ANGEL MARIA
CARRACEDO ALVAREZ
Catedrático de universidade
Universidade de Vigo
Vigo, EspañaPublicacións en colaboración con investigadores/as de Universidade de Vigo (14)
2024
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Cognitive and clinical predictors of a long-term course in obsessive compulsive disorder: A machine learning approach in a prospective cohort study
Journal of Affective Disorders, Vol. 350, pp. 648-655
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Is There a Bias Towards Males in the Diagnosis of Autism? A Systematic Review and Meta-Analysis
Neuropsychology Review
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Population-based detection of children ASD/ADHD comorbidity from atypical sensory processing
Applied Intelligence, Vol. 54, Núm. 20, pp. 9906-9923
2023
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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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Rare coding variation provides insight into the genetic architecture and phenotypic context of autism
Nature Genetics, Vol. 54, Núm. 9, pp. 1320-1331
2021
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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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LIPG endothelial lipase and breast cancer risk by subtypes
Scientific Reports, Vol. 11, Núm. 1
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Obesity-related genetic determinants of stroke
Brain Communications, Vol. 3, Núm. 2
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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
2019
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Spatially explicit analysis reveals complex human genetic gradients in the Iberian Peninsula
Scientific Reports, Vol. 9, Núm. 1
2017
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Forensic genetics and genomics: Much more than just a human affair
PLoS Genetics, Vol. 13, Núm. 9
2015
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Investigation of gene-environment interactions between 47 newly identified breast cancer susceptibility loci and environmental risk factors
International Journal of Cancer, Vol. 136, Núm. 6, pp. E685-E696
2006
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Distinct phenotypic features and gender-specific disease manifestations in a Spanish family with desmin L370P mutation
Neuromuscular Disorders, Vol. 16, Núm. 8, pp. 498-503