Evidence map›Paper›PMID 24809478›Full record

ArticlePloS one2014

Implications of the admixture process in skin color molecular assessment.

Caio Cesar Silva de Cerqueira, Tábita Hünemeier, Jorge Gomez-Valdés, Virgínia Ramallo, Carla Daiana Volasko-Krause, Ana Angélica Leal Barbosa, Pedro Vargas-Pinilla, Rodrigo Ciconet Dornelles, Danaê Longo, Francisco Rothhammer and 12 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
1.4field-weighted citation impact, top 22% 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

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 39 citations in OpenAlex.

  1. Pooled it
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  7. Controlling my genome with my smartphone: first clinical experiences of the PROMISE system.Clinical research in cardiology : official journal of the German Cardiac Society · 2022
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4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

22 authors at 10 institutions in 7 countries.

Caio Cesar Silva de CerqueiraDepartamento de Genética, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil.
Tábita HünemeierDepartamento de Genética, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil.
Jorge Gomez-ValdésLaboratorio de Antropología Física, Departamento de Anatomía, Facultad de Medicina, Universidad Nacional Autónoma de Mexico, Mexico City, Mexico.
Virgínia RamalloDepartamento de Genética, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil.
Carla Daiana Volasko-KrauseDepartamento de Genética, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil.
Ana Angélica Leal BarbosaDepartamento de Ciências Biológicas, Universidade Estadual do Sudoeste da Bahia, Jequié, Brazil.
Pedro Vargas-PinillaDepartamento de Genética, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil.
Rodrigo Ciconet DornellesDepartamento de Genética, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil.
Danaê LongoInstituto Federal de Educação, Ciência e Tecnologia Farroupilha, Alegrete, Brazil.
Francisco RothhammerInstituto de Alta Investigación, Universidad de Tarapacá, Facultad de Medicina, Universidad de Chile and Centro de Investigaciones del Hombre en el Desierto, Arica, Chile.
Gabriel BedoyaUniversidad de Antioquia, Medellín, Colombia.
Samuel Canizales-QuinterosUnidad de Genómica de Poblaciones Aplicada a la Salud, Facultad de Química, Universidad Nacional Autónoma de México, Mexico City, Mexico; Instituto Nacional de Medicina Genómica, Mexico City, Mexico.
Victor Acuña-AlonzoMolecular Genetics Laboratory, Escuela Nacional de Antropología e Historia, Mexico City, Mexico.
Carla GalloLaboratorio de Investigación y Desarrollo, Facultad de Ciencias y Filosofía, Universidad Peruana Cayetano Heredia, Lima, Perú
Giovanni PolettiLaboratorio de Investigación y Desarrollo, Facultad de Ciencias y Filosofía, Universidad Peruana Cayetano Heredia, Lima, Perú
Rolando González-JoséCentro Nacional Patagónico, CONICET, Puerto Madryn, Argentina.
Francisco Mauro SalzanoDepartamento de Estatística, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil.
Sídia Maria Callegari-JacquesDepartamento de Genética, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil; Departamento de Estatística, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil.
Lavínia Schuler-FacciniDepartamento de Genética, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil; INAGEMP - Instituto Nacional de Genética Médica Populacional, Porto Alegre, Brazil.
Andrés Ruiz-LinaresDepartment of Genetics, Evolution and Environment and UCL Genetics Institute, University College London, London, United Kingdom.
Maria Cátira BortoliniDepartamento de Genética, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil.
for CANDELA (Consortium for the Analysis of the Diversity and Evolution of Latin America)
Universidade Federal do Rio Grande do Sul · BRUniversidad Nacional Autónoma de México · MXUniversidad Peruana Cayetano Heredia · PECentro Científico Tecnológico Patagónico · ARInstituto Federal Farroupilha · BRNational Institute of Anthropology and History · MXSouthwest Bahia State University · BRUniversidad de Antioquia · COUniversity College London · GBUniversity of Chile · CL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The understanding of the complex genotype-phenotype architecture of human pigmentation has clear implications for the evolutionary history of humans, as well as for medical and forensic practices. Although dozens of genes have previously been associated with human skin color, knowledge about this trait remains incomplete. In particular, studies focusing on populations outside the European-North American axis are rare, and, until now, admixed populations have seldom been considered. The present study was designed to help fill this gap. Our objective was to evaluate possible associations of 18 single nucleotide polymorphisms (SNPs), located within nine genes, and one pseudogene with the Melanin Index (MI) in two admixed Brazilian populations (Gaucho, N = 352; Baiano, N = 148) with different histories of geographic and ethnic colonization. Of the total sample, four markers were found to be significantly associated with skin color, but only two (SLC24A5 rs1426654, and SLC45A2 rs16891982) were consistently associated with MI in both samples (Gaucho and Baiano). Therefore, only these 2 SNPs should be preliminarily considered to have forensic significance because they consistently showed the association independently of the admixture level of the populations studied. We do not discard that the other two markers (HERC2 rs1129038 and TYR rs1126809) might be also relevant to admixed samples, but additional studies are necessary to confirm the real importance of these markers for skin pigmentation. Finally, our study shows associations of some SNPs with MI in a modern Brazilian admixed sample, with possible applications in forensic genetics. Some classical genetic markers in Euro-North American populations are not associated with MI in our sample. Our results point out the relevance of considering population differences in selecting an appropriate set of SNPs as phenotype predictors in forensic practice.

Indexed as

BreedingAdolescentAdultAgedAged, 80 and overFemaleGene FrequencyGenotypeHumansMaleMelaninsMiddle AgedSkin PigmentationYoung AdultMelanins

Identifiers

PMID24809478
PMCPMC4014568
OpenAlexW2012911342

What OpenQuestion holds

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LicenceCC BY
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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.