Ruth O. Braden
Melbourne, VIC, Australia
Last Updated: 09/26/2026
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Found 25 publications
Speech, language, social communication, and communication assessments in Rett syndrome: A systematic review.
Journal: Developmental medicine and child neurology
Published: March 11, 2026
Improving prognostication for individuals with FOXP1 syndrome: Parent-reported practical and social skills in 52 individuals.
Journal: Research in developmental disabilities
Published: June 17, 2025
Speech and Language Disorders Associated With 7q31 Deletions Implicating FOXP2.
Journal: American journal of medical genetics. Part A
Published: March 21, 2025
Understanding speech and language in KIF1A-associated neurological disorder.
Journal: European journal of human genetics : EJHG
Published: March 02, 2025
Speech, Language and Non-verbal Communication in CLN2 and CLN3 Batten Disease.
Journal: Journal of inherited metabolic disease
Published: September 01, 2024
Inherited PURA Pathogenic Variant Associated With a Mild Neurodevelopmental Disorder.
Journal: Neurology. Genetics
Published: April 16, 2024
Adaptive functioning in children and young adults with monogenic neurodevelopmental disorders.
Journal: Developmental medicine and child neurology
Published: March 21, 2024
Clinician Awareness of Stickler Syndromes Among Australian Allied Health Care Professionals.
Journal: Journal of multidisciplinary healthcare
Published: December 11, 2023
Self-Reported Stuttering Severity Is Accurate: Informing Methods for Large-Scale Data Collection in Stuttering.
Journal: Journal of speech, language, and hearing research : JSLHR
Published: December 05, 2023
Perisylvian and Hippocampal Anomalies in Individuals With Pathogenic GRIN2A Variants.
Journal: Neurology. Genetics
Published: October 04, 2023
Clinical phenotype of FOXP1 syndrome: parent-reported medical signs and symptoms in 40 individuals.
Journal: Journal of medical genetics
Published: July 26, 2023
SETBP1 variants outside the degron disrupt DNA-binding, transcription and neuronal differentiation capacity to cause a heterogeneous neurodevelopmental disorder.
Journal: Nature communications
Published: January 25, 2023
Last Updated: 09/26/2026