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Progress in Genomic Medicine
From Research to Clinical Application
Offers a careful synthesis of the history, foundations, evolving trends and ongoing challenges in genomic medicine
Moyra Smith (Author)
9780323915472, Elsevier Science
Paperback / softback, published 4 November 2021
396 pages, 60 illustrations (30 in full color)
23.4 x 19 x 2.5 cm, 0.81 kg
Progress in Genomic Medicine: From Research to Clinical Application provides a careful synthesis of the foundations, current trends and translational challenges in genomic medicine, clarifying pathways forward and enabling genomic medicine research and implementation across clinical settings and treatment development. Sections address the history and growth of genetic medicine, with a discussion of key studies in syndrome delineations, inherited diseases, biochemical genetics, and chromosome abnormalities, overview clinical applications made possible through genomic advances, with chapters on DNA sequencing for clinical genetic diagnosis, genotype-phenotype correlations in individuals and across populations, new-born screening for treatable genetic disorders, and more. In addition, social, ethical and public health aspects of applying genomic technologies are included throughout. Here, Dr. Smith applies her experience and participation in the field, across its major milestones, to put current research, clinical advances, and ongoing questions in context.
Part I. History and Growth of Genetic Medicine 1. Documentation of units of inheritance and their contribution to phenotype2. Early documentation of inherited disorders through family studies 3. Discoveries in physiology, biochemistry, protein and enzyme studies between 1920-19704. Early translation of biochemical, metabolic and genetic discoveries into clinical medicine5. Advances in methods of genome analyses, nucleotide analyses and implications of variants Part II. Clinical Applications of Genomic Medicine6. Expansion of use of genome analyses and sequencing to diagnosis of genetic diseases 7. Improved analyses of regulatory genome, transcriptome and gene function, mutation penetrance and clinical applications 8. Standardized phenotype documentation, documentation of genotype phenotype correlations9. Expansion of methods of gene editing therapy and analysis of safety and efficacy10. Public health applications of genetics including newborn screening and documentation of gene environment interactions 11. Analysis of variants associated with abnormal drug responses, genetics and genomics in drug design12. Genetic and genomic medicine relevance to cancer prevention, diagnosis, and treatment13. Benefits of the incorporation of genomic medicine in clinical practice14. Using insights from genomics to increase possibilities for treatment of genetic diseases
Subject Areas: DNA & Genome [PSAK1], Genetics [non-medical PSAK]
