| Mutations in dynein link motor neuron degeneration to defects in retrograde transport M Hafezparast, R Klocke, C Ruhrberg, A Marquardt, A Ahmad-Annuar, ... Science 300 (5620), 808-812, 2003 | 840 | 2003 |
| Signaling across the synapse: a role for Wnt and Dishevelled in presynaptic assembly and neurotransmitter release A Ahmad-Annuar, L Ciani, I Simeonidis, J Herreros, NB Fredj, SB Rosso, ... The Journal of cell biology 174 (1), 127-139, 2006 | 296 | 2006 |
| Parkinson's disease in the Western Pacific Region SY Lim, AH Tan, A Ahmad-Annuar, C Klein, LCS Tan, RL Rosales, ... The Lancet Neurology 18 (9), 865-879, 2019 | 161 | 2019 |
| Genome-wide association study of Parkinson’s disease in East Asians JN Foo, LC Tan, ID Irwan, WL Au, HQ Low, KM Prakash, A Ahmad-Annuar, ... Human Molecular Genetics 26 (1), 226-232, 2017 | 134 | 2017 |
| Spina bifida: pathogenesis, mechanisms, and genes in mice and humans SW Mohd-Zin, AI Marwan, MK Abou Chaar, A Ahmad-Annuar, ... Scientifica 2017 (1), 5364827, 2017 | 103 | 2017 |
| DRD and GRIN2B polymorphisms and their association with the development of impulse control behaviour among Malaysian Parkinson’s disease patients S Zainal Abidin, EL Tan, SC Chan, A Jaafar, AX Lee, MHN Abd Hamid, ... BMC neurology 15, 1-10, 2015 | 95 | 2015 |
| Improved inherited peripheral neuropathy genetic diagnosis by whole‐exome sequencing AP Drew, D Zhu, A Kidambi, C Ly, S Tey, MH Brewer, A Ahmad‐Annuar, ... Molecular genetics & genomic medicine 3 (2), 143-154, 2015 | 83 | 2015 |
| Mouse models for neurological disease M Hafezparast, A Ahmad-Annuar, NW Wood, SJ Tabrizi, EMC Fisher The Lancet Neurology 1 (4), 215-224, 2002 | 60 | 2002 |
| Quantitative magnetic resonance imaging and radiogenomic biomarkers for glioma characterisation: a systematic review P Seow, JHD Wong, A Ahmad-Annuar, A Mahajan, NA Abdullah, N Ramli The British journal of radiology 91 (1092), 20170930, 2018 | 51 | 2018 |
| Contextual modulation of visuomotor associations in bumble‐bees (Bombus terrestris) M Colborn, A Ahmad-Annuar, K Fauria, TS Collett Proceedings of the Royal Society of London. Series B: Biological Sciences …, 1999 | 51 | 1999 |
| The prevalence and distribution of spina bifida in a single major referral center in Malaysia A Sahmat, R Gunasekaran, SW Mohd-Zin, L Balachandran, MK Thong, ... Frontiers in Pediatrics 5, 237, 2017 | 44 | 2017 |
| LRRK2 G2385R and R1628P mutations are associated with an increased risk of Parkinson’s disease in the Malaysian population AA Gopalai, SY Lim, JY Chua, S Tey, TT Lim, N Mohamed Ibrahim, ... BioMed research international 2014 (1), 867321, 2014 | 42 | 2014 |
| Underrepresented populations in Parkinson's genetics research: current landscape and future directions AF Schumacher‐Schuh, A Bieger, O Okunoye, KY Mok, SY Lim, ... Movement Disorders 37 (8), 1593-1604, 2022 | 40 | 2022 |
| Multi-ancestry genome-wide association meta-analysis of Parkinson’s disease JJ Kim, D Vitale, DV Otani, MM Lian, K Heilbron, H Iwaki, J Lake, ... Nature genetics 56 (1), 27-36, 2024 | 39 | 2024 |
| Missense Mutation of Brain Derived Neurotrophic Factor (BDNF) Alters Neurocognitive Performance in Patients with Mild Traumatic Brain Injury: A Longitudinal Study V Narayanan, V Veeramuthu, A Ahmad-Annuar, N Ramli, V Waran, ... PLoS One 11 (7), e0158838, 2016 | 39 | 2016 |
| Identification of genetic risk loci and causal insights associated with Parkinson's disease in African and African admixed populations: a genome-wide association study M Rizig, S Bandres-Ciga, MB Makarious, OO Ojo, PW Crea, OV Abiodun, ... The Lancet Neurology 22 (11), 1015-1025, 2023 | 34 | 2023 |
| Using global team science to identify genetic Parkinson’s disease worldwide EJ Vollstedt, M Kasten, C Klein Annals of neurology 86 (2), 153, 2019 | 33 | 2019 |
| Paradigms for the identification of new genes in motor neuron degeneration M Hafezparast, A Ahmad‐Annuar, H Hummerich, P Shah, M Ford, ... Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders 4 (4), 249-257, 2003 | 33 | 2003 |
| Analysis of non-synonymous-coding variants of Parkinson's disease-related pathogenic and susceptibility genes in East Asian populations JN Foo, LC Tan, H Liany, TH Koh, ID Irwan, YY Ng, A Ahmad-Annuar, ... Human molecular genetics 23 (14), 3891-3897, 2014 | 32 | 2014 |
| Glucocerebrosidase (GBA) gene variants in a multi-ethnic Asian cohort with Parkinson’s disease: mutational spectrum and clinical features JL Lim, K Lohmann, AH Tan, YW Tay, KA Ibrahim, Z Abdul Aziz, ... Journal of Neural Transmission, 1-12, 2022 | 30 | 2022 |
