Jones, Julie

Clinical Genomic Sequencing Program Director

Jones, Julie

Dr. Jones came to the Greenwood Genetic Center (GGC) as a Clinical Molecular Fellow in 2003. After completing her fellowship, she became Assistant Director of the Molecular Diagnostic Laboratory and in 2008 assumed the position of Director.

In 2014, she became the Director of the Clinical Genomic Sequencing Program. In this new role, Dr. Jones’s primary responsibilities include the analysis of next generation sequencing data including whole exome sequencing and the pulmonary panels.

Dr. Jones is board certified by the American Board of Medical Genetics and Genomics. She is a member of the American Society of Human Genetics and the American College of Medical Genetics and Genomics.

Contact Information

Office (864) 678-7885
Fax (864) 941-8141
[email protected]


  • B.S. (Math and Biology), Birmingham Southern College, Birmingham, AL, 1990
  • Ph.D. (Medical Genetics), University of Alabama at Birmingham, Birmingham, AL, 1998
  • Postdoctoral Fellow, Cystic Fibrosis Research Center, University of Alabama at Birmingham, Birmingham, AL, 1998
  • Research Fellow, Department of Molecular Physiology and Biophysics, Vanderbilt University Medical Center, Nashville, TN, 1999-2003
  • Clinical Fellow, Molecular Diagnostic Laboratory, Greenwood Genetic Center, Greenwood, SC, 2003-2005
  • Asst. Director, Molecular Diagnostic Laboratory, Greenwood Genetic Center, Greenwood, SC, 2005-2008
  • Director, Molecular Diagnostic Laboratory, Greenwood Genetic Center, Greenwood, SC 2008-2012

