Emery and Rimoin’s Principles and Practice of Medical Genetics and Genomics (7th Ed.) Foundations
Coordonnateurs : Pyeritz Reed E., Korf Bruce R., Grody Wayne W.
For decades, Emery and Rimoin?s Principles and Practice of Medical Genetics and Genomics has served as the ultimate resource for clinicians integrating genetics into medical practice. With detailed coverage in contributions from over 250 of the world?s most trusted authorities in medical genetics and a series of 11 volumes available for individual sale, the Seventh Edition of this classic reference includes the latest information on seminal topics such as prenatal diagnosis, genome and exome sequencing, public health genetics, genetic counseling, and management and treatment strategies to complete its coverage of this growing field for medical students, residents, physicians, and researchers involved in the care of patients with genetic conditions. This comprehensive yet practical resource emphasizes theory and research fundamentals related to applications of medical genetics across the full spectrum of inherited disorders and applications to medicine more broadly.
This volume, Foundations, summarizes basic theories, concepts, research areas, and the history of medical genetics, providing a contextual framework for integrating genetics into medical practice. In this new edition, clinically oriented information is supported by full-color images and expanded sections on the foundations of genetic analytics, next generation sequencing, and therapeutics.
With regular advances in genomic technologies propelling precision medicine into the clinic, Emery and Rimoin?s Principles and Practice of Medical Genetics and Genomics: Seventh Edition bridges the gap between high-level molecular genetics and practical application and serves as an invaluable clinical tool for the health professionals and researchers.
1. Medicine in a Genetic and Genomic Context Reed E. Pyeritz
2. Foundations and Application of Precision Medicine Geoffrey S. Ginsburg and Susanne B. Haga
3. Nature and Frequency of Genetic Disease Bruce R. Korf, Reed E. Pyeritz and Wayne W. Grody
4. Genome and Gene Structure Madhuri R. Hegde and Michael R. Crowley
5. Epigenetics Rosanna Weksberg, Darci T. Butcher, Cheryl Cytrynbaum, Michelle T. Siu, Sanaa Choufani and Benjamin Tycko
6. Human Genomic Variants and Inherited Disease: Molecular Mechanisms and Clinical Consequences Stylianos E. Antonarakis and David N. Cooper
7. Genes in Families Jackie Cook
8. Analysis of Genetic Linkage Rita M. Cantor
9. Chromosomal Basis of Inheritance Fady M. Mikhail
10 Mitochondrial Biology and Medicine Douglas C. Wallace, Marie T. Lott and Vincent Procaccio
11. Multifactorial Inheritance and Complex Diseases Allison Fialkowski, T. Mark Beasley and Hemant K. Tiwari
12. Population Genetics H. Richard Johnston, Bronya J.B. Keats and Stephanie L. Sherman
13. Pathogenetics of Disease Reed E. Pyeritz
14. Twins and Twinning Mark P. Umstad, Lucas Calais-Ferreira, Katrina J. Scurrah, Judith G. Hall and Jeffrey M. Craig
15. The Biological Basis of Aging: Implications for Medical Genetics Junko Oshima, Fuki M. Hisama and George M. Martin
16. Pharmacogenomics Daniel W. Nebert and Ge Zhang
Students, physicians, and researchers in the field of medical genetics and personalized medicine; medical practitioners across medical disciplines as well as systems biology, molecular medicine, and genetic epidemiology; genetic counselors; genetic researchers in industry and pharma
Bruce R. Korf is the director of the Heflin Center for Human Genetics and chairman of the Department of Genetics at the University of Alabama at Birmingham. In April 2009, he began a two-year term as president of the American College of Medical Genetics (ACMG). Korf received his M.D. from Cornell University Medical College and his Ph.D. in genetics and cell biology from Rockefeller University. He completed a residency in pediatrics, pediatric neurology, and genetics at Children's Hospital, Boston. Prior to his appointment at the University of Alabama, he served as clinical director in the Division of Genetics at Children's Hospital from 1986 to 1999, and as the medical director of the Harvard-Partners Center for Genetics and Genomics fr
- Introduces genetic researchers, students, and health professionals to basic theories, concepts, research areas, and the history of medical genetics, offering a contextual framework for integrating genetics into medical practice
- Completely revised and up-to-date, this new edition highlights traditional approaches and new developments in the field of medical genetics, including cancer genetics, genomic technologies, genome and exome sequencing, prenatal diagnosis, public health genetics, genetic counseling, and single-cell analysis for diagnosis
- Includes color images supporting identification, concept illustration, and method processing
- Features contributions by leading international researchers and practitioners of medical genetics
Date de parution : 11-2018
Ouvrage de 572 p.
19x23.3 cm
Mots-clés :
Aging theory; Aging; Alzheimer disease; Alzheimer syndrome; Assortative mating; biology; Cancer; Carrier; Chromatin; Chromosome; Clinical utility; Complex disease; Complex traits; Copy number variation; DNA methylation; Dominant; Electron transport complex; Epigenetics; Epigenomics; Evolution; Evolutionary; Expressivity; Gene expression; Gene therapy; Gene; Genetic architecture; Genetic etiology; Genetic heterogeneity; Genetic linkage analysis; Genetic predisposition to disease; Genetic variation; Genetics; Genome variation; Genome; Genome-wide association studies (GWAS)Individualized drug therapy; GWAS; Hardy; Weinberg equilibrium; Histone modifications; homeostasis; Homeostasis; Human disease; Implementation; Imprinting; Inbreeding; Inheritance; Linkage disequilibrium; LOD scores; Mendelian diseases; Migration; Mitochondria; Mitochondrial disease; Mitochondrial DNA; Mitochondrial; Monogenic (Mendelian) traits; Mosaicism; Movement disorders; Multifactorial; Mutation