Application of quantile regression to recent genetic and -omic studies Laurent BriollaisGilles Durrieu Review Paper 26 April 2014 Pages: 951 - 966
Genome-wide association tests of inversions with application to psoriasis Jianzhong MaMomiao XiongChristopher I. Amos Original Investigation 13 March 2014 Pages: 967 - 974
Truncation of the E3 ubiquitin ligase component FBXO31 causes non-syndromic autosomal recessive intellectual disability in a Pakistani family Asif MirKumudesh SritharanJohn B. Vincent Original Investigation 13 March 2014 Pages: 975 - 984
Large multiethnic Candidate Gene Study for C-reactive protein levels: identification of a novel association at CD36 in African Americans Jaclyn EllisEthan M. LangeLeslie A. Lange Original Investigation 19 March 2014 Pages: 985 - 995
CHD7, the gene mutated in CHARGE syndrome, regulates genes involved in neural crest cell guidance Yvonne SchulzPeter WehnerSilke Pauli Original Investigation 13 April 2014 Pages: 997 - 1009
Conditions for the validity of SNP-based heritability estimation James J. LeeCarson C. Chow Original Investigation 18 April 2014 Pages: 1011 - 1022
Mutations in CENPE define a novel kinetochore-centromeric mechanism for microcephalic primordial dwarfism Ghayda M. MirzaaBenjamin VitreMark O’Driscoll Original Investigation 20 April 2014 Pages: 1023 - 1039
Homozygous truncating PTPRF mutation causes athelia Guntram BorckLiat de VriesLina Basel-Vanagaite Original Investigation 30 April 2014 Pages: 1041 - 1047
Metabolic heritability at birth: implications for chronic disease research Kelli K. RyckmanCaitlin J. SmithJeffrey C. Murray Original Investigation 22 May 2014 Pages: 1049 - 1057
CpG methylation regulates allelic expression of GDF5 by modulating binding of SP1 and SP3 repressor proteins to the osteoarthritis susceptibility SNP rs143383 Louise N. ReynardCatherine BuiJohn Loughlin Original Investigation Open access 27 May 2014 Pages: 1059 - 1073