Steve McCarroll
Overview
Explore the profile of Steve McCarroll including associated specialties, affiliations and a list of published articles.
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Articles
9
Citations
4927
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Recent Articles
1.
Li R, Gagliano Taliun S, Liao K, Flickinger M, Sobell J, Genovese G, et al.
medRxiv
. 2025 Jan;
PMID: 39763555
In studies of individuals of primarily European genetic ancestry, common and low-frequency variants and rare coding variants have been found to be associated with the risk of bipolar disorder (BD)...
2.
Wong W, Emdin C, Bick A, Zekavat S, Niroula A, Pirruccello J, et al.
Nature
. 2023 Jul;
619(7970):E47.
PMID: 37400552
No abstract available.
3.
Wong W, Emdin C, Bick A, Zekavat S, Niroula A, Pirruccello J, et al.
Nature
. 2023 Apr;
616(7958):747-754.
PMID: 37046084
Chronic liver disease is a major public health burden worldwide. Although different aetiologies and mechanisms of liver injury exist, progression of chronic liver disease follows a common pathway of liver...
4.
Stahl E, Breen G, Forstner A, McQuillin A, Ripke S, Trubetskoy V, et al.
Nat Genet
. 2019 May;
51(5):793-803.
PMID: 31043756
Bipolar disorder is a highly heritable psychiatric disorder. We performed a genome-wide association study (GWAS) including 20,352 cases and 31,358 controls of European descent, with follow-up analysis of 822 variants...
5.
Maussion G, Cruceanu C, Rosenfeld J, Bell S, Jollant F, Szatkiewicz J, et al.
Am J Med Genet A
. 2016 Oct;
173(2):395-406.
PMID: 27759917
We performed whole-genome sequencing on an individual from a family with variable psychiatric phenotypes that had a sensory processing disorder, apraxia, and autism. The proband harbored a maternally inherited balanced...
6.
Vilhjalmsson B, Yang J, Finucane H, Gusev A, Lindstrom S, Ripke S, et al.
Am J Hum Genet
. 2015 Oct;
97(4):576-92.
PMID: 26430803
Polygenic risk scores have shown great promise in predicting complex disease risk and will become more accurate as training sample sizes increase. The standard approach for calculating risk scores involves...
7.
Bhatia G, Patterson N, Pasaniuc B, Zaitlen N, Genovese G, Pollack S, et al.
Am J Hum Genet
. 2011 Sep;
89(3):368-81.
PMID: 21907010
The study of recent natural selection in human populations has important applications to human history and medicine. Positive natural selection drives the increase in beneficial alleles and plays a role...
8.
Sabeti P, Fry B, Lohmueller J, Hostetter E, Cotsapas C, Xie X, et al.
Nature
. 2007 Oct;
449(7164):913-8.
PMID: 17943131
With the advent of dense maps of human genetic variation, it is now possible to detect positive natural selection across the human genome. Here we report an analysis of over...
9.
Frazer K, Ballinger D, Cox D, Hinds D, Stuve L, Boudreau A, et al.
Nature
. 2007 Oct;
449(7164):851-61.
PMID: 17943122
We describe the Phase II HapMap, which characterizes over 3.1 million human single nucleotide polymorphisms (SNPs) genotyped in 270 individuals from four geographically diverse populations and includes 25-35% of common...