Evidence map›Paper›PMID 33270668›Full record

ArticlePloS one2020

Complex genetic dependencies among growth and neurological phenotypes in healthy children: Towards deciphering developmental mechanisms.

Lisa Uechi, Mahjoubeh Jalali, Jayson D Wilbur, Jonathan L French, N L Jumbe, Michael J Meaney, Peter D Gluckman, Neerja Karnani, Nikita A Sakhanenko, David J Galas and 1 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

9 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
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  6. Journal of computational biology : a journal of computational molecular cell biology · 2023
    Article
  7. Article
  8. AtypicalGenes · 2021
    Review
  9. 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

11 authors at 5 institutions in 4 countries.

Lisa UechiPacific Northwest Research Institute, Seattle, Washington, United States of America.ORCID 0000-0001-8215-6938
Mahjoubeh JalaliPacific Northwest Research Institute, Seattle, Washington, United States of America.
Jayson D WilburMetrum Research Group, Tariffville, CT, United States of America.
Jonathan L FrenchMetrum Research Group, Tariffville, CT, United States of America.ORCID 0000-0001-9649-169X
N L JumbePharmactuarials LLC, Mountain View, CA, United States of America.
Michael J MeaneyDouglas Mental Health University Institute, McGill University, Montreal, QC, Canada.
Peter D GluckmanCentre for Human Evolution, Adaptation and Disease, Liggins Institute, University of Auckland, Auckland, New Zealand.
Neerja KarnaniDepartment of Biochemistry, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
Nikita A SakhanenkoPacific Northwest Research Institute, Seattle, Washington, United States of America.ORCID 0000-0001-6256-4643
David J GalasPacific Northwest Research Institute, Seattle, Washington, United States of America.ORCID 0000-0001-8248-8617
GUSTO study group
Pacific Northwest Diabetes Research Institute · USMetrum Research Group (United States) · USCanadian Institute for Advanced Research · CANational University of Singapore · SGUniversity of Auckland · NZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The genetic mechanisms of childhood development in its many facets remain largely undeciphered. In the population of healthy infants studied in the Growing Up in Singapore Towards Healthy Outcomes (GUSTO) program, we have identified a range of dependencies among the observed phenotypes of fetal and early childhood growth, neurological development, and a number of genetic variants. We have quantified these dependencies using our information theory-based methods. The genetic variants show dependencies with single phenotypes as well as pleiotropic effects on more than one phenotype and thereby point to a large number of brain-specific and brain-expressed gene candidates. These dependencies provide a basis for connecting a range of variants with a spectrum of phenotypes (pleiotropy) as well as with each other. A broad survey of known regulatory expression characteristics, and other function-related information from the literature for these sets of candidate genes allowed us to assemble an integrated body of evidence, including a partial regulatory network, that points towards the biological basis of these general dependencies. Notable among the implicated loci are RAB11FIP4 (next to NF1), MTMR7 and PLD5, all highly expressed in the brain; DNMT1 (DNA methyl transferase), highly expressed in the placenta; and PPP1R12B and DMD (dystrophin), known to be important growth and development genes. While we cannot specify and decipher the mechanisms responsible for the phenotypes in this study, a number of connections for further investigation of fetal and early childhood growth and neurological development are indicated. These results and this approach open the door to new explorations of early human development.

Indexed as

Child DevelopmentChildChromatinEpistasis, GeneticFetal DevelopmentGene Expression ProfilingGene Expression Regulation, DevelopmentalGene Regulatory NetworksGenetic LociGenetic PleiotropyGenome-Wide Association StudyGenotypeHumansLinkage DisequilibriumNervous SystemPhenotypeChromatin

Identifiers

PMID33270668
PMCPMC7714163
OpenAlexW3107776007

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.