Search Results - Sébastien Jacquemont
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Genetic and phenotypic similarity across major psychiatric disorders: a systematic review and quantitative assessment by Vincent-Raphaël Bourque, Cécile Poulain, Catherine Proulx, Clara Moreau, Ridha Joober, Baudouin Forgeot d’Arc, Guillaume Huguet, Sébastien Jacquemont
Published 2024Revisão -
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In-vivo probabilistic atlas of human thalamic nuclei based on diffusion- weighted magnetic resonance imaging by Elena Najdenovska, Yasser Alemán‐Gómez, Giovanni Battistella, Maxime Descoteaux, Patric Hagmann, Sébastien Jacquemont, Philippe Maeder, Jean‐Philippe Thiran, Eleonora Fornari, Meritxell Bach Cuadra
Published 2018Artigo -
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Robust thalamic nuclei segmentation method based on local diffusion magnetic resonance properties by Giovanni Battistella, Elena Najdenovska, Philippe Maeder, Naghmeh Ghazaleh, Alessandro Daducci, Jean‐Philippe Thiran, Sébastien Jacquemont, Constantin Tuleasca, Marc Levivier, Meritxell Bach Cuadra, Eleonora Fornari
Published 2016Artigo -
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Genetic modulation of brain dynamics in neurodevelopmental disorders: the impact of copy number variations on resting-state EEG by 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
Published 2025Artigo -
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Mavoglurant in Fragile X Syndrome: Results of two open-label, extension trials in adults and adolescents by 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
Published 2018Artigo -
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Neuropathological, clinical and molecular pathology in female fragile X premutation carriers with and without FXTAS by 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
Published 2012Artigo -
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KCTD13 is a major driver of mirrored neuroanatomical phenotypes of the 16p11.2 copy number variant by 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
Published 2012Artigo
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Biology
Gene
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Copy-number variation
Autism
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Autism spectrum disorder
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Fragile X syndrome
Gene duplication
Developmental psychology
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Fragile x
Environmental health
FMR1
Genotype
Intellectual disability
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Schizophrenia (object-oriented programming)
Ataxia
Clinical psychology