Evidence map›Paper›PMID 32016392›Full record

ArticleHuman molecular genetics2020

Deficiency of FRAS1-related extracellular matrix 1 (FREM1) causes congenital diaphragmatic hernia in humans and mice.

Tyler F Beck, Danielle Veenma, Oleg A Shchelochkov, Zhiyin Yu, Bum Jun Kim, Hitisha P Zaveri, Yolande van Bever, Sunju Choi, Hannie Douben, Terry K Bertin and 7 more

Abstract readPublished Erratum
PubMed Full text at PMC Publisher
In one paragraph

Article in Human molecular genetics, 2020. 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

17 authors.

Tyler F BeckDepartment of Molecular and Human Genetics.
Danielle VeenmaDepartment of Pediatric Surgery.
Oleg A ShchelochkovDepartment of Pediatrics, The University of Iowa, Iowa City, IA 52242, USA.
Zhiyin YuDepartment of Molecular and Human Genetics.
Bum Jun KimDepartment of Molecular and Human Genetics.
Hitisha P ZaveriDepartment of Molecular and Human Genetics.
Yolande van BeverDepartment of Clinical Genetics, Erasmus Medical Center, Rotterdam 3015 GJ, The Netherlands.
Sunju ChoiInstitute for Genetic Medicine and Center for Craniofacial Molecular Biology, University of Southern California, Los Angeles, CA 90033, USA.
Hannie DoubenDepartment of Clinical Genetics, Erasmus Medical Center, Rotterdam 3015 GJ, The Netherlands.
Terry K BertinDepartment of Molecular and Human Genetics.
Pragna I PatelInstitute for Genetic Medicine and Center for Craniofacial Molecular Biology, University of Southern California, Los Angeles, CA 90033, USA.
Brendan LeeDepartment of Molecular and Human Genetics.
Dick TibboelDepartment of Pediatric Surgery.
Annelies de KleinDepartment of Clinical Genetics, Erasmus Medical Center, Rotterdam 3015 GJ, The Netherlands.
David W StocktonDepartment of Pediatrics.
Monica J JusticeDepartment of Molecular and Human Genetics.
Daryl A ScottDepartment of Molecular and Human Genetics.

Funding

UNDERSTANDING FXTAS AMONG MALES WITH THE FMR1 PREMUTATIONP30HD024064 · NICHD · BAYLOR COLLEGE OF MEDICINE · PI TOLIAS, KIMBERLY R · 1988 to 2013
$29.4M
Recessive Ocular Phenotypes from Murine ENU MutagenesisR03EY014854 · NEI · BAYLOR COLLEGE OF MEDICINE · PI STOCKTON, DAVID W · 2003 to 2005
$444k
NEI NIH HHS R03 EY014854NICHD NIH HHS P30 HD024064
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Identifiers

PMID32016392
PMCPMC8325106

What OpenQuestion holds

Textmetadata
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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.