Tariq O. Faquih

The paper identifies 16 genetic loci interacting with sleep duration to influence glycemic traits in over 480,000 individuals, revealing distinct biological mechanisms for short and long sleep.

This study identifies genetic variants associated with missing metabolite measurements in two population-based cohorts, suggesting missingness is partly genetic and relevant for clinical and epidemiological research.

This study examines how non-pathogenic CAG repeats in HTT, ATXN3, and CACNA1A genes affect sleep outcomes, finding sex- and depression-specific associations.

This study identifies twelve novel blood pressure loci and shows smoking modifies genetic effects on BP through immune-related pathways in over 1 million individuals.

This study identifies 22 novel gene-sleep duration interaction loci for blood pressure traits across 811,405 individuals, highlighting distinct genetic influences of short and long sleep on cardiovascular health.

This study performs genome-wide association analysis on composite sleep health scores, identifying 28 novel loci and confirming 341 previously reported loci, with insights into genetic mechanisms and pathways.

This study identifies gene-environment interactions between excessive daytime sleepiness and genetic variants linked to obstructive sleep apnea severity, revealing novel therapeutic targets.

This study identifies 17 genetic loci associated with sleep duration and lipid levels, offering potential druggable targets for dyslipidemia in individuals with sleep disturbances.

This study identifies genetic variants associated with income and shows they correlate with health outcomes and educational attainment.