Evidence map›Paper›PMID 30745909›Full record

ArticleFrontiers in genetics2018

Exome Sequencing Identifies

Chao-Biao Xue, Zhou-Heng Xu, Jun Zhu, Yu Wu, Xi-Hang Zhuang, Qu-Liang Chen, Cai-Ru Wu, Jin-Tao Hu, Hou-Shi Zhou, Wei-Hang Xie and 6 more

Abstract read
In one paragraph

Article in Frontiers in genetics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing 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

21 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Differential Association of theInternational journal of molecular sciences · 2025
    Article
  5. Rare Homozygous Variants inInternational journal of molecular sciences · 2025
    Article
  6. Article
  7. Article
  8. Genomic Loci Influencing Cue-Reactivity in Heterogeneous Stock Rats.bioRxiv : the preprint server for biology · 2024
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. 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

16 authors.

Chao-Biao XueMental Health Center, Shantou University Medical College, Shantou, China.
Zhou-Heng XuLaboratory of Genomic and Precision Medicine, Wuxi School of Medicine, Jiangnan University, Wuxi, China.
Jun ZhuMental Health Center, Shantou University Medical College, Shantou, China.
Yu WuMental Health Center, Shantou University Medical College, Shantou, China.
Xi-Hang ZhuangMental Health Center, Shantou University Medical College, Shantou, China.
Qu-Liang ChenMental Health Center, Shantou University Medical College, Shantou, China.
Cai-Ru WuMental Health Center, Shantou University Medical College, Shantou, China.
Jin-Tao HuMental Health Center, Shantou University Medical College, Shantou, China.
Hou-Shi ZhouShantou Central Hospital, Affiliated Shantou Hospital of Sun Yat-sen University, Shantou, China.
Wei-Hang XieShantou Central Hospital, Affiliated Shantou Hospital of Sun Yat-sen University, Shantou, China.
Xin YiBeijing Genomics Institute - Shenzhen, Shenzhen, China.
Shan-Shan YuBeijing Genomics Institute - Shenzhen, Shenzhen, China.
Zhi-Yu PengBeijing Genomics Institute - Shenzhen, Shenzhen, China.
Huan-Ming YangBeijing Genomics Institute - Shenzhen, Shenzhen, China.
Xiao-Hong HongMental Health Center, Shantou University Medical College, Shantou, China.
Jian-Huan ChenLaboratory of Genomic and Precision Medicine, Wuxi School of Medicine, Jiangnan University, Wuxi, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Schizophrenia is a complex psychiatric disorder with high genetic heterogeneity, however, the contribution of rare mutations to the disease etiology remains to be further elucidated. We herein performed exome sequencing in a Han Chinese schizophrenia family and identified a missense mutation (c.6724C>T, p.R2242C) in the teneurin transmembrane protein 4 (

Indexed as

associationco-segregationexome analysisrare mutationschizophrenia

Identifiers

PMID30745909
PMCPMC6360184

What OpenQuestion holds

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Registered trials

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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.