Dena G. Hernandez
Dena G. Hernandez
National Institutes of Health, National Institute on Aging
Verified email at mail.nih.gov
Title
Cited by
Cited by
Year
Heart disease and stroke statistics—2017 update: a report from the American Heart Association
EJ Benjamin, MJ Blaha, SE Chiuve, M Cushman, SR Das, R Deo, ...
circulation 135 (10), e146-e603, 2017
12708*2017
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
35702011
Discovery and refinement of loci associated with lipid levels
CJ Willer, EM Schmidt, S Sengupta, GM Peloso, S Gustafsson, S Kanoni, ...
Nature genetics 45 (11), 1274, 2013
19772013
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
GB Ehret, PB Munroe, KM Rice, M Bochud, AD Johnson, DI Chasman, ...
Nature 478 (7367), 103, 2011
19112011
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
17612009
Systematic identification of trans eQTLs as putative drivers of known disease associations
HJ Westra, MJ Peters, T Esko, H Yaghootkar, C Schurmann, J Kettunen, ...
Nature genetics 45 (10), 1238-1243, 2013
15062013
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
13762014
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
11752010
Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study
E Majounie, AE Renton, K Mok, EGP Dopper, A Waite, S Rollinson, ...
The Lancet Neurology 11 (4), 323-330, 2012
9912012
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
9192008
Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies
International Parkinson Disease Genomics Consortium
The Lancet 377 (9766), 641-649, 2011
8582011
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
7912010
Common variants associated with plasma triglycerides and risk for coronary artery disease
R Do, CJ Willer, EM Schmidt, S Sengupta, C Gao, GM Peloso, ...
Nature genetics 45 (11), 1345-1352, 2013
7802013
GWAS of 126,559 individuals identifies genetic variants associated with educational attainment
CA Rietveld, SE Medland, J Derringer, J Yang, T Esko, NW Martin, ...
science 340 (6139), 1467-1471, 2013
7702013
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
6472015
Lewy bodies and parkinsonism in families with parkin mutations
M Farrer, P Chan, R Chen, L Tan, S Lincoln, D Hernandez, L Forno, ...
Annals of Neurology: Official Journal of the American Neurological …, 2001
5742001
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
5402014
DNA methylation-based measures of biological age: meta-analysis predicting time to death
BH Chen, RE Marioni, E Colicino, MJ Peters, CK Ward-Caviness, PC Tsai, ...
Aging (Albany NY) 8 (9), 1844, 2016
5262016
Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies
CE Elks, JRB Perry, P Sulem, DI Chasman, N Franceschini, C He, ...
Nature genetics 42 (12), 1077-1085, 2010
5092010
Genetic screening for a single common LRRK2 mutation in familial Parkinson's disease
WC Nichols, N Pankratz, D Hernandez, C Paisán-Ruíz, S Jain, CA Halter, ...
The Lancet 365 (9457), 410-412, 2005
4932005
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Articles 1–20