Evidence map›Paper›PMID 32895925›Full record

ArticleThe British journal of dermatology2021

Comorbid acne inversa and Dowling-Degos disease due to a single NCSTN mutation: is there enough evidence? Reply from the authors.

S Garcovich, P M Tricarico, C N Meddour, G Giovanardi, K Peris, S Crovella, M Boniotto

Open access · bronzeAbstract readLetterComment
PubMed Publisher
In one paragraph

Article in The British journal of dermatology, 2021. 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
0.1field-weighted citation impact, top 55% 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, 2 citations in OpenAlex.

  1. Frontiers in medicine · 2025
    Article
  2. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 4 institutions in 2 countries.

S GarcovichDermatology, Department of Medical and Surgical Sciences, Fondazione Policlinico A. Gemelli IRCCS, Rome, Italy.ORCID 0000-0001-8967-6688
P M TricaricoDepartment of Advanced Diagnostics, Institute for Maternal and Child Health-IRCCS 'Burlo Garofolo', Trieste, Italy.
C N MeddourUniversity of Paris Est-Créteil, Créteil, France.
G GiovanardiDermatology, Department of Medical and Surgical Sciences, Fondazione Policlinico A. Gemelli IRCCS, Rome, Italy.
K PerisDermatology, Department of Medical and Surgical Sciences, Fondazione Policlinico A. Gemelli IRCCS, Rome, Italy.
S CrovellaDepartment of Advanced Diagnostics, Institute for Maternal and Child Health-IRCCS 'Burlo Garofolo', Trieste, Italy.
M BoniottoUniversity of Paris Est-Créteil, Créteil, France.ORCID 0000-0002-9548-2254
Università Cattolica del Sacro Cuore · ITInserm · FRIRCCS Materno Infantile Burlo Garofolo · ITUniversity of Trieste · IT

Funding

Austrian Science Fund FWF I 4229
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Hidradenitis SuppurativaSkin Diseases, PapulosquamousHumansHyperpigmentationMutationPhenotypeSkin Diseases, Genetic

Identifiers

PMID32895925
OpenAlexW3084025330

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.