ARTICLE IN ACADEMIC JOURNALS
| NO | DETAILS OF ARTICLE IN ACADEMIC JOURNALS |
|---|---|
| 1. |
Impact of BRCA1/2 cascade testing on anxiety, depression, and cancer worry levels among unaffected relatives in a multiethnic Asian cohort
2023
Author(s) : Thong Meow Keong Source :
JOURNAL OF GENETIC COUNSELING
DOI :
10.1002/jgc4.1619
|
| 2. |
The clinical utility of polygenic risk scores in genomic medicine practices: a systematic review
2022
Author(s) : Thong Meow Keong Source :
HUMAN GENETICS
DOI :
10.1007/s00439-022-02452-x
|
| 3. |
The clinical utility of polygenic risk scores in genomic medicine practices: a systematic review
2022
Author(s) : Thong Meow Keong Source :
Human Genetics
DOI :
10.1007/s00439-022-02452-x
|
| 4. |
Targeted Gene Sanger Sequencing Should Remain the First-Tier Genetic Test for Children Suspected to Have the Five Common X-Linked Inborn Errors of Immunity
2022
Author(s) : Thong Meow Keong Source :
Frontiers in Immunology
DOI :
10.3389/fimmu.2022.883446
|
| 5. |
Eph and Ephrin Variants in Malaysian Neural Tube Defect Families
2022
Source :
Genes
DOI :
10.3390/genes13060952
|
| 6. |
The clinical utility of polygenic risk scores in genomic medicine practices: a systematic review.
2022
Author(s) : Thong Meow Keong Source :
Human genetics [Hum Genet] NLMUID: 7613873
DOI :
10.1007/s00439-022-02452-x
|
| 7. |
Oncologist-led BRCA counselling improves access to cancer genetic testing in middle-income Asian country, with no significant impact on psychosocial outcomes
2022
Source :
JOURNAL OF MEDICAL GENETICS
DOI :
10.1136/jmedgenet-2020-107416
|
| 8. |
Psychosocial impact and health behaviour intent of breast cancer patients with BRCA1/2 and PALB2 pathogenic variants unselected by a priori risk.
2022
Author(s) : Thong Meow Keong Source :
PLOS ONE
DOI :
10.1371/journal.pone.0263675
|
| 9. |
Management of Multi-Drug Resistant Non-Tuberculous Mycobacteria Infection in Children with Cystic Fibrosis: Two Case Studies
2022
Source :
PEDIATRIC PULMONOLOGY
|
| 10. |
Ethical issues related to gene therapy with onasemnogene abeparvovec for spinal muscular atrophy type 1 in a developing country
2022
Source :
GENETICS IN MEDICINE
DOI :
10.1016/j.gim.2022.01.472
|
| 11. |
Psychosocial outcome and health behaviour intent of breast cancer patients with BRCA1/2 and PALB2 pathogenic variants unselected by a priori risk
2022
Author(s) : Thong Meow Keong, Nur Aishah Binti Mohd Taib Source :
PLOS ONE
DOI :
10.1371/journal.pone.0263675
|
| 12. |
Eph and Ephrin Variants in Malaysian Neural Tube Defect Families
2022
Source :
GENES
DOI :
10.3390/genes13060952
|
| 13. |
Attitudes and training needs of oncologists and surgeons in mainstreaming breast cancer genetic counseling in a low-to-middle income Asian country
2022
Author(s) : Thong Meow Keong, Nur Aishah Binti Mohd Taib Source :
JOURNAL OF GENETIC COUNSELING
DOI :
10.1002/jgc4.1579
|
| 14. |
Oncologist-led BRCA counselling improves access to cancer genetic testing in middle-income Asian country, with no significant impact on psychosocial outcomes
2022
Source :
Journal of Medical Genetics
DOI :
10.1136/jmedgenet-2020-107416
|
| 15. |
Targeted Gene Sanger Sequencing Should Remain the First-Tier Genetic Test for Children Suspected to Have the Five Common X-Linked Inborn Errors of Immunity
2022
Author(s) : Lee Way Seah, Thong Meow Keong Source :
FRONTIERS IN IMMUNOLOGY
DOI :
10.3389/fimmu.2022.883446
|
| 16. |
Attitudes and training needs of oncologists and surgeons in mainstreaming breast cancer genetic counseling in a low-to-middle income Asian country
2022
Author(s) : Thong Meow Keong Source :
Journal of Genetic Counseling
DOI :
10.1002/jgc4.1579
|
| 17. |
Psychosocial outcome and health behaviour intent of breast cancer patients with BRCA1/2 and PALB2 pathogenic variants unselected by a priori risk
2022
Author(s) : Thong Meow Keong Source :
PloS one
DOI :
10.1371/journal.pone.0263675
|
| 18. |
Beta-thalassemias
2021
Author(s) : Thong Meow Keong Source :
NEW ENGLAND JOURNAL OF MEDICINE
DOI :
10.1056/NEJMc2105064
|
| 19. |
beta-Thalassemias
2021
Author(s) : Thong Meow Keong Source :
NEW ENGLAND JOURNAL OF MEDICINE
DOI :
10.1056/NEJMc2105064
|
| 20. |
Communication about positive BRCA1 and BRCA2 genetic test results and uptake of testing in relatives in a diverse Asian setting
2021
Author(s) : Thong Meow Keong Source :
Journal of Genetic Counseling
DOI :
10.1002/jgc4.1360
|
| 21. |
Oncologist-led BRCA counselling improves access to cancer genetic testing in middle-income Asian country, with no significant impact on psychosocial outcomes
2021
Author(s) : Thong Meow Keong, Woo Yin Ling Source :
Journal of Medical Genetics
DOI :
10.1136/jmedgenet-2020-107416
|
| 22. |
Communication about positive BRCA1 and BRCA2 genetic test results and uptake of testing in relatives in a diverse Asian setting
2021
Author(s) : Thong Meow Keong, Nur Aishah Binti Mohd Taib Source :
JOURNAL OF GENETIC COUNSELING
DOI :
10.1002/jgc4.1360
|
| 23. |
International perspectives on the implementation of reproductive carrier screening
2020
Author(s) : Thong Meow Keong Source :
PRENATAL DIAGNOSIS
|
| 24. |
Congenital myasthenic syndrome with novel pathogenic variants in the COLQ gene associated with the presence of antibodies to acetylcholine receptors
2020
Source :
JOURNAL OF CLINICAL NEUROSCIENCE
|
| 25. |
Growth hormone therapy for people with thalassaemia
2020
Author(s) : Thong Meow Keong Source :
COCHRANE DATABASE OF SYSTEMATIC REVIEWS
DOI :
10.1002/14651858.CD012284.pub3
|
| 26. |
Infantile neuroaxonal dystrophy in a pair of Malaysian siblings with progressive cerebellar atrophy: Description of an expanded phenotype with novel PLA2G6 variants
2020
Source :
Journal of Clinical Neuroscience
DOI :
10.1016/j.jocn.2019.08.111
|
| 27. |
Infantile neuroaxonal dystrophy in a pair of Malaysian siblings with progressive cerebellar atrophy: Description of an expanded phenotype with novel PLA2G6 variants
2020
Author(s) : Thong Meow Keong Source :
JOURNAL OF CLINICAL NEUROSCIENCE
|
| 28. |
Rare disease in Malaysia: Challenges and solutions
2020
Author(s) : Thong Meow Keong Source :
PLOS ONE
|
| 29. |
Rare disease in Malaysia: Challenges and solutions
2020
Author(s) : Thong Meow Keong Source :
PLOS ONE
DOI :
10.1371/journal.pone.0230850
|
| 30. |
Rare disease in Malaysia: Challenges and solutions.
