Associated Papers
Sex differences in the developing human cortex intersect with genetic risk of neurodevelopmental disorders.
Hennick K et al.
Biorxiv : the Preprint Server for Biology, 2025
40950053 (PubMed )
Supplement: media-31.xlsx › sex-gene-DNMs
Genetic variants and phenotypic data curated for the CAGI6 intellectual disability panel challenge.
Aspromonte MC et al.
Human Genetics, 2025
The missing link: ARID1B non-truncating variants causing Coffin-Siris syndrome due to protein aggregation.
Bosch E et al.
Human Genetics, 2024
39028335 (PubMed )
Supplement: 439_2024_2688_MOESM1_ESM.xlsx › missense_clinvar
Select a paper to view details