ARTICLE IN ACADEMIC JOURNALS
NO | DETAILS OF ARTICLE IN ACADEMIC JOURNALS |
---|---|
1. |
Establishing an online resource to facilitate global collaboration and inclusion of underrepresented populations: Experience from the MJFF Global Genetic Parkinson's Disease Project
2023
Source : PLOS ONE DOI : 10.1371/journal.pone.0292180 |
2. |
Genetic Testing for Parkinson's Disease and Movement Disorders in Less Privileged Areas: Barriers and Opportunities
2023
Source : MOVEMENT DISORDERS CLINICAL PRACTICE DOI : 10.1002/mdc3.13903 |
3. |
Embracing Monogenic Parkinson's Disease: The MJFF Global Genetic PD Cohort
2023
Source : MOVEMENT DISORDERS DOI : 10.1002/mds.29288 |
4. |
Genetic study of early-onset Parkinson's disease in the Malaysian population
2023
Source : PARKINSONISM & RELATED DISORDERS DOI : 10.1016/j.parkreldis.2023.105399 |
5. |
Single-center Experience of Deep Brain Stimulation (DBS) Surgery in Malaysia
2023
Author(s) : Azlina Binti Ahmad Annuar,Lim Shen-yang Source : MOVEMENT DISORDERS |
6. |
Clinical Outcomes After Ventriculo-Peritoneal Shunting in Patients With Classic vs. Complex NPH
2022
Source : FRONTIERS IN NEUROLOGY DOI : 10.3389/fneur.2022.868000 |
7. |
A mixed method study on the impact of living with spinal muscular atrophy in Malaysia from patients' and caregivers' perspectives
2022
Author(s) : Azlina Binti Ahmad Annuar Source : ORPHANET JOURNAL OF RARE DISEASES DOI : 10.1186/s13023-022-02351-4 |
8. |
Rare homozygous PRKN exon 7 duplication in a Ibanese patient from Northwestern Borneo with young onset Parkinson?s disease
2022
Source : NEUROLOGY ASIA DOI : 10.54029/2022frs |
9. |
Underrepresented Populations in Parkinson's Genetics Research: Current Landscape and Future Directions
2022
Author(s) : Azlina Binti Ahmad Annuar,Lim Shen-yang Source : MOVEMENT DISORDERS DOI : 10.1002/mds.29126 |
10. |
Glucocerebrosidase (GBA) gene variants in a multi-ethnic Asian cohort with Parkinson's disease: mutational spectrum and clinical features
2022
Author(s) : Azlina Binti Ahmad Annuar,Kamal Azrin Bin Abdullah @ Kalai Arasu A/l Muthusamy,Lim Shen-yang,Tan Ai Huey Source : JOURNAL OF NEURAL TRANSMISSION DOI : 10.1007/s00702-021-02421-0 |
11. |
Clinical phenotype of Parkinson's disease with a homozygous PRKN p.Cys441Arg mutation
2021
Source : NEUROLOGY ASIA |
12. |
Hereditary Transthyretin Amyloidosis in Multi-Ethnic Malaysians
2021
Source : NEUROMUSCULAR DISORDERS DOI : 10.1016/j.nmd.2021.03.008 |
13. |
Association study of MCCC1/LAMP3 and DGKQ variants with Parkinson's disease in patients of Malay ancestry
2021
Author(s) : Azlina Binti Ahmad Annuar Source : NEUROLOGICAL SCIENCES |
14. |
Parkinson s disease with homozygous PINK1 p.Leu489Pro mutations in two Indian sisters.
