(Q63916494)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20664646%20AND%20SRC:MED&resulttype=core&format=json

8 February 2020

title

Variation across the allele frequency spectrum (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20664646%20AND%20SRC:MED&resulttype=core&format=json

8 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A20664646

11 June 2024

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20664646%20AND%20SRC:MED&resulttype=core&format=json

8 February 2020

Mark McCarthy

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20664646%20AND%20SRC:MED&resulttype=core&format=json

8 February 2020

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=20664646

11 June 2024

publication date

1 August 2010

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20664646%20AND%20SRC:MED&resulttype=core&format=json

full work available at URL

8 February 2020

http://www.nature.com/articles/ng0810-648.pdf

file format

Portable Document Format

1 reference

https://api.crossref.org/works/10.1038/NG0810-648

http://www.nature.com/articles/ng0810-648

11 June 2024

1 reference

https://api.crossref.org/works/10.1038/NG0810-648

11 June 2024

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20664646%20AND%20SRC:MED&resulttype=core&format=json

8 February 2020

volume

42

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20664646%20AND%20SRC:MED&resulttype=core&format=json

8 February 2020

issue

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20664646%20AND%20SRC:MED&resulttype=core&format=json

8 February 2020

page(s)

648-650

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20664646%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1038/ng0810-648

8 February 2020

exact match

0 references

cites work

Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels

1 reference

12 December 2020

The P446L variant in GCKR associated with fasting plasma glucose and triglyceride levels exerts its effect through increased glucokinase activity in liver

1 reference

12 December 2020

Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia

1 reference

12 December 2020

Rare loss-of-function mutations in ANGPTL family members contribute to plasma triglyceride levels in humans.

1 reference

12 December 2020

Uncovering the roles of rare variants in common disease through whole-genome sequencing

1 reference

12 December 2020

Sequence variations in PCSK9, low LDL, and protection against coronary heart disease

1 reference

12 December 2020

Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts

1 reference

12 December 2020

Finding the missing heritability of complex diseases

1 reference

12 December 2020

Common variants at 30 loci contribute to polygenic dyslipidemia

1 reference

12 December 2020

Common missense variant in the glucokinase regulatory protein gene is associated with increased plasma triglyceride and C-reactive protein but lower fasting glucose concentrations

1 reference

12 December 2020

Exome sequencing identifies the cause of a mendelian disorder

1 reference

12 December 2020

New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk

1 reference

12 December 2020

Journal of Clinical Investigation

5

119

70

S Romeo

2009

1 reference

https://api.crossref.org/works/10.1038/NG0810-648