Personalized Psychiatry

Our research in Personalized Psychiatry focuses on understanding individual variability in response to stress and how this variability shapes vulnerability or resilience to psychiatric disorders, including depression, anxiety, and substance abuse. We combine unique behavioral models of dominance and submissiveness with human studies to investigate the molecular, genetic, and hormonal mechanisms underlying stress-related psychopathology.

Using a wide range of molecular and genetic tools, we identify biomarkers and biological signatures (genomic and hormonal) that distinguish between stress-resilient and stress-vulnerable individuals. We further explore key pathways, including the hypothalamic–pituitary–adrenal (HPA) axis, dopaminergic signaling, and genes involved in synaptic plasticity, to better understand their role in shaping behavioral and emotional outcomes.

Our approach aims to move beyond a one-size-fits-all understanding of psychiatric disorders toward the identification of individual risk profiles, laying the foundation for early diagnosis and the development of prognostic tools for populations at risk of depression, anxiety, and addiction.

This study investigates how stress and personality traits influence vulnerability to drug addiction. Using a mouse model of dominance and submissiveness, we identify genomic and hormonal signatures underlying differential responses to drugs, aiming to develop personalized prognostic tools for addiction risk.
This study explores the biological mechanisms underlying depression and anxiety through animal models and human research. By comparing stress-resilient and vulnerable mouse strains, we identify biomarkers and assess their relevance to human psychiatric disorders, including MDD and bipolar disorder.
Exploring how stress, depression, and personality traits contribute to age-related cognitive decline, this research uses stress-resilient and vulnerable mouse models to identify underlying molecular mechanisms and genes, aiming to support early diagnosis and prevention of cognitive impairment in humans.
Prenatal stress shapes lifelong vulnerability to behavioral disorders. Using mouse models of stress resilience and susceptibility, we show that offspring of stressed, vulnerable mothers exhibit heightened stress responses and depressive traits, and identify placental glucocorticoid receptor pathways as targets for early diagnosis.
This research investigates molecular and functional mechanisms underlying learning, memory formation, and cognitive decline. Focusing on synaptic plasticity, signaling networks, and aging-related impairments, the study aims to identify key molecular regulators involved in memory deterioration, neurodegeneration, and depressive-like behavior.