Gordon Worley | Scholars@Duke

Gordon Worley
Professor Emeritus of Pediatrics

Dr. Gordon Worley specializes in Neurodevelopmental Disabilities, a sub-specialty of Pediatrics focusing on the management of the medical problems of children with physical disabilities. The principal diagnoses he treats are cerebral palsy, spina bifida, and Down syndrome. HIs research pertains to clinical problems of children with these conditions. Current research interests include genetic factors influencing outcomes of Extremely Low Birth Weight Infants using analyses of a large data set; comparison of outcomes of prenatal (in utero) surgery vs postnatal for lesion closure in meningomyelocele using the National Spina Bifida Patient Registry; Down Syndrome Disintegrative Disorder; and associations of ADHD with high risk sexual behaviors using analyses of a large data set.

Office Hours

Tuesdays usually

Current Appointments & Affiliations

Professor Emeritus of Pediatrics, Pediatrics, Neurology, Pediatrics 2017

Contact Information

408 Deming Road, Chapel Hill, NC 27514
408 Deming Road, Chapel Hill, NC 27514
worle001@mc.duke.edu (919) 967-4476

Background
Education, Training, & Certifications
- M.D., Harvard University 1973
- B.M.S., Dartmouth College 1971
- B.A., University of Wisconsin at Madison 1969
Duke Appointment History
- Professor of Pediatrics, Pediatrics, Neurology, Pediatrics 2014 - 2017
- Professor of Pediatrics, Pediatrics, Clinical Science Departments 2006 - 2014
- Clinical Professor of Pediatrics, Pediatrics, Clinical Science Departments 2005 - 2006
- Associate Clinical Professor of Pediatrics, Pediatrics, Clinical Science Departments 1997 - 2005
- Associate Clinical Professor of Pediatrics, Pediatrics, Primary Care Pediatrics, Pediatrics 1994 - 1997
- Assistant Clinical Professor of Pediatrics, Pediatrics, Primary Care Pediatrics, Pediatrics 1994
- Assistant Professor of Pediatrics, Pediatrics, Primary Care Pediatrics, Pediatrics 1984 - 1994
- Associate in the Department of Pediatrics, Pediatrics, Clinical Science Departments 1980 - 1984
Research
Selected Grants
- National Spina Bifida Patient Registry - Duke Clinic Demonstration Project 2011 - 2014
Publications & Artistic Works
Selected Publications
- Academic Articles
  - Hart, Sarah J., Kanecia Zimmerman, Corinne M. Linardic, Sheila Cannon, Anna Pastore, Vasiliki Patsiogiannis, Paolo Rossi, et al. “Detection of iron deficiency in children with Down syndrome..” Genet Med, August 16, 2019. https://doi.org/10.1038/s41436-019-0637-4.
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  - Cardinale, Kathleen M., Alexandra Bocharnikov, Sarah J. Hart, Jane Ann Baker, Christopher Eckstein, Joan M. Jasien, William Gallentine, Gordon Worley, Priya S. Kishnani, and Heather Van Mater. “Immunotherapy in selected patients with Down syndrome disintegrative disorder..” Dev Med Child Neurol 61, no. 7 (July 2019): 847–51. https://doi.org/10.1111/dmcn.14127.
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  - Worley, Gordon. “A clinician's concerns about motor function outcomes of fetal surgery for myelomeningocele..” Am J Obstet Gynecol 220, no. 1 (January 2019). https://doi.org/10.1016/j.ajog.2018.09.020.
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  - Mori, Mari, Naoko Kurokawa, and Gordon Worley. “Speculation on the naming of Moyamoya disease..” J Neuroradiol 45, no. 4 (July 2018): 261–62. https://doi.org/10.1016/j.neurad.2018.03.004.
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  - Sun, Jessica M., Allen W. Song, Laura E. Case, Mohamad A. Mikati, Kathryn E. Gustafson, Ryan Simmons, Ricki Goldstein, et al. “Effect of Autologous Cord Blood Infusion on Motor Function and Brain Connectivity in Young Children with Cerebral Palsy: A Randomized, Placebo-Controlled Trial..” Stem Cells Transl Med 6, no. 12 (December 2017): 2071–78. https://doi.org/10.1002/sctm.17-0102.