2021
Author(s) : Goh Khean Jin,Tan Chong Tin,Norlisah Binti Mohd Ramli,Azlina Binti Ahmad Annuar,Lim Shen-yang,Tan Ai Huey Source : Neurology Asia |
15. |
Glucocerebrosidase (GBA) gene variants in a multi-ethnic Asian cohort with Parkinson's disease: mutational spectrum and clinical features
2021
Author(s) : Azlina Binti Ahmad Annuar Source : JOURNAL OF NEURAL TRANSMISSION |
16. |
A survey on patients' disease perception and the impact of the COVID-19 pandemic on persons living with amyotrophic lateral sclerosis in Malaysia
2021
Author(s) : Azlina Binti Ahmad Annuar Source : NEURODEGENERATIVE DISEASE MANAGEMENT |
17. |
Parkinson's disease with homozygous PINK1 p.Leu489Pro mutations in two Indian sisters
2021
Author(s) : Goh Khean Jin,Tan Chong Tin,Norlisah Binti Mohd Ramli,Azlina Binti Ahmad Annuar,Lim Shen-yang,Tan Ai Huey Source : NEUROLOGY ASIA |
18. |
Mutation analysis of SOD1, C9orf72, TARDBP and FUS genes in ethnically-diverse Malaysian patients with Amyotrophic Lateral Sclerosis (ALS),
2021
Author(s) : Azlina Binti Ahmad Annuar Source : NEUROBIOLOGY OF AGING |
19. |
Rare homozygous PRKN exon 8 and 9 deletion in Malay familial early-onset Parkinson's disease
2021
Author(s) : Azlina Binti Ahmad Annuar Source : ANNALS ACADEMY OF MEDICINE SINGAPORE |
20. |
Mutation analysis of SOD1, C9orf72, TARDBP and FUS genes in ethnically-diverse Malaysian patients with amyotrophic lateral sclerosis (ALS)
2021
Source : NEUROBIOLOGY OF AGING DOI : 10.1016/j.neurobiolaging.2021.07.008 |
21. |
A survey on patients' disease perception and the impact of the COVID-19 pandemic on persons living with amyotrophic lateral sclerosis in Malaysia
2021
Source : NEURODEGENERATIVE DISEASE MANAGEMENT DOI : 10.2217/nmt-2021-0004 |
22. |
Hereditary transthyretin amyloidosis in multi-ethnic Malaysians
2021
Author(s) : Goh Khean Jin,Azlina Binti Ahmad Annuar,Nortina Shahrizaila,Nor Ashikin Binti Md Sari,Tan Cheng Yin,Low Soon Chai Source : NEUROMUSCULAR DISORDERS DOI : 10.1016/j.nmd.2021.03.008 |
23. |
Association study of MCCC1/LAMP3 and DGKQ variants with Parkinson's disease in patients of Malay ancestry
2021
Source : NEUROLOGICAL SCIENCES DOI : 10.1007/s10072-021-05056-x |
24. |
Lack of diversity in Parkinson's disease genetic research: current landscape and future directions
2021
Author(s) : Azlina Binti Ahmad Annuar,Lim Shen-yang Source : MOVEMENT DISORDERS |
25. |
GBA variants in a multi-ethnic Parkinson's disease (PD) cohort in Malaysia
2021
Source : MOVEMENT DISORDERS |
26. |
Rare homozygous PRKN exon 8 and 9 deletion in Malay familial early-onset Parkinson's disease
2021
Source : ANNALS ACADEMY OF MEDICINE SINGAPORE DOI : 10.47102/annals-acadmed.sg.2020508 |
27. |
Improved spinal cord gray matter morphology induced by Spirulina platensis following spinal cord injury in rat models.
2020
Author(s) : Azlina Binti Ahmad Annuar Source : Ultrastructural Pathology |
28. |
Clinical Phenotype ofLRRK2R1441C in 2 Chinese Sisters
2020
Author(s) : Azlina Binti Ahmad Annuar,Kamal Azrin Bin Abdullah @ Kalai Arasu A/l Muthusamy,Lim Shen-yang,Tan Ai Huey Source : NEURODEGENERATIVE DISEASES DOI : 10.1159/000508131 |
29. |
Identification of Risk Loci for Parkinson Disease in Asians and Comparison of Risk Between Asians and Europeans A Genome-Wide Association Study
2020
Author(s) : Azlina Binti Ahmad Annuar,Tan Ai Huey Source : JAMA NEUROLOGY DOI : 10.1001/jamaneurol.2020.0428 |
30. |
Identification of Risk Loci for Parkinson Disease in Asians and Comparison of Risk Between Asians and Europeans: A Genome-Wide Association Study
2020
Author(s) : Azlina Binti Ahmad Annuar Source : JAMA Neurology DOI : 10.1001/jamaneurol.2020.0428 |
31. |
Glucocerebrosidase genetic variants in Malays with early and late-onset Parkinson's disease.
2020
Author(s) : Azlina Binti Ahmad Annuar Source : Neurology Asia |
32. |
Clinical Phenotype of LRRK2 R1441C in 2 Chinese Sisters
2020
Author(s) : Azlina Binti Ahmad Annuar Source : Neurodegenerative Diseases DOI : 10.1159/000508131 |
33. |
PINK1 p.Leu347Pro mutations in Malays: Prevalence and illustrative cases
2020
Source : PARKINSONISM & RELATED DISORDERS DOI : 10.1016/j.parkreldis.2020.08.015 |
34. |
PINK1 p.Leu347Pro mutations in malays: Prevalence and illustrative cases. Parkinsonism & Related Disorders (Impact Factor: 4.3).
