- Medical School - UT Southwestern Medical School (1998-2007)
- Residency - UT Southwestern Medical School (2010-2012), Genetics
- Residency - Children's Health Dallas (2007-2010), Pediatrics
Garrett Gotway, M.D., Ph.D.
- Pediatrics - Genetics and Metabolism
Education & Training
Honors & Awards
- D Magazine Best Doctor 2022
- D Magazine Best Pediatric Specialist, (2015-2016, 2020-2021)
- Texas Super Doctors 2017, Texas Monthly Magazine
Books & Publications
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Publications
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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 Clinical genetics 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 American journal of human genetics 2016 Sep -
IKBKG Mutation With Incontinentia Pigmenti and Ring-Enhancing Encephalopathy.
Eksambe D, Agim N, Uddin N, Gotway G, Pascual JM JAMA neurology 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 Molecular genetics and metabolism 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 journal of rare diseases 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 deformity 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 neurology 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 American journal of medical genetics. Part 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 Journal of the Association of Genetic Technologists 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 Proceedings of the National Academy of Sciences of the United States of America 1999 Oct 96 21 11922-7 -
Report of the fourth international workshop on human chromosome 15 mapping 1997.
Morton CC, Christian SL, Donlon TA, Driscoll DJ, Fink JK, Gabriel JM, Gotway G, Greally JM, Hitchins MP, Howard HC, Ji Y, Leonard S, Lerner T, Magenis E, Malcolm S, Ohta T, Rainier S, Rees M, Riley B, Robinson WP, Saitoh S, Schultz R, Sell S, Sharp JD, Nicholls RD Cytogenetics and cell genetics 1999 84 1-2 12-21 -
Chromosomal localization of a human mucin gene (MUC8) and cloning of the cDNA corresponding to the carboxy terminus.
Shankar V, Pichan P, Eddy RL, Tonk V, Nowak N, Sait SN, Shows TB, Schultz RE, Gotway G, Elkins RC, Gilmore MS, Sachdev GP American journal of respiratory cell and molecular biology 1997 Mar 16 3 232-41
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FBXL4 defects are common in patients with congenital lactic acidemia and encephalomyopathic mitochondrial DNA depletion syndrome.
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