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  - Worley, Gordon. “Case 14-2016: A Woman with a Thyroid Nodule and Psychosis..” The New England Journal of Medicine 375, no. 9 (September 2016). https://doi.org/10.1056/nejmc1607733.
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  - MacIver, Nancie J., Steven M. Thomas, Cynthia L. Green, and Gordon Worley. “Increased leptin levels correlate with thyroid autoantibodies in nonobese males..” Clin Endocrinol (Oxf) 85, no. 1 (July 2016): 116–21. https://doi.org/10.1111/cen.12963.
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  - Carpenter, Kimberly L. H., Wei Li, Hongjiang Wei, Bing Wu, Xue Xiao, Chunlei Liu, Gordon Worley, and Helen Link Egger. “Magnetic susceptibility of brain iron is associated with childhood spatial IQ..” Neuroimage 132 (May 15, 2016): 167–74. https://doi.org/10.1016/j.neuroimage.2016.02.028.
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  - Worley, Gordon, Blythe G. Crissman, Emily Cadogan, Christie Milleson, Deanna W. Adkins, and Priya S. Kishnani. “Down Syndrome Disintegrative Disorder: New-Onset Autistic Regression, Dementia, and Insomnia in Older Children and Adolescents With Down Syndrome..” J Child Neurol 30, no. 9 (August 2015): 1147–52. https://doi.org/10.1177/0883073814554654.
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  - Worley, Gordon. “Can more urological deaths in spina bifida be prevented?.” Dev Med Child Neurol 57, no. 7 (July 2015): 594–95. https://doi.org/10.1111/dmcn.12720.
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  - Englander, Zoë A., Carolyn E. Pizoli, Anastasiya Batrachenko, Jessica Sun, Gordon Worley, Mohamad A. Mikati, Joanne Kurtzberg, and Allen W. Song. “Diffuse reduction of white matter connectivity in cerebral palsy with specific vulnerability of long range fiber tracts..” Neuroimage Clin 2 (2013): 440–47. https://doi.org/10.1016/j.nicl.2013.03.006.
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  - Dixon, Natalia E., Blythe G. Crissman, P Brian Smith, Sherri A. Zimmerman, Gordon Worley, and Priya S. Kishnani. “Prevalence of iron deficiency in children with Down syndrome..” J Pediatr 157, no. 6 (December 2010): 967-971.e1. https://doi.org/10.1016/j.jpeds.2010.06.011.
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  - Yanovitch, Tammy, David K. Wallace, Sharon F. Freedman, Laura B. Enyedi, Priya Kishnani, Gordon Worley, Blythe Crissman, Erica Burner, and Terri L. Young. “The accuracy of photoscreening at detecting treatable ocular conditions in children with Down syndrome..” J Aapos 14, no. 6 (December 2010): 472–77. https://doi.org/10.1016/j.jaapos.2010.09.016.
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  - Gregory, Simon G., Jessica J. Connelly, Aaron J. Towers, Jessica Johnson, Dhani Biscocho, Christina A. Markunas, Carla Lintas, et al. “Genomic and epigenetic evidence for oxytocin receptor deficiency in autism..” Bmc Med 7 (October 22, 2009). https://doi.org/10.1186/1741-7015-7-62.
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  - Deak, Kristen L., Deborah G. Siegel, Timothy M. George, Simon Gregory, Allison Ashley-Koch, Marcy C. Speer, and Marcy C. NTD Collaborative Group. “Further evidence for a maternal genetic effect and a sex-influenced effect contributing to risk for human neural tube defects..” Birth Defects Res a Clin Mol Teratol 82, no. 10 (October 2008): 662–69. https://doi.org/10.1002/bdra.20511.
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  - Stamm, Demetra S., Deborah G. Siegel, Lorraine Mehltretter, Jessica J. Connelly, Alison Trott, Nathen Ellis, Victoria Zismann, et al. “Refinement of 2q and 7p loci in a large multiplex NTD family..” Birth Defects Res a Clin Mol Teratol 82, no. 6 (June 2008): 441–52. https://doi.org/10.1002/bdra.20462.
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  - Jha, Amitabh, Daniel P. Lammertse, Joseph R. Coll, Susan Charlifue, Christopher T. Coughlin, Gale G. Whiteneck, and Gordon Worley. “Apolipoprotein E epsilon4 allele and outcomes of traumatic spinal cord injury..” J Spinal Cord Med 31, no. 2 (2008): 171–76. https://doi.org/10.1080/10790268.2008.11760708.
