Evidence map›Paper›PMID 32908133›Full record

ArticleTranslational psychiatry2020

Polygenic risk for schizophrenia and subcortical brain anatomy in the UK Biobank cohort.

Steluta Grama, Isabella Willcocks, John J Hubert, Antonio F Pardiñas, Sophie E Legge, Matthew Bracher-Smith, Georgina E Menzies, Lynsey S Hall, Andrew J Pocklington, Richard J L Anney and 3 more

Open access · goldAbstract read
In one paragraph

Article in Translational psychiatry, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
4.3field-weighted citation impact, top 5% of its field
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

20 citing papers in PubMed, 1 synthesis or guideline pooled it, 35 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. The impact of polygenic risk for alzheimer's disease on neurotransmitter-related grey matter atrophy in the alzheimer continuum.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2025
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  15. The neural signatures of psychoses in Alzheimer's disease: a neuroimaging genetics approach.European archives of psychiatry and clinical neuroscience · 2023
    Article
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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

13 authors at 2 institutions in 1 country.

Steluta Grama *MRC Centre for Neuropsychiatric Genetics and Genomics, Division of Psychiatry and Clinical Neurosciences, Cardiff University, Cardiff, CF10 3AT, UK.
Isabella Willcocks *MRC Centre for Neuropsychiatric Genetics and Genomics, Division of Psychiatry and Clinical Neurosciences, Cardiff University, Cardiff, CF10 3AT, UK.
John J HubertMRC Centre for Neuropsychiatric Genetics and Genomics, Division of Psychiatry and Clinical Neurosciences, Cardiff University, Cardiff, CF10 3AT, UK.
Antonio F PardiñasMRC Centre for Neuropsychiatric Genetics and Genomics, Division of Psychiatry and Clinical Neurosciences, Cardiff University, Cardiff, CF10 3AT, UK.ORCID http://orcid.org/0000-0001-6845-7590
Sophie E LeggeMRC Centre for Neuropsychiatric Genetics and Genomics, Division of Psychiatry and Clinical Neurosciences, Cardiff University, Cardiff, CF10 3AT, UK.ORCID http://orcid.org/0000-0001-6617-0289
Matthew Bracher-SmithMRC Centre for Neuropsychiatric Genetics and Genomics, Division of Psychiatry and Clinical Neurosciences, Cardiff University, Cardiff, CF10 3AT, UK.ORCID http://orcid.org/0000-0002-0531-6309
Georgina E MenziesUK Dementia Research Institute, Cardiff University, Cardiff, CF10 3AT, UK.ORCID http://orcid.org/0000-0002-6600-6507
Lynsey S HallMRC Centre for Neuropsychiatric Genetics and Genomics, Division of Psychiatry and Clinical Neurosciences, Cardiff University, Cardiff, CF10 3AT, UK.ORCID http://orcid.org/0000-0002-0624-5303
Andrew J PocklingtonMRC Centre for Neuropsychiatric Genetics and Genomics, Division of Psychiatry and Clinical Neurosciences, Cardiff University, Cardiff, CF10 3AT, UK.ORCID http://orcid.org/0000-0002-2137-0452
Richard J L AnneyMRC Centre for Neuropsychiatric Genetics and Genomics, Division of Psychiatry and Clinical Neurosciences, Cardiff University, Cardiff, CF10 3AT, UK.
Nicholas J BrayMRC Centre for Neuropsychiatric Genetics and Genomics, Division of Psychiatry and Clinical Neurosciences, Cardiff University, Cardiff, CF10 3AT, UK.ORCID http://orcid.org/0000-0002-4357-574X
Valentina Escott-PriceMRC Centre for Neuropsychiatric Genetics and Genomics, Division of Psychiatry and Clinical Neurosciences, Cardiff University, Cardiff, CF10 3AT, UK.ORCID http://orcid.org/0000-0003-1784-5483
Xavier CaserasMRC Centre for Neuropsychiatric Genetics and Genomics, Division of Psychiatry and Clinical Neurosciences, Cardiff University, Cardiff, CF10 3AT, UK. CaserasX@cardiff.ac.uk.ORCID http://orcid.org/0000-0002-8490-6891
Cardiff University · GBUK Dementia Research Institute · GB

Funding

Medical Research Council G0801418Medical Research Council MC_PC_17212Medical Research Council MR/L010305/1Medical Research Council MR/L023784/2Medical Research Council MR/T04604X/1
6 · The paper itself

Abstract

Research has shown differences in subcortical brain volumes between participants with schizophrenia and healthy controls. However, none of these differences have been found to associate with schizophrenia polygenic risk. Here, in a large sample (n = 14,701) of unaffected participants from the UK Biobank, we test whether schizophrenia polygenic risk scores (PRS) limited to specific gene-sets predict subcortical brain volumes. We compare associations with schizophrenia PRS at the whole genome level ('genomic', including all SNPs associated with the disorder at a p-value threshold < 0.05) with 'genic' PRS (based on SNPs in the vicinity of known genes), 'intergenic' PRS (based on the remaining SNPs), and genic PRS limited to SNPs within 7 gene-sets previously found to be enriched for genetic association with schizophrenia ('abnormal behaviour,' 'abnormal long-term potentiation,' 'abnormal nervous system electrophysiology,' 'FMRP targets,' '5HT2C channels,' 'CaV2 channels' and 'loss-of-function intolerant genes'). We observe a negative association between the 'abnormal behaviour' gene-set PRS and volume of the right thalamus that survived correction for multiple testing (ß = -0.031, p

Indexed as

SchizophreniaBiological Specimen BanksBrainGenetic Predisposition to DiseaseGenome-Wide Association StudyHumansMultifactorial InheritanceUnited Kingdom

Identifiers

PMID32908133
PMCPMC7481214
OpenAlexW3084046914

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.