2020
Author(s) : Thong Meow Keong Source :
PLoS ONE
DOI :
10.1371/journal.pone.0230850
|
| 31. |
Congenital myasthenic syndrome with novel pathogenic variants in the COLQ gene associated with the presence of antibodies to acetylcholine receptors
2020
Author(s) : Thong Meow Keong, Gan Chin Seng Source :
Journal of Clinical Neuroscience
DOI :
10.1016/j.jocn.2019.12.007
|
| 32. |
Rare disease in Malaysia: Challenges and solutions
2020
Author(s) : Thong Meow Keong Source :
PLoS ONE
|
| 33. |
Congenital myasthenic syndrome with novel pathogenic variants in the COLQ gene associated with the presence of antibodies to acetylcholine receptors.
2020
Author(s) : Thong Meow Keong Source :
J Clin Neurosciences
DOI :
10.1016/j.jocn.2019.12.007
|
| 34. |
Rubinstein-Taybisyndrome in diverse populations
2020
Author(s) : Thong Meow Keong Source :
AMERICAN JOURNAL OF MEDICAL GENETICS PART A
DOI :
10.1002/ajmg.a.61888
|
| 35. |
International perspectives on the implementation of reproductive carrier screening
2020
Author(s) : Thong Meow Keong Source :
PRENATAL DIAGNOSIS
|
| 36. |
Turner syndrome in diverse populations
2020
Author(s) : Thong Meow Keong Source :
AMERICAN JOURNAL OF MEDICAL GENETICS PART A
|
| 37. |
Turner syndrome in diverse populations
2020
Author(s) : Thong Meow Keong Source :
AMERICAN JOURNAL OF MEDICAL GENETICS PART A
|
| 38. |
Growth hormone therapy for people with thalassaemia.
2020
Author(s) : Thong Meow Keong Source :
Cochrane Database of Systematic Reviews
DOI :
10.1002/14651858.CD012284.pub3.
|
| 39. |
Rubinstein-Taybi syndrome in diverse populations
2020
Author(s) : Thong Meow Keong Source :
American Journal of Medical Genetics A
DOI :
10.1002/ajmg.a.61888.
|
| 40. |
Infantile neuroaxonal dystrophy in a pair of Malaysian siblings with progressive cerebellar atrophy: Description of an expanded phenotype with novel PLA2G6 variants
2020
Source :
JOURNAL OF CLINICAL NEUROSCIENCE
|
| 41. |
Turner syndrome in diverse populations.
2020
Author(s) : Thong Meow Keong Source :
Am J Med Genet A
DOI :
10.1002/ajmg.a.61461
|
| 42. |
Congenital myasthenic syndrome with novel pathogenic variants in the COLQ gene associated with the presence of antibodies to acetylcholine receptors
2020
Source :
JOURNAL OF CLINICAL NEUROSCIENCE
|
| 43. |
Effects of Digital game-based learning on elementary science learning: A systematic review.
2019
Author(s) : Loh Sau Cheong, Thong Meow Keong Source :
IEEE Access
DOI :
10.1109/ACCESS.2019.2916324
|
| 44. |
Cornelia de Lange syndrome in diverse populations
2019
Author(s) : Thong Meow Keong Source :
AMERICAN JOURNAL OF MEDICAL GENETICS PART A
|
| 45. |
A Digital Game-Based Learning Method to Improve Students Critical Thinking Skills in Elementary Science
2019
Author(s) : Thong Meow Keong Source :
IEEE ACCESS
|
| 46. |
A comparative study of patients' perceptions of genetic and genomic medicine services in California and Malaysia
2019
Author(s) : Thong Meow Keong Source :
J Community Genet
DOI :
10.1007/s12687-018-0399-8.
|
| 47. |
Effects of Digital Game-Based Learning on Elementary Science Learning: A Systematic Review
2019
Author(s) : Thong Meow Keong Source :
IEEE ACCESS
|
| 48. |
Psychosocial impact of undergoing prostate cancer screening for men with BRCA1 or BRCA2 mutations
2019
Author(s) : Thong Meow Keong Source :
BJU INTERNATIONAL
|
| 49. |
International perspectives on the implementation of reproductive carrier screening
2019
Author(s) : Thong Meow Keong Source :
Prenatal Diagnosis
DOI :
10.1002/pd.5611
|
| 50. |
Quality of life of children with tuberous sclerosis complex
2019
Source :
ARCHIVES OF DISEASE IN CHILDHOOD
|
| 51. |
Training in clinical genetics and genetic counseling in Asia
2019
Author(s) : Thong Meow Keong Source :
Am J Med Genet C Semin Med Genet.
DOI :
10.1002/ajmg.c.31703
|
| 52. |
Asia Pacific Society of Human Genetics (APSHG) from conception to 2019: 13 years of collaboration to tackle congenital malformation and genetic disorders in Asia
2019
Author(s) : Thong Meow Keong Source :
Am J Med Genet C Semin Med Genet.
