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Tan, Ai Huey and Cornejo-Olivas, Mario and Okubadejo, Njideka and Pal, Pramod Kumar and Saranza, Gerard and Saffie-Awad, Paula and Ahmad-Annuar, Azlina and Schumacher-Schuh, Artur F. and Okeng'o, Kigocha and Mata, Ignacio F. and Gatto, Emilia M. and Lim, Shen-Yang (2024) Genetic testing for parkinson's disease and movement disorders in less privileged areas: Barriers and opportunities. Movement Disorders Clinical Practice, 11 (1). 14 – 20. ISSN 2330-1619, DOI https://doi.org/10.1002/mdc3.13903.
Ibrahim, Kamariah and Ahmad-Annuar, Azlina (2022) COVID-19 pandemic: Lessons learned for undergraduate research training. Biochemistry and Molecular Biology Education, 50 (5). pp. 476-478. ISSN 1470-8175, DOI https://doi.org/10.1002/bmb.21665.
Schumacher-Schuh, Artur Francisco and Bieger, Andrei and Okunoye, Olaitan and Mok, Kin Ying and Lim, Shen-Yang and Bardien, Soraya and Ahmad-Annuar, Azlina and Santos-Lobato, Bruno Lopes and Strelow, Matheus Zschornack and Salama, Mohamed and Rao, Shilpa C. and Zewde, Yared Zenebe and Dindayal, Saiesha and Azar, Jihan and Prashanth, Lingappa Kukkle and Rajan, Roopa and Noyce, Alastair J. and Okubadejo, Njideka and Rizig, Mie and Lesage, Suzanne and Mata, Ignacio Fernandez and Progra, Global Parkinson's Genetics (2022) Underrepresented populations in Parkinson's genetics research: Current landscape and future directions. Movement Disorders, 37 (8). pp. 1593-1604. ISSN 0885-3185, DOI https://doi.org/10.1002/mds.29126.
Ch'ng, Gaik Siew and Koh, Karina and Ahmad-Annuar, Azlina and Taib, Fahisham and Koh, Cha Ling and Lim, Edmund Soon Chin (2022) A mixed method study on the impact of living with spinal muscular atrophy in Malaysia from patients' and caregivers' perspectives. Orphanet Journal of Rare Diseases, 17 (1). ISSN 1750-1172, DOI https://doi.org/10.1186/s13023-022-02351-4.
Lim, Jia Lun and Lohmann, Katja and Tan, Ai Huey and Tay, Yi Wen and Ibrahim, Khairul Azmi and Aziz, Zariah Abdul and Mawardi, Ahmad Shahir and Puvanarajah, Santhi Datuk and Lim, Thien Thien and Looi, Irene and Ooi, Joshua Chin Ern and Chia, Yuen Kang and Muthusamy, Kalai Arasu and Bauer, Peter and Rolfs, Arndt and Klein, Christine and Ahmad-Annuar, Azlina and Lim, Shen-Yang (2022) Glucocerebrosidase (GBA) gene variants in a multi-ethnic Asian cohort with Parkinson's disease: Mutational spectrum and clinical features. Journal of Neural Transmission, 129 (1). pp. 37-48. ISSN 0300-9564, DOI https://doi.org/10.1007/s00702-021-02421-0.
Edgar, Suzanna and Ellis, Melina and Abdul-Aziz, Nur Adilah and Goh, Khean-Jin and Shahrizaila, Nortina and Kennerson, Marina L. and Ahmad-Annuar, Azlina (2021) Mutation analysis of SOD1, C9orf72, TARDBP and FUS genes in ethnically-diverse Malaysian patients with amyotrophic lateral sclerosis (ALS). Neurobiology of Aging, 108. pp. 200-206. ISSN 0197-4580, DOI https://doi.org/10.1016/j.neurobiolaging.2021.07.008.
Lim, Jia Lun and Ng, Ebonne Yulin and Lim, Shen-Yang and Tan, Ai Huey and Abdul-Aziz, Zariah and Ibrahim, Khairul Azmi and Gopalai, Aroma Agape and Tay, Yi Wen and Vijayanathan, Yuganthini and Toh, Tzi Shin and Lim, Soo Kun and Bee, Ping-Chong and Puvanarajah, Santhi Datuk and Viswanathan, Shanthi and Looi, Irene and Lim, Thien Thien and Eow, Gaik Bee and Cheah, Wee Kooi and Tan, Eng-King and Ahmad-Annuar, Azlina (2021) Association study of MCCC1/LAMP3 and DGKQ variants with Parkinson's disease in patients of Malay ancestry. Neurological Sciences, 42 (10). pp. 4203-4207. ISSN 1590-1874, DOI https://doi.org/10.1007/s10072-021-05056-x.
Edgar, Suzanna and Abdul-Aziz, Nur Adilah and Loh, Ee Chin and Capelle, David Paul and Goh, Khean-Jin and Latif, Lydia Abdul and Shahrizaila, Nortina and Ahmad-Annuar, Azlina (2021) A survey on patients' disease perception and the impact of the COVID-19 pandemic on persons living with amyotrophic lateral sclerosis in Malaysia. Neurodegenerative Disease Management, 11 (04). pp. 307-314. ISSN 1758-2024, DOI https://doi.org/10.2217/nmt-2021-0004.
