Evidence map›Paper›PMID 30900988›Full record

ArticleeLife2019

Analysis of the genomic architecture of a complex trait locus in hypertensive rat models links

Angela Schulz, Nicola Victoria Müller, Nina Anne van de Lest, Andreas Eisenreich, Martina Schmidbauer, Andrei Barysenka, Bettina Purfürst, Anje Sporbert, Theodor Lorenzen, Alexander M Meyer and 9 more

Open access · goldAbstract read
In one paragraph

Article in eLife, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

21 citing papers in PubMed, 42 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

19 authors at 8 institutions in 4 countries.

Angela Schulz *Charité - Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, Berlin, Germany.ORCID 0000-0002-4576-8035
Nicola Victoria Müller *Charité - Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, Berlin, Germany.ORCID 0000-0001-7261-830X
Nina Anne van de LestDepartment of Pathology, Leiden University Medical Center (LUMC), Leiden, The Netherlands.
Andreas EisenreichCharité - Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, Berlin, Germany.
Martina SchmidbauerCharité - Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, Berlin, Germany.
Andrei BarysenkaWestfälische Wilhelms University, Genetic Epidemiology, Institute for Human Genetics, Münster, Germany.
Bettina PurfürstMax Delbrück Center for Molecular Medicine in the Helmholtz Association, Core Facility Electron Microscopy, Berlin, Germany.
Anje SporbertMax Delbrück Center for Molecular Medicine in the Helmholtz Association, Advanced Light Microscopy, Berlin, Germany.
Theodor LorenzenInstitute of Clinical Pharmacology and Toxicology, Berlin Institute of Health, Berlin, Germany.
Alexander M Meyer
Laura HerlanInstitute of Clinical Pharmacology and Toxicology, Berlin Institute of Health, Berlin, Germany.
Anika WittenWestfälische Wilhelms University, Genetic Epidemiology, Institute for Human Genetics, Münster, Germany.
Frank RühleWestfälische Wilhelms University, Genetic Epidemiology, Institute for Human Genetics, Münster, Germany.
Weibin ZhouDivision of Nephrology, Department of Medicine, Center for Human Disease Modeling, Duke University School of Medicine, Durham, United States.
Emile de HeerDepartment of Pathology, Leiden University Medical Center (LUMC), Leiden, The Netherlands.
Marion ScharpfeneckerDepartment of Pathology, Leiden University Medical Center (LUMC), Leiden, The Netherlands.
Daniela PanákováDZHK (German Centre for Cardiovascular Research), Partner site Berlin, Berlin, Germany.ORCID 0000-0002-8739-6225
Monika Stoll *Westfälische Wilhelms University, Genetic Epidemiology, Institute for Human Genetics, Münster, Germany.
Reinhold Kreutz *Institute of Clinical Pharmacology and Toxicology, Berlin Institute of Health, Berlin, Germany.ORCID 0000-0002-4818-211X
University of Münster · DEHumboldt-Universität zu Berlin · DELeiden University Medical Center · NLMax Delbrück Center · DEBerlin Institute of Health at Charité - Universitätsmedizin Berlin · DEGerman Centre for Cardiovascular Research · DEDuke University · USUniversity of Edinburgh · GB

Funding

Deutsche Forschungsgemeinschaft DFG KR 1152-3-1Deutsche Forschungsgemeinschaft Project number 394046635 - SFB 1365Deutsche Forschungsgemeinschaft SCHU 2604/1-1Deutsche Hochdrckliga (DHL) Stiftungsprofessur HypertensiologieEuropean Commission WNT/CALCIUM IN HEART-322189Helmholtz-Gemeinschaft VH-NG-736
6 · The paper itself

Abstract

Unraveling the genetic susceptibility of complex diseases such as chronic kidney disease remains challenging. Here, we used inbred rat models of kidney damage associated with elevated blood pressure for the comprehensive analysis of a major albuminuria susceptibility locus detected in these models. We characterized its genomic architecture by congenic substitution mapping, targeted next-generation sequencing, and compartment-specific RNA sequencing analysis in isolated glomeruli. This led to prioritization of transmembrane protein

Indexed as

Genetic LociGenetic Predisposition to DiseaseMultifactorial InheritanceAlbuminuriaAnimalsDisease Models, AnimalHumansHypertensionHypertension, RenalNephritisRatsZebrafishalbuminuriablood pressuregeneticsgenomicshumannext generation sequencingratRNA sequencingzebrafish

Identifiers

PMID30900988
PMCPMC6478434
OpenAlexW2922807795

What OpenQuestion holds

Textmetadata
LicenceCC BY
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 OpenQuestion graph.