- D Magazine Best Doctor 2022-2025
- D Magazine Best Pediatric Specialist, 2015-2016, 2020-2021
- Texas Super Doctors 2017, Texas Monthly Magazine
Garrett Gotway, M.D., Ph.D.
Interim Chief, Division of Pediatric Genetics and Metabolism
- Pediatrics - Genetics and Metabolism
Education & Training
- Residency - Children's Medical Center Dallas (2007-2010), Pediatrics
- Residency - UT Southwestern Medical School (2010-2012), Genetics
- Medical School - UT Southwestern Medical School (1998-2007)
Honors & Awards
Books & Publications
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Publications
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Partial N-acetyl glutamate synthase deficiency presenting as postpartum hyperammonemia: Diagnosis and subsequent pregnancy management
Abou Haidar L, Pachnis P, Gotway GK, Ni M, DeBerardinis RJ, McNutt MC JIMD Reports 2023 Nov 64 403-409 -
Novel pathogenic UQCRC2 variants in a female with normal neurodevelopment
Haidar LA, Harris RC, Pachnis P, Chen H, Gotway GK, Ni M, DeBerardinis RJ Cold Spring Harbor Molecular Case Studies 2023 9 -
Arginase 1 Deficiency in Patients Initially Diagnosed with Hereditary Spastic Paraplegia
McNutt MC, Foreman N, Gotway G Movement Disorders Clinical Practice 2023 Jan 10 109-114 -
The roles of homocysteinemia and methylmalonic acidemia in kidney injury in atypical hemolytic uremic syndrome caused by cobalamin C deficiency
Wood WD, Elmaghrabi A, Gotway G, Wolf MT Pediatric Nephrology 2022 Jun 37 1415-1418 -
Chromosomal Microarray Reinterpretation: Applications to Pediatric Practice
Shi G, Xu J, Barnes SF, Farooqi MS, Luu HS, Gotway G, Park JY Journal of Pediatrics 2022 Apr 243 219-223 -
Infigratinib in children with achondroplasia: the PROPEL and PROPEL 2 studies
Savarirayan R, De Bergua JM, Arundel P, McDevitt H, Cormier-Daire V, Saraff V, Skae M, Delgado B, Leiva-Gea A, Santos-Simarro F, Salles JP, Nicolino M, Rossi M, Kannu P, Bober MB, Phillips J, Saal H, Harmatz P, Burren C, Gotway G, Cho T, Muslimova E, Weng R, Rogoff D, Hoover-Fong J, Irving M Therapeutic Advances in Musculoskeletal Disease 2022 Mar 14 -
Histone H3.3 beyond cancer: Germline mutations in Histone 3 Family 3A and 3B cause a previously unidentified neurodegenerative disorder in 46 patients
Author Collaboration DS, Author Collaboration CC, Author Collaboration CS, Author Collaboration UD, Bryant L, Li D, Cox SG, Marchione D, Joiner EF, Wilson K, Janssen K, Lee P, March ME, Nair D, Sherr E, Fregeau B, Wierenga KJ, Wadley A, Mancini GM, Powell-Hamilton N, van de Kamp J, Grebe T, Dean J, Ross A, Crawford HP, Powis Z, Cho MT, Willing MC, Manwaring L, Schot R, Nava C, Afenjar A, Lessel D, Wagner M, Klopstock T, Winkelmann J, Catarino CB, Retterer K, Schuette JL, Innis JW, Pizzino A, Lüttgen S, Denecke J, Strom TM, Monaghan KG, Yuan ZF, Dubbs H, Bend R, Lee JA, Lyons MJ, Hoefele J, Günthner R, Umana L, Gotway G Science Advances 2020 Dec 6 -
Reinterpretation of Chromosomal Microarrays with Detailed Medical History
Farooqi MS, Figueroa S, Gotway G, Wang J, Luu HS, Park JY Journal of Pediatrics 2020 Jul 222 180-185.e1 -
Assessment of Interlaboratory Variation in the Interpretation of Genomic Test Results in Patients with Epilepsy
Sorelle JA, Pascual JM, Gotway G, Park JY JAMA Network Open 2020 Apr 3 -
Clinical exome studies have inconsistent coverage
Gotway G, Crossley E, Kozlitina J, Xing C, Fan J, Hornbuckle C, Thies J, Michel D, Quinn C, Scheuerle AE, Umana LA, Uhles CL, Park JY Clinical chemistry 2020 Jan 66 199-206 -
A Novel Homozygous Deletion within the FRY Gene Associated with Nonsyndromic Developmental Delay
Paulraj P, Bosworth M, Longhurst M, Hornbuckle C, Gotway G, Lamb AN, Andersen EF Cytogenetic and Genome Research 2019 Nov 159 19-25 -
Functional Assessment of Lipoyltransferase-1 Deficiency in Cells, Mice, and Humans
Ni M, Solmonson A, Pan C, Yang C, Li D, Notzon A, Cai L, Guevara G, Zacharias LG, Faubert B, Vu HS, Jiang L, Ko B, Morales NM, Pei J, Vale G, Rakheja D, Grishin NV, McDonald JG, Gotway GK, McNutt MC, Pascual JM, DeBerardinis RJ Cell Reports 2019 Apr 27 1376-1386.e6 -
Clinical Utility of Reinterpreting Previously Reported Genomic Epilepsy Test Results for Pediatric Patients
Sorelle JA, Thodeson DM, Arnold S, Gotway G, Park JY JAMA Pediatrics 2019 Jan 173 -
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 91 634-639 -
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 Oct 99 934-941 -
IKBKG mutation with incontinentia pigmenti and ring-enhancing encephalopathy
Eksambe D, Agim N, Uddin N, Gotway G, Pascual JM JAMA neurology 2015 Dec 72 1533-1535 -
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 Aug 10 -
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 116 269-274 -
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 2 324-332 -
Diagnostic yield of clinical next-generation sequencing panels for epilepsy
Wang J, Gotway G, Pascual JM, Park JY JAMA neurology 2014 May 71 650-651 -
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 158 A 206-214 -
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 11922-11927 -
Fourth International Workshop on Human Chromosome 15 Mapping, Genome Database, Baltimore, MD, October 28 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, Talbot C, Trent R, Wevrick R, Nicholls RD Cytogenetics and Cell Genetics 1999 84 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 16 232-241
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Partial N-acetyl glutamate synthase deficiency presenting as postpartum hyperammonemia: Diagnosis and subsequent pregnancy management
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