Genetics and Genomics in Medicine
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Genetics and Genomics in Medicine
Book Hero Magic created this recommendation. While it's new and still learning, it may not be perfect - your feedback is welcome! IS THIS YOUR NEXT READ?
The second edition of this popular textbook written for undergraduates, graduate students, and medical researchers, Genetics and Genomics in Medicine explains the science behind the uses of genetics and genomics in medicine today. This second edition has been thoroughly updated in line with the latest developments in the field.
The second edition of this textbook written for undergraduate students, graduate students and medical researchers, Genetics and Genomics in Medicine explains the science behind the uses of genetics and genomics in medicine today, and how it is being applied.
Maintaining the features that made the first edition so popular, this second edition has been thoroughly updated in line with the latest developments in the field. DNA technologies are explained, with emphasis on the modern techniques that are revolutionising the use of genetic information in medicine and indicating the role of genetics in common diseases. Epigenetics and non-coding RNA are covered in-depth, as are genetic approaches to treatment and prevention, including pharmacogenomics, genetic testing, and personalised medicine.
A dedicated chapter charts the latest insights into the molecular basis of cancers, cancer genomics, and novel approaches to cancer detection. Coverage of genetic testing at the level of genes, chromosomes, and genomes has been significantly expanded and updated. Extra prominence has been given to additional genomic analyses, ethical aspects, and novel therapeutic approaches. Various case studies illustrate selected clinical applications.
Key Features
- Comprehensive and integrated account of how genetics and genomics affect the entire spectrum of human health and disease
- Exquisite artwork illuminates the key concepts and mechanisms
- Summary points at the end of each chapter help to consolidate learning
- For each chapter, an abundance of further reading to help provide the reader with direction for further study
- Inclusive online question bank to test understanding
- Standard boxes summarise certain key principles in genetics
- Clinical boxes summarise selected case studies, pathogenesis mechanisms, or novel therapies for selected diseases
This book is equally suited for newcomers to the field as well as for engineers and scientists that have basic knowledge in this field but are interested in obtaining more information about specific future applications.
Book Hero Magic summarised reviews for this book. While it's new and still learning, it may not be perfect - your feedback is welcome! HOW HAS THIS BEEN REVIEWED?
This second edition is praised as an essential resource that is both detailed and accessible. It offers a comprehensive and well-executed update that enhances understanding of genetics and genomics in medicine, recommended for libraries and individuals interested in the subject. Mark F. Sanders, PhD, UC Davis College of Biological Sciences, endorses the clarity and depth of the writing.
Book Details
INFORMATION
ISBN: 9780367490812
Publisher: Taylor & Francis Ltd
Format: Paperback / softback
Date Published: 31 October 2022
Country: United Kingdom
Imprint: CRC Press
Edition: 2nd edition
Illustration: 86 Tables, color; 253 Line drawings, color; 26 Halftones, color; 279 Illustrations, color
Audience: Tertiary education
DIMENSIONS
Width: 210.0mm
Height: 280.0mm
Weight: 1480g
Pages: 552
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About the Author
Tom Strachan is Emeritus Professor of Human Molecular Genetics at Newcastle University, UK. Together with a former colleague, Andrew Read, he writes the popular Human Molecular Genetics textbook, now in its Fifth Edition.
Anneke Lucassen is Professor of Genomic Medicine and Director of the Centre for Personalised Medicine at the University of Oxford, UK
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