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Lista de obras de Dena G. Hernandez

35th Annual Meeting of the European Association for the Study of Diabetes

artículo científico

35th Annual Meeting of the European Association for the Study of Diabetes : Brussels, Belgium, 28 September-2 October 1999

article

52 Genetic Loci Influencing Myocardial Mass

artículo científico publicado en 2016

A 6.4 Mb duplication of the α-synuclein locus causing frontotemporal dementia and Parkinsonism: phenotype-genotype correlations

artículo científico publicado en 2014

A 7.5-Mb duplication at chromosome 11q21-11q22.3 is associated with a novel spastic ataxia syndrome

artículo científico publicado en 2014

A C6orf10/LOC101929163 locus is associated with age of onset in C9orf72 carriers

A SINE-VNTR-Alu in the LRIG2 Promoter Is Associated with Gene Expression at the Locus

artículo científico publicado en 2020

A candidate gene for autoimmune myasthenia gravis ⬇️

artículo científico publicado el 27 de junio de 2012

A candidate gene study of risk for dementia in older, postmenopausal women: Results from the Women's Health Initiative Memory Study

scientific article published on 07 March 2019

A common variation in deiodinase 1 gene DIO1 is associated with the relative levels of free thyroxine and triiodothyronine

artículo científico publicado en 2008

A comprehensive screening of copy number variability in dementia with Lewy bodies

scientific article published on 24 October 2018

A consanguineous Turkish family with early-onset Parkinson's disease and an exon 4 parkin deletion

artículo científico publicado en 2004

A dominant mutation in FBXO38 causes distal spinal muscular atrophy with calf predominance

scientific journal article

A duplication at chromosome 11q12.2-11q12.3 is associated with spinocerebellar ataxia type 20

artículo científico publicado en 2008

A genome-wide association study identifies protein quantitative trait loci (pQTLs)

artículo científico publicado en 2008

A genome-wide association study identifies susceptibility loci for ovarian cancer at 2q31 and 8q24.

artículo científico publicado en 2010

A genome-wide association study of myasthenia gravis

artículo científico publicado en 2015

A genome-wide association study of sporadic ALS in a homogenous Irish population

artículo científico publicado en 2007

A genome-wide genotyping study in patients with ischaemic stroke: initial analysis and data release

artículo científico publicado en 2007

A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD

artículo científico publicado en 2011

A meta-analysis identifies new loci associated with body mass index in individuals of African ancestry

artículo científico publicado en 2013

A meta-analysis of 120 246 individuals identifies 18 new loci for fibrinogen concentration

artículo científico publicado en 2015

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

artículo científico publicado en 2010

A meta-analysis of gene expression signatures of blood pressure and hypertension

artículo científico publicado en 2015

A paradoxical relationship between family history, onset age, and genetic risk in Parkinson's disease

scholarly article by Madeleine Kristiansen et al published February 2019 in Movement Disorders

A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinson's disease

artículo científico publicado en 2012

A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinson's disease

artículo científico publicado en 2013

A polymorphism in the GALNT2 gene and ovarian cancer risk in four population based case-control studies

artículo científico publicado en 2010

A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis

artículo científico publicado en 2009

A whole-blood transcriptome meta-analysis identifies gene expression signatures of cigarette smoking

artículo científico publicado en 2016

ABSTRACTS

scholarly article

ADORA1 mutations are not a common cause of Parkinson's disease and dementia with Lewy bodies

artículo científico publicado en 2016

APOE and AβPP gene variation in cortical and cerebrovascular amyloid-β pathology and Alzheimer's disease: a population-based analysis

artículo científico publicado en 2011

Abundant quantitative trait loci exist for DNA methylation and gene expression in human brain

artículo científico publicado en 2010

Advancing age is associated with gene expression changes resembling mTOR inhibition: evidence from two human populations

scientific article published on 16 July 2012

Allelic heterogeneity and more detailed analyses of known loci explain additional phenotypic variation and reveal complex patterns of association

artículo científico publicado en 2011

Alzheimer risk variant CLU and brain function during aging

artículo científico publicado en 2012

An exploratory analysis on gene-environment interactions for Parkinson disease

artículo científico publicado en 2012

Analysis of C9orf72 repeat expansions in a large international cohort of dementia with Lewy bodies.