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  - Cohen-Wolkowiez, Michael, Daniel K. Benjamin, Vance G. Fowler, Kelly C. Wade, Barbara D. Alexander, Gordon Worley, Ricki F. Goldstein, and P Brian Smith. “Mortality and neurodevelopmental outcome after Staphylococcus aureus bacteremia in infants..” Pediatr Infect Dis J 26, no. 12 (December 2007): 1159–61. https://doi.org/10.1097/INF.0b013e31814620a6.
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  - Ashley-Koch, Allison E., James Jaworski, De Qiong Ma, Hao Mei, Marylyn D. Ritchie, David A. Skaar, G. Robert Delong, et al. “Investigation of potential gene-gene interactions between APOE and RELN contributing to autism risk..” Psychiatr Genet 17, no. 4 (August 2007): 221–26. https://doi.org/10.1097/YPG.0b013e32809c2f75.
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  - O’Grady, Gwen, Abee L. Boyles, Marcy Speer, Frank DeRuyter, Warren Strittmatter, and Gordon Worley. “Apolipoprotein E alleles and sensorineural hearing loss..” Int J Audiol 46, no. 4 (April 2007): 183–86. https://doi.org/10.1080/14992020601145294.
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  - Worley, G., R. D. Stevenson, L. Rosenbloom, and P. B. Sullivan. “Castang and Novartis Foundation Conference on Undernutrition in Children with Cerebral Palsy: Survey of participants about decision-making for enteral (gastrostomy) feeding.” Journal of Nutritional and Environmental Medicine 16, no. 1 (February 1, 2007): 75–81. https://doi.org/10.1080/13590840601016445.
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  - Attis, M Gallego, A. Selim, J. Segal, N. Prose, and G. Worley. “Mycobacterium avium-complex: A rare cutaneous presentation.” Journal of Cutaneous Pathology 34, no. 1 (January 1, 2007): 118–19.
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  - Boyles, Abee L., Ashley V. Billups, Kristen L. Deak, Deborah G. Siegel, Lorraine Mehltretter, Susan H. Slifer, Alexander G. Bassuk, et al. “Neural tube defects and folate pathway genes: family-based association tests of gene-gene and gene-environment interactions..” Environ Health Perspect 114, no. 10 (October 2006): 1547–52. https://doi.org/10.1289/ehp.9166.
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  - Stevenson, Richard D., Mark Conaway, John W. Barrington, Sara L. Cuthill, Gordon Worley, and Richard C. Henderson. “Fracture rate in children with cerebral palsy..” Pediatr Rehabil 9, no. 4 (October 2006): 396–403.
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  - Stevenson, Richard D., Mark Conaway, W Cameron Chumlea, Peter Rosenbaum, Ellen B. Fung, Richard C. Henderson, Gordon Worley, et al. “Growth and health in children with moderate-to-severe cerebral palsy..” Pediatrics 118, no. 3 (September 2006): 1010–18. https://doi.org/10.1542/peds.2006-0298.
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  - Crissman, Blythe G., Gordon Worley, Nancy Roizen, and Priya S. Kishnani. “Current perspectives on Down syndrome: selected medical and social issues..” Am J Med Genet C Semin Med Genet 142C, no. 3 (August 15, 2006): 127–30.
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  - Crissman, Blythe G., Gordon Worley, Nancy Roizen, and Priya S. Kishnani. “Current perspectives on Down syndrome: selected medical and social issues..” American Journal of Medical Genetics. Part C, Seminars in Medical Genetics 142C, no. 3 (August 2006): 127–30. https://doi.org/10.1002/ajmg.c.30099.
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  - Stamm, Demetra S., Evadnie Rampersaud, Susan H. Slifer, Lorraine Mehltretter, Deborah G. Siegel, Jianzhen Xie, Diane Hu-Lince, et al. “High-density single nucleotide polymorphism screen in a large multiplex neural tube defect family refines linkage to loci at 7p21.1-pter and 2q33.1-q35..” Birth Defects Res a Clin Mol Teratol 76, no. 6 (June 2006): 499–505. https://doi.org/10.1002/bdra.20272.
