Genetics of Frontotemporal Dementia (Q39017699)

8 September 2017

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title

Genetics of Frontotemporal Dementia (English)

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8 September 2017

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frontotemporal dementia

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Tim Lynch

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8 September 2017

Diana A Olszewska

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8 September 2017

Roisin Lonergan

series ordinal

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8 September 2017

Emer M Fallon

series ordinal

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8 September 2017

publication date

1 December 2016

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Current Neurology and Neuroscience Reports

8 September 2017

published in

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8 September 2017

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8 September 2017

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8 September 2017

page(s)

107

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The heritability and genetics of frontotemporal lobar degeneration.

8 September 2017

cites work

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https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

Phenotypic Heterogeneity of Monogenic Frontotemporal Dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

21 January 2018

Frontotemporal dementia.

1 reference

https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

A stop-codon mutation in the BRI gene associated with familial British dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

A decamer duplication in the 3' region of the BRI gene originates an amyloid peptide that is associated with dementia in a Danish kindred

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

Clinical, genetic and pathological heterogeneity of frontotemporal dementia: a review

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

Spinocerebellar ataxia 17 (SCA17) and Huntington's disease-like 4 (HDL4).

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

Dentatorubral–pallidoluysian atrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

Clinical characteristics of a family with chromosome 17-linked disinhibition-dementia-parkinsonism-amyotrophy complex.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

Rapidly progressive autosomal dominant parkinsonism and dementia with pallido-ponto-nigral degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

Familial multiple system tauopathy with presenile dementia: a disease with abundant neuronal and glial tau filaments

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

Frontotemporal dementia and parkinsonism linked to chromosome 17: a consensus conference. Conference Participants

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

Association of missense and 5'-splice-site mutations in tau with the inherited dementia FTDP-17

21 January 2018

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https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

Tau is a candidate gene for chromosome 17 frontotemporal dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

Dementia in 2013: frontotemporal lobar degeneration-building on breakthroughs

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

Closing the tau loop: the missing tau mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

A distinct familial presenile dementia with a novel missense mutation in the tau gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

5' splice site mutations in tau associated with the inherited dementia FTDP-17 affect a stem-loop structure that regulates alternative splicing of exon 10.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

Progressive supranuclear palsy pathology caused by a novel silent mutation in exon 10 of the tau gene: expansion of the disease phenotype caused by tau gene mutations.

21 January 2018

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https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

Regulation of alternative splicing of tau exon 10.

21 January 2018

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https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

Association of an extended haplotype in the tau gene with progressive supranuclear palsy

21 January 2018

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https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

Association between the extended tau haplotype and frontotemporal dementia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

Tau haplotype frequency in frontotemporal lobar degeneration and amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

Association between tau H2 haplotype and age at onset in frontotemporal dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

MAPT H1 Haplotype is Associated with Late-Onset Alzheimer's Disease Risk in APOEɛ4 Noncarriers: Results from the Dementia Genetics Spanish Consortium

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

Invited review: Frontotemporal dementia caused by microtubule-associated protein tau gene (MAPT) mutations: a chameleon for neuropathology and neuroimaging

21 January 2018

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https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

The genetics and neuropathology of frontotemporal lobar degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

Pallidopontonigral degeneration: a deceptive familial tauopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

Frontotemporal lobar degeneration: a consensus on clinical diagnostic criteria

21 January 2018

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https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

Sensitivity of revised diagnostic criteria for the behavioural variant of frontotemporal dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

Presymptomatic cognitive and neuroanatomical changes in genetic frontotemporal dementia in the Genetic Frontotemporal dementia Initiative (GENFI) study: a cross-sectional analysis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

Longitudinal neuroimaging and neuropsychological profiles of frontotemporal dementia with C9ORF72 expansions.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

The tauopathy associated with mutation +3 in intron 10 of Tau: characterization of the MSTD family

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

Trajectories of brain and hippocampal atrophy in FTD with mutations in MAPT or GRN

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

Longitudinal diffusion tensor imaging in frontotemporal dementia.

21 January 2018

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https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

Profiles of white matter tract pathology in frontotemporal dementia

21 January 2018

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https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

Structural and functional brain connectivity in presymptomatic familial frontotemporal dementia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

Interaction of the amyloid imaging tracer FDDNP with hallmark Alzheimer's disease pathologies

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

Comparison of the binding characteristics of [18F]THK-523 and other amyloid imaging tracers to Alzheimer's disease pathology

21 January 2018

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https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

Imaging of tau pathology in a tauopathy mouse model and in Alzheimer patients compared to normal controls

21 January 2018

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https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

18F-AV-1451 tau PET imaging correlates strongly with tau neuropathology in MAPT mutation carriers

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

Validating novel tau positron emission tomography tracer [F-18]-AV-1451 (T807) on postmortem brain tissue

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

Assessing THK523 selectivity for tau deposits in Alzheimer's disease and non-Alzheimer's disease tauopathies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

Novel 18F-labeled arylquinoline derivatives for noninvasive imaging of tau pathology in Alzheimer disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

Structure-Activity Relationship Study of Heterocyclic Phenylethenyl and Pyridinylethenyl Derivatives as Tau-Imaging Agents That Selectively Detect Neurofibrillary Tangles in Alzheimer's Disease Brains.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

The neuropathology of chromosome 17-linked dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

Molecular neuropathology of frontotemporal dementia: insights into disease mechanisms from postmortem studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

Pathological inclusion bodies in tauopathies contain distinct complements of tau with three or four microtubule-binding repeat domains as demonstrated by new specific monoclonal antibodies

