Evidence map›Paper›PMID 29283788›Full record

ArticleOphthalmic genetics2018

Investigating the disease association of USH2A p.C759F variant by leveraging large retinitis pigmentosa cohort data.

Mariana DuPont, Evan M Jones, Mingchu Xu, Rui Chen

Abstract read
In one paragraph

Article in Ophthalmic genetics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. A Comparative Evaluation of the Genetic Variant Spectrum in theInternational journal of molecular sciences · 2024
    Article
  2. Review
  3. Article
  4. Article
  5. Truncating Variants Contribute to Hearing Loss and Severe Retinopathy inInternational journal of molecular sciences · 2020
    Article
  6. Article
  7. Structural modeling, mutation analysis, andComputational and structural biotechnology journal · 2020
    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

4 authors.

Mariana DuPonta College of Arts and Sciences , Dillard University , New Orleans , LA , USA.
Evan M Jonesb Department of Molecular and Human Genetics , Baylor College of Medicine , Houston , TX , USA.
Mingchu Xub Department of Molecular and Human Genetics , Baylor College of Medicine , Houston , TX , USA.
Rui Chenb Department of Molecular and Human Genetics , Baylor College of Medicine , Houston , TX , USA.

Funding

VISION RESEARCH CENTERP30EY002520 · NEI · BAYLOR COLLEGE OF MEDICINE · PI Samuel M Wu · 1985 to 2026
$14.8M
GENETICS OF EARLY ONSET RETINAL DISEASESR01EY018571 · NEI · UNIVERSITY OF CALIFORNIA-IRVINE · PI RUI CHEN · 2008 to 2026
$7.2M
PROGRAM IN HUMAN MOLECULAR GENETICST32GM008307 · NIGMS · BAYLOR COLLEGE OF MEDICINE · PI SHAULSKY, GAD · 1990 to 2020
$6.6M
Molecular Basis of Human Visual System DisordersR01EY022356 · NEI · UNIVERSITY OF CALIFORNIA-IRVINE · PI RUI CHEN · 2012 to 2026
$6.1M
FGI: Acquisition of an Illumina Genome Analyzer System for Functional Genomic ResS10RR026550 · NCRR · BAYLOR COLLEGE OF MEDICINE · PI CHEN, RUI · 2010 to 2010
$500k
NCRR NIH HHS S10 RR026550NEI NIH HHS P30 EY002520NEI NIH HHS R01 EY018571NEI NIH HHS R01 EY022356NIGMS NIH HHS T32 GM008307
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Cohort StudiesExtracellular Matrix ProteinsGene FrequencyGenetic VariationHumansMutationRetinitis PigmentosaRNA, MessengerExtracellular Matrix ProteinsRNA, MessengerUSH2A protein, human

Identifiers

PMID29283788
PMCPMC6084783

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.