Lauren Margolin
Overview
Explore the profile of Lauren Margolin including associated specialties, affiliations and a list of published articles.
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Articles
17
Citations
1359
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0
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Recent Articles
1.
Collins R, Brand H, Karczewski K, Zhao X, Alfoldi J, Francioli L, et al.
Nature
. 2021 Feb;
590(7846):E55.
PMID: 33536627
No abstract available.
2.
Collins R, Brand H, Karczewski K, Zhao X, Alfoldi J, Francioli L, et al.
Nature
. 2020 May;
581(7809):444-451.
PMID: 32461652
Structural variants (SVs) rearrange large segments of DNA and can have profound consequences in evolution and human disease. As national biobanks, disease-association studies, and clinical genetic testing have grown increasingly...
3.
Artomov M, Joseph V, Tiao G, Thomas T, Schrader K, Klein R, et al.
Eur J Hum Genet
. 2019 Feb;
27(5):824-828.
PMID: 30718883
Along with traditional effects of aging and carcinogen exposure-inherited DNA variation has substantial contribution to cancer risk. Extraordinary progress made in analysis of common variation with GWAS methodology does not...
4.
Choi S, Weng L, Roselli C, Lin H, Haggerty C, Shoemaker M, et al.
JAMA
. 2018 Dec;
320(22):2354-2364.
PMID: 30535219
Importance: Atrial fibrillation (AF) is the most common arrhythmia affecting 1% of the population. Young individuals with AF have a strong genetic association with the disease, but the mechanisms remain...
5.
Roselli C, Chaffin M, Weng L, Aeschbacher S, Ahlberg G, Albert C, et al.
Nat Genet
. 2018 Jun;
50(9):1225-1233.
PMID: 29892015
Atrial fibrillation (AF) affects more than 33 million individuals worldwide and has a complex heritability. We conducted the largest meta-analysis of genome-wide association studies (GWAS) for AF to date, consisting...
6.
Collins R, Brand H, Redin C, Hanscom C, Antolik C, Stone M, et al.
Genome Biol
. 2017 Mar;
18(1):36.
PMID: 28260531
Background: Structural variation (SV) influences genome organization and contributes to human disease. However, the complete mutational spectrum of SV has not been routinely captured in disease association studies. Results: We...
7.
Saxena R, Plenge R, Bjonnes A, Dashti H, Okada Y, Gad El Haq W, et al.
Arthritis Rheumatol
. 2017 Jan;
69(5):976-985.
PMID: 28118524
Objective: Genetic factors underlying susceptibility to rheumatoid arthritis (RA) in Arab populations are largely unknown. This genome-wide association study (GWAS) was undertaken to explore the generalizability of previously reported RA...
8.
Redin C, Brand H, Collins R, Kammin T, Mitchell E, Hodge J, et al.
Nat Genet
. 2016 Nov;
49(1):36-45.
PMID: 27841880
Despite the clinical significance of balanced chromosomal abnormalities (BCAs), their characterization has largely been restricted to cytogenetic resolution. We explored the landscape of BCAs at nucleotide resolution in 273 subjects...
9.
Brand H, Collins R, Hanscom C, Rosenfeld J, Pillalamarri V, Stone M, et al.
Am J Hum Genet
. 2015 Jun;
97(1):170-6.
PMID: 26094575
Copy-number variants (CNVs) have been the predominant focus of genetic studies of structural variation, and chromosomal microarray (CMA) for genome-wide CNV detection is the recommended first-tier genetic diagnostic screen in...
10.
Kiwelu I, Novitsky V, Kituma E, Margolin L, Baca J, Manongi R, et al.
PLoS One
. 2014 Jul;
9(7):e102258.
PMID: 25003939
A national ART program was launched in Tanzania in October 2004. Due to the existence of multiple HIV-1 subtypes and recombinant viruses co-circulating in Tanzania, it is important to monitor...