Jan 19–22, 2027 | Beaver Run Conference Center, Breckenridge, CO, United States
Scientific Organizers:
Tomasz Nowakowski, Xin Jin, Stephan Sanders, and Zhaolan (Joe) Zhou
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Scientific Organizers: Tomasz Nowakowski, Xin Jin, Stephan Sanders, and Zhaolan (Joe) Zhou
Tomasz Nowakowski, PhD
University of California, San Francisco
Xin Jin, PhD
Scripps Research Institute
Stephan Sanders, PhD
University of Oxford
Zhaolan (Joe) Zhou, PhD
University of Pennsylvania
***Meeting program subject to change.
Available Formats: = Livestream = In Person = On DemandBooking Function
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Tuesday, January 19, 2027
Fundraising
Wednesday, January 20, 2027
A Journey in Rett Syndrome: From Basic Science Discovery of Causal Gene to Therapies of Patients
Experimental Validation of Common Variants of Neurodevelopmental Disorders
Massively Parallel Dissection of Gene to Phenotype Relationships Using Perturb-seq
The Genetic Orchestra of Autism: From Medicine to Neurodiversity
Short Talk: Genomic Configurations Model the Systems-Level Organization of Autism-Associated Variation
Short Talk: Multimodal Spatial Functional Genomics in Neurodevelopmental Disorders
Short Talk: Parallel CRISPRi Screening of 204 SPARK Cohort Autism Risk Genes Reveals Cell-type-specific Gene Programs in Human Cortical Neurons and Microglia
Short Talk: Rice University, Intrinsic Coordination of Dynamic Molecular Signatures Shape the Human Prefrontal Cortex
Short Talk: Postnatal Reconfiguration of the Human Neuronal Epigenome Via Hydroxymethylation
Short Talk: CRISPR screens identify CSNK2A1 as a Druggable Regulator of MeCP2 and Highlight Molecular Convergence Across Okur-Chung Neurodevelopmental Syndrome and MECP2-Related Disorders
Short Talk: Membrane Cytoskeletal Aggregation Drives Proteotoxic and Network Dysfunction in SPTBN1 Syndrome
Short Talk: Histone Serotonylation Recruitment of KMT2E Regulates Chromatin Dynamics In Neurodevelopment
Short Talk: Understanding Reversibility of Developmental Disorders: Towards a Tissue-Specific, Reversible Mouse Model of Cornelia De Lange Syndrome
Genetic and Epigenetic Mechanisms of Cortical Development
Deep Mutational Scanning Approaches to Correlate Structure and Function of Proteins
Kinase Signaling in Neurodevelopmental Disorders
Short Talk: Neuronal Primary Cilia Modulate Excitatory Synapses Formation and Plasticity
Short Talk: Brain-Wide Cellular-Resolution Mapping Of Cortical Defects In A Mouse Model of 22q11.2 Deletion Syndrome
Thursday, January 21, 2027
Transient Connectivity and Circuit Reprogramming in Cortical Development
Spontaneous Activity–Gene Program Interplay in Circuits Development: Implications for Neurodevelopmental Disorders
Wiring Specificity of Neural Circuits
The Neuroscience of Prosocial Behavior: From Helping and Cooperation to Social AI
Short Talk: Intrinsic Excitability Deficits Precede Synaptic Dysfunction in the Developing mPFC of Shank3B−/− Mice
Short Talk: Cross-Species Analyses Reveal Disturbance of Cortical Functional Hierarchy in Rett Syndrome
Establishing Tools for Human Neuroscience
Interrogating Human Specific and Neurodevelopmental Risk Genes using Chimeric Models
Brain Organoids to Study Neurodevelopmental Disorders
Short Talk: Transcriptomic Convergence and the Female Protective Effect in Autism
Short Talk: Spatial Single-Cell Omics Reveals Selective Neuronal Vulnerability and Pathological Cell States in Focal Cortical Dysplasia Type 2
Friday, January 22, 2027
Epigenetic Dissection of Mechanisms underlying Neurodevelopmental Disorders
Insights into Gene-Environment Interactions in Neurodevelopmental Disorders
Cytokine Regulation of Brain and Behavior
Neonatal Hypoxia and Pediatric Risk Factors
Short Talk: A Tale of Two Risks: Early-Life Adversity Shapes the Expression of SCHEMA Schizophrenia Risk Genes
Short Talk: Using Human Stem Cell-Based Organoid Models to Understand Neurodevelopmental Disorders
Short Talk: Genetic Disruption of Developmental Scaling in Chiari I Malformation
Short Talk: Investigating Astrocyte Contributions to TSC Using Human Brain Organoid Models
Short Talk: Spliceosome Malfunction Leads to Neurodevelopmental Disorders With Overlapping Features
Short Talk: MYT1L Haploinsufficiency Profoundly Dysregulates Transcription, Circuitry, and Behavior across Multiple Brain Regions
Short Talk: Gene Replacement in Neurodevelopmental Disorders: Reversing Metabolic and Neuronal Altered Function in SSADH Deficiency
Short Talk: A Conserved Molecular Signature of CHD8 Haploinsufficiency Across Diverse Neurodevelopmental Contexts
Short Talk: Distinct Molecular Mechanisms Define Classes of Pathogenic Variants in TBR1 Syndrome
Short Talk: An Innovative RNA Technology Targeting the Reversal of Neurodevelopmental Conditions Stemming from Haploinsufficiency
Gene Targeting Strategies for Autism and Neurodevelopmental Disorders
Lessons from Neurodevelopmental Disease
Short Talk: Making Sense Out of Nonsense: Switching Poison Exons to Modify Neurodevelopmental Disorders
The Parents’ Journey through Drug Development: Making the IMPOSSIBLE POSSIBLE-The Angelman Syndrome Story
Saturday, January 23, 2027
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