Alison R Barton
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Explore the profile of Alison R Barton including associated specialties, affiliations and a list of published articles.
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16
Citations
639
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Recent Articles
1.
Barton A, Santander C, Skoglund P, Moltke I, Reich D, Mathieson I
Nature
. 2025 Feb;
638(8051):E19-E22.
PMID: 39972236
No abstract available.
2.
Akbari A, Barton A, Gazal S, Li Z, Kariminejad M, Perry A, et al.
bioRxiv
. 2024 Sep;
PMID: 39314480
We present a method for detecting evidence of natural selection in ancient DNA time-series data that leverages an opportunity not utilized in previous scans: testing for a consistent trend in...
3.
Hujoel M, Handsaker R, Sherman M, Kamitaki N, Barton A, Mukamel R, et al.
Nat Genet
. 2024 Mar;
56(4):569-578.
PMID: 38548989
Copy number variants (CNVs) are among the largest genetic variants, yet CNVs have not been effectively ascertained in most genetic association studies. Here we ascertained protein-altering CNVs from UK Biobank...
4.
Zhang M, Durvasula A, Chiang C, Koch E, Strober B, Shi H, et al.
Res Sq
. 2024 Jan;
PMID: 38168385
The genetic architecture of human diseases and complex traits has been extensively studied, but little is known about the relationship of causal disease effect sizes between proximal SNPs, which have...
5.
Zhang M, Durvasula A, Chiang C, Koch E, Strober B, Shi H, et al.
medRxiv
. 2023 Dec;
PMID: 38106023
The genetic architecture of human diseases and complex traits has been extensively studied, but little is known about the relationship of causal disease effect sizes between proximal SNPs, which have...
6.
Mukamel R, Handsaker R, Sherman M, Barton A, Hujoel M, McCarroll S, et al.
Cell
. 2023 Aug;
186(17):3659-3673.e23.
PMID: 37527660
Many regions in the human genome vary in length among individuals due to variable numbers of tandem repeats (VNTRs). To assess the phenotypic impact of VNTRs genome-wide, we applied a...
7.
Hujoel M, Handsaker R, Sherman M, Kamitaki N, Barton A, Mukamel R, et al.
bioRxiv
. 2023 Jun;
PMID: 37333244
Structural variants (SVs) comprise the largest genetic variants, altering from 50 base pairs to megabases of DNA. However, SVs have not been effectively ascertained in most genetic association studies, leaving...
8.
Barton A, Santander C, Skoglund P, Moltke I, Reich D, Mathieson I
bioRxiv
. 2023 Mar;
PMID: 36993413
Klunk et al. analyzed ancient DNA data from individuals in London and Denmark before, during and after the Black Death [1], and argued that allele frequency changes at immune genes...
9.
Hujoel M, Sherman M, Barton A, Mukamel R, Sankaran V, Terao C, et al.
Cell
. 2022 Oct;
185(22):4233-4248.e27.
PMID: 36306736
The human genome contains hundreds of thousands of regions harboring copy-number variants (CNV). However, the phenotypic effects of most such polymorphisms are unknown because only larger CNVs have been ascertainable...
10.
Barton A, Hujoel M, Mukamel R, Sherman M, Loh P
Am J Hum Genet
. 2022 Jun;
109(7):1298-1307.
PMID: 35649421
Recent work has found increasing evidence of mitigated, incompletely penetrant phenotypes in heterozygous carriers of recessive Mendelian disease variants. We leveraged whole-exome imputation within the full UK Biobank cohort (n...