Lista de obras -

A second X chromosome contributes to resilience in a mouse model of Alzheimer's disease

scientific article published on 01 August 2020

APOE Genotype Affects Cognitive Training Response in Healthy Shanghai Community-Dwelling Elderly Individuals

artículo científico publicado en 2015

Age-dependent effects of APOE ε4 in preclinical Alzheimer's disease

artículo científico publicado en 2016

Altered network connectivity in frontotemporal dementia with C9orf72 hexanucleotide repeat expansion

artículo científico publicado en 2014

Alzheimer Disease-associated Cortical Atrophy Does not Differ Between Chinese and Whites

scientific article published on 01 July 2019

Amyloid in dementia associated with familial FTLD: not an innocent bystander

artículo científico publicado en 2015

Apolipoprotein ε4 is associated with lower brain volume in cognitively normal Chinese but not white older adults

artículo científico publicado en 2015

Association Between Genetic Traits for Immune-Mediated Diseases and Alzheimer Disease

artículo científico publicado en 2016

Association of Alzheimer Disease Susceptibility Variants and Gene Expression in the Human Brain-Reply

artículo científico publicado en 2016

Atypical, slowly progressive behavioural variant frontotemporal dementia associated with C9ORF72 hexanucleotide expansion

artículo científico publicado en 2012

Brain volumetric deficits in MAPT mutation carriers: a multisite study

artículo científico publicado en 2020

C9ORF72 hexanucleotide repeats in behavioral and motor neuron disease: clinical heterogeneity and pathological diversity

artículo científico

C9orf72, AAO and ancestry help discriminating behavioural from language variants in FTLD cohorts

scientific article published on 17 September 2020

C9orf72-FTD/ALS pathogenesis: evidence from human neuropathological studies

article

CXCR4 involvement in neurodegenerative diseases.

artículo científico publicado en 2018

Correction: Immune-related genetic enrichment in frontotemporal dementia: An analysis of genome-wide association studies

artículo científico publicado en 2018

Damage to left frontal regulatory circuits produces greater positive emotional reactivity in frontotemporal dementia

artículo científico publicado en 2014

Decision tree analysis of genetic risk for clinically heterogeneous Alzheimer's disease

artículo científico publicado en 2015

Depressive symptoms in Chinese-American subjects with cognitive impairment

artículo científico publicado en 2013

Dissecting the genetic relationship between cardiovascular risk factors and Alzheimer's disease

scientific article published on 09 November 2018

Fine-mapping of the human leukocyte antigen locus as a risk factor for Alzheimer disease: A case-control study.

artículo científico publicado en 2017

Frequency of frontotemporal dementia gene variants in , , and in academic versus commercial laboratory cohorts

article

Frequency of the TREM2 R47H Variant in Various Neurodegenerative Disorders

artículo científico publicado en 2019

Frontotemporal dementia due to C9ORF72 mutations: clinical and imaging features

artículo científico publicado en 2012

Frontotemporal dementia in a Brazilian kindred with the c9orf72 mutation

artículo científico publicado en 2012

Gene-based aggregate SNP associations between candidate AD genes and cognitive decline

artículo científico publicado en 2016

Genetic Variation in the Androgen Receptor and Measures of Plasma Testosterone Levels Suggest Androgen Dysfunction in Alzheimer's Disease

artículo científico publicado en 2018

Genetic architecture of sporadic frontotemporal dementia and overlap with Alzheimer's and Parkinson's diseases

artículo científico publicado en 2016

Genetic assessment of age-associated Alzheimer disease risk: Development and validation of a polygenic hazard score

artículo científico publicado en 2017

Genetic modifiers of cognitive maintenance among older adults

artículo científico publicado en 2014

Genetic origin of a large family with a novel PSEN1 mutation (Ile416Thr)

artículo científico publicado en 2019

Genetic variation across RNA metabolism and cell death gene networks is implicated in the semantic variant of primary progressive aphasia

