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Jose C. Florez

Researcher at Harvard University

Publications -  414
Citations -  58686

Jose C. Florez is an academic researcher from Harvard University. The author has contributed to research in topics: Type 2 diabetes & Diabetes mellitus. The author has an hindex of 87, co-authored 357 publications receiving 50750 citations. Previous affiliations of Jose C. Florez include George Washington University & University of California, Davis.

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Rare coding variants in 35 genes associate with circulating lipid levels – a multi-ancestry analysis of 170,000 exomes

George Hindy, +225 more
- 26 Aug 2021 - 
TL;DR: In this article, gene-based association testing of blood lipid levels with rare (minor allele frequency 170,000 individuals from multiple ancestries: 97,493 European, 30,025 South Asian, 16,507 African, 16.440 Hispanic/Latino, 10,420 East Asian, and 1,182 Samoan was performed.
Journal ArticleDOI

Pharmacogenetic Perturbations in Humans as a Tool to Generate Mechanistic Insight

TL;DR: Although GWAS constitute a powerful approach to rapidly and systematically uncover associations that may open new windows into T2D pathophysiology, they do not circumvent the need to refine the associated loci to find the precise “causal” DNA sequences—causal in the sense that altering these sequences would eliminate the clinical phenotype.
Posted ContentDOI

Random glucose GWAS in 493,036 individuals provides insights into diabetes pathophysiology, complications and treatment stratification

Lagou, +116 more
- 20 Apr 2021 - 
TL;DR: In this paper, a meta-analysis of random glucose measurements in 493,036 individuals without diabetes of diverse ethnicities was conducted to identify 128 associated loci represented by 162 distinct signals, including 14 with sex-dimorphic effects, 9 discovered through trans-ethnic analysis and 70 novel signals for glycaemic traits.

Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

Valérie Turcot, +399 more
TL;DR: Pathway analyses based on the variants associated with BMI 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.