Publicacións nas que colabora con Montserrat Fernández Prieto (22)

2023

  1. 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

  2. The genomics of visuospatial neurocognition in obsessive-compulsive disorder: A preliminary GWAS

    Journal of Affective Disorders, Vol. 333, pp. 365-376

2022

  1. A Machine Learning Approach in Autism Spectrum Disorders: From Sensory Processing to Behavior Problems

    Frontiers in Molecular Neuroscience, Vol. 15

  2. 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

  3. Neuropsychological performance and predictors of pharmacological treatment response in obsessive compulsive disorder

    Journal of Affective Disorders, Vol. 317, pp. 52-58

  4. Rare coding variation provides insight into the genetic architecture and phenotypic context of autism

    Nature Genetics, Vol. 54, Núm. 9, pp. 1320-1331

  5. 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

  1. 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

  2. Exploring the biological role of postzygotic and germinal de novo mutations in ASD

    Scientific Reports, Vol. 11, Núm. 1

  3. 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

  4. 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

  1. Cerebellar Cognitive Affective Syndrome in Costa da Morte Ataxia (SCA36)

    Cerebellum, Vol. 19, Núm. 4, pp. 501-509

  2. Executive impairments in Obsessive Compulsive Disorder: A systematic review with emotional and non-emotional paradigms

    Psicothema, Vol. 32, Núm. 1, pp. 24-32

  3. 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

  4. Psychiatric comorbidities in Asperger syndrome are related with polygenic overlap and differ from other Autism subtypes

    Translational Psychiatry, Vol. 10, Núm. 1

2017

  1. Touch Processing and Social Behavior in ASD

    Journal of Autism and Developmental Disorders, Vol. 47, Núm. 8, pp. 2425-2433

2015

  1. 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

  2. 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

  1. Fenotipo Neuroanatómico y Neurocognitivo en el Síndrome de Williams

    Revista de Investigación en Logopedia, Vol. 3, Núm. 1, pp. 18-33

2012

  1. Cognitive functioning in children and adults with Smith-Magenis syndrome

    European Journal of Medical Genetics, Vol. 55, Núm. 6-7, pp. 394-399