UCLA is home to one of the largest neurology programs in the country. Our expertise spans all aspects of brain disease and includes research initiatives to improve care and outcomes. Our Clinical Neurogenomics Research Center (CNRC) represents one of our most ambitious efforts to date.
We are among the first programs in the country exploring how specific genes and genetic pathways influence the course of brain diseases, many of which are currently untreatable. UCLA is uniquely positioned to uncover new care possibilities and improve quality of life for the people we serve.
CNRC builds off the momentum and infrastructure of UCLA’s precision medicine initiative, which uses sophisticated new technology to identify the right treatment for each patient. As a result of this work, scientists across multiple specialties have access to data points from thousands of patients to establish potential hypotheses. UCLA’s expertise in bioinformatics helps us analyze and present this genomic sequencing data in ways that accelerate research.
We are leveraging these resources to facilitate large-scale genomic studies for brain disease. This infrastructure is accelerating the pace of scientific discovery so that we may someday have the ability to develop unique treatments for every patient with neurological disease.
We have also established a universal consent process that enables us to be transparent with research participants about our studies while still facilitating novel research. Applying precision
health tools and learning to CNRC efforts brings us closer to our goal of changing the landscape for select medical conditions. Read more about our Institute for Precision Health.
Additional UCLA capabilities that support our neurogenomics research include:
UCLA is experienced in creating biobanks to support clinical research. Our biobanks house hundreds of thousands of records.
Biobanks differ from other biospecimen repositories, like blood or tissue banks, in their ability to house vast quantities of samples and multiple types of data. Our dedicated neurogenomics biobank is the first of its kind and is growing by thousands of records each year.
We start by collecting blood or saliva samples for genomic analysis. For some studies, we may also request blood, skin, muscle or lumbar puncture samples. The infrastructure established by our precision medicine program makes it possible to link biosamples with a patient’s phenotype (electronic health record data). These linkages allow researchers to learn more about research participants’ health histories when necessary.
Partnerships with other UCLA scientists are speeding discovery by allowing us to test hypotheses about brain disease. These scientists include renowned researchers in areas such as genetics, neurobiology and pharmacology.
We share observations with these scientists, who explore the data further in their labs to help us answer important questions. For example, we can learn more about the biologic mechanisms affected by a mutation that causes brain disease by collaborating with UCLA’s molecular neurobiologists.
Our departments’ close geographic proximity to each other fosters a level of collaboration that few academic medical centers can match. Find out more about why innovation lives here.
We have taken steps to give researchers access to necessary patient data, and patients access to medically actionable findings:
Learn more about the Clinical Neurogenomics Research Center, including how to become a research participant, by calling us at [contact info].