Dena G. Hernandez
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Neurogeneticist
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Genetics
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Biology
Dena G. Hernandez's Degrees
- PhD Neuroscience Stanford University
Why Is Dena G. Hernandez Influential?
(Suggest an Edit or Addition)According to Wikipedia, Dena Michelle Godwin Hernandez is a neurogeneticist. She is head of the genomic technologies group in the laboratory of neurogenetics at the National Institute on Aging. Hernandez completed a Ph.D. at the UCL Queen Square Institute of Neurology in 2016. Her dissertation was titled Genetic variation and DNA methylation in the context of neurological disease. Hernandez's doctoral advisors were Andrew Singleton and John Hardy.
Dena G. Hernandez's Published Works
Number of citations in a given year to any of this author's works
Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author
Published Works
- A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD (2011) (3746)
- Discovery and Refinement of Loci Associated with Lipid Levels (2013) (2475)
- Genetic Variants in Novel Pathways Influence Blood Pressure and Cardiovascular Disease Risk (2011) (1928)
- Genome-Wide Association Study reveals genetic risk underlying Parkinson’s disease (2009) (1770)
- Systematic identification of trans eQTLs as putative drivers of known disease associations (2013) (1593)
- Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson’s disease (2014) (1591)
- Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study (2012) (1007)
- Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies (2011) (873)
- Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies (2019) (871)
- Genotype, haplotype and copy-number variation in worldwide human populations (2008) (866)
- GWAS of 126,559 Individuals Identifies Genetic Variants Associated with Educational Attainment (2013) (803)
- Abundant Quantitative Trait Loci Exist for DNA Methylation and Gene Expression in Human Brain (2010) (794)
- Common variants associated with plasma triglycerides and risk for coronary artery disease (2013) (767)
- Exome Sequencing Reveals VCP Mutations as a Cause of Familial ALS (2011) (763)
- Common genetic variants influence human subcortical brain structures (2015) (731)
- DNA methylation-based measures of biological age: meta-analysis predicting time to death (2016) (699)
- Epigenetic Signatures of Cigarette Smoking (2016) (574)
- Exome Sequencing Reveals VCP Mutations as a Cause of Familial ALS (2010) (548)
- The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study (2015) (532)
- Lewy bodies and parkinsonism in families with parkin mutations (2001) (488)
- Identification of common variants influencing risk of the tauopathy Progressive Supranuclear Palsy (2011) (481)
- Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies (2010) (477)
- Characterization of PLA2G6 as a locus for dystonia‐parkinsonism (2008) (466)
- A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs) (2008) (460)
- Genetic screening for a single common LRRK2 mutation in familial Parkinson's disease (2005) (459)
- The transcriptional landscape of age in human peripheral blood (2015) (450)
- Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure (2011) (424)
- Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes. (2008) (424)
- Rare coding variants in the phospholipase D3 gene confer risk for Alzheimer’s disease (2013) (418)
- Genome-wide Analyses Identify KIF5A as a Novel ALS Gene (2018) (414)
- Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data (2006) (412)
- Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function (2016) (388)
- Genetics in Parkinson disease: Mendelian versus non‐Mendelian inheritance (2016) (374)
- Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium (2009) (369)
- Genomic Variation in Seven Khoe-San Groups Reveals Adaptation and Complex African History (2012) (369)
- Distinct DNA methylation changes highly correlated with chronological age in the human brain. (2011) (360)
- A genome-wide association study identifies susceptibility loci for ovarian cancer at 2q31 and 8q24 (2010) (341)
- α-synuclein gene haplotypes are associated with Parkinson’s disease (2001) (334)
- Multiple Genetic Loci Influence Serum Urate Levels and Their Relationship With Gout and Cardiovascular Disease Risk Factors (2010) (323)
- Association of vitamin D status with arterial blood pressure and hypertension risk: a mendelian randomisation study (2014) (318)
- Menopause accelerates biological aging (2016) (295)
- Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy. (2016) (292)
- A Two-Stage Meta-Analysis Identifies Several New Loci for Parkinson's Disease (2011) (278)
- Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study (2010) (278)
- Excessive burden of lysosomal storage disorder gene variants in Parkinson’s disease (2017) (278)
- Deletion at ITPR1 Underlies Ataxia in Mice and Spinocerebellar Ataxia 15 in Humans (2007) (272)
