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Sebastian Guelfi
Sebastian Guelfi
Verge Genomics
Verified email at ucl.ac.uk
Title
Cited by
Cited by
Year
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
15292019
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
8342015
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
6752014
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
2982017
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
2712015
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
2452016
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
2392017
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
2352016
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
1242017
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
1152021
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
812019
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
782019
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
712017
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
612020
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
552020
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
542019
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
512016
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
492019
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
472020
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
412021
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