Genetic alterations of δ-catenin/NPRAP/Neurojungin (CTNND2): functional implications in complex human diseases Qun LuByron J. AguilarYan-Hua Chen Review 05 July 2016 Pages: 1107 - 1116
Identity by descent fine mapping of familial adult myoclonus epilepsy (FAME) to 2p11.2–2q11.2 Lyndal HendenSaskia FreytagMelanie Bahlo Original Investigation 01 July 2016 Pages: 1117 - 1125
The genetic history of Cochin Jews from India Yedael Y. WaldmanArjun BiddandaAlon Keinan Original Investigation Open access 04 July 2016 Pages: 1127 - 1143
Genetic variants in microRNA and microRNA biogenesis pathway genes and breast cancer risk among women of African ancestry Frank QianYe FengDezheng Huo Original Investigation 05 July 2016 Pages: 1145 - 1159
Nonrecurrent PMP22-RAI1 contiguous gene deletions arise from replication-based mechanisms and result in Smith–Magenis syndrome with evident peripheral neuropathy Bo YuanJuanita NeiraJames R. Lupski Original Investigation 07 July 2016 Pages: 1161 - 1174
Immunoglobulin G genotypes and the risk of schizophrenia Janardan P. PandeyAryan M. NamboodiriRobert C. Elston Original Investigation 08 July 2016 Pages: 1175 - 1179
Three novel missense mutations in the filamin B gene are associated with isolated congenital talipes equinovarus Haiou YangZhaojing ZhengQihua Fu Original Investigation 09 July 2016 Pages: 1181 - 1189
Mutations in CIT, encoding citron rho-interacting serine/threonine kinase, cause severe primary microcephaly in humans Ranad ShaheenAmal HashemFowzan S. Alkuraya Original Investigation 08 August 2016 Pages: 1191 - 1197
CIT, a gene involved in neurogenic cytokinesis, is mutated in human primary microcephaly Sulman BasitKhalid M. Al-HarbiMohammed I. Samman Original Investigation 12 August 2016 Pages: 1199 - 1207
A lethal phenotype associated with tissue plasminogen deficiency in humans Hanan E. ShamseldinAbdulrahman AldeeriFowzan S. Alkuraya Short Communication 14 July 2016 Pages: 1209 - 1211