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Faculty

Elizabeth Sellars, M.D.

Picture of Picture ofElizabeth  Sellars
  • College of Health Related Professions
  • Assistant Professor, College of Medicine, Department of Pediatrics
  • Assistant Professor, College of Medicine

Sections

  • Genetics & Metabolism

Specialties

  • Genetics

Contact Information

  • Email: EASellars@uams.edu
    Phone: 501-364-2966
    Address: Arkansas Children's Hospital
    1 Children's Way
    Little Rock, AR 72202

Education

  • B.S., Davidson College, 2002
  • M.D., University of Arkansas for Medical Sciences, 2007

Licensure and Board Certification

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

Recent Publications

  • Journal Article, Sellars EA,Sullivan BR,Schaefer GB Whole exome sequencing reveals EP300 mutation in mildly affected female: expansion of the spectrum. Clin Case Rep 2016 Jul 4 (7): 696-8.
  • Journal Article, Zarate YA,Clingenpeel R,Sellars EA,Tang X,Kaylor JA,Bosanko K,Linam LE,Byers PH COL1A1 and COL1A2 sequencing results in cohort of patients undergoing evaluation for potential child abuse. Am J Med Genet A 2016 Jul 170 (7): 1858-62.
  • Journal Article, Zarate YA,Sellars E,Lepard T,Tang X,Collins RT 2nd Aortic dilation, genetic testing, and associated diagnoses. Genet Med 2016 Apr 18 (4): 356-63.
  • Journal Article, Zarate YA,Sellars E,Lepard T,Carlo WF,Tang X,Collins RT 2nd Aortic dilation in pediatric patients. Eur J Pediatr 2015 Dec 174 (12): 1585-92.
  • Journal Article, Zarate YA,Perry H,Ben-Omran T,Sellars EA,Stein Q,Almureikhi M,Simmons K,Klein O,Fish J,Feingold M,Douglas J,Kruer MC,Si Y,Mao R,McKnight D,Gibellini F,Retterer K,Slavotinek A Further supporting evidence for the SATB2-associated syndrome found through whole exome sequencing. Am J Med Genet A 2015 May 167A (5): 1026-32.
  • Journal Article, Wong D,Tortorelli S,Bishop L,Sellars EA,Schimmenti LA,Gallant N,Prada CE,Hopkin RJ,Leslie ND,Berry SA,Rosenblatt DS,Fair AL,Matern D,Raymond K,Oglesbee D,Rinaldo P,Gavrilov D Outcomes of four patients with homocysteine remethylation disorders detected by newborn screening. Genet Med 2015 Apr 9.
  • Journal Article, Sellars EA,Bosanko KA,Lepard T,Garnica A,Schaefer GB A newborn with complex skeletal abnormalities, joint contractures, and bilateral corneal clouding with sclerocornea. Semin Pediatr Neurol 2014 Jun 21 (2): 84-7.
  • Journal Article, Zarate YA,Lepard T,Sellars E,Kaylor JA,Alfaro MP,Sailey C,Schaefer GB,Collins RT 2nd Cardiovascular and genitourinary anomalies in patients with duplications within the Williams syndrome critical region: phenotypic expansion and review of the literature. Am J Med Genet A 2014 Aug 164A (8): 1998-2002.
  • Journal Article, Keppler-Noreuil KM,Sapp JC,Lindhurst MJ,Parker VE,Blumhorst C,Darling T,Tosi LL,Huson SM,Whitehouse RW,Jakkula E,Grant I,Balasubramanian M,Chandler KE,Fraser JL,Gucev Z,Crow YJ,Brennan LM,Clark R,Sellars EA,Pena LD,Krishnamurty V,Shuen A,Braverman N,Cunningham ML,Sutton VR,Tasic V,Graham JM Jr,Geer J Jr,Henderson A,Semple RK,Biesecker LG Clinical delineation and natural history of the PIK3CA-related overgrowth spectrum. Am J Med Genet A 2014 Jul 164A (7): 1713-33.
  • Journal Article, Sellars EA,Wusik K,Weaver KN,Hopkin RJ Variable presentation between a mother and a fetus with Goltz syndrome. Prenat Diagn 2013 Dec 33 (12): 1211-3.

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