artículo científico publicado en 2019

Genome sequencing for early-onset or atypical dementia: high diagnostic yield and frequent observation of multiple contributory alleles

scientific article published on 13 December 2019

Genome-wide analyses as part of the international FTLD-TDP whole-genome sequencing consortium reveals novel disease risk factors and increases support for immune dysfunction in FTLD

scientific article published on 09 February 2019

Genome-wide association study identifies MAPT locus influencing human plasma tau levels

artículo científico publicado en 2017

Heightened emotional contagion in mild cognitive impairment and Alzheimer's disease is associated with temporal lobe degeneration

artículo científico publicado en 2013

Identification of a rare coding variant in TREM2 in a Chinese individual with Alzheimer's disease

artículo científico publicado en 2017

Immune-related genetic enrichment in frontotemporal dementia: An analysis of genome-wide association studies

artículo científico publicado en 2018

Immunological signatures in frontotemporal lobar degeneration

scientific article published on 01 April 2019

Increased prevalence of autoimmune disease within C9 and FTD/MND cohorts: Completing the picture

scientific article published on 28 October 2016

Insulin-Like Growth Factor Binding Protein 2 Is Associated With Biomarkers of Alzheimer's Disease Pathology and Shows Differential Expression in Transgenic Mice.

artículo científico publicado en 2018

Joint genome-wide association study of progressive supranuclear palsy identifies novel susceptibility loci and genetic correlation to neurodegenerative diseases

scholarly article by Jason A Chen published in August 2018

Lack of Association Between the CCR5-delta32 Polymorphism and Neurodegenerative Disorders

scientific article published on 17 January 2020

Life extension factor klotho enhances cognition

artículo científico publicado en 2014

Longevity Gene KLOTHO and Alzheimer Disease-A Better Fate for Individuals Who Carry APOE ε4

scientific article published on 13 April 2020

Mitochondrial DNA sequence associations with dementia and amyloid-β in elderly African Americans

artículo científico publicado en 2013

Mitochondrial DNA sequence variation associated with dementia and cognitive function in the elderly

artículo científico publicado en 2012

Mitochondrial DNA sequence variation is associated with free-living activity energy expenditure in the elderly

artículo científico publicado en 2012

Neurotransmitter Pathway Genes in Cognitive Decline During Aging: Evidence for GNG4 and KCNQ2 Genes

artículo científico publicado en 2018

No association between the COMT Val158Met polymorphism and cognitive training response in healthy Shanghai community-dwelling elderly individuals

scientific article published on 14 July 2020

Non-Coding and Loss-of-Function Coding Variants in TET2 are Associated with Multiple Neurodegenerative Diseases

artículo científico publicado en 2020

Polygenic hazard score, amyloid deposition and Alzheimer's neurodegeneration

scientific article published on 01 February 2019

Polygenic hazard score: an enrichment marker for Alzheimer's associated amyloid and tau deposition

artículo científico publicado en 2017

Progranulin mutations as risk factors for Alzheimer disease

scientific article published on June 2013

Protein network analysis reveals selectively vulnerable regions and biological processes in FTD

Rare TREM2 variants associated with Alzheimer's disease display reduced cell surface expression

artículo científico publicado en 2016

Rare variants in the neuronal ceroid lipofuscinosis gene MFSD8 are candidate risk factors for frontotemporal dementia

article

Recent advances in the genetics of frontotemporal dementia

artículo científico publicado en 2019

Regionally specific TSC1 and TSC2 gene expression in tuberous sclerosis complex

scientific article published in Scientific Reports

Response to Holstege et al

artículo científico publicado en 2020

Selective Genetic Overlap Between Amyotrophic Lateral Sclerosis and Diseases of the Frontotemporal Dementia Spectrum.