Selected Publications

  • Louie, R.J., Tan, Q.K., Gilner, J.B., Rogers, R.C., Younge, N., Wechsler, S.B., McDonald, M.T., Gordon, B., Saski, C.A.,Jones, J.R., Chapman, S.J., Stevenson, R.E., Sleasman, J.W., Friez, M.J. Novel pathogenic variants in FOXP3 in fetuses with echogenic bowel and skin desquamation identified by ultrasound. Am J Med Genet A. 2017 173(5):1219-1225.
  • Zarate, Y.A., Kalsner, L., Basinger, A., Jones, J.R., Li, C., Szybowska, M., Xu, Z.L., Vergano, S., Caffrey, A.R., Gonzalez, C.V., Dubbs, H., Zackai, E., Millan, F., Telegrafi, A., Baskin, B., Person, R., Fish, J.L., Everman, D.B. Genotype and Phenotype in 12 additional individuals with SATB2-Associated Syndrome. Clin Genet. 2017.
  • Smith, J.A., Holden, K.R., Friez, M.J., Jones, J.R., Lyons, M.J. A novel familial autosomal dominant mutation in ARID1B causing neurodevelopmental delays, short stature, and dysmorphic features. Am J Med Genet A. 2016 170(12):3313-3318.
  • Stolerman, E.S., Smith, B., Chaubey, A., Jones, J.R. CHD8 intragenic deletion associated with autism spectrum disorder. Eur J Med Genet. 2016 59(4):189-94.
  • Tanaka, A.J., Cho, M.T., Retterer, K., Jones, J.R., Nowak, C., Douglas, J., , Y.H., McConkie-Rosell, A., Schaefer, G.B., Kaylor, J., Rahman, O.A., Telegrafi, A., Friedman, B., Douglas, G., Monaghan, K.G., Chung, W.K. De novo pathogenic variants in CHAMP1 are associated with global developmental delay, intellectual disability, and dysmorphic facial features. Cold Spring Harb Mol Case Stud. 2016 2(1):a000661.
  • Bronicki, L.M., Redin, C., Drunat, S., Piton, A., Lyons, M., Passemard, S., Baumann, C., Faivre, L., Thevenon, J., Rivière, J.B., Isidor, B., Gan, G., Francannet, C., Willems, M., Gunel, M., Jones, J.R., Gleeson, J.G., Mandel, J.L., Stevenson, R.E., Friez, M.J., Aylsworth, A.S. Ten new cases further delineate the syndromic intellectual disability phenotype caused by mutations in DYRK1A. European Journal of Human Genetics 2015 23(11):1482-7.
  • Rojnueangnit, K., Jones, J.R., Basehore, M.J., Robin, N.H. Classic phenotype of Coffin-lowry syndrome in a female with stimulus-induced drop episodes and a genotype with preserved N-terminal kinase domain. American Journal of Medical Genetics Part A 2014 164(2):516-21.
  • Pollard, L.M., Jones, J.R., Wood, T.C. Molecular characterization of 355 mucopolysaccharidosis patients reveals 104 novel mutations. Journal of Inherited Metabolic Disease 2013 6(2):179-87.
  • Giampietro, P.F., Baker, M.W., Basehore, M.J., Jones, JR, Seroogy, C.M. Novel mutation in TP63 associated with Ectrodactyly Ectodermal Dysplasia and Clefting syndrome and T cell lymphopenia. American Journal of Medical Genetics Part A 2013 161A(6):1432-5.
  • Zarate, Y.A., Zhan, H., Jones, JR. Infrequent Manifestations of Kabuki Syndrome in a Patient with Novel MLL2 Mutation. Molecular Syndromology 2012 3(4):180-4.
  • Basehore MJ, Marlowe NM, Jones JR, Behlendorf DE, Laver TA, Friez MJ. Validation of a Screening Tool for the Rapid and Reliable Detection of CGG Trinucleotide Repeat Expansions in FMR1. Genet Test Mol Biomarkers. 2012 June 16(6):465-70.
  • Takano K, Tan WH, Irons MB, Jones JR, Schwartz CE. Pitt-Hopkins syndrome should be in the differential diagnosis for males presenting with an ATR-X phenotype. Clinical Genet Dec. 2011: 80: 600-01.
  • Fusco F, Paciolla M, Chen E, Li X, Genesio R, Conti A, Jones J, Poeta L, Lioi MB, Ursini MV, Miano MG.Genetic and molecular analysis of a new unbalanced X;18 rearrangement: localization of the diminished ovarian reserve disease locus in the distal Xq POF1 region. Hum Reprod. 2011 Nov 26(11):3186-96.
  • Champion, KJ, Bunag, C, Estep, AL,Jones, JR, Bolt, CH, Rogers, RC, Rauen, KA, Everman, DB. Germline mutation in BRAF codon 600 is compatible with human development: de novo p.V600G mutation identified in a patient with CFC syndrome. Clinical Genetics 79(5):468-474, 2010.
  • Takano K, Lyons M, Moyes C, Jones J, Schwartz C. Two percent of patients suspected of having Angelman syndrome have TCF4 mutations. Clinical Genetics 78(3):282-288, 2010.
  • Jones JR, Skinner C, Friez MJ, Schwartz CE, Stevenson RE. Hypothesis: Dysregulation of methylation of brain-expressed genes on the X chromosome and autism spectrum disorders. American Journal of Medical Genetics Part A 146A: 2213-2220, 2008.
  • Schwartz CE, Tarpey PS, Lubs HA, Verloes A, May MM, Risheg H, Friez MJ, Futreal PA, Edkins S, Teague J, Briault S, Skinner C, Bauer-Carlin A, Simensen RJ, Joseph SM, Jones JR, Gecz J, Stratton MR, Raymond FL, Stevenson RE. The original Lujan syndrome family has a novel missense mutation (p.N1007S) in the MED12 gene. Journal of Medical Genetics 44:472-477, 2007.
  • Friez MJ, Jones JR, Clarkson K, Lubs H, Abuelo D, Blaymore Bier J, Shashidhar P, Simensen R, Williams C, Giampietro PF, Schwartz CE, Stevenson RE. Recurrent infections, hypotonia, and mental retardation caused by duplication of MECP2 and adjacent region in Xq28. Pediatrics 118: e1687-e1695, 2006.
  • Wang RY, Jones JR, Chen S, Rogers RC, Friez MJ, Schwartz CE, Graham JM. A previously unreported mutation in a Currarino syndrome kindred. American Journal of Medical Genetics Part A 140A: 1923-1930, 2006.
  • Jones JR, Barrick C, Blondeau B, Shiota M, Kahn BB, Magnuson MA. Deletion of PPAR gamma in adipose tissues of mice protects against high fat diet-induced obesity and insulin resistance. PNAS 102: 6207-6212, 2005.
  • Mnatzakanian GN, Lohi H, Munteanu I, Alfred SE, Yamada T, MacLeod PJM, Jones JR, Scherer SW, Schanen NC, Friez MJ, Vincent JB, Minassian BA. A previously unidentified MECP2 open reading frame defines a new protein isoform relevant to Rett syndrome. Nature Genetics 36: 339-341, 2004.
  • Jones JR, Schwiebert EM, DuVall MD, Venglarik CJ, Wen H, Braunstein G, Bates E, Maddry JA, Greer H, Sorscher EJ. Activation of chloride secretion in cystic fibrosis cells and tissues by the substituted imidazole SRI 2931. Biochemistry 42: 13241-13249, 2003.
  • Du M,Jones JR, Lanier J, Keeling KM, Lindsey JR, Tousson A, Bëbok Z, Whitsett JA, Dey CR, Colledge WH, Evans MJ, Sorscher EJ, Bedwell DM. Aminoglycoside suppression of a premature stop mutation in a cftr -/- mouse carrying a human CFTR-G542X transgene. Journal of Molecular Medicine 80: 595-604, 2002.
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