scispace - formally typeset
G

Gonçalo R. Abecasis

Researcher at University of Michigan

Publications -  629
Citations -  271012

Gonçalo R. Abecasis is an academic researcher from University of Michigan. The author has contributed to research in topics: Genome-wide association study & Population. The author has an hindex of 179, co-authored 595 publications receiving 230323 citations. Previous affiliations of Gonçalo R. Abecasis include Johns Hopkins University School of Medicine & Wellcome Trust Centre for Human Genetics.

Papers
More filters
Journal ArticleDOI

Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease.

Jonas B. Nielsen, +119 more
TL;DR: In this article, the authors performed genome-wide analyses of participants in the HUNT Study in Norway to search for protein-altering variants with beneficial impact on quantitative blood traits related to cardiovascular disease, but without detrimental impact on liver function.
Journal ArticleDOI

Sequence data and association statistics from 12,940 type 2 diabetes cases and controls

Jason Flannick, +352 more
- 19 Dec 2017 - 
TL;DR: The GoT2D and T2D-GENES consortia catalogued variation from whole-genome sequencing and exome sequencing of 12,940 individuals of multiple ancestries as mentioned in this paper.
Posted ContentDOI

GWAS meta-analysis (N=279,930) identifies new genes and functional links to intelligence

Jeanne E. Savage, +138 more
- 06 Sep 2017 - 
TL;DR: The largest genetic association study of intelligence to date is presented, identifying 206 genomic loci and implicating 1,041 genes (963 novel) via positional mapping, expression quantitative trait locus (eQTL) mapping, chromatin interaction mapping, and gene-based association analysis.
Journal ArticleDOI

Evaluating the contribution of rare variants to type 2 diabetes and related traits using pedigrees.

Goo Jun, +84 more
TL;DR: The results from deep whole-genome analysis of large Mexican-American pedigrees are described, suggesting that large-effect rare variants account for only a modest fraction of the genetic risk of these traits in this sample of families.