Lista de obras -

A blood gene expression marker of early Alzheimer's disease

artículo científico publicado en 2013

A152T tau allele causes neurodegeneration that can be ameliorated in a zebrafish model by autophagy induction

artículo científico publicado en 2017

Activity-Dependent Regulation of Alternative Cleavage and Polyadenylation During Hippocampal Long-Term Potentiation.

artículo científico publicado en 2017

Adult rat myelin enhances axonal outgrowth from neural stem cells.

artículo científico publicado en 2018

Altered network connectivity in frontotemporal dementia with C9orf72 hexanucleotide repeat expansion

artículo científico publicado en 2014

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

artículo científico publicado en 2015

Ancient hybridization and strong adaptation to viruses across African vervet monkey populations.

artículo científico publicado en 2017

ApoE ε4 Is Associated With Cognition, Brain Integrity, and Atrophy in HIV Over Age 60. ⬇️

artículo científico publicado en 2016

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

artículo científico publicado en 2015

Assessment of executive function declines in presymptomatic and mildly symptomatic familial frontotemporal dementia: NIH-EXAMINER as a potential clinical trial endpoint

scientific article published on 01 January 2020

Astrocyte molecular signatures in Huntington's disease

scientific article published on 01 October 2019

Brain volumetric deficits in MAPT mutation carriers: a multisite study

artículo científico publicado en 2020

C9ORF72 repeat expansions in cases with previously identified pathogenic mutations

artículo científico publicado en 2013

CREB controls cortical circuit plasticity and functional recovery after stroke.

artículo científico publicado en 2018

Clinical and volumetric changes with increasing functional impairment in familial frontotemporal lobar degeneration

artículo científico publicado en 2020

Clinicopathological correlations in behavioural variant frontotemporal dementia.

artículo científico publicado en 2017

Contribution of common and rare variants to bipolar disorder susceptibility in extended pedigrees from population isolates

artículo científico publicado en 2020

DNA methylation study of Huntington's disease and motor progression in patients and in animal models

scientific article published on 10 September 2020

Distinct Subtypes of Behavioral Variant Frontotemporal Dementia Based on Patterns of Network Degeneration

artículo científico publicado en 2016

Evidence for a role of the rare p.A152T variant in MAPT in increasing the risk for FTD-spectrum and Alzheimer's diseases

artículo científico publicado en 2012

Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS

artículo científico publicado en 2011

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

artículo científico publicado en 2017

ForestQC: Quality control on genetic variants from next-generation sequencing data using random forest

artículo científico publicado en 2019

Frequency of the TREM2 R47H Variant in Various Neurodegenerative Disorders

artículo científico publicado en 2019

GDF10 is a signal for axonal sprouting and functional recovery after stroke.

artículo científico publicado en 2015

Genetic screening of a large series of North American sporadic and familial frontotemporal dementia cases

artículo científico publicado en 2020

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

artículo científico publicado en 2017

Identification of common variants associated with human hippocampal and intracranial volumes

artículo científico publicado en 2012

Immunosuppressive effect and global dysregulation of blood transcriptome in response to psychosocial stress in vervet monkeys (Chlorocebus sabaeus)

artículo científico publicado en 2020

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

scientific article published on 28 October 2016

Individualized atrophy scores predict dementia onset in familial frontotemporal lobar degeneration

artículo científico publicado en 2020

Injured adult neurons regress to an embryonic transcriptional growth state

scientific article published on 15 April 2020

Integrated genomics and proteomics define huntingtin CAG length-dependent networks in mice.