artículo científico publicado en 2016

Analysis of SCA-2 and SCA-3 repeats in Parkinsonism: evidence of SCA-2 expansion in a family with autosomal dominant Parkinson's disease

artículo científico publicado en 2005

Analysis of genome-wide association studies of Alzheimer disease and of Parkinson disease to determine if these 2 diseases share a common genetic risk

artículo científico publicado en 2013

Analysis of neurodegenerative disease-causing genes in dementia with Lewy bodies

scientific article published on 29 January 2020

Analysis of repeated leukocyte DNA methylation assessments reveals persistent epigenetic alterations after an incident myocardial infarction

Another explanation for apparent epistasis

artículo científico publicado en 2014

ApoE epsilon3-haplotype modulates Alzheimer beta-amyloid deposition in the brain

artículo científico publicado en 2002

Are myocardial infarction--associated single-nucleotide polymorphisms associated with ischemic stroke?

artículo científico publicado en 2012

Assessment of APOE in atypical parkinsonism syndromes

artículo científico publicado en 2019

Assessment of Parkinson's disease risk loci in Greece

scientific article published on 27 September 2013

Association of Methylation Signals With Incident Coronary Heart Disease in an Epigenome-Wide Assessment of Circulating Tumor Necrosis Factor α.

artículo científico publicado en 2018

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

scientific article published on 01 August 2019

Association of hippocampal volume polygenic predictor score with baseline and change in brain volumes and cognition among cognitively healthy older adults

artículo científico publicado en 2020

Association of vitamin D status with arterial blood pressure and hypertension risk: a mendelian randomisation study

artículo científico publicado en 2014

Baseline genetic associations in the Parkinson's Progression Markers Initiative (PPMI)

artículo científico publicado en 2016

Blood DNA Methylation and Aging: A Cross-Sectional Analysis and Longitudinal Validation in the InCHIANTI Study

artículo científico publicado en 2020

Blood Leukocyte DNA Methylation Predicts Risk of Future Myocardial Infarction and Coronary Heart Disease

scientific article published on 19 August 2019

CCAAT-enhancer-binding protein-beta expression in vivo is associated with muscle strength

artículo científico publicado en 2012

CUBN is a gene locus for albuminuria

artículo científico publicado en 2011

Canine hereditary ataxia in old english sheepdogs and gordon setters is associated with a defect in the autophagy gene encoding RAB24

artículo científico publicado en 2014

Case-control study of the ?-synuclein interacting protein gene and Parkinson's disease

article

Case-control study of the extended tau gene haplotype in Parkinson's disease

article

Cell Specific eQTL Analysis without Sorting Cells

artículo científico publicado en 2015

Cell specific eQTL analysis without sorting cells

Change in Epigenome-Wide DNA Methylation Over 9 Years and Subsequent Mortality: Results From the InCHIANTI Study

artículo científico publicado en 2015

Characterization of PLA2G6 as a locus for dystonia-parkinsonism

artículo científico publicado en 2009

Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study

artículo científico publicado en 2010

Clinical and positron emission tomography of Parkinson's disease caused by LRRK2.

artículo científico publicado en 2005

Coding variation in GBA explains the majority of the SYT11-GBA Parkinson's disease GWAS locus

artículo científico publicado en 2018

Common genetic variants influence human subcortical brain structures

artículo científico publicado en 2015

Common genetic variation and susceptibility to partial epilepsies: a genome-wide association study

scientific journal article

Common variants associated with plasma triglycerides and risk for coronary artery disease

artículo científico publicado en 2013

Common variants at 19p13 are associated with susceptibility to ovarian cancer

artículo científico publicado en 2010

Comparison of HapMap and 1000 Genomes Reference Panels in a Large-Scale Genome-Wide Association Study

artículo científico publicado en 2017

Comprehensive promoter level expression quantitative trait loci analysis of the human frontal lobe

artículo científico publicado en 2016

Correction: Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults

artículo científico publicado en 2017

Correction: Identification, Replication, and Fine-Mapping of Loci Associated with Adult Height in Individuals of African Ancestry.

