ArticleEuropean journal of human genetics : EJHG2022
The 2019 and 2021 International Workshops on Alport Syndrome.
Erratum issuedAbstract read
In one paragraph
Article in European journal of human genetics : EJHG, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 26 papers, 1 of them a synthesis that pooled it.
0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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.
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.
Who cites it
26 citing papers in PubMed, 1 synthesis or guideline pooled it.
- Potential Renal Damage Biomarkers in Alport Syndrome-A Review of the Literature.International journal of molecular sciences · 2022Pooled it
- New therapeutic hope for rare podocytopathies.Pediatric nephrology (Berlin, Germany) · 2026Article
- Systematic Review of IgA Nephropathy Coexisting With Alport Syndrome.Kidney international reports · 2026Article
- Accelerated basement membrane remodeling and serum matrix fragments as biomarkers of fibrosis in Alport syndrome.Cell reports · 2026Article
- Clinical value of luciferase-based bioluminescence assay in diagnosis of Alport syndrome.Frontiers in pediatrics · 2026Article
- Collagen IV in Gould syndrome and Alport syndrome.Nature reviews. Nephrology · 2025Review
- A 15-year experience highlighting the spectrum of Alport kidney disease in the pediatric population and novel genetic variants in COL4A3-5.Pediatric nephrology (Berlin, Germany) · 2025Article
- Pathological diagnosis of Alport syndrome.Kidney research and clinical practice · 2025Article
- Prospective Cohort Study in Alport Syndrome Patients Under Standard Therapy.Kidney international reports · 2025Article
- Endoplasmic reticulum stress as a driver and therapeutic target for kidney disease.Nature reviews. Nephrology · 2025Review
- Slowly progressive autosomal dominant Alport Syndrome due to COL4A3 splicing variant.European journal of human genetics : EJHG · 2025Article
- A retrospective study of kidney disease in Alport syndrome during and after pregnancy.Journal of nephrology · 2025Observational
- Candidate Genetic Modifiers in Alport Syndrome: A Case Series.Life (Basel, Switzerland) · 2025Article
- Framework for standardized genetic testing recommendations for chronic kidney disease in Ontario.Genetics in medicine open · 2025Article
- SGLT2-Inhibition in Patients With Alport Syndrome.Kidney international reports · 2024Article
- Increased prevalence of kidney cysts in individuals carrying heterozygous COL4A3 or COL4A4 pathogenic variants.Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association · 2024Article
- Genetic reprogramming with stem cells regenerates glomerular epithelial podocytes in Alport syndrome.Life science alliance · 2024Article
- A case report: Alport syndrome and growth hormone deficiency associated with a newTranslational pediatrics · 2024Article
- Exploration of Gene Therapy for Alport Syndrome.Biomedicines · 2024Review
- A NovelGenes · 2024Article
Corrections and comments
- Erratum issued
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
Extracellular vesicles derived from amniotic fluid stem cells normalize glomerular function during progressive kidney disease.R01DK121037 · NIDDK · CHILDREN'S HOSPITAL OF LOS ANGELES · PI PERIN, LAURA · 2020 to 2023
$2.2MNovel mechanisms of glomerular injury in primary membranous nephropathyR01DK123234 · NIDDK · CHILDREN'S HOSPITAL OF LOS ANGELES · PI DA SACCO, STEFANO · 2020 to 2024
$1.9MNIDDK NIH HHS R01 DK121037NIDDK NIH HHS R01 DK123234
Abstract
PubMed holds no abstract for this paper.
Indexed as
Nephritis, HereditaryCollagen Type IVFemaleHumansMaleCollagen Type IV
Identifiers
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.