Evidence map›Paper›PMID 34853632›Full record

ReviewInternational journal of molecular epidemiology and genetics2021

Melanoma susceptibility: an update on genetic and epigenetic findings.

Ole Ah Truderung, Judit C Sagi, Agnes F Semsei, Csaba Szalai

Open access · greenAbstract readReview
In one paragraph

Review in International journal of molecular epidemiology and genetics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.4field-weighted citation impact, top 37% 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

6 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Frontiers in oncology · 2022
    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.

Ole Ah TruderungDepartment of Genetics, Cell- and Immunobiology, Semmelweis University H-1089 Budapest, Hungary.
Judit C SagiDepartment of Genetics, Cell- and Immunobiology, Semmelweis University H-1089 Budapest, Hungary.
Agnes F SemseiDepartment of Genetics, Cell- and Immunobiology, Semmelweis University H-1089 Budapest, Hungary.
Csaba SzalaiDepartment of Genetics, Cell- and Immunobiology, Semmelweis University H-1089 Budapest, Hungary.
Semmelweis University · HU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Malignant melanoma is one of the most highly ranked cancers in terms of years of life lost. Hereditary melanoma with its increased familial susceptibility is thought to affect up to 12% of all melanoma patients. In the past, only a few high-penetrance genes associated with familial melanoma, such as

Indexed as

epigeneticsfamilial melanomagermline mutationhereditary melanomamelanoma geneticsMelanoma susceptibilitypolygenic risk score

Identifiers

PMID34853632
PMCPMC8611230
OpenAlexW3216855297

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.