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Movement Disorders : Official Journal of the Movement Disorder Society
|
November 7, 2020
Expanded CAG Repeats in ATXN1, ATXN2, ATXN3, and HTT in the 1000 Genomes Project
Fulya Akçimen, Jay P Ross, Calwing Liao, et al.
Molecular Psychiatry
|
April 7, 2026
Convergent coexpression reveals shared biological mechanisms underlying common and rare variant risk in six neuropsychiatric disorders
Hanna Abe, Calwing Liao, Lide Han, et al.
Nature Communications
|
October 3, 2019
Transcriptome-wide association study of attention deficit hyperactivity disorder identifies associated genes and phenotypes
Calwing Liao, Alexandre D Laporte, Dan Spiegelman, et al.
Nature Protocols
|
March 29, 2025
Tutorial: guidelines for quality filtering of whole-exome and whole-genome sequencing data for population-scale association analyses
Julia M Sealock, Franjo Ivankovic, Calwing Liao, et al.
Communications Biology
|
July 12, 2020
Transcriptome-wide association study for restless legs syndrome identifies new susceptibility genes
Fulya Akçimen, Faezeh Sarayloo, Calwing Liao, et al.
Communications Biology
|
March 31, 2022
Transcriptome-wide association study reveals increased neuronal FLT3 expression is associated with Tourette's syndrome
Calwing Liao, Veikko Vuokila, Hélène Catoire, et al.
NPJ Genomic Medicine
|
August 4, 2022
Transcriptomic effects of propranolol and primidone converge on molecular pathways relevant to essential tremor
Charles-Etienne Castonguay, Calwing Liao, Anouar Khayachi, et al.
Journal of Psychiatry & Neuroscience : JPN
|
June 2, 2021
Chronic lithium treatment alters the excitatory/ inhibitory balance of synaptic networks and reduces mGluR5-PKC signalling in mouse cortical neurons
Anouar Khayachi, Ariel Ase, Calwing Liao, et al.
Scientific Reports
|
October 30, 2025
Lithium partially rescues gene expression and enhancer activity from heterozygous knockout of AKAP11 while inducing novel differential changes
Nargess Farhangdoost, Alessia Pietrantonio, Yumin Liu, et al.
Neurology. Genetics
|
August 4, 2022
Questioning the Association of the <i>STMN2</i> Dinucleotide Repeat With Amyotrophic Lateral Sclerosis
Jay P Ross, Fulya Akçimen, Calwing Liao, et al.
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of 4
Search research articles
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Showing results (1-10 of 35) with videos related to
Sort By:
Page
of 4
Movement Disorders : Official Journal of the Movement Disorder Society
|
November 7, 2020
Expanded CAG Repeats in ATXN1, ATXN2, ATXN3, and HTT in the 1000 Genomes Project
Fulya Akçimen, Jay P Ross, Calwing Liao, et al.
Molecular Psychiatry
|
April 7, 2026
Convergent coexpression reveals shared biological mechanisms underlying common and rare variant risk in six neuropsychiatric disorders
Hanna Abe, Calwing Liao, Lide Han, et al.
Nature Communications
|
October 3, 2019
Transcriptome-wide association study of attention deficit hyperactivity disorder identifies associated genes and phenotypes
Calwing Liao, Alexandre D Laporte, Dan Spiegelman, et al.
Nature Protocols
|
March 29, 2025
Tutorial: guidelines for quality filtering of whole-exome and whole-genome sequencing data for population-scale association analyses
Julia M Sealock, Franjo Ivankovic, Calwing Liao, et al.
Communications Biology
|
July 12, 2020
Transcriptome-wide association study for restless legs syndrome identifies new susceptibility genes
Fulya Akçimen, Faezeh Sarayloo, Calwing Liao, et al.
Communications Biology
|
March 31, 2022
Transcriptome-wide association study reveals increased neuronal FLT3 expression is associated with Tourette's syndrome
Calwing Liao, Veikko Vuokila, Hélène Catoire, et al.
NPJ Genomic Medicine
|
August 4, 2022
Transcriptomic effects of propranolol and primidone converge on molecular pathways relevant to essential tremor
Charles-Etienne Castonguay, Calwing Liao, Anouar Khayachi, et al.
Journal of Psychiatry & Neuroscience : JPN
|
June 2, 2021
Chronic lithium treatment alters the excitatory/ inhibitory balance of synaptic networks and reduces mGluR5-PKC signalling in mouse cortical neurons
Anouar Khayachi, Ariel Ase, Calwing Liao, et al.
Scientific Reports
|
October 30, 2025
Lithium partially rescues gene expression and enhancer activity from heterozygous knockout of AKAP11 while inducing novel differential changes
Nargess Farhangdoost, Alessia Pietrantonio, Yumin Liu, et al.
Neurology. Genetics
|
August 4, 2022
Questioning the Association of the <i>STMN2</i> Dinucleotide Repeat With Amyotrophic Lateral Sclerosis
Jay P Ross, Fulya Akçimen, Calwing Liao, et al.
Page
of 4