Elise Brimble

Publication Activity (10 Years)

Years Active: 2023-2024
Publications (10 Years): 6

Top Topics

Intellectual Disability

Autism Spectrum Disorder

Top Venues

Orphanet journal of rare diseases

bioRxiv : the preprint server for biology

This page only lists publications with an associated author ORCID identifier.

Publications

Kimberly Wiltrout, Elise Brimble, Annapurna H Poduri
Comprehensive phenotypes of patients with SYNGAP1-related disorder reveals high rates of epilepsy and autism. Epilepsia (2024)
Kimberly Wiltrout, Elise Brimble, Annapurna H Poduri
Comprehensive phenotypes of patients with SYNGAP1-related disorder reveals high rates of epilepsy and autism. Epilepsia 65 (5) (2024)
Kimberly Wiltrout, Elise Brimble, Annapurna H Poduri
Comprehensive phenotypes of patients with SYNGAP1-related disorder reveals high rates of epilepsy and autism. Epilepsia 65 (5) (2024)
Kimberly Wiltrout, Elise Brimble, Annapurna H Poduri
Comprehensive phenotypes of patients with SYNGAP1-related disorder reveals high rates of epilepsy and autism. Epilepsia 65 (5) (2024)
Kate E McCluskey, Katherine M Stovell, Karen Law, Elina Kostyanovskaya, James Schmidt, Cameron R T Exner, Jeanselle Dea, Elise Brimble, Matthew W State, A Jeremy Willsey, Helen Rankin Willsey
Autism gene variants disrupt enteric neuron migration and cause gastrointestinal dysmotility. bioRxiv : the preprint server for biology (2024)
Elise Brimble, Kathryn G Reyes, Kopika Kuhathaas, Orrin Devinsky, Maura R Z Ruzhnikov, Xilma R Ortiz-Gonzalez, Ingrid Scheffer, Nadia Bahi-Buisson, Heather Olson, null null
Expanding genotype-phenotype correlations in FOXG1 syndrome: results from a patient registry. Orphanet journal of rare diseases 18 (1) (2023)