ArticleInternational journal of legal medicine2008
Analysis of Y-chromosomal SNP haplogroups and STR haplotypes in an Algerian population sample.
Article in International journal of legal medicine, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.
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Who cites it
27 citing papers in PubMed.
- Deciphering the genetic diversity in the Arabian Peninsula and Africa: insights from Y-STR data.Forensic science, medicine, and pathology · 2026Article
- The North African maternal genetic diversity enriched by historical migrations: insights from a comprehensive analysis of complete mitogenomes.Mammalian genome : official journal of the International Mammalian Genome Society · 2026Article
- Impact of patrilocality on contrasting patterns of paternal and maternal heritage in Central-West Africa.Scientific reports · 2024Article
- Insights into the Middle Eastern paternal genetic pool in Tunisia: high prevalence of T-M70 haplogroup in an Arab population.Scientific reports · 2021Article
- Genetic Relationship Among the Kazakh People Based on Y-STR Markers Reveals Evidence of Genetic Variation Among Tribes and Zhuz.Frontiers in genetics · 2021Article
- Genetic structure in the paternal lineages of South East Spain revealed by the analysis of 17 Y-STRs.Scientific reports · 2019Article
- The peopling of the last Green Sahara revealed by high-coverage resequencing of trans-Saharan patrilineages.Genome biology · 2018Article
- Dissecting the influence of Neolithic demic diffusion on Indian Y-chromosome pool through J2-M172 haplogroup.Scientific reports · 2016Article
- Sousse: extreme genetic heterogeneity in North Africa.Journal of human genetics · 2015Article
- Genetic Heterogeneity in Algerian Human Populations.PloS one · 2015Article
- Determination of population origin: a comparison of autosomal SNPs, Y-chromosomal and mtDNA haplogroups using a Malagasy population as example.European journal of human genetics : EJHG · 2013Article
- Introducing the Algerian mitochondrial DNA and Y-chromosome profiles into the North African landscape.PloS one · 2013Article
- Understanding the Y chromosome variation in Korea--relevance of combined haplogroup and haplotype analyses.International journal of legal medicine · 2012Article
- Allele and haplotype diversity of X-chromosomal STRs in Ivory Coast.International journal of legal medicine · 2011Article
- A major Y-chromosome haplogroup R1b Holocene era founder effect in Central and Western Europe.European journal of human genetics : EJHG · 2011Article
- Y-chromosome R-M343 African lineages and sickle cell disease reveal structured assimilation in Lebanon.Journal of human genetics · 2011Article
- Y chromosome homogeneity in the Korean population.International journal of legal medicine · 2010Article
- Y-STR variation in Albanian populations: implications on the match probabilities and the genetic legacy of the minority claiming an Egyptian descent.International journal of legal medicine · 2010Article
- Human genetic differentiation across the Strait of Gibraltar.BMC evolutionary biology · 2010Article
- Human Y chromosome haplogroup R-V88: a paternal genetic record of early mid Holocene trans-Saharan connections and the spread of Chadic languages.European journal of human genetics : EJHG · 2010Article
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9 authors.
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Abstract
The distribution of Y-chromosomal single nucleotide polymorphism (SNP) haplogroups and short tandem repeat (STR) haplotypes was determined in a sample of 102 unrelated men of Arab origin from northwestern Algeria (Oran area). A total of nine different haplogroups were identified by a panel of 22 binary markers. The most common haplogroups observed in the Algerian population were E3b2 (45.1%) and J1 (22.5%). Y-STR typing by a 17-loci multiplex system allowed 93 haplotypes to be defined (88 were unique). Striking differences in the allele distribution and gene diversity of Y-STR markers between haplogroups could be found. In particular, intermediate alleles at locus DYS458 specifically characterized the haplotypes of individuals carrying haplogroup J1. All the intermediate alleles shared a common repeat sequence structure, supporting the hypothesis that the variant originated from a single mutational event.
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