- Correction: Corrigendum: Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis (2015) (268)
- Frontotemporal dementia and its subtypes: a genome-wide association study (2014) (262)
- Common variants at 19p13 are associated with susceptibility to ovarian cancer (2010) (262)
- Genome-wide SNP assay reveals structural genomic variation, extended homozygosity and cell-line induced alterations in normal individuals. (2007) (249)
- A Meta-Analysis Identifies New Loci Associated with Body Mass index in Individuals of African Ancestry (2013) (244)
- New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk (2016) (242)
- Novel genetic loci associated with hippocampal volume (2017) (238)
- Early‐onset Parkinson's disease caused by a compound heterozygous DJ‐1 mutation (2003) (237)
- A DNA methylation biomarker of alcohol consumption (2016) (236)
- Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data (2007) (233)
- Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders. (2018) (221)
- Human aging is characterized by focused changes in gene expression and deregulation of alternative splicing (2011) (218)
- DNA methylation signatures of chronic low-grade inflammation are associated with complex diseases (2016) (215)
- CUBN is a gene locus for albuminuria. (2011) (214)
- A genome-wide genotyping study in patients with ischaemic stroke: initial analysis and data release (2007) (207)
- A genome-wide association study of sporadic ALS in a homogenous Irish population. (2007) (199)
- DYT16, a novel young-onset dystonia-parkinsonism disorder: identification of a segregating mutation in the stress-response protein PRKRA (2008) (196)
- Splice mutation in the iron-sulfur cluster scaffold protein ISCU causes myopathy with exercise intolerance. (2008) (195)
- Novel genetic loci underlying human intracranial volume identified through genome-wide association (2016) (192)
- Parkinson's disease age at onset genome‐wide association study: Defining heritability, genetic loci, and α‐synuclein mechanisms (2019) (189)
- Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource study (2011) (185)
- Genome-wide Pleiotropy Between Parkinson Disease and Autoimmune Diseases (2017) (185)
- Genetic analysis implicates APOE, SNCA and suggests lysosomal dysfunction in the etiology of dementia with Lewy bodies (2014) (185)
- MAPT expression and splicing is differentially regulated by brain region: relation to genotype and implication for tauopathies (2012) (176)
- Genome-wide association study confirms extant PD risk loci among the Dutch (2011) (175)
- Mutations in TTBK2, encoding a kinase implicated in tau phosphorylation, segregate with spinocerebellar ataxia type 11 (2007) (173)
- Diagnosis of Parkinson's disease on the basis of clinical and genetic classification: a population-based modelling study (2015) (172)
- Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis (2014) (170)
- Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease. (2013) (169)
- alpha-Synuclein gene haplotypes are associated with Parkinson's disease. (2001) (164)
- Investigating the genetic architecture of dementia with Lewy bodies: a two-stage genome-wide association study (2018) (163)
- DNA Methylation of Lipid-Related Genes Affects Blood Lipid Levels (2015) (153)
- Genome-wide physical activity interactions in adiposity ― A meta-analysis of 200,452 adults (2017) (153)
- Common genetic variation and susceptibility to partial epilepsies: a genome-wide association study (2010) (152)
- Identification and functional characterization of a novel R621C mutation in the synphilin-1 gene in Parkinson's disease. (2003) (150)
- Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits (2017) (149)
- Genome-wide meta-analysis uncovers novel loci influencing circulating leptin levels (2016) (147)
- A meta-analysis of four genome-wide association studies of survival to age 90 years or older: the Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium. (2010) (139)
- Genome-Wide Association Study of White Blood Cell Count in 16,388 African Americans: the Continental Origins and Genetic Epidemiology Network (COGENT) (2011) (136)
- A common variation in deiodinase 1 gene DIO1 is associated with the relative levels of free thyroxine and triiodothyronine. (2008) (134)
- A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis. (2009) (133)
- Meta-Analysis of Genome-Wide Association Studies Identifies Six New Loci for Serum Calcium Concentrations (2013) (130)
- Genome-wide screen identifies rs646776 near sortilin as a regulator of progranulin levels in human plasma. (2010) (129)
- Integration of GWAS SNPs and tissue specific expression profiling reveal discrete eQTLs for human traits in blood and brain (2012) (126)
- A genome-wide association study of myasthenia gravis. (2015) (124)
- Multiple Loci Are Associated with White Blood Cell Phenotypes (2011) (123)
- Large proportion of amyotrophic lateral sclerosis cases in Sardinia due to a single founder mutation of the TARDBP gene. (2011) (116)
