Evidence map›Paper›PMID 29539633›Full record

ArticleNature2018

Placentation defects are highly prevalent in embryonic lethal mouse mutants.

Vicente Perez-Garcia, Elena Fineberg, Robert Wilson, Alexander Murray, Cecilia Icoresi Mazzeo, Catherine Tudor, Arnold Sienerth, Jacqueline K White, Elizabeth Tuck, Edward J Ryder and 15 more

Open access · greenAbstract read
In one paragraph

Article in Nature, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 221 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
221citing papers in PubMed, 2 pooled it
60.2field-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

221 citing papers in PubMed, 2 syntheses or guidelines pooled it, 377 citations in OpenAlex.

  1. Pooled it
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  7. Brain volumes in fetuses with congenital heart disease and placental vascular abnormalities.Journal of perinatology : official journal of the California Perinatal Association · 2026
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161 more citing papers are in PubMed but not listed here.

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

25 authors at 6 institutions in 2 countries.

Vicente Perez-GarciaThe Babraham Institute, Babraham Research Campus, Cambridge CB22 3AT, UK.
Elena FinebergThe Babraham Institute, Babraham Research Campus, Cambridge CB22 3AT, UK.
Robert WilsonThe Francis Crick Institute, 1 Midland Road, London NW1 1AT, UK.
Alexander MurrayThe Babraham Institute, Babraham Research Campus, Cambridge CB22 3AT, UK.
Cecilia Icoresi MazzeoWellcome Trust Sanger Institute, Cambridge CB10 1SA, UK.
Catherine TudorWellcome Trust Sanger Institute, Cambridge CB10 1SA, UK.
Arnold SienerthThe Babraham Institute, Babraham Research Campus, Cambridge CB22 3AT, UK.
Jacqueline K WhiteWellcome Trust Sanger Institute, Cambridge CB10 1SA, UK.
Elizabeth TuckWellcome Trust Sanger Institute, Cambridge CB10 1SA, UK.
Edward J RyderWellcome Trust Sanger Institute, Cambridge CB10 1SA, UK.
Diane GleesonWellcome Trust Sanger Institute, Cambridge CB10 1SA, UK.
Emma SiragherWellcome Trust Sanger Institute, Cambridge CB10 1SA, UK.
Hannah Wardle-JonesWellcome Trust Sanger Institute, Cambridge CB10 1SA, UK.
Nicole StaudtWellcome Trust Sanger Institute, Cambridge CB10 1SA, UK.
Neha WaliWellcome Trust Sanger Institute, Cambridge CB10 1SA, UK.
John CollinsWellcome Trust Sanger Institute, Cambridge CB10 1SA, UK.
Stefan GeyerDivision of Anatomy, Center for Anatomy & Cell Biology, Medical University of Vienna, Waehringerstrasse 13, A-1090 Vienna, Austria.
Elisabeth M Busch-NentwichWellcome Trust Sanger Institute, Cambridge CB10 1SA, UK.
Antonella GalliWellcome Trust Sanger Institute, Cambridge CB10 1SA, UK.
James C SmithThe Francis Crick Institute, 1 Midland Road, London NW1 1AT, UK.
Elizabeth RobertsonSir William Dunn School of Pathology, University of Oxford, Oxford OX1 3RE, UK.
David J AdamsWellcome Trust Sanger Institute, Cambridge CB10 1SA, UK.
Wolfgang J WeningerDivision of Anatomy, Center for Anatomy & Cell Biology, Medical University of Vienna, Waehringerstrasse 13, A-1090 Vienna, Austria.
Timothy MohunThe Francis Crick Institute, 1 Midland Road, London NW1 1AT, UK.
Myriam HembergerThe Babraham Institute, Babraham Research Campus, Cambridge CB22 3AT, UK.
Wellcome Sanger Institute · GBBabraham Institute · GBThe Francis Crick Institute · GBMedical University of Vienna · ATUniversity of Cambridge · GBUniversity of Oxford · GB

Funding

Medical Research Council MC_U117597140Wellcome Trust
6 · The paper itself

Abstract

Large-scale phenotyping efforts have demonstrated that approximately 25-30% of mouse gene knockouts cause intrauterine lethality. Analysis of these mutants has largely focused on the embryo and not the placenta, despite the crucial role of this extraembryonic organ for developmental progression. Here we screened 103 embryonic lethal and sub-viable mouse knockout lines from the Deciphering the Mechanisms of Developmental Disorders program for placental phenotypes. We found that 68% of knockout lines that are lethal at or after mid-gestation exhibited placental dysmorphologies. Early lethality (embryonic days 9.5-14.5) is almost always associated with severe placental malformations. Placental defects correlate strongly with abnormal brain, heart and vascular development. Analysis of mutant trophoblast stem cells and conditional knockouts suggests that a considerable number of factors that cause embryonic lethality when ablated have primary gene function in trophoblast cells. Our data highlight the hugely under-appreciated importance of placental defects in contributing to abnormal embryo development and suggest key molecular nodes that govern placenta formation.

Indexed as

MutationAnimalsEmbryo LossFemaleMiceMice, KnockoutPlacentaPlacentationPregnancyStem CellsTrophoblasts

Identifiers

PMID29539633
PMCPMC5866719
OpenAlexW2789302016

What OpenQuestion holds

Textmetadata
LicenceTDM
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.