檢索結果 - Sébastien Jacquemont
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In-vivo probabilistic atlas of human thalamic nuclei based on diffusion- weighted magnetic resonance imaging 由 Elena Najdenovska, Yasser Alemán‐Gómez, Giovanni Battistella, Maxime Descoteaux, Patric Hagmann, Sébastien Jacquemont, Philippe Maeder, Jean‐Philippe Thiran, Eleonora Fornari, Meritxell Bach Cuadra
出版 2018Artigo -
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Robust thalamic nuclei segmentation method based on local diffusion magnetic resonance properties 由 Giovanni Battistella, Elena Najdenovska, Philippe Maeder, Naghmeh Ghazaleh, Alessandro Daducci, Jean‐Philippe Thiran, Sébastien Jacquemont, Constantin Tuleasca, Marc Levivier, Meritxell Bach Cuadra, Eleonora Fornari
出版 2016Artigo -
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Genetic modulation of brain dynamics in neurodevelopmental disorders: the impact of copy number variations on resting-state EEG 由 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
出版 2025Artigo -
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Mavoglurant in Fragile X Syndrome: Results of two open-label, extension trials in adults and adolescents 由 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
出版 2018Artigo -
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Neuropathological, clinical and molecular pathology in female fragile X premutation carriers with and without FXTAS 由 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
出版 2012Artigo -
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KCTD13 is a major driver of mirrored neuroanatomical phenotypes of the 16p11.2 copy number variant 由 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
出版 2012Artigo
相關主題
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