Evidence map›Paper›PMID 23273769›Full record

ArticleJournal of genetics and genomics = Yi chuan xue bao2012

Clue to a new deafness gene: a large Chinese nonsyndromic hearing loss family linked to DFNA4.

Liang Zong, Chunye Lu, Yali Zhao, Qian Li, Dongyi Han, Weiyan Yang, Yan Shen, Qingyin Zheng, Qiuju Wang

Abstract readLetter
In one paragraph

Article in Journal of genetics and genomics = Yi chuan xue bao, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Comparative proteomic analysis of human lung telocytes with fibroblasts.Journal of cellular and molecular medicine · 2014
    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

9 authors.

Liang Zong
Chunye Lu
Yali Zhao
Qian Li
Dongyi Han
Weiyan Yang
Yan Shen
Qingyin Zheng
Qiuju Wang

Funding

Deciphering the Usher I protein interactome using a genetic approachR01DC009246 · NIDCD · CASE WESTERN RESERVE UNIVERSITY · PI ZHENG, QING Y · 2009 to 2013
$1.6M
NIDCD NIH HHS R01 DC009246
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Asian PeopleChinaChromosome MappingChromosomes, Human, Pair 19DeafnessDNA Mutational AnalysisFamily HealthFemaleGenetic Predisposition to DiseaseHearing Loss, SensorineuralHumansMaleMyosin Heavy ChainsMyosin Type IIPedigreeMYH7b protein, humanMyosin Heavy ChainsMyosin Type II

Identifiers

PMID23273769
PMCPMC3685490

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.