Projects per year
Personal profile
Area of Expertise
My research interests focus on translating genetic and genomic advances into patient care. My projects include the implementation of family health history tools for improvement of patient care and the creation of tools that explain genetic and genomic advances to diverse patient populations. I work to identify and eliminate barriers to the implementation of genetic and genomic medicine in populations that have been traditionally underrepresented in genomic research and medical testing. With rapidly growing fields such as epigenetics and genomic sequencing there is a need to determine the clinical utility of burgeoning tests. In order to achieve this goal, I utilize large patient populations to interrogate real world applications for genetics in healthcare. I focus on the application of genetic testing throughout a patient’s life, from pre-conception through healthy aging.
Education/Academic qualification
BS in Bioenvironmental Sciences, Texas A & M University
PhD in Plant Pathology, Texas A & M University
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Projects
- 2 Finished
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Pharmacogenomics in pediatric populations (For: Pruthali Kulkarni)
5/06/17 → 31/05/18
Project: Research
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Stakeholder Perspectives for the Consent into a Multiuse, Multi-Institution Biobank
1/09/14 → 31/12/15
Project: Research
Research Output
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Differentiation of Hispanic biogeographic ancestry with 80 ancestry informative markers
Setser, C. H., Planz, J. V., Barber, R. C., Phillips, N. R., Chakraborty, R. & Cross, D. S., 1 Dec 2020, In: Scientific Reports. 10, 1, 7745.Research output: Contribution to journal › Article › peer-review
Open Access -
Affordable Care Act and cancer stage at diagnosis in an underserved population
Lu, Y., Jackson, B. E., Gehr, A. W., Cross, D., Neerukonda, L., Tanna, B., Ghabach, B. & Ojha, R. P., Sep 2019, In: Preventive Medicine. 126, 105748.Research output: Contribution to journal › Article › peer-review
Open Access1 Scopus citations -
Diversity in the era of precision medicine - From bench to bedside implementation
Mamun, A., Nsiah, N. Y., Srinivasan, M., Chaturvedula, A., Basha, R., Cross, D., Jones, H. P., Nandy, K. & Vishwanatha, J. K., 2019, In: Ethnicity and Disease. 29, 3, p. 517-524 8 p.Research output: Contribution to journal › Article › peer-review
4 Scopus citations -
Implementation, adoption, and utility of family health history risk assessment in diverse care settings: evaluating implementation processes and impact with an implementation framework
Wu, R. R., Myers, R. A., Sperber, N., Voils, C. I., Neuner, J., McCarty, C. A., Haller, I. V., Harry, M., Fulda, K. G., Cross, D., Dimmock, D., Rakhra-Burris, T., Buchanan, A. H., Ginsburg, G. S. & Orlando, L. A., 1 Feb 2019, In: Genetics in Medicine. 21, 2, p. 331-338 8 p.Research output: Contribution to journal › Article › peer-review
8 Scopus citations -
A SMAD4 mutation indicative of juvenile polyposis syndrome in a family previously diagnosed with Menetrier's disease
Burmester, J. K., Bell, L. N., Cross, D., Meyer, P. & Yale, S. H., 1 Oct 2016, In: Digestive and Liver Disease. 48, 10, p. 1255-1259 5 p.Research output: Contribution to journal › Article › peer-review
3 Scopus citations