DOI :
10.1002/ajmg.c.31701
|
| 53. |
Ten-year trend in prevalence and outcome of Down syndrome with congenital heart disease in a middle-income country
2019
Author(s) : Thong Meow Keong, Norazah Binti Zahari Source :
European Journal of Pediatrics
DOI :
10.1007/s00431-019-03403-x
|
| 54. |
A Digital Game-Based Learning Method to Improve Students Critical Thinking Skills in Elementary Science
2019
Source :
IEEE ACCESS
|
| 55. |
Effects of Digital Game-Based Learning on Elementary Science Learning: A Systematic Review
2019
Source :
IEEE ACCESS
|
| 56. |
Clinical, biochemical and genetic profiles of patients with mucopolysaccharidosis type IVA (Morquio A syndrome) in Malaysia: the first national natural history cohort study
2019
Author(s) : Thong Meow Keong Source :
ORPHANET JOURNAL OF RARE DISEASES
|
| 57. |
Training in clinical genetics and genetic counseling in Asia
2019
Author(s) : Thong Meow Keong Source :
AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS
|
| 58. |
Cornelia de Lange syndrome in diverse populations.
2019
Author(s) : Thong Meow Keong Source :
Am J Med Genet A
DOI :
10.1002/ajmg.a.61033.
|
| 59. |
Clinical, biochemical and genetic profiles of patients with mucopolysaccharidosis type IVA (Morquio A syndrome) in Malaysia: the first national natural history cohort study.
2019
Author(s) : Thong Meow Keong Source :
Orphanet J Rare Dis.
DOI :
10.1186/s13023-019-1105-6.
|
| 60. |
Ten-year trend in prevalence and outcome of Down syndrome with congenital heart disease in a middle-income country.
2019
Author(s) : Thong Meow Keong Source :
Eur J Pediatr
DOI :
10.1007/s00431-019-03403-x
|
| 61. |
Ten-year trend in prevalence and outcome of Down syndrome with congenital heart disease in a middle-income country
2019
Author(s) : Thong Meow Keong Source :
EUROPEAN JOURNAL OF PEDIATRICS
|
| 62. |
Introducing clinical ethics consultation service in Malaysia: A SWOT analysis.
2019
Author(s) : Thong Meow Keong Source :
Clinical Ethics
DOI :
10.1177/1477750919839913
|
| 63. |
Quality of life of children with tuberous sclerosis complex
2019
Author(s) : Thong Meow Keong Source :
ARCHIVES OF DISEASE IN CHILDHOOD
|
| 64. |
Achieving the targets of sustainable development goals (2030 agenda) for congenital disorders in Asia: Bottlenecks and interventions
2019
Author(s) : Thong Meow Keong Source :
AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS
|
| 65. |
Asia Pacific Society of Human Genetics (APSHG) from conception to 2019: 13 years of collaboration to tackle congenital malformation and genetic disorders in Asia
2019
Author(s) : Thong Meow Keong Source :
AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS
|
| 66. |
Achieving the targets of sustainable development goals (2030 agenda) for congenital disorders in Asia: Bottlenecks and interventions.
2019
Author(s) : Thong Meow Keong Source :
Am J Med Genet C Semin Med Genet.
DOI :
10.1002/ajmg.c.31690.
|
| 67. |
Quality of life of children with tuberous sclerosis complex.
2019
Author(s) : Thong Meow Keong Source :
Arch Dis Child
DOI :
10.1136/archdischild-2018-316394
|
| 68. |
Medical genetics in developing countries in the Asia-Pacific region: challenges and opportunities
2018
Source :
Genet Med
DOI :
10.1038/s41436-018-0135-0.
|
| 69. |
An audiological evaluation of syndromic and non-syndromic craniosynostosis in pre-school going children
2018
Source :
International Journal of Pediatric Otorhinolaryngology
DOI :
10.1016/j.ijporl.2018.03.010
|
| 70. |
A case-control study of breast cancer risk factors in 7,663 women in Malaysia
2018
Author(s) : Thong Meow Keong Source :
PLOS ONE
|
| 71. |
A Report on Ten Asia Pacific Countries on Current Status and Future Directions of the Genetic Counseling Profession: The Establishment of the Professional Society of Genetic Counselors in Asia
2018
Author(s) : Thong Meow Keong Source :
Journal of Genetic Counseling
DOI :
10.1007/s10897-017-0115-6.
|
| 72. |
Cranial neural tube defect after trimethoprim exposure
2018
Author(s) : Thong Meow Keong, Noraishah Mydin Binti Haji Abdul Aziz, Dharmendra A/l Ganesan, Zamri Bin Chik, Julia Anak Patrick Engkasan, Noreena Binti Nordin Source :
BMC Research Notes
DOI :
10.1186/s13104-018-3593-1
|
| 73. |
GWAS signals revisited using human knockouts.
2018
Author(s) : Thong Meow Keong Source :
Genet Med.
DOI :
doi: 10.1038/gim.2017.78.
|
| 74. |
A case-control study of breast cancer risk factors in 7,663 women in Malaysia.
2018
Author(s) : Thong Meow Keong Source :
PLoS One
DOI :
10.1371/journal.pone.0203469
|
| 75. |
Williams-Beuren syndrome in diverse populations
2018
Source :
Am J Med Genet A.
DOI :
10.1002/ajmg.a.38672.
|
| 76. |
Down Syndrome in Diverse Populations
2017
Author(s) : Thong Meow Keong Source :
AMERICAN JOURNAL OF MEDICAL GENETICS PART A
|
| 77. |
Deregulation of microRNAs in blood and skeletal muscles of myotonic dystrophy type 1 patients
2017
Source :
Neurology India
DOI :
10.4103/neuroindia.NI_237_16
|
| 78. |
Family history of early infant death correlates with earlier age at diagnosis but not shorter time to diagnosis for severe combined immunodeficiency.
2017
Author(s) : Thong Meow Keong Source :
Frontiers in Immunology
DOI :
10.3389/fimmu.2017.00808.
|
| 79. |
Noonan Syndrome in Diverse Populations
2017
Author(s) : Thong Meow Keong, Premala A/p Muthukumarasamy Source :
Am J Med Genet A
DOI :
10.1002/ajmg.a.38362.
|
| 80. |
22q11.2 deletion syndrome in diverse populations
2017
Author(s) : Thong Meow Keong Source :
AMERICAN JOURNAL OF MEDICAL GENETICS PART A
|
| 81. |
Growth hormone therapy for people with thalassaemia.
