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English
Genomics: The search for association
scientific article published in Nature
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
20981103
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20981103%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 January 2020
title
Genomics: The search for association
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
20981103
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20981103%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 January 2020
main subject
genomics
1 reference
based on heuristic
inferred from title
author
Monya Baker
series ordinal
1
object named as
Monya Baker
1 reference
stated in
Europe PubMed Central
PubMed publication ID
20981103
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20981103%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 January 2020
language of work or name
English
0 references
publication date
1 October 2010
1 reference
stated in
Europe PubMed Central
PubMed publication ID
20981103
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20981103%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 January 2020
published in
Nature
1 reference
stated in
Europe PubMed Central
PubMed publication ID
20981103
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20981103%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 January 2020
volume
467
1 reference
stated in
Europe PubMed Central
PubMed publication ID
20981103
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20981103%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 January 2020
issue
7319
1 reference
stated in
Europe PubMed Central
PubMed publication ID
20981103
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20981103%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 January 2020
page(s)
1135-1138
1 reference
stated in
Europe PubMed Central
PubMed publication ID
20981103
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20981103%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 January 2020
exact match
https://scigraph.springernature.com/pub.10.1038/4671135a
0 references
cites work
Towards a comprehensive structural variation map of an individual human genome
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/20981103
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/20981103
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Biological, clinical and population relevance of 95 loci for blood lipids
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/20981103
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Common SNPs in HMGCR in micronesians and whites associated with LDL-cholesterol levels affect alternative splicing of exon13
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/20981103
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Integrating common and rare genetic variation in diverse human populations
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/20981103
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/20981103
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/20981103
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Exome sequencing identifies the cause of a mendelian disorder
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/20981103
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Estimation of effect size distribution from genome-wide association studies and implications for future discoveries
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/20981103
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Functional impact of global rare copy number variation in autism spectrum disorders
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/20981103
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1038/4671135A
1 reference
stated in
Europe PubMed Central
PubMed publication ID
20981103
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20981103%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 January 2020
Dimensions Publication ID
1036294055
0 references
PubMed publication ID
20981103
1 reference
stated in
Europe PubMed Central
PubMed publication ID
20981103
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20981103%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 January 2020
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