Evidence map›Paper›PMID 28794556›Full record

ArticleIndian journal of dermatology

Keratin 17 Mutations in Four Families from India with Pachyonychia Congenita.

Manoj Agarwala, Pankaj Salphale, Dincy Peter, Neil J Wilson, Susanne Pulimood, Mary E Schwartz, Frances J D Smith

Open access · diamondAbstract read
In one paragraph

Article in Indian journal of dermatology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.4field-weighted citation impact, top 41% 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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. 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

7 authors at 4 institutions in 3 countries.

Manoj AgarwalaDepartment of Dermatology, Christian Medical College, Vellore, Tamil Nadu, India.
Pankaj SalphaleDepartment of Dermatology, Christian Medical College, Vellore, Tamil Nadu, India.
Dincy PeterDepartment of Dermatology, Christian Medical College, Vellore, Tamil Nadu, India.
Neil J WilsonSchool of Life Sciences, Division of Biological Chemistry and Drug Discovery, Dermatology and Genetic Medicine, University of Dundee, Dundee, UK.
Susanne PulimoodDepartment of Dermatology, Christian Medical College, Vellore, Tamil Nadu, India.
Mary E SchwartzPachyonychia Congenita Project, Salt Lake City, UT, USA.
Frances J D SmithSchool of Life Sciences, Division of Biological Chemistry and Drug Discovery, Dermatology and Genetic Medicine, University of Dundee, Dundee, UK.
Christian Medical College · INChristian Medical College & Hospital · INUniversity of Dundee · GBPachyonychia Congenita Project · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pachyonychia congenita (PC) is a rare autosomal dominant genetic skin disorder due to a mutation in any one of the five keratin genes,

Indexed as

Cystskeratinkeratin mutationnail dystrophypachyonychia congenitapalmoplantar keratodermaplantar pain

Identifiers

PMID28794556
PMCPMC5527726
OpenAlexW2737036600

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.