(Q36742669)

16 August 2017

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

1 reference

16 August 2017

1 reference

30

1 reference

16 August 2017

Sruti Rayaprolu

6

0 references

Elizabeth Finger

Elizabeth Finger

8

0 references

Michael J Strong

Michael J Strong

23

0 references

Charles L White

Charles L White

20

0 references

Catherine Lomen-Hoerth

12

Catherine Lomen-Hoerth

1 reference

16 August 2017

26

Ryan J Uitti

1 reference

16 August 2017

28

Zbigniew K Wszolek

1 reference

16 August 2017

18

Manuela Neumann

1 reference

16 August 2017

32

Rosa Rademakers

1 reference

16 August 2017

22

Ronald C Petersen

1 reference

16 August 2017

24

Bruce L Miller

1 reference

16 August 2017

31

Owen A Ross

1 reference

16 August 2017

10

William W Seeley

1 reference

16 August 2017

16

David S Knopman

1 reference

16 August 2017

25

Bradley F Boeve

1 reference

16 August 2017

Neill R Graff-Radford

29

Neill R Graff-Radford

1 reference

16 August 2017

2

Michael G Heckman

1 reference

16 August 2017

27

Kevin B Boylan

1 reference

16 August 2017

4

Matt C Baker

1 reference

16 August 2017

7

Heather Stewart

1 reference

16 August 2017

15

Carol Lippa

1 reference

16 August 2017

14

Eileen H Bigio

1 reference

16 August 2017

11

Kimmo J Hatanpaa

1 reference

Alexandra I Soto-Ortolaza

16 August 2017

5

Alexandra I Soto-Ortolaza

1 reference

16 August 2017

9

Kathryn Volkening

1 reference

16 August 2017

17

Hans A Kretzschmar

1 reference

Mariely DeJesus-Hernandez

16 August 2017

3

Mariely Dejesus-Hernandez

1 reference

16 August 2017

Nicola J Rutherford

1

1 reference

16 August 2017

Andrew Kertesz

13

1 reference

16 August 2017

Richard J Caselli

19

1 reference

16 August 2017

Ian R Mackenzie

21

1 reference

16 August 2017

26 July 2012

1 reference

16 August 2017

Neurobiology of Aging

1 reference

16 August 2017

33

1 reference

16 August 2017

12

1 reference

16 August 2017

2950.e5-7

1 reference

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

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

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