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An estimate of amyotrophic lateral sclerosis heritability using twin data.
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scholarly article
1 reference
stated in
Europe PubMed Central
PMC publication ID
2988617
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20861059%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 February 2020
meta-analysis
0 references
title
An estimate of amyotrophic lateral sclerosis heritability using twin data
(English)
1 reference
stated in
Europe PubMed Central
PMC publication ID
2988617
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20861059%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 February 2020
main subject
amyotrophic lateral sclerosis
0 references
heritability
1 reference
based on heuristic
inferred from title
author
Ammar Al-Chalabi
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMC publication ID
2988617
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20861059%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 February 2020
Fang Fang
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMC publication ID
2988617
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20861059%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 February 2020
Christopher Shaw
series ordinal
5
1 reference
stated in
Europe PubMed Central
PMC publication ID
2988617
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20861059%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 February 2020
Weimin Ye
series ordinal
6
1 reference
stated in
Europe PubMed Central
PMC publication ID
2988617
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20861059%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 February 2020
Fruhling Rijsdijk
series ordinal
7
1 reference
stated in
Europe PubMed Central
PMC publication ID
2988617
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20861059%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 February 2020
P Nigel Leigh
series ordinal
4
object named as
P N Leigh
1 reference
stated in
Europe PubMed Central
PMC publication ID
2988617
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20861059%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 February 2020
author name string
M F Hanby
series ordinal
3
1 reference
stated in
Europe PubMed Central
PMC publication ID
2988617
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20861059%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 February 2020
language of work or name
English
0 references
publication date
22 September 2010
1 reference
stated in
Europe PubMed Central
PMC publication ID
2988617
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20861059%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 February 2020
published in
Journal of Neurology, Neurosurgery and Psychiatry
1 reference
stated in
Europe PubMed Central
PMC publication ID
2988617
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20861059%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 February 2020
volume
81
1 reference
stated in
Europe PubMed Central
PMC publication ID
2988617
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20861059%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 February 2020
issue
12
1 reference
stated in
Europe PubMed Central
PMC publication ID
2988617
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20861059%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 February 2020
page(s)
1324-1326
1 reference
stated in
Europe PubMed Central
PMC publication ID
2988617
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20861059%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 February 2020
cites work
Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2988617
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28 July 2018
Natural history and clinical features of the flail arm and flail leg ALS variants
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2988617
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28 July 2018
Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2988617
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28 July 2018
TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2988617
retrieved
28 July 2018
TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2988617
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28 July 2018
The epidemiology of ALS and the role of population-based registries
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28 July 2018
A mutation in the vesicle-trafficking protein VAPB causes late-onset spinal muscular atrophy and amyotrophic lateral sclerosis
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2988617
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28 July 2018
The Swedish Twin Registry: a unique resource for clinical, epidemiological and genetic studies
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2988617
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28 July 2018
British motor neuron disease twin study
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2988617
retrieved
28 July 2018
Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2988617
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28 July 2018
Autism as a strongly genetic disorder: evidence from a British twin study
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2988617
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28 July 2018
Mutations of optineurin in amyotrophic lateral sclerosis
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PubMed Central
reference URL
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30 October 2018
Genetics of motor neuron disorders: new insights into pathogenic mechanisms
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PubMed Central
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30 October 2018
Familial aggregation of amyotrophic lateral sclerosis
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2988617
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30 October 2018
Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2988617
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30 October 2018
Epidemiology of ALS in Italy: a 10-year prospective population-based study.
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PubMed Central
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30 October 2018
ANG mutations segregate with familial and 'sporadic' amyotrophic lateral sclerosis.
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2988617
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30 October 2018
Comparison of analysis of variance and maximum likelihood based path analysis of twin data: partitioning genetic and environmental sources of covariance
1 reference
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PubMed Central
reference URL
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30 October 2018
Path analysis in genetic epidemiology: a critique
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PubMed Central
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30 October 2018
Amyotrophic lateral sclerosis in an urban setting
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2988617
retrieved
30 October 2018
Age at onset in sod1-mediated amyotrophic lateral sclerosis shows familiality
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/20861059
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1136/JNNP.2010.207464
1 reference
stated in
Europe PubMed Central
PMC publication ID
2988617
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20861059%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 February 2020
PMC publication ID
2988617
1 reference
stated in
Europe PubMed Central
PMC publication ID
2988617
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20861059%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 February 2020
PubMed publication ID
20861059
1 reference
stated in
Europe PubMed Central
PMC publication ID
2988617
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20861059%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 February 2020
ResearchGate publication ID
46403093
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