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Linkage analysis identifies a locus for plasma von Willebrand factor undetected by genome-wide association

Overview of attention for article published in Proceedings of the National Academy of Sciences of the United States of America, December 2012
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  • In the top 25% of all research outputs scored by Altmetric
  • High Attention Score compared to outputs of the same age (93rd percentile)
  • Good Attention Score compared to outputs of the same age and source (70th percentile)

Mentioned by

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1 news outlet
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4 X users
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2 patents
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1 Wikipedia page

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96 Mendeley
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Article details
Title
Linkage analysis identifies a locus for plasma von Willebrand factor undetected by genome-wide association
Published in
Proceedings of the National Academy of Sciences of the United States of America, December 2012
DOI 10.1073/pnas.1219885110
Pubmed ID
Authors
Abstract

The plasma glycoprotein von Willebrand factor (VWF) exhibits fivefold antigen level variation across the normal human population determined by both genetic and environmental factors. Low levels of VWF are associated with bleeding and elevated levels with increased risk for thrombosis, myocardial infarction, and stroke. To identify additional genetic determinants of VWF antigen levels and to minimize the impact of age and illness-related environmental factors, we performed genome-wide association analysis in two young and healthy cohorts (n = 1,152 and n = 2,310) and identified signals at ABO (P < 7.9E-139) and VWF (P < 5.5E-16), consistent with previous reports. Additionally, linkage analysis based on sibling structure within the cohorts, identified significant signals at chromosome 2q12-2p13 (LOD score 5.3) and at the ABO locus on chromosome 9q34 (LOD score 2.9) that explained 19.2% and 24.5% of the variance in VWF levels, respectively. Given its strong effect, the linkage region on chromosome 2 could harbor a potentially important determinant of bleeding and thrombosis risk. The absence of a chromosome 2 association signal in this or previous association studies suggests a causative gene harboring many genetic variants that are individually rare, but in aggregate common. These results raise the possibility that similar loci could explain a significant portion of the "missing heritability" for other complex genetic traits.

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X Demographics

X Demographics

The data shown below were collected from the profiles of 4 X users who shared this research output. Click here to find out more about how the information was compiled.
Mendeley demographics

Mendeley demographics

The data shown below were compiled from readership statistics for 96 Mendeley readers of this research output. Click here to see the associated Mendeley record.
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Geographical breakdown

Geographical breakdown
Country Count As %
United States 1 1%
Sweden 1 1%
Portugal 1 1%
United Kingdom 1 1%
France 1 1%
Belgium 1 1%
Unknown 90 94%

Demographic breakdown

Readers by professional status
Readers by professional status Count As %
Researcher 26 27%
Student > Ph. D. Student 22 23%
Student > Bachelor 13 14%
Professor 5 5%
Other 4 4%
Other 14 15%
Unknown 12 13%
Readers by discipline
Readers by discipline Count As %
Agricultural and Biological Sciences 35 36%
Medicine and Dentistry 15 16%
Biochemistry, Genetics and Molecular Biology 10 10%
Nursing and Health Professions 5 5%
Computer Science 2 2%
Other 15 16%
Unknown 14 15%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 18. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 16 December 2025.
All research outputs
#2,668,321
of 34,518,147 outputs
Outputs from Proceedings of the National Academy of Sciences of the United States of America
#30,372
of 119,104 outputs
Outputs of similar age
#21,668
of 347,629 outputs
Outputs of similar age from Proceedings of the National Academy of Sciences of the United States of America
#285
of 985 outputs
Altmetric has tracked 34,518,147 research outputs across all sources so far. Compared to these this one has done particularly well and is in the 92nd percentile: it's in the top 10% of all research outputs ever tracked by Altmetric.
So far Altmetric has tracked 119,104 research outputs from this source. They typically receive a lot more attention than average, with a mean Attention Score of 40.1. This one has gotten more attention than average, scoring higher than 74% of its peers.
Older research outputs will score higher simply because they've had more time to accumulate mentions. To account for age we can compare this Altmetric Attention Score to the 347,629 tracked outputs that were published within six weeks on either side of this one in any source. This one has done particularly well, scoring higher than 93% of its contemporaries.
We're also able to compare this research output to 985 others from the same source and published within six weeks on either side of this one. This one has gotten more attention than average, scoring higher than 70% of its contemporaries.