Shane E McCarthy
Overview
Explore the profile of Shane E McCarthy including associated specialties, affiliations and a list of published articles.
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Articles
12
Citations
1881
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Recent Articles
1.
Hooper A, Somersan-Karakaya S, McCarthy S, Mylonakis E, Ali S, Mei J, et al.
mBio
. 2022 Oct;
13(6):e0169922.
PMID: 36255239
We conducted a analysis in seropositive patients who were negative or borderline for functional neutralizing antibodies (NAbs) against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) at baseline from a phase...
2.
Horowitz J, Kosmicki J, Damask A, Sharma D, Roberts G, Justice A, et al.
Nat Genet
. 2022 Mar;
54(4):382-392.
PMID: 35241825
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) enters human host cells via angiotensin-converting enzyme 2 (ACE2) and causes coronavirus disease 2019 (COVID-19). Here, through a genome-wide association study, we identify...
3.
Kosmicki J, Horowitz J, Banerjee N, Lanche R, Marcketta A, Maxwell E, et al.
Am J Hum Genet
. 2021 Jun;
108(7):1350-1355.
PMID: 34115965
Severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) causes coronavirus disease 2019 (COVID-19), a respiratory illness that can result in hospitalization or death. We used exome sequence data to investigate associations between...
4.
Harold D, Connolly S, Riley B, Kendler K, McCarthy S, McCombie W, et al.
Am J Med Genet B Neuropsychiatr Genet
. 2019 Feb;
180(3):223-231.
PMID: 30801977
Genome-wide association studies (GWASs) are highly effective at identifying common risk variants for schizophrenia. Rare risk variants are also important contributors to schizophrenia etiology but, with the exception of large...
5.
Staples J, Maxwell E, Gosalia N, Gonzaga-Jauregui C, Snyder C, Hawes A, et al.
Am J Hum Genet
. 2018 May;
102(5):874-889.
PMID: 29727688
Large-scale human genetics studies are ascertaining increasing proportions of populations as they continue growing in both number and scale. As a result, the amount of cryptic relatedness within these study...
6.
McCartney D, Walker R, Morris S, Anderson S, Duff B, Marioni R, et al.
NPJ Schizophr
. 2018 Mar;
4(1):5.
PMID: 29555928
Recent work has highlighted a possible role for altered epigenetic modifications, including differential DNA methylation, in susceptibility to psychiatric illness. Here, we investigate blood-based DNA methylation in a large family...
7.
McCarthy S, McCombie W, Corvin A
Schizophr Bull
. 2014 Mar;
40(3):492-6.
PMID: 24674812
Significant progress is being made in defining the genetic etiology of schizophrenia. As the list of implicated genes grows, parallel developments in gene editing technology provide new methods to investigate...
8.
Nord A, Roeb W, Dickel D, Walsh T, Kusenda M, OConnor K, et al.
Eur J Hum Genet
. 2011 Mar;
19(6):727-31.
PMID: 21448237
Individuals with autism are more likely to carry rare inherited and de novo copy number variants (CNVs). However, further research is needed to establish which CNVs are causal and the...
9.
Girirajan S, Rosenfeld J, Cooper G, Antonacci F, Siswara P, Itsara A, et al.
Nat Genet
. 2010 Feb;
42(3):203-9.
PMID: 20154674
We report the identification of a recurrent, 520-kb 16p12.1 microdeletion associated with childhood developmental delay. The microdeletion was detected in 20 of 11,873 cases compared with 2 of 8,540 controls...
10.
Sebat J, Levy D, McCarthy S
Trends Genet
. 2009 Nov;
25(12):528-35.
PMID: 19883952
Recent studies have established an important role for rare genomic deletions and duplications in the etiology of schizophrenia. This research suggests that the genetic architecture of neuropsychiatric disorders includes a...