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Morgan Cook was diagnosed with short telomeres syndrome, caused by inherited gene mutations.
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.
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.
Living better, living longer
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
Michael C. Stephens, M.D. - Concerns of PGx Testing
Michael C. Stephens, M.D. - New Clinical Tool for Patient Care
Michael C. Stephens, M.D. - Traditional Use of PGx Testing
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
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