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  - Rampersaud, E., A. G. Bassuk, D. S. Enterline, T. M. George, D. G. Siegel, E. C. Melvin, J. Aben, et al. “Whole genomewide linkage screen for neural tube defects reveals regions of interest on chromosomes 7 and 10..” J Med Genet 42, no. 12 (December 2005): 940–46. https://doi.org/10.1136/jmg.2005.031658.
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  - Deak, Kristen L., Margaret E. Dickerson, Elwood Linney, David S. Enterline, Timothy M. George, Elizabeth C. Melvin, Felicia L. Graham, et al. “Analysis of ALDH1A2, CYP26A1, CYP26B1, CRABP1, and CRABP2 in human neural tube defects suggests a possible association with alleles in ALDH1A2..” Birth Defects Res a Clin Mol Teratol 73, no. 11 (November 2005): 868–75. https://doi.org/10.1002/bdra.20183.
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  - Lark, Robert K., Cherise L. Williams, Diane Stadler, Sean L. Simpson, Richard C. Henderson, Lisa Samson-Fang, and Gordon Worley. “Serum prealbumin and albumin concentrations do not reflect nutritional state in children with cerebral palsy..” J Pediatr 147, no. 5 (November 2005): 695–97. https://doi.org/10.1016/j.jpeds.2005.05.029.
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  - Deak, Kristen L., Abee L. Boyles, Heather C. Etchevers, Elizabeth C. Melvin, Deborah G. Siegel, Felicia L. Graham, Susan H. Slifer, et al. “SNPs in the neural cell adhesion molecule 1 gene (NCAM1) may be associated with human neural tube defects..” Hum Genet 117, no. 2–3 (July 2005): 133–42. https://doi.org/10.1007/s00439-005-1299-7.
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  - Henderson, Richard C., Shawn R. Gilbert, Meagan E. Clement, Almas Abbas, Gordon Worley, and Richard D. Stevenson. “Altered skeletal maturation in moderate to severe cerebral palsy..” Dev Med Child Neurol 47, no. 4 (April 2005): 229–36. https://doi.org/10.1017/s0012162205000459.
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  - Blackman, James A., Gordon Worley, and Warren J. Strittmatter. “Apolipoprotein E and brain injury: implications for children..” Dev Med Child Neurol 47, no. 1 (January 2005): 64–70. https://doi.org/10.1017/s0012162205000113.
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  - Benz, Lisa P., Frances E. Swift, Felicia L. Graham, David S. Enterline, Elizabeth C. Melvin, Preston Hammock, John R. Gilbert, et al. “TERC is not a major gene in human neural tube defects..” Birth Defects Res a Clin Mol Teratol 70, no. 8 (August 2004): 531–33. https://doi.org/10.1002/bdra.20057.
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  - Worley, Gordon, Rolla Shbarou, Amy N. Heffner, Karin M. Belsito, George T. Capone, and Priya S. Kishnani. “New onset focal weakness in children with Down syndrome..” Am J Med Genet A 128A, no. 1 (July 1, 2004): 15–18. https://doi.org/10.1002/ajmg.a.30067.
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  - Raiford, K. L., Y. Shao, I. C. Allen, E. R. Martin, M. M. Menold, H. H. Wright, R. K. Abramson, et al. “No association between the APOE gene and autism..” Am J Med Genet B Neuropsychiatr Genet 125B, no. 1 (February 15, 2004): 57–60. https://doi.org/10.1002/ajmg.b.20104.
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  - Hardy, O., G. Worley, M. M. Lee, S. Chaing, J. Mackey, B. Crissman, and P. S. Kishnani. “Hypothyroidism in Down Syndrome: Screening Guidelines and Testing Methodology [4].” American Journal of Medical Genetics 124 A, no. 4 (February 1, 2004): 436–37.
  - Worley, Gordon, David L. Witsell, and Gregory F. Hulka. “Laryngeal dystonia causing inspiratory stridor in children with cerebral palsy..” Laryngoscope 113, no. 12 (December 2003): 2192–95. https://doi.org/10.1097/00005537-200312000-00028.
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  - Worley, Gordon. “A new look at meningomyeloceles..” Pediatrics 111, no. 6 Pt 1 (June 2003): 1494–95. https://doi.org/10.1542/peds.111.6.1494.
