Rudy, Natasha

Genetic Counselor

Rudy, Natasha

Natasha joined the Greenwood Genetic Center in 2022 from the University of Alabama at Birmingham where she was a clinical genetic counselor for general genetics and cancer genetics. Natasha is a graduate of the Genetic Counseling Program at the University of South Carolina. She works in GGC’s Greenville office providing general genetic counseling for pediatric and adult patients. Natasha is a member of the National Society of Genetic Counselors and is certified by the American Board of Genetic Counseling.

Education

  • B.S., Biology, Wofford College, 2014
  • B.A., Mathematics, Wofford College, 2014
  • M.S., Genetic Counseling, University of South Carolina, 2016

Contact Information

Office : (864) 678-7890
[email protected]

Publications

  • Upadia, J., Gonzales, P. R., Atkinson, T. P., Schroeder, H. W., Robin, N. H., Rudy, N. L., & Mikhail, F. M. (2018). A previously unrecognized 22q13.2 microdeletion syndrome that encompasses TCF20 and TNFRSF13C. American Journal of Medical Genetics. Part A176(12), 2791–2797. https://doi.org/10.1002/ajmg.a.40492
  • Gonzales, P. R., Andersen, E. F., Brown, T. R., Horner, V. L., Horwitz, J., Rehder, C. W., Rudy, N. L., Robin, N. H., Thorland, E. C., & On Behalf Of The ACMG Laboratory Quality Assurance Committee (2022). Interpretation and reporting of large regions of homozygosity and suspected consanguinity/uniparental disomy, 2021 revision: A technical standard of the American College of Medical Genetics and Genomics (ACMG). Genetics in Medicine : Official Journal of the American College of Medical Genetics24(2), 255–261. https://doi.org/10.1016/j.gim.2021.10.004
  • Asif, M., Kaygusuz, E., Shinawi, M., Nickelsen, A., Hsieh, T. C., Wagle, P., Budde, B. S., Hochscherf, J., Abdullah, U., Höning, S., Nienberg, C., Lindenblatt, D., Noegel, A. A., Altmüller, J., Thiele, H., Motameny, S., Fleischer, N., Segal, I., Pais, L., Tinschert, S., …Rudy, N. L.,… Hussain, M. S. (2022). De novo variants of CSNK2B cause a new intellectual disability-craniodigital syndrome by disrupting the canonical Wnt signaling pathway. HGG Advances3(3), 100111. https://doi.org/10.1016/j.xhgg.2022.100111
  • Isidor, B., Ebstein, F., Hurst, A., Vincent, M., Bader, I., Rudy, N. L., Cogne, B., Mayr, J., Brehm, A., Bupp, C., Warren, K., Bacino, C. A., Gerard, A., Ranells, J. D., Metcalfe, K. A., van Bever, Y., Jiang, Y. H., Mendelssohn, B. A., Cope, H., Rosenfeld, J. A., … Stankiewicz, P. (2022). Stankiewicz-Isidor syndrome: expanding the clinical and molecular phenotype. Genetics in Medicine : Official Journal of the American College of Medical Genetics24(1), 179–191. https://doi.org/10.1016/j.gim.2021.09.005
Family of 5 smiling and waving

Meet the Hunt Family

Meet the Hunt Family! Two of their children, Madison and Levi, were diagnosed with PKU by newborn screening. GGC's Metabolic Treatment Team has become part of their extended family by providing expertise, compassionate care, and vital treatments for these precious children!...

In The News