artículo científico publicado en 2018

Shared genetic risk between corticobasal degeneration, progressive supranuclear palsy, and frontotemporal dementia

artículo científico publicado en 2017

Systemic klotho is associated with KLOTHO variation and predicts intrinsic cortical connectivity in healthy human aging

scientific article published on 06 October 2016

The 5-HTTLPR variant in the serotonin transporter gene modifies degeneration of brain regions important for emotion in behavioral variant frontotemporal dementia

artículo científico publicado en 2015

The Chinese Verbal Learning Test specifically assesses hippocampal state

artículo científico publicado en 2014

The Radiogenomics of Late-onset Alzheimer Disease

scientific article published on 01 December 2019

The Transcriptional Landscape of Microglial Genes in Aging and Neurodegenerative Disease.

artículo científico publicado en 2019

The relationship between complement factor C3, APOE ε4, amyloid and tau in Alzheimer's disease

artículo científico publicado en 2016

Variation in longevity gene KLOTHO is associated with greater cortical volumes

artículo científico publicado en 2015

Youthful Processing Speed in Older Adults: Genetic, Biological, and Behavioral Predictors of Cognitive Processing Speed Trajectories in Aging

artículo científico publicado en 2017

Lista de obras de

A second X chromosome contributes to resilience in a mouse model of Alzheimer's disease

APOE Genotype Affects Cognitive Training Response in Healthy Shanghai Community-Dwelling Elderly Individuals

Age-dependent effects of APOE ε4 in preclinical Alzheimer's disease

Altered network connectivity in frontotemporal dementia with C9orf72 hexanucleotide repeat expansion

Alzheimer Disease-associated Cortical Atrophy Does not Differ Between Chinese and Whites

Amyloid in dementia associated with familial FTLD: not an innocent bystander

Apolipoprotein ε4 is associated with lower brain volume in cognitively normal Chinese but not white older adults

Association Between Genetic Traits for Immune-Mediated Diseases and Alzheimer Disease

Association of Alzheimer Disease Susceptibility Variants and Gene Expression in the Human Brain-Reply

Atypical, slowly progressive behavioural variant frontotemporal dementia associated with C9ORF72 hexanucleotide expansion

Brain volumetric deficits in MAPT mutation carriers: a multisite study

C9ORF72 hexanucleotide repeats in behavioral and motor neuron disease: clinical heterogeneity and pathological diversity

C9orf72, AAO and ancestry help discriminating behavioural from language variants in FTLD cohorts

C9orf72-FTD/ALS pathogenesis: evidence from human neuropathological studies

CXCR4 involvement in neurodegenerative diseases.

Correction: Immune-related genetic enrichment in frontotemporal dementia: An analysis of genome-wide association studies

Damage to left frontal regulatory circuits produces greater positive emotional reactivity in frontotemporal dementia

Decision tree analysis of genetic risk for clinically heterogeneous Alzheimer's disease

Depressive symptoms in Chinese-American subjects with cognitive impairment

Dissecting the genetic relationship between cardiovascular risk factors and Alzheimer's disease

Fine-mapping of the human leukocyte antigen locus as a risk factor for Alzheimer disease: A case-control study.

Frequency of frontotemporal dementia gene variants in , , and in academic versus commercial laboratory cohorts

Frequency of the TREM2 R47H Variant in Various Neurodegenerative Disorders

Frontotemporal dementia due to C9ORF72 mutations: clinical and imaging features

Frontotemporal dementia in a Brazilian kindred with the c9orf72 mutation

Gene-based aggregate SNP associations between candidate AD genes and cognitive decline

Genetic Variation in the Androgen Receptor and Measures of Plasma Testosterone Levels Suggest Androgen Dysfunction in Alzheimer's Disease

Genetic architecture of sporadic frontotemporal dementia and overlap with Alzheimer's and Parkinson's diseases

Genetic assessment of age-associated Alzheimer disease risk: Development and validation of a polygenic hazard score

