Evidence map›Paper›PMID 38559031›Full record

ArticlemedRxiv : the preprint server for health sciences2024

A framework for conducting time-varying genome-wide association studies: An application to body mass index across childhood in six multiethnic cohorts.

Kimberley Burrows, Anni Heiskala, Jonathan P Bradfield, Zhanna Balkhiyarova, Lijiao Ning, Mathilde Boissel, Yee-Ming Chan, Philippe Froguel, Amelie Bonnefond, Hakon Hakonarson and 10 more

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In one paragraph

Article in medRxiv : the preprint server for health sciences, 2024. 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

5 · Who and what money

Authors and funding

20 authors.

Kimberley BurrowsMRC Integrative Epidemiology Unit at the University of Bristol, Bristol, UK.ORCID 0000-0002-3208-0389
Anni HeiskalaResearch Unit of Population Health, University of Oulu, Oulu, Finland.
Jonathan P BradfieldCenter for Applied Genomics, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.
Zhanna BalkhiyarovaDepartment of Clinical and Experimental Medicine, School of Biosciences and Medicine, University of Surrey, Guildford, UK.
Lijiao NingUniv Lille, INSERM/CNRS UMR1283/8199, EGID, Institut Pasteur de Lille, Lille University Hospital, Lille, France.
Mathilde BoisselUniv Lille, INSERM/CNRS UMR1283/8199, EGID, Institut Pasteur de Lille, Lille University Hospital, Lille, France.
Yee-Ming ChanDivision of Endocrinology, Department of Pediatrics, Boston Children's Hospital.
Philippe FroguelUniv Lille, INSERM/CNRS UMR1283/8199, EGID, Institut Pasteur de Lille, Lille University Hospital, Lille, France.
Amelie BonnefondUniv Lille, INSERM/CNRS UMR1283/8199, EGID, Institut Pasteur de Lille, Lille University Hospital, Lille, France.
Hakon HakonarsonCenter for Applied Genomics, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.
Alessander Couto AlvesSchool of Biosciences and Medicine, University of Surrey, Guildford, UK.
Deborah A LawlorMRC Integrative Epidemiology Unit at the University of Bristol, Bristol, UK.
Marika KaakinenDepartment of Clinical and Experimental Medicine, School of Biosciences and Medicine, University of Surrey, Guildford, UK.
Marjo-Riitta JärvelinResearch Unit of Population Health, University of Oulu, Oulu, Finland.
Struan F A GrantCenter for Applied Genomics, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.
Kate TillingMRC Integrative Epidemiology Unit at the University of Bristol, Bristol, UK.
Inga ProkopenkoDepartment of Clinical and Experimental Medicine, School of Biosciences and Medicine, University of Surrey, Guildford, UK.
Sylvain SebertResearch Unit of Population Health, University of Oulu, Oulu, Finland.
Mickaël CanouilUniv Lille, INSERM/CNRS UMR1283/8199, EGID, Institut Pasteur de Lille, Lille University Hospital, Lille, France.
Nicole M WarringtonInstitute for Molecular Bioscience, University of Queensland, Brisbane, Australia.

Funding

Genome Wide Association Study for Childhood ObesityR01HD056465 · NICHD · CHILDREN'S HOSP OF PHILADELPHIA · PI GRANT, STRUAN F A · 2008 to 2024
$9.5M
NICHD NIH HHS R01 HD056465
6 · The paper itself

Abstract

Genetic effects on changes in human traits over time are understudied and may have important pathophysiological impact. We propose a framework that enables data quality control, implements mixed models to evaluate trajectories of change in traits, and estimates phenotypes to identify age-varying genetic effects in genome-wide association studies (GWASs). Using childhood body mass index (BMI) as an example, we included 71,336 participants from six cohorts and estimated the slope and area under the BMI curve within four time periods (infancy, early childhood, late childhood and adolescence) for each participant, in addition to the age and BMI at the adiposity peak and the adiposity rebound. GWAS on each of the estimated phenotypes identified 28 genome-wide significant variants at 13 loci across the 12 estimated phenotypes, one of which was novel (in

Identifiers

PMID38559031
PMCPMC10980110

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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.