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Sergey Kisselev
Sergey Kisselev
Data Manager, Columbia University Irving Medical Center
Verified email at cumc.columbia.edu
Title
Cited by
Cited by
Year
Cognitive performance of GBA mutation carriers with early-onset PD: The CORE-PD study
RN Alcalay, E Caccappolo, H Mejia-Santana, MX Tang, L Rosado, ...
Neurology 78 (18), 1434-1440, 2012
2962012
Acute kidney injury due to collapsing glomerulopathy following COVID-19 infection
Y Peleg, S Kudose, V D’Agati, E Siddall, S Ahmad, T Nickolas, S Kisselev, ...
Kidney international reports 5 (6), 940-945, 2020
2762020
Association of glucocerebrosidase mutations with dementia with lewy bodies
LN Clark, LA Kartsaklis, RW Gilbert, B Dorado, BM Ross, S Kisselev, ...
Archives of neurology 66 (5), 578-583, 2009
2192009
Genome-wide association study identifies candidate genes for Parkinson's disease in an Ashkenazi Jewish population
X Liu, R Cheng, M Verbitsky, S Kisselev, A Browne, H Mejia-Sanatana, ...
BMC medical genetics 12, 1-16, 2011
2012011
Frequency of known mutations in early-onset Parkinson disease: implication for genetic counseling: the consortium on risk for early onset Parkinson disease study
RN Alcalay, E Caccappolo, H Mejia-Santana, MX Tang, L Rosado, ...
Archives of neurology 67 (9), 1116-1122, 2010
1832010
COVID-19–associated glomerular disease
AA Shetty, I Tawhari, L Safar-Boueri, N Seif, A Alahmadi, R Gargiulo, ...
Journal of the American Society of Nephrology 32 (1), 33-40, 2021
1742021
Predictors of parkin mutations in early-onset Parkinson disease: the consortium on risk for early-onset Parkinson disease study
KS Marder, MX Tang, H Mejia-Santana, L Rosado, ED Louis, CL Comella, ...
Archives of neurology 67 (6), 731-738, 2010
1222010
Exome sequencing identified MYO1E and NEIL1 as candidate genes for human autosomal recessive steroid-resistant nephrotic syndrome
S Sanna-Cherchi, KE Burgess, SN Nees, G Caridi, PL Weng, M Dagnino, ...
Kidney international 80 (4), 389-396, 2011
952011
Replication of the LINGO1 gene association with essential tremor in a North American population
LN Clark, N Park, S Kisselev, E Rios, JH Lee, ED Louis
European journal of human genetics 18 (7), 838-843, 2010
882010
Reorganization of corticostriatal circuits in healthy G2019S LRRK2 carriers
RC Helmich, A Thaler, BFL Van Nuenen, T Gurevich, A Mirelman, ...
Neurology 84 (4), 399-406, 2015
802015
Fall risk and gait in Parkinson's disease: the role of the LRRK2 G2019S mutation
A Mirelman, T Heman, K Yasinovsky, A Thaler, T Gurevich, K Marder, ...
Movement Disorders 28 (12), 1683-1690, 2013
802013
Lower cognitive performance in healthy G2019S LRRK2 mutation carriers
A Thaler, A Mirelman, T Gurevich, E Simon, A Orr-Urtreger, K Marder, ...
Neurology 79 (10), 1027-1032, 2012
742012
Motor phenotype of LRRK2 G2019S carriers in early-onset Parkinson disease
RN Alcalay, H Mejia-Santana, MX Tang, L Rosado, M Verbitsky, ...
Archives of neurology 66 (12), 1517-1522, 2009
722009
Self-report of cognitive impairment and mini-mental state examination performance in PRKN, LRRK2, and GBA carriers with early onset Parkinson's disease
RN Alcalay, H Mejia-Santana, MX Tang, B Rakitin, L Rosado, B Ross, ...
Journal of clinical and experimental neuropsychology 32 (7), 775-779, 2010
712010
Gene-wise association of variants in four lysosomal storage disorder genes in neuropathologically confirmed Lewy body disease
LN Clark, R Chan, R Cheng, X Liu, N Park, N Parmalee, S Kisselev, ...
PLoS One 10 (5), e0125204, 2015
652015
Olfaction in Parkin heterozygotes and compound heterozygotes: The CORE-PD study
RN Alcalay, A Siderowf, R Ottman, E Caccappolo, H Mejia-Santana, ...
Neurology 76 (4), 319-326, 2011
542011
Identification of candidate genes for familial early-onset essential tremor
X Liu, N Hernandez, S Kisselev, A Floratos, A Sawle, I Ionita-Laza, ...
European Journal of Human Genetics 24 (7), 1009-1015, 2016
452016
Promoter methylation‐mediated inactivation of PCDH10 in acute lymphoblastic leukemia contributes to chemotherapy resistance
G Narayan, AJ Freddy, D Xie, H Liyanage, L Clark, S Kisselev, J Un Kang, ...
Genes, Chromosomes and Cancer 50 (12), 1043-1053, 2011
452011
Genetic analysis of the FUS/TLS gene in essential tremor
N Parmalee, K Mirzozoda, S Kisselev, N Merner, P Dion, G Rouleau, ...
European journal of neurology 20 (3), 534-539, 2013
412013
Candidate sequence variants and fetal hemoglobin in children with sickle cell disease treated with hydroxyurea
NS Green, KL Ender, F Pashankar, C Driscoll, PJ Giardina, CA Mullen, ...
PLoS One 8 (2), e55709, 2013
362013
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