Steven A. Wall
Oxford, ENG OX39DS, United Kingdom
Last Updated: 09/26/2026
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Found 73 publications
Evaluating the pathogenic significance of unique chromosomal variants in craniosynostosis using patient-derived induced pluripotent stem cells and mouse modelling.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: March 03, 2026
Regulatory elements in SEM1-DLX5-DLX6 (7q21.3) locus contribute to genetic control of coronal nonsyndromic craniosynostosis and bone density-related traits.
Journal: Genetics in medicine open
Published: September 30, 2024
Reassessing the association: Evaluation of a polyalanine deletion variant of RUNX2 in non-syndromic sagittal and metopic craniosynostosis.
Journal: Journal of anatomy
Published: February 13, 2024
A European Multicenter Outcome Study of Perioperative Airway Management Policies following Midface Surgery in Syndromic Craniosynostosis.
Journal: Plastic and reconstructive surgery
Published: January 30, 2024
Pathogenic variants in the paired-related homeobox 1 gene (PRRX1) cause craniosynostosis with incomplete penetrance.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: December 22, 2022
Neoforehead Remodelling Techniques for Fronto-Orbital Advancement and Remodelling in the Oxford Craniofacial Unit: Lateral Remodelling and a Novel Central Self-Stabilizing S-Osteotomy Technique.
Journal: The Journal of craniofacial surgery
Published: November 16, 2021
Psychosocial Impact of Coronal Access Scars in Craniosynostosis Procedures on Patients and Their Families.
Journal: The Journal of craniofacial surgery
Published: September 24, 2021
Parent and Patient Reported Outcomes for Head Shape in Children Undergoing Surgery for Single Suture Synostosis.
Journal: The Journal of craniofacial surgery
Published: September 14, 2021
Cognitive, Behavioural, Speech, Language and Developmental Outcomes Associated with Pathogenic Variants in the ERF Gene.
Journal: The Journal of craniofacial surgery
Published: July 27, 2021
Hearing, Speech, Language, and Communicative Participation in Patients With Apert Syndrome: Analysis of Correlation With Fibroblast Growth Factor Receptor 2 Mutation.
Journal: The Journal of craniofacial surgery
Published: July 26, 2021
Neurodevelopmental, Cognitive, and Psychosocial Outcomes for Individuals With Pathogenic Variants in the TCF12 Gene and Associated Craniosynostosis.
Journal: The Journal of craniofacial surgery
Published: April 27, 2021
Last Updated: 09/26/2026