Evidence map›Paper›PMID 42205162›Full record

ArticleBrain communications2026

The contribution of apolipoprotein E genetic variation to dementia risk in British South Asians.

Benjamin M Jacobs, Avinash Chandra, Isabelle Francesca Foote, Faiza Durrani, Sheena Waters, Yue Liu, Petroula Proitsi, Genes & Health Research Team, Cara L Croft, Dylan M Williams and 6 more

Abstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Brain communications, 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.

Benjamin M JacobsWolfson Institute of Population Health, Queen Mary University of London, London EC1M 6BQ, UK.ORCID https://orcid.org/0000-0002-6023-6010
Avinash ChandraWolfson Institute of Population Health, Queen Mary University of London, London EC1M 6BQ, UK.
Isabelle Francesca FooteWolfson Institute of Population Health, Queen Mary University of London, London EC1M 6BQ, UK.
Faiza DurraniWolfson Institute of Population Health, Queen Mary University of London, London EC1M 6BQ, UK.
Sheena WatersWolfson Institute of Population Health, Queen Mary University of London, London EC1M 6BQ, UK.
Yue LiuWolfson Institute of Population Health, Queen Mary University of London, London EC1M 6BQ, UK.
Petroula ProitsiWolfson Institute of Population Health, Queen Mary University of London, London EC1M 6BQ, UK.
Genes & Health Research Team
Cara L CroftCentre for Neuroscience, Surgery & Trauma, The Blizard Institute, Queen Mary University of London, London E1 2AT, UK.
Dylan M WilliamsDivision of Psychiatry, University College London, London W1T 7NF, UK.
Sarah FinerWolfson Institute of Population Health, Queen Mary University of London, London EC1M 6BQ, UK.ORCID https://orcid.org/0000-0002-2684-4653
Stuart RisonWolfson Institute of Population Health, Queen Mary University of London, London EC1M 6BQ, UK.
Arnab MandalWolfson Institute of Population Health, Queen Mary University of London, London EC1M 6BQ, UK.ORCID https://orcid.org/0009-0008-5107-4487
Moneeza SiddiquiWolfson Institute of Population Health, Queen Mary University of London, London EC1M 6BQ, UK.
David A van HeelCentre for Neuroscience, Surgery & Trauma, The Blizard Institute, Queen Mary University of London, London E1 2AT, UK.ORCID https://orcid.org/0000-0002-0637-2265
Charles R MarshallWolfson Institute of Population Health, Queen Mary University of London, London EC1M 6BQ, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Understanding the genetic basis of dementia in diverse populations is essential to ensure that efforts to predict, prevent and treat dementia are equitable. The strongest genetic risk factor for dementia-

Indexed as

ancestryAPOEdementiageneticssouth Asian

Identifiers

PMID42205162
PMCPMC13202451

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.