Evidence map›Paper›PMID 29441215›Full record

ArticleJournal of pediatric genetics2018

Pycnodysostosis: Novel Variants in

Arya Shambhavi, Smrithi Salian, Hitesh Shah, Mohandas Nair, Krishna Sharan, Dong-Kyu Jin, Sung Yoon Cho, Mary Mathew, Anju Shukla, Katta M Girisha

Abstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Journal of pediatric genetics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Article
  3. A Novel Variant c.847T>C inClinical medicine insights. Case reports · 2019
    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

10 authors.

Arya ShambhaviDepartment of Medical Genetics, Kasturba Medical College, Manipal University, Manipal, Karnataka, India.
Smrithi SalianDepartment of Medical Genetics, Kasturba Medical College, Manipal University, Manipal, Karnataka, India.
Hitesh ShahDepartment of Orthopaedics, Kasturba Medical College, Manipal University, Manipal, Karnataka, India.
Mohandas NairDepartment of Pediatrics, Government Medical College, Kozhikode, India.
Krishna SharanDepartment of Radiotherapy, Kasturba Medical College, Manipal University, Manipal, Karnataka, India.
Dong-Kyu JinDepartment of Pediatrics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea.
Sung Yoon ChoDepartment of Pediatrics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea.
Mary MathewDepartment of Pathology, Kasturba Medical College, Manipal University, Manipal, Karnataka, India.
Anju ShuklaDepartment of Medical Genetics, Kasturba Medical College, Manipal University, Manipal, Karnataka, India.
Katta M GirishaDepartment of Medical Genetics, Kasturba Medical College, Manipal University, Manipal, Karnataka, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pycnodysostosis is an autosomal recessive skeletal dysplasia caused by pathogenic variants in the cathepsin K (

Indexed as

cathepsin Kgiant cell tumorpycnodysostosis

Identifiers

PMID29441215
PMCPMC5809170

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.