ArticleJournal of the Royal Society of New Zealand2025
The role of clinical genetics in integrating cancer genetics care in Aotearoa New Zealand: improved access for improved outcomes.
Article in Journal of the Royal Society of New Zealand, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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
1 citing paper in PubMed.
- Genetic Counseling in Aotearoa New Zealand: Context, Practice and the Future of Genomic Healthcare.Journal of genetic counseling · 2026Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
This viewpoint explores the current state of cancer genetics care in Aotearoa and how appropriate resourcing could lead to improved outcomes in individuals with an underlying cancer predisposition. There is increasing demand for genetic results at the point at which they may have a clinical impact in patients diagnosed with cancer, highlighting the need for improved access to genetic testing. For those cancers that are heritable, genetic test results can also inform appropriate management for at-risk relatives, including screening, risk-reducing surgery and prophylactic medical therapy, leading to an expected decrease in cancer incidence. We explore barriers to cancer genetics care and offer potential solutions to ensure equitable service delivery.
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Registered trials
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.