Evidence map›Paper›PMID 39310605›Full record

ReviewCureus2024

A Review of Genetic Diversity Based on the Y Chromosome in the Romanian Population.

Ramona Hodișan, Dana C Zaha, Claudia Jurca, Codruta D Petchesi, Marius Bembea

Abstract readReview
In one paragraph

Review in Cureus, 2024. 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
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. 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

5 authors.

Ramona HodișanDoctoral School of Biomedical Sciences, University of Oradea, Oradea, ROU.
Dana C ZahaDepartment of Preclinical Disciplines, University of Oradea, Faculty of Medicine and Pharmacy, Oradea, ROU.
Claudia JurcaDepartment of Preclinical Disciplines, University of Oradea, Faculty of Medicine and Pharmacy, Oradea, ROU.
Codruta D PetchesiDepartment of Preclinical Disciplines, University of Oradea, Faculty of Medicine and Pharmacy, Oradea, ROU.
Marius BembeaDoctoral School of Biomedical Sciences, University of Oradea, Oradea, ROU.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Y chromosome analysis is used in a number of practical applications, including investigations of criminal cases, establishment of paternity, searching for missing persons, studies on human migration, evolutionary research, and historical and genealogical investigations. Questions about the origin of individual ethnic groups are addressed not only through archaeological, linguistic, and ethnographic methods but also through molecular genetics methods. The study of genetic diversity in Romania is particularly interesting from several perspectives because Romania, located in Southeast Europe, is distinguished by the fact that the Carpathians and the Danube served as natural barriers against the migrations of peoples for centuries, thus influencing the genetic mixture of the population. This is relevant for understanding the history and formation of ethnic groups in the region. In addition, many ethnic minorities live in Romania, which adds an additional dimension of genetic and cultural diversity. This article aims to provide an updated picture of the genetic diversity in Romania and to highlight the significant studies carried out among the Romanian population. By analyzing the articles published in the Web of Science, Scopus, or PubMed databases, which explore genetic diversity using the Y chromosome, the aim is to better understand the current genetic panorama in Romania.

Indexed as

genetic diversityhaplogrouphaplotypehumanromanian populationy chromosome

Identifiers

PMID39310605
PMCPMC11416838

What OpenQuestion holds

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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.