(Q24630410)

Jonathan D Rohrer

3

0 references

Jason D. Warren

Jason D Warren

16

0 references

Nick C. Fox

Nick C Fox

10

0 references

Martin Rossor

Martin N Rossor

11

0 references

John Anthony Hardy

12

John Hardy

0 references

Tammaryn Lashley

4

Tammaryn Lashley

0 references

Colin J Mahoney

1

Colin J Mahoney

0 references

Jonathan M Schott

9

Jonathan M Schott

0 references

Tom Yeatman

7

Tom Yeatman

0 references

Jon R Beck

2

Jon Beck

0 references

Tim J Shakespeare

6

Tim Shakespeare

0 references

John Collinge

13

John Collinge

0 references

Simon Mead

15

Simon Mead

0 references

author name string

Elizabeth K Warrington

8

0 references

Tamas Revesz

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

14

0 references

language of work or name

English

0 references

publication date

March 2012

0 references

published in

Brain

0 references

volume

135

0 references

issue

Pt 3

0 references

page(s)

736-50

0 references

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3286330

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

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3286330

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

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3286330

A harmonized classification system for FTLD-TDP pathology

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3286330

Classification of primary progressive aphasia and its variants

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3286330

Strongly reduced volumes of putamen and thalamus in Alzheimer's disease: an MRI study

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3286330

Analysis of IFT74 as a candidate gene for chromosome 9p-linked ALS-FTD

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3286330

Cortical Surface-Based Analysis

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3286330

Comparison of family histories in FTLD subtypes and related tauopathies

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3286330

Tract-based spatial statistics: voxelwise analysis of multi-subject diffusion data

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3286330

Measuring the thickness of the human cerebral cortex from magnetic resonance images

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3286330

Clinical and neuropathologic heterogeneity of c9FTD/ALS associated with hexanucleotide repeat expansion in C9ORF72

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3286330

Phenotypic signatures of genetic frontotemporal dementia

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3286330

Clinical and neuroanatomical signatures of tissue pathology in frontotemporal lobar degeneration

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3286330

A comparative clinical, pathological, biochemical and genetic study of fused in sarcoma proteinopathies

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3286330

Semantic dementia: a specific network-opathy

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3286330

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

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3286330

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

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3286330

Neurobehavioral features in frontotemporal dementia with amyotrophic lateral sclerosis

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3286330

Clinical, neuroimaging and neuropathological features of a new chromosome 9p-linked FTD-ALS family

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3286330

How preserved is episodic memory in behavioral variant frontotemporal dementia?

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3286330

Distinct profiles of brain atrophy in frontotemporal lobar degeneration caused by progranulin and tau mutations

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3286330

The heritability and genetics of frontotemporal lobar degeneration.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3286330

Delusions in frontotemporal lobar degeneration

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3286330

Dopamine D2 receptor levels in striatum, thalamus, substantia nigra, limbic regions, and cortex in schizophrenic subjects

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3286330

Pedigree with frontotemporal lobar degeneration--motor neuron disease and Tar DNA binding protein-43 positive neuropathology: genetic linkage to chromosome 9.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3286330

Disconnection syndromes of basal ganglia, thalamus, and cerebrocerebellar systems

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3286330

Parietal lobe deficits in frontotemporal lobar degeneration caused by a mutation in the progranulin gene

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3286330

A distinct clinical, neuropsychological and radiological phenotype is associated with progranulin gene mutations in a large UK series

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3286330

Corticobasal degeneration and its relationship to progressive supranuclear palsy and frontotemporal dementia

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3286330

The prevalence of frontotemporal dementia

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3286330

Schizophrenia and cognitive dysmetria: a positron-emission tomography study of dysfunctional prefrontal-thalamic-cerebellar circuitry

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3286330

Clinical research criteria for the diagnosis of progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome): report of the NINDS-SPSP international workshop

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3286330

The boundary shift integral: an accurate and robust measure of cerebral volume changes from registered repeat MRI.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3286330

Interactive algorithms for the segmentation and quantitation of 3-D MRI brain scans.

30 May 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWR361

Identification of 2 Loci at chromosomes 9 and 14 in a multiplex family with frontotemporal lobar degeneration and amyotrophic lateral sclerosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWR361

Visual presentation of phobic stimuli: amygdala activation via an extrageniculostriate pathway?

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWR361

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWR361

The case of a 48 year-old woman with bizarre and complex delusions.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWR361

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWR361

Issues with threshold masking in voxel-based morphometry of atrophied brains.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWR361

Cognition, emotion and the cerebellum.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWR361

Threshold-free cluster enhancement: addressing problems of smoothing, threshold dependence and localisation in cluster inference.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWR361

Waiting for spiders: brain activation during anticipatory anxiety in spider phobics.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWR361

Three families with amyotrophic lateral sclerosis and frontotemporal dementia with evidence of linkage to chromosome 9p.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWR361

Deficits of memory, executive functioning and attention following infarction in the thalamus; a study of 22 cases with localised lesions.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWR361

Familial amyotrophic lateral sclerosis with frontotemporal dementia is linked to a locus on chromosome 9p13.2-21.3.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWR361

Chromosome 9p-linked families with frontotemporal dementia associated with motor neuron disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWR361

A locus on chromosome 9p confers susceptibility to ALS and frontotemporal dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWR361

A C9orf72 promoter repeat expansion in a Flanders-Belgian cohort with disorders of the frontotemporal lobar degeneration-amyotrophic lateral sclerosis spectrum: a gene identification study.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3286330

The cerebellar cognitive profile.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3286330

Neuropathologic features of frontotemporal lobar degeneration with ubiquitin-positive inclusions visualized with ubiquitin-binding protein p62 immunohistochemistry

28 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22366791

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Ubiquitinated, p62 immunopositive cerebellar cortical neuronal inclusions are evident across the spectrum of TDP-43 proteinopathies but are only rarely additionally immunopositive for phosphorylation-dependent TDP-43

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22366791

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

p62 positive, TDP-43 negative, neuronal cytoplasmic and intranuclear inclusions in the cerebellum and hippocampus define the pathology of C9orf72-linked FTLD and MND/ALS

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22366791

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1093/BRAIN/AWR361

1 reference

2008073

2008073

1 reference

1 reference

1 reference