Elena Grechanina
A5053276208- Forensic and Genetic Research
- Yersinia bacterium, plague, ectoparasites research
- Metabolism and Genetic Disorders
- Forensic Anthropology and Bioarchaeology Studies
- Mitochondrial Function and Pathology
- Advanced MRI Techniques and Applications
- Hereditary Neurological Disorders
- Amino Acid Enzymes and Metabolism
- Genomics and Rare Diseases
- History of Medical Practice
- Genetics and Neurodevelopmental Disorders
- Medical and Biological Sciences
- Genetic diversity and population structure
- Genomic variations and chromosomal abnormalities
Kharkiv National Medical University
2006-2021
University of Calabar
2004
It has been often stated that the overall pattern of human maternal lineages in Europe is largely uniform. Yet this uniformity may also result from an insufficient depth and width phylogenetic analysis, particular predominant western Eurasian haplogroup (Hg) H comprises nearly a half European mitochondrial DNA (mtDNA) pool. Making use coding sequence information 267 mtDNA Hg sequences, we have analyzed 830 genomes, 11 European, Near Middle Eastern, Central Asian, Altaian populations. In...
Abstract Human mitochondrial DNA haplogroup U is among the initial maternal founders in Southwest Asia and Europe one that best indicates matrilineal genetic continuity between late Pleistocene hunter-gatherer groups present-day populations of Europe. While most subclades are older than 30 thousand years, comparatively recent coalescence time extant variation U7 (~16–19 years ago) suggests its current distribution consequence more dispersal events, despite wide geographical range across...
Hereditary motor and sensory neuropathies are one of the most common diseases among monogenic hereditary nervous system. group clinically genetically heterogeneous characterized by peripheral nerve damage. have little effect on life expectancy, this leads to their significant accumulation in individual families populations as a whole. The form disorder is neuropathy with an autosomal dominant type inheritance - 1A, caused mutation gene myelin protein 22 (PMP22) chromosome 17p11.2-12....