artículo científico publicado en 2011

Correction: The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study

artículo científico publicado en 2016

Correction: The complex genetics of gait speed: genome-wide meta-analysis approach

artículo científico publicado en 2017

Corrigendum: Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis

artículo científico publicado en 2015

DNA methylation of lipid-related genes affects blood lipid levels

scientific article published on 12 January 2015

DNA methylation signatures of chronic low-grade inflammation are associated with complex diseases

artículo científico publicado en 2016

DNA methylation-based measures of biological age: meta-analysis predicting time to death

artículo científico publicado en 2016

DYT16, a novel young-onset dystonia-parkinsonism disorder: identification of a segregating mutation in the stress-response protein PRKRA

artículo científico publicado en 2008

Deletion at ITPR1 underlies ataxia in mice and humans (SCA15)

Deletion at ITPR1 underlies ataxia in mice and spinocerebellar ataxia 15 in humans

artículo científico publicado en 2007

Diagnosis of Parkinson's disease on the basis of clinical and genetic classification: a population-based modelling study

artículo científico publicado en 2015

Differences in the Presentation and Progression of Parkinson's Disease by Sex

artículo científico publicado en 2020

Discovery and refinement of loci associated with lipid levels

artículo científico publicado en 2013

Distinct DNA methylation changes highly correlated with chronological age in the human brain

artículo científico publicado en 2011

EIF4G1 mutations do not cause Parkinson's disease

artículo científico publicado en 2015

Early-onset Parkinson's disease caused by a compound heterozygous DJ-1 mutation

article

Epigenetic Signatures of Cigarette Smoking

artículo científico publicado en 2016

Erratum: Corrigendum: Common variants at 19p13 are associated with susceptibility to ovarian cancer

scholarly article published in Nature Genetics

Erratum: Mutations in TTBK2, encoding a kinase implicated in tau phosphorylation, segregate with spinocerebellar ataxia type 11

scholarly article published in Nature Genetics

Ethnic differences in the expression of neurodegenerative disease: Machado-Joseph disease in Africans and Caucasians

artículo científico publicado en 2002

Exome Sequencing Reveals VCP Mutations as a Cause of Familial ALS

Exome sequencing in an SCA14 family demonstrates its utility in diagnosing heterogeneous diseases

artículo científico publicado en 2012

Exome sequencing reveals VCP mutations as a cause of familial ALS

artículo científico publicado en 2010

Exome sequencing reveals riboflavin transporter mutations as a cause of motor neuron disease

artículo científico publicado en 2012

Familial frontotemporal dementia with amyotrophic lateral sclerosis and a shared haplotype on chromosome 9p

artículo científico publicado en 2010

Fine-mapping, gene expression and splicing analysis of the disease associated LRRK2 locus

artículo científico publicado en 2013

Finnish Parkinson's disease study integrating protein-protein interaction network data with exome sequencing analysis

scientific article published on 11 December 2019

Frequency of Loss of Function Variants in LRRK2 in Parkinson Disease

artículo científico publicado en 2018

Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study

artículo científico publicado en 2012

Frontotemporal dementia and its subtypes: a genome-wide association study

artículo científico publicado en 2014

GWAS of 126,559 individuals identifies genetic variants associated with educational attainment

artículo científico publicado en 2013

Gene expression markers of age-related inflammation in two human cohorts

artículo científico publicado en 2015

Gene transcripts associated with muscle strength: a CHARGE meta-analysis of 7,781 persons

artículo científico publicado en 2015

Genetic analysis implicates APOE, SNCA and suggests lysosomal dysfunction in the etiology of dementia with Lewy bodies.

