| Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies MA Nalls, C Blauwendraat, CL Vallerga, K Heilbron, S Bandres-Ciga, ... The Lancet Neurology 18 (12), 1091-1102, 2019 | 1702 | 2019 |
| Common genetic variants influence human subcortical brain structures DP Hibar, JL Stein, ME Renteria, A Arias-Vasquez, S Desrivières, ... Nature 520 (7546), 224-229, 2015 | 859 | 2015 |
| Genetic variability in the regulation of gene expression in ten regions of the human brain A Ramasamy, D Trabzuni, S Guelfi, V Varghese, C Smith, R Walker, T De, ... Nature neuroscience 17 (10), 1418-1428, 2014 | 692 | 2014 |
| Novel genetic loci associated with hippocampal volume DP Hibar, HHH Adams, N Jahanshad, G Chauhan, JL Stein, E Hofer, ... Nature communications 8 (1), 13624, 2017 | 315 | 2017 |
| A genome-wide gene-expression analysis and database in transgenic mice during development of amyloid or tau pathology M Matarin, DA Salih, M Yasvoina, DM Cummings, S Guelfi, W Liu, ... Cell reports 10 (4), 633-644, 2015 | 277 | 2015 |
| Novel genetic loci underlying human intracranial volume identified through genome-wide association HHH Adams, DP Hibar, V Chouraki, JL Stein, PA Nyquist, ME Rentería, ... Nature neuroscience 19 (12), 1569-1582, 2016 | 252 | 2016 |
| An additional k-means clustering step improves the biological features of WGCNA gene co-expression networks JA Botía, J Vandrovcova, P Forabosco, S Guelfi, K D’Sa, ... BMC systems biology 11, 1-16, 2017 | 251 | 2017 |
| Genetic influences on schizophrenia and subcortical brain volumes: large-scale proof of concept B Franke, JL Stein, S Ripke, V Anttila, DP Hibar, KJE Van Hulzen, ... Nature neuroscience 19 (3), 420-431, 2016 | 238 | 2016 |
| Identification of candidate Parkinson disease genes by integrating genome-wide association study, expression, and epigenetic data sets DA Kia, D Zhang, S Guelfi, C Manzoni, L Hubbard, RH Reynolds, J Botía, ... JAMA neurology 78 (4), 464-472, 2021 | 130 | 2021 |
| Genetic architecture of sporadic frontotemporal dementia and overlap with Alzheimer's and Parkinson's diseases R Ferrari, Y Wang, J Vandrovcova, S Guelfi, A Witeolar, CM Karch, ... Journal of Neurology, Neurosurgery & Psychiatry 88 (2), 152-164, 2017 | 128 | 2017 |
| Genetic variability in response to amyloid beta deposition influences Alzheimer’s disease risk DA Salih, S Bayram, S Guelfi, RH Reynolds, M Shoai, M Ryten, ... Brain communications 1 (1), fcz022, 2019 | 90 | 2019 |
| The endocytic membrane trafficking pathway plays a major role in the risk of Parkinson's disease S Bandres‐Ciga, S Saez‐Atienzar, L Bonet‐Ponce, K Billingsley, D Vitale, ... Movement Disorders 34 (4), 460-468, 2019 | 82 | 2019 |
| Increased brain expression of GPNMB is associated with genome wide significant risk for Parkinson’s disease on chromosome 7p15.3 MN Murthy, C Blauwendraat, Ukbec, S Guelfi, IPDGC, J Hardy, PA Lewis, ... neurogenetics 18 (3), 121-133, 2017 | 75 | 2017 |
| Penetrance of Parkinson's Disease in LRRK2 p.G2019S Carriers Is Modified by a Polygenic Risk Score H Iwaki, C Blauwendraat, MB Makarious, S Bandrés‐Ciga, HL Leonard, ... Movement Disorders 35 (5), 774-780, 2020 | 64 | 2020 |
| Dystonia genes functionally converge in specific neurons and share neurobiology with psychiatric disorders NE Mencacci, RH Reynolds, SG Ruiz, J Vandrovcova, P Forabosco, ... Brain 143 (9), 2771-2787, 2020 | 57 | 2020 |
| The genetic architecture of Parkinson disease in Spain: characterizing population‐specific risk, differential haplotype structures, and providing etiologic insight S Bandres‐Ciga, S Ahmed, MS Sabir, C Blauwendraat, ... Movement Disorders 34 (12), 1851-1863, 2019 | 56 | 2019 |
| Transcriptomic and genetic analyses reveal potential causal drivers for intractable partial epilepsy S Guelfi, JA Botia, M Thom, A Ramasamy, M Perona, L Stanyer, ... Brain 142 (6), 1616-1630, 2019 | 52 | 2019 |
| Frontotemporal dementia: insights into the biological underpinnings of disease through gene co-expression network analysis R Ferrari, P Forabosco, J Vandrovcova, JA Botía, S Guelfi, JD Warren, ... Molecular neurodegeneration 11, 1-19, 2016 | 51 | 2016 |
| Incomplete annotation has a disproportionate impact on our understanding of Mendelian and complex neurogenetic disorders D Zhang, S Guelfi, S Garcia-Ruiz, B Costa, RH Reynolds, K D’Sa, W Liu, ... Science Advances 6 (24), eaay8299, 2020 | 50 | 2020 |
| Investigation of autosomal genetic sex differences in Parkinson's disease C Blauwendraat, H Iwaki, MB Makarious, S Bandres‐Ciga, HL Leonard, ... Annals of neurology 90 (1), 35-42, 2021 | 49 | 2021 |
