Steven McCarroll
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Explore the profile of Steven McCarroll including associated specialties, affiliations and a list of published articles.
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22
Citations
9078
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Recent Articles
11.
Zekavat S, Ruotsalainen S, Handsaker R, Alver M, Bloom J, Poterba T, et al.
Nat Commun
. 2018 Aug;
9(1):3493.
PMID: 30140049
The original version of this article contained an error in the name of the author Ramachandran S. Vasan, which was incorrectly given as Vasan S. Ramachandran. This has now been...
12.
Zekavat S, Ruotsalainen S, Handsaker R, Alver M, Bloom J, Poterba T, et al.
Nat Commun
. 2018 Jul;
9(1):2606.
PMID: 29973585
Lipoprotein(a), Lp(a), is a modified low-density lipoprotein particle that contains apolipoprotein(a), encoded by LPA, and is a highly heritable, causal risk factor for cardiovascular diseases that varies in concentrations across...
13.
Gusev A, Mancuso N, Won H, Kousi M, Finucane H, Reshef Y, et al.
Nat Genet
. 2018 Apr;
50(4):538-548.
PMID: 29632383
Genome-wide association studies (GWAS) have identified over 100 risk loci for schizophrenia, but the causal mechanisms remain largely unknown. We performed a transcriptome-wide association study (TWAS) integrating a schizophrenia GWAS...
14.
Finucane H, Reshef Y, Anttila V, Slowikowski K, Gusev A, Byrnes A, et al.
Nat Genet
. 2018 Apr;
50(4):621-629.
PMID: 29632380
We introduce an approach to identify disease-relevant tissues and cell types by analyzing gene expression data together with genome-wide association study (GWAS) summary statistics. Our approach uses stratified linkage disequilibrium...
15.
McCarthy S, Das S, Kretzschmar W, Delaneau O, Wood A, Teumer A, et al.
Nat Genet
. 2016 Aug;
48(10):1279-83.
PMID: 27548312
We describe a reference panel of 64,976 human haplotypes at 39,235,157 SNPs constructed using whole-genome sequence data from 20 studies of predominantly European ancestry. Using this resource leads to accurate...
16.
Lek M, Karczewski K, Minikel E, Samocha K, Banks E, Fennell T, et al.
Nature
. 2016 Aug;
536(7616):285-91.
PMID: 27535533
Large-scale reference data sets of human genetic variation are critical for the medical and functional interpretation of DNA sequence changes. Here we describe the aggregation and analysis of high-quality exome...
17.
Padmanabhan J, Nanda P, Tandon N, Mothi S, Bolo N, McCarroll S, et al.
J Psychiatr Res
. 2016 Mar;
77:52-8.
PMID: 26978185
Background: An elevated prevalence of Type 2 diabetes (T2D) has been observed in people with psychotic disorders and their relatives compared to the general population. It is not known whether...
18.
Minikel E, Vallabh S, Lek M, Estrada K, Samocha K, Sathirapongsasuti J, et al.
Sci Transl Med
. 2016 Jan;
8(322):322ra9.
PMID: 26791950
More than 100,000 genetic variants are reported to cause Mendelian disease in humans, but the penetrance-the probability that a carrier of the purported disease-causing genotype will indeed develop the disease-is...
19.
Song J, Bergen S, Di Florio A, Karlsson R, Charney A, Ruderfer D, et al.
Mol Psychiatry
. 2015 Oct;
21(9):1290-7.
PMID: 26503763
Lithium is the mainstay prophylactic treatment for bipolar disorder (BD), but treatment response varies considerably across individuals. Patients who respond well to lithium treatment might represent a relatively homogeneous subtype...
20.
Brand H, Pillalamarri V, Collins R, Eggert S, ODushlaine C, Braaten E, et al.
Am J Hum Genet
. 2014 Oct;
95(4):454-61.
PMID: 25279985
Structural variation (SV) is a significant component of the genetic etiology of both neurodevelopmental and psychiatric disorders; however, routine guidelines for clinical genetic screening have been established only in the...