ARTICLE IN ACADEMIC JOURNALS
| NO | DETAILS OF ARTICLE IN ACADEMIC JOURNALS |
|---|---|
| 1. |
Single-center Experience of Deep Brain Stimulation (DBS) Surgery in Malaysia
2023
Author(s) : Azlina Binti Ahmad Annuar, Lim Shen-yang Source :
MOVEMENT DISORDERS
|
| 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. |
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
|
| 6. |
Glucocerebrosidase (GBA) gene variants in a multi-ethnic Asian cohort with Parkinson's disease: mutational spectrum and clinical features
2022
Source :
JOURNAL OF NEURAL TRANSMISSION
DOI :
10.1007/s00702-021-02421-0
|
| 7. |
Clinical Outcomes After Ventriculo-Peritoneal Shunting in Patients With Classic vs. Complex NPH
2022
Source :
FRONTIERS IN NEUROLOGY
DOI :
10.3389/fneur.2022.868000
|
| 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. |
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
|
| 10. |
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
|
| 11. |
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
|
| 12. |
GBA variants in a multi-ethnic Parkinson's disease (PD) cohort in Malaysia
2021
Source :
MOVEMENT DISORDERS
|
| 13. |
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
|
| 14. |
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
|
| 15. |
Parkinson s disease with homozygous PINK1 p.Leu489Pro mutations in two Indian sisters.
2021
Author(s) : Norlisah Binti Mohd Ramli, Lim Shen-yang, Tan Chong Tin, Goh Khean Jin, Tan Ai Huey, Azlina Binti Ahmad Annuar Source :
Neurology Asia
|
| 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. |
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
|
| 18. |
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
|
| 19. |
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
|
| 20. |
Hereditary Transthyretin Amyloidosis in Multi-Ethnic Malaysians
2021
Source :
NEUROMUSCULAR DISORDERS
DOI :
10.1016/j.nmd.2021.03.008
|
| 21. |
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
|
| 22. |
Clinical phenotype of Parkinson's disease with a homozygous PRKN p.Cys441Arg mutation
2021
Source :
NEUROLOGY ASIA
|
| 23. |
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
|
| 24. |
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
|
| 25. |
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
|
| 26. |
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
|
| 27. |
Clinical Phenotype of LRRK2 R1441C in 2 Chinese Sisters
2020
Author(s) : Azlina Binti Ahmad Annuar Source :
Neurodegenerative Diseases
DOI :
10.1159/000508131
|
| 28. |
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
|
| 29. |
Glucocerebrosidase genetic variants in Malays with early and late-onset Parkinson's disease.
2020
Author(s) : Azlina Binti Ahmad Annuar Source :
Neurology Asia
|
| 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. |
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
|
| 32. |
Clinical Phenotype ofLRRK2R1441C in 2 Chinese Sisters
2020
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. |
Linkage analysis and whole exome sequencing reveals AHNAK2 as a novel genetic cause for autosomal recessive CMT in a Malaysian family
2019
Source :
NEUROGENETICS
DOI :
10.1007/s10048-019-00576-3
|
| 35. |
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
|
| 36. |
Ala97Ser mutation is common among ethnic Chinese Malaysians with transthyretin familial amyloid polyneuropathy
2019
Source :
Amyloid
|
| 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. |
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
|
| 39. |
DTI Profiles for Rapid Description of Cohorts at the Clinical-Research Interface
2019
Source :
Frontiers in Medicine
DOI :
10.3389/fmed.2018.00357
|
| 40. |
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
|
| 41. |
Parkinsons disease in the Western Pacific Region
2019
Source :
LANCET NEUROLOGY
|
| 42. |
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
|
| 43. |
DTI Profiles for Rapid Description of Cohorts at the Clinical-Research Interface.
2019
Author(s) : Azlina Binti Ahmad Annuar Source :
Frontiers in Medicine
|
| 44. |
Parkinson's disease in the Western Pacific Region
2019
Author(s) : Azlina Binti Ahmad Annuar, Tan Chong Tin Source :
Lancet Neurology
|
| 45. |
Association of LRRK2 Haplotype With Age at Onset in Parkinson Disease
2018
Author(s) : Azlina Binti Ahmad Annuar Source :
JAMA Neurology
|
| 46. |
Evaluation of novel Parkinson’s disease candidate genes in the Chinese population
2018
Author(s) : Azlina Binti Ahmad Annuar Source :
Neurobiology of Aging
|
| 47. |
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
|
| 48. |
A Patient with Beta-Propeller Protein-Associated Neurodegeneration (BPAN): Treatment with Iron Chelation Therapy
2018
Author(s) : Tan Ai Huey, Azlina Binti Ahmad Annuar, Lim Shen-yang, Bee Ping Chong, Norlisah Binti Mohd Ramli Source :
Journal of Movement disorders
|
| 49. |
Purposeless Groaning in Parkinson’s Disease
2018
Author(s) : Azlina Binti Ahmad Annuar Source :
Journal of Movement Disorders
|
| 50. |
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
|
| 51. |
Genome-wide association study of Parkinson's disease in East Asians
2017
Author(s) : Azlina Binti Ahmad Annuar Source :
HUMAN MOLECULAR GENETICS
|
| 52. |
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.
|
| 53. |
Congenital myasthenic syndrome due to novel CHAT mutations in an ethnic Kadazandusun family.
