Common variations in the ALMS1 gene do not contribute to susceptibility to type 2 diabetes in a large white UK population. (Q52569872)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16601972%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

title

Common variations in the ALMS1 gene do not contribute to susceptibility to type 2 diabetes in a large white UK population (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16601972%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

1 reference

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16601972%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

Michael N Weedon

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16601972%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

Mark McCarthy

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16601972%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

Timothy Barrett

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16601972%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

author name string

J A L Minton

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16601972%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

T M Frayling

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16601972%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

C Ricketts

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16601972%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

G A Hitman

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16601972%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

A T Hattersley

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16601972%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

M Walker

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16601972%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

publication date

7 April 2006

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16601972%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16601972%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

volume

49

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16601972%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

issue

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16601972%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

page(s)

1209-1213

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16601972%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/s00125-006-0227-2

19 January 2020

exact match

0 references

cites work

Mutation of ALMS1, a large gene with a tandem repeat encoding 47 amino acids, causes Alström syndrome

1 reference

12 December 2020

A meta-analysis of four European genome screens (GIFT Consortium) shows evidence for a novel region on chromosome 17p11.2-q22 linked to type 2 diabetes.

1 reference

12 December 2020

Retinal degeneration combined with obesity, diabetes mellitus and neurogenous deafness: a specific syndrome (not hitherto described) distinct from the Laurence-Moon-Bardet-Biedl syndrome: a clinical, endocrinological and genetic examination based on

1 reference

12 December 2020

A sibship test for linkage in the presence of association: the sib transmission/disequilibrium test

1 reference

12 December 2020

New Alström syndrome phenotypes based on the evaluation of 182 cases

1 reference

12 December 2020

Mutations in ALMS1 cause obesity, type 2 diabetes and neurosensory degeneration in Alström syndrome

1 reference

12 December 2020

Subcellular localization of ALMS1 supports involvement of centrosome and basal body dysfunction in the pathogenesis of obesity, insulin resistance, and type 2 diabetes

1 reference

12 December 2020

Common Variants of the Hepatocyte Nuclear Factor-4 P2 Promoter Are Associated With Type 2 Diabetes in the U.K. Population

1 reference

12 December 2020

Parent-offspring trios: a resource to facilitate the identification of type 2 diabetes genes.

1 reference

12 December 2020

Lack of association between gene variants in the ALMS1 gene and Type 2 diabetes mellitus

1 reference

12 December 2020

A genomewide scan for loci predisposing to type 2 diabetes in a U.K. population (the Diabetes UK Warren 2 Repository): analysis of 573 pedigrees provides independent replication of a susceptibility locus on chromosome 1q

1 reference

12 December 2020

10.1007/S00125-006-0227-2

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16601972%20AND%20SRC:MED&resulttype=core&format=json

release_bjwvm4shqzfohb4s5qbvhfwzkq

19 January 2020

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/bjwvm4shqzfohb4s5qbvhfwzkq

24 November 2022

mapped directly with Wikidata item

1 reference