2017
Author(s) : Thong Meow Keong Source :
Cochrane Database Syst Rev
DOI :
10.1002/14651858.CD012284.pub2
|
| 82. |
3-methylglutaconic aciduria, a frequent but underrecognized finding in carbamoyl phosphate synthetase I deficiency
2017
Source :
Clinica Chimica Acta
DOI :
10.1016/j.cca.2017.05.023
|
| 83. |
Analysis of CTG repeat length variation in the DMPK gene in the general population and the molecular diagnosis of myotonic dystrophy type 1 in Malaysia
2017
Author(s) : Thong Meow Keong Source :
BMJ OPEN
|
| 84. |
A Report on Ten Asia Pacific Countries on Current Status and Future Directions of the Genetic Counseling Profession: The Establishment of the Professional Society of Genetic Counselors in Asia
2017
Author(s) : Thong Meow Keong Source :
Journal of Genetic Counseling
DOI :
10.1007/s10897-017-0115-6.
|
| 85. |
Sandhoff disease in two siblings of a Malaysian family: Description of novel beta hexosaminidase mutations, magnetic resonance imaging, and spectroscopic findings.
2017
Source :
Neurology India
|
| 86. |
The Prevalence and Distribution of Spina Bifida in a Single Major Referral Center in Malaysia
2017
Source :
Frontiers in Pediatrics
DOI :
10.3389/fped.2017.00237
|
| 87. |
Congenital muscular dystrophy due to laminin 2 (merosin) deficiency (MDC1A) in an ethnic Malay girl.
2017
Source :
Neurology Asia
|
| 88. |
Analysis of CTG repeat length variation in the DMPK gene in the general population and the molecular diagnosis of myotonic dystrophy type 1 in Malaysia.
2017
Author(s) : Thong Meow Keong, Mohd Taufik Bin Ishak, Wong Kum Thong, Azlina Binti Ahmad Annuar, Goh Khean Jin Source :
BMJ Open
DOI :
10.1136/bmjopen-2015-010711.
|
| 89. |
Effects of sharing information on drug administration errors in pediatric wards: a pre-post intervention study
2017
Author(s) : Thong Meow Keong Source :
THERAPEUTICS AND CLINICAL RISK MANAGEMENT
|
| 90. |
Down syndrome in diverse populations.
2017
Author(s) : Premala A/p Muthukumarasamy, Thong Meow Keong Source :
American Journal of Medical Genetics Part A
DOI :
doi: 10.1002/ajmg.a.38043
|
| 91. |
Effects of Sharing Information on Drug Administration Errors in Paediatric Wards: A Pre-Post Intervention Study.
2017
Author(s) : Thong Meow Keong, Asma Binti Omar Source :
Therapeutics and Clinical Risk Management
DOI :
10.2147/TCRM.S128504
|
| 92. |
22q11.2 deletion syndrome in diverse populations
2017
Author(s) : Premala A/p Muthukumarasamy, Thong Meow Keong Source :
American Journal of Medical Genetics A
DOI :
10.1002/ajmg.a.38199
|
| 93. |
Identification of germline alterations in breast cancer predisposition genes among Malaysian breast cancer patients using panel testing
2016
Author(s) : Nur Aishah Binti Mohd Taib, Thong Meow Keong Source :
Clinical Genetics
|
| 94. |
Identification of germline alterations in breast cancer predisposition genes among Malaysian breast cancer patients using panel testing. Ng PS1, Wen WX2, Fadlullah MZ3, Yoon SY4, Lee SY5, Thong MK6, Yip CH7, Mohd Taib NA8,9, Teo SH10,11,12.
2016
Author(s) : Ng Pei Sze, Wen Wei Xiong, Yoon Sook Yee, Yip Cheng Har, Teo Soo Hwang, Thong Meow Keong, Nur Aishah Binti Mohd Taib Source :
Clinical Genetics
|
| 95. |
Erratum to: Recurrent mutation testing of BRCA1 and BRCA2 in Asian breast cancer patients identify carriers in those with presumed low risk by family history
2015
Author(s) : Peter Choon Eng Kang, Phuah Sze Yee, Kavitta Sivanandan, Kang In Nee , Eswary Thirthagiri, Jian Jun Liu, Norhashimah Hassan, Sook-yee Yoon, Miao Hui, A.prof Mikael Hartman, Prof Adjung Yip Cheng Har, Teo Soo Hwang, Thong Meow Keong, Nur Aishah Binti Mohd Taib Source :
Breast Cancer Research and Treatment
|
| 96. |
Compound Heterozygous Mutations in TTC7A cause familial multiple intestinal atresias and severe combined immunedeficiency
2015
Author(s) : Amira Sariyati Binti Firdaus, Mahmoud Danaee Source :
CLINICAL GENETICS
|
| 97. |
Identifying the need for a multidisciplinary approach for early recognition of mucopolysaccharidosis VI (MPS VI)
2015
Author(s) : Thong Meow Keong Source :
Molecular Genetics and Metabolism
|
| 98. |
The first Malay database toward the ethnic- specific target molecular variation.
2015
Author(s) : Thong Meow Keong Source :
BMC Res Notes
|
| 99. |
Beyond Critical Congenital Heart Disease: Newborn Screening Using Pulse Oximetry for Neonatal Sepsis and Respiratory Diseases in a Middle-Income Country.
2015
Source :
PLoS One.
|
| 100. |
Identifying the need for a multidisciplinary approach for early recognition of mucopolysaccharidosis VI (MPS VI).
2015
Author(s) : Kaustuv Bhattacharya, Michael Fietz, Shanti Balasubramaniam, Thong Meow Keong Source :
Mol Genet Metab.
|
| 101. |
Birth defects registries in the genomics era: challenges and opportunities for developing countries
2014
Author(s) : Thong Meow Keong Source :
Frontiers in Pediatrics
|
| 102. |
Recurrent mutation testing of BRCA1 and BRCA2 in Asian breast cancer patients identify carriers in those with presumed low risk by family history
2014
Author(s) : Thong Meow Keong Source :
Breast Cancer Research and Treatment
|
| 103. |
Single mitochondrial DNA deletions in chronic progressive external ophthalmoplegia (CPEO) and Kearns-Sayre syndrome (KSS) patients from a multiethnic Asian population
2014
Author(s) : Thong Meow Keong Source :
Neurology Asia
|
| 104. |
Compound heterozygous mutations in TTC7A cause familial multiple intestinal atresia and severe combined Deficiency immunodeficiency.
