COVID-19 pandemic: Lessons learned for undergraduate research training

by Ibrahim, Kamariah, Ahmad-Annuar, Azlina
Published 2022

A Perspective on the Role of microRNA-128 Regulation in Mental and Behavioral Disorders

by Ching, Ai Sze, Ahmad-Annuar, Azlina
Published 2015

Developing a model for studying complex brain function using zebrafish (Danio rerio) and cavefish (Mexican tetra)

by Ahmad, Hafandi, Ahmad Zaki, Nabila Irqin, Ahmad Annuar, Azlina, Mohd Daud, Hassan
Published 2015

A mixed method study on the impact of living with spinal muscular atrophy in Malaysia from patients' and caregivers' perspectives

by Ch'ng, Gaik Siew, Koh, Karina, Ahmad-Annuar, Azlina, Taib, Fahisham, Koh, Cha Ling, Lim, Edmund Soon Chin
Published 2022

Mutation analysis of SOD1, C9orf72, TARDBP and FUS genes in ethnically-diverse Malaysian patients with amyotrophic lateral sclerosis (ALS)

by Edgar, Suzanna, Ellis, Melina, Abdul-Aziz, Nur Adilah, Goh, Khean-Jin, Shahrizaila, Nortina, Kennerson, Marina L., Ahmad-Annuar, Azlina
Published 2021

Rare homozygous PRKN exon 7 duplication in a Ibanese patient from Northwestern Borneo with young onset Parkinson's disease

by Wong, Siaw Cheng, Tan, Zhun Foo, Tay, Yi-Wen, Law, Wan Chung, Ahmad Annuar, Azlina, Tan, Ai Huey, Lim, Shen-Yang
Published 2022

A survey on patients' disease perception and the impact of the COVID-19 pandemic on persons living with amyotrophic lateral sclerosis in Malaysia

by Edgar, Suzanna, Abdul-Aziz, Nur Adilah, Loh, Ee Chin, Capelle, David Paul, Goh, Khean-Jin, Latif, Lydia Abdul, Shahrizaila, Nortina, Ahmad-Annuar, Azlina
Published 2021

Editorial: genetic and molecular diversity in Parkinson's disease

by Abdul Murad, Nor Azian, Sulaiman, Siti Aishah, Ahmad-Annuar, Azlina, Mohamed Ibrahim, Norlinah, Mohamed, Wael Mohamed Yousef, Md Rani, Shahrul Azmin, Mok, Kin Ying
Published 2022

Glucocerebrosidase genetic variants in Malays with early and late-onset Parkinson’s disease

by Pakarulrazy, Nur Fadhlina Mohamad, Syafruddin, Saiful Effendi, Mutalib, Nurul Syakima Ab, Ahmad-Annuar, Azlina, Lim, Shen Yang, Jamal, Rahman, Abdul Murad, Nor Azian, Ibrahim, Norlinah M.
Published 2020

Clinical phenotype of Parkinson's disease with a homozygous PRKN p.Cys441Arg mutation

by Lim, Shen-Yang, Ahmad-Annuar, Azlina, Lohmann, Katja, Tan, Ai Huey, Tay, Yi Wen, Lim, Jia Lun, Lim, Kai Bin, Lit, Lei Cheng, Bauer, Peter, Rolfs, Arndt, Klein, Christine
Published 2021

A KMT2B frameshift variant causing focal dystonia restricted to the oromandibular region after long-term follow-up

by Closas, Alfand Marl F. Dy, Lohmann, Katja, Tan, Ai Huey, Ibrahim, Norlinah Mohamed, Lim, Jia Lun, Tay, Yi Wen, Muthusamy, Kalai Arasu, Ahmad Annuar, Azlina, Klein, Christine, Lim, Shen -Yang
Published 2023

Hereditary transthyretin amyloidosis in multi-ethnic Malaysians

by Low, Soon-Chai, Md Sari, Nor Ashikin, Tan, Cheng-Yin, Ahmad-Annuar, Azlina, Wong, Kum-Thong, Law, Wan-Chung, Sim, Rachel Siew-Hung, Lin, Kon-Ping, Shahrizaila, Nortina, Goh, Khean-Jin
Published 2021

