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Journal of Lipid Research|June 23, 2019
Rare DEGS1 variant significantly alters de novo ceramide synthesis pathwayNicholas B Blackburn, Laura F Michael, Peter J Meikle, et al.
Frontiers in Genetics|April 24, 2025
Disentangling effects of the DR and DQ isomers encoded by the HLA class II haplotype DRB1*15:01/DQB1*06:02 to help establish the true risk allele for FVIII inhibitor development in Hemophilia AVincent P Diego, Bernadette W Luu, Marcio A Almeida, et al.
Molecular Human Reproduction|May 22, 2013
Localization of a major susceptibility locus influencing preterm birthG Chittoor, V S Farook, S Puppala, et al.
Frontiers in Genetics|June 16, 2012
Variants in CPT1A, FADS1, and FADS2 are Associated with Higher Levels of Estimated Plasma and Erythrocyte Delta-5 Desaturases in Alaskan EskimosV Saroja Voruganti, Paul B Higgins, Sven O E Ebbesson, et al.
Journal of Lipid Research|April 11, 2025
Statin effects on the lipidome: Predicting statin usage and implications for cardiovascular risk predictionChangyu Yi, Kevin Huynh, Yvette Schooneveldt, et al.
Scientific Reports|January 22, 2021
Further evidence supporting a potential role for ADH1B in obesityLiza D Morales, Douglas T Cromack, Devjit Tripathy, et al.
Human Molecular Genetics|November 8, 2014
Whole-genome sequencing to understand the genetic architecture of common gene expression and biomarker phenotypesAndrew R Wood, Marcus A Tuke, Mike Nalls, et al.
Human Molecular Genetics|July 6, 2010
Bivariate genetic association of KIAA1797 with heart rate in American Indians: the Strong Heart Family StudyPhillip E Melton, Sue Rutherford, Venkata Saroja Voruganti, et al.
Genetic Epidemiology|January 15, 2025
General Kernel Machine Methods for Multi-Omics Integration and Genome-Wide Association Testing With Related IndividualsAmarise Little, Ni Zhao, Anna Mikhaylova, et al.
BMC Proceedings|December 17, 2016
Omics-squared: human genomic, transcriptomic and phenotypic data for genetic analysis workshop 19John Blangero, Tanya M Teslovich, Xueling Sim, et al.
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