2014
Author(s) : Thong Meow Keong, Koh Mia Tuang Source :
Clinical Genetics
|
| 105. |
Prevalence of PALB2 Mutations in Breast Cancer Patients in Multi-Ethnic Asian Population in Malaysia and Singapore
2013
Author(s) : Thong Meow Keong Source :
Plos One
|
| 106. |
Neural Tube Defects in Malaysia: Data from the Malaysian National Neonatal Registry
2013
Author(s) : Thong Meow Keong Source :
Journal of Tropical Pediatrics
|
| 107. |
Genetic Polymorphisms in LDLR, APOB, PCSK9 and Other Lipid Related Genes Associated with Familial Hypercholesterolemia in Malaysia
2013
Author(s) : Thong Meow Keong Source :
Plos One
|
| 108. |
Genetic polymorphisms in LDLR, APOB, PCSK9 and other lipid related genes associated with Familial hypercholesterolemia in Malaysia
2013
Author(s) : Thong Meow Keong, Rosmawati Binti Mohamed, Wan Azman Bin Wan Ahmad, Jamunarani A/p S Vadivelu Source :
Plos One
|
| 109. |
Genetic Counseling Services and Development of Training Programs in Malaysia.
2013
Author(s) : Thong Meow Keong Source :
Journal of Genetic Counseling
|
| 110. |
Prevalence of PALB2 mutations in breast cancer patients in multi- ‐ethnic Asian population in Malaysia and Singapore
2013
Author(s) : Teo Soo Hwang, Yip Cheng Har, Phuah Sze Yee, Lee Sheau Yee, Peter Kang, Kang In Nee, Yoon Sook-yee, Thong Meow Keong, Nur Aishah Binti Mohd Taib Source :
PlosOne
|
| 111. |
Genetic Counseling Services and Development of Training Programs in Malaysia
2013
Author(s) : Thong Meow Keong Source :
Journal of Genetic Counseling
|
| 112. |
Neural Tube Defects in Malaysia: Data from the Malaysian National Neonatal Registry.
2013
Author(s) : Thong Meow Keong Source :
J Trop Pediatr.
DOI :
10.1093/tropej/fmt026
|
| 113. |
Genetic Counseling/Consultation in South-East Asia: A Report from the Workshop at the 10th Asia Pacific Conference on Human Genetics
2013
Author(s) : Thong Meow Keong Source :
Journal of Genetic Counseling
|
| 114. |
Tropical distal renal tubular acidosis: clinical and
epidemiological studies in 78 patients.
2012
Author(s) : Thong Meow Keong Source :
QJM
|
| 115. |
A tribute to Keiko Kobayashi and her work on citrin
deficiency.
2012
Author(s) : Thong Meow Keong Source :
Molecular Genetics and Metabolism
|
| 116. |
Current diagnosis and management of mucopolysaccharidosis VI in the Asia-Pacific region
2012
Author(s) : Thong Meow Keong Source :
Molecular Genetics and Metabolism
|
| 117. |
Tropical distal renal tubular acidosis: clinical and epidemiological studies in 78 patients
2012
Author(s) : Thong Meow Keong Source :
Qjm-an International Journal of Medicine
|
| 118. |
Comparable frequency of BRCA1, BRCA2 and TP53 germline
mutations in a multi-ethnic Asian cohort suggests TP53
screening should be offered together with BRCA1/2
screening to early-onset breast cancer patients.
2012
Author(s) : Chin Kin Fah, Nur Aishah Binti Mohd Taib, Hany Binti Mohd Ariffin, Thong Meow Keong, Teo Soo Hwang Source :
Breast Cancer Research
|
| 119. |
Current diagnosis and management of mucopolysaccharidosis
VI in the Asia-Pacific region.
2012
Author(s) : Thong Meow Keong Source :
Mol Genet Metab
|
| 120. |
Comparable frequency of BRCA1, BRCA2 and TP53 germline mutations in a multi-ethnic Asian cohort suggests TP53 screening should be offered together with BRCA1/2 screening to early-onset breast cancer patients
2012
Author(s) : Thong Meow Keong Source :
Breast Cancer Research
|
| 121. |
The frequency of common mitochondrial DNA mutations in
a cohort of Malaysian patients with specific
mitochondrial encephalomyopathy syndromes
2011
Author(s) : Wong Kum Thong, Chong Jia Woei, Thong Meow Keong, Azlina Binti Ahmad Annuar, Goh Khean Jin Source :
Neurology Asia
|
| 122. |
Genetic counseling for patients and families with hereditary breast and ovarian cancer in a developing Asian country: an observational descriptive study.
2011
Source :
Familial Cancer
|
| 123. |
Genetic counseling for patients and families with hereditary breast and ovarian cancer in a developing Asian country: an observational descriptive study
2011
Author(s) : Thong Meow Keong Source :
Familial Cancer
|
| 124. |
Genetic Counseling For Patients and Families with
Hereditary Breast and Ovarian Cancer in a
Developing
Asian Country: An Observational Descriptive Study.
2011
Author(s) : Thong Meow Keong, Sook-yee Yoon, Yip Cheng Har, Teo Soo Hwang, Nur Aishah Binti Mohd Taib Source :
Familial Cancer
|
| 125. |
Students¿f Perception and Acceptance of Problem-based
Learning (PBL) in a Hybrid Traditional-PBL Curriculum
2011
Author(s) : Thong Meow Keong Source :
J Med Education
|
| 126. |
Neonatal intrahepatic cholestasis caused by citrin
deficiency in two Malaysian Chinese siblings: outcome
at one year of life.
2010
Author(s) : Keiko Kobayashi, Thong Meow Keong Source :
Singapore Medical Journal
|
| 127. |
Large BRCA1 and BRCA2 genomic rearrangements in Malaysian high risk breast-ovarian cancer families
2010
Author(s) : Thong Meow Keong Source :
Breast Cancer Research and Treatment
|
| 128. |
Exercise induced cramps and myoglobinuria in
dystrophinopathy - a report of three Malaysian cases.
2010
Source :
Neurology Asia
|
| 129. |
Adenylosuccinate lyase deficiency in a Malaysian
patient, with novel adenylosuccinate lyase gene
mutations.
