Jérémy Hall

This study uses MEA assays to show that L-type calcium channel inhibitors affect synchronous firing in hiPSC-derived neuronal networks, suggesting their utility for studying psychiatric risk genes.

This study uses a rat model to show that Cyfip1 haploinsufficiency causes white matter changes, myelin thinning, reduced mature oligodendrocytes, and behavioural inflexibility.

This study examines genotype-phenotype relationships in children with copy number variants (CNVs) associated with high neuropsychiatric risk, finding similar adverse effects across different CNVs with some qualitative differences.

The paper investigates how genetic risk for schizophrenia and developmental delay relates to structural brain abnormalities in midline white matter.

This study evaluates parental satisfaction with genetic counseling and information about psychiatric risks in children with rare disorders, finding dissatisfaction with communication and reliance on non-professional sources for information.

This study shows that enhancing ERK2 signalling protects neurons and improves memory in mouse models of neurodegenerative diseases.

This study examines phenotypic and genetic characteristics of adults diagnosed with ASD, finding high psychiatric comorbidity and increased polygenic risk for common ASD variants.

The paper examines the dynamic expression of risk genes for schizophrenia and bipolar disorder across developmental stages in brain regions, finding distinct expression patterns between the two disorders.

This study investigates how NMDAR hypofunction affects sensory processing in mice by altering top-down and bottom-up cortical activity.