Kathleen E Stirrups
Overview
Explore the profile of Kathleen E Stirrups including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
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29
Citations
3517
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Recent Articles
11.
Turcot V, Lu Y, Highland H, Schurmann C, Justice A, Fine R, et al.
Nat Genet
. 2019 Jun;
51(7):1191-1192.
PMID: 31160809
An amendment to this paper has been published and can be accessed via a link at the top of the paper.
12.
Wei W, Tuna S, Keogh M, Smith K, Aitman T, Beales P, et al.
Science
. 2019 May;
364(6442.
PMID: 31123110
Approximately 2.4% of the human mitochondrial DNA (mtDNA) genome exhibits common homoplasmic genetic variation. We analyzed 12,975 whole-genome sequences to show that 45.1% of individuals from 1526 mother-offspring pairs harbor...
13.
Justice A, Karaderi T, Highland H, Young K, Graff M, Lu Y, et al.
Nat Genet
. 2019 Feb;
51(3):452-469.
PMID: 30778226
Body-fat distribution is a risk factor for adverse cardiovascular health consequences. We analyzed the association of body-fat distribution, assessed by waist-to-hip ratio adjusted for body mass index, with 228,985 predicted...
14.
Turcot V, Lu Y, Highland H, Schurmann C, Justice A, Fine R, et al.
Nat Genet
. 2018 Mar;
50(5):766-767.
PMID: 29549330
In the version of this article originally published, one of the two authors with the name Wei Zhao was omitted from the author list and the affiliations for both authors...
15.
Turcot V, Lu Y, Highland H, Schurmann C, Justice A, Fine R, et al.
Nat Genet
. 2018 Mar;
50(5):765-766.
PMID: 29549329
In the published version of this paper, the name of author Emanuele Di Angelantonio was misspelled. This error has now been corrected in the HTML and PDF versions of the...
16.
Turcot V, Lu Y, Highland H, Schurmann C, Justice A, Fine R, et al.
Nat Genet
. 2017 Dec;
50(1):26-41.
PMID: 29273807
Genome-wide association studies (GWAS) have identified >250 loci for body mass index (BMI), implicating pathways related to neuronal biology. Most GWAS loci represent clusters of common, noncoding variants from which...
17.
Liu D, Peloso G, Yu H, Butterworth A, Wang X, Mahajan A, et al.
Nat Genet
. 2017 Oct;
49(12):1758-1766.
PMID: 29083408
We screened variants on an exome-focused genotyping array in >300,000 participants (replication in >280,000 participants) and identified 444 independent variants in 250 loci significantly associated with total cholesterol (TC), high-density-lipoprotein...
18.
Kraja A, Cook J, Warren H, Surendran P, Liu C, Evangelou E, et al.
Circ Cardiovasc Genet
. 2017 Oct;
10(5).
PMID: 29030403
Background: Genome-wide association studies have recently identified >400 loci that harbor DNA sequence variants that influence blood pressure (BP). Our earlier studies identified and validated 56 single nucleotide variants (SNVs)...
19.
van den Berg M, Warren H, Cabrera C, Verweij N, Mifsud B, Haessler J, et al.
Hum Mol Genet
. 2017 Apr;
26(12):2346-2363.
PMID: 28379579
Resting heart rate is a heritable trait, and an increase in heart rate is associated with increased mortality risk. Genome-wide association study analyses have found loci associated with resting heart...
20.
Manning A, Highland H, Gasser J, Sim X, Tukiainen T, Fontanillas P, et al.
Diabetes
. 2017 Mar;
66(7):2019-2032.
PMID: 28341696
To identify novel coding association signals and facilitate characterization of mechanisms influencing glycemic traits and type 2 diabetes risk, we analyzed 109,215 variants derived from exome array genotyping together with...