2010
Author(s) : Chen Bee Chin, Thong Meow Keong, Ivan Mcgown Source :
J Inherit Metab Dis
DOI :
10.1007/s10545-010-9056-z.
|
| 130. |
Exercise induced cramps and myoglobinuria in dystrophinopathy - a report of three Malaysian patients
2010
Author(s) : Thong Meow Keong Source :
Neurology Asia
|
| 131. |
Neonatal intrahepatic cholestasis caused by citrin deficiency in two Malaysian siblings: outcome at one year of life
2010
Author(s) : Thong Meow Keong Source :
Singapore Medical Journal
|
| 132. |
Congenital disorder of glycosylation type Ia in
a Malaysian family: Clinical outcome and
description of a novel PMM2 mutation
2009
Author(s) : Thong Meow Keong, Michael Fietz Source :
Journal of Inherited Metabolic Disease
|
| 133. |
Clinical and Pathologic Differences Between BRCA1-, BRCA2-, and Non-BRCA-Associated Breast Cancers in a Multiracial Developing Country
2009
Author(s) : Thong Meow Keong Source :
World Journal of Surgery
|
| 134. |
MECP2 Mutations in Malaysian Rett Syndrome Patients
2009
Source :
Singapore Medical Journal
|
| 135. |
MECP2 mutations in Malaysian Rett syndrome patients
2009
Author(s) : Thong Meow Keong Source :
Singapore Medical Journal
|
| 136. |
Evaluation of BRCA1 and BRCA2 mutations and risk-prediction models in a typical Asian country (Malaysia) with a relatively low incidence of breast cancer
2008
Author(s) : Thong Meow Keong Source :
Breast Cancer Research
|
| 137. |
An Overview of Computer-Aided Medical Pedigree
Drawing Systems.
2008
Author(s) : Thong Meow Keong Source :
Chiang Mai University Journal of Natural Sciences
|
| 138. |
Evaluation of BRCA1 and BRCA2 risk prediction
models in a typical Asian country (Malaysia) with
relatively low incidence of breast cancer.
2008
Author(s) : Thong Meow Keong Source :
Breast Cancer Research
|
| 139. |
Spectrum of Inherited Metabolic Disorders in Malaysia.
2008
Author(s) : Thong Meow Keong Source :
Annals Academy of Medicine, Singapore
|
| 140. |
Reducing the Impact of Genetic Diseases: Curative and
Preventive Aspects.
2006
Author(s) : Thong Meow Keong Source :
JUMMEC- Journal of the University of Malaya Medical Center
|
| 141. |
Prenatal detection of birth defects in a Malaysian population: Estimation of the influence of termination of pregnancy on birth prevalence in a developing country
2006
Author(s) : Thong Meow Keong Source :
Australian New Zealand Journal of Obstetrics Gynaecology
|
| 142. |
Prenatal detection of birth defects in a
Malaysian population: Estimation of the influence
of termination of pregnancy on birth prevalence
in a developing country.
2006
Author(s) : Thong Meow Keong Source :
Australian & New Zealand J of Obstetrics & Gynaecology
|
| 143. |
Further delineation of Al-Gazali syndrome (multiple sketetal abnormalities with anterior segment anomalies of the eye and early lethality) in a Malaysian family
2005
Author(s) : Thong Meow Keong Source :
Clinical Dysmorphology
|
| 144. |
Diagnosis and management of Duchenne Muscular Dystrophy in a developing country over a 10-year period.
2005
Author(s) : Thong Meow Keong, Wong Kum Thong Source :
Developmental Medicine and Child Neurology
|
| 145. |
Diagnosis and management of Duchenne muscular dystrophy in a developing country over a 10-year period
2005
Author(s) : Thong Meow Keong Source :
Developmental Medicine and Child Neurology
|
| 146. |
The spectrum of beta globin gene mutations in
children with beta- thalassaemia major from Kota
Kinabalu, Sabah, Malaysia.
2005
Author(s) : Thong Meow Keong Source :
Singapore Medical Journal
|
| 147. |
A population-based study of birth defects in Malaysia.
2005
Author(s) : Thong Meow Keong Source :
Annals of Human Biology
|
| 148. |
Characterisation of beta-globin gene mutations in Malaysian children: A Strategy for the control of beta-thalassaemia in a developing country.
2005
Author(s) : Thong Meow Keong Source :
Journal of Tropical Paediatrics
|
| 149. |
Further delineation of Al-Gazali syndrome in a Malaysian family
2005
Author(s) : Thong Meow Keong Source :
Clinical Dysmorphology
|
| 150. |
A population-based study of birth defects in Malaysia
2005
Author(s) : Thong Meow Keong Source :
Annals of Human Biology
|
| 151. |
Characterisation of beta-globin gene mutations in malaysian children: A strategy for the control of beta-thalassaemia in a developing country
2005
Author(s) : Thong Meow Keong Source :
Journal of Tropical Pediatrics
|
| 152. |
Effects of MECP2 mutation type, location and X-inactivation in modulating Rett Syndrome phenotype.
2003
Author(s) : Thong Meow Keong Source :
American Journal of Medical Genetics
|
| 153. |
Mucopolysaccharidosis: airway risk to
anaesthetists. Asean Journal of Anaesthesiology
2003
Author(s) : Thong Meow Keong Source :
Asean Journal of Anaesthesiology
|
| 154. |
Problem-Based Learning: Monitoring and Searching for an Appropriate Tune.
2002
Author(s) : Junedah Binti Sanusi, Thong Meow Keong, Christina Tan Phoay Lay, Nor Azila Binti Mohd Adnan, Sim Si Mui, Tan Nget Hong, Atiya Bin Abdul Sallam, John George Source :
Journal of Medical Education (Taiwan)
|
| 155. |
Ten novel FBN2 mutations in congenital contractural arachnodactyly: delineation of the molecular pathogenesis and clinical phenotype.
2002
Author(s) : Thong Meow Keong Source :
Human Mutation
|
| 156. |
Combine-ARMS: A rapid and cost-effective protocol for molecular characterization of beta-thalassemia in Malaysia
2001
Author(s) : Thong Meow Keong Source :
Genetic Testing
|
| 157. |
Combine-ARMS: A rapid and cost-effective protocol for molecular characterization of beta-thalassaemia in Malaysia
2001
Source :
Genetic Testing
|
| 158. |
Acampomelic campomelic dysplasia with SOX9
mutation.
