Evidence map›Paper›PMID 36690832›Full record

ArticleEuropean journal of human genetics : EJHG2024

Correction: The 2019 and 2021 International workshops on Alport syndrome.

Sergio Daga, Jie Ding, Constantinos Deltas, Judy Savige, Beata S Lipska-Ziętkiewicz, Julia Hoefele, Frances Flinter, Daniel P Gale, Marina Aksenova, Hirofumi Kai and 16 more

Abstract readPublished Erratum
PubMed Full text at PMC Publisher
In one paragraph

Article in European journal of human genetics : EJHG, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

26 authors.

Sergio DagaMedical Genetics, University of Siena, Siena, Italy.
Jie DingPeking University First Hospital, Beijing, China.
Constantinos DeltasBiobank.cy Center of Excellence in Biobanking and Biomedical Research and University of Cyprus Medical School, Nicosia, Cyprus.ORCID http://orcid.org/0000-0001-5549-9169
Judy SavigeDepartment of Medicine, Melbourne and Northern Health, The University of Melbourne, Parkville, VIC, 3050, Australia.
Beata S Lipska-ZiętkiewiczRare Diseases Centre, Clinical Genetics Unit, Department of Biology and Medical Genetics, Medical University of Gdańsk, Gdansk, Poland.ORCID http://orcid.org/0000-0002-4169-9685
Julia HoefeleInstitute of Human Genetics, Klinikum rechts der Isar, Technical University of Munich, School of Medicine, Munich, Germany.ORCID http://orcid.org/0000-0002-7917-7129
Frances FlinterDepartment of Clinical Genetics, Guys' and St Thomas' NHS Foundation Trust, London, UK.
Daniel P GaleDepartment of Renal Medicine, University College London, London, UK.
Marina AksenovaY. Veltischev Research and Clinical Institute for Pediatrics at the Pirogov Russian National Research Medical University, Taldomskaya Street, 2, Moscow, 125412, Russia.ORCID http://orcid.org/0000-0002-3699-1884
Hirofumi KaiDepartment of Molecular Medicine, Kumamoto University, Kumamoto, Japan.
Laura PerinGOFARR Laboratory for Organ Regenerative Research and Cell Therapeutics in Urology, Saban Research Institute, Division of Urology, Children's Hospital Los Angeles, Los Angeles, CA, USA.
Moumita BaruaToronto General Hospital, Toronto General Research Institute, University of Toronto, Toronto, ON, Canada.
Roser TorraInherited Kidney Diseases, Nephrology Department, Fundació Puigvert, IIB-Sant Pau, Medicine Department, Universitat Autónoma de Barcelona, Barcelona, Spain.
Jeff H MinerDivision of Nephrology, Washington University School of Medicine, St. Louis, MO, 63110, USA.ORCID http://orcid.org/0000-0002-1510-8714
Laura MassellaDivision of Nephrology, Department of Pediatric Subspecialties, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Danica Galešić LjubanovićUniversity of Zagreb School of Medicine, Department of Pathology and Department of Nephropathology and Electron Microscopy Dubrava University Hospital, Zagreb, Croatia.
Rachel LennonWellcome Centre for Cell-Matrix Research, Division of Cell-Matrix Biology and Regenerative Medicine, School of Biological Sciences, Faculty of Biology Medicine and Health, The University of Manchester, Manchester Academic Health Science Centre, Manchester, UK.ORCID http://orcid.org/0000-0001-6400-0227
Andrè B WeinstockAlport Syndrome Foundation, Phoenix, AZ, USA.
Bertrand KnebelmannNephrology Department, Reference Center for Inherited Kidney Diseases (MARHEA), APHP, Necker Hospital, Paris University, Paris, France.
Agne CerkauskaiteFaculty of Medicine, Vilnius University, Vilnius, Lithuania.
Susie GearAlport UK, Tetbury, UK.
Oliver GrossDepartment of Nephrology and Rheumatology, University Medicine Goettingen, Gottingen, Germany.
A Neil TurnerCentre for Inflammation, University of Edinburgh, Edinburgh, UK.ORCID http://orcid.org/0000-0003-4547-873X
Margherita BaldassarriMedical Genetics, University of Siena, Siena, Italy.
Anna Maria PintoGenetica Medica, Azienda Ospedaliero-Universitaria Senese, Siena, Italy.ORCID http://orcid.org/0000-0001-6259-6901
Alessandra RenieriMedical Genetics, University of Siena, Siena, Italy. alessandra.renieri@unisi.it.ORCID http://orcid.org/0000-0002-0846-9220

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Identifiers

PMID36690832
PMCPMC10772067

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.