- Clinical and positron emission tomography of Parkinson's disease caused by LRRK2 (2005) (115)
- Exome sequencing reveals riboflavin transporter mutations as a cause of motor neuron disease. (2012) (114)
- Mutations in GBA2 cause autosomal-recessive cerebellar ataxia with spasticity. (2013) (112)
- A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinson's disease. (2013) (112)
- Contribution of APOE promoter polymorphisms to Alzheimer’s disease risk (2002) (112)
- Genome-Wide Meta-Analysis for Serum Calcium Identifies Significantly Associated SNPs near the Calcium-Sensing Receptor (CASR) Gene (2010) (110)
- A Meta-analysis of Gene Expression Signatures of Blood Pressure and Hypertension (2015) (108)
- Genome-wide meta-analyses of smoking behaviors in African Americans (2012) (106)
- Cell Specific eQTL Analysis without Sorting Cells (2014) (105)
- NeuroX, a fast and efficient genotyping platform for investigation of neurodegenerative diseases (2015) (104)
- Novel Loci Associated with Usual Sleep Duration: The CHARGE Consortium Genome-Wide Association Study (2014) (104)
- Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture (2021) (99)
- Blood Leukocyte DNA Methylation Predicts Risk of Future Myocardial Infarction and Coronary Heart Disease. (2019) (99)
- Familial frontotemporal dementia with amyotrophic lateral sclerosis and a shared haplotype on chromosome 9p (2011) (98)
- Habitual sleep duration is associated with BMI and macronutrient intake and may be modified by CLOCK genetic variants. (2015) (98)
- 52 Genetic Loci Influencing Myocardial Mass. (2016) (98)
- Shared polygenic risk and causal inferences in amyotrophic lateral sclerosis (2019) (98)
- Genomewide association study of Parkinson's disease clinical biomarkers in 12 longitudinal patients' cohorts (2019) (97)
- The dardarin G2019S mutation is a common cause of Parkinson's disease but not other neurodegenerative diseases (2005) (96)
- Expanding Parkinson’s disease genetics: novel risk loci, genomic context, causal insights and heritable risk (2018) (94)
- Genetic modifiers of risk and age at onset in GBA associated Parkinson's disease and Lewy body dementia. (2019) (92)
- NeuroChip, an updated version of the NeuroX genotyping platform to rapidly screen for variants associated with neurological diseases (2017) (92)
- Phenomenology of “Lubag” or X‐linked dystonia–parkinsonism (2002) (86)
- Discovery and functional prioritization of Parkinson’s disease candidate genes from large-scale whole exome sequencing (2017) (85)
- Identification, Replication, and Fine-Mapping of Loci Associated with Adult Height in Individuals of African Ancestry (2011) (83)
- Parkinson’s disease genetics: identifying novel risk loci, providing causal insights and improving estimates of heritable risk (2018) (81)
- Identification of evolutionarily conserved gene networks mediating neurodegenerative dementia. (2018) (81)
- Identification of Nine Novel Loci Associated with White Blood Cell Subtypes in a Japanese Population (2011) (80)
- Resolving the polymorphism-in-probe problem is critical for correct interpretation of expression QTL studies (2013) (79)
- Identification of a common variant in the TFR2 gene implicated in the physiological regulation of serum iron levels. (2011) (79)
- Causal Effect of Plasminogen Activator Inhibitor Type 1 on Coronary Heart Disease (2017) (78)
- Allelic heterogeneity and more detailed analyses of known loci explain additional phenotypic variation and reveal complex patterns of association (2011) (76)
- A meta-analysis of 120 246 individuals identifies 18 new loci for fibrinogen concentration. (2016) (75)
- A whole-blood transcriptome meta-analysis identifies gene expression signatures of cigarette smoking. (2016) (75)
- Genome-wide analysis of genetic correlation in dementia with Lewy bodies, Parkinson's and Alzheimer's diseases (2016) (74)
- Ethnic differences in the expression of neurodegenerative disease: Machado‐Joseph disease in Africans and Caucasians (2002) (73)
- Alzheimer Risk Variant CLU and Brain Function During Aging (2013) (71)
- Genetic comorbidities in Parkinson's disease. (2014) (67)
- Analysis of genome-wide association studies of Alzheimer disease and of Parkinson disease to determine if these 2 diseases share a common genetic risk. (2013) (63)
- Meta-analysis of epigenome-wide association studies of cognitive abilities (2018) (62)
- Baseline genetic associations in the Parkinson's Progression Markers Initiative (PPMI) (2016) (61)
- Frequency of Loss of Function Variants in LRRK2 in Parkinson Disease (2018) (61)
- Another explanation for apparent epistasis (2014) (60)
- SCA15 due to large ITPR1 deletions in a cohort of 333 white families with dominant ataxia. (2011) (60)
- Genomewide SNP assay reveals mutations underlying Parkinson disease (2008) (60)
- Genetic variation associated with circulating monocyte count in the eMERGE Network. (2013) (59)
