Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Gabrielle Houle"'
Autor:
Charles-Etienne Castonguay, Calwing Liao, Anouar Khayachi, Yumin Liu, Miranda Medeiros, Gabrielle Houle, Jay P. Ross, Patrick A. Dion, Guy A. Rouleau
Publikováno v:
npj Genomic Medicine, Vol 7, Iss 1, Pp 1-13 (2022)
Abstract Essential tremor (ET) is one of the most common movement disorders, affecting nearly 5% of individuals over 65 years old. Despite this, few genetic risk loci for ET have been identified. Recent advances in pharmacogenomics have previously be
Externí odkaz:
https://doaj.org/article/a039ede0ce6a42c794df849f2ee72262
Autor:
Qin He, Célia Jantac Mam-Lam-Fook, Julie Chaignaud, Charlotte Danset-Alexandre, Anton Iftimovici, Johanna Gradels Hauguel, Gabrielle Houle, Calwing Liao, ICAAR study group, Patrick A. Dion, Guy A. Rouleau, Oussama Kebir, Marie-Odile Krebs, Boris Chaumette
Publikováno v:
Translational Psychiatry, Vol 11, Iss 1, Pp 1-9 (2021)
Abstract Cognitive impairment is a core feature of schizophrenia which precedes the onset of full psychotic symptoms, even in the ultra-high-risk stage (UHR). Polygenic risk scores (PRS) can be computed for many psychiatric disorders and phenotyping
Externí odkaz:
https://doaj.org/article/175a1bb7257548a3b8336d9bb1081eb3
Autor:
Calwing Liao, Faezeh Sarayloo, Veikko Vuokila, Daniel Rochefort, Fulya Akçimen, Simone Diamond, Gabrielle Houle, Alexandre D. Laporte, Dan Spiegelman, Qin He, Hélène Catoire, Patrick A. Dion, Guy A. Rouleau
Publikováno v:
Frontiers in Genetics, Vol 11 (2020)
Objective: Essential tremor (ET) is a common movement disorder that has a high heritability. A number of genetic studies have associated different genes and loci with ET, but few have investigated the biology of any of these genes. STK32B was signifi
Externí odkaz:
https://doaj.org/article/1b7dca9c79064eee9686d420cea20d75
Autor:
Faezeh Sarayloo, Alexandre Dionne-Laporte, Helene Catoire, Daniel Rochefort, Gabrielle Houle, Jay P Ross, Fulya Akçimen, Rachel De Barros Oliveira, Gustavo Turecki, Patrick A Dion, Guy A Rouleau
Publikováno v:
PLoS ONE, Vol 14, Iss 11, p e0225186 (2019)
Restless legs syndrome is a common complex disorder with different genetic and environmental risk factors. Here we used human cell lines to conduct an RNA-Seq study and observed how the gene showing the most significant association with RLS, MEIS1, a
Externí odkaz:
https://doaj.org/article/c09c9e6260a54b268d5adb635aca985a
Autor:
Patrick A. Dion, Anouar Khayachi, Gabrielle Houle, Guy A. Rouleau, Charles-Etienne Castonguay, Jay P. Ross, Calwing Liao
Essential tremor (ET) is one of the most common movement disorders, affecting nearly 5% of individuals over 65 years old. Despite its high heritability, few genetic risk loci for ET have been identified. Recent advances in pharmacogenomics have gener
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::724dfdce8121c2706158420a8efaff3e
https://doi.org/10.1101/2021.09.13.460137
https://doi.org/10.1101/2021.09.13.460137
Autor:
Christian Martel, Guy A. Rouleau, Nicolas Dupré, Leila Sellami, Lydia Touzel-Deschênes, Kevin Lacroix, Robert Laforce, François Gros-Louis, Laurence Martineau, Andréane Lavallée, Gabrielle Houle, Marie Beaudin, Nicolas Chrestian
Publikováno v:
Neurology: Genetics
ObjectiveTo better characterize the neurologic and cognitive profile of patients with spinocerebellar ataxia 34 (SCA34) caused by ELOVL4 mutations and to demonstrate the presence of ELOVL4 cellular localization and distribution abnormalities in skin-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::08a0ec7a813cf582d867b0a39f84074a
http://europepmc.org/articles/PMC7073455
http://europepmc.org/articles/PMC7073455
Autor:
Alex Rajput, Sandra B. Laurent, Claire S. Leblond, Gabrielle Houle, Carles Vilariño-Güell, Cynthia V. Bourassa, Guy A. Rouleau, Jean-François Schmouth, Amirthagowri Ambalavanan, Sylvain Chouinard, Dan Spiegelman, Patrick A. Dion, Michel Panisset, Nicolas Dupré
Publikováno v:
Molecular Neurobiology. 56:4317-4321
Essential Tremor is a prevalent neurological disorder of unknown etiology. Studies suggest that genetic factors contribute to this pathology. To date, no causative mutations in a gene have been reproducibly reported. All three structures of the olivo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::83a961e1f3b0a0b4f48dbc29b814ffd5
https://doi.org/10.1007/s12035-018-1369-1
https://doi.org/10.1007/s12035-018-1369-1
Dramaturgy of the Body: Marcello Moretti's Construction of Arlecchino at the Piccolo Teatro of Milan
Autor:
Gabrielle Houle
Publikováno v:
New Theatre Quarterly. 34:130-144
In this article Gabrielle Houle examines the dramaturgical process that actor Marcello Moretti applied to his creation of Arlecchino's body in Giorgio Strehler's globally acclaimed productions of The Servant of Two Masters at the Piccolo Teatro of Mi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::05017446d1f60a6099a463e399be90d5
https://doi.org/10.1017/s0266464x18000040
https://doi.org/10.1017/s0266464x18000040
Autor:
Gabrielle Houle, Jennifer Heywood
Publikováno v:
Theatre Research in Canada. 38:250-259
In April 2016, we attended the final presentations of our students in a first-year acting course at Glendon College, which is the bilingual faculty of York University.1As a part of the course evaluation, the instructor, Jennifer Heywood, asked the st
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e3519dd7ff130880e029d43fa3435d6f
https://doi.org/10.3138/tric.38.2.250
https://doi.org/10.3138/tric.38.2.250