artículo científico publicado en 2016

Longitudinal RNA-Seq analysis of acute and chronic neurogenic skeletal muscle atrophy

scientific article published on 24 September 2019

Loss of functional connectivity is greater outside the default mode network in nonfamilial early-onset Alzheimer's disease variants

artículo científico publicado en 2015

Mitochondrial dysfunction and immune activation are detectable in early Alzheimer's disease blood

artículo científico publicado en 2012

Mutations in XPR1 cause primary familial brain calcification associated with altered phosphate export

artículo científico publicado en 2015

Network degeneration and dysfunction in presymptomatic C9ORF72 expansion carriers

artículo científico publicado en 2016

No Evidence to Suggest that the Use of Acetylcholinesterase Inhibitors Confounds the Results of Two Blood-Based Biomarker Studies in Alzheimer's Disease

artículo científico publicado en 2015

Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C-->T (Arg493X) mutation: an international initiative

artículo científico publicado en 2007

Plasma tau and neurofilament light in frontotemporal lobar degeneration and Alzheimer's disease

artículo científico publicado en 2020

Primary brain calcification: an international study reporting novel variants and associated phenotypes

artículo científico publicado en 2018

Publisher Correction: Ancient hybridization and strong adaptation to viruses across African vervet monkey populations

artículo científico publicado en 2018

Quality of life and caregiver burden in familial frontotemporal lobar degeneration: Analyses of symptomatic and asymptomatic individuals within the LEFFTDS cohort

artículo científico publicado en 2020

Signaling to transcription networks in the neuronal retrograde injury response.

artículo científico publicado en 2010

TDP-43 frontotemporal lobar degeneration and autoimmune disease

artículo científico publicado en 2013

Temporal variant of frontotemporal dementia in C9orf72 repeat expansion carriers: two case studies

scientific article published on 16 March 2020

Tet3 regulates synaptic transmission and homeostatic plasticity via DNA oxidation and repair

artículo científico publicado en 2015

The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data

artículo científico publicado en 2014

The Longitudinal Trajectory of Default Mode Network Connectivity in Healthy Older Adults Varies as a Function of Age and is Associated with Changes in Episodic Memory and Processing Speed.

artículo científico publicado en 2018

The longitudinal evaluation of familial frontotemporal dementia subjects protocol: Framework and methodology

scientific article published on 06 January 2020

Therapeutic targeting of oxygen-sensing prolyl hydroxylases abrogates ATF4-dependent neuronal death and improves outcomes after brain hemorrhage in several rodent models

scientific article published on March 2016

Timing of Smarcb1 and Nf2 inactivation determines schwannoma versus rhabdoid tumor development.

artículo científico publicado en 2017

Tracking white matter degeneration in asymptomatic and symptomatic MAPT mutation carriers

artículo científico publicado en 2019

Transcriptional profiling of isogenic Friedreich ataxia neurons and effect of an HDAC inhibitor on disease signatures

artículo científico publicado en 2018

Utility of the global CDR® plus NACC FTLD rating and development of scoring rules: Data from the ARTFL/LEFFTDS Consortium

scientific article published on 01 January 2020

White Matter Stroke Induces a Unique Oligo-Astrocyte Niche That Inhibits Recovery

artículo científico publicado en 2019

hnRNPs Interacting with mRNA Localization Motifs Define Axonal RNA Regulons

artículo científico publicado en 2018

Lista de obras de

A blood gene expression marker of early Alzheimer's disease

A152T tau allele causes neurodegeneration that can be ameliorated in a zebrafish model by autophagy induction

Activity-Dependent Regulation of Alternative Cleavage and Polyadenylation During Hippocampal Long-Term Potentiation.

Adult rat myelin enhances axonal outgrowth from neural stem cells.

Altered network connectivity in frontotemporal dementia with C9orf72 hexanucleotide repeat expansion

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

Ancient hybridization and strong adaptation to viruses across African vervet monkey populations.

ApoE ε4 Is Associated With Cognition, Brain Integrity, and Atrophy in HIV Over Age 60. ⬇️

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

Assessment of executive function declines in presymptomatic and mildly symptomatic familial frontotemporal dementia: NIH-EXAMINER as a potential clinical trial endpoint

Astrocyte molecular signatures in Huntington's disease

Brain volumetric deficits in MAPT mutation carriers: a multisite study

C9ORF72 repeat expansions in cases with previously identified pathogenic mutations

CREB controls cortical circuit plasticity and functional recovery after stroke.

