Goncalo R Abecasis
Overview
Explore the profile of Goncalo R Abecasis including associated specialties, affiliations and a list of published articles.
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341
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93862
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Recent Articles
1.
Kessler M, Damask A, OKeeffe S, Banerjee N, Li D, Watanabe K, et al.
Nature
. 2025 Jan;
637(8047):E27.
PMID: 39779868
No abstract available.
2.
Borda V, Loesch D, Guo B, Laboulaye R, Veliz-Otani D, French J, et al.
Cell Genom
. 2024 Nov;
4(11):100692.
PMID: 39486408
Latin Americans are underrepresented in genetic studies, increasing disparities in personalized genomic medicine. Despite available genetic data from thousands of Latin Americans, accessing and navigating the bureaucratic hurdles for consent...
3.
Annis A, Gunaseelan V, Smith A, Abecasis G, Larach D, Zawistowski M, et al.
Genet Epidemiol
. 2024 Oct;
49(1):e22588.
PMID: 39385445
Persistent opioid use after surgery is a common morbidity outcome associated with subsequent opioid use disorder, overdose, and death. While phenotypic associations have been described, genetic associations remain unidentified. Here,...
4.
Gaynor S, Joseph T, Bai X, Zou Y, Boutkov B, Maxwell E, et al.
Nat Genet
. 2024 Sep;
56(11):2345-2351.
PMID: 39322778
Whole-genome sequencing (WGS), whole-exome sequencing (WES) and array genotyping with imputation (IMP) are common strategies for assessing genetic variation and its association with medically relevant phenotypes. To date, there has...
5.
Weinstock J, Chaudhry S, Ioannou M, Viskadourou M, Reventun P, Jakubek Y, et al.
medRxiv
. 2024 Sep;
PMID: 39228737
Clonal hematopoiesis (CH) is defined by the expansion of a lineage of genetically identical cells in blood. Genetic lesions that confer a fitness advantage, such as point mutations or mosaic...
6.
Kosmicki J, Marcketta A, Sharma D, Di Gioia S, Batista S, Yang X, et al.
Nat Genet
. 2024 Aug;
56(8):1592-1596.
PMID: 39103650
Coronavirus disease 2019 (COVID-19) and influenza are respiratory illnesses caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and influenza viruses, respectively. Both diseases share symptoms and clinical risk...
7.
Kwong A, Zawistowski M, Fritsche L, Zhan X, Bragg-Gresham J, Branham K, et al.
Hum Mol Genet
. 2023 Nov;
33(4):374-385.
PMID: 37934784
Genome-wide association studies have contributed extensively to the discovery of disease-associated common variants. However, the genetic contribution to complex traits is still largely difficult to interpret. We report a genome-wide...
8.
Zhou S, Sosina O, Bovijn J, Laurent L, Sharma V, Akbari P, et al.
Nat Genet
. 2023 Aug;
55(8):1277-1287.
PMID: 37558884
In this study, we leveraged the combined evidence of rare coding variants and common alleles to identify therapeutic targets for osteoporosis. We undertook a large-scale multiancestry exome-wide association study for...
9.
Rajagopal V, Watanabe K, Mbatchou J, Ayer A, Quon P, Sharma D, et al.
Nat Genet
. 2023 Jun;
55(7):1138-1148.
PMID: 37308787
Human genetic studies of smoking behavior have been thus far largely limited to common variants. Studying rare coding variants has the potential to identify drug targets. We performed an exome-wide...
10.
Weinstock J, Laurie C, Broome J, Taylor K, Guo X, Shuldiner A, et al.
Sci Adv
. 2023 May;
9(17):eabm4945.
PMID: 37126548
Nononcogenic somatic mutations are thought to be uncommon and inconsequential. To test this, we analyzed 43,693 National Heart, Lung and Blood Institute Trans-Omics for Precision Medicine blood whole genomes from...