Evidence map›Paper›PMID 7977362›Full record

ArticleAmerican journal of human genetics1994

Genetic epidemiology of vitiligo: multilocus recessivity cross-validated.

S K Nath, P P Majumder, J J Nordlund

Open access · greenAbstract read
In one paragraph

Article in American journal of human genetics, 1994. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed, 1 pooled it
0.9field-weighted citation impact, top 28% 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

40 citing papers in PubMed, 1 synthesis or guideline pooled it, 163 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Vitiligo, from Pathogenesis to Therapeutic Advances: State of the Art.International journal of molecular sciences · 2023
    Review
  5. Review
  6. Review
  7. Article
  8. A Rare Case of Congenital Vitiligo in a Neonate.The Journal of clinical and aesthetic dermatology · 2021
    Article
  9. Translational Research in Vitiligo.Frontiers in immunology · 2021
    Review
  10. Article
  11. Review
  12. Article
  13. Genetics of Vitiligo.Dermatologic clinics · 2017
    Review
  14. Article
  15. Highlights in pathogenesis of vitiligo.World journal of clinical cases · 2015
    Review
  16. Melanocyte stem cells as potential therapeutics in skin disorders.Expert opinion on biological therapy · 2014
    Review
  17. Current aspects of vitiligo genetics.Postepy dermatologii i alergologii · 2014
    Review
  18. Involvement of interferon-gamma genetic variants and intercellular adhesion molecule-1 in onset and progression of generalized vitiligo.Journal of interferon & cytokine research : the official journal of the International Society for Interferon and Cytokine Research · 2013
    Article
  19. Review
  20. 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

3 authors at 1 institution in 1 country.

S K NathAnthropometry and Human Genetics Unit, Indian Statistical Institute, Calcutta.
P P Majumder
J J Nordlund
Indian Statistical Institute · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Vitiligo is a dermatological disorder characterized by hypopigmentary patches that tend to become progressive over time. There are reports of extensive familial aggregation. A genetic model for this disorder was earlier proposed by us. This model postulates that recessive alleles at multiple unlinked autosomal loci interact epistatically in the pathogenesis of vitiligo. The present family study was primarily undertaken to cross-validate the proposed genetic model. Data on 194 families from the United States were collected. Each family was ascertained through an affected proband. Analyses of these data reveal that approximately 20% of probands have at least one first-degree relative afflicted with vitiligo. All types of first-degree relatives of probands show a significant risk of developing vitiligo. Results of segregation and robustness analyses reveal that the genetic model postulated by us previously is the most parsimonious model for the present family data set.

Indexed as

AdolescentAdultAgedAge of OnsetChildChild, PreschoolFemaleGenes, RecessiveGenotypeHumansMaleMiddle AgedModels, GeneticPhenotypeRisk FactorsSurveys and Questionnaires

Identifiers

PMID7977362
PMCPMC1918341
OpenAlexW1540646219

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.