Cowles Library: Pharmacogenomics & Personalized Medicine: Pharmacogenomics

Books & Ebooks

Emery's Elements of Medical Genetics and Genomics by Peter D. Turnpenny; Sian Ellard; Ruth Cleaver
Call Number: RB155 .E5 2022

ISBN: 9780702079665

Publication Date: 2021-02-13

Long recognized as a leading textbook in this fast-moving field, Emery's Elements of Medical Genetics and Genomics offers current, complete information with a strong basis in practical clinical genetics and genomics for medical school and beyond.
Pharmacogenomics: A Primer for Clinicians by Lam, Jerika T.; Gutierrez, Mary A.; and Shah, Samit
ISBN: 1260457117

Publication Date: 2021

An invaluable resource to the rapidly emerging field of pharmacogenomics—complete with case studies, clinical pearls, and treatment recommendations.
Pharmacogenomics: Challenges and Opportunities in Therapeutic Implementation by Yui-Wing Francis Lam (Editor); Stuart R. Scott (Editor)
ISBN: 9780128126264

Publication Date: 2018-12-06

Pharmacogenomics: Challenges and Opportunities in Therapeutic Implementation, Second Edition, provides comprehensive coverage of the challenges and opportunities facing the therapeutic implications of pharmacogenomics from academic, regulatory, pharmaceutical, socio-ethical and economic perspectives.
Pharmacogenomics: Foundations, Competencies, and the Pharmacists' Patient Care Process by David Kisor (Editor); David Bright (Editor); Thomas Smith (Editor); Kristin Wiisanen (Editor)
ISBN: 9781582123851

Publication Date: 2022-09-15

Second Edition provides a basic and clinical foundation for the application of drug-gene interactions in clinical therapeutics.
Precision Medicine: a Guide to Genomics in Clinical Practice by Jeanette J. McCarthy; Bryce A. Mendelsohn
Call Number: RB155 .M33 2017

ISBN: 9781259644139

Publication Date: 2016-12-23

A complete how-to-guide for incorporating precision medicine into any type of practice The Application of Precision Medicine is a practical, succinct, high-yield book for medical professionals who want to learn how genomic medicine can and should be practiced in their specific field of interest. Unlike similar books on the subject, this unique text bypasses the basic science and more advance genetic science, and focuses solely on what a practitioner needs to know on a daily basis.
Combining Human Genetics and Causal Inference to Understand Human Disease and Development by George Davey Smith (Editor); Rebecca Richmond (Editor); Jean-Baptiste Pingault (Editor)
Call Number: RB155 .C589 2022

ISBN: 9781621823810

Publication Date: 2022-01-31

In human genetics, causal inference methods leverage large omics data sets and phenotypic information to decipher various cause-and-effect relationships in human health and disease (e.g., smoking and lung cancer). The focus of such work is typically on modifiable variables (e.g., behavior or environmental exposure) that impact disease onset, progression, and outcome. A better understanding of these variables can lead to interventions and therapeutics that have a desirable impact on public health.

Other Resources

National Resources

Clinical Pharmacogenetics Implementation Consortium (CPIC) Guidelines
Learn Genetics - Genetic Science Learning Center
National Center for Biotechnology Information (NCBI) Databases
(Scroll down page to see the various different resources available via NCBI.)
National Human Genome Research Institute
PharmGKB The Pharmacogenomics Knowledgebase

Databases

PubMed (MEDLINE)
SciFinder Scholar
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You must create your own username and password to access SciFinder Scholar

With a single source, you can explore scientific information in journal and patent literature from around the world. SciFinder Scholar contains:

-More than 15 million single- and multi-step reactions
-More than 1 billion predicted and experimental properties
-The CAS REGISTRY database - the original source and final authority for CAS Registry Numbers - updated daily
-Patent records
-Sequences combined from CAS and GenBank databases

Scopus

Abstract and citation database covering the natural sciences, social sciences, and the humanities back to 1970.

More information about Scopus can be found at https://www.elsevier.com/products/scopus

ChEMBL Database
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ChEMBL is a database of ca. 500,000 bioactive compounds, their quantitative properties and bioactivities (binding constants, pharmacology and ADMET, etc). The data is abstracted and curated from the primary scientific literature and the data made available due to funding by the Wellcome Trust.

Journals

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Pharmacogenomics & Personalized Medicine: Pharmacogenomics

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