(Q56968845)

8

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Casper G. Schalkwijk

5

object named as

Casper G. Schalkwijk

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author name string

Steven J.R. Meex

1

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Jana V. van Vliet-Ostaptchouk

2

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Carla J.H. van der Kallen

3

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Marleen M.J. van Greevenbroek

4

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Ellen E. Blaak

7

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Marten H. Hofker

9

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Coen D.A. Stehouwer

10

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Tjerk W.A. de Bruin

Molecular Genetics and Metabolism

11

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publication date

July 2008

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published in

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volume

94

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issue

3

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page(s)

352-355

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cites work

Linkage of familial combined hyperlipidaemia to chromosome 1q21-q23

1 reference

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Familial combined hyperlipidemia is associated with upstream transcription factor 1 (USF1).

7 January 2021

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Familial combined hyperlipidemia in Mexicans: association with upstream transcription factor 1 and linkage on chromosome 16q24.1.

7 January 2021

1 reference

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Upstream stimulatory factor 1 associated with familial combined hyperlipidemia, LDL cholesterol, and triglycerides

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2008.03.011

Variation in USF1 shows haplotype effects, gene : gene and gene : environment associations with glucose and lipid parameters in the European Atherosclerosis Research Study II.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2008.03.011

The linkage and association of the gene encoding upstream stimulatory factor 1 with type 2 diabetes and metabolic syndrome in the Chinese population

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2008.03.011

Upstream transcription factor-1 gene polymorphism is associated with increased adipocyte lipolysis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2008.03.011

Risk alleles of USF1 gene predict cardiovascular disease of women in two prospective studies

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2008.03.011

Support for linkage of familial combined hyperlipidemia to chromosome 1q21-q23 in Chinese and German families

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2008.03.011

Contribution of chromosome 1q21-q23 to familial combined hyperlipidemia in Mexican families

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2008.03.011

Replication of Linkage of Familial Combined Hyperlipidemia to Chromosome 1q With Additional Heterogeneous Effect of Apolipoprotein A-I/C-III/A-IV Locus

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YMGME.2008.03.011

A genome-wide search for type 2 diabetes susceptibility genes in Utah Caucasians

7 January 2021

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Genome-wide and fine-mapping linkage studies of type 2 diabetes and glucose traits in the Old Order Amish: evidence for a new diabetes locus on chromosome 14q11 and confirmation of a locus on chromosome 1q21-q24.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2008.03.011

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

7 January 2021

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A genome-wide scan for loci linked to plasma levels of glucose and HbA(1c) in a community-based sample of Caucasian pedigrees: The Framingham Offspring Study

7 January 2021

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2008.03.011

Linkage of the metabolic syndrome to 1q23-q31 in Hispanic families: the Insulin Resistance Atherosclerosis Study Family Study

7 January 2021

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

7 January 2021

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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.

7 January 2021

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Genome-wide search for type 2 diabetes/impaired glucose homeostasis susceptibility genes in the Chinese: significant linkage to chromosome 6q21-q23 and chromosome 1q21-q24.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2008.03.011

Common polymorphisms in the USF1 gene are not associated with type 2 diabetes in French Caucasians

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2008.03.011

Variation Within the Gene Encoding the Upstream Stimulatory Factor 1 Does Not Influence Susceptibility to Type 2 Diabetes in Samples From Populations With Replicated Evidence of Linkage to Chromosome 1q

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2008.03.011

A genome-wide scan in type 2 diabetes mellitus provides independent replication of a susceptibility locus on 18p11 and suggests the existence of novel Loci on 2q12 and 19q13.

7 January 2021

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Myosin IXB variant increases the risk of celiac disease and points toward a primary intestinal barrier defect

7 January 2021

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Common variants in the ATP-sensitive K+ channel genes KCNJ11 (Kir6.2) and ABCC8 (SUR1) in relation to glucose intolerance: population-based studies and meta-analyses

7 January 2021

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Validation of capillary glucose measurements to detect glucose intolerance or type 2 diabetes mellitus in the general population

7 January 2021

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2008.03.011

USF1 and dyslipidemias: converging evidence for a functional intronic variant

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2008.03.011

Essential role in vivo of upstream stimulatory factors for a normal dietary response of the fatty acid synthase gene in the liver

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2008.03.011

The involvement of upstream stimulatory factor 1 in Dutch patients with familial combined hyperlipidemia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2008.03.011

USF1 implicated in the aetiology of familial combined hyperlipidaemia and the metabolic syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2008.03.011

Associations between USF1 gene variants and cardiovascular risk factors in the Quebec Family Study

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2008.03.011

Upstream transcription factor 1 gene polymorphisms are associated with high antilipolytic insulin sensitivity and show gene-gene interactions.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2008.03.011

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2008.03.011