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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 | 201 | 2011 |
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 | 183 | 2010 |
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 | 174 | 2021 |
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 | 122 | 2010 |
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 | 95 | 2011 |
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 | 88 | 2010 |
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 | 80 | 2015 |
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 | 80 | 2013 |
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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 | 72 | 2009 |
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 | 71 | 2010 |
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 | 65 | 2015 |
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 | 54 | 2011 |
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 | 45 | 2016 |
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 | 45 | 2011 |
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 | 41 | 2013 |
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