artículo científico publicado en 2014

Genetic comorbidities in Parkinson's disease

artículo científico publicado en 2013

Genetic modifiers of risk and age at onset in GBA associated Parkinson's disease and Lewy body dementia

artículo científico publicado en 2020

Genetic risk of Parkinson disease and progression:: An analysis of 13 longitudinal cohorts

artículo científico publicado en 2019

Genetic screening for a single common LRRK2 mutation in familial Parkinson's disease

artículo científico publicado en 2005

Genetic variants associated with physical performance and anthropometry in old age: a genome-wide association study in the ilSIRENTE cohort

artículo científico publicado en 2017

Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk

artículo científico publicado en 2011

Genetic variation associated with circulating monocyte count in the eMERGE Network

artículo científico publicado en 2013

Genetics in Parkinson disease: Mendelian versus non-Mendelian inheritance

artículo científico publicado en 2016

Genetics of early-onset Parkinson's disease in Finland: exome sequencing and genome-wide association study

artículo científico publicado en 2017

Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders

artículo científico publicado en 2018

Genome wide assessment of young onset Parkinson's disease from Finland

artículo científico publicado en 2012

Genome-wide Analyses Identify KIF5A as a Novel ALS Gene

artículo científico publicado en 2018

Genome-wide Pleiotropy Between Parkinson Disease and Autoimmune Diseases

artículo científico publicado en 2017

Genome-wide SNP assay reveals structural genomic variation, extended homozygosity and cell-line induced alterations in normal individuals

artículo científico publicado en 2006

Genome-wide analysis of genetic correlation in dementia with Lewy bodies, Parkinson's and Alzheimer's diseases

artículo científico publicado en 2015

Genome-wide assessment of Parkinson's disease in a Southern Spanish population

artículo científico publicado en 2016

Genome-wide association meta-analysis of fish and EPA+DHA consumption in 17 US and European cohorts.

artículo científico publicado en 2017

Genome-wide association study confirms extant PD risk loci among the Dutch

artículo científico publicado en 2011

Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure

artículo científico publicado en 2011

Genome-wide association study of white blood cell count in 16,388 African Americans: the continental origins and genetic epidemiology network (COGENT).

artículo científico publicado en 2011

Genome-wide association study reveals genetic risk underlying Parkinson's disease

artículo científico publicado en 2009

Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data

scientific journal article

Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data

scientific journal article

Genome-wide meta-analyses of smoking behaviors in African Americans

artículo científico publicado en 2012

Genome-wide meta-analysis for serum calcium identifies significantly associated SNPs near the calcium-sensing receptor (CASR) gene

artículo científico publicado en 2010

Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits.

artículo científico publicado en 2017

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

artículo científico publicado en 2018

Genome-wide meta-analysis uncovers novel loci influencing circulating leptin levels

artículo científico publicado en 2016

Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults

artículo científico publicado en 2017

Genome-wide screen identifies rs646776 near sortilin as a regulator of progranulin levels in human plasma

artículo científico publicado en 2010

Genomewide SNP assay reveals mutations underlying Parkinson disease

scientific article published on 01 February 2008

Genomewide association study of Parkinson's disease clinical biomarkers in 12 longitudinal patients' cohorts

scientific article published on 10 September 2019

Genomic risk profiling of ischemic stroke: results of an international genome-wide association meta-analysis

artículo científico publicado en 2011

Genomic variation in seven Khoe-San groups reveals adaptation and complex African history

artículo científico publicado en 2012

Genotype, haplotype and copy-number variation in worldwide human populations

artículo científico publicado en 2008

Habitual sleep duration is associated with BMI and macronutrient intake and may be modified by CLOCK genetic variants

artículo científico publicado en 2014

Heritability and genetic variance of dementia with Lewy bodies

scientific article published on 03 April 2019

High-resolution inference of genetic relationships among Jewish populations

scientific article published on 09 January 2020

Human aging is characterized by focused changes in gene expression and deregulation of alternative splicing

artículo científico publicado en 2011

Identification and functional characterization of a novel R621C mutation in the synphilin-1 gene in Parkinson's disease

artículo científico publicado en 2003

Identification of a common variant in the TFR2 gene implicated in the physiological regulation of serum iron levels

artículo científico publicado en 2010

Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy

artículo científico publicado en 2011

Identification of nine novel loci associated with white blood cell subtypes in a Japanese population

artículo científico publicado en 2011

Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies

artículo científico publicado en 2019

Identification, replication, and fine-mapping of Loci associated with adult height in individuals of african ancestry

artículo científico publicado en 2011

Identifying likely causal connections between gene expression levels using a Mendelian randomization approach

article

Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies

artículo científico publicado en 2011

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

artículo científico publicado en 2013

Initial assessment of the pathogenic mechanisms of the recently identified Alzheimer risk Loci

