
Advances in ADHD and Co-Occurring Disorders: Genetics & Beyond
Advances in ADHD and Co-Occurring Disorders: Genetics & Beyond
Pricing
Information
Date & Time
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Learning Objectives
Participants will be able to:
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Identify the current genetic and neurobiological underpinnings of ADHD and its comorbidities based on large-scale consortia research
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Evaluate the clinical relevance of biological markers for improved diagnosis and treatment response prediction in neurodevelopmental disorders.
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Translate insights from molecular and neuroimaging studies into potential applications for therapeutic development and precision medicine.
Educational Goal
Description
Over the past two decades, our understanding of neurodevelopmental psychiatric disorders—particularly ADHD and its frequent comorbidities—has moved from symptom-based models toward biologically-grounded frameworks. This session outlines the progress in psychiatric genetics, highlighting validated insights from large-scale international collaborations and translational research.
Initial genome-wide association studies (GWAS) involving ADHD identified significant heritability but lacked the statistical power to define underlying mechanisms. Today, through efforts like the Psychiatric Genomics Consortium (PGC), IMpACT, and ENIGMA, large meta-analyses have consistently uncovered common and rare genetic variants linked to ADHD. These findings are now being integrated with neuroimaging data and experimental models to define biological pathways.
This presentation explores how these converging methods—including iPSC-derived neurons, bioinformatics, and neuroimaging genetics—are mapping the path from genotype to phenotype. It also reviews how these advances inform our understanding of comorbidities (e.g., autism, mood disorders), treatment response variability, and the goal of biologically anchored diagnosis and therapeutic innovation. Special attention is given to the urgent clinical relevance of these findings: ADHD is a family illness with profound long-term impact if left untreated. Timely diagnosis and interventions require a scientific and therapeutic model that reflects the complexity of its etiology.