2000
Author(s) : Thong Meow Keong Source :
Am J Med Genet
|
| 159. |
Screening for undetected beta-globin gene mutations using chemical cleavage of mismatch method in patients registered with the Thalassaemia Registry, University Hospital Kuala Lumpur
1999
Author(s) : Thong Meow Keong Source :
Asia-Pacific Journal of Molecular Biology and Biotechnology
|
| 160. |
Screening for undetected beta-globin gene mutations
using chemical cleavage of mutation method in patients
registered with the Thalassaemia Registry, University
Hospital Kuala Lumpur
1999
Author(s) : Thong Meow Keong Source :
Asia-Pacific Journal of Molecular Biology and Biotechnology
|
| 161. |
A child with hemimegalencephaly, hemihypertrophy, macrocephaly, cutaneous vascular malformation, psychomotor retardation and intestinal lymphangiectasia a diagnostic dilemma.
1999
Author(s) : Thong Meow Keong Source :
Clinical Dysmorphology
|
| 162. |
A single large deletion accounts for all beta-globin gene mutations in twenty families in Sabah (north Borneo), Malaysia
1999
Author(s) : Thong Meow Keong Source :
Human Mutation
|
| 163. |
Undescended testes: incidence in 1002 consecutive male infants and outcome at one year of age.
1998
Author(s) : Thong Meow Keong Source :
Pediatr Surg Int
|
| 164. |
Dengue shock syndrome and acute respiratory distress syndrome
1998
Author(s) : Thong Meow Keong Source :
Lancet
|
| 165. |
Undescended testes: incidence in 1,002 consecutive male infants and outcome at 1 year of age
1998
Author(s) : Thong Meow Keong Source :
Pediatric Surgery International
|
| 166. |
Memorable patients - Down but not out
1998
Author(s) : Thong Meow Keong Source :
British Medical Journal
|
| 167. |
Distal renal tubular acidosis and hereditary elliptocytosis in a single family.
1997
Author(s) : Thong Meow Keong Source :
Singapore Medical Journal
|
| 168. |
B Streptococcus: Maternal carriage rate and early neonatal septicaemia.
1997
Author(s) : Thong Meow Keong, Lim Chin Theam Source :
Annals Academy of Medicine, Singapore
|
| 169. |
Supernumerary chromosomes in mosaic Turner Syndrome.
1996
Author(s) : Thong Meow Keong Source :
Med J Malaysia
|
| 170. |
X-linked lymphoproliferative disease in a
Malaysian
family
1996
Author(s) : Thong Meow Keong, Hany Binti Mohd Ariffin Source :
Singapore Med. Journal
|
| 171. |
The Lissencephalic Syndromes.
1996
Author(s) : Thong Meow Keong Source :
Med J Malaysia
|
| 172. |
Dengue-associated adult respiratory distress syndrome.
1995
Author(s) : Thong Meow Keong, Lam Sai Kit Source :
Annals of Tropical Paediatrics
|
| 173. |
DENGUE-ASSOCIATED ADULT-RESPIRATORY-DISTRESS-SYNDROME
1995
Author(s) : Thong Meow Keong Source :
Annals of Tropical Paediatrics
|
| 174. |
Malignant Rhabdoid Tumour of the Kidney.
1994
Author(s) : Thong Meow Keong Source :
Singapore Paediatr J
|
BOOK
| NO | DETAILS OF BOOK |
|---|---|
| 1. |
White Paper: Rare Diseases in Malaysia.
2019
Author(s) : Thong Meow Keong |
| 2. |
Apakah itu sindrom Down? Edisi Kedua
2016
Author(s) : Thong Meow Keong |
| 3. |
Problem-Based Learning in Medical Sciences.
2012
Author(s) : Thong Meow Keong, Lian Lay Hoong, Christina Tan Phoay Lay, Sim Si Mui, Jamunarani A/p S Vadivelu, Kanthimathi A/p M S Subramaniam |
| 4. |
Rare Journeys of Love
2011
Author(s) : Thong Meow Keong |
| 5. |
Handbook of Hospital Paediatrics Second Edition
2009
Author(s) : Thong Meow Keong |
| 6. |
Management of Birth Defects and Haemoglobin
Disorders
2006
Author(s) : Thong Meow Keong |
| 7. |
Handbook of Hospital Paediatrics
2005
Author(s) : Thong Meow Keong |
| 8. |
From peas to chips: the globalisation of genetics.
2003
Author(s) : Thong Meow Keong |
| 9. |
Health Technology Assessment Report on Management of
Thalassaemia, Ministry of Health Malaysia
2003
Author(s) : Thong Meow Keong |
CHAPTER IN BOOK
| NO | DETAILS OF CHAPTER IN BOOK |
|---|---|
| 1. |
Clinical Genetics
2019
Author(s) : Thong Meow Keong |
| 2. |
Problem-Based Learning in the Clinical Years.
2012
Author(s) : Thong Meow Keong, Lian Lay Hoong |
| 3. |
Development and Design of Case Scenarios.
2012
|
| 4. |
Clinical Dysmorphology and Birth Defects Registry in
the Asia-Pacific Region
2012
Author(s) : Thong Meow Keong |
| 5. |
What are Rare Disorders
2011
Author(s) : Thong Meow Keong |
| 6. |
Birth Defects, Genetics and the Last Best Hope on
Earth.
2010
Author(s) : Thong Meow Keong |
| 7. |
Clinical Genetics & Genetic Counselling
2009
Author(s) : Thong Meow Keong |
| 8. |
Cardiorespiratory arrest.
2009
Author(s) : Thong Meow Keong |
| 9. |
Birth Defects & Skeletal Dysplasias
2009
Author(s) : Thong Meow Keong |
| 10. |
Poisoning in Children
2009
Author(s) : Thong Meow Keong |
| 11. |
Genetic Testing and Metabolic Evaluation.
2009
Author(s) : Thong Meow Keong |
PROCEEDING
| NO | DETAILS OF PROCEEDING |
|---|---|
| 1. |
Genetic and genomic testing in children: clinical, laboratory and ethical issues.
