Risk alleles of USF1 gene predict cardiovascular disease of women in two prospective studies (Q34598124)

3 August 2017

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

1 reference

cardiovascular disease in women

3 August 2017

cardiovascular disease

1 reference

based on heuristic

inferred from title

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author

Kari Kuulasmaa

10

1 reference

3 August 2017

Mervi Alanne

2

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Janna Saarela

object named as

Janna Saarela

6

0 references

Markus Perola

13

object named as

Markus Perola

1 reference

3 August 2017

12

Veikko Salomaa

1 reference

3 August 2017

Leena Peltonen-Palotie

14

object named as

Leena Peltonen

1 reference

3 August 2017

11

Kaisa Silander

1 reference

3 August 2017

5

Päivi Pajukanta

1 reference

3 August 2017

7

Pekka Ellonen

1 reference

3 August 2017

3

Kirsi Auro

1 reference

3 August 2017

1

Kati Komulainen

1 reference

3 August 2017

Riika Kilpikari

4

1 reference

3 August 2017

Kaisa Salminen

8

1 reference

3 August 2017

Sangita Kulathinal

9

1 reference

3 August 2017

12 May 2006

1 reference

3 August 2017

1 reference

3 August 2017

2

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3 August 2017

5

1 reference

3 August 2017

e69

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Creative Commons Attribution 4.0 International

3 August 2017

start time

12 May 2006

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

USF1 and dyslipidemias: converging evidence for a functional intronic variant

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1458962

The validity of the Finnish Hospital Discharge Register and Causes of Death Register data on coronary heart disease

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1458962

MORGAM (an international pooling of cardiovascular cohorts).

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1458962

Haploview: analysis and visualization of LD and haplotype maps

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1458962

A system for specific, high-throughput genotyping by allele-specific primer extension on microarrays

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1458962

Validation of stroke diagnosis in the National Hospital Discharge Register and the Register of Causes of Death in Finland

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1458962

Validity of diagnoses of major coronary events in national registers of hospital diagnoses and deaths in Finland

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1458962

Blot hybridisation analysis of genomic DNA

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1458962

Evaluating whole genome amplification via multiply-primed rolling circle amplification for SNP genotyping of samples with low DNA yield.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1458962

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

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1458962

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

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1458962

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

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1458962

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

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1458962

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

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1458962

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

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1458962

Continuous 15-year decrease in incidence and mortality of stroke in Finland: the FINSTROKE study.

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1458962

Trends in coronary events in Finland during 1983-1997. The FINAMI study

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1458962

Robust variance estimation for the case-cohort design.

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1458962

Cardiovascular risk factor changes in Finland, 1972-1997

26 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16699592

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1371/JOURNAL.PGEN.0020069

1 reference

3 August 2017

1 reference

3 August 2017

1 reference