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Clinical Applications of Cancer Genetic Testing | P. Sharma | Standard Edition, 2026 | Taylor & Francis Group (English Medium)
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| 5469-6536 |
The book "Clinical Applications of Cancer Genetic Testing" by P. Sharma is a comprehensive guide to understanding the role of genetic testing in the diagnosis and treatment of cancer. This standard edition, published in 2026 by Taylor & Francis Group, provides a thorough overview of the latest advancements in genetic testing technology and how it is being used to personalize cancer treatment for patients. In this book, readers will learn about the different types of genetic tests available for cancer screening, including hereditary cancer risk assessments and somatic mutation testing. The author, P. Sharma, a renowned expert in the field of cancer genetics, explains how these tests can help identify individuals at high risk for developing certain types of cancer and guide treatment decisions based on their unique genetic makeup. The book also covers important topics such as the ethical implications of genetic testing, insurance coverage for testing services, and how to interpret test results. With detailed case studies and practical examples, readers will gain a deeper understanding of how genetic testing is revolutionizing cancer care and improving patient outcomes. Whether you are a healthcare professional looking to expand your knowledge of cancer genetics or a patient interested in learning more about personalized medicine options, "Clinical Applications of Cancer Genetic Testing" is an essential resource that will empower you to make informed decisions about your health.
Clinical Applications of Cancer Genetic Testing (2026) is an advanced medical and oncology reference textbook written by P. Sharma and published by Taylor & Francis Group. This book provides a comprehensive overview of how genetic testing is transforming modern cancer diagnosis, risk assessment, and personalized treatment strategies.
Cancer genetics is one of the fastest-growing fields in medical science. With the rise of precision medicine, genetic profiling has become essential for identifying hereditary cancer risks, detecting mutations, and guiding targeted therapies. This book explains these concepts in a structured, clinically relevant manner suitable for both students and healthcare professionals.
The book focuses on the integration of molecular genetics with clinical oncology, helping readers understand how laboratory findings translate into real-world patient care. It highlights how genetic testing is used not only for diagnosis but also for prevention and treatment planning.
Key topics covered include:
- Fundamentals of cancer genetics and molecular biology
- Principles of genetic testing and sequencing technologies
- BRCA1/BRCA2 and hereditary breast-ovarian cancer syndromes
- Lynch syndrome and colorectal cancer genetics
- Tumor biomarkers and predictive genetic markers
- Role of next-generation sequencing (NGS) in oncology
- Personalized and targeted cancer therapies
- Ethical, legal, and counseling aspects of genetic testing
A major strength of this book is its clinical application-based approach, which connects genetic theory with practical oncology decision-making. It helps clinicians understand how to interpret genetic reports and apply them in treatment planning.
This 2026 edition includes updated advancements in genomic medicine, including next-generation sequencing technologies, liquid biopsy applications, and emerging targeted therapies in oncology. It also emphasizes the importance of genetic counseling in patient care and family risk assessment.
The book is especially useful for:
- Oncologists and cancer specialists
- Medical geneticists and researchers
- Pathologists and laboratory professionals
- MBBS and postgraduate medical students
- Healthcare professionals involved in precision medicine
With 240 pages of well-structured and updated content, this paperback edition serves as a valuable reference for understanding how genetic testing is reshaping cancer diagnosis and treatment in modern clinical practice.
| SKU / BOOK Code: | TFR-CANCER-GENETICS-SHARMA-202 |
| Publisher: | Taylor & Francis Group |
| Author: | Sharma P |
| Binding Type: | Paperback |
| No. of Pages: | 240 |
| ISBN-10: | NA |
| ISBN-13: | NA |
| Edition: | Standard |
| Language: | English Medium |
| Publish Year: | 2026-01 |
| Weight (g): | 300 |
| Product Condition: | New |
| Reading Age: | Above 18 Years |
| Country of Origin: | India |
| Genre: | Medical Books |
| Manufacturer: | Taylor & Francis Group |
| Importer: | Taylor & Francis Group |
| Packer: | Fullfilled by Supplier |
The book "Clinical Applications of Cancer Genetic Testing" by P. Sharma is a comprehensive guide to understanding the role of genetic testing in the diagnosis and treatment of cancer. This standard edition, published in 2026 by Taylor & Francis Group, provides a thorough overview of the latest advancements in genetic testing technology and how it is being used to personalize cancer treatment for patients. In this book, readers will learn about the different types of genetic tests available for cancer screening, including hereditary cancer risk assessments and somatic mutation testing. The author, P. Sharma, a renowned expert in the field of cancer genetics, explains how these tests can help identify individuals at high risk for developing certain types of cancer and guide treatment decisions based on their unique genetic makeup. The book also covers important topics such as the ethical implications of genetic testing, insurance coverage for testing services, and how to interpret test results. With detailed case studies and practical examples, readers will gain a deeper understanding of how genetic testing is revolutionizing cancer care and improving patient outcomes. Whether you are a healthcare professional looking to expand your knowledge of cancer genetics or a patient interested in learning more about personalized medicine options, "Clinical Applications of Cancer Genetic Testing" is an essential resource that will empower you to make informed decisions about your health.
Clinical Applications of Cancer Genetic Testing (2026) is an advanced medical and oncology reference textbook written by P. Sharma and published by Taylor & Francis Group. This book provides a comprehensive overview of how genetic testing is transforming modern cancer diagnosis, risk assessment, and personalized treatment strategies.
Cancer genetics is one of the fastest-growing fields in medical science. With the rise of precision medicine, genetic profiling has become essential for identifying hereditary cancer risks, detecting mutations, and guiding targeted therapies. This book explains these concepts in a structured, clinically relevant manner suitable for both students and healthcare professionals.
The book focuses on the integration of molecular genetics with clinical oncology, helping readers understand how laboratory findings translate into real-world patient care. It highlights how genetic testing is used not only for diagnosis but also for prevention and treatment planning.
Key topics covered include:
- Fundamentals of cancer genetics and molecular biology
- Principles of genetic testing and sequencing technologies
- BRCA1/BRCA2 and hereditary breast-ovarian cancer syndromes
- Lynch syndrome and colorectal cancer genetics
- Tumor biomarkers and predictive genetic markers
- Role of next-generation sequencing (NGS) in oncology
- Personalized and targeted cancer therapies
- Ethical, legal, and counseling aspects of genetic testing
A major strength of this book is its clinical application-based approach, which connects genetic theory with practical oncology decision-making. It helps clinicians understand how to interpret genetic reports and apply them in treatment planning.
This 2026 edition includes updated advancements in genomic medicine, including next-generation sequencing technologies, liquid biopsy applications, and emerging targeted therapies in oncology. It also emphasizes the importance of genetic counseling in patient care and family risk assessment.
The book is especially useful for:
- Oncologists and cancer specialists
- Medical geneticists and researchers
- Pathologists and laboratory professionals
- MBBS and postgraduate medical students
- Healthcare professionals involved in precision medicine
With 240 pages of well-structured and updated content, this paperback edition serves as a valuable reference for understanding how genetic testing is reshaping cancer diagnosis and treatment in modern clinical practice.
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