Evidence map›Paper›PMID 36117978›Full record

ArticleFrontiers in medicine2022

The multifaceted phenotypic and genotypic spectrum of type-IV-collagen-related nephropathy-A human genetics department experience.

Jasmina Ćomić, Korbinian M Riedhammer, Roman Günthner, Christian W Schaaf, Patrick Richthammer, Hannes Simmendinger, Donald Kieffer, Riccardo Berutti, Velibor Tasic, Nora Abazi-Emini and 10 more

Open access · goldAbstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Frontiers in medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.6field-weighted citation impact, top 37% 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

6 citing papers in PubMed, 6 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

20 authors at 7 institutions in 4 countries.

Jasmina ĆomićInstitute of Human Genetics, Klinikum rechts der Isar, Technical University of Munich, School of Medicine, Munich, Germany.
Korbinian M RiedhammerInstitute of Human Genetics, Klinikum rechts der Isar, Technical University of Munich, School of Medicine, Munich, Germany.
Roman GünthnerDepartment of Nephrology, Klinikum rechts der Isar, Technical University of Munich, School of Medicine, Munich, Germany.
Christian W SchaafInstitute of Human Genetics, Klinikum rechts der Isar, Technical University of Munich, School of Medicine, Munich, Germany.
Patrick RichthammerInstitute of Human Genetics, Klinikum rechts der Isar, Technical University of Munich, School of Medicine, Munich, Germany.
Hannes SimmendingerInstitute of Human Genetics, Klinikum rechts der Isar, Technical University of Munich, School of Medicine, Munich, Germany.
Donald KiefferInstitute of Human Genetics, Klinikum rechts der Isar, Technical University of Munich, School of Medicine, Munich, Germany.
Riccardo BeruttiInstitute of Human Genetics, Klinikum rechts der Isar, Technical University of Munich, School of Medicine, Munich, Germany.
Velibor TasicUniversity Children's Hospital, Medical Faculty of Skopje, Skopje, North Macedonia.
Nora Abazi-EminiUniversity Children's Hospital, Medical Faculty of Skopje, Skopje, North Macedonia.
Valbona Nushi-StavileciPediatric Clinic, University Clinical Center of Kosovo, Prishtina, Serbia.
Jovana PutnikInstitute for Mother and Child Health Care of Serbia "Dr. Vukan Čupić", Department of Nephrology, University of Belgrade, Faculty of Medicine, Belgrade, Serbia.
Nataša StajicInstitute for Mother and Child Health Care of Serbia "Dr. Vukan Čupić", Department of Nephrology, University of Belgrade, Faculty of Medicine, Belgrade, Serbia.
Adrian LunguUniversity Children's Hospital, Medical Faculty of Skopje, Skopje, North Macedonia.
Oliver GrossClinic of Nephrology and Rheumatology, University Medical Center Göttingen, University of Göttingen, Göttingen, Germany.
Lutz RendersDepartment of Nephrology, Klinikum rechts der Isar, Technical University of Munich, School of Medicine, Munich, Germany.
Uwe HeemannDepartment of Nephrology, Klinikum rechts der Isar, Technical University of Munich, School of Medicine, Munich, Germany.
Matthias C BraunischDepartment of Nephrology, Klinikum rechts der Isar, Technical University of Munich, School of Medicine, Munich, Germany.
Thomas MeitingerInstitute of Human Genetics, Klinikum rechts der Isar, Technical University of Munich, School of Medicine, Munich, Germany.
Julia HoefeleInstitute of Human Genetics, Klinikum rechts der Isar, Technical University of Munich, School of Medicine, Munich, Germany.
Klinikum rechts der Isar · DETechnical University of Munich · DEPHI University Psychiatric Clinic - Skopje · MKInstitute of Public Health of Serbia · RSUniversity Clinical Center of Kosovo · XKUniversity of Belgrade · RSUniversity of Göttingen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Disease-causing variants in

Indexed as

Alport syndromeCOL4A3COL4A4COL4A5type-IV-collagen-related nephropathy

Identifiers

PMID36117978
PMCPMC9470833
OpenAlexW4293715049

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.