GGrantIndex
← Search

Genetic Epidemiology and Risk Assessment Program

$99,278P30FY2022CANIH

Mayo Clinic Rochester, Rochester MN

Investigators

Linked publications, trials & patents

Trial NCT06508463Trial NCT06387979Trial NCT06381154Trial NCT06353191Trial NCT06315595Trial NCT06271291Trial NCT06238648Trial NCT06207188Trial NCT06160206Trial NCT06115772Trial NCT06078709Trial NCT06075524Trial NCT06073951Trial NCT06058663Trial NCT05917145Trial NCT05910801Trial NCT05720624Trial NCT05717153Trial NCT05704283Trial NCT05703399Trial NCT05674123Trial NCT05653661Trial NCT05640765Trial NCT05612100Trial NCT05591092Trial NCT05584449Trial NCT05575440Trial NCT05560009Trial NCT05557877Trial NCT05556525Trial NCT05549661Trial NCT05547386Trial NCT05547347Trial NCT05541016Trial NCT05530759Trial NCT05526417Trial NCT05523154Trial NCT05518903Trial NCT05512767Trial NCT05507879Trial NCT05507541Trial NCT05497804Trial NCT05465954Trial NCT05465941Trial NCT05447923Trial NCT05447910Trial NCT05443971Trial NCT05438563Trial NCT05417867Trial NCT05416983Trial NCT05412953Trial NCT05411523Trial NCT05411497Trial NCT05410977Trial NCT05407038Trial NCT05407025Trial NCT05403580Trial NCT05399004Trial NCT05393713Trial NCT05392946Trial NCT05388877Trial NCT05388851Trial NCT05388058Trial NCT05388006Trial NCT05356897Trial NCT05294367Trial NCT05288062Trial NCT05269381Trial NCT05246670Trial NCT05232851Trial NCT05224271Trial NCT05222620Trial NCT05212428Trial NCT05199285Trial NCT05194293Trial NCT05176223Trial NCT05168163Trial NCT05130060Trial NCT05112627Trial NCT05112614Trial NCT05111314Trial NCT05077735Trial NCT05075980Trial NCT05053100Trial NCT05045066Trial NCT05033288Trial NCT05030298Trial NCT05018208Trial NCT05005182Trial NCT04999826Trial NCT04975516Trial NCT04967196Trial NCT04926948Trial NCT04925817Trial NCT04917744Trial NCT04906369Trial NCT04897009Trial NCT04895735Trial NCT04892277Trial NCT04892264

Abstract

GENETIC EPIDEMIOLOGY AND RISK ASSESSMENT PROGRAM PROJECT SUMMARY The unifying goal of the Genetic Epidemiology and Risk Assessment (GERA) Program is the application of genetic and molecular epidemiology methods to the study of critical questions addressing the etiology, prognosis, and survivorship of cancer in human populations. More specifically, GERA members leverage the combination of epidemiologic methods with high-resolution molecular techniques in order to identify risk and prognostic factors; improve risk stratification; and provide an evidence base for primary, secondary, and tertiary prevention strategies. This goal is further accelerated by applying novel and innovative methods from statistics and informatics. To address these fundamental questions, 3 scientific aims have been developed: 1) To use the tremendous advances in genetics and molecular biology to understand genetic, environmental, and gene–environment interactions in the etiology of cancer in human populations; 2) To use these same advances to understand the molecular epidemiology of cancer prognosis and survivorship; and 3) To develop and apply novel statistical and informatics methods for the design and analysis of genetic and molecular epidemiology studies. The GERA Program's cancer etiology studies use family-based, case-control, and cohort study designs and focus on the genetic epidemiology of cancer, premalignant conditions, and intermediate phenotypes, as well as nongenetic risk factors and descriptive epidemiology. Etiologic heterogeneity based on tumor phenotype is also being addressed. Cancer prognosis research focuses on host factors, including genetic and serum biomarkers as well as lifestyle factors that influence prognosis; tumor biomarkers; and survivorship. Novel methods for the design and analysis of genetic and molecular epidemiologic studies are being developed, building on our expertise in biostatistics, medical informatics, and bioinformatics. To achieve these goals we have assembled a team of 29 multidisciplinary members from 4 departments from all 3 campuses. Total direct peer-reviewed funding is $3.6M (79% from the NCI), with total direct funding of $5.4M. Since 2013, the program has generated 744 publications, 36% reflecting intraprogrammatic collaborations and 59% reflecting interprogrammatic collaborations. Notable contributions have been made in the epidemiology of pancreatic, lung, ovarian, breast, colon, prostate, and lymphoproliferative malignancies as well as to the statistical genetics and medical and bioinformatics literature. Leadership of the program is provided by Drs. Cerhan, Parker, and Yang. The Program makes extensive use of Shared Resources. In the next 5 years, we will facilitate innovative research in cancer etiology and prognosis with a focus on genomics and related omics fields, development and application of novel technologies and methods, and translation to the clinic and population as well as back to the lab to inform biology.

View original record on NIH RePORTER →