Evidence map›Paper›PMID 35511163›Full record

ArticleG3 (Bethesda, Md.)2022

Demographic history differences between Hispanics and Brazilians imprint haplotype features.

Pedro Rodrigues Sousa da Cruz, Galina Ananina, Rodrigo Secolin, Vera Lúcia Gil-da-Silva-Lopes, Carmen Silvia Passos Lima, Paulo Henrique Condeixa de França, Amanda Donatti, Gustavo Jacob Lourenço, Tânia Kawasaki de Araujo, Milena Simioni and 3 more

Open access · goldAbstract read
In one paragraph

Article in G3 (Bethesda, Md.), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
0.9field-weighted citation impact, top 23% 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

4 citing papers in PubMed, 1 synthesis or guideline pooled it, 6 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Association Between Genetic Variants inDiagnostics (Basel, Switzerland) · 2025
    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

13 authors at 2 institutions in 1 country.

Pedro Rodrigues Sousa da CruzLaboratory of Human Genetics, Center for Molecular Biology and Genetic Engineering (CBMEG), University of Campinas-UNICAMP, Campinas, SP 13083-875, Brazil.ORCID 0000-0002-0133-8439
Galina AnaninaLaboratory of Human Genetics, Center for Molecular Biology and Genetic Engineering (CBMEG), University of Campinas-UNICAMP, Campinas, SP 13083-875, Brazil.ORCID 0000-0002-4347-5079
Rodrigo SecolinDepartment of Medical Genetics and Genomic Medicine, School of Medical Sciences, University of Campinas-UNICAMP, Campinas, SP 13083-887, Brazil.ORCID 0000-0002-2485-9560
Vera Lúcia Gil-da-Silva-LopesDepartment of Medical Genetics and Genomic Medicine, School of Medical Sciences, University of Campinas-UNICAMP, Campinas, SP 13083-887, Brazil.ORCID 0000-0003-1288-0554
Carmen Silvia Passos LimaClinical Oncology Service, Department of Internal Medicine, School of Medical Sciences, University of Campinas-UNICAMP, Campinas, SP 13083-887, Brazil.ORCID 0000-0002-1314-2345
Paulo Henrique Condeixa de FrançaJoinville Stroke Biobank, University of Region of Joinville-UNIVILLE, Joinville, SC 89202-190, Brazil.ORCID 0000-0002-1750-9132
Amanda DonattiDepartment of Medical Genetics and Genomic Medicine, School of Medical Sciences, University of Campinas-UNICAMP, Campinas, SP 13083-887, Brazil.ORCID 0000-0002-0535-3724
Gustavo Jacob LourençoLaboratory of Cancer Genetics, School of Medical Sciences, University of Campinas-UNICAMP, Campinas, SP 13083-887, Brazil.ORCID 0000-0002-5944-0305
Tânia Kawasaki de AraujoDepartment of Medical Genetics and Genomic Medicine, School of Medical Sciences, University of Campinas-UNICAMP, Campinas, SP 13083-887, Brazil.ORCID 0000-0003-3056-3894
Milena SimioniDepartment of Medical Genetics and Genomic Medicine, School of Medical Sciences, University of Campinas-UNICAMP, Campinas, SP 13083-887, Brazil.ORCID 0000-0003-3604-3099
Iscia Lopes-CendesDepartment of Medical Genetics and Genomic Medicine, School of Medical Sciences, University of Campinas-UNICAMP, Campinas, SP 13083-887, Brazil.ORCID 0000-0002-6221-6822
Fernando Ferreira CostaHematology and Hemotherapy Center, University of Campinas-UNICAMP, Campinas, SP, 13083-878, Brazil.ORCID 0000-0002-4632-572X
Mônica Barbosa de MeloLaboratory of Human Genetics, Center for Molecular Biology and Genetic Engineering (CBMEG), University of Campinas-UNICAMP, Campinas, SP 13083-875, Brazil.ORCID 0000-0002-1801-5441
Universidade Estadual de Campinas (UNICAMP) · BRUniversidade da Região de Joinville · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Admixture is known to greatly impact the genetic landscape of a population and, while genetic variation underlying human phenotypes has been shown to differ among populations, studies on admixed subjects are still scarce. Latin American populations are the result of complex demographic history, such as 2 or 3-way admixing events, bottlenecks and/or expansions, and adaptive events unique to the American continent. To explore the impact of these events on the genetic structure of Latino populations, we evaluated the following haplotype features: linkage disequilibrium, shared identity by descent segments, runs of homozygosity, and extended haplotype homozygosity (integrated haplotype score) in Latinos represented in the 1000 Genome Project along with array data from 171 Brazilians sampled in the South and Southeast regions of Brazil. We found that linkage disequilibrium decay relates to the amount of American and African ancestry. The extent of identity by descent sharing positively correlates with historical effective population sizes, which we found to be steady or growing, except for Puerto Ricans and Colombians. Long runs of homozygosity, a particular instance of autozygosity, was only enriched in Peruvians and Native Americans. We used simulations to account for random sampling and linkage disequilibrium to filter positive selection indexes and found 244 unique markers under selection, 26 of which are common to 2 or more populations. Some markers exhibiting positive selection signals had estimated time to the most recent common ancestor consistent with human adaptation to the American continent. In conclusion, Latino populations present highly divergent haplotype characteristics that impact genetic architecture and underlie complex phenotypes.

Indexed as

Genetics, PopulationHispanic or LatinoBrazilDemographyHaplotypesHumansLinkage DisequilibriumPolymorphism, Single NucleotidediversityhaplotypesIBD sharingLatinoslinkage disequilibriumpopulationROHselection

Identifiers

PMID35511163
PMCPMC9258545
OpenAlexW4229049850

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.