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  - Samson-Fang, Lisa, Ellen Fung, Virginia A. Stallings, Mark Conaway, Gordon Worley, Peter Rosenbaum, Randy Calvert, et al. “Relationship of nutritional status to health and societal participation in children with cerebral palsy..” J Pediatr 141, no. 5 (November 2002): 637–43. https://doi.org/10.1067/mpd.2002.129888.
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  - Worley, Gordon, Christine M. Houlihan, Marcia E. Herman-Giddens, Maureen E. O’Donnell, Mark Conaway, Virginia A. Stallings, W Cameron Chumlea, et al. “Secondary sexual characteristics in children with cerebral palsy and moderate to severe motor impairment: a cross-sectional survey..” Pediatrics 110, no. 5 (November 2002): 897–902. https://doi.org/10.1542/peds.110.5.897.
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  - Worley, Gordon, Harmony Garges, Anne Marie Valente, and Deborah W. Kredich. “Hypothyroidism in house officers..” Lancet 360, no. 9336 (September 14, 2002). https://doi.org/10.1016/S0140-6736(02)09988-9.
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  - Worley, G. “Diagnosis of psychogenic paralysis by observation of patient movement in sleep..” J Neurol 249, no. 9 (September 2002). https://doi.org/10.1007/s00415-002-0782-5.
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  - Henderson, Richard C., Robert K. Lark, Matthew J. Gurka, Gordon Worley, Ellen B. Fung, Mark Conaway, Virginia A. Stallings, and Richard D. Stevenson. “Bone density and metabolism in children and adolescents with moderate to severe cerebral palsy..” Pediatrics 110, no. 1 Pt 1 (July 2002). https://doi.org/10.1542/peds.110.1.e5.
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  - Speer, Marcy C., Elizabeth C. Melvin, Kristi D. Viles, Kim A. Bauer, Evadnie Rampersaud, Courtney Drake, Timothy M. George, et al. “T locus shows no evidence for linkage disequilibrium or mutation in American Caucasian neural tube defect families..” Am J Med Genet 110, no. 3 (July 1, 2002): 215–18. https://doi.org/10.1002/ajmg.10436.
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  - Houlihan, C. M., G. Worley, M. Conaway, J. Roemmich, A. Rogol, M. O’Donnell, R. Henderson, and R. Stevenson. “Longitudinal study of the progression of secondary sexual characteristics in children with cerebral palsy.” Pediatric Research 51, no. 4 (April 1, 2002): 26A-26A.
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  - Stevenson, R. D., M. Conaway, G. Worley, M. O’Donnell, and R. C. Henderson. “Stability of nutrition and growth in children with moderate/severe cerebral palsy.” Pediatric Research 51, no. 4 (April 1, 2002): 438A-438A.
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  - Fung, Ellen B., Lisa Samson-Fang, Virginia A. Stallings, Mark Conaway, Gregory Liptak, Richard C. Henderson, Gordon Worley, et al. “Feeding dysfunction is associated with poor growth and health status in children with cerebral palsy..” J Am Diet Assoc 102, no. 3 (March 2002): 361–73. https://doi.org/10.1016/s0002-8223(02)90084-2.
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  - Siegel, D. G., E. C. Melvin, H. Cukier, T. M. George, J. F. Mackey, G. Worley, J. S. Nye, and M. C. Speer. “No evidence for involvement of PPARG in neural tube defect families..” American Journal of Human Genetics 69, no. 4 (October 1, 2001): 656–656.
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  - Kenter, K., G. Worley, T. Griffin, and R. D. Fitch. “Pediatric traumatic atlanto-occipital dislocation: five cases and a review..” J Pediatr Orthop 21, no. 5 (September 2001): 585–89.
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  - Worley, G., J. S. Wiener, T. M. George, H. E. Fuchs, J. F. Mackey, R. D. Fitch, and K. T. Oldham. “Acute abdominal symptoms and signs in children and young adults with spina bifida: ten years' experience..” J Pediatr Surg 36, no. 9 (September 2001): 1381–86. https://doi.org/10.1053/jpsu.2001.26375.
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  - Liptak, G. S., M. O’Donnell, M. Conaway, W. C. Chumlea, G. Wolrey, R. C. Henderson, E. Fung, et al. “Health status of children with moderate to severe cerebral palsy..” Dev Med Child Neurol 43, no. 6 (June 2001): 364–70. https://doi.org/10.1017/s001216220100069x.