Genetic modifiers of cognitive maintenance among older adults

Genetic origin of a large family with a novel PSEN1 mutation (Ile416Thr)

Genetic variation across RNA metabolism and cell death gene networks is implicated in the semantic variant of primary progressive aphasia

Genome sequencing for early-onset or atypical dementia: high diagnostic yield and frequent observation of multiple contributory alleles

Genome-wide analyses as part of the international FTLD-TDP whole-genome sequencing consortium reveals novel disease risk factors and increases support for immune dysfunction in FTLD

Genome-wide association study identifies MAPT locus influencing human plasma tau levels

Heightened emotional contagion in mild cognitive impairment and Alzheimer's disease is associated with temporal lobe degeneration

Identification of a rare coding variant in TREM2 in a Chinese individual with Alzheimer's disease

Immune-related genetic enrichment in frontotemporal dementia: An analysis of genome-wide association studies

Immunological signatures in frontotemporal lobar degeneration

Increased prevalence of autoimmune disease within C9 and FTD/MND cohorts: Completing the picture

Insulin-Like Growth Factor Binding Protein 2 Is Associated With Biomarkers of Alzheimer's Disease Pathology and Shows Differential Expression in Transgenic Mice.

Joint genome-wide association study of progressive supranuclear palsy identifies novel susceptibility loci and genetic correlation to neurodegenerative diseases

Lack of Association Between the CCR5-delta32 Polymorphism and Neurodegenerative Disorders

Life extension factor klotho enhances cognition

Longevity Gene KLOTHO and Alzheimer Disease-A Better Fate for Individuals Who Carry APOE ε4

Mitochondrial DNA sequence associations with dementia and amyloid-β in elderly African Americans

Mitochondrial DNA sequence variation associated with dementia and cognitive function in the elderly

Mitochondrial DNA sequence variation is associated with free-living activity energy expenditure in the elderly

Neurotransmitter Pathway Genes in Cognitive Decline During Aging: Evidence for GNG4 and KCNQ2 Genes

No association between the COMT Val158Met polymorphism and cognitive training response in healthy Shanghai community-dwelling elderly individuals

Non-Coding and Loss-of-Function Coding Variants in TET2 are Associated with Multiple Neurodegenerative Diseases

Polygenic hazard score, amyloid deposition and Alzheimer's neurodegeneration

Polygenic hazard score: an enrichment marker for Alzheimer's associated amyloid and tau deposition

Progranulin mutations as risk factors for Alzheimer disease

Protein network analysis reveals selectively vulnerable regions and biological processes in FTD

Rare TREM2 variants associated with Alzheimer's disease display reduced cell surface expression

Rare variants in the neuronal ceroid lipofuscinosis gene MFSD8 are candidate risk factors for frontotemporal dementia

Recent advances in the genetics of frontotemporal dementia

Regionally specific TSC1 and TSC2 gene expression in tuberous sclerosis complex

Response to Holstege et al

Selective Genetic Overlap Between Amyotrophic Lateral Sclerosis and Diseases of the Frontotemporal Dementia Spectrum.

Shared genetic risk between corticobasal degeneration, progressive supranuclear palsy, and frontotemporal dementia

Systemic klotho is associated with KLOTHO variation and predicts intrinsic cortical connectivity in healthy human aging

The 5-HTTLPR variant in the serotonin transporter gene modifies degeneration of brain regions important for emotion in behavioral variant frontotemporal dementia

The Chinese Verbal Learning Test specifically assesses hippocampal state

The Radiogenomics of Late-onset Alzheimer Disease

The Transcriptional Landscape of Microglial Genes in Aging and Neurodegenerative Disease.

The relationship between complement factor C3, APOE ε4, amyloid and tau in Alzheimer's disease

Variation in longevity gene KLOTHO is associated with greater cortical volumes

Youthful Processing Speed in Older Adults: Genetic, Biological, and Behavioral Predictors of Cognitive Processing Speed Trajectories in Aging