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Rebecca Linn Schaub, MD, MS, CCD
Pediatrics

Rebecca Linn Schaub, MD, MS, CCD

Assistant Professor
Director, Pediatric Bone Metabolic Clinic

1200 Children's Ave,Suite 4D,Oklahoma City, OK 73104

572-244-0043

rebecca-schaub@ou.edu

Academic Section(s):

Diabetes and Endocrinology

Education:

Bachelor of Science - Texas Christian University

Master of Science/Genetics – Texas A&M University

Doctor of Medicine from University of Texas Health Sciences Center at San Antonio

Board Certification(s):

American Board of Pediatrics, General Pediatrics

American Board of Pediatrics, Pediatric Endocrinology

Residency:

 University of Texas Health Sciences Center atSan Antonio

Fellowship:

 Baylor College of Medicine/Texas Children's Hospital, Houston, Tx

Clinical/Research Interests:

Bone Metabolic disease

  • Type 1 Diabetes
  • Autoimmune thyroid disease and thyroid cancer
  • Endocrine disorder associated with congenital genetic syndromes

Select Publications:

  1. Schaub, R. L.# (2017). Racial and ethnic differences among children with new onset autoimmune Type 1 diabetes. Diabetic Medicine/Wiley, 34(10), 1435-1439. PMID: 28626948. DOI: 10.1111/dme.13408.
  2. Schaub, R. L. (2012). Deep vein thrombosis and septic pulmonary emboli with MRSA osteomyelitis in a pediatric patient. Pediatric Emergency Care/Wolters Kluwer, 28(9), 911-912. PMID: 22940890. DOI: 10.1097/PEC.0b013e318267ea4e
  3. Schaub, R. L.# (2009). Narrowing critical regions and determining penetrance for selected 18q- phenotypes. American Journal of Medical Genetics/Wiley, 149A(7), 1421-1430. PMID: 19533771. DOI: 10.1002/ajmg.a.32899
  4. Schaub, R. L.# (2005). Cognitive ability predicts degree of genetic abnormality in participants with 18q deletions. Journal of the International Neuropsychological Society, 11(5), 584-590. PMID: 16212685. DOI: 10.1017/S1355617705050691
  5. Schaub, R. L. (2005). The spectrum of thyroid abnormalities in individuals with 18q deletions. Journal of Clinical Endocrinology and Metabolism/The Endocrine Society, 90(4), 2259-2263. PMID: 15671099. DOI: doi: 10.1210/jc.2004-1630.
  6. Schaub, R. L. (2002). Molecular characterization of 18p deletions: Evidence for a breakpoint cluster. Genetics in Medicine/Elsevier, 4(1), 15-19. PMID: 11839953. DOI: 10.1097/00125817-200201000-00003.
  7. Schaub, R. L.# (2000). The spectrum of growth abnormalities in children with 18q deletions. Journal of Clinical Endocrinology and Metabolism/The Endocrine Society, 85(12), 4450-4. PMID: PMID: 11134092. DOI: 10.1210/jcem.85.12.7016.
  8. Schaub, R. L.# (1999). Congenital anomalies and anthropometry of individuals with deletions of chromosome 18q. American Journal of Medical Genetics/Wiley-Liss, 85(5), 455-462. PMID: 10405442. DOI: 10.1002/(sici)1096-8628(19990827)85:5<455::aid-ajmg5>3.0.co;2-z.
  9. Schaub, R. L.# (1996). Mapping 638 STSs to regions of human chromosome 3. Cytogenetics and Cell Genetics/Karger Online, 72(1), 90-94. PMID: 8565645. DOI: 10.1159/000134170
  10. Schaub, R. L.# (1993). Characterization of mouse tartrate-resistant acid phosphatase (TRAP) gene promoter. Journal of Bone and Mineral Research/Oxford Academic/Oxford University Press, 8(10), 1263-1270. PMID: 8256664.