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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)
  • High Attention Score compared to outputs of the same age and source (87th percentile)

Readers on

mendeley
635 Mendeley
citeulike
1 CiteULike
connotea
1 Connotea
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Article details
Title
Genome-Wide Association Analysis Identifies Variants Associated with Nonalcoholic Fatty Liver Disease That Have Distinct Effects on Metabolic Traits
Published in
PLoS Genetics, March 2011
DOI 10.1371/journal.pgen.1001324
Pubmed ID
Authors
Abstract

Nonalcoholic fatty liver disease (NAFLD) clusters in families, but the only known common genetic variants influencing risk are near PNPLA3. We sought to identify additional genetic variants influencing NAFLD using genome-wide association (GWA) analysis of computed tomography (CT) measured hepatic steatosis, a non-invasive measure of NAFLD, in large population based samples. Using variance components methods, we show that CT hepatic steatosis is heritable (∼26%-27%) in family-based Amish, Family Heart, and Framingham Heart Studies (n = 880 to 3,070). By carrying out a fixed-effects meta-analysis of genome-wide association (GWA) results between CT hepatic steatosis and ∼2.4 million imputed or genotyped SNPs in 7,176 individuals from the Old Order Amish, Age, Gene/Environment Susceptibility-Reykjavik study (AGES), Family Heart, and Framingham Heart Studies, we identify variants associated at genome-wide significant levels (p<5×10(-8)) in or near PNPLA3, NCAN, and PPP1R3B. We genotype these and 42 other top CT hepatic steatosis-associated SNPs in 592 subjects with biopsy-proven NAFLD from the NASH Clinical Research Network (NASH CRN). In comparisons with 1,405 healthy controls from the Myocardial Genetics Consortium (MIGen), we observe significant associations with histologic NAFLD at variants in or near NCAN, GCKR, LYPLAL1, and PNPLA3, but not PPP1R3B. Variants at these five loci exhibit distinct patterns of association with serum lipids, as well as glycemic and anthropometric traits. We identify common genetic variants influencing CT-assessed steatosis and risk of NAFLD. Hepatic steatosis associated variants are not uniformly associated with NASH/fibrosis or result in abnormalities in serum lipids or glycemic and anthropometric traits, suggesting genetic heterogeneity in the pathways influencing these traits.

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X Demographics

X Demographics

The data shown below were collected from the profiles of 3 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 635 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Geographical breakdown
Country Count As %
United States 4 <1%
Italy 3 <1%
Germany 3 <1%
Netherlands 1 <1%
United Kingdom 1 <1%
France 1 <1%
Spain 1 <1%
Canada 1 <1%
Belgium 1 <1%
Other 0 0%
Unknown 619 97%

Demographic breakdown

Readers by professional status
Readers by professional status Count As %
Researcher 136 21%
Student > Ph. D. Student 89 14%
Professor 58 9%
Student > Master 48 8%
Other 41 6%
Other 113 18%
Unknown 150 24%
Readers by discipline
Readers by discipline Count As %
Medicine and Dentistry 174 27%
Biochemistry, Genetics and Molecular Biology 105 17%
Agricultural and Biological Sciences 97 15%
Nursing and Health Professions 10 2%
Pharmacology, Toxicology and Pharmaceutical Science 8 1%
Other 53 8%
Unknown 188 30%
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 14 April 2026.
All research outputs
#2,491,179
of 31,634,113 outputs
Outputs from PLoS Genetics
#1,631
of 9,542 outputs
Outputs of similar age
#9,918
of 146,502 outputs
Outputs of similar age from PLoS Genetics
#11
of 91 outputs
Altmetric has tracked 31,634,113 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 9,542 research outputs from this source. They typically receive a lot more attention than average, with a mean Attention Score of 16.9. This one has done well, scoring higher than 82% 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 146,502 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 91 others from the same source and published within six weeks on either side of this one. This one has done well, scoring higher than 87% of its contemporaries.