Evidence map›Paper›PMID 26015711›Full record

ReviewJournal of pharmacy & bioallied sciences2015

Genodermatoses.

N Aravindha Babu, E Rajesh, Jayasri Krupaa, G Gnananandar

Open access · goldAbstract readReview
In one paragraph

Review in Journal of pharmacy & bioallied sciences, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.5field-weighted citation impact, top 34% 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

11 citing papers in PubMed, 19 citations in OpenAlex.

  1. Decoding Genetic Disease Through the Skin: Lessons From the UDN.International journal of dermatology · 2026
    Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Introduction to phacomatoses (neurocutaneous disorders) in childhood.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2020
    Article
  9. Review
  10. Periocular dermatoses.International journal of women's dermatology · 2017
    Review
  11. Incontinentia Pigmenti: A Case Report of a Complex Systemic Disease.Open access Macedonian journal of medical sciences · 2017
    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

4 authors at 1 institution in 1 country.

N Aravindha BabuDepartment of Oral pathology and Microbiology, Sree Balaji Dental College and Hospital, Bharath University, Chennai, Tamil Nadu, India.
E RajeshDepartment of Oral pathology and Microbiology, Sree Balaji Dental College and Hospital, Bharath University, Chennai, Tamil Nadu, India.
Jayasri KrupaaDepartment of Oral pathology and Microbiology, Sree Balaji Dental College and Hospital, Bharath University, Chennai, Tamil Nadu, India.
G GnananandarDepartment of Oral pathology and Microbiology, Sree Balaji Dental College and Hospital, Bharath University, Chennai, Tamil Nadu, India.
Sree Balaji Dental College and Hospital · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Genodermatoses are an inherited disorder, present with multisystem involvement. Help us to identify regular mutations and appalling skin diseases with recessive inheritance. Genetic heterogeneity is very common, and molecular diagnosis requires a broad effort. Recurrent mutations in unrelated families were seen in families with xeroderma, Griscelli. It seems likely that eventually oligonucleotide arrays will replace most other methods for routine mutation scanning of the more common diseases and planned sequencing will be increasingly used for rarer diseases.

Indexed as

Benigndyskeratosis congenitalectodermal dysplasiaEhlers–Danlos syndromeepidermolysis bullosahereditaryhidrotic ectodermal dysplasiahypohidrotic ectodermal dysplasiaincontinentia pigmentiintraepithelial-dyskeratosiskeratosis follicularismultiple hamartoma syndromepachyonychia congenitalPeutz–Jeghers syndrometuberous sclerosisWarty dyskeratomawhite sponge nevusxeroderma pigmentosum

Identifiers

PMID26015711
PMCPMC4439671
OpenAlexW4253322180

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.