Antonio Benítez‐Burraco

This study links bipolar disorder to human self-domestication by showing overlapping genes and differential expression in brain regions associated with the disorder.

The paper tests if self-domestication and neural crest loci contribute to neurodevelopmental disorder heritability, finding significant enrichments that disappear when other genomic annotations are included.

The paper identifies overlapping patterns of abnormal gene expression in blood samples from individuals with autism and Williams syndrome, with similar trends but greater dysregulation in Williams syndrome.

The paper reports on a girl with a 1q42.3q43 duplication, describing her severe speech and language impairments and identifying potential candidate genes.

The paper describes a child with a 9p24.3 duplication causing language impairment, highlighting deficits in language structure and function and potential molecular mechanisms involving the SLIT/ROBO/FOXP2 network and DOCK8-CDC42 interaction.

The paper identifies enrichment of MER41 LTR sequences in promoters of intellectual disability-associated genes, linking immune pathways to cognitive evolution.

The paper identifies genes related to language development and evolution that are dysregulated in WS blood samples, suggesting they may contribute to language dysfunction in the condition.

The paper proposes a set of candidate genes, the language oscillogenome, that link genetic factors to brain rhythms involved in language processing.

The paper infers Neanderthal language-related neural oscillation properties by analyzing methylation differences in genes associated with language oscillogenome.

The paper reports a novel MED13L mutation associated with language impairment, cognitive delay, and behavioral issues in a child.

This paper explores how developmental dyslexia may arise from impaired brain rhythms during speech and reading tasks, linking genetic factors to neural oscillations and potential diagnostic applications.

This paper explores the hypothesis that schizophrenia may be linked to human self-domestication, suggesting a connection between domestication syndrome genes and schizophrenia-related brain expression changes.

The paper reports a family with a 15q11.2 BP1-BP2 duplication showing variable phenotypes, suggesting gene expression level changes may affect cognitive development.