Genetics and Genomics in Medicine

Genetics and Genomics in Medicine, Second Edition is a comprehensive textbook that explains the science behind the uses of genetics and genomics in medicine today. It has been thoroughly updated in line with the latest developments in the field, including DNA technologies, epigenetics, non-coding RNA, genetic approaches to treatment and prevention, and cancer genomics. It also includes case studies and an online question bank to test understanding.

Format: Paperback / softback
Length: 534 pages
Publication date: 31 October 2022
Publisher: Taylor & Francis Ltd

Genetics and Genomics in Medicine, the second edition, is a comprehensive textbook designed for undergraduate students, graduate students, and medical researchers. Written by renowned experts in the field, this textbook delves into the science behind the applications of genetics and genomics in modern medicine.

The first edition of this textbook gained popularity for its clear and concise explanations, and the second edition maintains these qualities while incorporating the latest developments in the field. The book begins by providing an overview of DNA technologies, emphasizing the modern techniques that are revolutionizing the use of genetic information in medicine. It also highlights the role of genetics in common diseases, such as cancer.

In-depth coverage is given to epigenetics and non-coding RNA, which play crucial roles in gene regulation and disease development. Genetic approaches to treatment and prevention, including pharmacogenomics, genetic testing, and personalized medicine, are explored. A dedicated chapter explores the molecular basis of cancers, cancer genomics, and novel approaches to cancer detection.

The 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, making the textbook more relatable and practical.

Key Features:

Comprehensive and Integrated Account: The textbook provides a comprehensive and integrated account of how genetics and genomics affect the entire spectrum of human health and disease. It covers various topics, including inheritance patterns, genetic mutations, gene expression, and the role of genetics in various diseases.

Exquisite Artwork: The book is accompanied by exquisite artwork that visually illustrates the key concepts and mechanisms discussed in each chapter. This artwork enhances the understanding and retention of the material.

Summary Points: At the end of each chapter, summary points help to consolidate learning. These points summarize the main ideas and provide a quick reference for future review.

Further Reading: For each chapter, an abundance of further reading is provided to help the reader explore the topic in more depth. These resources include journal articles, research papers, and online resources.

Inclusive Online Question Bank: An inclusive online question bank is available to test understanding of the material covered in the textbook. This question bank provides a platform for self-assessment and helps the reader gauge their knowledge.

Standard Boxes: Standard boxes summarize certain key principles in genetics, providing a concise overview of important concepts.

Clinical Boxes: Clinical boxes summarize selected case studies, pathogen interactions, and genetic disorders. These boxes provide real-world examples and help the reader apply the theoretical knowledge to clinical scenarios.

Genetics and Genomics in Medicine is an essential resource for students, researchers, and healthcare professionals interested in understanding the role of genetics and genomics in modern medicine. With its comprehensive coverage, exquisite artwork, and practical applications, this textbook is a valuable tool for advancing knowledge in the field.

Weight: 1502g
Dimension: 212 x 283 x 29 (mm)
ISBN-13: 9780367490812
Edition number: 2 ed