artículo científico publicado en 2013

Insufficient evidence for pathogenicity of SNCA His50Gln (H50Q) in Parkinson's disease

artículo científico publicado en 2017

Integration of GWAS SNPs and tissue specific expression profiling reveal discrete eQTLs for human traits in blood and brain

artículo científico publicado en 2012

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

artículo científico publicado en 2016

Investigating the genetic architecture of dementia with Lewy bodies: a two-stage genome-wide association study

artículo científico publicado en 2017

Kinesin-associated protein 3 (KIFAP3) has no effect on survival in a population-based cohort of ALS patients

artículo científico publicado en 2010

Kohlschütter-Tönz syndrome: mutations in ROGDI and evidence of genetic heterogeneity

artículo científico publicado en 2012

Lack of G2019S LRRK2 mutation in a cohort of Taiwanese with sporadic Parkinson's disease

scientific article published on 01 June 2006

Large proportion of amyotrophic lateral sclerosis cases in Sardinia due to a single founder mutation of the TARDBP gene

artículo científico publicado en 2011

Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease

artículo científico publicado en 2014

Leukocyte CCR2 expression is associated with mini-mental state examination score in older adults

artículo científico publicado en 2012

Linkage and association analyses of type 2 diabetes/impaired glucose metabolism and adiponectin serum levels in Japanese Americans from Hawaii

artículo científico publicado en 2007

Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy

scientific journal article

MAPT expression and splicing is differentially regulated by brain region: relation to genotype and implication for tauopathies

artículo científico publicado en 2012

MIDN locus structural variants and Parkinson's Disease risk

artículo científico publicado en 2020

Menopause accelerates biological aging

artículo científico publicado en 2016

Meta-analysis of epigenome-wide association studies of cognitive abilities

artículo científico publicado en 2018

Meta-analysis of genome-wide association studies identifies six new Loci for serum calcium concentrations

artículo científico publicado en 2013

Multiple genetic loci influence serum urate levels and their relationship with gout and cardiovascular disease risk factors

artículo científico publicado en 2010

Multiple loci are associated with white blood cell phenotypes

artículo científico publicado en 2011

Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium

artículo científico publicado en 2009

Mutation analysis of sporadic early-onset Alzheimer's disease using the NeuroX array

artículo científico publicado en 2016

Mutation at the SCA17 locus is not a common cause of parkinsonism

scientific article published on 01 August 2003

Mutation of the Parkin gene in a Persian family: clinical progression over a 40-year period

artículo científico publicado en 2005

Mutations in GBA2 cause autosomal-recessive cerebellar ataxia with spasticity

artículo científico publicado en 2013

Mutations in TTBK2, encoding a kinase implicated in tau phosphorylation, segregate with spinocerebellar ataxia type 11.

artículo científico publicado en 2007

Mutations in neurofilament genes are not a significant primary cause of non-SOD1-mediated amyotrophic lateral sclerosis

artículo científico publicado en 2005

NeuroChip, an updated version of the NeuroX genotyping platform to rapidly screen for variants associated with neurological diseases

artículo científico publicado en 2017

NeuroX, a fast and efficient genotyping platform for investigation of neurodegenerative diseases

artículo científico publicado en 2015

Neurofibrillary tau pathology modulated by genetic variation of alpha-synuclein

artículo científico publicado en 2008

New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk ⬇️

artículo científico publicado en 2016

Next-generation sequencing reveals substantial genetic contribution to dementia with Lewy bodies

artículo científico publicado en 2016

Normal localization of deltaF323-Y328 mutant torsinA in transfected human cells

artículo científico publicado en 2002

Novel age-associated DNA methylation changes and epigenetic age acceleration in middle-aged African Americans and whites

artículo científico publicado en 2019

Novel genetic loci associated with hippocampal volume

scientific article published on 18 January 2017

Novel genetic loci underlying human intracranial volume identified through genome-wide association

artículo científico publicado en 2016

Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis

artículo científico publicado en 2014

Novel loci associated with usual sleep duration: the CHARGE Consortium Genome-Wide Association Study

artículo científico publicado en 2014

Parkinson's disease age at onset genome-wide association study: Defining heritability, genetic loci, and α-synuclein mechanisms

