Dena G. Hernandez

Alıntı yapanlar

	Hepsi	2020 yılından bugüne
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Genel erişim

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274 makale

3 makale

genel erişime açık olanlar

genel erişime açık olmayanlar

Finansman sağlayan kuruluşun getirdiği zorunluluğa dayalı olarak

Katkıda bulunan yazarlar

Andrew SingletonNational Institute on Agingmail.nih.gov üzerinde doğrulanmış e-posta adresine sahip
Mike A. NallsFounder/consultant with Data Tecnica International + Data science lead at NIH’s Center for Alzheimermail.nih.gov üzerinde doğrulanmış e-posta adresine sahip
Sonja W. ScholzNational Institute of Neurological Disorders and Strokenih.gov üzerinde doğrulanmış e-posta adresine sahip
Bryan TraynorLaboratory of Neurogenetics, National Institute on Agingmail.nih.gov üzerinde doğrulanmış e-posta adresine sahip
Javier Simón-SánchezHertie Institute for Clinical Brain Research (HIH)dzne.de üzerinde doğrulanmış e-posta adresine sahip
Jose BrasRegeneron Genetics Center, Regeneron Pharmaceuticalsregeneron.com üzerinde doğrulanmış e-posta adresine sahip
Rita GuerreiroVan Andel Research Institutevai.org üzerinde doğrulanmış e-posta adresine sahip
Allissa DillmanMontgomery Collegemontgomerycollege.edu üzerinde doğrulanmış e-posta adresine sahip
Coro Paisán RuizAssociate Professor, Icahn School of Medicine at Mount Sinaimssm.edu üzerinde doğrulanmış e-posta adresine sahip
Juan TroncosoProfessor of Pathology, Johns Hopkins University School of Medicinejhmi.edu üzerinde doğrulanmış e-posta adresine sahip
Daniah TrabzuniSenior research fellowucl.ac.uk üzerinde doğrulanmış e-posta adresine sahip
Marcel van der BrugGenentechgene.com üzerinde doğrulanmış e-posta adresine sahip
Dr Luke C PillingUniversity of Exeter Medical School, U.K.exeter.ac.uk üzerinde doğrulanmış e-posta adresine sahip
Vincent PlagnolChief Scientific Officer, Genomics plcgenomicsplc.com üzerinde doğrulanmış e-posta adresine sahip
Peter HeutinkIndependant consultant

Takip et

Dena G. Hernandez

National Institutes of Health, National Institute on Aging

mail.nih.gov üzerinde doğrulanmış e-posta adresine sahip

Genomics Neuroscience Disease


Başlık Alıntılara göre sırala Yıla göre sırala Başlığa göre sırala	Alıntı yapanlar Alıntı yapanlar	Yıl
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	39367*	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	5011	2011
Discovery and refinement of loci associated with lipid levels Nature genetics 45 (11), 1274-1283, 2013	3104	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	2361	2011
Genome-wide association study reveals genetic risk underlying Parkinson's disease J Simón-Sánchez, C Schulte, JM Bras, M Sharma, JR Gibbs, D Berg, ... Nature genetics 41 (12), 1308-1312, 2009	2260	2009
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	2078	2014
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	1968	2019
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	1937	2013
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	1496	2010
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	1403	2012
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	1064	2016
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	1060	2013
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	1041	2013
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	1039	2008
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	1029	2011
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	916	2010
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	897	2015
Epigenetic signatures of cigarette smoking R Joehanes, AC Just, RE Marioni, LC Pilling, LM Reynolds, ... Circulation: cardiovascular genetics 9 (5), 436-447, 2016	877	2016
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	721	2014
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), 8570, 2015	676	2015

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