David Johnson

Mutations in TCF12, encoding a basic helix-loop-helix partner of TWIST1, are a frequent cause of coronal craniosynostosis

John Broxholme, Elizabeth Sweeney, Angela F Brady, 2013, Nature Genetics.

The Aesthetic Outcome of Surgical Correction for Sagittal Synostosis Can Be Reliably Scored by a Novel Method of Preoperative and Postoperative Visual Assessment

David W. Johnson, S. Wall, David Johnson, 2014, Plastic and reconstructive surgery.

Missense mutations in the homeodomain of HOXD13 are associated with brachydactyly types D and E.

Richard C Trembath, Henk Giele, Robert M Esnouf, 2003, American journal of human genetics.

Long-Term Morphological Outcomes in Nonsyndromic Sagittal Craniosynostosis: a Comparison of 2 Techniques

J. Jayamohan, David W. Johnson, S. Wall, 2015, The Journal of craniofacial surgery.

Clinical genetics of craniosynostosis

Steven A. Wall, A. Wilkie, David W. Johnson, 2017, Current opinion in pediatrics.