Lista de obras - Denise Harold - Dominio Público Uruguay

A genome-wide study shows a limited contribution of rare copy number variants to Alzheimer's disease risk

artículo científico publicado en 2012

A modifier of Huntington's disease onset at the MLH1 locus

artículo científico publicado en 2017

A novel Alzheimer disease locus located near the gene encoding tau protein.

artículo científico publicado en 2015

Alpha-T-catenin is expressed in human brain and interacts with the Wnt signaling pathway but is not responsible for linkage to chromosome 10 in Alzheimer's disease

artículo científico publicado en 2004

Alzheimer's disease and age-related macular degeneration have different genetic models for complement gene variation

article

Alzheimer's disease genetics: current knowledge and future challenges

artículo científico publicado en 2010

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 shared heritability in common disorders of the brain

artículo científico publicado en 2018

Association analysis of 528 intra-genic SNPs in a region of chromosome 10 linked to late onset Alzheimer's disease

artículo científico publicado en 2008

Author Correction: Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

scientific article published on 01 September 2019

Can Studies of Neuroinflammation in a TSPO Genetic Subgroup (HAB or MAB) Be Applied to the Entire AD Cohort?

artículo científico publicado en 2015

Characterisation and validation of insertions and deletions in 173 patient exomes

artículo científico publicado en 2012

Characterization of a family with rare deletions in CNTNAP5 and DOCK4 suggests novel risk loci for autism and dyslexia

artículo científico publicado en 2010

Cognitive Characterization of Schizophrenia Risk Variants Involved in Synaptic Transmission: Evidence of CACNA1C's Role in Working Memory

artículo científico publicado en 2017

Cognitive analysis of schizophrenia risk genes that function as epigenetic regulators of gene expression

artículo científico publicado en 2016

Common polygenic variation enhances risk prediction for Alzheimer's disease

artículo científico publicado en 2015

Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease

artículo científico publicado en 2011

Corrigendum to "Genome-wide association interaction analysis for Alzheimer's disease." [Neurobiol. Aging 35 (2014) 2436-2443].

artículo científico publicado en 2015

Deep sequencing of the Nicastrin gene in pooled DNA, the identification of genetic variants that affect risk of Alzheimer's disease

artículo científico publicado en 2011

Effects of MiR-137 genetic risk score on brain volume and cortical measures in patients with schizophrenia and controls

artículo científico publicado en 2018

Erratum to "Polymorphisms in BACE2 may affect the age of onset Alzheimer's dementia in Down syndrome" [Neurobiol. Aging 35 (2014) 1513.e1-1513.e5].

artículo científico publicado en 2014

Erratum to "Polymorphisms in BACE2 may affect the age of onset Alzheimer's dementia in Down syndrome" [Neurobiol. Aging 35 (2014) 1513.e1-1513.e5].

artículo científico publicado en 2014

Erratum: Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease

scholarly article published in Nature Genetics

Erratum: Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease

article

Erratum: Genome-wide haplotype association study identifies the FRMD4A gene as a risk locus for Alzheimer's disease

article

Estimation and partitioning of polygenic variation captured by common SNPs for Alzheimer's disease, multiple sclerosis and endometriosis

artículo científico publicado en 2012

Evidence that PICALM affects age at onset of Alzheimer's dementia in Down syndrome

artículo científico publicado en 2013

Follow-up of loci from the International Genomics of Alzheimer's Disease Project identifies TRIP4 as a novel susceptibility gene

artículo científico publicado en 2014

From molecule to clinic and community for neurodegeneration: research to bridge translational gaps

artículo científico

Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexia

artículo científico publicado en 2006

GWAS of cerebrospinal fluid tau levels identifies risk variants for Alzheimer's disease

artículo científico publicado en 2013

Gene-wide analysis detects two new susceptibility genes for Alzheimer's disease

artículo científico publicado en 2014

Genetic evidence for the involvement of lipid metabolism in Alzheimer's disease

artículo científico publicado en 2010

Genetic evidence implicates the immune system and cholesterol metabolism in the aetiology of Alzheimer's disease

artículo científico publicado en 2010

Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

artículo científico publicado en 2019

Genetic overlap between Alzheimer's disease and Parkinson's disease at the MAPT locus

artículo científico publicado en 2015

Genetic variation at the CELF1 (CUGBP, elav-like family member 1 gene) locus is genome-wide associated with Alzheimer's disease and obesity

artículo científico publicado en 2014

Genetically predicted complement component 4A expression: effects on memory function and middle temporal lobe activation.

