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Faculty

G. Bradley Schaefer, M.D.

Picture of Picture ofG. Bradley Schaefer
  • Professor, College of Medicine, Department of Pediatrics
  • Section Chief, Genetics & Metabolism
  • Arkansas Children's Hospital Committee for the Future Endowed Chair in Genetics

Sections

  • Genetics & Metabolism

Specialties

  • Genetics

Contact Information

  • Email: SchaeferGB@uams.edu
    Phone: 501-364-2971
    Fax: 501-364-1564
    Address: Arkansas Children's Hospital
    1 Children's Way
    Little Rock, AR 72202

Education

  • BS, University of Oklahoma, 1978
  • M.D., Oklahoma University Health Sciences Center, 1982

Training

  • Fellow, Genetics, Endocrinology & Metabolism, Oklahoma University Health Sciences Center, 1984-1986
  • Resident, Pediatrics, Oklahoma University Health Sciences Center, 1982-1984

Licensure and Board Certification

  • American Board of Medical Specialties, Medical Genetics, Clinical Genetics (M.D.)
  • American Board of Medical Specialties, Pediatrics, Pediatric Endocrinology
  • American Board of Medical Specialties, Pediatrics, Pediatrics

Clinical & Research Interests

  • Clinical Research, Quantitative neuroimaging

Recent Honors

  • Golden Apple Teaching Award, Sophomore Medical Class UAMS, 2011
  • Red Sash Teaching Award, Senior Medical Class, UAMS, 2011
  • Invited Faculty Speaker, Medical School Convocation, 2013
  • Gold Sash Teaching Award, Senior Medical School Class, UAMS, 2013, 2013
  • Invited Faculty Speaker , UAMS Medical School Convocation, 2013, 2013
  • Gold Sash Teaching Award, Senior Medical School Class, UAMS, 2013, 2013
  • Paul R. Dyken Scholarship Lecture Genetics in Pediatric Neurology March 22, 2014, Southern Society of Pediatric Nuerology New Orleans, LA, 2014
  • Invited Keynote Speaker, Annual Meeting, Oklahoma Speech-Language Hearing Association Tulsa, OK, 2014
  • Red Sash Teaching Award, Senior Medical Student Class, UAMS 2014, 2014
  • Red Sash Teaching Awarad , Senior Medical Student Class, UAMS, 2015, 2015

Recent Publications

  • Journal Article, Steinfeld, H., Cho, M.T., Retterer, K., Person, R., Schaefer, GB., Danylchuk, N., Malik, S., Wechsler, S., Monaghan, G., Henderson, L., Chung, W.K. Mutations in HIVEP2 are Associated with Developmenal Delay, Intellectual Disability, and Dysmorphic Features. Neurogenetics 2016 Mar;
  • Journal Article, Schaefer, GB., Olney, A.H., Nowak, C. In Memory of Murray Feingold (1930-2015).. Am. J. Med. Genet. A. 2016 170 A(7):1727-1731.
  • Journal Article, Schaefer, GB., Larson, I., Bolick, J. ., Williamson-Dean, L. What is the Role of Clinical Genetics in the Patient-Centered Medical Home?. Genet. Med. 2016 18(5):440-442.
  • Journal Article, Lam, W.W.K., Millichap, J.J., Soares, D.C., Chin, R., McLellan, A., FitzPatrick, D.R., Elmslie, F., Lees, M.M., Schaefer, GB., Abbot, C.M. Novel de novo EEF1A2 Missense Mutations Causing Epilepsy and Intellectual Disability.. Mol. Genet. Genom. Med. Open Access. 2016 4(4):465-474.
  • Journal Article, Zarate, Y.A., Bosanko, K.A., Bhoj, E., Ganetzky, R., Starr, L.J. ., Zackai, E.H., Schaefer, GB. Phenotypic Modifications of Patiens with Full Chromosome Aneuploidies and Concurrent Suspected or Confirmed Second Diagnoses.. Am. J. Med. Genet. A. 2016 24:1080-1083.
  • Journal Article, Sellars, E.A., Sullivan, B.R., Schaefer, GB. Whole Exome Sequencing Reveals EP300 mutation in a Mildly Affected Female.. Clin. Case Reports 2016 4(7):696-698.
  • Journal Article, Steinfeld, H., Cho, M.T., Retterer, K., Person, R., Schaefer, GB., Danylchuk, N., Malik, S., Wechsler, S., Monaghan, G., Henderson, L., Chung, W.K. Mutations in HIVEP2 are Associated with Developmenal Delay, Intellectual Disability, and Dysmorphic Features. Neurogenetics 2016 17(3):159-164.
  • Journal Article, Heinen, C.A., Jongejan, A., Watson, P.J., Redeker, B., Boelen, A., Forzano, F., Kelley, R., Olney, A.H., Pierpont, M.E., Schaefer, GB., Stewart, F., vanTrotsenburg, P., Fliers, E., Mannens, M.M., Schwabe, J.W., Hennekam, R.C. A Specific Mutation in TBL1XR1 Causes Pierpont Syndrome.. J Med Genet. 2016 53(5):330-337.
  • Journal Article, Zarate, Y.A., Jones, J.R., Jones, M.A., Millan, F., Juusola, J., Vertino-Bell ,A., Schaefer, GB., Kruer, M.C. Lessons From the First Pair of Siblings with BPAN.. Eur. J. Hum. Genet. 2016 24(7):1080-1083.
  • Journal Article, Tanaka, J.T., Cho, M.T., Retterer, K., Jones, J., Nowak, C., Douglas, J., Jiang, Y., McConkie-Rosell, A., Schaefer, GB., Kaylor, J., Telerafi, A., Friedman, B., Douglas, G., Monaghan, K.A., 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 doi: 10.1101(mcs.a000661)

Recent Grant Awards

  • Heartland Genetics and Newborn Screening Collaborative, HRSA, 2012-06-01 00:00:00-2017-05-31 00:00:00
  • Heartland Genetics and Newborn Screening Collaborative, HRSA, 5 H46MC24089-02-00, 2012-06-01 00:00:00-2017-05-31 00:00:00
  • Heartland Genetics and Newborn Screening Collaborative, HRSA, 5 H46MC24089-03-00, 2012-06-01 00:00:00-2017-05-31 00:00:00
  • Heartland Genetics and Newborn Screening Collaborative, HRSA, 5 H46MC240890400, 2012-06-01 00:00:00-2017-05-31 00:00:00
  • Heartland Genetics and Newborn Screening Collaborative, HRSA, 5 H46MC240890500, 2012-06-01 00:00:00-2017-05-31 00:00:00
  • Schaefer General Research Account, 2014-09-09 00:00:00-2021-12-31 00:00:00

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