Evidence map›Paper›PMID 36267860›Full record

ArticleJournal of pediatric genetics2022

Exome Sequencing Reveals De Novo Variants in Congenital Scoliosis.

Kohei Murakami, Shingo Kikugawa, Shoji Seki, Hidetomi Terai, Takako Suzuki, Masaki Nakano, Jun Takahashi, Yukio Nakamura

Open access · greenAbstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Journal of pediatric genetics, 2022. 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
0.1field-weighted citation impact, top 58% 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

4 citing papers in PubMed, 4 citations in OpenAlex.

  1. The role of genetics and molecular mechanisms in early onset scoliosis.Journal of clinical orthopaedics and trauma · 2026
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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

8 authors at 5 institutions in 1 country.

Kohei MurakamiDepartment of Orthopaedic Surgery, Shinshu University School of Medicine, Matsumoto, Nagano, Japan.ORCID 0000-0001-5458-410X
Shingo KikugawaDNA Chip Research Inc., Minato-ku, Tokyo, Japan.
Shoji SekiDepartment of Orthopedic Surgery, Faculty of Medicine, University of Toyama, Toyama, Japan.
Hidetomi TeraiDepartment of Orthopedics, Osaka City University Graduate School of Medicine, Osaka, Japan.ORCID 0000-0001-9183-3363
Takako SuzukiDepartment of Orthopaedic Surgery, Shinshu University School of Medicine, Matsumoto, Nagano, Japan.
Masaki NakanoDepartment of Orthopaedic Surgery, Shinshu University School of Medicine, Matsumoto, Nagano, Japan.
Jun TakahashiDepartment of Orthopaedic Surgery, Shinshu University School of Medicine, Matsumoto, Nagano, Japan.
Yukio NakamuraDepartment of Orthopaedic Surgery, Shinshu University School of Medicine, Matsumoto, Nagano, Japan.ORCID 0000-0002-3911-7180
Shinshu University · JPDNA Chip Research (Japan) · JPOkayama University of Science · JPOsaka City University · JPUniversity of Toyama · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Congenital scoliosis (CS) is a lateral curvature of the spine characterized by the presence of vertebral anomalies. Pathogenic genetic variants in the

Indexed as

congenital scoliosisde novo variantsexome sequencing

Identifiers

PMID36267860
PMCPMC9578779
OpenAlexW3152874940

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.