Evidence map›Paper›PMID 21807117›Full record

ArticleBiochimica et biophysica acta2012

A systems genetic analysis of high density lipoprotein metabolism and network preservation across mouse models.

Peter Langfelder, Lawrence W Castellani, Zhiqiang Zhou, Eric Paul, Richard Davis, Eric E Schadt, Aldons J Lusis, Steve Horvath, Margarete Mehrabian

Abstract read
In one paragraph

Article in Biochimica et biophysica acta, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.6field-weighted citation impact, top 16% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

20 citing papers in PubMed, 28 citations in OpenAlex.

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  12. An Integrative Genomic Study Implicates the Postsynaptic Density in the Pathogenesis of Bipolar Disorder.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2016
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  16. Multi-omic network signatures of disease.Frontiers in genetics · 2014
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 2 institutions in 1 country.

Peter LangfelderDepartment of Human Genetics, David Geffen School of Medicine at UCLA, Gonda (Goldschmied) Neuroscience and Genetics Research Center, 695 Charles E. Young Drive South, Box 708822, Los Angeles, CA 90095-7088, USA. peter.langfelder@gmail.com
Lawrence W Castellani
Zhiqiang Zhou
Eric Paul
Richard Davis
Eric E Schadt
Aldons J Lusis
Steve Horvath
Margarete Mehrabian
University of California, Los Angeles · USPacific Biosciences (United States) · US

Funding

ULTRASTRUCTURE OF THE INTIMA IN EARLY LESION FORMATIONP01HL030568 · NHLBI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI IRUELA-ARISPE, M. LUISA · 1985 to 2019
$55.2M
Systems genomics of metabolic syndrome traitsP01HL028481 · NHLBI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI LUSIS, ALDONS JAKE · 1985 to 2019
$50.2M
MAPPING THE GENES FOR ATHEROSCLEROSIS AND INSULIN RESISTANCEP01HL060030 · NHLBI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI HSUEH, WILLA A. · 1999 to 2003
$7.2M
Novel Models of Cardiovascular Complications of DiabetesU01HL070526 · NHLBI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI HSUEH, WILLA A. · 2001 to 2005
$3.8M
Dissection of HDL function using mouse modelsR01HL094322 · NHLBI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI LUSIS, ALDONS JAKE · 2009 to 2013
$1.9M
Integrative genetic approaches to AtherosclerosisR01HL095154 · NHLBI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI LUSIS, ALDONS JAKE · 2009 to 2010
$967k
NHLBI NIH HHS HL28481NHLBI NIH HHS HL30568NHLBI NIH HHS HL60030NHLBI NIH HHS HL70526NHLBI NIH HHS P01 HL028481NHLBI NIH HHS P01 HL060030NHLBI NIH HHS R01 HL094322NHLBI NIH HHS R01 HL095154NHLBI NIH HHS U01 HL070526
6 · The paper itself

Abstract

We report a systems genetic analysis of high density lipoprotein (HDL) levels in an F2 intercross between inbred strains CAST/EiJ and C57BL/6J. We previously showed that there are dramatic differences in HDL metabolism in a cross between these strains, and we now report co-expression network analysis of HDL that integrates global expression data from liver and adipose with relevant metabolic traits. Using data from a total of 293 F2 intercross mice, we constructed weighted gene co-expression networks and identified modules (subnetworks) associated with HDL and clinical traits. These were examined for genes implicated in HDL levels based on large human genome-wide associations studies (GWAS) and examined with respect to conservation between tissue and sexes in a total of 9 data sets. We identify genes that are consistently ranked high by association with HDL across the 9 data sets. We focus in particular on two genes, Wfdc2 and Hdac3, that are located in close proximity to HDL QTL peaks where causal testing indicates that they may affect HDL. Our results provide a rich resource for studies of complex metabolic interactions involving HDL. This article is part of a Special Issue entitled Advances in High Density Lipoprotein Formation and Metabolism: A Tribute to John F. Oram (1945-2010).

Indexed as

Adipose TissueAnalysis of VarianceAnimalsCholesterolCrosses, GeneticDiet, High-FatFemaleGene Regulatory NetworksHistone Deacetylase 3Histone DeacetylasesHybridization, GeneticLipoproteins, HDLLiverLod ScoreMaleMiceCholesterolHistone Deacetylase 3Histone DeacetylasesLipoproteins, HDLProteinsWAP Four-Disulfide Core Domain Protein 2Wfdc2 protein, mouse

Identifiers

PMID21807117
PMCPMC3265689
OpenAlexW2017685968

What Socratic holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.