Colby Chiang
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Explore the profile of Colby Chiang including associated specialties, affiliations and a list of published articles.
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28
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3030
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Recent Articles
1.
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...
2.
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...
3.
Scott A, Chiang C, Hall I
Genome Res
. 2021 Sep;
31(12):2249-2257.
PMID: 34544830
Structural variants (SVs) are an important source of human genome diversity, but their functional effects are poorly understood. We mapped 61,668 SVs in 613 individuals from the GTEx project and...
4.
Chen L, Abel H, Das I, Larson D, Ganel L, Kanchi K, et al.
Am J Hum Genet
. 2021 Apr;
108(4):583-596.
PMID: 33798444
The contribution of genome structural variation (SV) to quantitative traits associated with cardiometabolic diseases remains largely unknown. Here, we present the results of a study examining genetic association between SVs...
5.
Abel H, Larson D, Regier A, Chiang C, Das I, Kanchi K, et al.
Nature
. 2020 May;
583(7814):83-89.
PMID: 32460305
A key goal of whole-genome sequencing for studies of human genetics is to interrogate all forms of variation, including single-nucleotide variants, small insertion or deletion (indel) variants and structural variants....
6.
Larson D, Abel H, Chiang C, Badve A, Das I, Eldred J, et al.
Bioinformatics
. 2019 Jun;
35(22):4782-4787.
PMID: 31218349
Summary: Large-scale human genetics studies are now employing whole genome sequencing with the goal of conducting comprehensive trait mapping analyses of all forms of genome variation. However, methods for structural...
7.
Pfister K, Pipka J, Chiang C, Liu Y, Clark R, Keller R, et al.
Cell Rep
. 2018 May;
23(9):2758-2769.
PMID: 29847804
Although aneuploidy is found in the majority of tumors, the degree of aneuploidy varies widely. It is unclear how cancer cells become aneuploid or how highly aneuploid tumors are different...
8.
Li X, Kim Y, Tsang E, Davis J, Damani F, Chiang C, et al.
Nature
. 2017 Oct;
550(7675):239-243.
PMID: 29022581
Rare genetic variants are abundant in humans and are expected to contribute to individual disease risk. While genetic association studies have successfully identified common genetic variants associated with susceptibility, these...
9.
Shaw N, Brand H, Kupchinsky Z, Bengani H, Plummer L, Jones T, et al.
Nat Genet
. 2017 May;
49(6):969.
PMID: 28546579
No abstract available.
10.
Chiang C, Scott A, Davis J, Tsang E, Li X, Kim Y, et al.
Nat Genet
. 2017 Apr;
49(5):692-699.
PMID: 28369037
Structural variants (SVs) are an important source of human genetic diversity, but their contribution to traits, disease and gene regulation remains unclear. We mapped cis expression quantitative trait loci (eQTLs)...