(Q80540707)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17597769%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

title

Conjuring SNPs to detect associations (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17597769%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

author name string

Andrew G Clark

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17597769%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

Jian Li

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17597769%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

publication date

1 July 2007

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17597769%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17597769%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

volume

39

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17597769%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

issue

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17597769%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

page(s)

815-816

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17597769%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1038/ng0707-815

1 January 2020

exact match

0 references

cites work

A new multipoint method for genome-wide association studies by imputation of genotypes

1 reference

https://api.crossref.org/works/10.1038%2FNG0707-815

7 January 2021

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

1 reference

https://api.crossref.org/works/10.1038%2FNG0707-815

7 January 2021

A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants

1 reference

https://api.crossref.org/works/10.1038%2FNG0707-815

7 January 2021

Score tests for association between traits and haplotypes when linkage phase is ambiguous

1 reference

https://api.crossref.org/works/10.1038%2FNG0707-815

7 January 2021

Evaluating and improving power in whole-genome association studies using fixed marker sets.

1 reference

https://api.crossref.org/works/10.1038%2FNG0707-815

7 January 2021

Contrasting linkage-disequilibrium patterns between cases and controls as a novel association-mapping method

1 reference

https://api.crossref.org/works/10.1038%2FNG0707-815

7 January 2021

Statistical significance for genomewide studies

1 reference

https://api.crossref.org/works/10.1038%2FNG0707-815

7 January 2021

Genome-wide detection of human copy number variations using high-density DNA oligonucleotide arrays

1 reference

https://api.crossref.org/works/10.1038%2FNG0707-815

7 January 2021

Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol

1 reference

https://api.crossref.org/works/10.1038%2FNG0707-815

7 January 2021

Population-based resequencing of ANGPTL4 uncovers variations that reduce triglycerides and increase HDL.

1 reference

https://api.crossref.org/works/10.1038%2FNG0707-815

7 January 2021

Identifiers

DOI

10.1038/NG0707-815

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17597769%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

1 reference