Výsledky vyhledávání - Sébastien Jacquemont
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Genetic and phenotypic similarity across major psychiatric disorders: a systematic review and quantitative assessment Autor Vincent-Raphaël Bourque, Cécile Poulain, Catherine Proulx, Clara Moreau, Ridha Joober, Baudouin Forgeot d’Arc, Guillaume Huguet, Sébastien Jacquemont
Vydáno 2024Revisão -
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In-vivo probabilistic atlas of human thalamic nuclei based on diffusion- weighted magnetic resonance imaging Autor Elena Najdenovska, Yasser Alemán‐Gómez, Giovanni Battistella, Maxime Descoteaux, Patric Hagmann, Sébastien Jacquemont, Philippe Maeder, Jean‐Philippe Thiran, Eleonora Fornari, Meritxell Bach Cuadra
Vydáno 2018Artigo -
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Robust thalamic nuclei segmentation method based on local diffusion magnetic resonance properties Autor Giovanni Battistella, Elena Najdenovska, Philippe Maeder, Naghmeh Ghazaleh, Alessandro Daducci, Jean‐Philippe Thiran, Sébastien Jacquemont, Constantin Tuleasca, Marc Levivier, Meritxell Bach Cuadra, Eleonora Fornari
Vydáno 2016Artigo -
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Genetic modulation of brain dynamics in neurodevelopmental disorders: the impact of copy number variations on resting-state EEG Autor Adrien E. E. Dubois, Elisabeth Audet-Duchesne, Inga Sophia Knoth, Charles-Olivier Martin, Khadijé Jizi, Petra Tamer, Nadine Younis, Sébastien Jacquemont, Guillaume Dumas, Sarah Lippé
Vydáno 2025Artigo -
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Mavoglurant in Fragile X Syndrome: Results of two open-label, extension trials in adults and adolescents Autor Randi Hagerman, Sébastien Jacquemont, Elizabeth Berry‐Kravis, Vincent des Portes, Andrew C. Stanfield, Barbara Koumaras, G. Rosenkranz, Alessandra Murgia, Christian Wolf, George Apostol, Florian von Raison
Vydáno 2018Artigo -
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Neuropathological, clinical and molecular pathology in female fragile X premutation carriers with and without FXTAS Autor Flora Tassone, Claudia Greco, Michael R. Hunsaker, Andreea L. Seritan, Robert F. Berman, Louise W. Gane, Sébastien Jacquemont, Kirin Basuta, Lee-Way Jin, Paul J. Hagerman, Randi J. Hagerman
Vydáno 2012Artigo -
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KCTD13 is a major driver of mirrored neuroanatomical phenotypes of the 16p11.2 copy number variant Autor Christelle Golzio, Jason R. Willer, Michael E. Talkowski, Edwin C. Oh, Yu Taniguchi, Sébastien Jacquemont, Alexandre Reymond, Mei Sun, Akira Sawa, James F. Gusella, Atsushi Kamiya, J. Beckmann, Nicholas Katsanis
Vydáno 2012Artigo
Vyhledávací nástroje:
Související témata
Biology
Gene
Genetics
Medicine
Psychology
Psychiatry
Genome
Copy-number variation
Autism
Neuroscience
Phenotype
Autism spectrum disorder
Cognition
Internal medicine
Fragile X syndrome
Gene duplication
Developmental psychology
Disease
Pathology
Computational biology
Fragile x
Environmental health
FMR1
Genotype
Intellectual disability
Pediatrics
Population
Schizophrenia (object-oriented programming)
Ataxia
Clinical psychology