Haplotype construction of the FRDA gene and evaluation of its role in type II diabetes (Q46435444)

22 December 2017

meta-analysis

0 references

title

Haplotype construction of the FRDA gene and evaluation of its role in type II diabetes (English)

1 reference

22 December 2017

0 references

5

1 reference

22 December 2017

Cecilia Lindgren

7

1 reference

22 December 2017

Leif Groop

6

Leif Groop

1 reference

22 December 2017

2

Peter Almgren

1 reference

22 December 2017

Marco Zucchelli

4

Marco Zucchelli

1 reference

22 December 2017

Johan Holmkvist

1

Johan Holmkvist

1 reference

22 December 2017

Hemang M Parikh

3

Hemang Parikh

1 reference

22 December 2017

publication date

1 July 2005

1 reference

22 December 2017

European Journal of Human Genetics

published in

1 reference

22 December 2017

volume

13

1 reference

22 December 2017

issue

7

1 reference

22 December 2017

page(s)

849-855

1 reference

22 December 2017

https://scigraph.springernature.com/pub.10.1038/sj.ejhg.5201413

exact match

0 references

cites work

Definition, diagnosis and classification of diabetes mellitus and its complications. Part 1: diagnosis and classification of diabetes mellitus provisional report of a WHO consultation

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201413

Glucose metabolism alterations in Friedreich's ataxia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201413

Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201413

A genome-wide search for human non-insulin-dependent (type 2) diabetes genes reveals a major susceptibility locus on chromosome 2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201413

Genomewide search for type 2 diabetes mellitus susceptibility loci in Finnish families: the Botnia study

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201413

An autosomal genomic scan for loci linked to prediabetic phenotypes in Pima Indians

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201413

Frataxin is reduced in Friedreich ataxia patients and is associated with mitochondrial membranes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201413

Regulation of mitochondrial iron accumulation by Yfh1p, a putative homolog of frataxin

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201413

PGC-1alpha-responsive genes involved in oxidative phosphorylation are coordinately downregulated in human diabetes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201413

Intermediate expansions of a GAA repeat in the frataxin gene are not associated with type 2 diabetes or altered glucose-induced beta-cell function in Danish Caucasians.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201413

Metabolic consequences of a family history of NIDDM (the Botnia study): evidence for sex-specific parental effects.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201413

Insulin secretion and insulin sensitivity in relation to glucose tolerance: lessons from the Botnia Study

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201413

Predictors of progression from impaired glucose tolerance to NIDDM: an analysis of six prospective studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201413

Impaired fasting glucose or impaired glucose tolerance. What best predicts future diabetes in Mauritius?

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201413

PedCheck: a program for identification of genotype incompatibilities in linkage analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201413

Genetic Power Calculator: design of linkage and association genetic mapping studies of complex traits

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201413

The structure of haplotype blocks in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201413

A generalization of the transmission/disequilibrium test for uncertain-haplotype transmission

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201413

GENECOUNTING: haplotype analysis with missing genotypes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201413

2LD, GENECOUNTING and HAP: Computer programs for linkage disequilibrium analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201413

Large-scale association studies of variants in genes encoding the pancreatic beta-cell KATP channel subunits Kir6.2 (KCNJ11) and SUR1 (ABCC8) confirm that the KCNJ11 E23K variant is associated with type 2 diabetes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201413

Linkage disequilibrium and the search for complex disease genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201413

Altered beta-cell characteristics in impaired glucose tolerant carriers of a GAA trinucleotide repeat polymorphism in the frataxin gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201413

An association between NIDDM and a GAA trinucleotide repeat polymorphism in the X25/frataxin (Friedreich's ataxia) gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201413

Intermediate expansions of a X25/frataxin gene GAA repeat and Type II diabetes: assessment using parent-offspring trios

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201413

A genome-wide search for type II diabetes susceptibility genes in Chinese Hans

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201413

7 January 2021

G130V, a common FRDA point mutation, appears to have arisen from a common founder

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201413

7 January 2021

No association between the Friedreich's ataxia gene and NIDDM in the French population

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201413

7 January 2021

The common PPARgamma Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201413

7 January 2021

Identifiers

DOI

10.1038/SJ.EJHG.5201413

1 reference

22 December 2017

PubMed ID

15827563

1 reference

22 December 2017