Svetlana Limborska
Overview
Explore the profile of Svetlana Limborska including associated specialties, affiliations and a list of published articles.
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22
Citations
1986
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Recent Articles
1.
Fedorova L, Khrunin A, Khvorykh G, Lim J, Thornton N, Mulyar O, et al.
Genes (Basel)
. 2022 Aug;
13(8).
PMID: 36011383
Common alleles tend to be more ancient than rare alleles. These common SNPs appeared thousands of years ago and reflect intricate human evolution including various adaptations, admixtures, and migration events....
2.
Mroczek M, Inashkina I, Stavusis J, Zayakin P, Khrunin A, Micule I, et al.
Hum Mutat
. 2022 Jun;
43(10):1347-1353.
PMID: 35731190
The investigated intronic CAPN3 variant NM_000070.3:c.1746-20C>G occurs in the Central and Eastern Europe with a frequency of >1% and there are conflicting interpretations on its pathogenicity. We collected data on...
3.
Trubetskoy V, Pardinas A, Qi T, Panagiotaropoulou G, Awasthi S, Bigdeli T, et al.
Nature
. 2022 Apr;
604(7906):502-508.
PMID: 35396580
Schizophrenia has a heritability of 60-80%, much of which is attributable to common risk alleles. Here, in a two-stage genome-wide association study of up to 76,755 individuals with schizophrenia and...
4.
Khvorykh G, Khrunin A, Filippenkov I, Stavchansky V, Dergunova L, Limborska S
Genes (Basel)
. 2021 Mar;
12(3).
PMID: 33668793
In this paper we propose a workflow for studying the genetic architecture of ischemic stroke outcomes. It develops further the candidate gene approach. The workflow is based on the animal...
5.
Zhernakova D, Brukhin V, Malov S, Oleksyk T, Koepfli K, Zhuk A, et al.
Genomics
. 2019 Mar;
112(1):442-458.
PMID: 30902755
The Russian Federation is the largest and one of the most ethnically diverse countries in the world, however no centralized reference database of genetic variation exists to date. Such data...
6.
Anttila V, Bulik-Sullivan B, Finucane H, Walters R, Bras J, Duncan L, et al.
Science
. 2018 Jun;
360(6395).
PMID: 29930110
Disorders of the brain can exhibit considerable epidemiological comorbidity and often share symptoms, provoking debate about their etiologic overlap. We quantified the genetic sharing of 25 brain disorders from genome-wide...
7.
Stavusis J, Inashkina I, Lace B, Pelnena D, Limborska S, Khrunin A, et al.
Hum Hered
. 2017 Nov;
82(3-4):140-146.
PMID: 29131013
Objectives: The PMCA gene family consists of 4 genes and at least 21 splice variants; among these, the Ca2+ ATPase 4 (PMCA4) gene encodes a plasma membrane protein abundantly expressed...
8.
Filatova E, Kasian A, Kolomin T, Rybalkina E, Alieva A, Andreeva L, et al.
Front Pharmacol
. 2017 Mar;
8:89.
PMID: 28293190
Clinical studies have shown that Selank had an anxiolytic effect comparable to that of classical benzodiazepine drugs, which can enhance the inhibitory effect of GABA by allosteric modulation of GABA...
9.
Wong E, Khrunin A, Nichols L, Pushkarev D, Khokhrin D, Verbenko D, et al.
Genome Res
. 2016 Dec;
27(1):1-14.
PMID: 27965293
Siberia and Northwestern Russia are home to over 40 culturally and linguistically diverse indigenous ethnic groups, yet genetic variation and histories of peoples from this region are largely uncharacterized. We...
10.
Mehta D, Tropf F, Gratten J, Bakshi A, Zhu Z, Bacanu S, et al.
JAMA Psychiatry
. 2016 Mar;
73(5):497-505.
PMID: 27007234
Importance: A recently published study of national data by McGrath et al in 2014 showed increased risk of schizophrenia (SCZ) in offspring associated with both early and delayed parental age,...