Genomics, Populations, and Society
- 1st Edition - November 14, 2024
- Latest edition
- Editors: Dhavendra Kumar, Ruth Chadwick
- Language: English
- Paperback ISBN:9 7 8 - 0 - 3 2 3 - 9 1 7 9 9 - 5
- eBook ISBN:9 7 8 - 0 - 3 2 3 - 9 7 1 9 9 - 7
Genomics, Populations, and Society, a new volume in the Genomic and Precision Medicine in Clinical Practice series, considers the vast and thorny web of ELSI topics in genomi… Read more
Genomics, Populations, and Society, a new volume in the Genomic and Precision Medicine in Clinical Practice series, considers the vast and thorny web of ELSI topics in genomics, from bioethics to healthcare applications, healthcare economics, genomic data management, and population dynamics. Emphasis is placed on the impact of rapid genomic advances on ethical, sociocultural and lifestyle dimensions. Healthcare and health economics topics include genomics and digital health, genome editing, and genomics and infectious disease management. Legal issues related to data ownership, equity, access, probity, consent, and confidentiality are also discussed in-depth, along with sociocultural topics such as community engagement, consanguinity, and more.Here, a range of readers from researchers to clinicians, policy administrators, lawyers, economists and social scientists will discover carefully crafted, synthesized discussions on ELSI topics in genomics to power new scientific advances and genomic medicine implementation.
- Includes more than twenty-four chapters across five integrated sections on scientific dilemmas in genomics, genomic healthcare applications, sociocultural aspects of genomics, ethical aspects and global health genomics
- Presents fundamental issues tied to biosociety, healthcare, law, and the bioeconomy as genomic medicine moves from research lab to the clinic
- Features chapter contributions from international experts
Active researchers in the areas of genetics, human genomics, economy, law, ethics, and public health, public health officials and clinical administrators, Students and clinicians
Section I Scientific aspects
1. From the double helix to personal genomes
2. Genetic and genomic technologies-an introduction
3. Computational genomics and bioinformatics
4. Bio-banks- organisation and the role ‘Biopreservation & Biobanking
Section II Healthcare applications
5. The genomic and precision medicine in clinical practice- Current perspectives and future directions
6. Genomic Healthcare & Genomic health screening
7. Genomics and Digital health
8. Genetics, genomics and drug prescribing
9. Genomics and Infectious diseases: Lessons learnt from Covid-19 pandemic
Section III Socio-Cultural Aspects
10. Rethinking individual and community engagement with genomics in a digital world
11. Consanguinity in the Genomic Era - requirement of focused counseling
12. Aging genomics and society
Section IV Ethical Aspects
13. The environment population health ethics, & genomics
14. The expanding scope of gen-ethics: Harmonization of genetic and environmental concerns
15. Biobanks providing a trusted research environment for health data to advance collaborative research and digital transformation of health systems
16. Beyond the central dogma: ecogenomics and the implication for bioethics.
Section V Global health genomics
17. Global Globin Network (GGN)
18. Genome databases- challenges and expectations
19. Commercialization of genetic samples and information
20. The governance of international genomics' collaborations: Opportunities and challenges
1. From the double helix to personal genomes
2. Genetic and genomic technologies-an introduction
3. Computational genomics and bioinformatics
4. Bio-banks- organisation and the role ‘Biopreservation & Biobanking
Section II Healthcare applications
5. The genomic and precision medicine in clinical practice- Current perspectives and future directions
6. Genomic Healthcare & Genomic health screening
7. Genomics and Digital health
8. Genetics, genomics and drug prescribing
9. Genomics and Infectious diseases: Lessons learnt from Covid-19 pandemic
Section III Socio-Cultural Aspects
10. Rethinking individual and community engagement with genomics in a digital world
11. Consanguinity in the Genomic Era - requirement of focused counseling
12. Aging genomics and society
Section IV Ethical Aspects
13. The environment population health ethics, & genomics
14. The expanding scope of gen-ethics: Harmonization of genetic and environmental concerns
15. Biobanks providing a trusted research environment for health data to advance collaborative research and digital transformation of health systems
16. Beyond the central dogma: ecogenomics and the implication for bioethics.
Section V Global health genomics
17. Global Globin Network (GGN)
18. Genome databases- challenges and expectations
19. Commercialization of genetic samples and information
20. The governance of international genomics' collaborations: Opportunities and challenges
- Edition: 1
- Latest edition
- Published: November 14, 2024
- Language: English
DK
Dhavendra Kumar
Professor Kumar has considerable previous experience in writing and editing books and journals related to genetics and genomics. His books include Genomics and Clinical Medicine and Genomics and Health in the Developing World. He founded and leads the new open access journal Applied and Translational Genomics, published by Elsevier. He has published 40 articles in the journals literature.
