Burns, Will

Assistant Clinical Geneticist

Burns, Will

Dr. Burns completed his Medial Genetics residency through the Greenwood Genetic Center in 2021. He rejoined the Center as a clinical geneticist in 2022 following a fellowship in Medical Biochemical Genetics at Nationwide Children’s Hospital. Dr. Burns has a special interest in metabolic disorders, and he sees patients in both general genetics and metabolic clinics through the Columbia office.  He is board certified in Medical Genetics (2021) and board eligible in General Pediatrics and Medical Biochemical Genetics.

Contact Information

Office: 803-799-5390


  • BS, Cell and Molecular Biology and History, Tulane University, New Orleans, LA, 2011
  • MS, Human Genetics, Tulane University, New Orleans, LA, 2012
  • MD, University of South Carolina School of Medicine, Columbia, SC, 2016
  • Residency, Pediatrics, Palmetto Health Richland, Columbia, SC, 2016-2019. Chief in 3rd year
  • Residency, Medical Genetics, Greenwood Genetic Center, 2019-2021
  • Fellowship, Medical Biochemical Genetics, Nationwide Children’s Hospital, Columbus, Ohio, 2021-2022
  • Assistant Clinical Geneticist, Greenwood Genetic Center, 2022-present

Selected Publications

  • Burns, W., Chaudhari, B. P., & Haffner, D. N. (2022). Neurogenetic and Metabolic Mimics of Common Neonatal Neurological Disorders. Seminars in Pediatric Neurology, 42, 100972. https://doi.org/10.1016/j.spen.2022.100972
  • Castle, A., Salian, S., Bassan, H., Sofrin-Drucker, E., Cusmai, R., Herman, K. C., Heron, D., Keren, B., Johnstone, D. L., Mears, W., Morlot, S., Nguyen, T., Rock, R., Stolerman, E., Russo, J., Burns, W. B., Jones, J. R., Serpieri, V., Wallaschek, H., Zanni, G., … Campeau, P. M. (2021). Expanding the Phenotypic Spectrum of GPI Anchoring Deficiency Due to Biallelic Variants in GPAA1. Neurology. Genetics, 7(6), e631. https://doi.org/10.1212/NXG.0000000000000631
  • Ziats, C. A., Burns, W. B., Tedder, M. L., Pollard, L., Wood, T., & Champaigne, N. L. (2021). 3-Methylglutaconic aciduria in carriers of primary carnitine deficiency. European Journal of Medical Genetics, 64(12), 104365. https://doi.org/10.1016/j.ejmg.2021.104365
  • Burns, W., Bird, L. M., Heron, D., Keren, B., Ramachandra, D., Thiffault, I., Del Viso, F., Amudhavalli, S., Engleman, K., Parenti, I., Kaiser, F. J., Wierzba, J., Riedhammer, K. M., Liptay, S., Zadeh, N., Porrmann, J., Fischer, A., Gößwein, S., McLaughlin, H. M., Telegrafi, A., … Lyons, M. J. (2021). Syndromic neurodevelopmental disorder associated with de novo variants in DDX23. American Journal of Medical Genetics. Part A, 185(10), 2863–2872. https://doi.org/10.1002/ajmg.a.62359


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 Noon...

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