Evidence map›Paper›PMID 29760202›Full record

ArticleG3 (Bethesda, Md.)2018

Survey of Human Chromosome 21 Gene Expression Effects on Early Development in

Sarah Edie, Norann A Zaghloul, Carmen C Leitch, Donna K Klinedinst, Janette Lebron, Joey F Thole, Andrew S McCallion, Nicholas Katsanis, Roger H Reeves

Abstract read
In one paragraph

Article in G3 (Bethesda, Md.), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing 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

26 citing papers in PubMed.

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  16. A single intranasal dose of a live-attenuated parainfluenza virus-vectored SARS-CoV-2 vaccine is protective in hamsters.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  17. A serum-stable RNA aptamer specific for SARS-CoV-2 neutralizes viral entry.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  18. Article
  19. Article
  20. Review
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

9 authors.

Sarah EdieJohns Hopkins University School of Medicine, Institute of Genetic Medicine, Baltimore, MD 21205.ORCID 0000-0003-2823-7571
Norann A ZaghloulUniversity of Maryland School of Medicine, Department of Medicine, Division of Endocrinology, Diabetes and Nutrition, Baltimore, MD 21201.
Carmen C LeitchUniversity of Maryland School of Medicine, Department of Medicine, Division of Endocrinology, Diabetes and Nutrition, Baltimore, MD 21201.
Donna K KlinedinstJohns Hopkins University School of Medicine, Department of Physiology, Baltimore, MD 21205.
Janette LebronJohns Hopkins University School of Medicine, Department of Physiology, Baltimore, MD 21205.
Joey F TholeJohns Hopkins University School of Medicine, Institute of Genetic Medicine, Baltimore, MD 21205.
Andrew S McCallionJohns Hopkins University School of Medicine, Institute of Genetic Medicine, Baltimore, MD 21205.
Nicholas KatsanisCenter for Human Disease Modeling, Duke University, Durham, NC 27701.
Roger H ReevesJohns Hopkins University School of Medicine, Institute of Genetic Medicine, Baltimore, MD 21205 rreeves@jhmi.edu.ORCID 0000-0002-3581-0850

Funding

GENOMIC APPROACHES TO ANEUPLOIDYR01HD038384 · NICHD · JOHNS HOPKINS UNIVERSITY · PI REEVES, ROGER H · 2000 to 2020
$11.0M
Development of a Neuronal Regulatory LexiconR01NS062972 · NINDS · JOHNS HOPKINS UNIVERSITY · PI MCCALLION, ANDREW S · 2009 to 2018
$4.1M
Neuropsychiatric Disease-focused Exploration of Neuronal Regulatory LandscapesR01MH106522 · NIMH · JOHNS HOPKINS UNIVERSITY · PI MCCALLION, ANDREW S · 2016 to 2021
$3.0M
NICHD NIH HHS R01 HD038384NIMH NIH HHS R01 MH106522NINDS NIH HHS R01 NS062972
6 · The paper itself

Abstract

Trisomy for human chromosome 21 (Hsa21) results in Down syndrome (DS), one of the most genetically complex conditions compatible with human survival. Assessment of the physiological consequences of dosage-driven overexpression of individual Hsa21 genes during early embryogenesis and the resulting contributions to DS pathology in mammals are not tractable in a systematic way. A recent study looked at loss-of-function of a subset of

Indexed as

Chromosomes, Human, Pair 21Gene Expression Regulation, DevelopmentalAnimalsDisease Models, AnimalDown SyndromeGene DosageGene LibraryGenetic Association StudiesGenetic Complementation TestHumansPhenotypeZebrafishHsa21over expressionzebrafish

Identifiers

PMID29760202
PMCPMC6027891

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.