Evidence map›Paper›PMID 40486211›Full record

ArticleResearch and practice in thrombosis and haemostasis2025

The diagnostic utility of genetic testing in inherited thrombocytopenia: regional multicenter tertiary experience.

Eman Hassan, Carl Fratter, Will Lester, Charles Percy, Walaa Saad, Afrah Alkhedir, Jayashree Motwani, Patricia Bignell, Phillip L R Nicolson, Neil V Morgan and 2 more

Abstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Research and practice in thrombosis and haemostasis, 2025. 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. Is genetic testing for heritable thrombocytopenia coming of age?Research and practice in thrombosis and haemostasis · 2025
    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

12 authors.

Eman HassanDepartment of Cardiovascular Sciences, College of Medicine and Health, University of Birmingham, UK.
Carl FratterOxford Centre for Genomic Medicine, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.
Will LesterDepartment of Cardiovascular Sciences, College of Medicine and Health, University of Birmingham, UK.
Charles PercyDepartment of Haematology, Queen Elizabeth Hospital, Birmingham, UK.
Walaa SaadDepartment of Haematology, Queen Elizabeth Hospital, Birmingham, UK.
Afrah AlkhedirDepartment of Haematology, Birmingham Children's Hospital, Birmingham, UK.
Jayashree MotwaniDepartment of Haematology, Birmingham Children's Hospital, Birmingham, UK.
Patricia BignellOxford Centre for Genomic Medicine, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.
Phillip L R NicolsonDepartment of Cardiovascular Sciences, College of Medicine and Health, University of Birmingham, UK.
Neil V MorganDepartment of Cardiovascular Sciences, College of Medicine and Health, University of Birmingham, UK.
Sandeep PotluriDepartment of Haematology, Birmingham Children's Hospital, Birmingham, UK.
Gillian LoweDepartment of Cardiovascular Sciences, College of Medicine and Health, University of Birmingham, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Identifiers

PMID40486211
PMCPMC12145818

What OpenQuestion holds

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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.