Latest
SRF | Dreem EEG Headband to Assess Sleep EEG Biomarkers in SYNGAP1
Virtual and experimental approaches to the pathogenicity of SynGAP1 missense mutations
Targeting gamma oscillations to improve cognition
SYNGAP1 Natural History Study/ Multidisciplinary Clinic at Children’s Hospital Colorado
Beyond the synapse: SYNGAP1 in primary and motile cilia
The Roles of Distinct Functions of SynGAP1 in SYNGAP1-Related Disorders
Quantifying perturbed SynGAP1 function caused by coding mutations
Therapeutic Strategies for Autism: Targeting Three Levels of the Central Dogma of Molecular Biology with a Focus on SYNGAP1
Involvement of the brain endothelium in neurodevelopmental disorders
Catatonia in Neurodevelopmental Conditions
A Data-Driven Approach to Reconstructing Disease Trajectories in SYNGAP1-Related Disorders
Harnessing mRNA metabolism for the development of precision gene therapy
Linking SYNGAP1 with Human-Specific Mechanisms of Neuronal Development
SYNGAP1 and Epilepsy SurgerySYNGAP1 and Epilepsy Surgery
Untitled Seminar
Giordano Lippi – Beyond transcription – microRNA mechanisms of brain development; Maria Isabel Carreño-Muñoz– Role of GABAergic circuits in the generation of sensory processing dysregulations in SYNGAP1 haploinsufficiency; Rhys Knowles-TBA; Nigel Kee- That other half: Derivation of posterior axial tissues from human stem cells
Targeting alternative splicing of SYNGAP1 using antisense oligonucleotides
The use of milk exosomes to increase the expression of SYNGAP1 expression in SYNGAP1 mice
Investigating the functional single-cell biology of SynGAP1 pathways
Untitled Seminar
Interpretation of SYNGAP1 Variants
Improving the assessment of SYNGAP1 and related genetic conditions by creating online measures for parents and patients
SynGAP modulates the body's biological clock: What Syngap1 mice can tell us about light & sleep
Types of seizures and EEG patterns in SYNGAP1
Sensory brain responses alterations as translational markers for SynGAP1 haploinsufficiency
Cómo y por qué utilizar modelos celulares humanos para estudiar Syngap1
Alteraciones en los patrones electrofisiológicos subyacentes a la percepción sensorial y su uso como biomarcadores de Syngap1
Interpretación de variantes en SYNGAP1
Desarrollo de tratamientos para síndromes de epilepsia: oportunidades para SYNGAP1
Alteraciones moleculares en el proteoma sináptico causadas por la deficiencia de SYNGAP1
Proyecto: Registro español SYNGAP1 - historia natural y estudio del sueño, Share4Rareplatform
Tipos de crisis epilépticas y patrones en electroencefalografía en SYNGAP1
Características generales de la encefalopatía epiléptica y desarrollo en SYNGAP1
Behavioural and cellular pathophysiology in a rat model of SYNGAP1 haploinsufficiency
Cannabinoids: What do we know
Cognition, behaviour and clinical trials in SYNGAP1
SYNGAP1 in translation: from deep phenotyping to human neurons
SYNGAP1 in the Developing Human Cortex
How and why to use human cellular models to study SYNGAP1
SYNGAP1: The road from gene discovery to targeted therapy
Towards therapeutics for Autism Spectrum Disorder using Syngap1 heterozygous mouse model
Rescue of SynGAP expression in SYNGAP1 Syndrome: Antisense Oligonucleotides (ASOs), small molecules, & viral genetic rescue
DEVELOPMENT OF AN OPTICAL ACTUATOR-REPORTER TOOLSET AND MOLECULAR-COMPUTATIONAL WORKFLOW TO PHENOTYPE PATHOGENICITY OF MISSENSE VARIANTS OF THE RARE MONOGENIC DISEASE GENE SYNGAP1
FENS Forum 2026
IMMUNOLIPOSOMES – A NEW THERAPEUTIC OPTION TO TREAT SYNGAP1-ASSOCIATED EPILEPSY
FENS Forum 2026
ELUCIDATING SYNGAP1 ISOFORM FUNCTIONS IN HUMAN NEURODEVELOPMENT USING CEREBRAL ORGANOIDS
FENS Forum 2026
DISTINCT SPECTRAL, CONNECTIVITY, AND FIRING DYNAMICS AROUND SEIZURES IN RAT MODELS OF SYNGAP1 AND GRIN2B NEURODEVELOPMENTAL DISORDERS
FENS Forum 2026
RECOMBINASE-ORTHOGONAL MONOSYNAPTIC RABIES VIRUS TRACING TOOLS FOR INTRA-BRAIN SYNAPTIC NETWORK COMPARISONS: A CASE STUDY OF SYNGAP1 HAPLOINSUFFICIENCY
FENS Forum 2026
INVESTIGATING THE RELATIONSHIPS BETWEEN ABSENCE SEIZURES, SLEEP, AND COGNITION IN A RAT MODEL OF <EM >SYNGAP1</EM>-RELATED INTELLECTUAL DISABILITY
FENS Forum 2026
PATIENT-SPECIFIC NEURODEVELOPMENTAL PHENOTYPES AND PHARMACOLOGICAL STRATEGIES IN SYNGAP1 SYNDROME
FENS Forum 2026
INVESTIGATING EARLY NEURODEVELOPMENTAL DISRUPTIONS IN <EM>SYNGAP1</EM> PATIENT IPSC-DERIVED NEURAL MODELS
FENS Forum 2026
Absence-seizure blockade rescues REM sleep impairment in a rat model of SYNGAP1 haploinsufficiency
Elucidating the role of FUS and FMRP in regulating SYNGAP1 expression in human iPSC-derived neurons
Mnk1/2 kinases regulate memory and autism-related behaviours via Syngap1
Reduced social interaction in two rat models of SYNGAP1 haploinsufficiency
Understanding the role of SYNGAP1 in Parvalbumin-expressing GABAergic circuit development and function
Brain-state dependent deficit in visual discrimination in a mouse model of SYNGAP1-related intellectual disability and autism
FENS Forum 2024
Establishment of an in vitro patient-derived hiPSC-based blood-brain barrier model of SYNGAP1 disorder
FENS Forum 2024
Exploring patient-specific mechanisms in SYNGAP1-related pathology to develop targeted therapeutic strategies
FENS Forum 2024
SYNGAP coverage
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