ArticleInternational journal of legal medicine2012
Analysis of 12 X-STRs in Greenlanders, Danes and Somalis using Argus X-12.
Article in International journal of legal medicine, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.
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.
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.
Who cites it
27 citing papers in PubMed, 77 citations in OpenAlex.
- Swedish population data for 37 autosomal, 12 X-chromosomal and 23 Y-chromosomal STR loci.International journal of legal medicine · 2026Article
- Integrative linkage and recombination analysis of 25 X-STRs across 7 linkage groups using pedigree-based and SNP-based strategies.Frontiers in genetics · 2025Article
- Characterization of a novel unliked 12 X-STR typing assay for forensic purposes in an admixed Rio de Janeiro population sample.Genetics and molecular biology · 2025Article
- Variability and forensic efficiency of 12 X-STR markers in Namibian populations.International journal of legal medicine · 2024Article
- Article
- Linkage, recombination and mutation rate analyses of 16 X-chromosomal STR loci in Sri Lankan Sinhalese pedigrees.International journal of legal medicine · 2022Article
- Genetic polymorphisms of 16 X-STR loci in the Hani population from Southwest China.Forensic sciences research · 2022Article
- X-chromosomal STR based genetic polymorphisms and demographic history of Sri Lankan ethnicities and their relationship with global populations.Scientific reports · 2021Article
- Haplotype data and forensic evaluation of 23 Y-STR and 12 X-STR loci in eight ethnic groups from Eritrea.International journal of legal medicine · 2021Article
- Development of a 16 X-STR multiplex PCR system for kinship analysis and its applicability for the Sinhalese population in Sri Lanka.International journal of legal medicine · 2021Article
- Population genetic analysis of Chinese Zhuang and Mulao minorities using AGCU-X19 STR kit.International journal of legal medicine · 2020Article
- Twenty Years Later: A Comprehensive Review of the X Chromosome Use in Forensic Genetics.Frontiers in genetics · 2020Review
- Establishment of 11 linked X-STR loci within 1.1 Mb to assist with kinship testing.International journal of legal medicine · 2018Article
- Genetic analysis of 12 X-STR loci in the Serbian population from Vojvodina Province.International journal of legal medicine · 2018Article
- Curiosities of X chromosomal markers and haplotypes.International journal of legal medicine · 2018Article
- Genetic analysis of 19 X chromosome STR loci for forensic purposes in four Chinese ethnic groups.Scientific reports · 2017Article
- Analysis of 12 X-STR loci in the population of south Croatia.Molecular biology reports · 2017Article
- Genetic polymorphism analyses of a novel panel of 19 X-STR loci in the Chinese Uygur ethnic minority.Journal of Zhejiang University. Science. B · 2016Article
- Genetic analysis of 12 X-chromosome STRs in Western Mediterranean populations.International journal of legal medicine · 2015Article
- The peopling of Greenland: further insights from the analysis of genetic diversity using autosomal and X-chromosomal markers.European journal of human genetics : EJHG · 2015Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
3 authors at 1 institution in 2 countries.
Funding
No grant is acknowledged in the PubMed record.
Abstract
X-chromosome markers have become a useful set of markers of choice when certain complex kinship cases need to be unravelled. The Argus X-12 kit allows the co-amplification in a single PCR reaction of 12 X-chromosome short tandem repeats located in four linkage groups. A number of 507 unrelated individuals from Greenland, Denmark and Somalia together with two generation families were typed using the Argus X-12 kit. Silent alleles for the DXS10148 and DXS10146 systems were observed in males, mostly from Somalia. High levels of intrapopulation variability and therefore high forensic parameter values were calculated for the three studied populations. The population in Greenland showed a significantly lower intrapopulation variability and a high genetic differentiation compared with 13 other populations. Significant levels of linkage disequilibrium were observed between markers belonging to the same linkage group, mainly in the populations in Greenland and Somalia. Family studies allowed the calculation of mutation and recombination frequencies. A higher male versus female mutation rate was obtained, with an average value of 3.3 × 10(-3). Recombination fraction calculations performed on two generation families showed, as previously described, a not complete independence between X-chromosome linkage groups 3 and 4.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.