Evidence map›Paper›PMID 27082423›Full record

ArticleHuman genome variation2016

Erratum: Novel rare variations of the oxytocin receptor (OXTR) gene in autism spectrum disorder individuals.

Xiaoxi Liu, Minae Kawashima, Taku Miyagawa, Takeshi Otowa, Khun Zaw Latt, Myo Thiri, Hisami Nishida, Toshiro Sugiyama, Yoshinori Tsurusaki, Naomichi Matsumoto and 4 more

Abstract readPublished Erratum
PubMed Full text at PMC Publisher
In one paragraph

Article in Human genome variation, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors.

Xiaoxi LiuDepartment of Human Genetics, Graduate School of Medicine, University of Tokyo , Tokyo, Japan.
Minae KawashimaDepartment of Human Genetics, Graduate School of Medicine, University of Tokyo, Tokyo, Japan; Japan Science and Technology Agency (JST), Tokyo, Japan.
Taku MiyagawaDepartment of Human Genetics, Graduate School of Medicine, University of Tokyo , Tokyo, Japan.
Takeshi OtowaDepartment of Neuropsychiatry, Graduate School of Medicine, University of Tokyo , Tokyo, Japan.
Khun Zaw LattDepartment of Human Genetics, Graduate School of Medicine, University of Tokyo , Tokyo, Japan.
Myo ThiriDepartment of Human Genetics, Graduate School of Medicine, University of Tokyo , Tokyo, Japan.
Hisami NishidaAsunaro Hospital for Child and Adolescent Psychiatry , Tsu, Japan.
Toshiro SugiyamaDepartment of Child and Adolescent Psychiatry, Hamamatsu University School of Medicine , Hamamatsu, Japan.
Yoshinori TsurusakiDepartment of Human Genetics, Graduate School of Medicine, Yokohama City University , Yokohama, Japan.
Naomichi MatsumotoDepartment of Human Genetics, Graduate School of Medicine, Yokohama City University , Yokohama, Japan.
Akihiko MabuchiDepartment of Human Genetics, Graduate School of Medicine, University of Tokyo , Tokyo, Japan.
Nobumasa KatoMedical Institute of Developmental Disabilities Research, Showa University , Tokyo, Japan.
Katsushi TokunagaDepartment of Human Genetics, Graduate School of Medicine, University of Tokyo , Tokyo, Japan.
Tsukasa SasakiDepartment of Physical and Health Education, Graduate School of Education, The University of Tokyo , Tokyo, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

[This corrects the article DOI: 10.1038/hgv.2015.24.][This corrects the article DOI: 10.1038/hgv.2015.24.].

Identifiers

PMID27082423
PMCPMC4785588

What OpenQuestion holds

Textmetadata
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.