artículo científico publicado en 2019

Penetrance of Parkinson's Disease in LRRK2 p.G2019S Carriers Is Modified by a Polygenic Risk Score

scientific article published on 20 January 2020

Peripheral Blood Transcriptomic Signatures of Fasting Glucose and Insulin Concentrations

artículo científico publicado en 2016

Phenomenology of ?Lubag? or X-linked dystonia-parkinsonism

article

Polygenic risk score in postmortem diagnosed sporadic early-onset Alzheimer's disease

artículo científico publicado en 2017

Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes

artículo científico publicado en 2008

Practice patterns and outcomes after stroke across countries at different economic levels (INTERSTROKE): an international observational study

artículo científico publicado en 2018

Principal-component analysis for assessment of population stratification in mitochondrial medical genetics

artículo científico publicado en 2010

Race-specific alterations in DNA methylation among middle-aged African Americans and Whites with metabolic syndrome

scientific article published on 04 December 2019

Rare coding variants in the phospholipase D3 gene confer risk for Alzheimer's disease

artículo científico publicado en 2014

Resolving the polymorphism-in-probe problem is critical for correct interpretation of expression QTL studies

artículo científico publicado en 2013

SCA15 due to large ITPR1 deletions in a cohort of 333 white families with dominant ataxia

artículo científico publicado en 2011

SLC25A46 Mutations Associated with Autosomal Recessive Cerebellar Ataxia in North African Families

artículo científico publicado en 2017

SNCA multiplication is not a common cause of Parkinson disease or dementia with Lewy bodies.

artículo científico publicado en 2004

Screening exons 16 and 17 of the amyloid precursor protein gene in sporadic early-onset Alzheimer's disease

artículo científico publicado en 2015

Siblings with ischemic stroke study: results of a genome-wide scan for stroke loci

artículo científico publicado en 2011

Splice mutation in the iron-sulfur cluster scaffold protein ISCU causes myopathy with exercise intolerance

artículo científico publicado en 2008

Splicing factor 3B1 hypomethylation is associated with altered SF3B1 transcript expression in older humans

artículo científico publicado en 2014

Structural genomic variation in ischemic stroke

artículo científico publicado en 2008

Systematic identification of trans eQTLs as putative drivers of known disease associations

artículo científico publicado en 2013

The Genetic Architecture of Parkinson Disease in Spain: Characterizing Population-Specific Risk, Differential Haplotype Structures, and Providing Etiologic Insight

scientific article published on 29 October 2019

The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study

artículo científico publicado en 2015

The complex genetics of gait speed: genome-wide meta-analysis approach

scientific article published on 10 January 2017

The dardarin G 2019 S mutation is a common cause of Parkinson's disease but not other neurodegenerative diseases

artículo científico publicado en 2005

Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies

artículo científico publicado en 2010

Towards a gene expression biomarker set for human biological age.

artículo científico publicado en 2013

Transcriptomic profiling of the human brain reveals that altered synaptic gene expression is associated with chronological aging

artículo científico publicado en 2017

Use of support vector machines for disease risk prediction in genome-wide association studies: concerns and opportunities

artículo científico publicado en 2012

Using DNA Methylation to Understand Biological Consequences of Genetic Variability ⬇️

artículo científico publicado el 26 de noviembre de 2011

Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease

artículo científico publicado en 2012

Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease

scholarly article by M. F. Keller et al published 5 May 2013 in Human Molecular Genetics

Using genome-wide complex trait analysis to quantify ‘missing heritability’ in Parkinson's disease

artículo científico publicado en 2013

WITHDRAWN: Familial Degenerative Encephalopathy with Intracranial Calcification and Metaphyseal Dysplasia

retracted scientific article published on 18 November 2008

Whole blood gene expression and interleukin-6 levels

artículo científico publicado en 2014

Whole-genome sequencing to understand the genetic architecture of common gene expression and biomarker phenotypes

artículo científico publicado en 2014

X-linked dystonia (“Lubag”) presenting predominantly with parkinsonism: A more benign phenotype?

article

X-linked recessive dystonia parkinsonism (XDP; Lubag; DYT3)

artículo científico publicado el 1 de enero de 2004

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