| Year |
Citation |
Score |
| 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 |
0.816 |
|
| 2023 |
Docherty AR, Mullins N, Ashley-Koch AE, Qin X, Coleman JRI, Shabalin A, Kang J, Murnyak B, Wendt F, Adams M, Campos AI, DiBlasi E, Fullerton JM, Kranzler HR, Bakian AV, ... ... Liao C, et al. GWAS Meta-Analysis of Suicide Attempt: Identification of 12 Genome-Wide Significant Loci and Implication of Genetic Risks for Specific Health Factors. The American Journal of Psychiatry. 180: 723-738. PMID 37777856 DOI: 10.1176/appi.ajp.21121266 |
0.596 |
|
| 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 |
0.806 |
|
| 2023 |
Liao C, Moyses-Oliveira M, De Esch CEF, Bhavsar R, Nuttle X, Li A, Yu A, Burt ND, Erdin S, Fu JM, Wang M, Morley T, Han L, Dion PA, Rouleau GA, et al. Convergent coexpression of autism-associated genes suggests some novel risk genes may not be detectable in large-scale genetic studies. Cell Genomics. 3: 100277. PMID 37082147 DOI: 10.1016/j.xgen.2023.100277 |
0.503 |
|
| 2022 |
Castonguay CE, Liao C, Khayachi A, Liu Y, Medeiros M, Houle G, Ross JP, Dion PA, Rouleau GA. Transcriptomic effects of propranolol and primidone converge on molecular pathways relevant to essential tremor. Npj Genomic Medicine. 7: 46. PMID 35927430 DOI: 10.1038/s41525-022-00318-9 |
0.811 |
|
| 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 |
0.787 |
|
| 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 |
0.796 |
|
| 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 |
Mullins N, Kang J, Campos AI, Coleman JRI, Edwards AC, Galfalvy H, Levey DF, Lori A, Shabalin A, Starnawska A, Su MH, Watson HJ, Adams M, Awasthi S, Gandal M, ... ... Liao C, et al. Dissecting the Shared Genetic Architecture of Suicide Attempt, Psychiatric Disorders, and Known Risk Factors. Biological Psychiatry. PMID 34861974 DOI: 10.1016/j.biopsych.2021.05.029 |
0.535 |
|
| 2021 |
He Q, Jantac Mam-Lam-Fook C, Chaignaud J, Danset-Alexandre C, Iftimovici A, Gradels Hauguel J, Houle G, Liao C, Dion PA, Rouleau GA, Kebir O, Krebs MO, Chaumette B. Influence of polygenic risk scores for schizophrenia and resilience on the cognition of individuals at-risk for psychosis. Translational Psychiatry. 11: 518. PMID 34628483 DOI: 10.1038/s41398-021-01624-z |
0.653 |
|
| 2021 |
Khayachi A, Ase A, Liao C, Kamesh A, Kuhlmann N, Schorova L, Chaumette B, Dion P, Alda M, Séguéla P, Rouleau G, Milnerwood A. Chronic lithium treatment alters the excitatory/ inhibitory balance of synaptic networks and reduces mGluR5-PKC signalling in mouse cortical neurons. Journal of Psychiatry & Neuroscience : Jpn. 46: E402-E414. PMID 34077150 DOI: 10.1503/jpn.200185 |
0.329 |
|
| 2021 |
Mullins N, Forstner AJ, O'Connell KS, Coombes B, Coleman JRI, Qiao Z, Als TD, Bigdeli TB, Børte S, Bryois J, Charney AW, Drange OK, Gandal MJ, Hagenaars SP, Ikeda M, ... ... Liao C, et al. Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology. Nature Genetics. PMID 34002096 DOI: 10.1038/s41588-021-00857-4 |
0.619 |
|
| 2021 |
Alfradique-Dunham I, Al-Ouran R, von Coelln R, Blauwendraat C, Hill E, Luo L, Stillwell A, Young E, Kaw A, Tan M, Liao C, Hernandez D, Pihlstrom L, Grosset D, Shulman LM, et al. Genome-Wide Association Study Meta-Analysis for Parkinson Disease Motor Subtypes. Neurology. Genetics. 7: e557. PMID 33987465 DOI: 10.1212/NXG.0000000000000557 |
0.399 |
|
| 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 |
0.762 |
|
| 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 |
0.723 |
|
| 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 |
0.766 |
|
| 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 |
0.77 |
|
| 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 |
0.759 |
|
| 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 |
0.787 |
|
| 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 |
0.771 |
|
| 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 |
0.753 |
|
| 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 |
0.772 |
|
| 2019 |
He Q, Kebir O, Houle G, Liao C, Dion PA, Rouleau GA, Krebs M, Chaumette B. T80SCHIZOPHRENIA POLYGENIC RISK SCORE CORRELATES WITH DECREASED COGNITIVE FUNCTIONS IN ULTRA-HIGH-RISK INDIVIDUALS FOR PSYCHOSIS European Neuropsychopharmacology. 29: S258-S259. DOI: 10.1016/J.Euroneuro.2019.08.279 |
0.673 |
|
| 2018 |
Liao C, Houle G, He Q, Laporte AD, Girard SL, Dion PA, Rouleau GA. Investigating the association and causal relationship between restless legs syndrome and essential tremor. Parkinsonism & Related Disorders. PMID 30366831 DOI: 10.1016/J.Parkreldis.2018.10.022 |
0.7 |
|
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