artículo científico publicado en 2018

Genome-wide analysis of genetic loci associated with Alzheimer disease

artículo científico publicado en 2010

Genome-wide association interaction analysis for Alzheimer's disease

artículo científico publicado en 2014

Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease

artículo científico publicado en 2009

Genome-wide association study of Alzheimer's disease with psychotic symptoms

artículo científico publicado en 2011

Genome-wide haplotype association study identifies the FRMD4A gene as a risk locus for Alzheimer's disease

artículo científico publicado en 2012

Haplotype-based stratification of Huntington's disease

artículo científico publicado en 2017

Increased expression of BIN1 mediates Alzheimer genetic risk by modulating tau pathology

artículo científico publicado en 2013

Interaction between the ADAM12 and SH3MD1 genes may confer susceptibility to late-onset Alzheimer's disease

artículo científico publicado en 2007

Linkage disequilibrium structure of KIAA0319 and DCDC2, two candidate susceptibility genes for developmental dyslexia

article

Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease

artículo científico publicado en 2013

Meta-analysis of the association between variants in SORL1 and Alzheimer disease

artículo científico publicado en 2011

MiR-137-derived polygenic risk: effects on cognitive performance in patients with schizophrenia and controls

artículo científico publicado en 2017

Missense variant in TREML2 protects against Alzheimer's disease

scientific article published on 21 December 2013

No consistent evidence for association between mtDNA variants and Alzheimer disease

artículo científico publicado en 2012

No evidence that extended tracts of homozygosity are associated with Alzheimer's disease.

artículo científico publicado en 2011

No support for association between dyslexia susceptibility 1 candidate 1 and developmental dyslexia

artículo científico publicado en 2005

Polymorphisms in BACE2 may affect the age of onset Alzheimer's dementia in Down syndrome

artículo científico publicado en 2013

Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease

artículo científico publicado en 2017

Remapping the insulin gene/IDDM2 locus in type 1 diabetes

artículo científico publicado en 2004

SNPs associated with cerebrospinal fluid phospho-tau levels influence rate of decline in Alzheimer's disease

artículo científico publicado en 2010

Sequence variation in the CHAT locus shows no association with late-onset Alzheimer's disease

artículo científico publicado en 2003

Shared genetic contribution to Ischaemic Stroke and Alzheimer's Disease

artículo científico publicado en 2016

Strong evidence that KIAA0319 on chromosome 6p is a susceptibility gene for developmental dyslexia

artículo científico publicado en 2005

Suggestive synergy between genetic variants in TF and HFE as risk factors for Alzheimer's disease

artículo científico publicado en 2010

The Genetic Modifiers of Motor OnsetAge (GeM MOA) Website: Genome-wide Association Analysis for Genetic Modifiers of Huntington's Disease

artículo científico publicado en 2015

The role of variation at AβPP, PSEN1, PSEN2, and MAPT in late onset Alzheimer's disease

artículo científico publicado en 2012

Lista de obras de Denise Harold

A genome-wide study shows a limited contribution of rare copy number variants to Alzheimer's disease risk

A modifier of Huntington's disease onset at the MLH1 locus

A novel Alzheimer disease locus located near the gene encoding tau protein.

Alpha-T-catenin is expressed in human brain and interacts with the Wnt signaling pathway but is not responsible for linkage to chromosome 10 in Alzheimer's disease

Alzheimer's disease and age-related macular degeneration have different genetic models for complement gene variation

Alzheimer's disease genetics: current knowledge and future challenges

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

Analysis of shared heritability in common disorders of the brain

Association analysis of 528 intra-genic SNPs in a region of chromosome 10 linked to late onset Alzheimer's disease

Author Correction: Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

Can Studies of Neuroinflammation in a TSPO Genetic Subgroup (HAB or MAB) Be Applied to the Entire AD Cohort?

