Evidence map›Paper›PMID 24500769›Full record

ArticleJournal of community genetics2014

Random inbreeding, isonymy, and population isolates in Argentina.

José Dipierri, Alvaro Rodríguez-Larralde, Italo Barrai, Jorge López Camelo, Esperanza Gutiérrez Redomero, Concepción Alonso Rodríguez, Virginia Ramallo, Rubén Bronberg, Emma Alfaro

Open access · bronzeAbstract read
In one paragraph

Article in Journal of community genetics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.2field-weighted citation impact, top 18% 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

2 citing papers in PubMed, 15 citations in OpenAlex.

  1. Clusters of rare disorders and congenital anomalies in South America.Revista panamericana de salud publica = Pan American journal of public health · 2023
    Review
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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

9 authors at 6 institutions in 4 countries.

José DipierriInstituto de Biología de la Altura, Universidad Nacional de Jujuy, Avda. Bolivia 1661, 4600, San Salvador de Jujuy, Argentina, dipierri@inbial.unju.edu.ar.
Alvaro Rodríguez-Larralde
Italo Barrai
Jorge López Camelo
Esperanza Gutiérrez Redomero
Concepción Alonso Rodríguez
Virginia Ramallo
Rubén Bronberg
Emma Alfaro
Consejo Nacional de Investigaciones Científicas y Técnicas · ARUniversidad de Alcalá · ESHospital Ramos Mejía · ARInstituto Venezolano de Investigaciones Científicas · VENational University of Jujuy · ARUniversity of Ferrara · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Population isolates are an important tool in identifying and mapping genes of Mendelian diseases and complex traits. The geographical identification of isolates represents a priority from a genetic and health care standpoint. The purpose of this study is to analyze the spatial distribution of consanguinity by random isonymy (F ST) in Argentina and its relationship with the isolates previously identified in the country. F ST was estimated from the surname distribution of 22.6 million electors registered for the year 2001 in the 24 provinces, 5 geographical regions, and 510 departments of the country. Statistically significant spatial clustering of F ST was determined using the SaTScan V5.1 software. F ST exhibited a marked regional and departamental variation, showing the highest values towards the North and West of Argentina. The clusters of high consanguinity by random isonymy followed the same distribution. Recognized Argentinean genetic isolates are mainly localized at the north of the country, in clusters of high inbreeding. Given the availability of listings of surnames in high-capacity storage devices for different countries, estimating F ST from them can provide information on inbreeding for all levels of administrative subdivisions, to be used as a demographic variable for the identification of isolates within the country for public health purposes.

Identifiers

PMID24500769
PMCPMC4059845
OpenAlexW2143556936

What OpenQuestion holds

Textmetadata
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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.