Valentina Moskvina
Overview
Explore the profile of Valentina Moskvina including associated specialties, affiliations and a list of published articles.
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62
Citations
6726
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Recent Articles
1.
Smith C, West H, Harris R, Idziaszczyk S, Maughan T, Kaplan R, et al.
J Natl Cancer Inst
. 2014 Apr;
106(5).
PMID: 24771876
No abstract available.
2.
Fogh I, Ratti A, Gellera C, Lin K, Tiloca C, Moskvina V, et al.
Hum Mol Genet
. 2013 Nov;
23(8):2220-31.
PMID: 24256812
Identification of mutations at familial loci for amyotrophic lateral sclerosis (ALS) has provided novel insights into the aetiology of this rapidly progressing fatal neurodegenerative disease. However, genome-wide association studies (GWAS)...
3.
Zammit S, Hamshere M, Dwyer S, Georgiva L, Timpson N, Moskvina V, et al.
Schizophr Bull
. 2013 Nov;
40(6):1254-62.
PMID: 24174267
Psychotic experiences are not uncommon in general population samples, but no studies have examined to what extent confirmed risk variants for schizophrenia are associated with such experiences. A total of...
4.
Lee S, Ripke S, Neale B, Faraone S, Purcell S, Perlis R, et al.
Nat Genet
. 2013 Aug;
45(9):984-94.
PMID: 23933821
Most psychiatric disorders are moderately to highly heritable. The degree to which genetic variation is unique to individual disorders or shared across disorders is unclear. To examine shared genetic etiology,...
5.
Moskvina V, Harold D, Russo G, Vedernikov A, Sharma M, Saad M, et al.
JAMA Neurol
. 2013 Aug;
70(10):1268-76.
PMID: 23921447
Importance: Despite Alzheimer disease (AD) and Parkinson disease (PD) being clinically distinct entities, there is a possibility of a pathological overlap, with some genome-wide association (GWA) studies suggesting that the...
6.
Walters J, Rujescu D, Franke B, Giegling I, Arias Vasquez A, Hargreaves A, et al.
Am J Psychiatry
. 2013 Aug;
170(8):877-85.
PMID: 23903335
OBJECTIVE The authors investigated the effects of recently identified genome-wide significant schizophrenia genetic risk variants on cognition and brain structure. METHOD A panel of six single-nucleotide polymorphisms (SNPs) was selected...
7.
Smith C, West H, Harris R, Idziaszczyk S, Maughan T, Kaplan R, et al.
J Natl Cancer Inst
. 2013 Jul;
105(16):1249-53.
PMID: 23852950
Biallelic inherited mutations in the oxidative DNA damage repair gene MUTYH predispose to colorectal adenomas and colorectal carcinoma (CRC) with high penetrance. We investigated whether rare inherited variants in other...
8.
Holmans P, Moskvina V, Jones L, Sharma M, Vedernikov A, Buchel F, et al.
Hum Mol Genet
. 2012 Dec;
22(5):1039-49.
PMID: 23223016
Parkinson's disease (PD) is the second most common neurodegenerative disease affecting 1-2% in people >60 and 3-4% in people >80. Genome-wide association (GWA) studies have now implicated significant evidence for...
9.
Keller M, Saad M, Bras J, Bettella F, Nicolaou N, Simon-Sanchez J, et al.
Hum Mol Genet
. 2012 Aug;
21(22):4996-5009.
PMID: 22892372
Genome-wide association studies (GWASs) have been successful at identifying single-nucleotide polymorphisms (SNPs) highly associated with common traits; however, a great deal of the heritable variation associated with common traits remains...
10.
Moskvina V, Schmidt K, Vedernikov A, Owen M, Craddock N, Holmans P, et al.
Eur J Hum Genet
. 2012 Feb;
20(8):890-6.
PMID: 22317971
Additional information about risk genes or risk pathways for diseases can be extracted from genome-wide association studies through analyses of groups of markers. The most commonly employed approaches involve combining...