| Association between alcoholism and γ‐amino butyric acid α2 receptor subtype in a Russian population J Lappalainen, E Krupitsky, M Remizov, S Pchelina, A Taraskina, ... Alcoholism: Clinical and Experimental Research 29 (4), 493-498, 2005 | 234 | 2005 |
| Paraoxonase 1 Met–Leu 54 polymorphism is associated with Parkinson’s disease SN Akhmedova, AK Yakimovsky, EI Schwartz Journal of the neurological sciences 184 (2), 179-182, 2001 | 125 | 2001 |
| Cryo-electron microscopy of extracellular vesicles from cerebrospinal fluid A Emelyanov, T Shtam, R Kamyshinsky, L Garaeva, N Verlov, I Miliukhina, ... PloS one 15 (1), e0227949, 2020 | 116 | 2020 |
| Oligomeric α-synuclein and glucocerebrosidase activity levels in GBA-associated Parkinson’s disease S Pchelina, A Emelyanov, G Baydakova, P Andoskin, K Senkevich, ... Neuroscience letters 636, 70-76, 2017 | 88 | 2017 |
| PDXK mutations cause polyneuropathy responsive to pyridoxal 5′‐phosphate supplementation V Chelban, MP Wilson, J Warman Chardon, J Vandrovcova, MN Zanetti, ... Annals of Neurology 86 (2), 225-240, 2019 | 67 | 2019 |
| Blood lysosphingolipids accumulation in patients with parkinson's disease with glucocerebrosidase 1 mutations S Pchelina, G Baydakova, M Nikolaev, K Senkevich, A Emelyanov, ... Movement disorders 33 (8), 1325-1330, 2018 | 58 | 2018 |
| Increased plasma oligomeric alpha-synuclein in patients with lysosomal storage diseases SN Pchelina, EP Nuzhnyi, AK Emelyanov, TM Boukina, TS Usenko, ... Neuroscience letters 583, 188-193, 2014 | 57 | 2014 |
| Gln→ Arg 191 polymorphism of paraoxonase and Parkinson’s disease S Akhmedova, S Anisimov, A Yakimovsky, E Schwartz Human heredity 49 (3), 178-180, 1999 | 56 | 1999 |
| Mutation analysis of Parkinson's disease genes in a Russian data set AK Emelyanov, TS Usenko, C Tesson, KA Senkevich, MA Nikolaev, ... Neurobiology of Aging 71, 267. e7-267. e10, 2018 | 55 | 2018 |
| Screening for LRRK2 mutations in patients with Parkinson’s disease in Russia: identification of a novel LRRK2 variant SN Pchelina, AF Yakimovskii, AK Emelyanov, ON Ivanova, ... European journal of neurology 15 (7), 692-696, 2008 | 54 | 2008 |
| Glucocerebrosidase gene mutations are associated with Parkinson's disease in Russia A Emelyanov, T Boukina, A Yakimovskii, T Usenko, A Drosdova, ... Movement Disorders 27 (1), 158-159, 2012 | 52 | 2012 |
| Selection of peptides binding to the amyloid b-protein reveals potential inhibitors of amyloid formation AL Schwarzman, M Tsiper, L Gregori, D Goldgaber, J Frakowiak, ... Amyloid 12 (4), 199-209, 2005 | 44 | 2005 |
| G2019S LRRK2 mutation in familial and sporadic Parkinson's disease in Russia SN Pchelina, AF Yakimovskii, ON Ivanova, AK Emelianov, AH Zakharchuk, ... Movement disorders: official journal of the Movement Disorder Society 21 (12 …, 2006 | 43 | 2006 |
| Ambroxol increases glucocerebrosidase (GCase) activity and restores GCase translocation in primary patient-derived macrophages in Gaucher disease and Parkinsonism AE Kopytova, GN Rychkov, MA Nikolaev, GV Baydakova, AA Cheblokov, ... Parkinsonism & related disorders 84, 112-121, 2021 | 41 | 2021 |
| Plasma O ligomeric A lpha‐S ynuclein I s A ssociated W ith G lucocerebrosidase A ctivity in G aucher D isease E Nuzhnyi, A Emelyanov, T Boukina, T Usenko, A Yakimovskii, ... Movement Disorders 30 (7), 989-991, 2015 | 40 | 2015 |
| Changing to interleaving stimulation might improve dystonia in cases not responding to pallidal stimulation N Kovács, J Janszky, F Nagy, I Balás Movement disorders 27 (1), 163-165, 2012 | 40 | 2012 |
| The frequency of cytochrome P450 2C9 genetic variants in the Russian population and their associations with individual sensitivity to warfarin therapy SN Pchelina, OV Sirotkina, AE Taraskina, TV Vavilova, AL Shwarzman, ... Thrombosis research 115 (3), 199-203, 2005 | 38 | 2005 |
| Mutation screen of the GAD2 gene and association study of alcoholism in three populations J Lappalainen, E Krupitsky, HR Kranzler, X Luo, M Remizov, S Pchelina, ... American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 144 …, 2007 | 34 | 2007 |
| Быстрые темпы насыщения варфарином-предиктор развития чрезмерной гипокоагуляции. Модернизация алгоритма подбора дозы варфарина ЕС Кропачева, НН Боровков, ТВ Вавилова, НК Вереина, ... Атеротромбоз, 74-86, 2015 | 31 | 2015 |
| Frequency of a specific cytochrome P4502D6B (CYP2D6B) mutant allele in clinically differentiated groups of patients with Parkinson disease SN Akhmedova, EA Pushnova, AF Yakimovsky, VV Avtonomov, ... Biochemical and molecular medicine 54 (2), 88-90, 1995 | 28 | 1995 |
Evgeny KrupitskyHead, Department of Addictions, V.M. Bekhterev National Medical Reserach Center for Psychiatry andVerified email at ek3506.spb.edu
