Fulya Akçimen

Affiliations: 
McGill University (Montreal Neurological Institute) 
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"Fulya Akçimen"
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Eubanks E, VanderSleen K, Mody J, et al. (2024) Increased burden of rare risk variants across gene expression networks predisposes to sporadic Parkinson's disease. Biorxiv : the Preprint Server For Biology
Akçimen F, Chia R, Saez-Atienzar S, et al. (2024) Genomic Analysis Identifies Risk Factors in Restless Legs Syndrome. Annals of Neurology
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
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