Danielle Mouhlas

Danielle Mouhlas works in genetics research focused on identifying and characterizing genetic and chromosomal abnormalities, including rare disease diagnostics and developmental disorders linked to gene mutations. Recent work includes studies on prenatal genetic diagnosis and a neurodevelopmental condition tied to a specific gene (MAPK1) within a group of related disorders called RASopathies. This research relates to understanding how genetic variations contribute to disease and how they can be detected before or after birth.

Publication output has been low and irregular over the last decade, with a peak in 2020 and generally fewer than two papers per year since then.

Generated by claude-sonnet-5 from public bibliographic data · Jul 20, 2026