Articles with public access mandates - Daniah TrabzuniLearn more
Available somewhere: 66
Review
A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD
AE Renton, E Majounie, A Waite, J Simón-Sánchez, S Rollinson, ...
Neuron 72 (2), 257-268, 2011
Mandates: US National Institutes of Health, German Research Foundation
Review
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
Mandates: US National Institutes of Health, UK Medical Research Council, Parkinson's …
Review
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
Mandates: US National Institutes of Health, UK Biotechnology and Biological Sciences …
Review
Identification of common variants associated with human hippocampal and intracranial volumes
JL Stein, SE Medland, AA Vasquez, DP Hibar, RE Senstad, AM Winkler, ...
Nature genetics 44 (5), 552-561, 2012
Mandates: US National Institutes of Health, Howard Hughes Medical Institute, Canadian …
Review
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
Mandates: US National Institutes of Health, UK Medical Research Council, National …
Review
The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data
PM Thompson, JL Stein, SE Medland, DP Hibar, AA Vasquez, ...
Brain imaging and behavior 8, 153-182, 2014
Mandates: US National Institutes of Health, UK Biotechnology and Biological Sciences …
Review
The transcriptional landscape of age in human peripheral blood
MJ Peters, R Joehanes, LC Pilling, C Schurmann, KN Conneely, J Powell, ...
Nature communications 6 (1), 1-14, 2015
Mandates: US National Institutes of Health, National Institute for Health Research, UK
Review
Rare coding variants in the phospholipase D3 gene confer risk for Alzheimer’s disease
C Cruchaga, CM Karch, SC Jin, BA Benitez, Y Cai, R Guerreiro, O Harari, ...
Nature 505 (7484), 550-554, 2014
Mandates: US National Institutes of Health, Canadian Institutes of Health Research, UK …
Review
Genome-wide meta-analysis identifies new susceptibility loci for migraine
V Anttila, BS Winsvold, P Gormley, T Kurth, F Bettella, G McMahon, ...
Nature genetics 45 (8), 912-917, 2013
Mandates: US National Institutes of Health, UK Medical Research Council, Wellcome Trust
Review
Loss of VPS13C function in autosomal-recessive parkinsonism causes mitochondrial dysfunction and increases PINK1/Parkin-dependent mitophagy
S Lesage, V Drouet, E Majounie, V Deramecourt, M Jacoupy, A Nicolas, ...
The American Journal of Human Genetics 98 (3), 500-513, 2016
Mandates: US National Institutes of Health, National Institute of Health and Medical …
Review
Excessive burden of lysosomal storage disorder gene variants in Parkinson’s disease
LA Robak, IE Jansen, J Van Rooij, AG Uitterlinden, R Kraaij, J Jankovic, ...
Brain 140 (12), 3191-3203, 2017
Mandates: US Department of Defense, US National Institutes of Health, Helmholtz …
Review
Genome-wide association study of obsessive-compulsive disorder
SE Stewart, D Yu, JM Scharf, BM Neale, JA Fagerness, CA Mathews, ...
Molecular psychiatry 18 (7), 788-798, 2013
Mandates: US National Institutes of Health, UK Medical Research Council
Review
Unbiased screen for interactors of leucine-rich repeat kinase 2 supports a common pathway for sporadic and familial Parkinson disease
A Beilina, IN Rudenko, A Kaganovich, L Civiero, H Chau, SK Kalia, ...
Proceedings of the National Academy of Sciences 111 (7), 2626-2631, 2014
Mandates: US National Institutes of Health, Research Foundation (Flanders), Fondazione …
Review
Major shifts in glial regional identity are a transcriptional hallmark of human brain aging
L Soreq, J Rose, E Soreq, J Hardy, D Trabzuni, MR Cookson, C Smith, ...
Cell reports 18 (2), 557-570, 2017
Mandates: US National Institutes of Health, Cancer Research UK, UK Medical Research …
Review
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
Mandates: US National Institutes of Health, Alzheimers's UK, UK Medical Research …
Review
Widespread sex differences in gene expression and splicing in the adult human brain
D Trabzuni, A Ramasamy, S Imran, R Walker, C Smith, ME Weale, ...
Nature communications 4 (1), 2771, 2013
Mandates: US National Institutes of Health, UK Medical Research Council, Parkinson's …
Review
Mutations in ANO3 cause dominant craniocervical dystonia: ion channel implicated in pathogenesis
G Charlesworth, V Plagnol, KM Holmström, J Bras, UM Sheerin, E Preza, ...
The American Journal of Human Genetics 91 (6), 1041-1050, 2012
Mandates: Parkinson's UK
Review
MAPT expression and splicing is differentially regulated by brain region: relation to genotype and implication for tauopathies
D Trabzuni, S Wray, J Vandrovcova, A Ramasamy, R Walker, C Smith, ...
Human molecular genetics 21 (18), 4094-4103, 2012
Mandates: US National Institutes of Health
Review
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
Mandates: US National Science Foundation, US Department of Energy, US National …
Review
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
Mandates: US National Science Foundation, US National Institutes of Health, US …
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