Characterisation and validation of insertions and deletions in 173 patient exomes

Characterization of a family with rare deletions in CNTNAP5 and DOCK4 suggests novel risk loci for autism and dyslexia

Cognitive Characterization of Schizophrenia Risk Variants Involved in Synaptic Transmission: Evidence of CACNA1C's Role in Working Memory

Cognitive analysis of schizophrenia risk genes that function as epigenetic regulators of gene expression

Common polygenic variation enhances risk prediction for Alzheimer's disease

Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease

Corrigendum to "Genome-wide association interaction analysis for Alzheimer's disease." [Neurobiol. Aging 35 (2014) 2436-2443].

Deep sequencing of the Nicastrin gene in pooled DNA, the identification of genetic variants that affect risk of Alzheimer's disease

Effects of MiR-137 genetic risk score on brain volume and cortical measures in patients with schizophrenia and controls

Erratum to "Polymorphisms in BACE2 may affect the age of onset Alzheimer's dementia in Down syndrome" [Neurobiol. Aging 35 (2014) 1513.e1-1513.e5].

Erratum to "Polymorphisms in BACE2 may affect the age of onset Alzheimer's dementia in Down syndrome" [Neurobiol. Aging 35 (2014) 1513.e1-1513.e5].

Erratum: Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease

Erratum: Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease

Erratum: Genome-wide haplotype association study identifies the FRMD4A gene as a risk locus for Alzheimer's disease

Estimation and partitioning of polygenic variation captured by common SNPs for Alzheimer's disease, multiple sclerosis and endometriosis

Evidence that PICALM affects age at onset of Alzheimer's dementia in Down syndrome

Follow-up of loci from the International Genomics of Alzheimer's Disease Project identifies TRIP4 as a novel susceptibility gene

From molecule to clinic and community for neurodegeneration: research to bridge translational gaps

Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexia

GWAS of cerebrospinal fluid tau levels identifies risk variants for Alzheimer's disease

Gene-wide analysis detects two new susceptibility genes for Alzheimer's disease

Genetic evidence for the involvement of lipid metabolism in Alzheimer's disease

Genetic evidence implicates the immune system and cholesterol metabolism in the aetiology of Alzheimer's disease

Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

Genetic overlap between Alzheimer's disease and Parkinson's disease at the MAPT locus

Genetic variation at the CELF1 (CUGBP, elav-like family member 1 gene) locus is genome-wide associated with Alzheimer's disease and obesity

Genetically predicted complement component 4A expression: effects on memory function and middle temporal lobe activation.

Genome-wide analysis of genetic loci associated with Alzheimer disease

Genome-wide association interaction analysis for Alzheimer's disease

Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease

Genome-wide association study of Alzheimer's disease with psychotic symptoms

Genome-wide haplotype association study identifies the FRMD4A gene as a risk locus for Alzheimer's disease

Haplotype-based stratification of Huntington's disease

Increased expression of BIN1 mediates Alzheimer genetic risk by modulating tau pathology

Interaction between the ADAM12 and SH3MD1 genes may confer susceptibility to late-onset Alzheimer's disease

Linkage disequilibrium structure of KIAA0319 and DCDC2, two candidate susceptibility genes for developmental dyslexia

Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease

Meta-analysis of the association between variants in SORL1 and Alzheimer disease

MiR-137-derived polygenic risk: effects on cognitive performance in patients with schizophrenia and controls

Missense variant in TREML2 protects against Alzheimer's disease

No consistent evidence for association between mtDNA variants and Alzheimer disease

No evidence that extended tracts of homozygosity are associated with Alzheimer's disease.

No support for association between dyslexia susceptibility 1 candidate 1 and developmental dyslexia

Polymorphisms in BACE2 may affect the age of onset Alzheimer's dementia in Down syndrome

Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease

Remapping the insulin gene/IDDM2 locus in type 1 diabetes

SNPs associated with cerebrospinal fluid phospho-tau levels influence rate of decline in Alzheimer's disease

Sequence variation in the CHAT locus shows no association with late-onset Alzheimer's disease

Shared genetic contribution to Ischaemic Stroke and Alzheimer's Disease

Strong evidence that KIAA0319 on chromosome 6p is a susceptibility gene for developmental dyslexia

Suggestive synergy between genetic variants in TF and HFE as risk factors for Alzheimer's disease

The Genetic Modifiers of Motor OnsetAge (GeM MOA) Website: Genome-wide Association Analysis for Genetic Modifiers of Huntington's Disease

The role of variation at AβPP, PSEN1, PSEN2, and MAPT in late onset Alzheimer's disease