Clinical and volumetric changes with increasing functional impairment in familial frontotemporal lobar degeneration

Clinicopathological correlations in behavioural variant frontotemporal dementia.

Contribution of common and rare variants to bipolar disorder susceptibility in extended pedigrees from population isolates

DNA methylation study of Huntington's disease and motor progression in patients and in animal models

Distinct Subtypes of Behavioral Variant Frontotemporal Dementia Based on Patterns of Network Degeneration

Evidence for a role of the rare p.A152T variant in MAPT in increasing the risk for FTD-spectrum and Alzheimer's diseases

Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS

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

ForestQC: Quality control on genetic variants from next-generation sequencing data using random forest

Frequency of the TREM2 R47H Variant in Various Neurodegenerative Disorders

GDF10 is a signal for axonal sprouting and functional recovery after stroke.

Genetic screening of a large series of North American sporadic and familial frontotemporal dementia cases

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

Identification of common variants associated with human hippocampal and intracranial volumes

Immunosuppressive effect and global dysregulation of blood transcriptome in response to psychosocial stress in vervet monkeys (Chlorocebus sabaeus)

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

Individualized atrophy scores predict dementia onset in familial frontotemporal lobar degeneration

Injured adult neurons regress to an embryonic transcriptional growth state

Integrated genomics and proteomics define huntingtin CAG length-dependent networks in mice.

Longitudinal RNA-Seq analysis of acute and chronic neurogenic skeletal muscle atrophy

Loss of functional connectivity is greater outside the default mode network in nonfamilial early-onset Alzheimer's disease variants

Mitochondrial dysfunction and immune activation are detectable in early Alzheimer's disease blood

Mutations in XPR1 cause primary familial brain calcification associated with altered phosphate export

Network degeneration and dysfunction in presymptomatic C9ORF72 expansion carriers

No Evidence to Suggest that the Use of Acetylcholinesterase Inhibitors Confounds the Results of Two Blood-Based Biomarker Studies in Alzheimer's Disease

Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C-->T (Arg493X) mutation: an international initiative

Plasma tau and neurofilament light in frontotemporal lobar degeneration and Alzheimer's disease

Primary brain calcification: an international study reporting novel variants and associated phenotypes

Publisher Correction: Ancient hybridization and strong adaptation to viruses across African vervet monkey populations

Quality of life and caregiver burden in familial frontotemporal lobar degeneration: Analyses of symptomatic and asymptomatic individuals within the LEFFTDS cohort

Signaling to transcription networks in the neuronal retrograde injury response.

TDP-43 frontotemporal lobar degeneration and autoimmune disease

Temporal variant of frontotemporal dementia in C9orf72 repeat expansion carriers: two case studies

Tet3 regulates synaptic transmission and homeostatic plasticity via DNA oxidation and repair

The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data

The Longitudinal Trajectory of Default Mode Network Connectivity in Healthy Older Adults Varies as a Function of Age and is Associated with Changes in Episodic Memory and Processing Speed.

The longitudinal evaluation of familial frontotemporal dementia subjects protocol: Framework and methodology

Therapeutic targeting of oxygen-sensing prolyl hydroxylases abrogates ATF4-dependent neuronal death and improves outcomes after brain hemorrhage in several rodent models

Timing of Smarcb1 and Nf2 inactivation determines schwannoma versus rhabdoid tumor development.

Tracking white matter degeneration in asymptomatic and symptomatic MAPT mutation carriers

Transcriptional profiling of isogenic Friedreich ataxia neurons and effect of an HDAC inhibitor on disease signatures

Utility of the global CDR® plus NACC FTLD rating and development of scoring rules: Data from the ARTFL/LEFFTDS Consortium

White Matter Stroke Induces a Unique Oligo-Astrocyte Niche That Inhibits Recovery

hnRNPs Interacting with mRNA Localization Motifs Define Axonal RNA Regulons