| Year |
Citation |
Score |
| 2024 |
Eubanks E, VanderSleen K, Mody J, Patel N, Sacks B, Farahani MD, Wang J, Elliott J, Jaber N, Akçimen F, Bandres-Ciga S, Helweh F, Liu J, Archakam S, Kimelman R, et al. Increased burden of rare risk variants across gene expression networks predisposes to sporadic Parkinson's disease. Biorxiv : the Preprint Server For Biology. PMID 39257816 DOI: 10.1101/2024.08.30.610195 |
0.334 |
|
| 2024 |
Akçimen F, Chia R, Saez-Atienzar S, Ruffo P, Rasheed M, Ross JP, Liao C, Ray A, Dion PA, Scholz SW, Rouleau GA, Traynor BJ. Genomic Analysis Identifies Risk Factors in Restless Legs Syndrome. Annals of Neurology. PMID 39078117 DOI: 10.1002/ana.27040 |
0.799 |
|
| 2024 |
Chia R, Ray A, Shah Z, Ding J, Ruffo P, Fujita M, Menon V, Saez-Atienzar S, Reho P, Kaivola K, Walton RL, Reynolds RH, Karra R, Sait S, Akcimen F, et al. Genome sequence analyses identify novel risk loci for multiple system atrophy. Neuron. PMID 38701790 DOI: 10.1016/j.neuron.2024.04.002 |
0.444 |
|
| 2023 |
Akçimen F, Chia R, Saez-Atienzar S, Ruffo P, Rasheed M, Ross JP, Liao C, Ray A, Dion PA, Scholz SW, Rouleau GA, Traynor BJ. Genomic analysis identifies risk factors in restless legs syndrome. Medrxiv : the Preprint Server For Health Sciences. PMID 38168192 DOI: 10.1101/2023.12.19.23300211 |
0.813 |
|
| 2023 |
Ross JP, Akçimen F, Liao C, Kwan K, Phillips DE, Schmilovich Z, Spiegelman D, Genge A, Dupré N, Dion PA, Farhan SMK, Rouleau GA. 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. PMID 37638500 DOI: 10.1016/j.gim.2023.100967 |
0.799 |
|
| 2023 |
Akçimen F, Lopez ER, Landers JE, Nath A, Chiò A, Chia R, Traynor BJ. Amyotrophic lateral sclerosis: translating genetic discoveries into therapies. Nature Reviews. Genetics. PMID 37024676 DOI: 10.1038/s41576-023-00592-y |
0.322 |
|
| 2022 |
Ross JP, Akçimen F, Liao C, Spiegelman D, Weisburd B, Dupré N, Dion PA, Rouleau GA, Farhan SMK. Questioning the Association of the Dinucleotide Repeat With Amyotrophic Lateral Sclerosis. Neurology. Genetics. 8: e678. PMID 35923349 DOI: 10.1212/NXG.0000000000000678 |
0.779 |
|
| 2022 |
Akçimen F, Dion PA, Rouleau GA. Progress in the genetics of RLS: the path ahead in the era of WGS. Sleep. PMID 35675840 DOI: 10.1093/sleep/zsac136 |
0.418 |
|
| 2022 |
Liao C, Vuokila V, Catoire H, Akçimen F, Ross JP, Bourassa CV, Dion PA, Meijer IA, Rouleau GA. Transcriptome-wide association study reveals increased neuronal FLT3 expression is associated with Tourette's syndrome. Communications Biology. 5: 289. PMID 35354918 DOI: 10.1038/s42003-022-03231-0 |
0.799 |
|
| 2022 |
Liao C, Castonguay CE, Heilbron K, Vuokila V, Medeiros M, Houle G, Akçimen F, Ross JP, Catoire H, Diez-Fairen M, Kang J, Mueller SH, Girard SL, Hopfner F, Lorenz D, et al. Association of Essential Tremor With Novel Risk Loci: A Genome-Wide Association Study and Meta-analysis. Jama Neurology. PMID 34982113 DOI: 10.1001/jamaneurol.2021.4781 |
