Liao C - Search Results

1

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. Mov Disord. 2020 Jul;35(7):1153-1162. doi: 10.1002/mds.28031. Epub 2020 Apr 6. Mov Disord. 2020. PMID: 32249994

2

Investigating the association and causal relationship between restless legs syndrome and essential tremor.

Liao C, Houle G, He Q, Laporte AD, Girard SL, Dion PA, Rouleau GA. Liao C, et al. Parkinsonism Relat Disord. 2019 Apr;61:238-240. doi: 10.1016/j.parkreldis.2018.10.022. Epub 2018 Oct 19. Parkinsonism Relat Disord. 2019. PMID: 30366831 No abstract available.

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. 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. Among authors: liao c. Sleep. 2020 Apr 15;43(4):zsz265. doi: 10.1093/sleep/zsz265. Sleep. 2020. PMID: 31665514

5

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. Among authors: liao c. Front Genet. 2019 Nov 22;10:1219. doi: 10.3389/fgene.2019.01219. eCollection 2019. Front Genet. 2019. PMID: 31824583 Free PMC article.

6

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. Among authors: liao c. 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.

7

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. Among authors: liao c. Commun Biol. 2020 Jul 10;3(1):373. doi: 10.1038/s42003-020-1105-z. Commun Biol. 2020. PMID: 32651461 Free PMC article.

8

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. Front Genet. 2020 Jul 31;11:813. doi: 10.3389/fgene.2020.00813. eCollection 2020. Front Genet. 2020. PMID: 32849812 Free PMC article.

9

Assessing the NOTCH2NLC GGC expansion in European patients with essential tremor.

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. Liao C, et al. Brain. 2020 Dec 5;143(11):e89. doi: 10.1093/brain/awaa291. Brain. 2020. PMID: 33146671 No abstract available.

10

Expanded CAG Repeats in ATXN1, ATXN2, ATXN3, and HTT in the 1000 Genomes Project.

Akçimen F, Ross JP, Liao C, Spiegelman D, Dion PA, Rouleau GA. Akçimen F, et al. Among authors: liao c. Mov Disord. 2021 Feb;36(2):514-518. doi: 10.1002/mds.28341. Epub 2020 Nov 7. Mov Disord. 2021. PMID: 33159825

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