1# Library to Find Best eBook for Read
Author : Andrew Howard
Release : 2019-01-13
Genre :
Kind : eBook
Book Rating : 799/5 ( reviews)
Book Synopsis Clinical Genomics by : Andrew Howard
Download or read book Clinical Genomics written by Andrew Howard. This book was released on 2019-01-13. Available in PDF, EPUB and Kindle. Book excerpt:
Author : Michael F. Murray (Physician)
Release : 2014
Genre : Medical
Kind : eBook
Book Rating : 446/5 ( reviews)
Book Synopsis Clinical Genomics: Practical Applications for Adult Patient Care by : Michael F. Murray (Physician)
Download or read book Clinical Genomics: Practical Applications for Adult Patient Care written by Michael F. Murray (Physician). This book was released on 2014. Available in PDF, EPUB and Kindle. Book excerpt: The first book on the clinical application of genetics in primary care medicine, Clinical Genomics focuses on the everyday application of genetic assessment and its diagnostic, therapeutic, and preventive implications in clinical practice. Unlike traditional textbooks on medical genetics and dysmorphology, this is a clinical reference that covers many of the common diseases seen in everyday medical practice. Features: endorsed by the American College of Physicians; addresses the genetic basis of common chronic diseases, not just the classic diseases of dysmorphology.
Author : Shweta Dhar
Release : 2020-04-10
Genre : Science
Kind : eBook
Book Rating : 459/5 ( reviews)
Book Synopsis Handbook of Clinical Adult Genetics and Genomics by : Shweta Dhar
Download or read book Handbook of Clinical Adult Genetics and Genomics written by Shweta Dhar. This book was released on 2020-04-10. Available in PDF, EPUB and Kindle. Book excerpt: Handbook of Clinical Adult Genetics and Genomics: A Practice-Based Approach provides a thorough overview of genetic disorders that are commonly encountered in adult populations and supports the full translation of adult genetic and genomic modalities into clinical practice. Expert chapter authors supplement foundational knowledge with case-based strategies for the evaluation and management of genetic disorders in each organ system and specialty area. Topics discussed include employing genetic testing technologies, reporting test results, genetic counseling for adult patients, medical genetics referrals, issues of complex inheritance, gene therapy, and diagnostic and treatment criteria for developmental, cardiovascular, gastrointestinal, neuropsychiatric, pulmonary issues, and much more. Employs clinical case studies to demonstrate how to evaluate, diagnosis and treat adult patients with genetic disorders Offers a practical framework for establishing an adult genetics clinic, addressing infrastructure, billing, counseling, and challenges unique to adult clinical genetics Features chapter contributions from authors at leading adult genetics institutions in the US and abroad
Author : National Academies of Sciences, Engineering, and Medicine
Release : 2018-05-16
Genre : Medical
Kind : eBook
Book Rating : 446/5 ( reviews)
Book Synopsis Implementing and Evaluating Genomic Screening Programs in Health Care Systems by : National Academies of Sciences, Engineering, and Medicine
Download or read book Implementing and Evaluating Genomic Screening Programs in Health Care Systems written by National Academies of Sciences, Engineering, and Medicine. This book was released on 2018-05-16. Available in PDF, EPUB and Kindle. Book excerpt: Genomic applications are being integrated into a broad range of clinical and research activities at health care systems across the United States. This trend can be attributed to a variety of factors, including the declining cost of genome sequencing and the potential for improving health outcomes and cutting the costs of care. The goals of these genomics-based programs may be to identify individuals with clinically actionable variants as a way of preventing disease, providing diagnoses for patients with rare diseases, and advancing research on genetic contributions to health and disease. Of particular interest are genomics- based screening programs, which will, in this publication, be clinical screening programs that examine genes or variants in unselected populations in order to identify individuals who are at an increased risk for a particular health concern (e.g., diseases, adverse drug outcomes) and who might benefit from clinical interventions. On November 1, 2017, the National Academies of Sciences, Engineering, and Medicine hosted a public workshop to explore the challenges and opportunities associated with integrating genomics-based screening programs into health care systems. This workshop was developed as a way to explore the challenges and opportunities associated with integrating genomics-based programs in health care systems in the areas of evidence collection, sustainability, data sharing, infrastructure, and equity of access. This publication summarizes the presentations and discussions from the workshop.
Author : Institute of Medicine
Release : 2014-08-19
Genre : Medical
Kind : eBook
Book Rating : 970/5 ( reviews)
Book Synopsis Assessing Genomic Sequencing Information for Health Care Decision Making by : Institute of Medicine
Download or read book Assessing Genomic Sequencing Information for Health Care Decision Making written by Institute of Medicine. This book was released on 2014-08-19. Available in PDF, EPUB and Kindle. Book excerpt: Rapid advances in technology have lowered the cost of sequencing an individual's genome from the several billion dollars that it cost a decade ago to just a few thousand dollars today and have correspondingly greatly expanded the use of genomic information in medicine. Because of the lack of evidence available for assessing variants, evaluation bodies have made only a few recommendations for the use of genetic tests in health care. For example, organizations, such as the Evaluation of Genomic Applications in Practice and Prevention working group, have sought to set standards for the kinds of evaluations needed to make population-level health decisions. However, due to insufficient evidence, it has been challenging to recommend the use of a genetic test. An additional challenge to using large-scale sequencing in the clinic is that it may uncover "secondary," or "incidental," findings - genetic variants that have been associated with a disease but that are not necessarily related to the conditions that led to the decision to use genomic testing. Furthermore, as more genetic variants are associated with diseases, new information becomes available about genomic tests performed previously, which raises issues about how and whether to return this information to physicians and patients and also about who is responsible for the information. To help develop a better understanding of how genomic information is used for healthcare decision making, the Roundtable on Translating Genomic-Based Research for Health of the Institute of Medicine held a workshop in Washington,DC in February 2014. Stakeholders, including clinicians, researchers, patients, and government officials, discussed the issues related to the use of genomic information in medical practice. Assessing Genomic Sequencing Information for Health Care Decision Making is the summary of that workshop. This report compares and contrasts evidence evaluation processes for different clinical indications and discusses key challenges in the evidence evaluation process.
