• 466 Citations
  • 9 h-Index
20022020

Research output per year

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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

Research Output

  • 466 Citations
  • 9 h-Index
  • 24 Article
  • 2 Review article
  • 1 Conference contribution
  • 1 Editorial

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 journalArticle

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 journalArticle

    Open Access
  • 1 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., 1 Jan 2019, In : Ethnicity and Disease. 29, 3, p. 517-524 8 p.

    Research output: Contribution to journalArticle

  • 3 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 journalArticle

  • 7 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 journalArticle

  • 3 Scopus citations