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Ingle, James

Mayo Clinic

Division of Medical Oncology, Department of Oncology, Mayo Clinic, Rochester, Minnesota, USA.

Citations 2

Aurora-A overexpression is linked to development of aggressive teratomas derived from humans iPS cells
Ohmine, Seiga, Salisbury, Jeffrey L., Pettinato, Giuseppe , Haddad, Tufia C. , D’Assoro, Antonino B. , Ingle, James, Haddad, Tufia, Galanis, Evanthia , D'Assoro, Antonino B, Ingle, James N. , Haddox, Candace L. , Ikeda, Yasuhiro

Oncology Reports | January 31, 2018 | Volume: No volume available | Issue: No issue available | Pages: No page available

10.3892/or.2018.6239 Get It

Pharmacogenomic Discovery to Function and Mechanism: Breast Cancer as a Case Study
Wang, Liewei , Weinshilboum, Richard M. , Ingle, James, Weinshilboum, Richard, Ingle, James N. , Weinshilboum, Richard M.

Clinical Pharmacology & Therapeutics | October 20, 2017 | Volume: 103 | Issue: 2 | Pages: 243-252

10.1002/cpt.915 Get It

Biomedical research is undergoing rapid change, with the development of a series of analytical omics techniques that are capable of generating Biomedical Big Data. These developments provide an unprecedented opportunity to gain novel insight into disease pathophysiology and mechanisms of drug action and response—but they also present significant challenges. Pharmacogenomics is a discipline within Clinical Pharmacology that has been at the forefront in defining, taking advantage of, and dealing with the opportunities and challenges of this aspect of the Post‐Genome Project world. This overview will describe the evolution of germline pharmacogenomic research strategies as we have moved from an era of candidate genes to agnostic genome‐wide association studies (GWAS) coupled with the functional and mechanistic pursuit of GWAS signals. Germline pharmacogenomic studies of breast cancer endocrine therapy will be used to illustrate research strategies that are being applied broadly to omics studies of drug response phenotypes.