2020
Source : Parkinsonism & Related Disorders DOI : doi.org/10.1016/j.parkreldis.2020.08.015 |
35. |
Ala97Ser mutation is common among ethnic Chinese Malaysians with transthyretin familial amyloid polyneuropathy
2019
Source : Amyloid |
36. |
Neuroprotective potential of Spirulina platensis on lesioned spinal cord corticospinal tract under experimental conditions in rat models
2019
Author(s) : Azlina Binti Ahmad Annuar Source : Ultrastructural Pathology |
37. |
Linkage analysis and whole exome sequencing reveals AHNAK2 as a novel genetic cause for autosomal recessive CMT in a Malaysian family
2019
Author(s) : Azlina Binti Ahmad Annuar Source : Neurogenetics |
38. |
DTI Profiles for Rapid Description of Cohorts at the Clinical-Research Interface
2019
Source : Frontiers in Medicine DOI : 10.3389/fmed.2018.00357 |
39. |
DTI Profiles for Rapid Description of Cohorts at the Clinical-Research Interface.
2019
Author(s) : Azlina Binti Ahmad Annuar Source : Frontiers in Medicine |
40. |
Parkinson's disease in the Western Pacific Region
2019
Author(s) : Tan Chong Tin,Azlina Binti Ahmad Annuar Source : Lancet Neurology |
41. |
MJFF Global Genetic Parkinson's Disease Study Group. Using global team science to identify genetic Parkinson's disease worldwide.
2019
Author(s) : Azlina Binti Ahmad Annuar Source : Annals of Neurology |
42. |
LRRK2 N551K and R1398H variants are protective in Malays and Chinese in Malaysia: a case-control association study for Parkinson s disease
2019
Author(s) : Azlina Binti Ahmad Annuar,Tan Ai Huey Source : Molecular Genetics and Genomics |
43. |
Linkage analysis and whole exome sequencing reveals AHNAK2 as a novel genetic cause for autosomal recessive CMT in a Malaysian family
2019
Source : NEUROGENETICS |
44. |
Parkinsons disease in the Western Pacific Region
2019
Source : LANCET NEUROLOGY |
45. |
Ala97Ser mutation is common among ethnic Chinese Malaysians with transthyretin familial amyloid polyneuropathy
2019
Author(s) : Goh Khean Jin,Tan Chong Tin,Wong Kum Thong,Azlina Binti Ahmad Annuar,Nortina Shahrizaila,Nor Ashikin Binti Md Sari,Tan Cheng Yin,Low Soon Chai Source : AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS |
46. |
LRRK2 N551K and R1398H variants are protective in Malays and Chinese in Malaysia: A case-control association study for Parkinsons disease
2019
Source : MOLECULAR GENETICS GENOMIC MEDICINE |
47. |
Purposeless Groaning in Parkinson’s Disease
2018
Author(s) : Azlina Binti Ahmad Annuar Source : Journal of Movement Disorders |
48. |
A Patient with Beta-Propeller Protein-Associated Neurodegeneration (BPAN): Treatment with Iron Chelation Therapy
2018
Author(s) : Norlisah Binti Mohd Ramli,Azlina Binti Ahmad Annuar,Bee Ping Chong,Lim Shen-yang,Tan Ai Huey Source : Journal of Movement disorders |
49. |
Quantitative Magnetic Resonance Imaging and radiogenomic biomarkers for glioma characterisation: A systematic review.
2018
Author(s) : Azlina Binti Ahmad Annuar Source : British Journal of Radiology |
50. |
Evaluation of novel Parkinson’s disease candidate genes in the Chinese population
2018
Author(s) : Azlina Binti Ahmad Annuar Source : Neurobiology of Aging |
51. |
Association of LRRK2 Haplotype With Age at Onset in Parkinson Disease
2018
Author(s) : Azlina Binti Ahmad Annuar Source : JAMA Neurology |
52. |
A Patient with Beta-Propeller Protein-Associated Neurodegeneration (BPAN): Treatment with Iron Chelation Therapy.
2018
Author(s) : Azlina Binti Ahmad Annuar Source : Journal of Movement Disorders |
53. |
Maternal intake of dietary virgin coconut oil modifies essential fatty acids and causes low body weight and spiky fur in mice
2017
Source : BMC Complementary and Alternative Medicine DOI : 10.1186/s12906-017-1600-z |
54. |
The Prevalence and Distribution of Spina Bifida in a Single Major Referral Center in Malaysia.
