(Q63916515)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19165915%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

title

Casting a wider net for diabetes susceptibility genes (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19165915%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19165915%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

publication date

1 September 2008

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19165915%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19165915%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

volume

40

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19165915%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

issue

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19165915%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

page(s)

1039-1040

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19165915%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1038/ng0908-1039

20 January 2020

exact match

0 references

cites work

Genome-wide association studies provide new insights into type 2 diabetes aetiology

1 reference

https://api.crossref.org/works/10.1038%2FNG0908-1039

7 January 2021

Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes

1 reference

https://api.crossref.org/works/10.1038%2FNG0908-1039

7 January 2021

SNPs in KCNQ1 are associated with susceptibility to type 2 diabetes in East Asian and European populations

1 reference

https://api.crossref.org/works/10.1038%2FNG0908-1039

7 January 2021

Variants in KCNQ1 are associated with susceptibility to type 2 diabetes mellitus.

1 reference

https://api.crossref.org/works/10.1038%2FNG0908-1039

7 January 2021

Genome-wide association studies for complex traits: consensus, uncertainty and challenges

1 reference

https://api.crossref.org/works/10.1038%2FNG0908-1039

7 January 2021

Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetes

1 reference

https://api.crossref.org/works/10.1038%2FNG0908-1039

7 January 2021

A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG0908-1039

7 January 2021

Effects of I(Ks) channel inhibitors in insulin-secreting INS-1 cells

1 reference

https://api.crossref.org/works/10.1038%2FNG0908-1039

7 January 2021

Common variants of the novel type 2 diabetes genes CDKAL1 and HHEX/IDE are associated with decreased pancreatic beta-cell function

1 reference

https://api.crossref.org/works/10.1038%2FNG0908-1039

7 January 2021

Human KVLQT1 gene shows tissue-specific imprinting and encompasses Beckwith-Wiedemann syndrome chromosomal rearrangements.

1 reference

https://api.crossref.org/works/10.1038%2FNG0908-1039

7 January 2021

A maternally methylated CpG island in KvLQT1 is associated with an antisense paternal transcript and loss of imprinting in Beckwith-Wiedemann syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG0908-1039

7 January 2021

Implication of genetic variants near TCF7L2, SLC30A8, HHEX, CDKAL1, CDKN2A/B, IGF2BP2, and FTO in type 2 diabetes and obesity in 6,719 Asians

1 reference

https://api.crossref.org/works/10.1038%2FNG0908-1039

7 January 2021

Association of CDKAL1, IGF2BP2, CDKN2A/B, HHEX, SLC30A8, and KCNJ11 with susceptibility to type 2 diabetes in a Japanese population.

1 reference

https://api.crossref.org/works/10.1038%2FNG0908-1039

7 January 2021

Impact of nine common type 2 diabetes risk polymorphisms in Asian Indian Sikhs: PPARG2 (Pro12Ala), IGF2BP2, TCF7L2 and FTO variants confer a significant risk

1 reference

https://api.crossref.org/works/10.1038%2FNG0908-1039

7 January 2021