Professor Dhavendra Kumar is a Visiting Professor, Genomic Policy Unit, Faculty of Life Sciences and Education, The University of South Wales and Consultant in Clinical Genetics at the University Hospital of Wales, Institute of Medical Genetics, Cardiff University, Cardiff, United Kingdom. He is one of the Consultants for the All Wales Medical Genetics Service and the lead Clinician for Clinical Cardiovascular Genetics. After qualifying in Medicine from the King George’s Medical College, University of Lucknow, India, he completed postgraduate training in Pediatrics with an MD. Since 1980 he has pursued a career in Medical Genetics in the UK. In 1990 he became a Diplomate of the American Board of Medical Genetics. He is a Fellow of the American College of Medical Genetics (FACMG) and as well as Royal Colleges of Physicians (FRCP-London and FRCP-Ireland) and Pediatrics and Child Health (FRCPCH-UK).
In 2015, he was conferred with the higher degree of DSc by his Alma Mater, King George’s Medical University, Lucknow (UP, India) based on his life-time contributions and achievements to genetic and genomic applications in medicine and health.
Affiliations and expertise
Honorary Clinical Professor, William Harvey Research Institute, Queen Mary University of London, UKRC
Ruth Chadwick
Ruth Chadwick is Distinguished Research Professor and Director of the ESRC (Economic and Social Sciences Research Council) Centre for Economic and Social Aspects of Genomics (Cesagen), at Cardiff University, UK and Link Chair between Cardiff Law School and the School of English, Communication and Philosophy (ENCAP). Professor Chadwick has coordinated a number of projects funded by the European Commission, including the EUROSCREEN projects and co-edits the journal Bioethics and the online journal Genomics, Society and Policy. She is Chair of the Human Genome Organisation Committee on Ethics, Law and Society, and has served as a member of several policy-making and advisory bodies, including the Panel of Eminent Ethical Experts of the Food and Agriculture Organisation of the United Nations (FAO), and the UK Advisory Committee on Novel Foods and Processes (ACNFP). She was editor-in-chief of the first edition of the award winning Encyclopedia of Applied Ethics. She is an Academician of the Academy of Social Sciences and a Fellow of the Hastings Center, New York; of the Royal Society of Arts; and of the Royal Society of Medicine. In 2005 she was the winner of the World Technology Network Award for Ethics for her work on the relationship between scientific developments and ethical frameworks. She graduated with first class Honours Literae Humaniores (Philosophy and Greek and Latin Literature) from the University of Oxford, and then went on to take the B.Phil. in Philosophy. She was awarded her D.Phil. on The Ethics of Eugenics and Genetic Engineering, supervised by Jonathan Glover. She completed an LL.B. (externally) at the University of London. She held positions at the University of Liverpool, St. Martins College, Lancaster, and University of Wales, Cardiff, before taking up her post as Professor of Moral Philosophy at the University of Central Lancashire. In June 1995 she became Head of the Centre for Professional Ethics at the University, a position she still holds. She has coordinated a number of multinational and multidisciplinary research projects funded by the European Union: Ethical Implications of Human Genome Analysis for Clinical Practice in Medical Genetics, with Special Reference to Genetic Counselling (1992); EUROSCREEN: Genetic Screening--Ethical and Philosophical Perspectives (1994–1996); BIOCULT: Cultural and Social Objections to Biotechnology, with Special Reference to the View of Young People (1995); EUROSCREEN 2: Genetic Screening--Towards Community Policy on Insurance, Commercialisation and Public Awareness (1996–1999). Her publications include the four volume edited collection, Kant: Critical Assessments (1992); Ethics, Reproduction and Genetic Control (Revised Edition, 1992);and a large number of papers in learned journals. She is joint series editor of the Routledge series on Professional Ethics. Professor Chadwick is secretary of the International Association of Bioethics and a member of the HUGO Ethics committee, the National Committee for Philosophy and the British Medical Association Steering Group on Human Genetics.
Affiliations and expertise
Distinguished Research Professor and Director, ESRC (Economic and Social Sciences Research Council) Centre for Economic and Social Aspects of Genomics (Cesagen), at Cardiff University, UKRead Genomics, Populations, and Society on ScienceDirect