Evidence map›Paper›PMID 23271015›Full record

ArticleJournal of genetics2012

Y-SNP haplogroups related to the Yqh+ heteromorphism in the Mexican northwestern population.

Enrique Jhonatan Romo-Martínez, Gabriela Martínez-Cortés, Reyna Lucía Barajas-Torres, Rodrigo Rubi-Castellanos, María Teresa Magaña-Torres, Héctor Rangel-Villalobos, Juan Ramón González-García

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In one paragraph

Article in Journal of genetics, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact, top 88% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Review
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

7 authors at 5 institutions in 2 countries.

Enrique Jhonatan Romo-MartínezDepartamento de Ingeniería en Biotecnología, Universidad Politécnica de Sinaloa, CP: 82199, Mazatlán, Sinaloa, México.
Gabriela Martínez-Cortés
Reyna Lucía Barajas-Torres
Rodrigo Rubi-Castellanos
María Teresa Magaña-Torres
Héctor Rangel-Villalobos
Juan Ramón González-García
Mexican Social Security Institute · MXAutonomous University of Yucatán · MXUniversidad de Guadalajara · MXUniversidad de la Ciénega · MXUniversidad Politécnica de Sinaloa

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Morphological variation of the Y chromosome has been observed in different populations. This variation is mostly related to the heteromorphic Yq12 band, which is composed of a variable block of constitutive heterochromatin. The Yqh+ heteromorphism has a worldwide frequency of 2.85% and is considered clinically innocuous. The aim of this study was to identify the ancestry of the Yqh+ heteromorphism present in individuals from western Mexico. For this purpose, 17 Y-chromosome single nucleotide polymorphisms were analysed by multiplex polymerase chain reaction and SNaPshot assays. In 28 Yqh+ males, only five haplogroups were observed; with a haplogroup diversity of 0.4841 ± 0.1094, which was less than that observed in a study of unselected Mexican mestizo population. Differences were specifically conferred by the high frequencies of haplogroups R1b1 and P*(xQ,R), and by the absence of the Amerindian haplogroup Q (Q*(xQ1a3a) plus Q1a3a) from the Yqh+ group. This study suggests a post-1492 incorporation for Yqh+ chromosomes into the Mexican northwestern population.

Indexed as

Polymorphism, Single NucleotideChromosomes, Human, YGene FrequencyGenetics, PopulationGeographyHaplotypesHumansKaryotypeMaleMexico

Identifiers

PMID23271015
OpenAlexW2072193842

What OpenQuestion holds

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Read underepoch 390

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.