Thompson and Thompson Genetics And Genomics In Medicine, 9th Edition (Original PDF From Publisher)

1.1.Description

First published in 1966, “Thompson and Thompson Genetics And Genomics In Medicine” has evolved into an indispensable textbook for a wide spectrum of learners, including medical students, genetic counseling students, and those in laboratory medicine.

Renowned for its emphasis on fundamental principles in human genetics and genomics and their applications in medicine, the book has become a trusted resource for countless individuals in various stages of their medical education.

“Thompson and Thompson Genetics And Genomics In Medicine”, now under an expanded title, undergoes a comprehensive revision by a new editorial team and a cadre of contributing authors.

This edition accommodates the evolving landscape of genetics and genomics, incorporating discoveries such as the functional roles of non-coding RNAs, chromatin regulation, and epigenetics, alongside the latest technologies and emerging diagnoses they facilitate.

The comprehensive coverage encompasses genomes in biology and medicine, copy number and structural genomic variation, and novel findings.

Enhanced by over 40 clinical case studies, full-color illustrations, updated diagrams, and clinical photos, the ninth edition ensures a contemporary and thorough exploration of genetic medicine.

Additionally, the updated terminology aligns with contemporary guidelines, and new sections highlight the growing role of sequencing and functional assays in diagnosis, including a dedicated chapter on Epigenetics.

The inclusion of content addressing the use of genetic information from diverse populations, including unique indigenous and founder populations, further emphasizes the book’s commitment to staying at the forefront of genetic medicine.

With end-of-chapter questions, comprehensive answers, and USMLE-style and multiple-choice questions available as part of the eBook, this edition continues to provide a robust learning experience.

The enhanced eBook version offers additional functionalities, allowing users to access content, customize, make notes, and highlights, and features updated clinical cases supported by photography from the not-for-profit organization, Positive Exposure.

“Thompson and Thompson Genetics And Genomics In Medicine” ensures that learners across various fields can navigate the complexities of genetics and genomics, making it an essential companion throughout basic science training, clinical placements, and beyond.

Thompson and Thompson Genetics And Genomics In Medicine

1.2.Key Features

The key features of “Thompson and Thompson Genetics And Genomics In Medicine” include its extensive coverage of fundamental principles in human genetics and genomics, catering to medical students, genetic counseling students, and those in laboratory medicine.

The ninth edition, under an expanded title, is thoroughly revised by a new editorial team and contributing authors, addressing the latest discoveries, technologies, and diagnoses in the field.

The inclusion of over 40 clinical case studies provides practical insights, and the full-color text, illustrations, diagrams, and clinical photos enhance comprehension.

The end-of-chapter questions with comprehensive answers, along with USMLE-style and multiple-choice questions in the eBook, offer valuable learning resources.

The updated terminology aligns with contemporary guidelines, and the new chapter on Epigenetics reflects current advancements.

“Thompson and Thompson Genetics And Genomics In Medicine” also emphasizes the growing role of sequencing and functional assays in diagnosis and features content on genetic information from diverse populations.

The enhanced eBook version adds interactive functionalities, and the collaboration with the not-for-profit organization, Positive Exposure, enhances clinical cases with photography.

Overall, these features make the “Thompson and Thompson Genetics And Genomics In Medicine” a comprehensive and contemporary resource in the realm of genetic medicine.

Thompson and Thompson Genetics And Genomics In Medicine

1.3. About Writer

Ronald Cohn is a distinguished physician-scientist recognized for his impactful contributions to the field of pediatrics and genomics.

Serving as the President and CEO of The Hospital for Sick Children (SickKids) in Toronto, Canada, Cohn has played a pivotal role in advancing pediatric healthcare.

His research focuses on rare genetic disorders and neuromuscular diseases, contributing significantly to the understanding and treatment of these conditions.

Stephen Scherer is a renowned geneticist and autism researcher.

As the Director of the Centre for Applied Genomics at SickKids and a Professor at the University of Toronto, Scherer has been instrumental in unraveling the genetic complexities of autism spectrum disorders. His work has led to groundbreaking discoveries, shedding light on the genetic basis of neurodevelopmental disorders and opening avenues for personalized treatments.

Ada Hamosh is a prominent clinical geneticist and researcher, known for her expertise in rare genetic diseases.

Serving as the Director of the McKusick-Nathans Institute of Genetic Medicine at Johns Hopkins University, Hamosh has dedicated her career to advancing clinical genetics and genomics.

Her research encompasses the discovery of disease-causing genetic variants and the implementation of genomic medicine to improve patient care.

Hamosh’s impactful contributions extend to her role as an editor for the widely used Online Mendelian Inheritance in Man (OMIM) database.

Thompson and Thompson Genetics And Genomics In Medicine

Summary

The ninth edition of “Thompson & Thompson Genetics And Genomics In Medicine” is an indispensable and thoroughly revised resource for medical students, genetic counseling students, and professionals in laboratory medicine.

Since its initial publication in 1966, this textbook has been a trusted guide, offering a comprehensive understanding of human genetics and genomics and their applications in the medical field.

Under the expanded title, the latest edition is curated by a new editorial team, featuring contributions from various authors.

The content encompasses the latest discoveries in genetics, including non-coding RNAs, chromatin regulation, and epigenetics, along with advancements in technologies and emerging genetic diagnoses.

With over 40 clinical case studies, full-color illustrations, updated diagrams, and clinical photos, the book provides a contemporary and practical approach to genetic medicine. “Thompson & Thompson Genetics And Genomics In Medicine” addresses variable expression, pleiotropy, and complex disorders through new diagnostic strategies, complemented by end-of-chapter questions and answers for consolidation and exam preparation.

The eBook version enhances the learning experience, offering additional features such as USMLE-style and multiple-choice questions, making it a comprehensive and up-to-date reference for genetic medicine education and practice.