Garrett Gotway, M.D., Ph.D. Associate Professor School Medical School Department Pediatrics | Eugene McDermott Center for Human Growth and Development | Internal Medicine You have reached the Academic Profile. For more information on the doctor and patient care, please visit the clinical profile. Education Medical School UT Southwestern Medical School (2007) Residency Children's Medical Center Dallas (2010), Pediatrics Residency UT Southwestern Medical School (2012), Genetics Publications Featured Publications FBXL4 defects are common in patients with congenital lactic acidemia and encephalomyopathic mitochondrial DNA depletion syndrome. Dai H, Zhang VW, El-Hattab AW, Ficicioglu C, Shinawi M, Lines M, Schulze A, McNutt M, Gotway G, Tian X, Chen S, Wang J, Craigen WJ, Wong LJ Clin. Genet. 2017 Apr 91 4 634-639 De Novo Mutations in CHD4, an ATP-Dependent Chromatin Remodeler Gene, Cause an Intellectual Disability Syndrome with Distinctive Dysmorphisms. Weiss K, Terhal PA, Cohen L, Bruccoleri M, Irving M, Martinez AF, Rosenfeld JA, Machol K, Yang Y, Liu P, Walkiewicz M, Beuten J, Gomez-Ospina N, Haude K, Fong CT, Enns GM, Bernstein JA, Fan J, Gotway G, Ghorbani M, van Gassen K, Monroe GR, van Haaften G, Basel-Vanagaite L, Yang XJ, Campeau PM, Muenke M Am. J. Hum. Genet. 2016 Sep IKBKG Mutation With Incontinentia Pigmenti and Ring-Enhancing Encephalopathy. Eksambe D, Agim N, Uddin N, Gotway G, Pascual JM JAMA Neurol 2015 Dec 72 12 1533-5 Adult-onset liver disease and hepatocellular carcinoma in S-adenosylhomocysteine hydrolase deficiency. Stender S, Chakrabarti RS, Xing C, Gotway G, Cohen JC, Hobbs HH Mol. Genet. Metab. 2015 Oct Mudd's disease (MAT I/III deficiency): a survey of data for MAT1A homozygotes and compound heterozygotes. Chien YH, Abdenur JE, Baronio F, Bannick AA, Corrales F, Couce M, Donner MG, Ficicioglu C, Freehauf C, Frithiof D, Gotway G, Hirabayashi K, Hofstede F, Hoganson G, Hwu WL, James P, Kim S, Korman SH, Lachmann R, Levy H, Lindner M, Lykopoulou L, Mayatepek E, Muntau A, Okano Y, Raymond K, Rubio-Gozalbo E, Scholl-Bürgi S, Schulze A, Singh R, Stabler S, Stuy M, Thomas J, Wagner C, Wilson WG, Wortmann S, Yamamoto S, Pao M, Blom HJ Orphanet J Rare Dis 2015 10 99 Genomic analyses of patients with unexplained early onset scoliosis. Gao X, Gotway G, Rathjen K, Johnston C, Sparagana S, Wise CA Spine Deform 2014 Sep 2 5 324-332 Diagnostic yield of clinical next-generation sequencing panels for epilepsy. Wang J, Gotway G, Pascual JM, Park JY JAMA Neurol 2014 May 71 5 650-1 Recombinant chromosome 7 in a mosaic 45,X/47,XXX patient. Tirado CA, Gotway G, Torgbe E, Iyer S, Dallaire S, Appleberry T, Suterwala M, Garcia R, Valdez F, Patel S, Koduru P Am. J. Med. Genet. A 2012 Jan 158A 1 206-14 8p11-12 FGFR1 rearrangements in hematological malignancies: review of the literature. Jose S, Gotway G, Garcia R, Vaziri A, Tirado CA J Assoc Genet Technol 2010 36 4 203-8 Human and mouse homologs of Escherichia coli DinB (DNA polymerase IV), members of the UmuC/DinB superfamily. Gerlach VL, Aravind L, Gotway G, Schultz RA, Koonin EV, Friedberg EC Proc. Natl. Acad. Sci. U.S.A. 1999 Oct 96 21 11922-7 Results 1-10 of 12 1 2 Next Last Honors & Awards Texas Super DoctorsTexas Monthly Magazine (2017) Best Pediatric Specialists/Doctors in DallasD Magazine (2015-2018)
