Evidence map›Paper›PMID 34282336›Full record

ArticleNature genetics2021

Distinction between the effects of parental and fetal genomes on fetal growth.

Thorhildur Juliusdottir, Valgerdur Steinthorsdottir, Lilja Stefansdottir, Gardar Sveinbjornsson, Erna V Ivarsdottir, Rosa B Thorolfsdottir, Jon K Sigurdsson, Vinicius Tragante, Kristjan E Hjorleifsson, Anna Helgadottir and 12 more

Abstract read
PubMed Publisher
In one paragraph

Article in Nature genetics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 62 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
62citing papers in PubMed, 3 pooled it
21.0field-weighted citation impact, top 1% 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

62 citing papers in PubMed, 3 syntheses or guidelines pooled it, 96 citations in OpenAlex.

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2 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

22 authors at 3 institutions in 2 countries.

Thorhildur Juliusdottir *deCODE genetics/Amgen, Reykjavik, Iceland.
Valgerdur Steinthorsdottir *deCODE genetics/Amgen, Reykjavik, Iceland. valgerdur.steinthorsdottir@decode.is.ORCID http://orcid.org/0000-0003-1846-6274
Lilja StefansdottirdeCODE genetics/Amgen, Reykjavik, Iceland.
Gardar SveinbjornssondeCODE genetics/Amgen, Reykjavik, Iceland.
Erna V IvarsdottirdeCODE genetics/Amgen, Reykjavik, Iceland.ORCID http://orcid.org/0000-0002-2069-0681
Rosa B ThorolfsdottirdeCODE genetics/Amgen, Reykjavik, Iceland.ORCID http://orcid.org/0000-0001-7475-0398
Jon K SigurdssondeCODE genetics/Amgen, Reykjavik, Iceland.
Vinicius TragantedeCODE genetics/Amgen, Reykjavik, Iceland.ORCID http://orcid.org/0000-0002-8223-8957
Kristjan E HjorleifssondeCODE genetics/Amgen, Reykjavik, Iceland.
Anna HelgadottirdeCODE genetics/Amgen, Reykjavik, Iceland.ORCID http://orcid.org/0000-0002-1806-2467
Michael L FriggedeCODE genetics/Amgen, Reykjavik, Iceland.ORCID http://orcid.org/0000-0003-2984-535X
Gudmundur ThorgeirssondeCODE genetics/Amgen, Reykjavik, Iceland.
Rafn BenediktssonFaculty of Medicine, University of Iceland, Reykjavik, Iceland.
Emil L SigurdssonDevelopment Centre for the Primary Care, Reykjavik, Iceland.
David O ArnardeCODE genetics/Amgen, Reykjavik, Iceland.
Thora SteingrimsdottirFaculty of Medicine, University of Iceland, Reykjavik, Iceland.
Ingileif JonsdottirdeCODE genetics/Amgen, Reykjavik, Iceland.ORCID http://orcid.org/0000-0001-8339-150X
Hilma HolmdeCODE genetics/Amgen, Reykjavik, Iceland.ORCID http://orcid.org/0000-0002-9517-6636
Daniel F GudbjartssondeCODE genetics/Amgen, Reykjavik, Iceland.ORCID http://orcid.org/0000-0002-5222-9857
Gudmar ThorleifssondeCODE genetics/Amgen, Reykjavik, Iceland.
Unnur ThorsteinsdottirdeCODE genetics/Amgen, Reykjavik, Iceland.
Kari StefanssondeCODE genetics/Amgen, Reykjavik, Iceland. kstefans@decode.is.ORCID http://orcid.org/0000-0003-1676-864X
deCODE Genetics (Iceland) · ISUniversity of Iceland · ISCalifornia Institute of Technology · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Birth weight is a common measure of fetal growth that is associated with a range of health outcomes. It is directly affected by the fetal genome and indirectly by the maternal genome. We performed genome-wide association studies on birth weight in the genomes of the child and parents and further analyzed birth length and ponderal index, yielding a total of 243 fetal growth variants. We clustered those variants based on the effects of transmitted and nontransmitted alleles on birth weight. Out of 141 clustered variants, 22 were consistent with parent-of-origin-specific effects. We further used haplotype-specific polygenic risk scores to directly test the relationship between adult traits and birth weight. Our results indicate that the maternal genome contributes to increased birth weight through blood-glucose-raising alleles while blood-pressure-raising alleles reduce birth weight largely through the fetal genome.

Indexed as

AdultBirth WeightBlood GlucoseBlood PressureBody HeightCardiovascular DiseasesFemaleFetal DevelopmentGenome-Wide Association StudyHaplotypesHumansIcelandInfant, NewbornMaleModels, GeneticPolymorphism, Single NucleotideBlood Glucose

Identifiers

PMID34282336
OpenAlexW3183211243

What OpenQuestion holds

Textmetadata
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.