Whole-genome sequencing in French Canadians from Quebec Cécile Low-KamDavid RhaindsGuillaume Lettre Original Investigation 04 July 2016 Pages: 1213 - 1221
FUS-linked essential tremor associated with motor dysfunction in Drosophila Murni TioRujing WenEng-King Tan Original Investigation Open access 09 July 2016 Pages: 1223 - 1232
ANKS3 is mutated in a family with autosomal recessive laterality defect Hanan E. ShamseldinToma Antonov YakulovFowzan S. Alkuraya Original Investigation 14 July 2016 Pages: 1233 - 1239
Multiple rare variants in high-risk pancreatic cancer-related genes may increase risk for pancreatic cancer in a subset of patients with and without germline CDKN2A mutations Xiaohong R. YangMelissa RotunnoAlisa M. Goldstein Original Investigation 23 July 2016 Pages: 1241 - 1249
Association of kidney structure-related gene variants with type 2 diabetes-attributed end-stage kidney disease in African Americans Meijian GuanJun MaMaggie C. Y. Ng Original Investigation 26 July 2016 Pages: 1251 - 1262
Mutation in SLC6A9 encoding a glycine transporter causes a novel form of non-ketotic hyperglycinemia in humans Majid AlfadhelMarwan NashabatQais Abu Ali Original Investigation Open access 01 August 2016 Pages: 1263 - 1268
A 1.35 Mb DNA fragment is inserted into the DHMN1 locus on chromosome 7q34–q36.2 Alexander P. DrewAnthony N. CutrupiMarina L. Kennerson Original Investigation 03 August 2016 Pages: 1269 - 1278
Genome-wide scans reveal variants at EDAR predominantly affecting hair straightness in Han Chinese and Uyghur populations Sijie WuJingze TanSijia Wang Original Investigation 03 August 2016 Pages: 1279 - 1286
Identification of susceptibility gene associated with female primary Sjögren’s syndrome in Han Chinese by genome-wide association study I-Wen SongHsiang-Cheng ChenJer-Yuarn Wu Original Investigation 08 August 2016 Pages: 1287 - 1294
Homozygous KCNMA1 mutation as a cause of cerebellar atrophy, developmental delay and seizures Brahim TabarkiNabil AlMajhadFowzan S. Alkuraya Short Communication 27 August 2016 Pages: 1295 - 1298