Fulya Akçimen

Affiliations: 
McGill University (Montreal Neurological Institute) 
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"Fulya Akçimen"
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Liao C, Sarayloo F, Vuokila V, et al. (2020) Transcriptomic Changes Resulting From Overexpression Identify Pathways Potentially Relevant to Essential Tremor. Frontiers in Genetics. 11: 813
Sarayloo F, Spiegelman D, Rochefort D, et al. (2020) SKOR1 has a transcriptional regulatory role on genes involved in pathways related to restless legs syndrome. European Journal of Human Genetics : Ejhg
Liao C, Sarayloo F, Rochefort D, et al. (2020) Multiomics Analyses Identify Genes and Pathways Relevant to Essential Tremor. Movement Disorders : Official Journal of the Movement Disorder Society
Akçimen F, Ross JP, Bourassa CV, et al. (2019) Investigation of the Repeat Expansion in a Canadian and a Brazilian Ataxia Cohort: Identification of Novel Conformations. Frontiers in Genetics. 10: 1219
Sarayloo F, Dionne-Laporte A, Catoire H, et al. (2019) Mineral absorption is an enriched pathway in a brain region of restless legs syndrome patients with reduced MEIS1 expression. Plos One. 14: e0225186
Akçimen F, Ross JP, Sarayloo F, et al. (2019) Genetic and epidemiological characterization of restless legs syndrome in Québec. Sleep
Liao C, Laporte AD, Spiegelman D, et al. (2019) Transcriptome-wide association study of attention deficit hyperactivity disorder identifies associated genes and phenotypes. Nature Communications. 10: 4450
Akçimen F, Spiegelman D, Dionne-Laporte A, et al. (2018) Screening of novel restless legs syndrome-associated genes in French-Canadian families. Neurology. Genetics. 4: e296
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