Evidence map›Paper›PMID 42381763›Full record

ArticleKidney international reports2026

Scoping Review of Global Kidney Genetics Clinic Models and Outcomes.

Ru Sin Lim, Trudie Harris, Julia Jefferis, Sadia Jahan, Regina Shaoying Lim, Louisa M D'Arrietta, Kar Hui Ng, Hui-Lin Chin, Liuh Ling Goh, Sanchalika Acharyya and 6 more

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Article in Kidney international reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Ru Sin LimDepartment of Renal Medicine, Tan Tock Seng Hospital, Novena, Singapore.
Trudie HarrisDepartment of Renal Medicine, Townsville University Hospital, Townsville, Queensland, Australia.
Julia JefferisCollege of Medicine and Dentistry, James Cook University, Townsville, Queensland, Australia.
Sadia JahanCollege of Medicine and Dentistry, James Cook University, Townsville, Queensland, Australia.
Regina Shaoying LimDepartment of Renal Medicine, Tan Tock Seng Hospital, Novena, Singapore.
Louisa M D'ArriettaCollege of Medicine and Dentistry, James Cook University, Townsville, Queensland, Australia.
Kar Hui NgDepartment of Pediatrics, Yong Loo Lin School of Medicine, National University of Singapore, Kent Ridge, Singapore.
Hui-Lin ChinDepartment of Pediatrics, Yong Loo Lin School of Medicine, National University of Singapore, Kent Ridge, Singapore.
Liuh Ling GohMolecular Diagnostic Laboratory, Tan Tock Seng Hospital, Novena, Singapore.
Sanchalika AcharyyaClinical Research & Innovation Office, Tan Tock Seng Hospital, Singapore.
Edwin Chan Shih-YenSingapore Clinical Research Institute, Queenstown, Singapore.
Chirag PatelGenetic Health Queensland, Royal Brisbane and Women's Hospital, Brisbane, Queensland, Australia.
Erik BirosCollege of Medicine and Dentistry, James Cook University, Townsville, Queensland, Australia.
Nick SevdalisCentre for Behavioral and Implementation Sciebnce Interventions, Yong Loo Lin School of Medicine, National University of Singapore, Kent Ridge, Singapore.
Andrew J MallettCollege of Medicine and Dentistry, James Cook University, Townsville, Queensland, Australia.
Global Kidney Genetics Clinic Leads Collaborators

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Genomic testing is reshaping nephrology practice, yet the implementation and outcomes of kidney genetics services remain poorly characterized. Methods: We conducted a 2-part scoping study comprising the following: (i) a literature review (Joanna Briggs Institute methodology, Preferred Reporting Items for Systematic reviews and Meta-Analyses extension for scoping reviews compliant; Open Science Framework registration doi.org/10.17605/OSF.IO/N32VA) of English-language publications (2000-2025) describing kidney genetics services and outcomes, and (ii) an international stakeholder consultation of clinic leads to capture real-world implementation experiences. Results: Sixty studies were included, predominantly from North America ( Conclusion: Kidney genetics care is expanding but remains unevenly implemented. Nephrologist-led models can be effective with support. Patient selection may influence diagnostic yield more than testing modality. Standardized outcome reporting and theory-driven implementation evaluation are essential for equitable and sustainable genomic services.

Indexed as

genetic kidney diseaseglobal kidney carekidney genetics clinic modelnephrogeneticsscoping review

Identifiers

PMID42381763
PMCPMC13314576

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Registered trials

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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.