关注
Dena G. Hernandez
Dena G. Hernandez
National Institutes of Health, National Institute on Aging
在 mail.nih.gov 的电子邮件经过验证
标题
引用次数
引用次数
年份
Heart disease and stroke statistics—2014 update: a report from the American Heart Association
AS Go, D Mozaffarian, VL Roger, EJ Benjamin, JD Berry, MJ Blaha, S Dai, ...
circulation 129 (3), e28-e292, 2014
42239*2014
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
47892011
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
2979*2013
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
CKDGen Consortium, KidneyGen Consortium, EchoGen consortium, ...
Nature 478 (7367), 103-109, 2011
23142011
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), 1308-1312, 2009
22182009
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
20242014
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
19132013
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
16672019
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
14512010
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
13362012
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
10382013
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
10232008
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
10132011
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
10062013
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
9842016
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 genetics 6 (5), e1000952, 2010
9042010
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
8502015
Epigenetic signatures of cigarette smoking
R Joehanes, AC Just, RE Marioni, LC Pilling, LM Reynolds, ...
Circulation: cardiovascular genetics 9 (5), 436-447, 2016
8212016
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
6912014
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), 699-705, 2011
6342011
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