Johnson D, Whitaker RH. A graphic, three-dimensional teaching model to demonstrate the topography of the human heart. Clin Anat 1995; 8: 407-411.

Johnson D, Cormack G, Abrahams PH, Dixon AK. Computed tomographic observations on subcutaneous fat: implications for liposuction. Plast Reconstr Surg 1996; 97: 387-395.

Johnson D, Dixon AK, Abrahams PH. The anatomical subcutaneous tissue: computed tomographic, magnetic resonance, and anatomical observations. Clin Anat 1996; 9: 19-24.

Johnson D, Hamer DB. Perforation of the transverse colon as a result of minor blunt abdominal trauma. [case report] Injury 1997; 28: 421-423.

Johnson D, Horsley SW, Moloney DM, Oldridge M, Twigg SRF, Walsh S, Barrow M, Njolstad PR, Kunz J. Ashworth GJ, Wall SA, Kearney L, Wilkie AOM. A comprehensive screen for TWIST mutations in patients with craniosynostosis identifies a new microdeletion syndrome of chromosome band 7p21.1. Am J Hum Genet 1998; 63: 1282-1293.

Johnson D, Coleman DJ. The selective use of a single stage and a two stage technique for hypospadias correction in 157 consecutive cases with the aim of normal appearance and function. Br J Plast Surg 1998; 51: 195-201.

Johnson D, Harrison DH. A technique for repairing massive ventral incisional hernias without the use of a mesh. Br J Plast Surg 1999; 52: 399-403.

Oldridge M, Zackai EH, McDonald-McGinn DM, Iseki S, Morriss-Kay GM, Twigg SRF, Johnson D, Wall SA, Jaing W, Theda C, Jabs EW Wilkie AOM. De novo Alu-element insertions in FGFR2 identify a distinct pathological basis for Apert syndrome. Am J Hum Genet 1999; 64: 446-461.

Johnson D, Iseki S, Wilkie AOM, Morriss-Kay GM. Expression patterns of Twist and Fgfr1, -2, and -3 in the developing mouse coronal suture suggest a key role for Twist in suture initiation and biogenesis. Mech Dev 2000; 91: 341-345.

Johnson D, Wall SA, Mann S, Wilkie AOM. A novel mutation, Ala315Ser, in FGFR2: a gene-environment interaction leading to craniosynostosis? Eur J Hum Genet 2000; 8: 571-577.

Johnson D, Coleman DJ. Ink used as first aid treatment of a scald. Burns 2000; 26: 507-508.

Glaser RL, Jaing W, Boyadjiev SA, Tran AK, Zachary AA, Maldergem LV Johnson D, Walsh S, Oldridge M, Wall SA Wilkie AOM Jabs EW. Paternal origin of FGFR2 mutations in sporadic cases of Crouzon syndrome and Pfeiffer syndrome. Am J Hum Genet 2000; 66: 768-777.

Johnson D, Wilkie AOM. Pfeiffer syndrome is not caused by haploinsufficient mutations of FGFR2. J Craniofac Genet Dev Biol 2000; 20: 109-111.

Johnson D, Pathirana PDR. Toxic shock syndrome following cessation of prophylactic antibiotics in a child with a 2% scald. Burns 2002, 28: 181-184.

Kan S, Elanko N, Johnson D, Cornejo-Roldan L, Cook J, Reich EW, Tomkins S, Verloes A, Twigg SRF, Rannan-Eliya S, McDonald-McGinn DM, Zackai EH, Wall SA, Muenke M, Wilkie AOM. Genomic screening of fibroblast growth factor receptor 2 reveals a wide spectrum of mutations in patients with syndromic craniosynostosis. Am J Hum Genet, 2002, 70: 472-486.

Johnson D, Whitworth IH. Recent developments in plastic surgery. BMJ, 2002, 325:319-322.

Kan S, Johnson D, Giele H, Wilkie AOM. An acceptor splice site mutation in HOXD13 results in variable hand but consistent foot malformations. Am J Med Genet, 2003, 121:69-74.

Johnson D, Kan S, Oldridge M, Trembath RC, Roche P, Esnouf RM, Giele H, Wilkie AOM. Missense mutations in the homeodomain of HOXD13 are associated with brachydactyly types D and E. Am J Hum Genet, 2003, 72:984-997.

Johnson D. A comprehensive screen of genes implicated in craniosynostosis. Ann R Coll Surg Engl. 2003,85:371-377.

Johnson D, Tiernan E, Richards AM, Cole RP. Dynamic external fixation for complex intra-articular phalangeal fractures. J Hand Surg, 2004, 29B1:76-81.

Jehee FS, Johnson D, Alonso LG, Cavalcanti DP, de Sa Moreira E, Alberto FL, Kok F, Kim C, Wall SA, Jab EW, Boyadjiev SA, Wilke AO, Passos-Bueno MR. Molecular screening for microdeletions at 9p22-p24 and 11q23-q24 in a large cohort of patients with trigonocephaly. Clin Genet. 2005, 67(6):503-10.


Gray's Anatomy 39th edition [Elsevier]. Editors: Standring S, Ellis H, Johnson D, Healy J, Williams A.2004.

Morriss-Kay GM, Iseki S, Johnson D. Genetic control of the cell proliferation-differentiation balance in the developing skull vault: roles of fibroblast growth factor receptor signalling pathways. In: The Molecular Basis of Skeletogenesis. (Ed. J Godde) Novartis Fnd Symp 232: 2001: 102 -116.

Johnson D, Wilkie AOM Wall SA. A comprehensive screen for TWIST mutations in Saethre-Chotzen syndrome identifies a new microdeletion disorder of chromosome 7. In: Proceedings of the VII International Congress of the International Society of Craniofacial Surgery: 2001, 53-56.

Johnson D, Kan S-h, Wilkie AOM, Giele H. A novel mutation in HOXD13 identifies a new polydactyly/brachydactyly phenotype. In: Proceedings of the VIIIth Congress of the Federation of the European Societies for Surgery of the Hand, 2002, 145-148.

Johnson D, Nugent M, Tan E, David DJ. A retrospective review of 203 patients with hemifacial microsomia implications for management. . In: Proceedings of the IX International Congress of the International Society of Craniofacial Surgery: 2006, in press.

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