2017
Author(s) : Azlina Binti Ahmad Annuar Source : Frontier in Paediatrics |
55. |
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 |
56. |
Genome-wide association study of Parkinson's disease in East Asians
2017
Author(s) : Azlina Binti Ahmad Annuar Source : HUMAN MOLECULAR GENETICS |
57. |
Spina Bifida: Pathogenesis, Mechanisms, and Genes in Mice and Humans
2017
Source : Scientifica DOI : 10.1155/2017/5364827 |
58. |
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) : Goh Khean Jin,Wong Kum Thong,Thong Meow Keong,Azlina Binti Ahmad Annuar,Mohd Taufik Bin Ishak Source : BMJ Open DOI : 10.1136/bmjopen-2015-010711. |
59. |
Identification of the genomic mutation in Epha4 (rb-2J/rb-2J) mice.
2016
Author(s) : Azlina Binti Ahmad Annuar Source : Genome |
60. |
Congenital myasthenic syndrome due to novel CHAT mutations in an ethnic Kadazandusun family.
2016
Author(s) : Azlina Binti Ahmad Annuar Source : Muscle and Nerve |
61. |
Mutation analysis of genes within the dynactin complex in a cohort of hereditary peripheral neuropathies.
2016
Author(s) : Azlina Binti Ahmad Annuar,Nortina Shahrizaila Source : Clinical Genetics |
62. |
Harmonizing the interpretation of genetic variants across the world: the Malaysian experience.
2016
Source : BMC Res Notes DOI : 10.1186/s13104-015-1798-0 |
63. |
PARK16 is associated with PD in the Malaysian population.
2016
Author(s) : Azlina Binti Ahmad Annuar,Lim Shen-yang Source : American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. |
64. |
Missense Mutation of Brain Derived Neurotrophic Factor (BDNF) Alters Neurocognitive Performance in Patients with Mild Traumatic Brain Injury: A Longitudinal Study.
2016
Author(s) : Azlina Binti Ahmad Annuar Source : PLoS One |
65. |
A perspective on the role of microRNA-128 regulation in mental and behavioural disorders.
2015
Author(s) : Azlina Binti Ahmad Annuar Source : Frontiers in Cellular Neuroscience |
66. |
Improved inherited peripheral neuropathy genetic diagnosis by whole-exome sequencing
2015
Author(s) : Azlina Binti Ahmad Annuar Source : Molecular Genetics & Genomic Medicine |
67. |
Improved inherited peripheral neuropathy genetic diagnosis by whole-exome sequencing
2015
Author(s) : Azlina Binti Ahmad Annuar Source : MOLECULAR GENETICS GENOMIC MEDICINE |
68. |
The first Malay database toward the ethnic-specific target molecular variation.
2015
Author(s) : Azlina Binti Ahmad Annuar Source : BMC Research Notes |
69. |
DRD and GRIN2B polymorphisms and their association with the development of impulse control behaviour among Malaysian Parkinson's disease patients
2015
Author(s) : Azlina Binti Ahmad Annuar Source : BMC Neurology |
70. |
LRRK2 G2385R and R1628P mutations are associated with an increased risk of Parkinson's disease in the Malaysian population
2014
Author(s) : Azlina Binti Ahmad Annuar Source : Biomed Research International |
71. |
Analysis of dynein intermediate chains, light intermediate chains and light chains in a cohort of hereditary peripheral neuropathies
2014
Author(s) : Azlina Binti Ahmad Annuar,Nortina Shahrizaila Source : Neurogenetics |
72. |
Rapid-Onset Dystonia-Parkinsonism in a Chinese Girl with a De Novo ATP1A3 c.2267G>A (p.R756H) Genetic Mutation
2014
Author(s) : Azlina Binti Ahmad Annuar Source : Muscle Disorders - Clinical Practice |
73. |
X-linked Charcot-Marie-Tooth disease predominates in a cohort of multi- ethnic Malaysian patients.
2014
Source : Muscle and Nerve |
74. |
Analysis of dynein intermediate chains, light intermediate chains and light chains in a cohort of hereditary peripheral neuropathies.
