Li Meng, Denise Goh

Goh Li Meng, Denise

Appointment(s)
  • Associate Professor, Department of Paediatrics
  • Senior Consultant, Khoo Teck Puat-National University Children's Medical Institute, National University Health System
Administrative Appointment(s)
  • Head, Division of Paediatric Genetics and Metabolism, Khoo Teck Puat-National University Children's Medical Institute, National University Health System
  • Director, Paediatric Undergraduate Medical Education
  • Chair, Faculty Assessment Committee
Joint Appointment(s)
  • Visiting Consultant, KK Women's and Children's Hospital, Singapore
Academic Qualifications
  • MMed, National University of Singapore, Singapore
  • MBBS (Honours), National University of Singapore, Singapore
  • FRCPCH, Royal College of Paediatrics and Child Health, United Kingdom
  • MD, National University of Singapore, Singapore
  • Dip ABMG, American College of Medical Genetics, USA
Research Interest(s)
  • Genetics
  • Inborn Error of Metabolism
  • Undiagnosed Cases
Recent Publications
  • 1. Chin HL, Aw MM, Quak SH, Huang J, Hart CE, Prabhakaran K, Goh DL. 2015 Jul. Molecular Genetics and Metabolism Reports. 4:49-52. doi: 10.1016/j.ymgmr.2015.06.003.
  • 2. Tan ML, Goh MC, Fu KX, Aw MH, Quak SH, Goh DL. 2015 Mar. Severe vitamin B12 deficiency in a 7-month-old boy. Ann Acad Med Singapore. 44(3):109-11.
  • 3. Denise Goh, et al. 2015 Jan. Implementing Entrustable Professional Activities at Yong Loo Lin School of Medicine Singapore Undergraduate Medical Education Program. South East Asian Journal of Medical Education.
  • 4. Lim JS, Tan ES, John CM, Poh S, Yeo SJ, Ang JS, Adakalaisamy P, Rozalli RA, Hart C, Tan ET, Ranieri E, Rajadurai VS, Cleary MA, Goh DL. 2014 Sep-Oct. Inborn Error of Metabolism (IEM) screening in Singapore by electrospray ionization-tandem mass spectrometry (ESI/MS/MS): An 8 year journey from pilot to current program. Mol Genet Metab. 113(1-2):53-61. doi: 10.1016/j.ymgme.2014.07.018.
  • 5. Cho SY, Goh DL, Lau KC, Ong HT, Lam CW. 2013 Nov. Microarray analysis unmasked paternal uniparental disomy of chromosome 12 in a patient with isolated sulfite oxidase deficiency. Clin Chim Acta. 426:13-7. doi: 10.1016/j.cca.2013.08.013.