Richard Gill

TL;DR: Depression symptoms are studied in families with an identified genetic form of epilepsy: autosomal dominant partial epilepsy with auditory features caused by mutations in the leucine‐rich, glioma inactivated 1 gene (LGI1).

TL;DR: Fine-mapping by targeted sequencing at WLS, MEF2C, ARHGAP1/F2 and JAG1 loci prioritized by eQTL and bioinformatic approaches identified less-common and rare non-coding SNVs associated with BMD independently from GWAS common SNPs, suggesting both common and less- common variants may associate with disease risks and phenotypes in the same loci.

TL;DR: Primary care physicians have underdeveloped knowledge of hyperbaric oxygen therapy, but their generally positive attitudes toward its use suggest that they might be receptive to educational interventions.

TL;DR: SNPs in the first intron of the fat mass and obesity-associated (FTO) gene represent the strongest genome-wide associations with adiposity and the molecular basis for body mass index disease.