The expanding phenotypic spectrum of female SLC9A6 mutation carriers: a case series and review of the literature Pierre SinajonDeborah VerbaanJoyce So Review 03 May 2016 Pages: 841 - 850
The hnRNP family: insights into their role in health and disease Thomas GeuensDelphine BouhyVincent Timmerman Review Open access 23 May 2016 Pages: 851 - 867
Mapping adipose and muscle tissue expression quantitative trait loci in African Americans to identify genes for type 2 diabetes and obesity Satria P. SajuthiNeeraj K. SharmaSwapan K. Das Original Investigation 19 May 2016 Pages: 869 - 880
IL8 gene as modifier of cystic fibrosis: unraveling the factors which influence clinical variability Larissa Lazzarini FurlanFernando Augusto Lima MarsonDorotéia Rossi Silva Souza Original Investigation 21 May 2016 Pages: 881 - 894
Epigenetic and genetic variation in GATA5 is associated with gastric disease risk Rafal S. SobotaNuri KodamanBarbara G. Schneider Original Investigation 25 May 2016 Pages: 895 - 906
Erratum to: Epigenetic and genetic variation in GATA5 is associated with gastric disease risk Rafal S. SobotaNuri KodamanBarbara G. Schneider Erratum 14 July 2016 Pages: 907 - 908
De novo RRAGC mutation activates mTORC1 signaling in syndromic fetal dilated cardiomyopathy Pamela A. LongMichael T. ZimmermannTimothy M. Olson Original Investigation 27 May 2016 Pages: 909 - 917
Identification of a homozygous nonsense mutation in KIAA0556 in a consanguineous family displaying Joubert syndrome Susanne RoosingRasim O. RostiJoseph G. Gleeson Original Investigation 31 May 2016 Pages: 919 - 921
Genome-wide association of familial prostate cancer cases identifies evidence for a rare segregating haplotype at 8q24.21 Craig C. TeerlinkDaniel LeongamornlertLisa Cannon-Albright Original Investigation 04 June 2016 Pages: 923 - 938
Differential frequency of NKG2C/KLRC2 deletion in distinct African populations and susceptibility to Trachoma: a new method for imputation of KLRC2 genotypes from SNP genotyping data Adriana GoncalvesPateh MakaloChrissy h. Roberts Original Investigation Open access 16 June 2016 Pages: 939 - 951
Spectrum of DNA variants for non-syndromic deafness in a large cohort from multiple continents Denise YanDemet TekinMustafa Tekin Original Investigation 25 June 2016 Pages: 953 - 961
Erratum to: Hierarchical modeling identifies novel lung cancer susceptibility variants in inflammation pathways among 10,140 cases and 11,012 controls Darren R. BrennerPaul BrennanRayjean J. Hung Erratum 06 June 2016 Pages: 963 - 963
Erratum to: Heritability and genome-wide analyses of problematic peer relationships during childhood and adolescence Beate St PourcainC. M. A. HaworthGeorge Davey Smith Erratum 14 June 2016 Pages: 965 - 965