0.798 |
|
| 2021 |
da Graça FF, Peluzzo TM, Bonadia LC, Martinez ARM, Diniz de Lima F, Pedroso JL, Barsottini OGP, Gama MTD, Akçimen F, Dion PA, Rouleau GA, Marques W, França MC. Diagnostic Yield of Whole Exome Sequencing for Adults with Ataxia: a Brazilian Perspective. Cerebellum (London, England). PMID 33956305 DOI: 10.1007/s12311-021-01268-1 |
0.497 |
|
| 2021 |
Estiar MA, Yu E, Haj Salem I, Ross JP, Mufti K, Akçimen F, Leveille E, Spiegelman D, Ruskey JA, Asayesh F, Dagher A, Yoon G, Tarnopolsky M, Boycott KM, Dupre N, et al. Evidence for Non-Mendelian Inheritance in Spastic Paraplegia 7. Movement Disorders : Official Journal of the Movement Disorder Society. PMID 33598982 DOI: 10.1002/mds.28528 |
0.692 |
|
| 2020 |
Akçimen F, Ross JP, Liao C, Spiegelman D, Dion PA, Rouleau GA. Expanded CAG Repeats in ATXN1, ATXN2, ATXN3, and HTT in the 1000 Genomes Project. Movement Disorders : Official Journal of the Movement Disorder Society. PMID 33159825 DOI: 10.1002/mds.28341 |
0.756 |
|
| 2020 |
Liao C, Akçimen F, Diez-Fairen M, Houle G, Ross JP, Schmilovich Z, Spiegelman D, Vuokila V, Catoire H, Meijer IA, Pastor P, Rajput A, Dion PA, Rouleau GA. Assessing the NOTCH2NLC GGC expansion in European patients with essential tremor. Brain : a Journal of Neurology. PMID 33146671 DOI: 10.1093/brain/awaa291 |
0.73 |
|
| 2020 |
Liao C, Sarayloo F, Vuokila V, Rochefort D, Akçimen F, Diamond S, Houle G, Laporte AD, Spiegelman D, He Q, Catoire H, Dion PA, Rouleau GA. Transcriptomic Changes Resulting From Overexpression Identify Pathways Potentially Relevant to Essential Tremor. Frontiers in Genetics. 11: 813. PMID 32849812 DOI: 10.3389/Fgene.2020.00813 |
0.776 |
|
| 2020 |
Kotan D, Özözen Ayas Z, Tunca C, Gungen BD, Akçimen F, Başak AN. Phenotypic and genotypic features of patients diagnosed with ALS in the city of Sakarya, Turkey. Acta Neurologica Belgica. PMID 32671691 DOI: 10.1007/s13760-020-01441-z |
0.322 |
|
| 2020 |
Akçimen F, Sarayloo F, Liao C, Ross JP, Oliveira RB, Dion PA, Rouleau GA. Transcriptome-wide association study for restless legs syndrome identifies new susceptibility genes. Communications Biology. 3: 373. PMID 32651461 DOI: 10.1038/s42003-020-1105-z |
0.784 |
|
| 2020 |
Tunca C, Şeker T, Akçimen F, Coşkun C, Bayraktar E, Palvadeau R, Zor S, Koçoğlu C, Kartal E, Şen NE, Hamzeiy H, Özoğuz Erimiş A, Norman U, Karakahya O, Olgun G, et al. Revisiting the complex architecture of ALS in Turkey: Expanding genotypes, shared phenotypes, molecular networks, and a public variant database. Human Mutation. PMID 32579787 DOI: 10.1002/Humu.24055 |
0.417 |
|
| 2020 |
Sarayloo F, Spiegelman D, Rochefort D, Akçimen F, De Barros Oliveira R, Dion PA, Rouleau GA. SKOR1 has a transcriptional regulatory role on genes involved in pathways related to restless legs syndrome. European Journal of Human Genetics : Ejhg. PMID 32572201 DOI: 10.1038/S41431-020-0670-4 |
