(Q52926370)

English

A German genome-wide linkage scan for type 2 diabetes supports the existence of a metabolic syndrome locus on chromosome 1p36.13 and a type 2 diabetes locus on chromosome 16p12.2.

scientific article published on 27 April 2007

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

9 May 2018

http://europepmc.org/abstract/MED/17464498

A German genome-wide linkage scan for type 2 diabetes supports the existence of a metabolic syndrome locus on chromosome 1p36.13 and a type 2 diabetes locus on chromosome 16p12.2. (English)

1 reference

Europe PubMed Central

PubMed publication ID

9 May 2018

http://europepmc.org/abstract/MED/17464498

type 2 diabetes

0 references

metabolic syndrome

1 reference

based on heuristic

inferred from title

Manuel Mattheisen

2

1 reference

Europe PubMed Central

PubMed publication ID

9 May 2018

http://europepmc.org/abstract/MED/17464498

Heinz Erich Wichmann

8

object named as

H E Wichmann

1 reference

Europe PubMed Central

PubMed publication ID

9 May 2018

7

object named as

N J Cox

1 reference

Europe PubMed Central

PubMed publication ID

9 May 2018

http://europepmc.org/abstract/MED/17464498

author name string

K Hoffmann

1

1 reference

Europe PubMed Central

PubMed publication ID

9 May 2018

http://europepmc.org/abstract/MED/17464498

S Dahm

3

1 reference

Europe PubMed Central

PubMed publication ID

9 May 2018

http://europepmc.org/abstract/MED/17464498

P Nürnberg

4

1 reference

Europe PubMed Central

PubMed publication ID

9 May 2018

http://europepmc.org/abstract/MED/17464498

C Roe

5

1 reference

Europe PubMed Central

PubMed publication ID

9 May 2018

http://europepmc.org/abstract/MED/17464498

J Johnson

6

1 reference

Europe PubMed Central

PubMed publication ID

9 May 2018

http://europepmc.org/abstract/MED/17464498

T F Wienker

9

1 reference

Europe PubMed Central

PubMed publication ID

9 May 2018

http://europepmc.org/abstract/MED/17464498

J Schulze

10

1 reference

Europe PubMed Central

PubMed publication ID

9 May 2018

http://europepmc.org/abstract/MED/17464498

P E Schwarz

11

1 reference

Europe PubMed Central

PubMed publication ID

9 May 2018

http://europepmc.org/abstract/MED/17464498

T H Lindner

12

1 reference

Europe PubMed Central

PubMed publication ID

9 May 2018

http://europepmc.org/abstract/MED/17464498

publication date

27 April 2007

1 reference

Europe PubMed Central

PubMed publication ID

9 May 2018

http://europepmc.org/abstract/MED/17464498

1 reference

Europe PubMed Central

PubMed publication ID

9 May 2018

http://europepmc.org/abstract/MED/17464498

50

1 reference

Europe PubMed Central

PubMed publication ID

9 May 2018

http://europepmc.org/abstract/MED/17464498

7

1 reference

Europe PubMed Central

PubMed publication ID

9 May 2018

http://europepmc.org/abstract/MED/17464498

1418-1422

1 reference

Europe PubMed Central

PubMed publication ID

9 May 2018

http://europepmc.org/abstract/MED/17464498

https://scigraph.springernature.com/pub.10.1007/s00125-007-0658-4

0 references

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

https://pubmed.ncbi.nlm.nih.gov/17464498

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17464498

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17464498

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

GRR: graphical representation of relationship errors

1 reference

https://pubmed.ncbi.nlm.nih.gov/17464498

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Allegro, a new computer program for multipoint linkage analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/17464498

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Principal component for metabolic syndrome risk maps to chromosome 4p in Mexican Americans: the San Antonio Family Heart Study.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17464498

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genomewide search for type 2 diabetes-susceptibility genes in French whites: evidence for a novel susceptibility locus for early-onset diabetes on chromosome 3q27-qter and independent replication of a type 2-diabetes locus on chromosome 1q21-q24.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17464498

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genome-wide Scan for Type 2 Diabetes Loci in Hong Kong Chinese and Confirmation of a Susceptibility Locus on Chromosome 1q21-q25

1 reference

https://pubmed.ncbi.nlm.nih.gov/17464498

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A genomewide search finds major susceptibility loci for gallbladder disease on chromosome 1 in Mexican Americans

1 reference

https://pubmed.ncbi.nlm.nih.gov/17464498

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mapping genes influencing type 2 diabetes risk and BMI in Japanese subjects

1 reference

https://pubmed.ncbi.nlm.nih.gov/17464498

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Loci on chromosomes 2 (NIDDM1) and 15 interact to increase susceptibility to diabetes in Mexican Americans

1 reference

https://pubmed.ncbi.nlm.nih.gov/17464498

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Efficiency of typing unaffected relatives in an affected-sib-pair linkage study with single-locus and multiple tightly linked markers.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17464498

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A common polymorphism in the upstream promoter region of the hepatocyte nuclear factor-4 alpha gene on chromosome 20q is associated with type 2 diabetes and appears to contribute to the evidence for linkage in an ashkenazi jewish population.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17464498

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A susceptibility locus for early-onset non-insulin dependent (type 2) diabetes mellitus maps to chromosome 20q, proximal to the phosphoenolpyruvate carboxykinase gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/17464498

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Asymptotic properties of affected-sib-pair linkage analysis.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17464498

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Merlin--rapid analysis of dense genetic maps using sparse gene flow trees

1 reference

https://pubmed.ncbi.nlm.nih.gov/17464498

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17464498

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evaluating the results of genomewide linkage scans of complex traits by locus counting

1 reference

https://pubmed.ncbi.nlm.nih.gov/17464498

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A Genome Scan for Type 2 Diabetes Susceptibility Loci in a Genetically Isolated Population

1 reference

https://pubmed.ncbi.nlm.nih.gov/17464498

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

https://pubmed.ncbi.nlm.nih.gov/17464498

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results

1 reference

https://pubmed.ncbi.nlm.nih.gov/17464498

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage and association of tumor necrosis factor receptor 2 locus with hypertension, hypercholesterolemia and plasma shed receptor

1 reference

https://pubmed.ncbi.nlm.nih.gov/17464498

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A comprehensive linkage analysis for myocardial infarction and its related risk factors

1 reference

https://pubmed.ncbi.nlm.nih.gov/17464498

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage of genetic markers on human chromosomes 20 and 12 to NIDDM in Caucasian sib pairs with a history of diabetic nephropathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/17464498

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17464498

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00125-007-0658-4

1 reference

Europe PubMed Central

PubMed publication ID

9 May 2018

http://europepmc.org/abstract/MED/17464498

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

9 May 2018

http://europepmc.org/abstract/MED/17464498

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q52926370&oldid=1424315346"