Length of normal alleles of C9ORF72 GGGGCC repeat do not influence disease phenotype (Q36742669)

16 August 2017

Length of normal alleles of C9ORF72 GGGGCC repeat do not influence disease phenotype (English)

1 reference

16 August 2017

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16 August 2017

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Catherine Lomen-Hoerth

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16 August 2017

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16 August 2017

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Manuela Neumann

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16 August 2017

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16 August 2017

22

Ronald C Petersen

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16 August 2017

24

Bruce L Miller

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16 August 2017

31

Owen A Ross

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16 August 2017

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William W Seeley

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16 August 2017

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16 August 2017

25

Bradley F Boeve

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16 August 2017

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Neill R Graff-Radford

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16 August 2017

2

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16 August 2017

27

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16 August 2017

4

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16 August 2017

7

Heather Stewart

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16 August 2017

15

Carol Lippa

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16 August 2017

14

Eileen H Bigio

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16 August 2017

11

Kimmo J Hatanpaa

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Alexandra I Soto-Ortolaza

16 August 2017

5

Alexandra I Soto-Ortolaza

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16 August 2017

9

Kathryn Volkening

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16 August 2017

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Hans A Kretzschmar

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Mariely DeJesus-Hernandez

16 August 2017

3

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16 August 2017

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1

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16 August 2017

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16 August 2017

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16 August 2017

26 July 2012

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16 August 2017

Neurobiology of Aging

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16 August 2017

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16 August 2017

2950.e5-7

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Frontotemporal lobar degeneration: current knowledge and future challenges.

16 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3617405

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3617405

Neuroimaging signatures of frontotemporal dementia genetics: C9ORF72, tau, progranulin and sporadics

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3617405

Characterization of frontotemporal dementia and/or amyotrophic lateral sclerosis associated with the GGGGCC repeat expansion in C9ORF72

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3617405

Clinical and pathological features of familial frontotemporal dementia caused by C9ORF72 mutation on chromosome 9p

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3617405

Clinical and pathological features of amyotrophic lateral sclerosis caused by mutation in the C9ORF72 gene on chromosome 9p

29 September 2017

1 reference

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3617405

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3617405

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3617405

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3617405

TDP-43 and FUS in amyotrophic lateral sclerosis and frontotemporal dementia

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3617405

Ataxin-2 intermediate-length polyglutamine expansions are associated with increased risk for ALS

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3617405

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3617405

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3617405

ALS: a disease of motor neurons and their nonneuronal neighbors

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3617405

Frontotemporal lobar degeneration: a consensus on clinical diagnostic criteria

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3617405

C9orf72 repeat expansions in patients with ALS and FTD.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3617405

Familial frontotemporal dementia and amyotrophic lateral sclerosis associated with the C9ORF72 hexanucleotide repeat

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3617405

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

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3617405

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

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3617405

5 September 2018

Frontotemporal dementia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3617405

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

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3617405

Interaction of normal and expanded CAG repeat sizes influences age at onset of Huntington disease

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3617405

NIPA1 polyalanine repeat expansions are associated with amyotrophic lateral sclerosis

4 December 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22840558

12 December 2020

inferred from PubMed ID database lookup

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

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22840558

12 December 2020

inferred from PubMed ID database lookup

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

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22840558

12 December 2020

inferred from PubMed ID database lookup

Identifiers

DOI

10.1016/J.NEUROBIOLAGING.2012.07.005

1 reference

release_hnbd4nbm6jfftowaltz2x3usoe

16 August 2017

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/hnbd4nbm6jfftowaltz2x3usoe

24 November 2022

mapped directly with Wikidata item

1 reference

16 August 2017

PubMed publication ID

22840558

1 reference