Johnson, David

Craniosynostosis

Johnson, D., & Wilkie, A. O. M. (2011) · European Journal of Human Genetics

Craniofacial Disorders and TreatmentsGenomics and Rare Diseases

Cited by 499

Hospitalization for Suicide Ideation or Attempt: 2008–2015

Plemmons, G., Hall, M., Doupnik, S., Gay, J., Brown, C., Browning, W., Casey, R., Freundlich, K., Johnson, D. P., Lind, C., et al. (2018) · Pediatrics

Suicide and Self-Harm StudiesHomicide, Infanticide, and Child Abuse

Cited by 405

Prevalence and Complications of Single-Gene and Chromosomal Disorders in Craniosynostosis

Wilkie, A. O. M., Byren, J. C., Hurst, J. A., Jayamohan, J., Johnson, D., Knight, S. J. L., Lester, T., Richards, P. G., Twigg, S. R. F., & Wall, S. A. (2010) · Pediatrics

Craniofacial Disorders and TreatmentsGenomics and Rare Diseases

Cited by 297

Genomic Screening of Fibroblast Growth-Factor Receptor 2 Reveals a Wide Spectrum of Mutations in Patients with Syndromic Craniosynostosis

Kan, S.-H., Elanko, N., Johnson, D., Cornejo-Roldan, L., Cook, J., Reich, E. W., Tomkins, S., Verloes, A., Twigg, S. R. F., Rannan-Eliya, S., et al. (2002) · The American Journal of Human Genetics

Craniofacial Disorders and TreatmentsConnective tissue disorders research

Cited by 265

A Comprehensive Screen for TWIST Mutations in Patients with Craniosynostosis Identifies a New Microdeletion Syndrome of Chromosome Band 7p21.1

Johnson, D., Horsley, S. W., Moloney, D. M., Oldridge, M., Twigg, S. R. F., Walsh, S., Barrow, M., Njølstad, P. R., Kunz, J., Ashworth, G. J., et al. (1998) · The American Journal of Human Genetics

Craniofacial Disorders and TreatmentsGenomic variations and chromosomal abnormalities

Cited by 230

The psychosocial impact of facial palsy: A systematic review

Hotton, M., Huggons, E., Hamlet, C., Shore, D., Johnson, D., Norris, J. H., Kilcoyne, S., & Dalton, L. (2020) · British Journal of Health Psychology

Facial Nerve Paralysis Treatment and ResearchFace Recognition and Perception

Cited by 141

The incidence of raised intracranial pressure in nonsyndromic sagittal craniosynostosis following primary surgery

Thomas, G. P. L., Johnson, D., Byren, J. C., Judge, A. D., Jayamohan, J., Magdum, S. A., Richards, P. G., & Wall, S. A. (2015) · Journal of Neurosurgery Pediatrics

Craniofacial Disorders and TreatmentsTraumatic Brain Injury and Neurovascular Disturbances

Cited by 81

Reoperation for Intracranial Hypertension in TWIST1-Confirmed Saethre-Chotzen Syndrome: A 15-Year Review

Woods, R. H., Ul-Haq, E., Wilkie, A. O. M., Jayamohan, J., Richards, P. G., Johnson, D., Lester, T., & Wall, S. A. (2009) · Plastic and Reconstructive Surgery

Craniofacial Disorders and TreatmentsTraumatic Brain Injury and Neurovascular Disturbances

Cited by 70

Rare mutations of FGFR2 causing apert syndrome: identification of the first partial gene deletion, and an Alu element insertion from a new subfamily

Bochukova, E. G., Roscioli, T., Hedges, D. J., Taylor, I. B., Johnson, D., David, D. J., Deininger, P. L., & Wilkie, A. O. M. (2009) · Human Mutation

Craniofacial Disorders and TreatmentsGenomics and Rare Diseases

Cited by 66

Molecular screening for microdeletions at 9p22‐p24 and 11q23‐q24 in a large cohort of patients with trigonocephaly

Jehee, F., Johnson, D., Alonso, L., Cavalcanti, D., De Sá Moreira, E., Alberto, F., Kok, F., Kim, C., Wall, S., Jabs, E., et al. (2005) · Clinical Genetics

Craniofacial Disorders and TreatmentsGenomic variations and chromosomal abnormalities

Cited by 55

Germline and somatic mosaicism for FGFR2 mutation in the mother of a child with Crouzon syndrome: Implications for genetic testing in “paternal age‐effect” syndromes

Goriely, A., Lord, H., Lim, J., Johnson, D., Lester, T., Firth, H. V., & Wilkie, A. O. M. (2010) · American Journal of Medical Genetics Part A

Craniofacial Disorders and TreatmentsGenomics and Rare Diseases

Cited by 41

Frank-ter Haar syndrome associated with sagittal craniosynostosis and raised intracranial pressure

Bendon, C. L., Fenwick, A. L., Hurst, J. A., Nürnberg, G., Nürnberg, P., Wall, S. A., Wilkie, A. O., & Johnson, D. (2012) · BMC Medical Genetics

Craniofacial Disorders and TreatmentsGenomics and Rare Diseases

Cited by 28

Evaluating the effectiveness and acceptability of information and therapy guides for improving the psychosocial well-being of people with facial palsy

Hotton, M., Johnson, D., Kilcoyne, S., & Dalton, L. (2022) · Journal of Plastic, Reconstructive & Aesthetic Surgery

Facial Nerve Paralysis Treatment and ResearchStroke Rehabilitation and Recovery

Cited by 12