Low, Soon-Chai and Md Sari, Nor Ashikin and Tan, Cheng-Yin and Ahmad-Annuar, Azlina and Wong, Kum-Thong and Law, Wan-Chung and Sim, Rachel Siew-Hung and Lin, Kon-Ping and Shahrizaila, Nortina and Goh, Khean-Jin (2021) Hereditary transthyretin amyloidosis in multi-ethnic Malaysians. Neuromuscular Disorders, 31 (7). pp. 642-650. ISSN 0960-8966, DOI https://doi.org/10.1016/j.nmd.2021.03.008.
Lim, Shen-Yang and Ahmad-Annuar, Azlina and Lohmann, Katja and Tan, Ai Huey and Tay, Yi Wen and Lim, Jia Lun and Lim, Kai Bin and Lit, Lei Cheng and Bauer, Peter and Rolfs, Arndt and Klein, Christine (2021) Clinical phenotype of Parkinson's disease with a homozygous PRKN p.Cys441Arg mutation. Neurology Asia, 26 (1). pp. 161-166. ISSN 1823-6138,
Lim, Shen-Yang and Ahmad-Annuar, Azlina and Lohmann, Katja and Tan, Ai Huey and Tay, Yi Wen and Lim, Jia Lun and Ramli, Norlisah and Teh, Pei Chiek and Kuppusamy, Rishikesan and Tan, Chong Tin and Goh, Khean Jin and Viswanathan, Shanthi and Bauer, Peter and Rolfs, Arndt and Klein, Christine (2021) Parkinson's disease with homozygous PINK1 p.Leu489Pro mutations in two Indian sisters. Neurology Asia, 26 (1). pp. 167-173. ISSN 1823-6138,
Lim, Shen-Yang and Lim, Jia Lun and Ahmad-Annuar, Azlina and Lohmann, Katja and Tan, Ai Huey and Lim, Kai Bin and Tay, Yi Wen and Shing, Yee Lee and Muthusamy, Kalai Arasu and Bauer, Peter and Rolfs, Arndt and Klein, Christine (2020) Clinical phenotype of LRRK2R1441C in 2 Chinese sisters. Neurodegenerative Diseases, 20 (1). pp. 39-45. ISSN 1660-2854, DOI https://doi.org/10.1159/000508131.
Pakarulrazy, Nur Fadhlina Mohamad and Syafruddin, Saiful Effendi and Mutalib, Nurul Syakima Ab and Ahmad-Annuar, Azlina and Lim, Shen Yang and Jamal, Rahman and Abdul Murad, Nor Azian and Ibrahim, Norlinah M. (2020) Glucocerebrosidase genetic variants in Malays with early and late-onset Parkinson’s disease. Neurology Asia, 25 (1). pp. 39-46. ISSN 1823-6138,
Tey, Shelisa and Shahrizaila, Nortina and Drew, Alexander P. and Samulong, Sarimah and Goh, Khean Jin and Battaloglu, Esra and Atkinson, Derek and Parman, Yesim and Jordanova, Albena and Chung, Ki Wha and Choi, Byung-Ok and Li, Yi-Chung and Auer-Grumbach, Michaela and Nicholson, Garth A. and Kennerson, Marina L. and Ahmad-Annuar, Azlina (2019) Linkage analysis and whole exome sequencing reveals AHNAK2 as a novel genetic cause for autosomal recessive CMT in a Malaysian family. Neurogenetics, 20 (3). pp. 117-127. ISSN 1364-6745, DOI https://doi.org/10.1007/s10048-019-00576-3.
Abdullah, Nor Linda and Gunasekaran, Renuka and Mohd-Zin, Siti Waheeda and Lim, Bee Hui and Maniam, Pramila and Mohd-Salleh, Anis Shuhada and Thong, Meow Keong and Chik, Zamri and Nordin, Noreena and Omar, Zaliha and Engkasan, Julia Patrick and Ganesan, Dharmendra and Aiezzah, Zakaria Nurul and Ahmad-Annuar, Azlina and Abdul-Aziz, Noraishah Mydin (2018) Cranial neural tube defect after trimethoprim exposure. BMC Research Notes, 11 (1). p. 475. ISSN 1756-0500, DOI https://doi.org/10.1186/s13104-018-3593-1.
Zainal Abidin, S. and Tan, E.L. and Chan, S.C. and Jaafar, Ameerah and Lee, A.X. and Abd Hamid, M.H.N. and Abdul Murad, N.A. and Pakarul Razy, N.F. and Azmin, S. and Ahmad-Annuar, Azlina and Lim, Shen Yang and Cheah, P.S. and Ling, K.H. and Mohamed Ibrahim, N. (2015) DRD and GRIN2B polymorphisms and their association with the development of impulse control behaviour among Malaysian Parkinson’s disease patients. BMC Neurology, 15 (1). p. 59. ISSN 1471-2377, DOI https://doi.org/10.1186/s12883-015-0316-2.
Ching, Ai Sze and Ahmad-Annuar, Azlina (2015) A Perspective on the Role of microRNA-128 Regulation in Mental and Behavioral Disorders. Frontiers in Cellular Neuroscience, 9. p. 465. ISSN 1662-5102, DOI https://doi.org/10.3389/fncel.2015.00465.
