Items where authors include "Morton, J."

Article

Brown, S.R. orcid.org/0000-0002-0980-2793, Hind, D. orcid.org/0000-0002-6409-4793, Strong, E. et al. (41 more authors) (2024) Real-world practice and outcomes in pilonidal surgery: pilonidal sinus treatment studying the options (PITSTOP) cohort. British Journal of Surgery, 111 (3). znae009. ISSN 0007-1323

Morton, J. orcid.org/0000-0002-4458-6256 (2024) Generative AI Adoption and Three Traps for Organizational Agility. California Management Review Insights. ISSN 0008-1256 (In Press)

Morton, J. orcid.org/0000-0002-4458-6256 (2024) Using Prompt Engineering to Better Communicate with People. Harvard Business Review. ISSN 0017-8012

Lee, S., Ochoa, E., Badura-Stronka, M. et al. (12 more authors) (2023) Germline pathogenic variants in HNRNPU are associated with alterations in blood methylome. European Journal of Human Genetics, 31 (9). pp. 1040-1047. ISSN 1018-4813

Morton, J. orcid.org/0000-0002-4458-6256, Zorina, A. and Kudaravalli, S. (2023) The Strategic Value of IT-Enabled Self-Organised Collectives During Crises. Journal of Strategic Information Systems, 32 (3). 101792. ISSN 0963-8687

Hill, J., Lee, S., Morton, D. et al. (543 more authors) (2022) Colorectal Endoscopic Stenting Trial (CReST) for obstructing left-sided colorectal cancer: randomized clinical trial. British Journal of Surgery, 109 (11). pp. 1073-1080. ISSN 0007-1323

Kettle, B., Hollatz, D., Gerstmayr, E. et al. (35 more authors) (2021) A laser-plasma platform for photon-photon physics : The two photon Breit-Wheeler process. New Journal of Physics. 115006. ISSN 1367-2630

Radley, J.A. orcid.org/0000-0002-0776-0091, O'Sullivan, R.B.G., Turton, S.E. et al. (14 more authors) (2019) Deep phenotyping of fourteen new patients with IQSEC2 variants, including monozygotic twins of discordant phenotype. Clinical Genetics, 95 (4). pp. 496-506. ISSN 0009-9163

Martin, H.C., Jones, W.D., McIntyre, R. et al. (37 more authors) (2018) Quantifying the contribution of recessive coding variation to developmental disorders. Science, 362 (6419). pp. 1161-1164. ISSN 0036-8075

Koczkowska, M., Chen, Y., Callens, T. et al. (72 more authors) (2018) Genotype-Phenotype Correlation in NF1: Evidence for a More Severe Phenotype Associated with Missense Mutations Affecting NF1 Codons 844-848. American Journal of Human Genetics, 102 (1). pp. 69-87. ISSN 0002-9297

Faundes, V., Newman, W.G., Bernardini, L. et al. (20 more authors) (2018) Histone lysine methylases and demethylases in the landscape of human developmental disorders. American Journal of Human Genetics, 102 (1). pp. 175-187. ISSN 0002-9297

McRae, J.F., Clayton, S., Fitzgerald, T.W. et al. (299 more authors) (2017) Prevalence and architecture of de novo mutations in developmental disorders. Nature, 542 (7642). pp. 433-438. ISSN 0028-0836

Fitzgerald, T.W., Gerety, S.S., Jones, W.D. et al. (263 more authors) (2015) Large-scale discovery of novel genetic causes of developmental disorders. Nature, 519. pp. 223-228. ISSN 0028-0836

Proceedings Paper

Golding, C., Morton, J. orcid.org/0000-0002-4458-6256 and Zorina, A. (2023) How Stakeholders' Emotions Can Shape Open Strategy Formulation. In: Taneja, S., (ed.) Academy of Management Proceedings. 83rd Annual Meeting of the Academy of Management, 04-08 Aug 2023, Boston, MA, USA. Academy of Management .