Fulya Akçimen
Affiliations: | McGill University (Montreal Neurological Institute) |
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Sign in to add mentor| Guy A. Rouleau | grad student | 2017- | McGill University (Montreal Neurological Institute) |
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| Chia R, Ray A, Shah Z, et al. (2024) Genome sequence analyses identify novel risk loci for multiple system atrophy. Neuron |
| Akçimen F, Chia R, Saez-Atienzar S, et al. (2023) Genomic analysis identifies risk factors in restless legs syndrome. Medrxiv : the Preprint Server For Health Sciences |
| Ross JP, Akçimen F, Liao C, et al. (2023) Rare variant and polygenic analyses of amyotrophic lateral sclerosis in the French-Canadian genome. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 100967 |
| Akçimen F, Lopez ER, Landers JE, et al. (2023) Amyotrophic lateral sclerosis: translating genetic discoveries into therapies. Nature Reviews. Genetics |
| Ross JP, Akçimen F, Liao C, et al. (2022) Questioning the Association of the Dinucleotide Repeat With Amyotrophic Lateral Sclerosis. Neurology. Genetics. 8: e678 |
| Akçimen F, Dion PA, Rouleau GA. (2022) Progress in the genetics of RLS: the path ahead in the era of WGS. Sleep |
| Liao C, Vuokila V, Catoire H, et al. (2022) Transcriptome-wide association study reveals increased neuronal FLT3 expression is associated with Tourette's syndrome. Communications Biology. 5: 289 |
| Liao C, Castonguay CE, Heilbron K, et al. (2022) Association of Essential Tremor With Novel Risk Loci: A Genome-Wide Association Study and Meta-analysis. Jama Neurology |
| da Graça FF, Peluzzo TM, Bonadia LC, et al. (2021) Diagnostic Yield of Whole Exome Sequencing for Adults with Ataxia: a Brazilian Perspective. Cerebellum (London, England) |
| Estiar MA, Yu E, Haj Salem I, et al. (2021) Evidence for Non-Mendelian Inheritance in Spastic Paraplegia 7. Movement Disorders : Official Journal of the Movement Disorder Society |