2019
Author(s) : Thong Meow Keong |
| 2. |
Ethical issues, genetic testing and screening in Paediatrics
2019
Author(s) : Thong Meow Keong |
| 3. |
Treatable inherited diseases revisited
2019
Author(s) : Thong Meow Keong |
| 4. |
Achieving SDGs for Congenital Disorders in Asia: Opportunities and Challenges
2019
Author(s) : Thong Meow Keong |
| 5. |
Genetics of thalassaemia and inherited conditions
2019
Author(s) : Thong Meow Keong |
| 6. |
Entrustable Professional Activities as an alternative assessment tool for entry into Malaysian Professional Paediatrics postgraduate training program
2019
Author(s) : Thong Meow Keong |
| 7. |
2nd UM-CUHK Certificate Course in Clinical Genetics and Genomics
2018
Author(s) : Thong Meow Keong |
| 8. |
Clinical utility and limitations of genetic and genomic testing.
2018
Author(s) : Thong Meow Keong |
| 9. |
Challenges in Interpretation of Genetic and Genomic Reports in the Clinic
2018
Author(s) : Thong Meow Keong |
| 10. |
Basic genetics with reference to muscle disease.
2018
Author(s) : Thong Meow Keong |
| 11. |
First UM-CUHK Certificate Course in Clinical Genetics and Genomics in conjunction with Paediatric Research Week 2017.
2017
Author(s) : Thong Meow Keong |
| 12. |
Treatment-focused genetic testing (TFGT)�is it too soon for Malaysia?
2015
Author(s) : Thong Meow Keong |
| 13. |
Comparative metabolomic analyses in term and preterm Malaysian infants.
2015
Author(s) : Thong Meow Keong |
| 14. |
Personalized and precision medicine: are we there yet?
2015
Author(s) : Thong Meow Keong |
| 15. |
Berardinelli-Seip congenital lipodystrophy and its diagnostic implications.
2015
Author(s) : Thong Meow Keong |
| 16. |
L-2-Hydroxyglutaric aciduria: a case report.
2015
|
| 17. |
Imprinting mutation of CDKN1C in Beckwith-Wiedemann Syndrome: inheritance, genetic counselling and surveillance.
2015
Author(s) : Thong Meow Keong |
| 18. |
Deregulation of specific microRNAs in whole blood and skeletal muscle of Myotonic Dystrophy type patients.
2014
Author(s) : Thong Meow Keong |
| 19. |
Characterisation of Malaysian children with Beckwith-Wiedemann syndrome and Russell-Silver syndrome using methylation-specific multiplex ligation-dependent probe amplification.
2014
Author(s) : Thong Meow Keong, Rozaida @ Poh Yuen Ying |
| 20. |
Methylation status in Malaysian children with Beckwith- Wiedemann Syndrome and Russell-Silver Syndrome.
2013
|
| 21. |
The Molecular Bases for Beckwith-Wiedemann Syndrome and Russell-Silver Syndrome.
2013
|
| 22. |
Early experience in a breast and ovarian cancer risk
management clinic in Malaysia.
2012
Author(s) : Thong Meow Keong, Nur Aishah Binti Mohd Taib |
| 23. |
BRCA1 & BRCA2 mutations in Malaysian breast cancer
patients.
2012
Author(s) : Thong Meow Keong, Nur Aishah Binti Mohd Taib |
| 24. |
Citrin Deficiency: Reflections on a Pan-Ethnic
Disorder and the Way Forward.
2012
Author(s) : Thong Meow Keong |
| 25. |
A Review of Genetic Counselling Service in 2005 and
2011 at the University of Malaya Medical Centre.
2012
Author(s) : Thong Meow Keong, Chew Hui Bein |
| 26. |
Classical Galactosemia with GALT mutations in a
Malaysian female: a 14-year follow-up.
2012
|
| 27. |
Citrin Deficiency in Malaysian Children: Clinical
&
Laboratory Presentation and Outcome.
2010
|
| 28. |
Genetic mutations in sarcoglycanopathies in a Malaysian population.
2010
Author(s) : Thong Meow Keong, Looi Ry, Goh Khean Jin, Azlina Binti Ahmad Annuar, Nortina Shahrizaila, Wong Kum Thong, Khoo Teik Beng, Terrence Thomas |
| 29. |
The Molecular Diagnosis of Myotonic Dystrophy in
Malaysia.
2010
Author(s) : Thong Meow Keong, Mohd Taufik Bin Ishak, Goh Khean Jin, Azlina Binti Ahmad Annuar, Wong Kum Thong |
| 30. |
PBL showing a P.B.L. (Positive, Buoyant, Lucid)
Trend? Graduating students self assessment
2008
Author(s) : Lian Lay Hoong, Thong Meow Keong |
| 31. |
Preimplantation Genetic Diagnosis and Controversies
2004
Author(s) : Thong Meow Keong |
| 32. |
Childhood renal cell carcinoma
2003
Author(s) : Thong Meow Keong, Yik Yee Ian |
| 33. |
Breast-feeding is possible even if mother and baby have phenylketonuria.
2000
Author(s) : Thong Meow Keong |
RESEARCH PROJECT
| GRANT | PROGRESS | STATUS |
|---|---|---|
|
Identification Of Candidate Gene Variants And Its Relevance In The Understanding Of Spina Bifida In Malaysia
Researcher(s) : Azizi Bin Abu Bakar, - |
|
end |
|
Creating New Learning Space In The Workplace: Entrustable Professional Activities (epas) As A Tool Of Learning And Assessment For Entry Into A Malaysian Professional Paediatric Training Program
|
|
end |
|
Metabolomic Analysis In Sick And Healthy Infants: A Novel Strategy In Personalized Medicine.
|
|
end |
RESEARCH COLLABORATOR
| GRANT | PROGRESS | STATUS |
|---|---|---|
|
Ephrinb1(efnb1), Ephb6 (ephb6) And Epha2 (epha2) As Gene Candidates For Spina Bifida
Researcher(s) : Associate Prof. Dr. Azlina Binti Ahmad Annuar, Prof. Dr. Thong Meow Keong |
|
end |
|
Molecular characterisation of Beckwith-Wiedemann syndrome and Russell-Silver syndrome affecting normal growth in Malaysian children
Researcher(s) : Prof. Dr. Thong Meow Keong, Mr. Mohd Taufik Bin Ishak |
|
end |
|
Pulse Oximetry Screening for Critical Congenital Heart Defects in apparently well term newborns
|
|
end |