Items where Author is "Prinsley, Peter"

Wilson, Emma, Jennings, Barbara ORCID: https://orcid.org/0000-0003-3792-9182, Khondoker, Mizanur ORCID: https://orcid.org/0000-0002-1801-1635, Philpott, Carl ORCID: https://orcid.org/0000-0002-1125-3236, Prinsley, Peter and Brewer, Daniel S. ORCID: https://orcid.org/0000-0003-4753-9794 (2024) Epidemiology of Cholesteatoma in the UK Biobank. Clinical Otolaryngology. ISSN 1749-4478 (In Press)

Cardenas, Ryan, Prinsley, Peter, Philpott, Carl ORCID: https://orcid.org/0000-0002-1125-3236, Bhutta, Mahmood F., Wilson, Emma, Brewer, Daniel ORCID: https://orcid.org/0000-0003-4753-9794 and Jennings, Barbara ORCID: https://orcid.org/0000-0003-3792-9182 (2024) Loss of function variants and locus heterogeneity in familial cholesteatoma. In: 56th European Society of Human Genetics (ESHG) Conference, 2023-06-10 - 2023-06-13.

Cardenas, Ryan, Prinsley, Peter, Philpott, Carl ORCID: https://orcid.org/0000-0002-1125-3236, Bhutta, Mahmood F., Wilson, Emma, Brewer, Daniel S. ORCID: https://orcid.org/0000-0003-4753-9794 and Jennings, Barbara A. ORCID: https://orcid.org/0000-0003-3792-9182 (2023) Whole exome sequencing study identifies candidate loss of function variants and locus heterogeneity in familial cholesteatoma. PLoS One, 18 (3). ISSN 1932-6203

Cardenas, Ryan, Prinsley, Peter, Philpott, Carl ORCID: https://orcid.org/0000-0002-1125-3236, Bhutta, Mahmood F, Wilson, Emma, Brewer, Daniel S. ORCID: https://orcid.org/0000-0003-4753-9794 and Jennings, Barbara A. ORCID: https://orcid.org/0000-0003-3792-9182 (2022) Whole exome sequencing study identifies candidate loss of function variants and locus heterogeneity in familial cholesteatoma.

Collins, Rachael, Hong Ta, Ngan, Jennings, Barbara A. ORCID: https://orcid.org/0000-0003-3792-9182, Prinsley, Peter, Philpott, Carl M. ORCID: https://orcid.org/0000-0002-1125-3236, Steel, Nick ORCID: https://orcid.org/0000-0003-1528-140X and Clark, Allan ORCID: https://orcid.org/0000-0003-2965-8941 (2020) Cholesteatoma and family history: An international survey. Clinical Otolaryngology, 45 (4). pp. 500-505. ISSN 1749-4478

Prinsley, Peter, Jennings, Barbara ORCID: https://orcid.org/0000-0003-3792-9182, Bhutta, Mahmood, Swan, Daniel, Willis, Gavin and Philpott, Carl ORCID: https://orcid.org/0000-0002-1125-3236 (2019) The genetics of cholesteatoma study. Loss‐of‐function variants in an affected family. Clinical Otolaryngology, 44 (5). ISSN 1749-4478

Ta, N. Hong, Jennings, B. ORCID: https://orcid.org/0000-0003-3792-9182, Philpott, C. ORCID: https://orcid.org/0000-0002-1125-3236 and Prinsley, P. (2019) Epidemiology of Cholesteatoma. British Journal of Surgery, 106. p. 15. ISSN 0007-1323

Jennings, Barbara ORCID: https://orcid.org/0000-0003-3792-9182, Philpott, Carl ORCID: https://orcid.org/0000-0002-1125-3236, Bhutta, Mahmood, Willis, Gavin, Swan, Daniel, Woods, Jane and Prinsley, Peter (2018) A study of the genetics of cholesteatoma through systematic review and whole exome sequencing. In: European Conference of Human Genetics 2018, 2018-06-16 - 2018-06-19. (In Press)

Jennings, Barbara A. ORCID: https://orcid.org/0000-0003-3792-9182, Prinsley, Peter, Philpott, Carl ORCID: https://orcid.org/0000-0002-1125-3236, Willis, Gavin and Bhutta, Mahmoud F (2018) The genetics of cholesteatoma. A systematic review using narrative synthesis. Clinical Otolaryngology, 43 (1). 55–67. ISSN 1749-4478

Philpott, C. M. ORCID: https://orcid.org/0000-0002-1125-3236, Rimal, D., Tassone, P., Prinsley, P. and Premachandra, D. J. (2008) A study of olfactory testing in patients with rhinological pathology in the ENT clinic. Rhinology, 46 (1). pp. 34-39.

Philpott, CM ORCID: https://orcid.org/0000-0002-1125-3236, Rimal, D, Tassone, P, Premachandra, D and Prinsley, P (2007) A study of olfactory testing in patients with rhinological pathology in the ENT Clinic. In: Section of Laryngology & Rhinology, Royal Society of Medicine London,, 2007-02-01.

Rimal, D, Philpott, CM ORCID: https://orcid.org/0000-0002-1125-3236, Tassone, P, Premachandra, DJ and Prinsley, PR (2006) An audit of olfactory testing in patients with rhinological disease. In: British Rhinological Society, 2007-05-01.