D. Goh

发表

Computer Calculated Dose in Paediatric Prescribing

R. C. Kirk, D. Goh, Jeya Packia, 2005, Drug safety.

Identification and molecular characterization of a novel PDE4D11 cAMP-specific phosphodiesterase isoform.

D. Goh, S. Tay, Clare N Lynex, 2008, Cellular signalling.

Implementing entrustable professional activities at Yong Loo Lin school of medicine Singapore undergraduate medical education program

D. Samarasekera, D. Goh, J. Jacobs, 2015 .

Response and Lessons Learnt Managing the COVID-19 Crisis by School of Medicine, National University of Singapore

Shuh Shing Lee, Mei Mei Lim, Y. Chong, 2020, MedEdPublish.

Genotype-phenotype correlation in patients with bicuspid aortic valve and aneurysm.

H. Dietz, Melissa L. Crenshaw, D. Goh, 2013, The Journal of thoracic and cardiovascular surgery.

Responsiveness of sphingosine phosphate lyase insufficiency syndrome to vitamin B6 cofactor supplementation

J. Hodgin, M. Wenk, F. Hildebrandt, 2020, Journal of inherited metabolic disease.

Effectively Attenuated by IL-35 Memory/Effector Th2 Cell Line Can Be Induced by Dust Mite Allergen-Specific Airway Inflammation and IgE Production

D. Goh, B. Lee, K. Chua, 2011 .

Airway Inflammation and IgE Production Induced by Dust Mite Allergen-Specific Memory/Effector Th2 Cell Line Can Be Effectively Attenuated by IL-35

D. Goh, B. Lee, K. Chua, 2011, The Journal of Immunology.

Cystic fibrosis transmembrane conductance regulator (CFTR) gene mutations in Asians with chronic pulmonary disease: a pilot study.

Daniel Y. T. Goh, L. Shek, S. Chong, 2006, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

The modulatory effects of lipopolysaccharide‐stimulated B cells on differential T‐cell polarization

D. Goh, K. Chua, I. Kuo, 2008, Immunology.

Clinical characteristics and genetic testing outcome of suspected hereditary peripheral nerve sheath tumours in a tertiary cancer institution in Singapore

D. Goh, Soo-Chin Lee, M. Puhaindran, 2022, Hereditary Cancer in Clinical Practice.

Using gene panels in the diagnosis of neuromuscular disorders: A mini-review

D. Goh, H. Chin, K. Ng, 2022, Frontiers in Neurology.

Analysis of clinically relevant variants from ancestrally diverse Asian genomes

A. Wilm, P. Gluckman, Y. Teo, 2022, Nature Communications.

Novel CFTR gene mutation in a patient with CBAVD.

Daniel Y. T. Goh, S. Chong, D. Goh, 2007, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Characterization of the human gene encoding alpha-aminoadipate aminotransferase (AADAT).

Ankita Patel, M. Geraghty, C. Jakobs, 2002, Molecular Genetics and Metabolism.

Parvalbumin – the major tropical fish allergen

Keng Hwee Neo, L. Shek, H. Van Bever, 2008, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.

Cholestatic Jaundice in Sulphite Oxidase Deficiency – An Unusual Association

D. Goh, M. Aw, S. Karthik, 2020, The Indian Journal of Pediatrics.

Molecular cytogenetic characterization of a subtle interstitial del(3)(p25.3p26.2) in a patient with deletion 3p syndrome.

Julie R Korenberg, J. Korenberg, G. Semenza, 2002, American journal of medical genetics.

Identification and characterization of novel mouse PDE4D isoforms: molecular cloning, subcellular distribution and detection of isoform-specific intracellular localization signals.

Sydney Brenner, D. Goh, S. Tay, 2008, Cellular signalling.

Microarray analysis unmasked paternal uniparental disomy of chromosome 12 in a patient with isolated sulfite oxidase deficiency.

C. Lam, D. Goh, H. Ong, 2013, Clinica chimica acta; international journal of clinical chemistry.

Reduced resource utilization with early use of next‐generation sequencing in rare genetic diseases in an Asian cohort

S. Jamuar, Nuraini Nazeha, Sylvia Kam, 2022, American journal of medical genetics. Part A.

Singapore Undiagnosed Disease Program: Genomic Analysis aids Diagnosis and Clinical Management

B. Venkatesh, Kanika Jain, S. Jamuar, 2020, Archives of Disease in Childhood.

A combination of two novel VARS2 variants causes a mitochondrial disorder associated with failure to thrive and pulmonary hypertension

C. Heng, O. Pines, D. Goh, 2019, Journal of Molecular Medicine.

CISH and susceptibility to infectious diseases.

S. Wong, J. Sung, D. Kwiatkowski, 2010, The New England journal of medicine.

Urea cycle disorder presenting as bilateral mesial temporal sclerosis – an unusual cause of seizures: a case report and review of the literature

D. Goh, H. Ong, F. Wang, 2018, Journal of Medical Case Reports.

Clinical report: a case of Williams Syndrome and Klinefelter Syndrome.

S. Chong, J. Lum, D. Goh, 2006, Annals of the Academy of Medicine, Singapore.

Ethnic differences in the time trend of female breast cancer incidence: Singapore, 1968 – 2002

P. Hall, X. Sim, K. Chia, 2006, BMC Cancer.

Strategies for identifying the genetic basis of dyslipidemia: genome-wide association studies vs. the resequencing of extremes

C. Khor, D. Goh, 2010, Current opinion in lipidology.

Pitfalls in clinical genetics

D. Goh, H. Chin, 2023, Singapore medical journal.

Unusually mild phenotype of AADC deficiency in 2 siblings.

D. Goh, S. Tay, P. Low, 2007, Molecular genetics and metabolism.

Missing parvalbumin: implications in diagnostic testing for tuna allergy.

Keng Hwee Neo, L. Shek, D. Goh, 2005, The Journal of allergy and clinical immunology.

Medical School Approach to Manage the Current COVID-19 Crisis

D. Samarasekera, D. Goh, T. Lau, 2020, Academic medicine : journal of the Association of American Medical Colleges.

Support for TGFB1 as a susceptibility gene for high myopia in individuals of Chinese descent.

S. Saw, C. Khor, D. Tan, 2010, Archives of ophthalmology.

cMET and refractive error progression in children.

S. Saw, C. Khor, K. Chia, 2009, Ophthalmology.

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.

D. Goh, J. S. Lim, E. Tan, 2014, Molecular genetics and metabolism.

Insulin resistance is associated with a metabolic profile of altered protein metabolism in Chinese and Asian-Indian men

E. Tai, Y. Low, O. Ilkayeva, 2010, Diabetologia.

Hepatocyte growth factor and retinal arteriolar diameter in Singapore Chinese.

E. Tai, Yi-Ju Li, N. Cheung, 2010, Ophthalmology.

Microarray analysis unmasked paternal uniparental disomy of chromosome 12 in a patient with isolated sulfite oxidase deficiency.

C. Lam, D. Goh, H. Ong, 2013, Clinica chimica acta; international journal of clinical chemistry.

Secondary Household Transmission of SARS, Singapore

Stefan Ma, K. Chia, B. Heng, 2004, Emerging infectious diseases.