Paola Niola

This study analyzes transcriptomic differences between 46,XY and 46,XX human fetal brain cortex samples to understand sex chromosome and hormone effects during early development.

This study uses single-nucleus and bulk RNA sequencing to identify novel pathogenic mechanisms of ovarian insufficiency in Turner Syndrome, beyond X chromosome haploinsufficiency.

This study maps the anatomical and transcriptional changes in human fetal ovaries during development using single-nuclei RNA sequencing and other techniques, identifying novel pathways and regulators.

This study creates a cell atlas of human adrenal cortex development using multi-omics approaches, revealing key developmental processes and potential therapeutic implications.