Using drug response data to identify molecular effectors, and molecular “omic” data to identify candidate drugs in cancer William C. ReinholdSudhir VarmaYves G. Pommier Review Paper 12 September 2014 Pages: 3 - 11
Mitochondrial dysfunction in schizophrenia: an evolutionary perspective Vanessa F. GonçalvesAna C. AndreazzaJames L. Kennedy Review Paper 14 October 2014 Pages: 13 - 21
Bayesian variable selection for hierarchical gene–environment and gene–gene interactions Changlu LiuJianzhong MaChristopher I. Amos Original Investigation 26 August 2014 Pages: 23 - 36
G-quadruplex formation enhances splicing efficiency of PAX9 intron 1 Mariana Martins RibeiroGleidson Silva TeixeiraSergio Roberto Peres Line Original Investigation 10 September 2014 Pages: 37 - 44
STIL mutation causes autosomal recessive microcephalic lobar holoprosencephaly Naseebullah KakarJamil AhmadGuntram Borck Original Investigation 14 September 2014 Pages: 45 - 51
Detection of SQSTM1/P392L post-zygotic mutations in Paget’s disease of bone Sabrina Guay-BélangerSylvain PicardLaëtitia Michou Original Investigation Open access 21 September 2014 Pages: 53 - 65
DUF1220 copy number is linearly associated with increased cognitive function as measured by total IQ and mathematical aptitude scores Jonathon M. DavisVeronica B. SearlesJames M. Sikela Original Investigation 07 October 2014 Pages: 67 - 75
Refinement of schizophrenia GWAS loci using methylome-wide association data Gaurav KumarShaunna L. ClarkEdwin J. C. G. van den Oord Original Investigation 07 October 2014 Pages: 77 - 87
The role of linkage disequilibrium in case-only studies of gene–environment interactions Pankaj YadavSandra Freitag-WolfMichael Krawczak Original Investigation 11 October 2014 Pages: 89 - 96
De novo mutations in beta-catenin (CTNNB1) appear to be a frequent cause of intellectual disability: expanding the mutational and clinical spectrum Alma KuechlerMarjolein H. WillemsenDagmar Wieczorek Original Investigation 19 October 2014 Pages: 97 - 109
Genetic variation of the transthyretin gene in wild-type transthyretin amyloidosis (ATTRwt) Jacquelyn L. SikoraMark W. LogueLawreen H. Connors Original Investigation 04 November 2014 Pages: 111 - 121
Oral-facial-digital syndrome type VI: is C5orf42 really the major gene? Marta RomaniFrancesca ManciniEnza Maria Valente Short Report Open access 19 November 2014 Pages: 123 - 126
A single codon insertion in the PICALM gene is not associated with subvalvular aortic stenosis in Newfoundland dogs Michaela DrögemüllerVidhya JagannathanTosso Leeb Letter to the Editor 13 November 2014 Pages: 127 - 129