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Human Molecular Genetics|May 1, 2012
Evaluation of copy number variations reveals novel candidate genes in autism spectrum disorder-associated pathwaysAnthony J Griswold, Deqiong Ma, Holly N Cukier, et al.Human Molecular Genetics|May 8, 2012
Loss of GM3 synthase gene, but not sphingosine kinase 1, is protective against murine nephronophthisis-related polycystic kidney diseaseThomas A Natoli, Hervé Husson, Kelly A Rogers, et al.Human Molecular Genetics|May 19, 2012
Novel association approach for variable number tandem repeats (VNTRs) identifies DOCK5 as a susceptibility gene for severe obesityJulia S El-Sayed Moustafa, Hariklia Eleftherohorinou, Adam J de Smith, et al.Human Molecular Genetics|September 16, 2015
Altered glycolipid and glycerophospholipid signaling drive inflammatory cascades in adrenomyeloneuropathyMontserrat Ruiz, Mariona Jové, Agatha Schlüter, et al.Human Molecular Genetics|September 16, 2015
A novel conditional knock-in approach defines molecular and circuit effects of the DYT1 dystonia mutationCorinne E Weisheit, William T DauerHuman Molecular Genetics|March 24, 2016
Genome wide association study identifies two loci associated with cadmium in erythrocytes among never-smokersYan Borné, Martin Söderholm, Lars Barregard, et al.Human Molecular Genetics|March 24, 2016
Molecular basis of classic galactosemia from the structure of human galactose 1-phosphate uridylyltransferaseThomas J McCorvie, Jolanta Kopec, Angel L Pey, et al.Human Molecular Genetics|March 24, 2016
Variation at 2q35 (PNKD and TMBIM1) influences colorectal cancer risk and identifies a pleiotropic effect with inflammatory bowel diseaseGiulia Orlando, Philip J Law, Kimmo Palin, et al.Human Molecular Genetics|March 25, 2016
Mutations in C8ORF37 cause Bardet Biedl syndrome (BBS21)Elise Heon, Gunhee Kim, Sophie Qin, et al.Human Molecular Genetics|March 25, 2016
GWAS meta-analysis of 16 852 women identifies new susceptibility locus for endometrial cancerMaxine M Chen, Tracy A O'Mara, Deborah J Thompson, et al.Pageof 1,195