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Kristin L. Young

Researcher at University of North Carolina at Chapel Hill

Publications -  78
Citations -  3432

Kristin L. Young is an academic researcher from University of North Carolina at Chapel Hill. The author has contributed to research in topics: Genome-wide association study & Medicine. The author has an hindex of 18, co-authored 66 publications receiving 2442 citations. Previous affiliations of Kristin L. Young include Lund University & University of Kansas.

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Genetic analyses of diverse populations improves discovery for complex traits

Genevieve L. Wojcik, +90 more
- 27 Jun 2019 - 
TL;DR: The value of diverse, multi-ethnic participants in large-scale genomic studies is demonstrated and evidence of effect-size heterogeneity across ancestries for published GWAS associations, substantial benefits for fine-mapping using diverse cohorts and insights into clinical implications are shown.

Rare and low-frequency coding variants alter human adult height

Eirini Marouli, +370 more
TL;DR: The results demonstrate that sufficiently large sample sizes can uncover rare and low-frequency variants of moderate-to-large effect associated with polygenic human phenotypes, and that these variants implicate relevant genes and pathways.
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Genome-wide physical activity interactions in adiposity. A meta-analysis of 200,452 adults

Mariaelisa Graff, +349 more
- 27 Apr 2017 - 
TL;DR: In additional genome-wide meta-analyses adjusting for PA and interaction with PA, 11 novel adiposity loci are identified, suggesting that accounting for PA or other environmental factors that contribute to variation in adiposity may facilitate gene discovery.
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Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

Valérie Turcot, +489 more
- 01 Jan 2018 - 
TL;DR: Exome-wide analysis identifies rare and low-frequency coding variants associated with body mass index that confirm enrichment of neuronal genes and provide new evidence for adipocyte and energy expenditure biology, widening the potential of genetically supported therapeutic targets in obesity.
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Fifteen new risk loci for coronary artery disease highlight arterial-wall-specific mechanisms.

Joanna M. M. Howson, +74 more
- 22 May 2017 - 
TL;DR: 25 new SNP–CAD associations are identified from 15 genomic regions, including SNPs in or near genes involved in cellular adhesion, leukocyte migration and atherosclerosis, coagulation and inflammation and vascular smooth muscle cell differentiation, which sheds light on potential disease mechanisms.