Аnastasia Levchenko

1.1k total citations
25 papers, 526 citations indexed

About

Аnastasia Levchenko is a scholar working on Neurology, Epidemiology and Genetics. According to data from OpenAlex, Аnastasia Levchenko has authored 25 papers receiving a total of 526 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Neurology, 9 papers in Epidemiology and 7 papers in Genetics. Recurrent topics in Аnastasia Levchenko's work include Restless Legs Syndrome Research (9 papers), Parkinson's Disease Mechanisms and Treatments (8 papers) and Genetics and Neurodevelopmental Disorders (5 papers). Аnastasia Levchenko is often cited by papers focused on Restless Legs Syndrome Research (9 papers), Parkinson's Disease Mechanisms and Treatments (8 papers) and Genetics and Neurodevelopmental Disorders (5 papers). Аnastasia Levchenko collaborates with scholars based in Russia, Canada and United States. Аnastasia Levchenko's co-authors include Guy A. Rouleau, Lan Xiong, Gustavo Turecki, Pascale Thibodeau, Judith St‐Onge, Alex Désautels, Marie‐Pierre Dubé, Alexander Kanapin, Cláudia Gaspar and Raul R. Gainetdinov and has published in prestigious journals such as Neurology, Annals of Neurology and Journal of Allergy and Clinical Immunology.

In The Last Decade

Аnastasia Levchenko

24 papers receiving 509 citations

Peers

Аnastasia Levchenko
Dean Foti Canada
Chieh-En Jane Tseng United States
Mayke Oosterloo Netherlands
J. Ding China
Joanne Doherty United Kingdom
Аnastasia Levchenko
Citations per year, relative to Аnastasia Levchenko Аnastasia Levchenko (= 1×) peers Élisabeth Ruppert

Countries citing papers authored by Аnastasia Levchenko

Since Specialization
Citations

This map shows the geographic impact of Аnastasia Levchenko's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Аnastasia Levchenko with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Аnastasia Levchenko more than expected).

Fields of papers citing papers by Аnastasia Levchenko

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Аnastasia Levchenko. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Аnastasia Levchenko. The network helps show where Аnastasia Levchenko may publish in the future.

