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Building genetic scores to predict risk of complex diseases in humans: is it possible?
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stated in
Europe PubMed Central
PMC publication ID
2963528
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20980472%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 January 2020
title
Building genetic scores to predict risk of complex diseases in humans: is it possible?
(English)
1 reference
stated in
Europe PubMed Central
PMC publication ID
2963528
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20980472%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 January 2020
author
Simin Liu
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMC publication ID
2963528
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20980472%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 January 2020
author name string
Yiqing Song
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMC publication ID
2963528
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20980472%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 January 2020
language of work or name
English
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publication date
1 November 2010
1 reference
stated in
Europe PubMed Central
PMC publication ID
2963528
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20980472%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 January 2020
published in
Diabetes
1 reference
stated in
Europe PubMed Central
PMC publication ID
2963528
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20980472%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 January 2020
volume
59
1 reference
stated in
Europe PubMed Central
PMC publication ID
2963528
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20980472%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 January 2020
issue
11
1 reference
stated in
Europe PubMed Central
PMC publication ID
2963528
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20980472%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 January 2020
page(s)
2729-2731
1 reference
stated in
Europe PubMed Central
PMC publication ID
2963528
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20980472%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 January 2020
copyright license
Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported
start time
27 August 2021
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April 2022 Public Data File from Crossref
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copyrighted
0 references
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Finding the missing heritability of complex diseases
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Sex hormone-binding globulin and risk of type 2 diabetes in women and men
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Genomic copy number variation, human health, and disease
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Genomewide association studies of stroke
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Clinical risk factors, DNA variants, and the development of type 2 diabetes
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FTO polymorphisms are associated with obesity but not diabetes risk in postmenopausal women
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Loci related to metabolic-syndrome pathways including LEPR,HNF1A, IL6R, and GCKR associate with plasma C-reactive protein: the Women's Genome Health Study
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retrieved
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based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.2337/DB10-1081
1 reference
stated in
Europe PubMed Central
PMC publication ID
2963528
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20980472%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 January 2020
PMC publication ID
2963528
1 reference
stated in
Europe PubMed Central
PMC publication ID
2963528
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20980472%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 January 2020
PubMed publication ID
20980472
1 reference
stated in
Europe PubMed Central
PMC publication ID
2963528
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20980472%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 January 2020
ResearchGate publication ID
47566464
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