Video Center

Patient Stories

  • Mallory Riggs shares her family’s struggle with having abnormally low platelets in the blood.
  • Larry Weakland's' pancreatic cancer was linked to an inherited gene mutation.
  • Genetic testing brings attention to individually rare, but collectively common genetic diseases.
  • Predictive genetic testing helps family of young patient battling ulcerative colitis.
  • Whole-exome sequencing probes into patient’s bone and joint pain.
  • RNA sequencing identifies DNA changes that caused genetic abnormalities.
  • Pharmacogenomic testing provided insight into why certain medications didn't work for Nicole.
  • Pharmacogenomic testing helps patient and her family members find answers to health-related questions.
  • Applied pharmacogenomics resolves patient's lifelong anxiety and depression.
  • Microbiome transplant clears antibiotic-resistant intestinal infection.
  • Genome sequencing reveals rare gene mutation.
  • Sequencing uncovers genetic makeup of aggressive tumor.
  • Whole-genome sequencing provides diagnosis for rare neurological disorder.
  • Obscure symptoms mapped to rare pediatric disorder.
  • Individualized Medicine and The Diagnostic Journey

Personalized Medicine Concepts

  • The Biomarker Discovery Program captures genetic information from cells and analyzes it, searching for genetic patterns to help physicians make more precise diagnoses and prescribe more effective, individualized treatments.
  • The Microbiome Program explores the genetic code of the body's microorganisms, using the latest techniques to profile an individual's microbiome to detect, prevent and diagnose infections and other diseases.
  • The Pharmacogenomics Program investigates how variations in genes affect response to medications, thereby using a patient's genetic profile to predict a drug's efficacy, guide dosage and improve patient safety.
  • Genomic sequencing is a process for analyzing a sample of DNA taken from your blood. In the lab, technicians extract DNA and prepare it for sequencing.
  • The Clinomics Program quickly moves discoveries from the research lab to the clinical setting, with practical, cost-efficient genomic tests for diagnosing and treating patients.
  • The Epigenomics Program investigates the role of the epigenome, examines which factors act on individual genes, and how certain changes in the epigenome affect our health.

Personalized Medicine 101

  • Personalizing care, preventing disease
  • Living better, living longer

Careers In Personalized Medicine

  • Katie Burbank, R.N., Genetic Nurse
  • Nicholas Chia, Ph.D., Scientist in Informatics and Microbiome
  • Margot Cousin, Ph.D., Genetic Scientist
  • Dusica Babovic-Vuksanovic, M.D., Medical Geneticist
  • Matthew J. Ferber, Ph.D., Clinical Genetic Scientist
  • Teresa M. Kruisselbrink, M.S., L.C.G.C., Genetic Counselor
  • Eric Matey, Pharm.D., R.Ph., Pharmacogenomics Pharmacist
  • Asha A. Nair, M.S., Ph.D., Bioinformatician

Personalized Medicine Provider Insights

  • Imad Absah, M.D. - Collaboration with Pharmacists
  • Imad Absah, M.D. - Implementing Pediatric Practice
  • Imad Absah, M.D. - Importance of PGx to Patient Care
  • Imad Absah, M.D. Patient Case – Crohn’s, Acid Reflux & Anxiety
  • Imad Absah, M.D. Patient Case – Esophagitis, Ulcers & Acid Reflux
  • Imad Absah, M.D. - When to Use PGx Testing
  • Stephanie L. Hines, M.D. - Advice for Colleague
  • Stephanie L. Hines, M.D. - Personal Testing
  • Konstantinos N Lazaridis, M.D. Provider Stories - Pharmacogenomics
  • Stephanie L. Hines, M.D. - Concerns of PGx Testing
  • Stephanie L. Hines, M.D. - New Clinical Tool for Patient Care
  • Stephanie L. Hines, M.D. - Traditional Use of PGx Testing

Center for Individualized Medicine Programs

  • George Vasmatzis, Ph.D., co-director, Biomarker Discovery Program
  • Matthew J. Ferber, Ph.D., and Eric D. Wieben, Ph.D., co-directors, Clinomics Program
  • Tamas Ordog, M.D., director, Epigenomics Program
  • Heidi Nelson, M.D., director, Microbiome Program
  • Richard Weinshilboum, M.D., director, Pharmacogenomics Program
  • Richard Sharp, Ph.D., director, Bioethics Program
  • Jean-Pierre A. Kocher, Ph.D., director, Bioinformatics Program
  • James R. Cerhan, M.D., Ph.D., co-director, Biorepositories Program
  • James D. Buntrock, director, Information Technology Program
  • Eric D. Wieben, Ph.D., director, Medical Genome Facility