Richardson, Ellen

Clinical Genetic Counselor

Richardson, Ellen

Ellen graduated from the University of South Carolina Genetic Counseling Program and joined the Greenwood Genetic Center in 2020. Ellen provides genetic counseling in general and metabolic clinics for pediatric and adult patients. She is a member of the National Society of Genetic Counselors.

Contact Information

Office (864) 388-1724
Fax (864) 941-8114
Email erichardson@ggc.org

Education

  • B.S. Biological Sciences, University of South Carolina, 2011
  • M.S. Biological Sciences, University of South Carolina, 2014
  • M.S. Genetic Counseling, University of South Carolina, 2020

Selected Publications

  • Yuqi Qiu, Thomas Arbogast, Sandra Martin Lorenzo, Hongying Li,1 Shih C. Tang, Ellen Richardson, Oanh Hong, Shawn Cho, Omar Shanta, Timothy Pang, Christina Corsello, Curtis K. Deutsch, Claire Chevalier, Erica E. Davis, Lilia M. Iakoucheva, Yann Herault, Nicholas Katsanis, Karen Messer, Jonathan Sebat, Oligogenic Effects of 16p11.2 Copy-Number Variation on Craniofacial Development, Cell Reports, Volume 28, Issue 13, 24 September 2019, Pages 3320-3328.

  • Anna Lindstrand, Stephan Frangakis, Claudia M.B. Carvalho, Ellen B. Richardson, Kelsey A. McFadden, Jason R. Willer, Davut Pehlivan, Pengfei Liu, Igor L. Pediaditakis, Aniko Sabo, Richard Alan Lewis, Eyal Banin, James R. Lupski, Erica E. Davis, Nicholas Katsanis, Copy-Number Variation Contributes to the Mutational Load of Bardet-Biedl Syndrome, The American Journal of Human Genetics, Volume 99, Issue 2, 4 August 2016, Pages 318-336, ISSN 0002-9297, http://dx.doi.org/10.1016/j.ajhg.2015.04.023
 

 

Meet Reggie Roper

Meet Reggie Roper

Reggie has been part of the GGC family for over 18 years. He has short stature, webbing of his hands, pulmonary stenosis, seizures and hydrocephalus along with developmental delay. He carried an initial diagnosis of cardiofaciocutaneous (CFC) syndrome; however, as genetic testing advanced, GGC made the diagnosis of Noonan-like syndrome with loose anagen hair by identifying a mutation in the SHOC2 gene. He is also an active participant in the Greenwood Community Theatre's Penguin Project. "GGC is...

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