C9orf72 and UNC13A are shared risk loci for amyotrophic lateral sclerosis and frontotemporal dementia: a genome-wide meta-analysis (Q34063137)

30 July 2017

0 references

C9orf72 and UNC13A are shared risk loci for amyotrophic lateral sclerosis and frontotemporal dementia: a genome-wide meta-analysis (English)

1 reference

amyotrophic lateral sclerosis and frontotemporal dementia

30 July 2017

0 references

amyotrophic lateral sclerosis

0 references

dementia

0 references

frontotemporal dementia

1 reference

7

1 reference

30 July 2017

15

1 reference

30 July 2017

17

André G Uitterlinden

0 references

Max Koppers

Max Koppers

12

0 references

Aleksey Shatunov

Aleksey Shatunov

21

0 references

Philip Van Damme

Philip van Damme

18

0 references

John Van Swieten

John C van Swieten

3

0 references

Vincenzo Silani

Vincenzo Silani

33

0 references

Pamela Shaw

Pamela J Shaw

24

0 references

Isabella Fogh

Isabella Fogh

26

0 references

Christopher Shaw

Christopher E Shaw

22

0 references

Karen E Morrison

Karen E Morrison

25

0 references

Albert Hofman

16

Albert Hofman

1 reference

30 July 2017

31

Peter Heutink

1 reference

30 July 2017

4

Ammar Al-Chalabi

1 reference

30 July 2017

20

Vincent Meininger

1 reference

30 July 2017

Leonard H van den Berg

35

Leonard H van den Berg

1 reference

30 July 2017

5

Albert C Ludolph

1 reference

30 July 2017

34

Wim Robberecht

1 reference

30 July 2017

27

Adriano Chiò

1 reference

30 July 2017

36

Jan H Veldink

1 reference

30 July 2017

13

Peter M Andersen

1 reference

30 July 2017

23

P Nigel Leigh

1 reference

30 July 2017

28

Bryan J Traynor

1 reference

30 July 2017

8

John E Landers

1 reference

30 July 2017

6

Jochen H Weishaupt

1 reference

30 July 2017

19

Judith Melki

1 reference

30 July 2017

1

Frank P Diekstra

1 reference

30 July 2017

Vivianna M Van Deerlin

2

Vivianna M Van Deerlin

1 reference

30 July 2017

11

R Jeroen Pasterkamp

1 reference

30 July 2017

14

Karol Estrada

1 reference

30 July 2017

29

David Czell

1 reference

30 July 2017

32

Paul I W de Bakker

1 reference

30 July 2017

9

Robert H Brown

1 reference

30 July 2017

Michael A van Es

10

1 reference

30 July 2017

Markus Weber

30

1 reference

30 July 2017

27 June 2014

1 reference

30 July 2017

1 reference

30 July 2017

76

1 reference

30 July 2017

120-133

1 reference

30 July 2017

1

1 reference

Stages of pTDP-43 pathology in amyotrophic lateral sclerosis

30 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4137231

The product of C9orf72, a gene strongly implicated in neurodegeneration, is structurally related to DENN Rab-GEFs

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4137231

Discovery of Novel DENN Proteins: Implications for the Evolution of Eukaryotic Intracellular Membrane Structures and Human Disease

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4137231

UNC13A influences survival in Italian amyotrophic lateral sclerosis patients: a population-based study

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4137231

Estimation of pleiotropy between complex diseases using single-nucleotide polymorphism-derived genomic relationships and restricted maximum likelihood

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4137231

Conditional and joint multiple-SNP analysis of GWAS summary statistics identifies additional variants influencing complex traits

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4137231

Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4137231

Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4137231

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4137231

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4137231

Involvement of Rab3A in vesicle priming during exocytosis: interaction with Munc13-1 and Munc18-1.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4137231

TMEM106B is associated with frontotemporal lobar degeneration in a clinically diagnosed patient cohort

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4137231

GCTA: a tool for genome-wide complex trait analysis

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4137231

Exome sequencing reveals VCP mutations as a cause of familial ALS

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4137231

Risk genotypes at TMEM106B are associated with cognitive impairment in amyotrophic lateral sclerosis

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4137231

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4137231

Strumpellin is a novel valosin-containing protein binding partner linking hereditary spastic paraplegia to protein aggregation diseases.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4137231

Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4137231

Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4137231

Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4137231

Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4137231

A flexible and accurate genotype imputation method for the next generation of genome-wide association studies

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4137231

Current hypotheses for the underlying biology of amyotrophic lateral sclerosis

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4137231

Practical aspects of imputation-driven meta-analysis of genome-wide association studies

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4137231

PLINK: a tool set for whole-genome association and population-based linkage analyses

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4137231

Establishing subtypes of the continuum of frontal lobe impairment in amyotrophic lateral sclerosis

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4137231

Mutations in the KIAA0196 gene at the SPG8 locus cause hereditary spastic paraplegia

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4137231

Principal components analysis corrects for stratification in genome-wide association studies

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4137231

Aberrant morphology and residual transmitter release at the Munc13-deficient mouse neuromuscular synapse

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4137231

Rank products: a simple, yet powerful, new method to detect differentially regulated genes in replicated microarray experiments

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4137231

Cognitive impairment, frontotemporal dementia, and the motor neuron diseases

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4137231

El Escorial revisited: revised criteria for the diagnosis of amyotrophic lateral sclerosis

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4137231

Prevalence and patterns of cognitive impairment in sporadic ALS.

5 July 2018

1 reference

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

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

UNC13A is a modifier of survival in amyotrophic lateral sclerosis

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24931836

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1002/ANA.24198

1 reference

30 July 2017

1 reference

30 July 2017

1 reference