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 A, 176(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 Genetics, 24(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 Advances, 3(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 Genetics, 24(1), 179–191. https://doi.org/10.1016/j.gim.2021.09.005