Publications by authors named "W Parson"

Article Synopsis
  • Southern Africa has a long history of human habitation, with diverse immigration affecting the original KhoeSan populations over thousands of years, leading to their decline or admixture, primarily involving KhoeSan women.
  • The study analyzed mitochondrial DNA from 247 South African individuals focused on groups with historical ties to KhoeSan populations to evaluate genetic diversity and connectivity among these groups.
  • Results showed 142 distinct haplotypes, predominantly haplogroup L0, especially within admixed populations, indicating significant population structure and limitations in using mtDNA analysis for forensic purposes due to observed regional variations and matrilocal patterns.
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Kaspar Hauser's parentage has been the subject of research and debate for nearly 200 years. As for his possible aristocratic descent through the House of Baden, there is suspicion that he was swapped as a baby, kidnapped, and kept in isolation to bring a collateral lineage to the throne. In the last 28 years, various genetic analyses have been carried out to investigate this possible aristocratic origin.

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Introduction: The acute antidepressant effect of sleep deprivation (SD) in patients with depressive disorders has been studied for more than 60 years. However, hypomanic mood swings after partial or total SD have also been described in people without diagnosed mental disorders. Studying this phenomenon in the general population may yield insights about the mechanisms of therapeutic SD, mania and bipolar disorders.

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The DNA Commission of the International Society for Forensic Genetics (ISFG) has developed a set of nomenclature recommendations for short tandem repeat (STR) sequences. These recommendations follow the 2016 considerations of the DNA Commission of the ISFG, incorporating the knowledge gained through research and population studies in the intervening years. While maintaining a focus on backward compatibility with the CE data that currently populate national DNA databases, this report also looks to the future with the establishment of recommended minimum sequence reporting ranges to facilitate interlaboratory comparisons, automated solutions for sequence-based allele designations, a suite of resources to support bioinformatic development, guidance for characterizing new STR loci, and considerations for incorporating STR sequences and other new markers into investigative databases.

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