Dr Ting Teck Wah

• MRCPCH (UK) 2012
• MBBS (Singapore) 2006

• Ministry of Health (MOH) Training Scholarship 2008

• Inborn errors of metabolism
• Genetics of neurodevelopmental delay

Peer reviewed publications

• Identification of KMT2D and KDM6A variants by targeted sequencing from patients with Kabuki syndrome and other congenital disorders. Yap CS, Shekhar Jamuar S, Lai AHM, Tan ES, Ng I, Ting TW, Tan EC. Gene. 2020 Jan 11:144360. In press
• The genotypic and phenotypic spectrum of MTO1 deficiency. O'Byrne JJ, Tarailo-Graovac M, Ghani A, Champion M, Deshpande C, Dursun A, Ozgul RK, Freisinger P, Garber I, Haack TB, Horvath R, Barić I, Husain RA, Kluijtmans LAJ, Kotzaeridou U, Morris AA, Ross CJ, Santra S, Smeitink J, Tarnopolsky M, Wortmann SB, Mayr JA, Brunner-Krainz M, Prokisch H, Wasserman WW, Wevers RA, Engelke UF, Rodenburg RJ, Ting TW, McFarland R, Taylor RW, Salvarinova R, van Karnebeek CDM. Molecular Genetics and Metabolism. 2018 Jan; 123(1):28-42.
• Acute lymphoblastic leukemia in a child with a de novo germline gnb1 mutation. Brett M, Lai AHM, Ting TW, Tan AM, Foo R, Jamuar S, Tan EC. American Journal of  Medical Genetics Part A. 2017 Feb;173(2):550-552.
• Milder Form of Urea Cycle Defect Revisited: Report and Review of Hyperornithinaemia-Hyperammonaemia-Homocitrullinuria (HHH) Syndrome Diagnosed in a Teenage Girl Presenting with Recurrent Encephalopathy. Qadri SK, Ting TW, Lim JS, Jamuar SS.  Annals Academy of Medicine Singapore. 2016 Dec;45(12):563-566
• Down syndrome increases hospital length of stay in children with bronchiolitis. Ting TW, Chan HY, Wong PPC, Tetsoni D, Lee JH. Proceedings of Singapore Healthcare. March 2016 25: 64-67
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• DICER1 deletion and 14q32 microdeletion syndrome: An additional case and review of literature. Ting TW, Brett M, Cham BWM, Lim JY, Law HY, Tan EC, Lai AHM, Jamuar SS. Clinical Dysmorphology. Jan 2016 ;25(1):37-40
• Left Ventricular Non-compaction: Is It Genetic? Ting TW, Jamuar SS, Brett MS, Tan ES, Cham BW, Lim JY, Law HY, Tan EC, Choo JT, Lai AH. Pediatric Cardiology. Dec 2015;36(8):1565-72. Epub Jun 2015.
• Cockayne Syndrome due to a maternally-inherited whole gene deletion of ERCC8 and a paternally-inherited ERCC8 exon 4 deletion. Ting TW, Brett MS, Tan ES, Shen Y, Lee SP, Lim EC, Vasanwala RF, Lek N, Thomas T, Lim KW, Tan EC. Gene. Nov 2015; 572(2):274-8
• Mosaicism in traditional mendelian diseases. Ting TW, Shahdadpuri R, Jamuar SS. Current Genetic Medicine Reports. Sept  2015; 3(3):101-109
• Loeys-Dietz Syndrome in a Southeast Asian Hospital: a case series. Ting TW, Lai AHM, Choo JTL, Tan TH. European Journal of Pediatrics. Mar 2014; 173(3):387-91
• Acute pancreatitis after propofol infusion in a teenage patient. Ting TW, Lee JH. Anaesthesia and Intensive Care. May 2012; 40 (3): 561-562
   
  
  Non-peer reviewed publications:

• On the fast track: Rapid genomic sequencing for critically-ill children. Ting TW, Jamuar S.  KK Women's and Children's Hospital Special Delivery. 2019 1: 5 – 7
• Citrin deficiency: A differential diagnosis. Ong C, Ting TW. KK Women's and Children's Hospital Special Delivery. 2018 2: 6 – 7.