J Raphael Gibbs
J Raphael Gibbs
Laboratory of Neurogenetics, NIA, NIH
Verified email at mail.nih.gov
Title
Cited by
Cited by
Year
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
31492011
TREM2 Variants in Alzheimer's Disease
R Guerreiro, A Wojtas, J Bras, M Carrasquillo, E Rogaeva, E Majounie, ...
New England Journal of Medicine 368 (2), 117-127, 2013
17502013
Genome-wide association study reveals genetic risk underlying Parkinson's disease
J Simon-Sanchez, C Schulte, JM Bras, M Sharma, JR Gibbs, D Berg, ...
Nature genetics 41 (12), 1308, 2009
16322009
Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease
MA Nalls, N Pankratz, CM Lill, CB Do, DG Hernandez, M Saad, ...
Nature genetics 46 (9), 989-993, 2014
11522014
Exome sequencing reveals VCP mutations as a cause of familial ALS
JO Johnson, J Mandrioli, M Benatar, Y Abramzon, VM Van Deerlin, ...
Neuron 68 (5), 857-864, 2010
10692010
Genotype, haplotype and copy-number variation in worldwide human populations
M Jakobsson, SW Scholz, P Scheet, JR Gibbs, JM VanLiere, HC Fung, ...
Nature 451 (7181), 998-1003, 2008
8862008
Abundant quantitative trait loci exist for DNA methylation and gene expression in human brain
JR Gibbs, MP van der Brug, DG Hernandez, BJ Traynor, MA Nalls, SL Lai, ...
PLoS Genet 6 (5), e1000952, 2010
7302010
Common genetic variants influence human subcortical brain structures
DP Hibar, JL Stein, ME Renteria, A Arias-Vasquez, S Desrivičres, ...
Nature 520 (7546), 224-229, 2015
5642015
A survey of genetic human cortical gene expression
AJ Myers, JR Gibbs, JA Webster, K Rohrer, A Zhao, L Marlowe, M Kaleem, ...
Nature genetics 39 (12), 1494-1499, 2007
5142007
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
4522014
Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy
GU Höglinger, NM Melhem, DW Dickson, PMA Sleiman, LS Wang, L Klei, ...
Nature genetics 43 (7), 699, 2011
4122011
A genome-wide association study identifies protein quantitative trait loci (pQTLs)
D Melzer, JRB Perry, D Hernandez, AM Corsi, K Stevens, I Rafferty, ...
PLoS Genet 4 (5), e1000072, 2008
4102008
Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data
HC Fung, S Scholz, M Matarin, J Simón-Sánchez, D Hernandez, A Britton, ...
The Lancet Neurology 5 (11), 911-916, 2006
3932006
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
3712014
Distinct DNA methylation changes highly correlated with chronological age in the human brain
DG Hernandez, MA Nalls, JR Gibbs, S Arepalli, M van der Brug, S Chong, ...
Human molecular genetics 20 (6), 1164-1172, 2011
3272011
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
3142013
Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis
JO Johnson, EP Pioro, A Boehringer, R Chia, H Feit, AE Renton, ...
Nature neuroscience 17 (5), 664-666, 2014
3122014
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
2742015
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
2632013
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
2632013
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