Evidence map›Paper›PMID 35710731›Full record

ArticleCommunications biology2022

Capturing additional genetic risk from family history for improved polygenic risk prediction.

Tianyuan Lu, Vincenzo Forgetta, J Brent Richards, Celia M T Greenwood

Abstract read
In one paragraph

Article in Communications biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Within-family analysis of PRSJournal, genetic engineering & biotechnology · 2025
    Article
  7. Article
  8. Article
  9. Effects of polygenic risk score and sodium and potassium intake on hypertension in Asians: A nationwide prospective cohort study.Hypertension research : official journal of the Japanese Society of Hypertension · 2024
    Article
  10. Article
  11. Article
  12. Article
  13. 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

4 authors.

Tianyuan LuLady Davis Institute for Medical Research, Jewish General Hospital, Montreal, QC, Canada. tianyuan.lu@mail.mcgill.ca.ORCID http://orcid.org/0000-0002-5664-5698
Vincenzo ForgettaLady Davis Institute for Medical Research, Jewish General Hospital, Montreal, QC, Canada.
J Brent RichardsLady Davis Institute for Medical Research, Jewish General Hospital, Montreal, QC, Canada.ORCID http://orcid.org/0000-0002-3746-9086
Celia M T GreenwoodLady Davis Institute for Medical Research, Jewish General Hospital, Montreal, QC, Canada. celia.greenwood@mcgill.ca.ORCID http://orcid.org/0000-0002-2427-5696

Funding

CIHR 365825CIHR 409511CIHR PJT-148620Medical Research Council MC_PC_17228Medical Research Council MC_QA137853Wellcome TrustWellcome Trust 076467/Z/05/ZWellcome Trust 217065/Z/19/Z
6 · The paper itself

Abstract

Family history of complex traits may reflect transmitted rare pathogenic variants, intra-familial shared exposures to environmental and lifestyle factors, as well as a common genetic predisposition. We developed a latent factor model to quantify trait heritability in excess of that captured by a common variant-based polygenic risk score, but inferable from family history. For 941 children in the Avon Longitudinal Study of Parents and Children cohort, a joint predictor combining a polygenic risk score for height and mid-parental height was able to explain

Indexed as

Genome-Wide Association StudyMultifactorial InheritanceAdultChildGenetic Predisposition to DiseaseHumansLongitudinal StudiesRisk Factors

Identifiers

PMID35710731
PMCPMC9203758

What OpenQuestion holds

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Registered trials

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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.