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Genetics Research

Genetics studies the genes and DNA coding that each person inherits from their parents and how these genes can lead to disease or better health. Some inherited genes cause diseases such as Tay-Sachs or sickle cell anemia, while mutations in genes can cause genetic disorders, such as Down syndrome. However, doctors also use genetics to understand which treatments may work best for an individual.
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Clinical Trials

City of Hope 96144 Molecular Genetics Studies of Cancer Patients and Their Relatives

STATUS: Active, Recruiting

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Publications

Beyond consent: building trusting relationships with diverse populations in precision medicine research.

Implementing universal Lynch syndrome screening (IMPULSS): protocol for a multi-site study to identify strategies to implement, adapt, and sustain genomic medicine programs in different organizational contexts.

Insights from a temporal assessment of increases in US private payer coverage of tumor sequencing from 2015 to 2019.

Selecting new upfront regimens for advanced ovarian cancer with biomarker guidance.

The Healthcare Systems Research Network (HCSRN) as an environment for dissemination and implementation research: a case study of developing a multi-site research study in precision medicine.

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Research Studies

Coverage, Price, and Reimbursement for Multigene Tests for Cancer and Related Conditions

Implementing Universal Lynch Syndrome Screening Across Multiple Healthcare Systems: Identifying Strategies to Facilitate and Maintain Programs in Different Organizations Contexts

Precision Medicine for Multiple Sclerosis: Making It Work (MS-SHARE)

Risk-Benefit Trade-Offs for Whole Genome Sequencing

Understanding the Experiences of Patients Undergoing Genetic Counseling and Testing for BRCA

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Featured Investigator

Kristin N. Arreola

Kristin N. Arreola

M.D.

Meet Kristin N. Arreola

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