Evidence map›Paper›PMID 26646939›Full record

ArticleScientific data2015

Multi-omic profiles of human non-alcoholic fatty liver disease tissue highlight heterogenic phenotypes.

Wasco Wruck, Karl Kashofer, Samrina Rehman, Andriani Daskalaki, Daniela Berg, Ewa Gralka, Justyna Jozefczuk, Katharina Drews, Vikash Pandey, Christian Regenbrecht and 7 more

Open access · goldAbstract readDataset
In one paragraph

Article in Scientific data, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed, 3 pooled it
3.7field-weighted citation impact, top 6% 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

31 citing papers in PubMed, 3 syntheses or guidelines pooled it, 61 citations in OpenAlex.

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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

17 authors at 7 institutions in 5 countries.

Wasco WruckMedical Faculty, Institute for Stem Cell Research and Regenerative Medicine, Heinrich Heine University, 40225 Düsseldorf, Germany.
Karl KashoferInstitute of Pathology, Medical University of Graz, Graz 8036, Austria.
Samrina RehmanThe Manchester Centre for Integrative Systems Biology, Manchester Institute of Biotechnology, University of Manchester, Manchester M1 7DN, UK.
Andriani DaskalakiDepartment of Vertebrate Genomics, Max Planck Institute for Molecular Genetics, Ihnestrasse 63, Berlin 14195, Germany.
Daniela BergDivision of Molecular Genome Analysis, German Cancer Research Center (DKFZ), 69120 Heidelberg, Germany.
Ewa GralkaMagnetic Resonance Center (CERM), University of Florence, 50019 Florence, Italy.
Justyna JozefczukDepartment of Vertebrate Genomics, Max Planck Institute for Molecular Genetics, Ihnestrasse 63, Berlin 14195, Germany.
Katharina DrewsDepartment of Vertebrate Genomics, Max Planck Institute for Molecular Genetics, Ihnestrasse 63, Berlin 14195, Germany.
Vikash PandeyDepartment of Vertebrate Genomics, Max Planck Institute for Molecular Genetics, Ihnestrasse 63, Berlin 14195, Germany.
Christian RegenbrechtInstitute for Pathology &Comprehensive Cancer Center, Cancer Stem Cell Group, Charité-Universitätsmedizin, 10117 Berlin, Germany.
Christoph WierlingDepartment of Vertebrate Genomics, Max Planck Institute for Molecular Genetics, Ihnestrasse 63, Berlin 14195, Germany.
Paola TuranoMagnetic Resonance Center (CERM), University of Florence, 50019 Florence, Italy.
Ulrike KorfDivision of Molecular Genome Analysis, German Cancer Research Center (DKFZ), 69120 Heidelberg, Germany.
Kurt ZatloukalInstitute of Pathology, Medical University of Graz, Graz 8036, Austria.
Hans LehrachDepartment of Vertebrate Genomics, Max Planck Institute for Molecular Genetics, Ihnestrasse 63, Berlin 14195, Germany.
Hans V WesterhoffThe Manchester Centre for Integrative Systems Biology, Manchester Institute of Biotechnology, University of Manchester, Manchester M1 7DN, UK.
James AdjayeMedical Faculty, Institute for Stem Cell Research and Regenerative Medicine, Heinrich Heine University, 40225 Düsseldorf, Germany.
Max Planck Institute for Molecular Genetics · DEGerman Cancer Research Center · DEMedical University of Graz · ATUniversity of Florence · ITUniversity of Manchester · GBCharité - Universitätsmedizin Berlin · DEHeinrich Heine University Düsseldorf · DE

Funding

Biotechnology and Biological Sciences Research Council BB/C008219/1Biotechnology and Biological Sciences Research Council BB/D019079/1Biotechnology and Biological Sciences Research Council BB/F003528/1Biotechnology and Biological Sciences Research Council BB/F003536/1Biotechnology and Biological Sciences Research Council BB/F003544/1Biotechnology and Biological Sciences Research Council BB/F003552/1Biotechnology and Biological Sciences Research Council BB/I004688/1Biotechnology and Biological Sciences Research Council BB/I004696/1Biotechnology and Biological Sciences Research Council BB/I00470X/1
6 · The paper itself

Abstract

Non-alcoholic fatty liver disease (NAFLD) is a consequence of sedentary life style and high fat diets with an estimated prevalence of about 30% in western countries. It is associated with insulin resistance, obesity, glucose intolerance and drug toxicity. Additionally, polymorphisms within, e.g., APOC3, PNPLA3, NCAN, TM6SF2 and PPP1R3B, correlate with NAFLD. Several studies have already investigated later stages of the disease. This study explores the early steatosis stage of NAFLD with the aim of identifying molecular mechanisms underlying the etiology of NAFLD. We analyzed liver biopsies and serum samples from patients with high- and low-grade steatosis (also pre-disease states) employing transcriptomics, ELISA-based serum protein analyses and metabolomics. Here, we provide a detailed description of the various related datasets produced in the course of this study. These datasets may help other researchers find new clues for the etiology of NAFLD and the mechanisms underlying its progression to more severe disease states.

Indexed as

Genetic Predisposition to DiseaseAcyltransferasesApolipoprotein C-IIIBiopsyChondroitin Sulfate ProteoglycansGenetic Association StudiesHumansLectins, C-TypeLipaseLiverMembrane ProteinsNerve Tissue ProteinsNeurocanNon-alcoholic Fatty Liver DiseasePhospholipases A2, Calcium-IndependentPolymorphism, Single NucleotideAcyltransferasesApolipoprotein C-IIIChondroitin Sulfate ProteoglycansLectins, C-TypeLipaseMembrane ProteinsNCAN protein, humanNerve Tissue ProteinsNeurocanPhospholipases A2, Calcium-IndependentPNPLA3 protein, humanPPP1R3B protein, humanProtein Phosphatase 1TM6SF2 protein, human

Identifiers

PMID26646939
PMCPMC4672680
OpenAlexW2196204028

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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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 OpenQuestion graph.