Montserrat
Fernández Prieto
Publicaciones en las que colabora con Montserrat Fernández Prieto (22)
2023
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Expanding the Clinical and Molecular Spectrum of FOXG1- and ZBTB18-Associated Neurodevelopmental Disorders
Cytogenetic and genome research, Vol. 163, Núm. 5-6, pp. 301-306
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The genomics of visuospatial neurocognition in obsessive-compulsive disorder: A preliminary GWAS
Journal of Affective Disorders, Vol. 333, pp. 365-376
2022
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A Machine Learning Approach in Autism Spectrum Disorders: From Sensory Processing to Behavior Problems
Frontiers in Molecular Neuroscience, Vol. 15
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How Executive Functions Correlate with Intelligence in Children and Adolescents in Autism Spectrum Disorders
Journal of Cognition and Development, Vol. 23, Núm. 5, pp. 776-790
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Neuropsychological performance and predictors of pharmacological treatment response in obsessive compulsive disorder
Journal of Affective Disorders, Vol. 317, pp. 52-58
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Rare coding variation provides insight into the genetic architecture and phenotypic context of autism
Nature Genetics, Vol. 54, Núm. 9, pp. 1320-1331
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Trio-based exome sequencing reveals a high rate of the de novo variants in intellectual disability
European Journal of Human Genetics, Vol. 30, Núm. 8, pp. 938-945
2021
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Executive Functioning: A Mediator Between Sensory Processing and Behaviour in Autism Spectrum Disorder
Journal of Autism and Developmental Disorders, Vol. 51, Núm. 6, pp. 2091-2103
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Exploring the biological role of postzygotic and germinal de novo mutations in ASD
Scientific Reports, Vol. 11, Núm. 1
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How is COVID-19 affecting patients with obsessive–compulsive disorder? A longitudinal study on the initial phase of the pandemic in a Spanish cohort
European Psychiatry, Vol. 64, Núm. 1
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Social Camouflaging in Females with Autism Spectrum Disorder: A Systematic Review
Journal of Autism and Developmental Disorders, Vol. 51, Núm. 7, pp. 2190-2199
2020
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Cerebellar Cognitive Affective Syndrome in Costa da Morte Ataxia (SCA36)
Cerebellum, Vol. 19, Núm. 4, pp. 501-509
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Executive impairments in Obsessive Compulsive Disorder: A systematic review with emotional and non-emotional paradigms
Psicothema, Vol. 32, Núm. 1, pp. 24-32
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Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism
Cell, Vol. 180, Núm. 3, pp. 568-584.e23
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Psychiatric comorbidities in Asperger syndrome are related with polygenic overlap and differ from other Autism subtypes
Translational Psychiatry, Vol. 10, Núm. 1
2017
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Touch Processing and Social Behavior in ASD
Journal of Autism and Developmental Disorders, Vol. 47, Núm. 8, pp. 2425-2433
2015
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Female patient with autistic disorder, intellectual disability, and co-morbid anxiety disorder: Expanding the phenotype associated with the recurrent 3q13.2-q13.31 microdeletion
American Journal of Medical Genetics, Part A, Vol. 167, Núm. 12, pp. 3121-3129
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Interstitial microdeletions including the chromosome band 4q13.2 and the UBA6 gene as possible causes of intellectual disability and behavior disorder
American Journal of Medical Genetics, Part A, Vol. 167, Núm. 12, pp. 3113-3120
2013
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Fenotipo Neuroanatómico y Neurocognitivo en el Síndrome de Williams
Revista de Investigación en Logopedia, Vol. 3, Núm. 1, pp. 18-33
2012
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Cognitive functioning in children and adults with Smith-Magenis syndrome
European Journal of Medical Genetics, Vol. 55, Núm. 6-7, pp. 394-399