Clinical phenotype of LRRK2R1441C in 2 Chinese sisters

by Lim, Shen-Yang, Lim, Jia Lun, Ahmad-Annuar, Azlina, Lohmann, Katja, Tan, Ai Huey, Lim, Kai Bin, Tay, Yi Wen, Shing, Yee Lee, Muthusamy, Kalai Arasu, Bauer, Peter, Rolfs, Arndt, Klein, Christine
Published 2020

Clinical phenotype ofLRRK2R1441C in 2 Chinese sisters

by Lim, Shen-Yang, Lim, Jia Lun, Ahmad-Annuar, Azlina, Lohmann, Katja, Tan, Ai Huey, Lim, Kai Bin, Tay, Yi Wen, Shing, Yee Lee, Muthusamy, Kalai Arasu, Bauer, Peter, Rolfs, Arndt, Klein, Christine
Published 2020

Identification of the genomic mutation in Epha4rb-2J/rb-2J mice

by Mohd Zin, Siti Waheeda, Abdullah, Nor Linda, Greene, Nicholas D. E., Cheah, Pike See, Ling, King Hwa, Yusof, Hadri, Marwan, Ahmed I., Williams, Sarah M., York, Kerri T., Ahmad Annuar, Azlina, Abdul Aziz, Noraishah Mydin
Published 2016

Genetic testing for parkinson's disease and movement disorders in less privileged areas: Barriers and opportunities

by Tan, Ai Huey, Cornejo-Olivas, Mario, Okubadejo, Njideka, Pal, Pramod Kumar, Saranza, Gerard, Saffie-Awad, Paula, Ahmad-Annuar, Azlina, Schumacher-Schuh, Artur F., Okeng'o, Kigocha, Mata, Ignacio F., Gatto, Emilia M., Lim, Shen-Yang
Published 2024

Parkinson's disease with homozygous PINK1 p.Leu489Pro mutations in two Indian sisters

by Lim, Shen-Yang, Ahmad-Annuar, Azlina, Lohmann, Katja, Tan, Ai Huey, Tay, Yi Wen, Lim, Jia Lun, Ramli, Norlisah, Teh, Pei Chiek, Kuppusamy, Rishikesan, Tan, Chong Tin, Goh, Khean Jin, Viswanathan, Shanthi, Bauer, Peter, Rolfs, Arndt, Klein, Christine
Published 2021

Linkage analysis and whole exome sequencing reveals AHNAK2 as a novel genetic cause for autosomal recessive CMT in a Malaysian family

by Tey, Shelisa, Shahrizaila, Nortina, Drew, Alexander P., Samulong, Sarimah, Goh, Khean Jin, Battaloglu, Esra, Atkinson, Derek, Parman, Yesim, Jordanova, Albena, Chung, Ki Wha, Choi, Byung-Ok, Li, Yi-Chung, Auer-Grumbach, Michaela, Nicholson, Garth A., Kennerson, Marina L., Ahmad-Annuar, Azlina
Published 2019

DRD and GRIN2B polymorphisms and their association with the development of impulse control behaviour among Malaysian Parkinson’s disease patients

by Zainal Abidin, S., Tan, E.L., Chan, S.C., Jaafar, Ameerah, Lee, A.X., Abd Hamid, M.H.N., Abdul Murad, N.A., Pakarul Razy, N.F., Azmin, S., Ahmad-Annuar, Azlina, Lim, Shen Yang, Cheah, P.S., Ling, K.H., Mohamed Ibrahim, N.
Published 2015

Cranial neural tube defect after trimethoprim exposure

by Abdullah, Nor Linda, Gunasekaran, Renuka, Mohd-Zin, Siti Waheeda, Lim, Bee Hui, Maniam, Pramila, Mohd-Salleh, Anis Shuhada, Thong, Meow Keong, Chik, Zamri, Nordin, Noreena, Omar, Zaliha, Engkasan, Julia Patrick, Ganesan, Dharmendra, Aiezzah, Zakaria Nurul, Ahmad-Annuar, Azlina, Abdul-Aziz, Noraishah Mydin
Published 2018