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  - Mackey, J., W. R. Treem, G. Worley, A. Boney, P. Hart, and P. S. Kishnani. “Frequency of celiac disease in individuals with Down syndrome in the United States..” Clin Pediatr (Phila) 40, no. 5 (May 2001): 249–52. https://doi.org/10.1177/000992280104000502.
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  - Melvin, E. C., T. M. George, G. Worley, A. Franklin, J. Mackey, K. Viles, N. Shah, et al. “Genetic studies in neural tube defects. NTD Collaborative Group..” Pediatr Neurosurg 32, no. 1 (January 2000): 1–9. https://doi.org/10.1159/000028889.
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  - Speer, M. C., J. Nye, D. McLone, G. Worley, E. C. Melvin, K. D. Viles, A. Franklin, C. Drake, J. Mackey, and T. M. George. “Possible interaction of genotypes at cystathionine beta-synthase and methylenetetrahydrofolate reductase (MTHFR) in neural tube defects. NTD Collaborative Group..” Clin Genet 56, no. 2 (August 1999): 142–44. https://doi.org/10.1034/j.1399-0004.1999.560208.x.
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  - Worley, G., S. J. Claerhout, and S. P. Combs. “Hypophosphatemia in malnourished children during refeeding..” Clin Pediatr (Phila) 37, no. 6 (June 1998): 347–52. https://doi.org/10.1177/000992289803700603.
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  - Melvin, E. C., K. D. Viles, J. F. Mackey, A. Lucas, A. Franklin, S. Albright, A. Aylsworth, et al. “Investigations of candidate genes for neural tube defects implicated from mouse models..” American Journal of Human Genetics 61, no. 4 (October 1, 1997): A286–A286.
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  - Speer, M. C., G. Worley, J. F. Mackey, E. Melvin, W. J. Oakes, and T. M. George. “The thermolabile variant of methylenetetrahydrofolate reductase (MTHFR) is not a major risk factor for neural tube defect in American Caucasians. The NTD Collaborative Group..” Neurogenetics 1, no. 2 (September 1997): 149–50.
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  - Sandler, A. D., G. Worley, E. C. Leroy, S. D. Stanley, and S. Kalman. “Sexual function and erection capability among young men with spina bifida..” Dev Med Child Neurol 38, no. 9 (September 1996): 823–29. https://doi.org/10.1111/j.1469-8749.1996.tb15117.x.
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  - Worley, G., J. M. Schuster, and W. J. Oakes. “Survival at 5 years of a cohort of newborn infants with myelomeningocele..” Dev Med Child Neurol 38, no. 9 (September 1996): 816–22. https://doi.org/10.1111/j.1469-8749.1996.tb15116.x.
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  - Worley, G., C. W. Erwin, R. F. Goldstein, J. M. Provenzale, and R. E. Ware. “Delayed development of sensorineural hearing loss after neonatal hyperbilirubinemia: a case report with brain magnetic resonance imaging..” Dev Med Child Neurol 38, no. 3 (March 1996): 271–77. https://doi.org/10.1111/j.1469-8749.1996.tb15090.x.
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  - Worley, G., J. M. Hoffman, S. S. Paine, S. L. Kalman, S. J. Claerhout, O. B. Boyko, R. S. Kandt, C. C. Santos, M. W. Hanson, and W. J. Oakes. “18-Fluorodeoxyglucose positron emission tomography in children and adolescents with traumatic brain injury..” Dev Med Child Neurol 37, no. 3 (March 1995): 213–20. https://doi.org/10.1111/j.1469-8749.1995.tb11994.x.
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  - Sandler, A. D., G. Worley, E. C. Leroy, S. D. Stanley, and S. Kalman. “Sexual knowledge and experience among young men with spina bifida..” Eur J Pediatr Surg 4 Suppl 1 (December 1994): 36–37.
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  - Worley, G., C. W. Erwin, J. M. Schuster, Y. Park, O. B. Boyko, M. L. Griebel, E. R. Weidman, R. A. Radtke, and W. J. Oakes. “BAEPs in infants with myelomeningocele and later development of Chiari II malformation-related brainstem dysfunction..” Dev Med Child Neurol 36, no. 8 (August 1994): 707–15. https://doi.org/10.1111/j.1469-8749.1994.tb11913.x.
