Scott E. Hickey, MD :: Nationwide Children’s Hospital, Columbus, Ohio

Scott E. Hickey, MD

Scott E. Hickey, MD

22q Center
Physician Team

Genetics (Molecular and Human)
Physician Team

Metabolic Bone Clinic
Physician Team

Prader-Willi Syndrome Clinic
Physician Team

Contact Information

Molecular & Human Genetics
700 Children's Dr
Columbus, OH 43205 [ map ]
PH: (614) 722-3535
FX: (614) 722-3546

Biography

Gender:

  • Male

Languages Spoken:

  • English

Education and Training

Medical School

  • University of Louisville School of Medicine
    Date Completed: 05/08/2004

Internship

  • Nationwide Children's Hospital
    Date Completed: 06/30/2007

Residency

  • Nationwide Children's Hospital
    Date Completed: 06/30/2009

Department:

  • Pediatrics

Section:

  • Molecular & Human Genetics

Specialty:

  • Clinical Genetics
  • Pediatrics

Date of Appointment at Nationwide Children’s Hospital:

  • 07/01/2009

Publications

  • Mori M, Mytinger J, Martin LC Bartholomew D, Hickey S. 2014. m.8993T>G-associated Leigh syndrome with hypocitrullinemia on newborn screening.  JIMD Rep. Vol. 17, no. September: 47-51.
  • 2014. Atypical breakpoint in a t(6;17) translocation case of acampomelic campomelic dysplasia.  EUROPEAN JOURNAL OF MEDICAL GENETICS. Vol. 57, no. 7. (July 1).
  • Walters-Sen LC, Thrush DL, Hickey SE, Hashimoto S, Reshmi S, Gastier-Foster JM, Pyatt RE, Astbury C. 2014. Atypical breakpoint in a t(6;17) translocation case of acampomelic campomelic dysplasia.  Eur J Med Genet. Vol. 57, no. July 1: 315-318-315-318.
  • Walters-Sen LC, Thrush DL, Hickey SE, Hashimoto S, Reshmi S, Gastier-Foster JM, Pyatt RE, Astbury C. 2014. Atypical breakpoint in a t(6;17) translocation case of acampomelic campomelic dysplasia.  Eur J Med Genet. Vol. 57, no. July: 315-318.
  • 2014. m.8993T>G-Associated Leigh Syndrome with Hypocitrullinemia on Newborn Screening.  JIMD reports. Vol. 17, no. January 1.
  • Bowden SA, Cozzi C, Hickey SE, Thrush DL, Astbury C, Nuthakki S. 2013. Autosomal dominant pseudohypoaldosteronism type 1 in an infant with salt wasting crisis associatd with urinary tract infection and obstructive uropathy.  Case Rep Endocrinol. Vol. 2013, no. December: e524647.
  • Hickey SE, Biswas S, Lamb Thrush D, et al. 2013. Multigeneration family with short stature, developmental delay, and dysmorphic features due to 4q27q28.1 microdeletion.  Eur J Med Genet. Vol. 56, no. 9. (September 1): 521-525-521-525.
  • Hickey SE, Lamb Thrush D, Walters L, et al. 2013. A case of an atypically large proximal 15q deletion as cause for Prader-Willi syndrome arising from a de novo unbalanced translocation.  Eur J Med Genet. Vol. 56, no. 9. (September): 510-514.
  • 2013. A case of an atypically large proximal 15q deletion as cause for Prader-Willi syndrome arising from a de novo unbalanced translocation.  EUROPEAN JOURNAL OF MEDICAL GENETICS. Vol. 56, no. 9. (September 1).
  • Hickey SE, Biswas S, Lamb Thrush D, et al. 2013. Multigeneration family with short stature, developmental delay, and dysmorphic features due to 4q27q28.1 microdeletion.  Eur J Med Genet. Vol. 56, no. 9. (September): 521-525.
  • Hickey SE, Walters Sen L, Pfau R, et al. 2013. Molecular resolution of an X-linked hypogonadism, gynecomastia, mental retardation, short stature, and obesity syndrome.  Am J Med Genet A. Vol. 161, no. 9. (September): 2294-2299.
  • Hickey SE, Walters Sen L, Pfau R, et al. 2013. Molecular resolution of an X-linked hypogonadism, gynecomastia, mental retardation, short stature, and obesity syndrome.  Am J Med Genet A. Vol. 161, no. 9. (September 1): 2294-2299-2294-2299.
  • 2013. ACMG Practice Guideline: lack of evidence for MTHFR polymorphism testing.  GENETICS IN MEDICINE. Vol. 15, no. 2. (February 1).
  • Hickey,Scott,E; Curry,Cynthia,J; Toriello,Helga,V. 2013. ACMG Practice Guideline: lack of evidence for MTHFR polymorphism testing.  GENETICS IN MEDICINE. Vol. 15, no. 2. (February): 153-156.
  • 2013. Autosomal dominant pseudohypoaldosteronism type 1 in an infant with salt wasting crisis associated with urinary tract infection and obstructive uropathy.  Case reports in endocrinology. Vol. 2013, no. January 1.
  • Hickey SE. 2009. Diagnosing rare metabolic diseases.  Critical Measures. Vol. 1, no. 10. (January 1): 2-5-2-5.
  • 2003. Malingering by proxy: A form of pediatric condition falsification.  JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS. Vol. 24, no. 4. (August 1).
  • 2002. Recurrent abdominal pain in children: past, present, and future.  The Journal of the Kentucky Medical Association. Vol. 100, no. 10. (October 1).
  • Kasdan ML, Hickey SE, Alexander JC, Higgins TS, Vender MI. 2001. Nocebo effect: perpetuation of factitious disorders.  Louisville Medicine.
  • 2000. Reflex sympathetic dystrophy: Misdiagnosis in patients with dysfunctional postures of the upper extremity.  JOURNAL OF HAND SURGERY-AMERICAN VOLUME. Vol. 25A, no. 6. (November 1).
  • Kasdan ML, Hickey SE. 2000. An inappropriate title: "Why most workers with occupational repetitive trauma do not file for workers' compensation." [Letter].  J Occup Environ Med. Vol. 6, no. 42. (January 1): 573-574-573-574.
  • Bowden SA, Cozzi C, Hickey SE, et al. Autosomal dominant pseudohypoaldosteronism type 1 in an infant with salt wasting crisis associated with urinary tract infection and obstructive uropathy.  Case Reports in Endocrinology.
  • Atypical breakpoint in a 6;17 translocation case of acampomelic campomelic dysplasia.
Nationwide Children's Hospital
700 Children's Drive Columbus, Ohio 43205 614.722.2000