Evidence map›Paper›PMID 33753502›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2021

Gain-of-function factor H-related 5 protein impairs glomerular complement regulation resulting in kidney damage.

Talat H Malik, Daniel P Gitterman, Deborah P Lavin, Hannah J Lomax-Browne, E Christina Hiemeyer, Linda B Moran, Katharina Boroviak, H Terence Cook, Alyssa C Gilmore, Mawj Mandwie and 6 more

Open access · hybridAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

16 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Association of Complement Genetics with Outcomes in IgA Nephropathy.Clinical journal of the American Society of Nephrology : CJASN · 2026
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. The human factor H protein family - an update.Frontiers in immunology · 2024
    Review
  10. Review
  11. Review
  12. Review
  13. C3 glomerulopathy: Understanding an ultra-rare complement-mediated renal disease.American journal of medical genetics. Part C, Seminars in medical genetics · 2022
    Review
  14. Review
  15. Homodimeric Minimal Factor H:Frontiers in immunology · 2021
    Article
  16. FHR-5 Serum Levels andFrontiers in immunology · 2021
    Article
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

16 authors at 5 institutions in 2 countries.

Talat H MalikCentre for Inflammatory Disease, Imperial College London, London W12 0NN, United Kingdom.ORCID 0000-0002-8127-6521
Daniel P GittermanWellcome Trust Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SA, United Kingdom.ORCID 0000-0002-3226-8429
Deborah P LavinCentre for Inflammatory Disease, Imperial College London, London W12 0NN, United Kingdom.ORCID 0000-0002-4994-3881
Hannah J Lomax-BrowneCentre for Inflammatory Disease, Imperial College London, London W12 0NN, United Kingdom.ORCID 0000-0002-5060-6137
E Christina HiemeyerCentre for Inflammatory Disease, Imperial College London, London W12 0NN, United Kingdom.
Linda B MoranNorth West London Pathology, Imperial College Healthcare National Health Service Trust, London W6 8RF, United Kingdom.
Katharina BoroviakWellcome Trust Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SA, United Kingdom.
H Terence CookCentre for Inflammatory Disease, Imperial College London, London W12 0NN, United Kingdom.ORCID 0000-0002-8950-1041
Alyssa C GilmoreCentre for Inflammatory Disease, Imperial College London, London W12 0NN, United Kingdom.
Mawj MandwieGene Therapy Research Unit, Children's Medical Research Institute and Sydney Children's Hospitals Network, The University of Sydney, NSW 2145 Westmead, Australia.ORCID 0000-0002-4165-4276
Amina AhmadGene Therapy Research Unit, Children's Medical Research Institute and Sydney Children's Hospitals Network, The University of Sydney, NSW 2145 Westmead, Australia.ORCID 0000-0002-8973-2085
Ian E AlexanderGene Therapy Research Unit, Children's Medical Research Institute and Sydney Children's Hospitals Network, The University of Sydney, NSW 2145 Westmead, Australia.ORCID 0000-0002-6213-5627
Grant J LoganGene Therapy Research Unit, Children's Medical Research Institute and Sydney Children's Hospitals Network, The University of Sydney, NSW 2145 Westmead, Australia.ORCID 0000-0001-9365-342X
Kevin J MarchbankTranslational and Clinical Research Institute, The Medical School, Newcastle University, Framlington Place, Newcastle-upon-Tyne NE2 4HH, United Kingdom.ORCID 0000-0003-1312-5411
Allan BradleyWellcome Trust Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SA, United Kingdom.
Matthew C PickeringCentre for Inflammatory Disease, Imperial College London, London W12 0NN, United Kingdom; matthew.pickering@imperial.ac.uk.ORCID 0000-0002-1153-0192
Imperial College London · GBThe University of Sydney · AUWellcome Sanger Institute · GBNational Health Service · GBNewcastle University · GB

Funding

Department of HealthMedical Research Council MC_PC_16054Medical Research Council MR/S025502/1Wellcome TrustWellcome Trust 212252/Z/18/Z
6 · The paper itself

Abstract

Genetic variation within the factor H-related (FHR) genes is associated with the complement-mediated kidney disease, C3 glomerulopathy (C3G). There is no definitive treatment for C3G, and a significant proportion of patients develop end-stage renal disease. The prototypical example is CFHR5 nephropathy, through which an internal duplication within a single

Indexed as

Gain of Function MutationAnimalsComplement C3Complement System ProteinsDisease Models, AnimalFemaleGlomerulonephritisHumansKidney GlomerulusMaleMiceMice, TransgenicSex FactorsCFHR5 protein, humanComplement C3Complement System Proteinscomplementimmunologykidney

Identifiers

PMID33753502
PMCPMC8020653
OpenAlexW3120740291

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.