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The resequencing imperative
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Europe PubMed Central
PubMed publication ID
17392801
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17392801%20AND%20SRC:MED&resulttype=core&format=json
retrieved
28 December 2019
title
The resequencing imperative
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17392801
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17392801%20AND%20SRC:MED&resulttype=core&format=json
retrieved
28 December 2019
author
Eric J. Topol
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1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17392801
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17392801%20AND%20SRC:MED&resulttype=core&format=json
retrieved
28 December 2019
Kelly A. Frazer
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Kelly A Frazer
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17392801
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17392801%20AND%20SRC:MED&resulttype=core&format=json
retrieved
28 December 2019
publication date
1 April 2007
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17392801
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17392801%20AND%20SRC:MED&resulttype=core&format=json
retrieved
28 December 2019
language of work or name
English
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published in
Nature Genetics
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17392801
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17392801%20AND%20SRC:MED&resulttype=core&format=json
retrieved
28 December 2019
volume
39
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17392801
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17392801%20AND%20SRC:MED&resulttype=core&format=json
retrieved
28 December 2019
issue
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17392801
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17392801%20AND%20SRC:MED&resulttype=core&format=json
retrieved
28 December 2019
page(s)
439-440
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17392801
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17392801%20AND%20SRC:MED&resulttype=core&format=json
retrieved
28 December 2019
cites work
GENE SEQUENCING: The Race for the $1000 Genome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0407-439
retrieved
7 January 2021
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inferred from DOI database lookup
Low LDL cholesterol in individuals of African descent resulting from frequent nonsense mutations in PCSK9.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0407-439
retrieved
7 January 2021
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inferred from DOI database lookup
Multiple rare variants in NPC1L1 associated with reduced sterol absorption and plasma low-density lipoprotein levels
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0407-439
retrieved
7 January 2021
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inferred from DOI database lookup
Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0407-439
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Population-based resequencing of ANGPTL4 uncovers variations that reduce triglycerides and increase HDL.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0407-439
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A "silent" polymorphism in the MDR1 gene changes substrate specificity
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0407-439
retrieved
7 January 2021
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inferred from DOI database lookup
Human catechol-O-methyltransferase haplotypes modulate protein expression by altering mRNA secondary structure.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0407-439
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A genome-wide association study identifies IL23R as an inflammatory bowel disease gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0407-439
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A genome-wide association scan of nonsynonymous SNPs identifies a susceptibility variant for Crohn disease in ATG16L1
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0407-439
retrieved
7 January 2021
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CFH haplotypes without the Y402H coding variant show strong association with susceptibility to age-related macular degeneration
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0407-439
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Common variation in three genes, including a noncoding variant in CFH, strongly influences risk of age-related macular degeneration
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0407-439
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0407-439
retrieved
7 January 2021
based on heuristic
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Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0407-439
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A genome-wide association study identifies novel risk loci for type 2 diabetes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0407-439
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A common haplotype of interferon regulatory factor 5 (IRF5) regulates splicing and expression and is associated with increased risk of systemic lupus erythematosus
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0407-439
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The genetics of health
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0407-439
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1038/NG0407-439
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17392801
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17392801%20AND%20SRC:MED&resulttype=core&format=json
retrieved
28 December 2019
PubMed publication ID
17392801
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17392801
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17392801%20AND%20SRC:MED&resulttype=core&format=json
retrieved
28 December 2019
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