ARTICLE IN ACADEMIC JOURNALS
| NO | DETAILS OF ARTICLE IN ACADEMIC JOURNALS |
|---|---|
| 1. |
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 |
| 2. |
Glucocerebrosidase genetic variants in Malays with early and late-onset Parkinson's disease.
2020
Author(s) : Azlina Binti Ahmad Annuar Source : Neurology Asia |
| 3. |
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 |
| 4. |
Clinical Phenotype of LRRK2 R1441C in 2 Chinese Sisters
2020
Author(s) : Azlina Binti Ahmad Annuar Source : Neurodegenerative Diseases DOI : 10.1159/000508131 |
| 5. |
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 |
| 6. |
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 |
| 7. |
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 |
| 8. |
DTI Profiles for Rapid Description of Cohorts at the Clinical-Research Interface.
2019
Author(s) : Azlina Binti Ahmad Annuar Source : Frontiers in Medicine |
| 9. |
Parkinson's disease in the Western Pacific Region
2019
Author(s) : Tan Chong Tin,Azlina Binti Ahmad Annuar Source : Lancet Neurology |
| 10. |
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 |
| 11. |
Ala97Ser mutation is common among ethnic Chinese Malaysians with transthyretin familial amyloid polyneuropathy
2019
Source : Amyloid |
| 12. |
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 |
| 13. |
DTI Profiles for Rapid Description of Cohorts at the Clinical-Research Interface
2019
Source : Frontiers in Medicine DOI : 10.3389/fmed.2018.00357 |
| 14. |
Cranial neural tube defect after trimethoprim exposure
2018
Author(s) : Thong Meow Keong,Zaliha Binti Omar,Azlina Binti Ahmad Annuar,Noraishah Mydin Binti Haji Abdul Aziz,Dharmendra A/l Ganesan,Zamri Bin Chik,Julia Anak Patrick Engkasan Source : BMC Research Notes DOI : 10.1186/s13104-018-3593-1 |
| 15. |
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 |
| 16. |
Association of LRRK2 Haplotype With Age at Onset in Parkinson Disease
2018
Author(s) : Azlina Binti Ahmad Annuar Source : JAMA Neurology |
| 17. |
Purposeless Groaning in Parkinson’s Disease
2018
Author(s) : Azlina Binti Ahmad Annuar Source : Journal of Movement Disorders |
| 18. |
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 |
| 19. |
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 |
| 20. |
Evaluation of novel Parkinson’s disease candidate genes in the Chinese population
2018
Author(s) : Azlina Binti Ahmad Annuar Source : Neurobiology of Aging |
| 21. |
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 |
| 22. |
Genome-wide association study of Parkinson's disease in East Asians
2017
Author(s) : Azlina Binti Ahmad Annuar Source : HUMAN MOLECULAR GENETICS |
| 23. |
Spina Bifida: Pathogenesis, Mechanisms, and Genes in Mice and Humans
2017
Source : Scientifica DOI : 10.1155/2017/5364827 |
| 24. |
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 |
| 25. |
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. |
| 26. |
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 |
| 27. |
Harmonizing the interpretation of genetic variants across the world: the Malaysian experience.
2016
Source : BMC Res Notes DOI : 10.1186/s13104-015-1798-0 |
| 28. |
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. |
| 29. |
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 |
| 30. |
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 |
| 31. |
Identification of the genomic mutation in Epha4 (rb-2J/rb-2J) mice.
2016
Author(s) : Azlina Binti Ahmad Annuar Source : Genome |
| 32. |
Congenital myasthenic syndrome due to novel CHAT mutations in an ethnic Kadazandusun family.
2016
Author(s) : Azlina Binti Ahmad Annuar Source : Muscle and Nerve |
| 33. |
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 |
| 34. |
The first Malay database toward the ethnic-specific target molecular variation.
2015
Author(s) : Azlina Binti Ahmad Annuar Source : BMC Research Notes |
| 35. |
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 |
| 36. |
Improved inherited peripheral neuropathy genetic diagnosis by whole-exome sequencing
2015
Author(s) : Azlina Binti Ahmad Annuar Source : Molecular Genetics & Genomic Medicine |
| 37. |
X-linked Charcot-Marie-Tooth disease predominates in a cohort of multi- ethnic Malaysian patients.
2014
Source : Muscle and Nerve |
| 38. |
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 |
| 39. |
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 |
| 40. |
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 |
| 41. |
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 |
| 42. |
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 |
| 43. |
Association of HLA locus variant in Parkinson disease.
2013
Author(s) : Azlina Binti Ahmad Annuar Source : Clinical Genetics |
| 44. |
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 |
| 45. |
The frequency of common mitochondrial DNA mutations in
a cohort of Malaysian patients with specific
mitochondrial encephalomyopathy syndromes
2011
Source : Neurology Asia |
| 46. |
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 |
|---|---|---|
|
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)) |
|
on going |
|
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 |
|
Ephrinb1(efnb1), Ephb6 (ephb6) And Epha2 (epha2) As Gene Candidates For Spina Bifida
(Bantuan Khas Penyelidikan (BKP Special)) |
|
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 |
|---|---|---|
|
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)) |
|
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)) |
|
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,Dr. Hong Yet Hoi
(International Funding) |
|
on going |
|
Ephrinb1(efnb1), Ephb6 (ephb6) And Epha2 (epha2) As Gene Candidates For Spina Bifida
(Bantuan Khas Penyelidikan (BKP Special)) |
|
end |
|
Ephrinb1(efnb1), Ephb6 (ephb6) And Epha2 (epha2) As Gene Candidates For Spina Bifida
(Bantuan Khas Penyelidikan (BKP Special)) |
|
end |