About: Dena G. Hernandez

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

neurogeneticist

Attributes	Values
rdf:type	Item
owl:sameAs	Dena G. Hernandez
description	onderzoeker (nl) neurogeneticist (en)
rdfs:label	Dena G Hernandez (nl) Dena G Hernandez (ast) Dena G. Hernandez (en) Dena G. Hernandez (es) Dena G. Hernandez (pl)
skos:prefLabel	Dena G Hernandez (nl) Dena G Hernandez (ast) Dena G. Hernandez (en) Dena G. Hernandez (es) Dena G. Hernandez (pl)
name	Dena G Hernandez (nl) Dena G Hernandez (ast) Dena G. Hernandez (en) Dena G. Hernandez (es) Dena G. Hernandez (pl)
Scopus author ID	wds:Q64856786-b780bac9-4494-01c2-fcc5-6c932274b949
Scopus author ID	7201790697
instance of	wds:Q64856786-59F659BB-9F36-4975-9540-C8CF450905CF
instance of	Homo sapiens
Google Knowledge Graph ID	wds:Q64856786-D12E5AC6-A46B-4CC2-A938-80317567D148
Google Knowledge Graph ID	http://g.co/kg/g/11fyyvw47g
Google Knowledge Graph ID	/g/11fyyvw47g
Semantic Scholar author ID	wds:Q64856786-A9F44188-C1E6-4714-B11F-1713D37B91A7
Semantic Scholar author ID	48350971
Google Scholar author ID	wds:Q64856786-EBEF4A6F-B4DF-40B1-811A-2B2062DC5BE4
Google Scholar author ID	-c2qYqYAAAAJ
skos:altLabel	D. Hernandez (en) Deana G. Hernández (en) Dena G Hernandez (en) Dena Hernandez (en)
occupation	wds:Q64856786-5F5E0E1E-D08B-44C2-8869-2A4B8218802E
sex or gender	wds:Q64856786-A9B9D5DE-F671-4A6B-8B00-095EBAF9866F
educated at	wds:Q64856786-09A2FE74-3742-4AD4-BCF4-1DBFA652E4BE
family name	wds:Q64856786-8CFC3443-A480-459C-A1D9-35B139F6B114
occupation	neurogeneticist
sex or gender	female organism
educated at	University College London
family name	Hernandez
ORCID iD	wds:Q64856786-32B4B8F6-6230-4D57-919C-F1ED08D42C7C
ORCID iD	https://orcid.org/0000-0002-0188-9927
ORCID iD	0000-0002-0188-9927
ResearcherID	wds:Q64856786-ef42c217-440d-2495-2352-d3880840a53a
Publons author ID	wds:Q64856786-34803002-4e12-e102-355a-aec5fd0689af
ResearcherID	D-6405-2015
Publons author ID	2422241
is owl:sameAs of	Dena G. Hernandez
is about of	Dena G. Hernandez https://www.wikidata.org/wiki/Special:EntityData/Q64856786 Dena G. Hernandez
is author of	Rare coding variants in the phospholipase D3 gene confer risk for Alzheimer's disease A genome-wide genotyping study in patients with ischaemic stroke: initial analysis and data release Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes Allelic heterogeneity and more detailed analyses of known loci explain additional phenotypic variation and reveal complex patterns of association A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinson's disease The dardarin G 2019 S mutation is a common cause of Parkinson's disease but not other neurodegenerative diseases DNA methylation signatures of chronic low-grade inflammation are associated with complex diseases Genome-wide screen identifies rs646776 near sortilin as a regulator of progranulin levels in human plasma Genome-wide association study of white blood cell count in 16,388 African Americans: the continental origins and genetic epidemiology network (COGENT). Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data Genome-wide association study confirms extant PD risk loci among the Dutch Systematic identification of trans eQTLs as putative drivers of known disease associations A meta-analysis identifies new loci associated with body mass index in individuals of African ancestry Large proportion of amyotrophic lateral sclerosis cases in Sardinia due to a single founder mutation of the TARDBP gene Early-onset Parkinson's disease caused by a compound heterozygous DJ-1 mutation Structural genomic variation in ischemic stroke Splice mutation in the iron-sulfur cluster scaffold protein ISCU causes myopathy with exercise intolerance Identification and functional characterization of a novel R621C mutation in the synphilin-1 gene in Parkinson's disease Mutations in neurofilament genes are not a significant primary cause of non-SOD1-mediated amyotrophic lateral sclerosis. Clinical and positron emission tomography of Parkinson's disease caused by LRRK2. A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD Common genetic variation and susceptibility to partial epilepsies: a genome-wide association study Multiple loci are associated with white blood cell phenotypes Genomic variation in seven Khoe-San groups reveals adaptation and complex African history Abundant quantitative trait loci exist for DNA methylation and gene expression in human brain Common genetic variants influence human subcortical brain structures Mutations in TTBK2, encoding a kinase implicated in tau phosphorylation, segregate with spinocerebellar ataxia type 11. Multiple genetic loci influence serum urate levels and their relationship with gout and cardiovascular disease risk factors A 6.4 Mb duplication of the α-synuclein locus causing frontotemporal dementia and Parkinsonism: phenotype-genotype correlations Genomewide SNP assay reveals mutations underlying Parkinson disease Genetic comorbidities in Parkinson's disease Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data Deletion at ITPR1 underlies ataxia in mice and spinocerebellar ataxia 15 in humans Genome-wide SNP assay reveals structural genomic variation, extended homozygosity and cell-line induced alterations in normal individuals Genotype, haplotype and copy-number variation in worldwide human populations Common variants associated with plasma triglycerides and risk for coronary artery disease Discovery and refinement of loci associated with lipid levels Common variants at 19p13 are associated with susceptibility to ovarian cancer Association of vitamin D status with arterial blood pressure and hypertension risk: a mendelian randomisation study Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis Kinesin-associated protein 3 (KIFAP3) has no effect on survival in a population-based cohort of ALS patients Identification of a common variant in the TFR2 gene implicated in the physiological regulation of serum iron levels A genome-wide association study of sporadic ALS in a homogenous Irish population. Habitual sleep duration is associated with BMI and macronutrient intake and may be modified by CLOCK genetic variants

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