- Imputation of Variants from the 1000 Genomes Project Modestly Improves Known Associations and Can Identify Low-frequency Variant - Phenotype Associations Undetected by HapMap Based Imputation (2013) (58)
- A duplication at chromosome 11q12.2–11q12.3 is associated with spinocerebellar ataxia type 20 (2008) (58)
- A 6.4 Mb duplication of the α-synuclein locus causing frontotemporal dementia and Parkinsonism: phenotype-genotype correlations. (2014) (58)
- Advancing age is associated with gene expression changes resembling mTOR inhibition: Evidence from two human populations (2012) (57)
- Next-generation sequencing reveals substantial genetic contribution to dementia with Lewy bodies (2016) (57)
- Case‐control study of the extended tau gene haplotype in Parkinson's disease (2001) (55)
- Genome-wide meta-analysis of macronutrient intake of 91,114 European ancestry participants from the cohorts for heart and aging research in genomic epidemiology consortium (2018) (54)
- Fine-Mapping, Gene Expression and Splicing Analysis of the Disease Associated LRRK2 Locus (2013) (53)
- Genetic risk of Parkinson disease and progression: (2019) (53)
- Lack of G2019S LRRK2 mutation in a cohort of Taiwanese with sporadic Parkinson's disease (2006) (52)
- Large-scale pathway specific polygenic risk and transcriptomic community network analysis identifies novel functional pathways in Parkinson disease (2020) (51)
- Initial Assessment of the Pathogenic Mechanisms of the Recently Identified Alzheimer Risk Loci (2013) (49)
- Use of support vector machines for disease risk prediction in genome‐wide association studies: Concerns and opportunities (2012) (48)
- Genetic modifiers of risk and age at onset in GBA associated Parkinson’s disease and Lewy body dementia (2019) (47)
- Principal-component analysis for assessment of population stratification in mitochondrial medical genetics. (2010) (46)
- Novel age-associated DNA methylation changes and epigenetic age acceleration in middle-aged African Americans and whites (2019) (46)
- Towards a gene expression biomarker set for human biological age (2013) (46)
- Gene-Environment Interactions of Circadian-Related Genes for Cardiometabolic Traits (2015) (45)
- A rare loss-of-function variant of ADAM17 is associated with late-onset familial Alzheimer disease (2018) (45)
- Genetics of early-onset Parkinson's disease in Finland: exome sequencing and genome-wide association study (2017) (43)
- A dominant mutation in FBXO38 causes distal spinal muscular atrophy with calf predominance. (2013) (43)
- An exploratory analysis on gene-environment interactions for Parkinson disease (2012) (43)
- Genome-wide estimate of the heritability of Multiple System Atrophy. (2016) (43)
- Kinesin-associated protein 3 (KIFAP3) has no effect on survival in a population-based cohort of ALS patients (2010) (42)
- Analysis of SCA-2 and SCA-3 repeats in Parkinsonism: Evidence of SCA-2 expansion in a family with autosomal dominant Parkinson's disease (2005) (41)
- Pathogenic Huntingtin Repeat Expansions in Patients with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis (2020) (40)
- Whole‐exome sequencing of the BDR cohort: evidence to support the role of the PILRA gene in Alzheimer's disease (2018) (39)
- Differences in the Presentation and Progression of Parkinson's Disease by Sex (2020) (39)
- Structural genomic variation in ischemic stroke (2008) (38)
- Mutations in neurofilament genes are not a significant primary cause of non-SOD1-mediated amyotrophic lateral sclerosis (2006) (38)
- Exome sequencing in an SCA14 family demonstrates its utility in diagnosing heterogeneous diseases (2012) (38)
- Correction: The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study (2016) (37)
- Association of dietary folate and vitamin B-12 intake with genome-wide DNA methylation in blood: a large-scale epigenome-wide association analysis in 5841 individuals. (2019) (36)
- Are Myocardial Infarction–Associated Single-Nucleotide Polymorphisms Associated With Ischemic Stroke? (2012) (35)
- Siblings With Ischemic Stroke Study: Results of a Genome-Wide Scan for Stroke Loci (2011) (35)
- Change in Epigenome-Wide DNA Methylation Over 9 Years and Subsequent Mortality: Results From the InCHIANTI Study. (2016) (35)
- Dairy Consumption and Body Mass Index Among Adults: Mendelian Randomization Analysis of 184802 Individuals from 25 Studies. (2018) (34)
- Transcriptomic profiling of the human brain reveals that altered synaptic gene expression is associated with chronological aging (2017) (33)
- Race-specific alterations in DNA methylation among middle-aged African Americans and Whites with metabolic syndrome (2019) (32)
- Genome Wide Assessment of Young Onset Parkinson’s Disease from Finland (2012) (32)
- Leukocyte CCR2 expression is associated with mini-mental state examination score in older adults. (2012) (31)
- Accelerating Medicines Partnership: Parkinson's Disease. Genetic Resource (2020) (31)
- Penetrance of Parkinson's Disease in LRRK2 p.G2019S Carriers Is Modified by a Polygenic Risk Score (2020) (31)
