Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Faezeh Sarayloo"'
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
Publikováno v:
Frontiers in Neurology, Vol 10 (2019)
Restless legs syndrome (RLS) is a common sleep-related disorder for which the underlying biological pathways and genetic determinants are not well understood. The genetic factors so far identified explain less than 10% of the disease heritability. Th
Externí odkaz:
https://doaj.org/article/1902ab8c7ad94a0c9d5150d1dea53441
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:
Calwing Liao, Guy A. Rouleau, Patrick A. Dion, Fulya Akçimen, Faezeh Sarayloo, Jay P. Ross, Rachel De Barros Oliveira
Publikováno v:
Communications Biology, Vol 3, Iss 1, Pp 1-5 (2020)
Communications Biology
Communications Biology
Restless legs syndrome (RLS) is a common neurological condition, with a prevalence of 5–15% in Central Europe and North America. Although genome-wide association studies (GWAS) have identified some common risk regions for RLS, the causal genes have
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::389aa0a5519bf032ac082765accd1bfe
http://link.springer.com/article/10.1038/s42003-020-1105-z
http://link.springer.com/article/10.1038/s42003-020-1105-z
Autor:
Guy A. Rouleau, Patrick A. Dion, Dan Spiegelman, Fulya Akçimen, Rachel De Barros Oliveira, Daniel Rochefort, Faezeh Sarayloo
Publikováno v:
Eur J Hum Genet
Restless legs syndrome (RLS) is a common sleep-related sensory-motor disorder. It is characterized by uncomfortable sensations in the legs during the evening or at night. The symptoms can be partially relieved by movement, so typically affected indiv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::806ebc6a2596a8725ee4510c41469adb
https://doi.org/10.1038/s41431-020-0670-4
https://doi.org/10.1038/s41431-020-0670-4
Autor:
Lan Xiong, Calwing Liao, Guy A. Rouleau, Ziv Gan-Or, Patrick A. Dion, Cynthia V. Bourassa, Jennifer A. Ruskey, Faezeh Sarayloo, Rachel De Barros Oliveira, Fulya Akçimen, Jay P. Ross
Publikováno v:
Sleep. 43
Currently, a total of 19 genetic loci are associated with the risk for developing RLS. This study aimed to assess these RLS predisposing genetic variants, as well as investigate the epidemiological profile and diagnostic features of individuals with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::526714d48078e172b31073be99b0c15b
https://doi.org/10.1093/sleep/zsz265
https://doi.org/10.1093/sleep/zsz265
Autor:
Daniel Rochefort, Hélène Catoire, Alexandre Dionne-Laporte, Faezeh Sarayloo, Rachel De Barros Oliveira, Guy A. Rouleau, Patrick A. Dion, Gabrielle Houle, Gustavo Turecki, Fulya Akçimen, Jay P. Ross
Publikováno v:
PLoS ONE
PLoS ONE, Vol 14, Iss 11, p e0225186 (2019)
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://explore.openaire.eu/search/publication?articleId=doi_dedup___::193609431c0c17ecfe966e0330b08985
https://pubmed.ncbi.nlm.nih.gov/31725784
https://pubmed.ncbi.nlm.nih.gov/31725784
Autor:
Alex Rajput, Dan Spiegelman, Fulya Akçimen, Alexandre D. Laporte, Patrick A. Dion, Daniel Rochefort, Calwing Liao, Faezeh Sarayloo, Gabrielle Houle, Guy A. Rouleau, Qin He
The genetic factors predisposing to essential tremor (ET), of one of the most common movement disorders, remains largely unknown. While current studies have examined the contribution of both common and rare genetic variants, very few have investigate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::abd2c74fdf631e5ad241ee77378f5f27
https://doi.org/10.1101/580753
https://doi.org/10.1101/580753
Autor:
Fulya Akçimen, Daniel Rochefort, Qin He, Faezeh Sarayloo, Alexandre D. Laporte, Patrick A. Dion, Hélène Catoire, Guy A. Rouleau, Dan Spiegelman, Simone Diamond, Calwing Liao
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.STK32Bwas significantly associ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e55d62948591fc1f74ef27975783b65e