Evidence map›Paper›PMID 41015616›Full record

ArticleEuropean journal of human genetics : EJHG2026

From screening to strategy: Clinical implications of COL4A3/COL4A4 variants found in reproductive genetic testing.

Gráinne Butler, David J Amor, Catherine Quinlan

Abstract read
In one paragraph

Article in European journal of human genetics : EJHG, 2026. 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. Alport: Renaming an Extended Clinical Spectrum.Journal of the American Society of Nephrology : JASN · 2026
    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

3 authors.

Gráinne ButlerDepartment of Paediatrics, University of Melbourne, Melbourne, VIC, Australia. grainne.butler@rch.org.au.ORCID 0000-0001-5966-4096
David J AmorDepartment of Paediatrics, University of Melbourne, Melbourne, VIC, Australia.ORCID 0000-0001-7191-8511
Catherine QuinlanDepartment of Paediatrics, University of Melbourne, Melbourne, VIC, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Reproductive genetic carrier screening (RGCS) is expanding in both public and private healthcare. The primary aim is to identify carrier status for genetic disorders, inform reproductive decision making and promote reproductive autonomy. As screening panels have increased, the potential for findings with personal health implications rises. We report the prevalence of COL4A3/COL4A4 heterozygous variants within a population undergoing RGCS in a private setting and propose a comprehensive management plan for the ongoing care of this patient cohort. Acknowledging that comprehensive guidelines exist for genetic testing and management of Alport syndrome as a broad patient group, this communication seeks to highlight the increasingly common finding of autosomal dominant Alport syndrome and proposes accessible and practical strategies for the clinicians encountering these patients.

Indexed as

AutoantigensCollagen Type IVGenetic Carrier ScreeningGenetic TestingNephritis, HereditaryAdultFemaleGenetic CounselingHeterozygoteHumansMaleAutoantigensCOL4A4 protein, humanCollagen Type IVtype IV collagen alpha3 chain

Identifiers

PMID41015616
PMCPMC12859056

What OpenQuestion holds

Textmetadata
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.