- A C6orf10/LOC101929163 locus is associated with age of onset in C9orf72 carriers (2018) (30)
- A C6orf10/LOC101929163 locus is associated with age of onset in C9orf72 carriers (2018) (30)
- X‐linked dystonia (“Lubag”) presenting predominantly with parkinsonism: A more benign phenotype? (2002) (29)
- Susceptible genes and disease mechanisms identified in frontotemporal dementia and frontotemporal dementia with Amyotrophic Lateral Sclerosis by DNA-methylation and GWAS (2017) (29)
- Interaction of methylation-related genetic variants with circulating fatty acids on plasma lipids: a meta-analysis of 7 studies and methylation analysis of 3 studies in the Cohorts for Heart and Aging Research in Genomic Epidemiology consortium. (2016) (29)
- Polygenic risk score in postmortem diagnosed sporadic early-onset Alzheimer's disease (2018) (28)
- Association of Methylation Signals With Incident Coronary Heart Disease in an Epigenome-Wide Assessment of Circulating Tumor Necrosis Factor &agr; (2018) (28)
- ApoE ϵ3‐haplotype modulates Alzheimer beta‐amyloid deposition in the brain (2002) (28)
- Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral Sclerosis (2021) (27)
- Genome-wide assessment of Parkinson's disease in a Southern Spanish population (2016) (27)
- Insufficient evidence for pathogenicity of SNCA His50Gln (H50Q) in Parkinson's disease (2017) (27)
- Coding variation in GBA explains the majority of the SYT11‐GBA Parkinson's disease GWAS locus (2018) (26)
- Neurofibrillary tau pathology modulated by genetic variation of α‐synuclein (2008) (26)
- Heritability and genetic variance of dementia with Lewy bodies (2018) (25)
- EIF4G1 mutations do not cause Parkinson's disease (2015) (25)
- The complex genetics of gait speed: genome-wide meta-analysis approach (2017) (25)
- Analysis of neurodegenerative disease-causing genes in dementia with Lewy bodies (2020) (25)
- Correction: Identification, Replication, and Fine-Mapping of Loci Associated with Adult Height in Individuals of African Ancestry (2011) (24)
- Comparison of HapMap and 1000 Genomes Reference Panels in a Large-Scale Genome-Wide Association Study (2017) (24)
- The Genetic Architecture of Parkinson Disease in Spain: Characterizing Population‐Specific Risk, Differential Haplotype Structures, and Providing Etiologic Insight (2019) (24)
- Normal localization of ΔF323-Y328 mutant torsinA in transfected human cells (2002) (23)
- A consanguineous Turkish family with early‐onset Parkinson's disease and an exon 4 parkin deletion (2004) (23)
- SLC25A46 Mutations Associated with Autosomal Recessive Cerebellar Ataxia in North African Families (2017) (22)
- Kohlschütter–Tönz Syndrome: Mutations in ROGDI and Evidence of Genetic Heterogeneity (2013) (22)
- Investigation of Autosomal Genetic Sex Differences in Parkinson's Disease (2021) (22)
- Whole blood gene expression and interleukin-6 levels. (2014) (22)
- Investigation of Autosomal Genetic Sex Differences in Parkinson's Disease (2021) (22)
- Assessment of Parkinson's disease risk loci in Greece (2014) (22)
- Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinsons disease (vol 22, pg 1696, 2013) (2013) (21)
- Mutation analysis of sporadic early-onset Alzheimer's disease using the NeuroX array (2017) (21)
- Assessment of a DJ-1 (PARK7) polymorphism in Finnish PD (2003) (21)
- Corrigendum to Using genome-wide complex trait analysis to quantify 'missing heritability' in parkinson's disease [Human Molecular Genetics, 21: 22 (2012) 4996-5009] doi: 10.1093/hmg/dds335] (2013) (21)
- Penetrance of Parkinson’s disease in LRRK2 p.G2019S carriers is modified by a polygenic risk score (2019) (21)
- Identification of sixteen novel candidate genes for late onset Parkinson’s disease (2021) (21)
- Genetic model of MS severity predicts future accumulation of disability (2020) (20)
- A candidate gene for autoimmune myasthenia gravis (2012) (20)
- APOE and AβPP gene variation in cortical and cerebrovascular amyloid-β pathology and Alzheimer's disease: a population-based analysis. (2011) (19)
- ApoE epsilon3-haplotype modulates Alzheimer beta-amyloid deposition in the brain. (2002) (17)
- Gene expression markers of age-related inflammation in two human cohorts (2015) (17)
- Peripheral Blood Transcriptomic Signatures of Fasting Glucose and Insulin Concentrations (2016) (17)
- A comprehensive screening of copy number variability in dementia with Lewy bodies (2019) (16)
- Genome-wide association meta-analysis of fish and EPA+DHA consumption in 17 US and European cohorts (2017) (16)
- Parkinson disease age of onset GWAS: defining heritability, genetic loci and a-synuclein mechanisms (2018) (16)
- Comprehensive promoter level expression quantitative trait loci analysis of the human frontal lobe (2016) (16)
- Assessment of APOE in atypical parkinsonism syndromes (2019) (16)
- Mutation at the SCA17 locus is not a common cause of parkinsonism. (2003) (16)
- Analysis of repeated leukocyte DNA methylation assessments reveals persistent epigenetic alterations after an incident myocardial infarction (2018) (16)
