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List of works by Dena G. Hernandez

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

article

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

scientific article

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

scientific article

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

scientific article

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

scientific article published on 11 November 2020

A candidate gene for autoimmune myasthenia gravis ⬇️

scientific article published on June 27, 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

scientific article published on 20 May 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

scientific article

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

scientific article published on 18 September 2008

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

scientific article

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

scientific article published on 19 September 2010

A genome-wide association study of myasthenia gravis

scientific article published on April 2015

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

scientific article published on 5 December 2007

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

scientific article

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

scientific article

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

scientific article

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

scientific article

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

scientific article

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

scientific article (publication date: March 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

scientific article published on 7 December 2012

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

scientific article published on 13 November 2013

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

scientific article

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

scientific article

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

scientific article

ABSTRACTS

scholarly article

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

scientific article published on 17 December 2016

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

scientific article

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

scientific article

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

scientific article

Alzheimer risk variant CLU and brain function during aging

scientific article

An exploratory analysis on gene-environment interactions for Parkinson disease

scientific article

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

scientific article

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

scientific article published in April 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

scientific article published on October 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

scientific article published in Nature

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

scientific article published in April 2002

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

scientific article published on 23 February 2012

Assessment of APOE in atypical parkinsonism syndromes

scientific article published on 21 February 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.

scientific article

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

scientific article published on 21 May 2020

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

scientific article

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

scientific article

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

scientific article published on 09 March 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

scientific article

CUBN is a gene locus for albuminuria

scientific article

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

scientific article (publication date: February 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

scientific article published on 8 May 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

scientific article published on 9 September 2015

Characterization of PLA2G6 as a locus for dystonia-parkinsonism

scientific article

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

scientific article

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

scientific article published in March 2005

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

scientific article published on 09 October 2018

Common genetic variants influence human subcortical brain structures

scientific article

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

scientific article

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

scientific article

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

scientific article

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

scientific article published on 10 June 2016

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

scientific article published on 23 August 2017

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

scientific article published on 21 November 2011

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

scientific article

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

scientific article published on 7 July 2017

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

scientific article published on 30 March 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

scientific article published on 12 December 2016

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

scientific article

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

scientific article

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

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

scientific article published in June 2007

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

scientific article

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

scientific article published on 01 October 2020

Discovery and refinement of loci associated with lipid levels

scientific article

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

scientific article

EIF4G1 mutations do not cause Parkinson's disease

scientific article published on 9 May 2015

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

article

Epigenetic Signatures of Cigarette Smoking

scientific article

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

scientific article published in September 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

scientific article

Exome sequencing reveals VCP mutations as a cause of familial ALS

scientific article

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

scientific article

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

scientific article

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

scientific article

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

scientific article published on 01 November 2018

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

scientific article

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

scientific article

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

scientific article published on 21 June 2013

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

scientific article

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

scientific article

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

scientific article

Genetic comorbidities in Parkinson's disease

scientific article published on 20 September 2013

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

scientific article published on 01 January 2020

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

scientific article published on 09 July 2019

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

scientific article published in The Lancet

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

scientific article published on 20 November 2017

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

scientific article published on 6 October 2011

Genetic variation associated with circulating monocyte count in the eMERGE Network

scientific article published on 12 January 2013

Genetics in Parkinson disease: Mendelian versus non-Mendelian inheritance

scientific article

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

scientific article

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

scientific article published in November 2018

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

scientific article

Genome-wide Analyses Identify KIF5A as a Novel ALS Gene

scientific article published in March 2018

Genome-wide Pleiotropy Between Parkinson Disease and Autoimmune Diseases

scientific article published on 05 June 2017

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

scientific article published on 20 November 2006

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

scientific article published on 2 November 2015

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

scientific article published on 11 June 2016

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

scientific article published on 13 December 2017

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

scientific article

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

scientific article

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

scientific article

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

scientific article

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

scientific article

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

scientific article

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

scientific article

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

scientific article published on 09 July 2018

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

scientific article published on February 2016

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

scientific article published on 27 April 2017

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

scientific article

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

scientific article published on 21 September 2011

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

scientific article

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

scientific article (publication date: 21 February 2008)

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

scientific article

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

scientific article

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

scientific article (publication date: June 2003)

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

scientific article

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

scientific article

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

scientific article

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

scientific article published on 01 December 2019

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

scientific article

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

scientific article

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

scientific article

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

scientific article published on 30 January 2013

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

scientific article published on 20 December 2017

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

scientific article

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

scientific article

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

scientific article published on 16 December 2017

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

scientific article

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

scientific article

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

scientific article

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

scientific article (publication date: September 2014)

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

scientific article

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

scientific article published on February 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

scientific article

MIDN locus structural variants and Parkinson's Disease risk

scientific article published on 24 March 2020

Menopause accelerates biological aging

scientific article

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

scientific article published on 8 January 2018

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

scientific article

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

scientific article

Multiple loci are associated with white blood cell phenotypes

scientific article

Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium

scientific article

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

scientific article published on 23 September 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

scientific article published in July 2005

Mutations in GBA2 cause autosomal-recessive cerebellar ataxia with spasticity

scientific article published on 17 January 2013

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

scientific article

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

scientific article published on 3 August 2005

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

scientific article published on 17 May 2017

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

scientific article

Neurofibrillary tau pathology modulated by genetic variation of alpha-synuclein

scientific article published in September 2008

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

scientific article published on February 2016

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

scientific article published on 13 June 2016

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

scientific article published on July 2002

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

scientific article published on 19 August 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

scientific article (publication date: 3 October 2016)

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

scientific article

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

scientific article published on 2 December 2014

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

scientific article published on 07 April 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

scientific article

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

article

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

scientific article published on 10 October 2017

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

scientific article

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

scientific article published in The Lancet

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

scientific article

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

scientific article

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

scientific article published on 21 February 2013

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

scientific article

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

scientific article published on 31 May 2017

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

scientific article

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

scientific article published on 29 December 2015

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

scientific article

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

scientific article

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

scientific article published on 23 January 2014

Structural genomic variation in ischemic stroke

scientific article

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

scientific article (publication date: October 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

scientific article

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

scientific article

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

scientific article

Towards a gene expression biomarker set for human biological age.

scientific article

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

scientific article published on 4 December 2017

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

scientific article published on 3 August 2012

Using DNA Methylation to Understand Biological Consequences of Genetic Variability ⬇️

scientific article published on November 26, 2011

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

scientific article published on 13 August 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

scientific article published on 14 February 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

scientific article

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

scientific article

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

article

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

scientific article published on January 1, 2004

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