0.791 |
|
| 2020 |
Liao C, Sarayloo F, Rochefort D, Houle G, Akçimen F, He Q, Laporte AD, Spiegelman D, Poewe W, Berg D, Müller S, Hopfner F, Deuschl G, Kuhlenbäeumer G, Rajput A, et al. Multiomics Analyses Identify Genes and Pathways Relevant to Essential Tremor. Movement Disorders : Official Journal of the Movement Disorder Society. PMID 32249994 DOI: 10.1002/Mds.28031 |
0.768 |
|
| 2020 |
Akçimen F, Martins S, Liao C, Bourassa CV, Catoire H, Nicholson GA, Riess O, Raposo M, França MC, Vasconcelos J, Lima M, Lopes-Cendes I, Saraiva-Pereira ML, Jardim LB, Sequeiros J, et al. Genome-wide association study identifies genetic factors that modify age at onset in Machado-Joseph disease. Aging. 12. PMID 32205469 DOI: 10.18632/aging.102825 |
0.756 |
|
| 2019 |
Akçimen F, Ross JP, Bourassa CV, Liao C, Rochefort D, Gama MTD, Dicaire MJ, Barsottini OG, Brais B, Pedroso JL, Dion PA, Rouleau GA. Investigation of the Repeat Expansion in a Canadian and a Brazilian Ataxia Cohort: Identification of Novel Conformations. Frontiers in Genetics. 10: 1219. PMID 31824583 DOI: 10.3389/Fgene.2019.01219 |
0.779 |
|
| 2019 |
Sarayloo F, Dionne-Laporte A, Catoire H, Rochefort D, Houle G, Ross JP, Akçimen F, Barros Oliveira R, Turecki G, Dion PA, Rouleau GA. Mineral absorption is an enriched pathway in a brain region of restless legs syndrome patients with reduced MEIS1 expression. Plos One. 14: e0225186. PMID 31725784 DOI: 10.1371/Journal.Pone.0225186 |
0.757 |
|
| 2019 |
Akçimen F, Ross JP, Sarayloo F, Liao C, De Barros Oliveira R, Ruskey JA, Bourassa CV, Dion PA, Xiong L, Gan-Or Z, Rouleau GA. Genetic and epidemiological characterization of restless legs syndrome in Québec. Sleep. PMID 31665514 DOI: 10.1093/Sleep/Zsz265 |
0.759 |
|
| 2019 |
Liao C, Laporte AD, Spiegelman D, Akçimen F, Joober R, Dion PA, Rouleau GA. Transcriptome-wide association study of attention deficit hyperactivity disorder identifies associated genes and phenotypes. Nature Communications. 10: 4450. PMID 31575856 DOI: 10.1038/S41467-019-12450-9 |
0.735 |
|
| 2018 |
Akçimen F, Spiegelman D, Dionne-Laporte A, Gan-Or Z, Dion PA, Rouleau GA. Screening of novel restless legs syndrome-associated genes in French-Canadian families. Neurology. Genetics. 4: e296. PMID 30637332 DOI: 10.1212/Nxg.0000000000000296 |
0.531 |
|
| 2017 |
Mitropoulos K, Merkouri Papadima E, Xiromerisiou G, Balasopoulou A, Charalampidou K, Galani V, Zafeiri KV, Dardiotis E, Ralli S, Deretzi G, John A, Kydonopoulou K, Papadopoulou E, di Pardo A, Akcimen F, et al. Genomic variants in the FTO gene are associated with sporadic amyotrophic lateral sclerosis in Greek patients. Human Genomics. 11: 30. PMID 29216901 DOI: 10.1186/S40246-017-0126-2 |
0.381 |
|
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