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The efficiency of molecular tests provides some accurate diagnoses for patients and is essential in the process of treatment and genetic counseling, and is very important for Personalized Genomic Medicine. The early and accurate diagnosis of a particular disease can improve quality of life of many patients, mainly with neurological morbidities. Our studies involve two investigative lines, including (1) the molecular diagnosis of genetic neurodegenerative diseases; (2) the role of single nucleotide polymorphisms (SNPs) in increasing the risk of neuropsychiatric diseases that affect human health, lifespan and longevity. From our genetic studies, we have detected many affected patients with autosomal dominant spinocerebellar ataxias (SCAs), a complex group of neurodegenerative diseases that share a similar molecular mechanism involving expansion of CAG repeats
(dynamic mutations). Over the generations, the symptoms can start early with more severe progression, depending on the size of the CAG repeats, a phenomenon called anticipation. In addition, we have developed a non-invasive early prenatal fetal gender determination, which is important in cases with risk of transmission of X-linked diseases. Our tests involve analysis of DYS14 gene and RhD diagnosis by rapid low-cost cell-free DNA extraction with conventional and multiplex PCR that are simple, fast, inexpensive, and highly sensitive techniques.(Alexis Trott, Molecular diagnostics and personalized genomic medicine applied to neurological disorders)