 1039 - 1046
Association of PDE4B polymorphisms and schizophrenia in Northwestern Han Chinese Fanglin GuanChen ZhangShengbin Li Original Investigation 11 December 2011 Pages: 1047 - 1056
Consistency of genome-wide associations across major ancestral groups Evangelia E. NtzaniGeorge LiberopoulosJohn P. A. Ioannidis Original Investigation 20 December 2011 Pages: 1057 - 1071
OPRM1 and EGFR contribute to skin pigmentation differences between Indigenous Americans and Europeans Ellen E. QuillenMarc BauchetMark D. Shriver Original Investigation 24 December 2011 Pages: 1073 - 1080
Effects of MAOA promoter methylation on susceptibility to paranoid schizophrenia Yanbo ChenJiexu ZhangQi Xu Original Investigation 24 December 2011 Pages: 1081 - 1087
GWAS-linked GAK locus in Parkinson’s disease in Han Chinese and meta-analysis Nan-Nan LiXue-Li ChangRong Peng Original Investigation 24 December 2011 Pages: 1089 - 1093
Validation of prostate cancer risk-related loci identified from genome-wide association studies using family-based association analysis: evidence from the International Consortium for Prostate Cancer Genetics (ICPCG) Guangfu JinLingyi LuInternational Consortium for Prostate Cancer Genetics Original Investigation 25 December 2011 Pages: 1095 - 1103
Genetic association between human chitinases and lung function in COPD F. AminuddinL. AkhabirA. J. Sandford Original Investigation 28 December 2011 Pages: 1105 - 1114
Mutation risk associated with paternal and maternal age in a cohort of retinoblastoma survivors Melissa B. MillsLouanne HudginsRuth A. Kleinerman Original Investigation 28 December 2011 Pages: 1115 - 1122
LG2 agrin mutation causing severe congenital myasthenic syndrome mimics functional characteristics of non-neural (z−) agrin Ricardo A. MaselliJose M. FernandezMichael J. Ferns Original Investigation 29 December 2011 Pages: 1123 - 1135
A functional variant of the collagen type III alpha1 gene modify risk of sporadic intracranial aneurysms Jingzhou ChenYufang ZhuRutai Hui Original Investigation 13 January 2012 Pages: 1137 - 1143
A multi-ethnic study of a PNPLA3 gene variant and its association with disease severity in non-alcoholic fatty liver disease Shamsul Mohd ZainRosmawati MohamedZahurin Mohamed Original Investigation Open access 19 January 2012 Pages: 1145 - 1152
The human lactase persistence-associated SNP −13910*T enables in vivo functional persistence of lactase promoter–reporter transgene expression Lin FangJong Kun AhnEric Sibley Original Investigation 19 January 2012 Pages: 1153 - 1159
Interaction between genetic and epigenetic variation defines gene expression patterns at the asthma-associated locus 17q12-q21 in lymphoblastoid cell lines Soizik BerlivetSanny MoussetteAnna K. Naumova Original Investigation Open access 24 January 2012 Pages: 1161 - 1171
Y chromosome haplogroups and prostate cancer in populations of European and Ashkenazi Jewish ancestry Zhaoming WangHemang ParikhLaufey Amundadottir Original Investigation Open access 24 January 2012 Pages: 1173 - 1185
Cognitive and serum BDNF correlates of BDNF Val66Met gene polymorphism in patients with schizophrenia and normal controls Xiang Yang ZhangDa Chun ChenThomas R. Kosten Original Investigation 24 February 2012 Pages: 1187 - 1195
Genetic variant in TP63 on locus 3q28 is associated with risk of lung adenocarcinoma among never-smoking females in Asia H. Dean Hosgood IIIWen-Chang WangQing Lan Original Investigation 25 February 2012 Pages: 1197 - 1203
Evolutionary genetics of the human Rh blood group system George H. PerryYali XueCharles Lee Original Investigation 25 February 2012 Pages: 1205 - 1216
NIPA2 located in 15q11.2 is mutated in patients with childhood absence epilepsy Yuwu JiangYuehua ZhangXiru Wu Original Investigation 26 February 2012 Pages: 1217 - 1224
Genome-wide two-locus epistasis scans in prostate cancer using two European populations Sha TaoJunjie FengJielin Sun Original Investigation 26 February 2012 Pages: 1225 - 1234
Polymorphisms in the XPG gene and risk of gastric cancer in Chinese populations Jing HeLi-Xin QiuJin Li Original Investigation 28 February 2012 Pages: 1235 - 1244
The prevalence of CD33 and MS4A6A variant in Chinese Han population with Alzheimer’s disease Yu-Lei DengLi-Hua LiuSheng-Di Chen Original Investigation 01 March 2012 Pages: 1245 - 1249
Genetic variants of the MRC1 gene and the IFNG gene are associated with leprosy in Han Chinese from Southwest China Dong WangJia-Qi FengYong-Gang Yao Original Investigation 06 March 2012 Pages: 1251 - 1260
Association between gout and polymorphisms in GCKR in male Han Chinese Jing WangShiguo LiuXu Ma Original Investigation 07 March 2012 Pages: 1261 - 1265
Erratum to: Association between gout and polymorphisms in GCKR in male Han Chinese Jing WangShiguo LiuXu Ma Publisher's Erratum 31 March 2012 Pages: 1267 - 1267
Loss-of-function mutations in filaggrin gene associate with psoriasis vulgaris in Chinese population Zhengmao HuZhimin XiongKun Xia Original Investigation 11 March 2012 Pages: 1269 - 1274
Randall H. Morse (ed.): Chromatin remodelling: methods and protocols Raymond Waters Book Review 06 April 2012 Pages: 1275 - 1275