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

ptl-1, a Caenorhabditis elegans gene whose products are homologous to the tau microtubule-associated proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

Knock-out and transgenic mouse models of tauopathies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

Immunotherapy targeting pathological tau conformers in a tangle mouse model reduces brain pathology with associated functional improvements.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

Immunotherapy Targeting Pathological Tau Prevents Cognitive Decline in a New Tangle Mouse Model

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

Immunotherapeutic approaches for Alzheimer's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

Tauopathy-like abnormalities and neurologic deficits in mice immunized with neuronal tau protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

Intracellular and extracellular microtubule associated protein tau as a therapeutic target in Alzheimer disease and other tauopathies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

Cellular Models of Aggregation-dependent Template-directed Proteolysis to Characterize Tau Aggregation Inhibitors for Treatment of Alzheimer Disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

Hereditary dysphasic disinhibition dementia: a frontotemporal dementia linked to 17q21-22.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

The granulin gene family: from cancer to dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

Recent insights into the involvement of progranulin in frontotemporal dementia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

Progranulin axis and recent developments in frontotemporal lobar degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

Progranulin Mutations are a Common Cause of FTLD in Northern Italy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

Phenotype variability in progranulin mutation carriers: a clinical, neuropsychological, imaging and genetic study

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

Multimodal FMRI resting-state functional connectivity in granulin mutations: the case of fronto-parietal dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

Alteration of behavioural phenotype in mice by targeted disruption of the progranulin gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

Exaggerated inflammation, impaired host defense, and neuropathology in progranulin-deficient mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

Accelerated lipofuscinosis and ubiquitination in granulin knockout mice suggest a role for progranulin in successful aging

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

Behavioral deficits and progressive neuropathology in progranulin-deficient mice: a mouse model of frontotemporal dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

HDAC2 negatively regulates memory formation and synaptic plasticity.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

Progranulin Levels in Plasma and Cerebrospinal Fluid in Granulin Mutation Carriers.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

Plasma progranulin levels predict progranulin mutation status in frontotemporal dementia patients and asymptomatic family members

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

C9ORF72 expansion in amyotrophic lateral sclerosis/frontotemporal dementia also causes parkinsonism

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

Early onset frontotemporal dementia with psychiatric presentation due to the C9ORF72 hexanucleotide repeat expansion: a case report

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

Frontotemporal dementia with the C9ORF72 hexanucleotide repeat expansion: clinical, neuroanatomical and neuropathological features

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

C9orf72 expansions in frontotemporal dementia and amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

Frontotemporal lobar degeneration: defining phenotypic diversity through personalized medicine

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

C9orf72 repeat expansions cause neurodegeneration in Drosophila through arginine-rich proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

Mutation within TARDBP leads to frontotemporal dementia without motor neuron disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

Clinical phenotypes and radiological findings in frontotemporal dementia related to TARDBP mutations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

FUS and TDP43 genetic variability in FTD and CBS

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

Chromosome 3 linked frontotemporal dementia (FTD-3).

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

Presymptomatic generalized brain atrophy in frontotemporal dementia caused by CHMP2B mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

Frontotemporal dementia caused by CHMP2B mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

Loss of TBK1 is a frequent cause of frontotemporal dementia in a Belgian cohort

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

Familial Presenile Dementia with Spastic Paralysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

Morphological basis for the spectrum of clinical deficits in spinocerebellar ataxia 17 (SCA17).

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

Loss of insight in frontotemporal dementia, corticobasal degeneration and progressive supranuclear palsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

Behavioral Disorder, Dementia, Ataxia, and Rigidity in a Large Family With TATA Box-Binding Protein Mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

18F-THK523: a novel in vivo tau imaging ligand for Alzheimer's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

Tau and transgenic animal models

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

The genetics of primary progressive aphasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-016-0707-9

From mild ataxia to huntington disease phenocopy: the multiple faces of spinocerebellar ataxia 17.

21 January 2018

1 reference

12 December 2020

A novel mutation at position +12 in the intron following exon 10 of the tau gene in familial frontotemporal dementia (FTD-Kumamoto)

1 reference

12 December 2020

Tau accumulation in astrocytes in progressive supranuclear palsy is a degenerative rather than a reactive process

1 reference

12 December 2020

Drosophila models of tauopathies: what have we learned?

1 reference

12 December 2020

Cortical volumes and atrophy rates in FTD-3 CHMP2B mutation carriers and related non-carriers

1 reference

12 December 2020

Progranulin: normal function and role in neurodegeneration

1 reference

12 December 2020

"Missing" tau mutation identified

1 reference

12 December 2020

Linkage of frontotemporal dementia to chromosome 17: clinical and neuropathological characterization of phenotype

1 reference

12 December 2020

Frontotemporal dementia and Parkinsonism linked to chromosome 17: a new group of tauopathies.

1 reference

12 December 2020

A highly selective and specific PET tracer for imaging of tau pathologies

1 reference

12 December 2020

Strong association of a novel Tau promoter haplotype in progressive supranuclear palsy

1 reference

12 December 2020

Localization of disinhibition-dementia-parkinsonism-amyotrophy complex to 17q21-22.

1 reference

12 December 2020

Corticobasal degeneration and progressive supranuclear palsy share a common tau haplotype

1 reference

12 December 2020

Neurodegenerative disorder FTDP-17-related tau intron 10 +16C → T mutation increases tau exon 10 splicing and causes tauopathy in transgenic mice

1 reference

12 December 2020

10.1007/S11910-016-0707-9

Identifiers

DOI

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8 September 2017

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