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Synopsis
The author reviews published research in functional genomics and phenotypic variation carried out primarily since 2006. Topics reviewed include investigations in genome architecture, gene structure, regulation and function of organelles including mitochondria and the endosome lysosome system. New insights into neurodevelopment and neurobehavioral disorders and aspects of genomic studies in complex common diseases are reviewed.
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About the Author
Moyra Smith, MD, PhD, has been conducting research in human genetics since 1965. She served as Clinical geneticist and Director of the Newborn screening Program at the University of California Irvine for 19 years and is currently Professor Emeritus at that institution. Her latest research includes studies of nuclear and mitochondrial genomics in autism
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Phenotypic Variation: Exploration and Functional Genomics
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Phenotypic Variation: Exploration and Functional Genomics
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