Evidence map›Paper›PMID 16897606›Full record

ArticleJournal of neural transmission (Vienna, Austria : 1996)2007

No association between the genetic polymorphisms in the RTN4R gene and schizophrenia in the Chinese population.

J Meng, Y Shi, X Zhao, S Guo, H Wang, Y Zheng, R Tang, G Feng, N Gu, H Liu and 2 more

Abstract read
PubMed Publisher
In one paragraph

Article in Journal of neural transmission (Vienna, Austria : 1996), 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.0field-weighted citation impact, top 27% 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

8 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Converging evidence for the Nogo-66 receptor gene in schizophrenia.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2009
    Review
  6. Genetic variants of Nogo-66 receptor with possible association to schizophrenia block myelin inhibition of axon growth.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2008
    Article
  7. Nogo-A and Nogo-66 receptor in amyotrophic lateral sclerosis.Journal of cellular and molecular medicine · 2008
    Review
  8. 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

12 authors at 6 institutions in 2 countries.

J MengBio-X Center, Shanghai Jiao Tong University, Shanghai, PR China.
Y Shi
X Zhao
S Guo
H Wang
Y Zheng
R Tang
G Feng
N Gu
H Liu
S Zhu
L He
Shanghai Jiao Tong University · CNChinese Academy of Sciences · CNHealth Commission of Jilin Province · CNInstitute of Mental Health · RSShanghai Institutes for Biological Sciences · CNShanghai Mental Health Center · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The RTN4R gene is located in the 22q11 region and it encodes a subunit of the receptor complex (RTN4R-p75NTR) which results in neuronal growth inhibitory signals in response to Nogo-66, MAG or OMG signaling. Previous studies have suggested that RTN4R might act as a potential candidate for schizophrenia susceptibility loci. We genotyped four SNPs within the gene and conducted a case-control study and TDT analysis, involving 707 schizophrenic patients, 689 controls and 372 unrelated small nuclear families with schizophrenic offspring in the Chinese population. We examined allele and genotype frequencies and haplotype distributions in both family- and nonfamily-based samples. Our results suggest that there is no significant association between the genetic polymorphisms and schizophrenia in the Han Chinese population.

Indexed as

Genetic Predisposition to DiseasePolymorphism, GeneticCase-Control StudiesChinaFemaleGPI-Linked ProteinsHumansMaleMiddle AgedMyelin ProteinsNogo Receptor 1Polymerase Chain ReactionReceptors, Cell SurfaceSchizophreniaGPI-Linked ProteinsMyelin ProteinsNogo Receptor 1Receptors, Cell SurfaceRTN4R protein, human

Identifiers

PMID16897606
OpenAlexW2092916024

What OpenQuestion holds

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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.