Evidence map›Paper›PMID 24073242›Full record

Trial reportPloS one2013

Revisiting the genetic ancestry of Brazilians using autosomal AIM-Indels.

Fernanda Saloum de Neves Manta, Rui Pereira, Romulo Vianna, Alfredo Rodolfo Beuttenmüller de Araújo, Daniel Leite Góes Gitaí, Dayse Aparecida da Silva, Eldamária de Vargas Wolfgramm, Isabel da Mota Pontes, José Ivan Aguiar, Milton Ozório Moraes and 2 more

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 68 papers.

0numbers the graph read from it
0cells of the map it votes in
68citing papers in PubMed
–field-weighted citation impact
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

68 citing papers in PubMed.

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  14. Human N-acetyltransferase 2 (Frontiers in pharmacology · 2023
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8 more citing papers are in PubMed but not listed here.

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

12 authors.

Fernanda Saloum de Neves MantaDNA Diagnostic Laboratory (LDD), State University of Rio de Janeiro (UERJ), Rio de Janeiro, Brazil.
Rui Pereira
Romulo Vianna
Alfredo Rodolfo Beuttenmüller de Araújo
Daniel Leite Góes Gitaí
Dayse Aparecida da Silva
Eldamária de Vargas Wolfgramm
Isabel da Mota Pontes
José Ivan Aguiar
Milton Ozório Moraes
Elizeu Fagundes de Carvalho
Leonor Gusmão

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

There are many different studies that contribute to the global picture of the ethnic heterogeneity in Brazilian populations. These studies use different types of genetic markers and are focused on the comparison of populations at different levels. In some of them, each geographical region is treated as a single homogeneous population, whereas other studies create different subdivisions: political (e.g., pooling populations by State), demographic (e.g., urban and rural), or ethnic (e.g., culture, self-declaration, or skin colour). In this study, we performed an enhanced reassessment of the genetic ancestry of ~ 1,300 Brazilians characterised for 46 autosomal Ancestry Informative Markers (AIMs). In addition, 798 individuals from twelve Brazilian populations representing the five geographical macro-regions of Brazil were newly genotyped, including a Native American community and a rural Amazonian community. Following an increasing North to South gradient, European ancestry was the most prevalent in all urban populations (with values up to 74%). The populations in the North consisted of a significant proportion of Native American ancestry that was about two times higher than the African contribution. Conversely, in the Northeast, Center-West and Southeast, African ancestry was the second most prevalent. At an intrapopulation level, all urban populations were highly admixed, and most of the variation in ancestry proportions was observed between individuals within each population rather than among population. Nevertheless, individuals with a high proportion of Native American ancestry are only found in the samples from Terena and Santa Isabel. Our results allowed us to further refine the genetic landscape of Brazilians while establishing the basis for the effective application of an autosomal AIM panel in forensic casework and clinical association studies within the highly admixed Brazilian populations.

Indexed as

Genetic MarkersGenetics, PopulationBrazilEthnicityGene FrequencyGenetic VariationGenotypeHumansRacial GroupsGenetic Markers

Identifiers

PMID24073242
PMCPMC3779230

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Registered trials

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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.