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  - Yancy, W. S., M. Fairchild, K. E. Gustafson, and G. Worley. “Book Reviews.” Journal of Developmental and Behavioral Pediatrics 14, no. 1 (January 1, 1993): 65–69.
  - Kreder, K. J., P. R. Young, G. Worley, and G. D. Webster. “Anomalies associated with myelodysplasia..” Urology 39, no. 3 (March 1992): 248–50. https://doi.org/10.1016/0090-4295(92)90299-c.
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  - Yancy, W. S., M. Fairchild, K. E. Gustafson, and G. Worley. “Journal article reviews.” Journal of Developmental and Behavioral Pediatrics 13, no. 5 (January 1, 1992): 376–80.
  - Worley, G., L. R. Rosenfeld, and J. Lipscomb. “Financial counseling for families of children with chronic disabilities..” Dev Med Child Neurol 33, no. 8 (August 1991): 679–89. https://doi.org/10.1111/j.1469-8749.1991.tb14945.x.
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  - Yancy, W. S., M. Fairchild, K. E. Gustafson, and G. Worley. “Journal article reviews.” Journal of Developmental and Behavioral Pediatrics 12, no. 5 (January 1, 1991): 342–46. https://doi.org/10.1097/00004703-199110000-00011.
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  - Yancy, W. S., M. Fairchild, K. E. Gustafson, and G. Worley. “Journal article reviews.” Journal of Developmental and Behavioral Pediatrics 12, no. 4 (January 1, 1991): 281–85. https://doi.org/10.1097/00004703-199108000-00011.
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  - Bangash, I. H., G. Worley, and R. S. Kandt. “Hysterical conversion reactions mimicking neurological disease..” Am J Dis Child 142, no. 11 (November 1988): 1203–6. https://doi.org/10.1001/archpedi.1988.02150110081024.
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  - Worley, G., B. Lipman, I. H. Gewolb, J. A. Green, D. E. Schmechel, C. R. Roe, and S. J. Gross. “Creatine kinase brain isoenzyme: relationship of cerebrospinal fluid concentration to the neurologic condition of newborns and cellular localization in the human brain..” Pediatrics 76, no. 1 (July 1985): 15–21.
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  - Worley, G., J. A. Green, T. E. Frothingham, R. A. Sturner, K. W. Walls, V. A. Pakalnis, and G. S. Ellis. “Toxocara canis infection: clinical and epidemiological associations with seropositivity in kindergarten children..” J Infect Dis 149, no. 4 (April 1984): 591–97. https://doi.org/10.1093/infdis/149.4.591.
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- Conference Papers
  - Sun, Jessica, Mohamad Mikati, Jesse D. Troy, Kathryn Gustafson, Ryan Simmons, Ricki Goldstein, Jodi Petry, et al. “Adequately Dosed Autologous Cord Blood Infusion Is Associated with Motor Improvement in Children with Cerebral Palsy.” In Biology of Blood and Marrow Transplantation, 22:S61–62. Elsevier BV, 2016. https://doi.org/10.1016/j.bbmt.2015.11.354.
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  - Sun, Jessica, Mohamad Mikati, Jesse Troy, Kathryn Gustafson, Ryan Simmons, Ricki Goldstein, Jodi Petry, et al. “Autologous Cord Blood Infusion for the Treatment of Brain Injury in Children with Cerebral Palsy.” In Blood, Vol. 126. AMER SOC HEMATOLOGY, 2015.
    Link to Item
  - Jha, A., J. R. Coll, D. P. Lammertse, S. W. Charlifue, G. G. Whiteneck, and G. Worley. “Apolipoprotein E polymorphism and spinal cord injury outcomes.” In Journal of Neurotrauma, 22:1237–1237. MARY ANN LIEBERT INC, 2005.
    Link to Item
  - Raiford, K. L., Y. Shao, I. C. Allen, M. M. Menold, M. L. Cuccaro, J. Gilbert, H. H. Wright, et al. “No association between the APOE gene and autistic disorder..” In American Journal of Human Genetics, 71:495–495. UNIV CHICAGO PRESS, 2002.
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Education, Training, & Certifications

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Conference Papers