2014
Author(s) : Azlina Binti Ahmad Annuar,Nortina Shahrizaila |
75. |
LRRK2 G2385R and R1628P Mutations Are Associated with an Increased Risk of Parkinson\s Disease in the Malaysian Population
2014
Author(s) : Azlina Binti Ahmad Annuar Source : Biomed Research International |
76. |
Analysis of non-synonymous-coding variants of Parkinson\s disease-related pathogenic and susceptibility genes in East Asian populations
2014
Author(s) : Azlina Binti Ahmad Annuar,Lim Shen-yang Source : Human Molecular Genetics |
77. |
Single mitochondrial DNA deletions in chronic progressive external ophthalmoplegia (CPEO) and Kearns- Sayre syndrome (KSS) patients from a multiethnic Asian population
2014
Source : Neurology Asia |
78. |
Analysis of non-synonymous-coding variants of Parkinson's disease- related pathogenic and susceptibility genes in East Asian populations.
2014
Author(s) : Azlina Binti Ahmad Annuar Source : Human Molecular Genetics |
79. |
Association of HLA locus variant in Parkinson\s disease
2013
Author(s) : Azlina Binti Ahmad Annuar,Lim Shen-yang Source : Clinical Genetics |
80. |
Association of HLA locus variant in Parkinson disease.
2013
Author(s) : Azlina Binti Ahmad Annuar Source : Clinical Genetics |
81. |
Lack of Association between the LRRK2 A419V Variant and Asian Parkinson\s Disease
2013
Source : Annals Academy of Medicine Singapore |
82. |
A family with inheritance of two X-linked disorders:
Charcot-Marie-Tooth Disease and Haemophilia A
2012
Author(s) : Goh Khean Jin,Azlina Binti Ahmad Annuar,Nortina Shahrizaila,Rabia Choudhry,Carolyn Lyn,Garth Nicholson,Marina Kennerson Source : Muscle and Nerve |
83. |
The frequency of common mitochondrial DNA mutations in
a cohort of Malaysian patients with specific
mitochondrial encephalomyopathy syndromes
2011
Source : Neurology Asia |
84. |
Exercise induced cramps and myoglobinuria in
dystrophinopathy - a report of three Malaysian cases.
2010
Source : Neurology Asia |
PROCEEDING
NO | DETAILS OF PROCEEDING |
---|---|
1. |
The Molecular Diagnosis of Myotonic Dystrophy in
Malaysia.
2010
Author(s) : Goh Khean Jin,Wong Kum Thong,Thong Meow Keong,Azlina Binti Ahmad Annuar,Mohd Taufik Bin Ishak |
2. |
Genetic mutations in sarcoglycanopathies in a Malaysian population.
2010
Author(s) : Goh Khean Jin,Wong Kum Thong,Thong Meow Keong,Azlina Binti Ahmad Annuar,Nortina Shahrizaila,Khoo Teik Beng,Terrence Thomas,Looi Ry |
RESEARCH PROJECT
GRANT | PROGRESS | STATUS |
---|---|---|
Characterisation of UHRF1BP1, a Potential New Candidate Gene for Amyotrophic Lateral Sclerosis
Researcher(s) : Prof. Dr. Nortina Shahrizaila
(University Grant) |
|
on going |
Identifying Disease-related Genomic Variation In Malaysian Amyotrophic Lateral Sclerosis Patients
(International Funding) |
|
on going |
A Clinicogenetic Study Of Parkinson's Disease In Malay Patients
Researcher(s) : Prof. Dr. Lim Shen-yang,Associate Prof. Dr. Tan Ai Huey
(Fundamental Research Grant Scheme (FRGS)) |
|
end |
Investigating The Genetics Of Amyotrophic Lateral Sclerosis (als) In Malaysia
Researcher(s) : Prof. Dr. Nortina Shahrizaila,Dr. Nur Izyani Binti Kamaruzman
(International Funding) |
|
end |
Investigating The Role Of Ahnak2, A Novel Cmt Gene, In Peripheral Neuropathy
(RU Geran - Fakulti Program) |
|
end |
Lrrk2 Genetic Variation In A Malay Parkinson's Disease Cohort
Researcher(s) : Associate Prof. Dr. Tan Ai Huey
(Private Funding) |
|
end |
The Role Of Cytoplasmic Dynein In Regulating Axonal Pathfinding And Synapse Formation
(High Impact Research - Ministry of Education (HIR-MOE) Cycle 1) |
|
end |
Is Cytoplasmic Dynein Associated With Disorders Of The Peripheral Nervous System?
