Akçimen F - Search Results

1

Transcriptomic Changes Resulting From STK32B Overexpression Identify Pathways Potentially Relevant to Essential Tremor.

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. Liao C, et al. Among authors: akcimen f. Front Genet. 2020 Jul 31;11:813. doi: 10.3389/fgene.2020.00813. eCollection 2020. Front Genet. 2020. PMID: 32849812 Free PMC article.

2

Screening of novel restless legs syndrome-associated genes in French-Canadian families.

Akçimen F, Spiegelman D, Dionne-Laporte A, Gan-Or Z, Dion PA, Rouleau GA. Akçimen F, et al. Neurol Genet. 2018 Dec 20;4(6):e296. doi: 10.1212/NXG.0000000000000296. eCollection 2018 Dec. Neurol Genet. 2018. PMID: 30637332 Free PMC article.

3

Transcriptome-wide association study of attention deficit hyperactivity disorder identifies associated genes and phenotypes.

Liao C, Laporte AD, Spiegelman D, Akçimen F, Joober R, Dion PA, Rouleau GA. Liao C, et al. Among authors: akcimen f. Nat Commun. 2019 Oct 1;10(1):4450. doi: 10.1038/s41467-019-12450-9. Nat Commun. 2019. PMID: 31575856 Free PMC article.

4

Genetic and epidemiological characterization of restless legs syndrome in Québec.

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. Akçimen F, et al. Sleep. 2020 Apr 15;43(4):zsz265. doi: 10.1093/sleep/zsz265. Sleep. 2020. PMID: 31665514

5

Mineral absorption is an enriched pathway in a brain region of restless legs syndrome patients with reduced MEIS1 expression.

Sarayloo F, Dionne-Laporte A, Catoire H, Rochefort D, Houle G, Ross JP, Akçimen F, Barros Oliveira R, Turecki G, Dion PA, Rouleau GA. Sarayloo F, et al. Among authors: akcimen f. PLoS One. 2019 Nov 14;14(11):e0225186. doi: 10.1371/journal.pone.0225186. eCollection 2019. PLoS One. 2019. PMID: 31725784 Free PMC article.

6

Investigation of the RFC1 Repeat Expansion in a Canadian and a Brazilian Ataxia Cohort: Identification of Novel Conformations.

Akçimen F, Ross JP, Bourassa CV, Liao C, Rochefort D, Gama MTD, Dicaire MJ, Barsottini OG, Brais B, Pedroso JL, Dion PA, Rouleau GA. Akçimen F, et al. Front Genet. 2019 Nov 22;10:1219. doi: 10.3389/fgene.2019.01219. eCollection 2019. Front Genet. 2019. PMID: 31824583 Free PMC article.

7

Genome-wide association study identifies genetic factors that modify age at onset in Machado-Joseph disease.

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, Dion PA, Rouleau GA. Akçimen F, et al. Aging (Albany NY). 2020 Mar 23;12(6):4742-4756. doi: 10.18632/aging.102825. Epub 2020 Mar 23. Aging (Albany NY). 2020. PMID: 32205469 Free PMC article.

8

Multiomics Analyses Identify Genes and Pathways Relevant to Essential Tremor.

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, Dion PA, Rouleau GA. Liao C, et al. Among authors: akcimen f. Mov Disord. 2020 Jul;35(7):1153-1162. doi: 10.1002/mds.28031. Epub 2020 Apr 6. Mov Disord. 2020. PMID: 32249994

9

SKOR1 has a transcriptional regulatory role on genes involved in pathways related to restless legs syndrome.

Sarayloo F, Spiegelman D, Rochefort D, Akçimen F, De Barros Oliveira R, Dion PA, Rouleau GA. Sarayloo F, et al. Among authors: akcimen f. Eur J Hum Genet. 2020 Nov;28(11):1520-1528. doi: 10.1038/s41431-020-0670-4. Epub 2020 Jun 22. Eur J Hum Genet. 2020. PMID: 32572201 Free PMC article.

10

Transcriptome-wide association study for restless legs syndrome identifies new susceptibility genes.

Akçimen F, Sarayloo F, Liao C, Ross JP, Oliveira RB, Dion PA, Rouleau GA. Akçimen F, et al. Commun Biol. 2020 Jul 10;3(1):373. doi: 10.1038/s42003-020-1105-z. Commun Biol. 2020. PMID: 32651461 Free PMC article.

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