- Screening exons 16 and 17 of the amyloid precursor protein gene in sporadic early-onset Alzheimer's disease (2016) (16)
- Case‐control study of the α‐synuclein interacting protein gene and Parkinson's disease (2003) (15)
- Genomic Risk Profiling of Ischemic Stroke: Results of an International Genome-Wide Association Meta-Analysis (2011) (15)
- The genetic architecture of Parkinson disease in Spain: characterizing population-specific risk, differential haplotype structures, and providing etiologic insight (2019) (15)
- A comprehensive assessment of benign genetic variability for neurodegenerative disorders (2018) (15)
- Erratum: Mutations in TTBK2, encoding a kinase implicated in tau phosphorylation, segregate with spinocerebellar ataxia type 11 (2008) (15)
- Regulatory sites for splicing in human basal ganglia are enriched for disease-relevant information (2020) (14)
- Genetic variants associated with physical performance and anthropometry in old age: a genome-wide association study in the ilSIRENTE cohort (2017) (13)
- Genome-Wide Association Study Meta-Analysis for Parkinson Disease Motor Subtypes (2020) (13)
- LRP10 in α-synucleinopathies (2018) (13)
- Analysis of C9orf72 repeat expansions in a large international cohort of dementia with Lewy bodies (2017) (13)
- A candidate gene study of risk for dementia in older, postmenopausal women: Results from the Women's Health Initiative Memory Study (2019) (12)
- Gene transcripts associated with muscle strength: a CHARGE meta-analysis of 7,781 persons (2015) (12)
- DNA methylation signatures reveal that distinct combinations of transcription factors specify human immune cell epigenetic identity. (2021) (12)
- LRP10 in α-synucleinopathies (2018) (12)
- Case-control study of the alpha-synuclein interacting protein gene and Parkinson's disease. (2003) (11)
- Normal localization of deltaF323-Y328 mutant torsinA in transfected human cells. (2002) (11)
- ADORA1 mutations are not a common cause of Parkinson's disease and dementia with Lewy bodies (2017) (11)
- Blood DNA Methylation and Aging: A Cross-Sectional Analysis and Longitudinal Validation in the InCHIANTI Study. (2020) (11)
- Linkage and Association Analyses of Type 2 Diabetes/Impaired Glucose Metabolism and Adiponectin Serum Levels in Japanese Americans From Hawaii (2007) (10)
- Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry. (2021) (10)
- Correction: Genome-wide physical activity interactions in adiposity ― A meta-analysis of 200,452 adults (2017) (9)
- Using DNA Methylation to Understand Biological Consequences of Genetic Variability (2011) (9)
- Mendelian Randomisation Study of Smoking, Alcohol, and Coffee Drinking in Relation to Parkinson's Disease. (2021) (9)
- Whole-genome sequencing to understand the genetic architecture of common gene expression and biomarker phenotypes (2014) (9)
- The Parkinson's Disease DNA Variant Browser (2020) (9)
- Gene Expression Imputation Across Multiple Tissue Types Provides Insight Into the Genetic Architecture of Frontotemporal Dementia and Its Clinical Subtypes (2021) (8)
- Splicing factor 3B1 hypomethylation is associated with altered SF3B1 transcript expression in older humans (2014) (8)
- Using genome-Wwide complex trait analysis to quantify 'missing heritability' in Parkinson's disease (2012) (8)
- A 7.5‐Mb duplication at chromosome 11q21‐11q22.3 is associated with a novel spastic ataxia syndrome (2015) (8)
- Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into the complex genetic architecture (2020) (7)
- Erratum: A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinson's disease [Human Molecular Genetics 22, 5, 2013, 1039-1049] doi:10.1093/hmg/dds492 (2014) (7)
- Genome-wide physical activity interactions in adiposity ― A meta-analysis of 200,452 adults (2016) (7)
- X-linked dystonia ("Lubag") presenting predominantly with parkinsonism: A more benign phenotype? (2002) (6)
- Mutation of the Parkin gene in a Persian family: Clinical progression over a 40‐year period (2005) (6)
- A polymorphism in the GALNT2 gene and ovarian cancer risk in four population based case-control studies. (2010) (6)
- A Mendelian randomisation study provides initial evidence that sex hormone binding globulin (SHBG) levels alter type 2 diabetes risk (2008) (6)
- Finnish Parkinson’s disease study integrating protein-protein interaction network data with exome sequencing analysis (2019) (5)
- The Foundational data initiative for Parkinson’s disease (FOUNDIN-PD): enabling efficient translation from genetic maps to mechanism (2021) (5)
- X-linked recessive dystonia parkinsonism (XDP; Lubag; DYT3). (2004) (4)
- The reported healthy ageing gene expression score: lack of association in two cohorts (2015) (4)
- Correction: Corrigendum: Common variants at 19p13 are associated with susceptibility to ovarian cancer (2016) (4)
- Dairy Intake and Parkinson's Disease: A Mendelian Randomization Study (2022) (4)