(High Impact Research - Ministry of Education (HIR-MOE) Cycle 1) |
|
end |
Whole Exome Sequencing In Families With Early Onset Parkinson's Disease
(Fundamental Research Grant Scheme (FRGS)) |
|
end |
NEURAL MICRORNA REGULATION OF CYTOSKELETAL DYNAMICS DURING AXONAL PATHFINDING
(Geran Penyelidikan Universiti Malaya (UMRG) - HTM (Wellness)) |
|
end |
RESEARCH COLLABORATOR
GRANT | PROGRESS | STATUS |
---|---|---|
Interrogating Lrrk2 Signalling In Biosamples Derived From Patients With Parkinson's Disease Carrying The Asian Lrrk2 G2385r And R1628p Variants For Biomarker Discovery
Researcher(s) : Prof. Dr. Lim Shen-yang,Associate Prof. Dr. Azlina Binti Ahmad Annuar,Associate Prof. Dr. Reena A/p Rajasuriar,Dr. Lit Lei Cheng
(International Funding) |
|
new |
Big Data Detection Of Cognitive Frailty
Researcher(s) : Irraivan A/l Elamvazuthi,Prof. Dr. Norlisah Binti Mohd Ramli,Azrina Binti Abd Aziz,Fakhrul Zaman Rokhani,Mazlyfarina Mohamad,Nor Fadilah Rajab,Associate Prof. Dr. Azlina Binti Ahmad Annuar,Lila Iznita Binti Izhar,Associate Prof. Dr. Nor 'izzati Binti Saedon,Prof. Dr. Kartini Binti Rahmat,Lim Weng Marc,Chengkai Lu,Dr. Sumaiyah Binti Mat,Hazlina Binti Mahadzir,Hazlina Binti Mahadzir
(Long Term Research Grant Scheme (LRGS)) |
|
on going |
Identifying Leucocyte And Urine Biomarkers In Pd Patients With Lrrk2 R1628p Variant
Researcher(s) : Prof. Dr. Lim Shen-yang,Associate Prof. Dr. Azlina Binti Ahmad Annuar,Dr. Lit Lei Cheng
(International Funding) |
|
on going |
Identifying Leucocyte And Urine Biomarkers In Pd Patients With Lrrk2 G2385r Variant
Researcher(s) : Dr. Lit Lei Cheng,Prof. Dr. Lim Shen-yang,Associate Prof. Dr. Azlina Binti Ahmad Annuar
(International Funding) |
|
on going |
To Investigate The Relationship Between Exposure To Tropical Infections And Als
Researcher(s) : Prof. Dr. Jamal I-ching Sam,Associate Prof. Dr. Azlina Binti Ahmad Annuar,Dr. David Paul Capelle,Dr. Soo Chun Ian
(International Funding) |
|
on going |
Genetic Testing in Parkinson's Disease: Patient Perspectives And Ethical Considerations
Researcher(s) : Associate Prof. Dr. Tan Ai Huey,Associate Prof. Dr. Azlina Binti Ahmad Annuar,Prof. Dr. Lim Shen-yang,Dr. Schee Jie Ping
(University Grant) |
|
on going |
Investigating The Genetic Causes For Early-onset Parkinson's Disease And Their Effects On Cellular Function In A Malaysian Cohort
(Fundamental Research Grant Scheme (FRGS)) |
|
on going |
Lipidomic Study Of Brain Cancer Cells: An In-vivo Study Towards Understanding The Underlying Lipogenesis And Lipid Metabolism Regulation Gliomas Growth
Researcher(s) : Associate Prof. Dr. Jeannie Wong Hsiu Ding,Dr. Tan Li Kuo,Associate Prof. Dr. N.vairavan A/l N.v.v.e Narayanan,Associate Prof. Dr. Azlina Binti Ahmad Annuar,Associate Prof. Dr. Man Kein Seong @ Mun Kein Seong,Dr. Aditya Tri Hernowo,Prof. Dr. Kartini Binti Rahmat
(Fundamental Research Grant Scheme (FRGS)) |
|
end |
Genetic Study Of Amyotrophic Lateral Sclerosis (als) In A Multi-ethnic Population
Researcher(s) : Prof. Dr. Goh Khean Jin,Associate Prof. Dr. Azlina Binti Ahmad Annuar,Marina Kennerson
(Fundamental Research Grant Scheme (FRGS)) |
|
end |
Genetic Study Of Als In A Multi-ethnic Asian Population
Researcher(s) : Associate Prof. Dr. Azlina Binti Ahmad Annuar
(International Funding) |
|
end |
Ephrinb1(efnb1), Ephb6 (ephb6) And Epha2 (epha2) As Gene Candidates For Spina Bifida
(Bantuan Khas Penyelidikan (BKP Special)) |
|
end |