(Q34569347)

3 August 2017

1 reference

title

Molecular diagnostics in monogenic and multifactorial forms of type 2 diabetes (English)

1 reference

3 August 2017

0 references

McCarthy MI

1

1 reference

PubMed ID

11901855

3 August 2017

Hattersley AT

series ordinal

2

1 reference

3 August 2017

1 November 2001

1 reference

Expert Review of Molecular Diagnostics: new diagnostic technologies are set to revolutionise healthcare

3 August 2017

1 reference

3 August 2017

1

1 reference

3 August 2017

4

1 reference

3 August 2017

403-412

1 reference

The dysmetabolic syndrome

3 August 2017

1 reference

https://api.crossref.org/works/10.1586%2F14737159.1.4.403

The perils of portliness: causes and consequences of visceral adiposity

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.1.4.403

Close linkage of glucokinase locus on chromosome 7p to early-onset non-insulin-dependent diabetes mellitus

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.1.4.403

Insulin secretory abnormalities in subjects with hyperglycemia due to glucokinase mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.1.4.403

HNF1alpha controls renal glucose reabsorption in mouse and man.

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.1.4.403

Abnormal nephron development associated with a frameshift mutation in the transcription factor hepatocyte nuclear factor-1 beta

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.1.4.403

beta-cell genes and diabetes: quantitative and qualitative differences in the pathophysiology of hepatic nuclear factor-1alpha and glucokinase mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.1.4.403

Predictive genetic testing in maturity-onset diabetes of the young (MODY).

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.1.4.403

A high prevalence of glucokinase mutations in gestational diabetic subjects selected by clinical criteria.

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.1.4.403

Mutations in the glucokinase gene of the fetus result in reduced birth weight

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.1.4.403

Searching for genetic determinants in the new millennium

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.1.4.403

Linkage disequilibrium in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.1.4.403

Pharmacogenetics and the practice of medicine

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.1.4.403

Multipoint quantitative-trait linkage analysis in general pedigrees

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.1.4.403

Genetic dissection of complex traits

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.1.4.403

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/10.1586%2F14737159.1.4.403

Genetic variation in the gene encoding calpain-10 is associated with type 2 diabetes mellitus

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.1.4.403

An autosomal genomic scan for loci linked to type II diabetes mellitus and body-mass index in Pima Indians

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.1.4.403

Genomewide linkage analysis of stature in multiple populations reveals several regions with evidence of linkage to adult height

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.1.4.403

The future of genetic studies of complex human diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.1.4.403

A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.1.4.403

Initial sequencing and analysis of the human genome

21 January 2018

1 reference

28 May 2022

https://opencitations.net/index/coci/api/v1/citations/10.1038/35057062

Dominant negative mutations in human PPARgamma associated with severe insulin resistance, diabetes mellitus and hypertension

1 reference

COCI

https://opencitations.net/index/coci/api/v1/citations/10.1038/47254

15 July 2023

Identifiers

DOI

10.1586/14737159.1.4.403

1 reference

3 August 2017

1 reference

PubMed ID

11901855