- Genome-wide Association and Meta-analysis of Age at Onset in Parkinson Disease (2022) (4)
- A SINE-VNTR-Alu in the LRIG2 Promoter Is Associated with Gene Expression at the Locus (2020) (4)
- Heterozygous PRKN mutations are common but do not increase the risk of Parkinson's disease (2021) (4)
- High-resolution inference of genetic relationships among Jewish populations (2020) (4)
- Genome-wide association study of Parkinson’s disease progression biomarkers in 12 longitudinal patients’ cohorts (2019) (3)
- Human-lineage-specific genomic elements are associated with neurodegenerative disease and APOE transcript usage (2021) (3)
- Discovery and functional prioritization of Parkinson’s disease candidate genes from large-scale whole exome sequencing (2017) (3)
- Correction: The complex genetics of gait speed: Genome-wide metaanalysis approach [Aging, (Albany NY), 9, 1, (2017), (209-246)]doi 10.18632/aging.101151 (2017) (3)
- MIDN locus structural variants and Parkinson's Disease risk (2020) (3)
- Mendelian randomization implies no direct causal association between leukocyte telomere length and amyotrophic lateral sclerosis (2020) (3)
- Author Correction: Susceptible genes and disease mechanisms identified in frontotemporal dementia and frontotemporal dementia with Amyotrophic Lateral Sclerosis by DNA-methylation and GWAS (2018) (2)
- The Interaction between HLA‐DRB1 and Smoking in Parkinson's Disease Revisited (2022) (2)
- Alzheimer Risk Variant Clusterin (CLU) and Brain Function During Aging (2011) (2)
- Large-scale pathway-specific polygenic risk, transcriptomic community networks and functional inferences in Parkinson disease (2020) (2)
- Large-scale Rare Variant Burden Testing in Parkinson's Disease Identifies Novel Associations with Genes Involved in Neuro-inflammation (2022) (2)
- Genome‐Wide Analysis of Structural Variants in Parkinson Disease (2023) (1)
- Transcriptomic profiling of the human brain reveals that altered synaptic gene expression is associated with chronological aging (2017) (1)
- A CANDIDATE GENE STUDY OF GENETIC RISK FOR DEMENTIA AND MILD COGNITIVE IMPAIRMENT (MCI) IN WOMEN AGED >65 YEARS: RESULTS FROM THE WOMEN’S HEALTH INITIATIVE MEMORY STUDY (WHIMS) (2014) (1)
- Biomarkers of Parkinson's Disease: Screening Vital Signs and Routine Blood Tests (2020) (1)
- Immune-related genetic enrichment in frontotemporal dementia (2017) (1)
- PLA2G6 as a locus for adult-onset dystonia-parkinsonism (2008) (1)
- LONGITUDINAL ANALYSIS OF DNA METHYLATION IN THE INCHIANTI AGING STUDY (2018) (1)
- Comprehensive promoter level expression quantitative trait loci analysis of the human frontal lobe (2016) (1)
- Deletion at ITPR1 underlies ataxia in mice and humans (SCA15) (2005) (1)
- Identification and single-base gene-editing functional validation of a cis-EPO variant as a genetic predictor for EPO-increasing therapies (2022) (1)
- Genome-wide analysis of Structural Variants in Parkinson’s Disease using Short-Read Sequencing data (2022) (1)
- Profiling the NOTCH2NLC GGC Repeat Expansion in Parkinson's Disease in the European Population (2022) (1)
- An Exploratory Analysis on Gene-Environment Interactions for Parkinson Disease (PD4.003) (2012) (1)
- Discovery and Refinement Supplementary (2015) (1)
- APOE E4 is associated with impaired self-declared cognition but not disease risk or age of onset in Nigerians with Parkinson’s disease (2022) (1)
- Correction: The complex genetics of gait speed: genome-wide meta-analysis approach (2017) (1)
- Genetics of Parkinson’s Disease (2015) (1)
- Genetic Loci In fl uencing Myocardial Mass (2016) (1)
- Genome-wide physical activity interactions in adiposity (2017) (1)
- Association of hippocampal volume polygenic predictor score with baseline and change in brain volumes and cognition among cognitively healthy older adults (2020) (1)
- Ischemic Stroke? Associated Single-Nucleotide Polymorphisms Associated With - Are Myocardial Infarction (2012) (0)
- OP-BRAI180237 2895..2907 (2018) (0)
- CALCULATING POLYGENIC RISK FOR INDIVIDUALS WITH SPORADIC EARLY ONSET ALZHEIMER’S DISEASE (2017) (0)
- Genome-wide physical activity interactions in adiposity A meta-analysis of 200,452 adults Genome-wide physical activity interactions in adiposity ― A meta-analysis of 200,452 adults (2017) (0)
- Original Article A polymorphism in the GALNT2 gene and ovarian cancer risk in four population based case-control studies (2010) (0)
- CHARGE meta-analysis of 7,781 persons Gene transcripts associated with muscle strength: a (2016) (0)
- Investigating the genetic architecture of Dementia with Lewy bodies: a genome-wide association study (2018) (0)
- Edinburgh Research Explorer Genetic risk of Parkinson disease and progression: (0)
- DNA methylation signatures of chronic low-grade inflammation are associated with complex diseases (2016) (0)
- [P3–107]: WITHDRAWN (2017) (0)
- EXOME SEQUENCING AS A RAPID AND COST EFFICIENT DIAGNOSTIC METHOD IN NEUROGENETIC DISORDERS (2011) (0)