2016
Author(s) : Azlina Binti Ahmad Annuar Source :
Muscle and Nerve
|
| 54. |
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
|
| 55. |
Mutation analysis of genes within the dynactin complex in a cohort of hereditary peripheral neuropathies.
2016
Author(s) : Nortina Shahrizaila, Azlina Binti Ahmad Annuar Source :
Clinical Genetics
|
| 56. |
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.
|
| 57. |
Improved inherited peripheral neuropathy genetic diagnosis by whole-exome sequencing
2015
Author(s) : Azlina Binti Ahmad Annuar Source :
MOLECULAR GENETICS GENOMIC MEDICINE
|
| 58. |
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
|
| 59. |
Improved inherited peripheral neuropathy genetic diagnosis by whole-exome sequencing
2015
Author(s) : Azlina Binti Ahmad Annuar Source :
Molecular Genetics & Genomic Medicine
|
| 60. |
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
|
| 61. |
X-linked Charcot-Marie-Tooth disease predominates in a cohort of multi- ethnic Malaysian patients.
2014
Source :
Muscle and Nerve
|
| 62. |
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, Wong Kum Thong, Wong Jia Woei, Goh Khean Jin, Azlina Binti Ahmad Annuar Source :
Neurology Asia
|
| 63. |
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
|
| 64. |
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
|
| 65. |
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
|
| 66. |
Analysis of dynein intermediate chains, light intermediate chains and light chains in a cohort of hereditary peripheral neuropathies.
2014
Author(s) : Nortina Shahrizaila, Azlina Binti Ahmad Annuar |
| 67. |
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
|
| 68. |
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
|
| 69. |
Lack of Association between the LRRK2 A419V Variant and Asian Parkinson\s Disease
2013
Source :
Annals Academy of Medicine Singapore
|
| 70. |
Association of HLA locus variant in Parkinson\s disease
2013
Author(s) : Azlina Binti Ahmad Annuar, Lim Shen-yang Source :
Clinical Genetics
|
| 71. |
Association of HLA locus variant in Parkinson disease.
2013
Author(s) : Azlina Binti Ahmad Annuar Source :
Clinical Genetics
|
| 72. |
A family with inheritance of two X-linked disorders:
Charcot-Marie-Tooth Disease and Haemophilia A
2012
Author(s) : Nortina Shahrizaila, Rabia Choudhry, Carolyn Lyn, Garth Nicholson, Marina Kennerson, Goh Khean Jin, Azlina Binti Ahmad Annuar Source :
Muscle and Nerve
|
| 73. |
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
|
| 74. |
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) : Thong Meow Keong, Mohd Taufik Bin Ishak, Goh Khean Jin, Azlina Binti Ahmad Annuar, Wong Kum Thong |
| 2. |
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 |
RESEARCH PROJECT
| GRANT | PROGRESS | STATUS |
|---|---|---|
|
Identifying Disease-related Genomic Variation In Malaysian Amyotrophic Lateral Sclerosis Patients
|
|
on going |
|
Characterisation Of Uhrf1bp1, A Potential New Candidate Gene For Amyotrophic Lateral Sclerosis
Researcher(s) : Prof. Dr. Nortina Shahrizaila |
|
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 |
|
end |
|
Investigating The Genetics Of Amyotrophic Lateral Sclerosis (als) In Malaysia
Researcher(s) : Prof. Dr. Nortina Shahrizaila, Dr. Nur Izyani Binti Kamaruzman |
|
end |
|
Investigating The Role Of Ahnak2, A Novel Cmt Gene, In Peripheral Neuropathy
|
|
end |
|
Lrrk2 Genetic Variation In A Malay Parkinson's Disease Cohort
Researcher(s) : Associate Prof. Dr. Tan Ai Huey |
|
end |
|
The Role Of Cytoplasmic Dynein In Regulating Axonal Pathfinding And Synapse Formation
|
|
end |
|
Is Cytoplasmic Dynein Associated With Disorders Of The Peripheral Nervous System?
|
|
end |
|
Whole Exome Sequencing In Families With Early Onset Parkinson's Disease
|
|
end |
|
NEURAL MICRORNA REGULATION OF CYTOSKELETAL DYNAMICS DURING AXONAL PATHFINDING
|
|
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
|
|
on going |
|
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, Dr. Kejal A/p Hasmukharay |
|
on going |
|
Genetic Testing In Parkinson's Disease: Patient Perspectives And Ethical Considerations
|
|
on going |
|
Identifying Leucocyte And Urine Biomarkers In Pd Patients With Lrrk2 R1628p Variant
|
|
on going |
|
Identifying Leucocyte And Urine Biomarkers In Pd Patients With Lrrk2 G2385r Variant
|
|
on going |
|
To Investigate The Relationship Between Exposure To Tropical Infections And Als
|
|
on going |
|
Investigating The Genetic Causes For Early-onset Parkinson's Disease And Their Effects On Cellular Function In A Malaysian Cohort
|
|
end |
|
Lipidomic Study Of Brain Cancer Cells: An In-vivo Study Towards Understanding The Underlying Lipogenesis And Lipid Metabolism Regulation Gliomas Growth
|
|
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 |
|
end |
|
Genetic Study Of Als In A Multi-ethnic Asian Population
Researcher(s) : Associate Prof. Dr. Azlina Binti Ahmad Annuar |
|
end |
|
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 |