Albert Vernon Smith
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Explore the profile of Albert Vernon Smith including associated specialties, affiliations and a list of published articles.
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Citations
15864
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Recent Articles
1.
Willems S, Ng N, Fernandez J, Fine R, Wheeler E, Wessel J, et al.
Wellcome Open Res
. 2024 Sep;
8():483.
PMID: 39280063
Background: Genome-wide association studies for glycemic traits have identified hundreds of loci associated with these biomarkers of glucose homeostasis. Despite this success, the challenge remains to link variant associations to...
2.
Shrine N, Izquierdo A, Chen J, Packer R, Hall R, Guyatt A, et al.
Nat Genet
. 2023 Sep;
55(10):1778-1779.
PMID: 37749248
No abstract available.
3.
Leiser C, Whitsel E, Reiner A, Rich S, Rotter J, Taylor K, et al.
Cancer Epidemiol Biomarkers Prev
. 2023 Jul;
32(10):1470-1473.
PMID: 37466697
Background: Clonal hematopoiesis of indeterminate potential (CHIP) is an age-related somatic mutation associated with incident hematologic cancer. Environmental stressors which, like air pollution, generate oxidative stress at the cellular level,...
4.
Einson J, Glinos D, Boerwinkle E, Castaldi P, Darbar D, de Andrade M, et al.
Genetics
. 2023 Jun;
224(4).
PMID: 37348055
Exonic variants present some of the strongest links between genotype and phenotype. However, these variants can have significant inter-individual pathogenicity differences, known as variable penetrance. In this study, we propose...
5.
Shrine N, Izquierdo A, Chen J, Packer R, Hall R, Guyatt A, et al.
Nat Genet
. 2023 Mar;
55(3):410-422.
PMID: 36914875
Lung-function impairment underlies chronic obstructive pulmonary disease (COPD) and predicts mortality. In the largest multi-ancestry genome-wide association meta-analysis of lung function to date, comprising 580,869 participants, we identified 1,020 independent...
6.
Einson J, Glinos D, Boerwinkle E, Castaldi P, Darbar D, de Andrade M, et al.
bioRxiv
. 2023 Feb;
PMID: 36778406
Exonic variants present some of the strongest links between genotype and phenotype. However, these variants can have significant inter-individual pathogenicity differences, known as variable penetrance. In this study, we propose...
7.
Yu K, Das S, LeFaive J, Kwong A, Pleiness J, Forer L, et al.
Am J Hum Genet
. 2022 May;
109(6):1007-1015.
PMID: 35508176
Genotype imputation is an integral tool in genome-wide association studies, in which it facilitates meta-analysis, increases power, and enables fine-mapping. With the increasing availability of whole-genome-sequence datasets, investigators have access...
8.
Kahali B, Chen Y, Feitosa M, Bielak L, OConnell J, Musani S, et al.
J Clin Endocrinol Metab
. 2020 Nov;
106(2):372-387.
PMID: 33231259
Context: Glycogen storage diseases are rare. Increased glycogen in the liver results in increased attenuation. Objective: Investigate the association and function of a noncoding region associated with liver attenuation but...
9.
Hahn J, Fu Y, Brown M, Bis J, de Vries P, Feitosa M, et al.
PLoS One
. 2020 Nov;
15(11):e0230035.
PMID: 33186364
Background: Genome-wide association studies have identified multiple genomic loci associated with coronary artery disease, but most are common variants in non-coding regions that provide limited information on causal genes and...
10.
Clark D, Okada Y, Moore K, Mason D, Pirastu N, Gandin I, et al.
Nat Commun
. 2019 Nov;
10(1):4957.
PMID: 31673082
In many species, the offspring of related parents suffer reduced reproductive success, a phenomenon known as inbreeding depression. In humans, the importance of this effect has remained unclear, partly because...