Zobrazeno 1 - 10
of 39
pro vyhledávání: '"Valérie, Côté"'
Autor:
Mélodie Proteau-Lemieux, Inga Sophia Knoth, Saeideh Davoudi, Charles-Olivier Martin, Anne-Marie Bélanger, Valérie Fontaine, Valérie Côté, Kristian Agbogba, Keely Vachon, Kerri Whitlock, Hazel Maridith Barlahan Biag, Angela John Thurman, Cory Rosenfelt, Flora Tassone, Julia Frei, Lucia Capano, Leonard Abbeduto, Sébastien Jacquemont, David Hessl, Randi Jenssen Hagerman, Andrea Schneider, Francois Bolduc, Evdokia Anagnostou, Sarah Lippe
Publikováno v:
Journal of Neurodevelopmental Disorders, Vol 16, Iss 1, Pp 1-17 (2024)
Abstract Background Fragile X syndrome (FXS) and autism spectrum disorder (ASD) are neurodevelopmental conditions that often have a substantial impact on daily functioning and quality of life. FXS is the most common cause of inherited intellectual di
Externí odkaz:
https://doaj.org/article/e9da68f609ee45e5ac044e74d9c0b585
Autor:
Florence Deguire, Gabriela López-Arango, Inga Sophia Knoth, Valérie Côté, Kristian Agbogba, Sarah Lippé
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-12 (2023)
Abstract Neurodevelopmental disorders (NDDs) are mostly diagnosed around the age of 4–5 years, which is too late considering that the brain is most susceptive to interventions during the first two years of life. Currently, diagnosis of NDDs is base
Externí odkaz:
https://doaj.org/article/f6c43cf671ee4b7fb461a56c33e7ece2
Autor:
Claudia Modenato, Kuldeep Kumar, Clara Moreau, Sandra Martin-Brevet, Guillaume Huguet, Catherine Schramm, Martineau Jean-Louis, Charles-Olivier Martin, Nadine Younis, Petra Tamer, Elise Douard, Fanny Thébault-Dagher, Valérie Côté, Audrey-Rose Charlebois, Florence Deguire, Anne M. Maillard, Borja Rodriguez-Herreros, Aurèlie Pain, Sonia Richetin, p11.2 European Consortium, Simons Searchlight Consortium, Lester Melie-Garcia, Leila Kushan, Ana I. Silva, Marianne B. M. van den Bree, David E. J. Linden, Michael J. Owen, Jeremy Hall, Sarah Lippé, Mallar Chakravarty, Danilo Bzdok, Carrie E. Bearden, Bogdan Draganski, Sébastien Jacquemont
Publikováno v:
Translational Psychiatry, Vol 11, Iss 1, Pp 1-10 (2021)
Abstract Many copy number variants (CNVs) confer risk for the same range of neurodevelopmental symptoms and psychiatric conditions including autism and schizophrenia. Yet, to date neuroimaging studies have typically been carried out one mutation at a
Externí odkaz:
https://doaj.org/article/3a9bd9d8d1da4a4690dbd8a4538abf20
Autor:
Gabriela López-Arango, Florence Deguire, Kristian Agbogba, Marc-Antoine Boucher, Inga S. Knoth, Ramy El-Jalbout, Valérie Côté, Amélie Damphousse, Samuel Kadoury, Sarah Lippé
Publikováno v:
Frontiers in Human Neuroscience, Vol 16 (2022)
Macrocephaly is present in about 2–5% of the general population. It can be found as an isolated benign trait or as part of a syndromic condition. Brain overgrowth has been associated with neurodevelopmental disorders such as autism during the first
Externí odkaz:
https://doaj.org/article/84dc2e1f92004c40a0db9efc956bc4bb
Publikováno v:
In International Journal of Nursing Studies Advances November 2020 2
Autor:
Mélodie Proteau-Lemieux, Inga Sophia Knoth, Kristian Agbogba, Valérie Côté, Hazel Maridith Barlahan Biag, Angela John Thurman, Charles-Olivier Martin, Anne-Marie Bélanger, Cory Rosenfelt, Flora Tassone, Leonard J. Abbeduto, Sébastien Jacquemont, Randi Hagerman, François Bolduc, David Hessl, Andrea Schneider, Sarah Lippé
Publikováno v:
Frontiers in Psychiatry, Vol 13 (2022)
Externí odkaz:
https://doaj.org/article/a9a990e624244ef78c52e61a01e7dd72
Autor:
Mélodie Proteau-Lemieux, Inga Sophia Knoth, Kristian Agbogba, Valérie Côté, Hazel Maridith Barlahan Biag, Angela John Thurman, Charles-Olivier Martin, Anne-Marie Bélanger, Cory Rosenfelt, Flora Tassone, Leonard J. Abbeduto, Sébastien Jacquemont, Randi Hagerman, François Bolduc, David Hessl, Andrea Schneider, Sarah Lippé
Publikováno v:
Frontiers in Psychiatry, Vol 12 (2021)
Introduction: Fragile X syndrome (FXS) is a genetic disorder caused by a mutation of the fragile X mental retardation 1 gene (FMR1). FXS is associated with neurophysiological abnormalities, including cortical hyperexcitability. Alterations in electro
Externí odkaz:
https://doaj.org/article/d93ca7bdf2524fd8a1e7d8324ddc4651
Antagonistic relationship of NuA4 with the non-homologous end-joining machinery at DNA damage sites.
Autor:
Salar Ahmad, Valérie Côté, Xue Cheng, Gaëlle Bourriquen, Vasileia Sapountzi, Mohammed Altaf, Jacques Côté
Publikováno v:
PLoS Genetics, Vol 17, Iss 9, p e1009816 (2021)
The NuA4 histone acetyltransferase complex, apart from its known role in gene regulation, has also been directly implicated in the repair of DNA double-strand breaks (DSBs), favoring homologous recombination (HR) in S/G2 during the cell cycle. Here,
Externí odkaz:
https://doaj.org/article/91831aa9281044388e22d5c6c7481cc1
Publikováno v:
PLoS Genetics, Vol 17, Iss 7, p e1009459 (2021)
Chromatin modifying complexes play important yet not fully defined roles in DNA repair processes. The essential NuA4 histone acetyltransferase (HAT) complex is recruited to double-strand break (DSB) sites and spreads along with DNA end resection. As
Externí odkaz:
https://doaj.org/article/c07c9a3c9fda49bf89c41828cf83325a
Sensory processing dysregulations as reliable translational biomarkers in SYNGAP1 haploinsufficiency
Autor:
Sarah Lippé, M. I. Carreno-Munoz, Jacques L. Michaud, Siyan Wang, G. Di Cristo, Kristian Agbogba, Maxime Lévesque, Massimo Avoli, Valérie Côté, Bidisha Chattopadhyaya
Publikováno v:
Brain. 145:754-769
Amongst the numerous genes associated with intellectual disability, SYNGAP1 stands out for its frequency and penetrance of loss-of-function variants found in patients, as well as the wide range of co-morbid disorders associated with its mutation. Mos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d01956815388ee7462fe40dde5fea73a
https://doi.org/10.1093/brain/awab329
https://doi.org/10.1093/brain/awab329