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Archives of Neurology|October 14, 2009
Association of intronic variants of the BTBD9 gene with Tourette syndromeJean-Baptiste Rivière, Lan Xiong, Anastasia Levchenko, et al.
Sleep Medicine|July 24, 2007
Genetic association studies of neurotensin gene and restless legs syndrome in French CanadiansLan Xiong, Anastasia Levchenko, Jacques Montplaisir, et al.
Annals of Neurology|June 3, 2004
The 14q restless legs syndrome locus in the French Canadian populationAnastasia Levchenko, Jacques-Yves Montplaisir, Marie-Pierre Dubé, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 19, 2007
Molecular genetic studies of DMT1 on 12q in French-Canadian restless legs syndrome patients and familiesLan Xiong, Patrick Dion, Jacques Montplaisir, et al.
Human Psychopharmacology|January 10, 2019
No evidence so far of a major role of AKT1 and GSK3B in the pathogenesis of antipsychotic-induced tardive dyskinesiaAnastasia Levchenko, Natalya Vyalova, Ivan V Pozhidaev, et al.
Progress in Neuro-Psychopharmacology & Biological Psychiatry|October 16, 2020
A genome-wide association study identifies a gene network associated with paranoid schizophrenia and antipsychotics-induced tardive dyskinesiaAnastasia Levchenko, Alexander Kanapin, Anastasia Samsonova, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 24, 2008
Autosomal-dominant locus for Restless Legs Syndrome in French-Canadians on chromosome 16p12.1Anastasia Levchenko, Jacques-Yves Montplaisir, Géraldine Asselin, et al.
Drug and Alcohol Dependence|May 29, 2025
Genetic analysis of alcohol use disorder: GWAS of alcohol use disorders identification test (AUDIT) and polygenic risk scores in an east slavic populationMichil Trofimov, Viacheslav Kudriavskii, Layal Shaheen, et al.
Human Molecular Genetics|January 8, 2009
MEIS1 intronic risk haplotype associated with restless legs syndrome affects its mRNA and protein expression levelsLan Xiong, Hélène Catoire, Patrick Dion, et al.
BMC Ophthalmology|October 9, 2021
Rare single nucleotide variants in COL5A1 promoter do not play a major role in keratoconus susceptibility associated with rs1536482Liubov O Skorodumova, Alexandra V Belodedova, Elena I Sharova, et al.
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