Co-authorship network of co-authors of Аnastasia Levchenko

This figure shows the co-authorship network connecting the top 25 collaborators of Аnastasia Levchenko. A scholar is included among the top collaborators of Аnastasia Levchenko based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Аnastasia Levchenko. Аnastasia Levchenko is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Levchenko, Аnastasia, et al.. (2023). Pilot Study to Detect the Repertoires of T-Cell Receptor Gamma Chains in Patients with Juvenile Schizophrenia. Russian Journal of Genetics. 59(7). 739–743. 1 indexed citations
2.
Levchenko, Аnastasia, Fedor Gusev, & Е. И. Рогаев. (2023). The evolutionary origin of psychosis. Frontiers in Psychiatry. 14. 1115929–1115929. 2 indexed citations
3.
Levchenko, Аnastasia, et al.. (2023). Genomic regulatory sequences in the pathogenesis of bipolar disorder. Frontiers in Psychiatry. 14. 1115924–1115924. 4 indexed citations
4.
Levchenko, Аnastasia, Alexander Kanapin, А. С. Благонравова, et al.. (2022). A Genome-Wide Association Study Reveals a BDNF-Centered Molecular Network Associated with Alcohol Dependence and Related Clinical Measures. Biomedicines. 10(12). 3007–3007. 5 indexed citations
5.
Skorodumova, Lyubov, Mukharram M. Bikbov, Oksana V. Selezneva, et al.. (2021). Rare single nucleotide variants in COL5A1 promoter do not play a major role in keratoconus susceptibility associated with rs1536482. BMC Ophthalmology. 21(1). 357–357. 1 indexed citations
6.
Levchenko, Аnastasia, et al.. (2020). Current challenges and possible future developments in personalized psychiatry with an emphasis on psychotic disorders. Heliyon. 6(5). e03990–e03990. 12 indexed citations
7.
Levchenko, Аnastasia, et al.. (2020). NRG1, PIP4K2A, and HTR2C as Potential Candidate Biomarker Genes for Several Clinical Subphenotypes of Depression and Bipolar Disorder. Frontiers in Genetics. 11. 936–936. 14 indexed citations
8.
Levchenko, Аnastasia, Alexander Kanapin, Anastasia Samsonova, et al.. (2020). A genome-wide association study identifies a gene network associated with paranoid schizophrenia and antipsychotics-induced tardive dyskinesia. Progress in Neuro-Psychopharmacology and Biological Psychiatry. 105. 110134–110134. 7 indexed citations
9.
Levchenko, Аnastasia, Г. Г. Симуткин, Н. А. Бохан, et al.. (2018). The functional variant rs334558 of <em>GSK3B</em> is associated with remission in patients with depressive disorders. Pharmacogenomics and Personalized Medicine. Volume 11. 121–126. 11 indexed citations
10.
Levchenko, Аnastasia, Alexander Kanapin, Anastasia Samsonova, & Raul R. Gainetdinov. (2017). Human Accelerated Regions and Other Human-Specific Sequence Variations in the Context of Evolution and Their Relevance for Brain Development. Genome Biology and Evolution. 10(1). 166–188. 52 indexed citations
11.
Levchenko, Аnastasia, et al.. (2015). Beta-catenin in schizophrenia: Possibly deleterious novel mutation. Psychiatry Research. 228(3). 843–848. 26 indexed citations
12.
Levchenko, Аnastasia, et al.. (2013). Sequencing of five left–right cerebral asymmetry genes in a cohort of schizophrenia and schizotypal disorder patients from Russia. Psychiatric Genetics. 24(2). 75–80. 6 indexed citations
13.
Xiong, Lan, Jacques Montplaisir, Alex Désautels, et al.. (2010). Family Study of Restless Legs Syndrome in Quebec, Canada. Archives of Neurology. 67(5). 617–22. 47 indexed citations
14.
Rivière, Jean‐Baptiste, Lan Xiong, Аnastasia Levchenko, et al.. (2009). Association of Intronic Variants of the BTBD9 Gene With Tourette Syndrome. Archives of Neurology. 66(10). 1267–72. 33 indexed citations
15.
Xiong, Lan, Hélène Catoire, Patrick A. Dion, et al.. (2009). MEIS1 intronic risk haplotype associated with restless legs syndrome affects its mRNA and protein expression levels. Human Molecular Genetics. 18(6). 1065–1074. 67 indexed citations
16.
Levchenko, Аnastasia, Géraldine Asselin, Sylvie Provost, et al.. (2008). Autosomal‐dominant locus for restless legs syndrome in French‐Canadians on chromosome 16p12.1. Movement Disorders. 24(1). 40–50. 36 indexed citations
17.
Xiong, Lan, Аnastasia Levchenko, Jacques Montplaisir, et al.. (2007). Genetic association studies of neurotensin gene and restless legs syndrome in French Canadians. Sleep Medicine. 9(3). 273–282. 4 indexed citations
18.
Xiong, Lan, Patrick A. Dion, Jacques Montplaisir, et al.. (2007). Molecular genetic studies ofDMT1on 12q in French‐Canadian restless legs syndrome patients and families. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 144B(7). 911–917. 20 indexed citations
19.
Levchenko, Аnastasia, Yves Robitaille, Michael J. Strong, & Guy A. Rouleau. (2004). TAU Mutations are not a Predominant Cause of Frontotemporal Dementia in Canadian Patients. Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 31(3). 363–367. 1 indexed citations
20.
Levchenko, Аnastasia, Marie‐Pierre Dubé, Jean‐Baptiste Rivière, et al.. (2004). The 14q restless legs syndrome locus in the French Canadian population. Annals of Neurology. 55(6). 887–891. 56 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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