- Unique and shared molecular features of human B and T lymphocyte memory differentiation (2022) (0)
- Tau tubulin kinase 2, implicated by tau phosphorylation, contains mutations that segregate with spinocerebellar ataxia type II (2008) (0)
- Polygenic Parkinson's disease genetic risk score as risk modifier of parkinsonism in Gaucher disease (2022) (0)
- Identification of a sex-specific genetic signature in dementia with Lewy bodies: a meta-analysis of genome-wide association studies (2022) (0)
- A candidate genes study of structural and functional brain aging in the Baltimore Longitudinal Study of Aging (2011) (0)
- Polygenic risk score in post-mortem diagnosed sporadic early onset Alzheimer’s disease (2017) (0)
- Front & Back Matter (2012) (0)
- Gastrectomy and Nigrostriatal Dopaminergic Depletion in De Novo Parkinson’s Disease (2019) (0)
- LINKING POLYGENIC RISK SCORES TO ALZHEIMER'S DISEASE GENES (2018) (0)
- Regulatory sites for splicing in human basal ganglia are enriched for disease-relevant information (2020) (0)
- Genetic variants associated with physical performance and anthropometry in old age: a genome-wide association study in the ilSIRENTE cohort (2017) (0)
- Analysis of repeated leukocyte DNA methylation assessments reveals persistent epigenetic alterations after an incident myocardial infarction (2018) (0)
- Genome-wide association analysis of Dementia with Lewy bodies reveals unique genetic architecture (2017) (0)
- A polymorphism in the GALNT 2 gene and ovarian cancer risk in four population based case-control studies (2011) (0)
- VKučinskas-2001-2016 (2016) (0)
- Genetic variation and DNA methylation in the context of neurological disease (2016) (0)
- Erratum: Author Correction: Susceptible genes and disease mechanisms identified in frontotemporal dementia and frontotemporal dementia with Amyotrophic Lateral Sclerosis by DNA-methylation and GWAS (Scientific reports (2017) 7 1 (8899)) (2018) (0)
- High-resolution inference of genetic relationships among Jewish populations (2020) (0)
- MAPT allele and haplotype frequencies in Nigerian Africans: population distribution and association with Parkinson’s disease risk and age at onset (2023) (0)
- AGenome-Wide Association Study ofMyasthenia Gravis (2015) (0)
- Epigenetic signature of human immune aging: the GESTALT study (2023) (0)
- Genome-wide Analyses Id entify KIF 5 A as a Novel ALS Gene Highlights (2018) (0)
- Running Title: Whole-exome sequencing of the BDR cohort: Evidence to support the role of the PILRA gene in Alzheimer’s disease (2017) (0)
- Identifying likely causal connections between gene expression levels using a Mendelian randomization approach (2011) (0)
- WITHDRAWN: Familial Degenerative Encephalopathy with Intracranial Calcification and Metaphyseal Dysplasia. (2008) (0)
- Ameta-analysis of 120 246 individuals identi fi es 18 new loci for fi brinogen concentration (2016) (0)
- Correction to: A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer’s disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity (2020) (0)
- A paradoxical relationship between family history, onset age, and genetic risk in Parkinson's disease (2018) (0)
- Analysis of neurodegenerative disease-causing genes in dementia with Lewy bodies (2020) (0)
- Investigation of Shared Genetic Risk Factors Between Parkinson's Disease and Cancers (2023) (0)
- Heterozygous PRKN mutations are common but do not increase the risk of Parkinson's disease. (2022) (0)
- Genome-wide Association and Meta-analysis of Age at Onset in Parkinson Disease (2022) (0)
- Methylomic and whole transcriptome analyses reveal several potential modifier genes in GBA1-associated Parkinson disease (2019) (0)
- Moving beyond neurons: the role of cell type-specific gene regulation in Parkinson’s disease heritability (2019) (0)
- A response to: A novel multi-tissue RNA diagnostic of healthy ageing relates to (2015) (0)
- Title : Polygenic risk score in post-mortem diagnosed sporadic early onset Alzheimer ’ s disease (2018) (0)
- Novel age-associated DNA methylation changes and epigenetic age acceleration in middle-aged African Americans and whites (2019) (0)
- Association of vitamin D status with arterial blood pressure and hypertension risk: A mendelian randomisation study (2014) (0)
- The Foundational Data Initiative for Parkinson Disease: Enabling efficient translation from genetic maps to mechanism (2023) (0)
- Mitochondria function associated genes contribute to Parkinson’s Disease risk and later age at onset (2019) (0)
- DNA methylation signatures reveal that distinct combinations of transcription factors specify human immune cell epigenetic identity. (2022) (0)
- Genome-wide DNA methylation analysis reveals several loci important for blood lipid levels (2015) (0)
- Identification of evolutionarily conserved gene networks mediating neurodegenerative dementia (2018) (0)
- APOE gene region methylation is associated with cognitive performance in middle-aged urban adults (2022) (0)
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