Items where authors include "Burn, J"

Article

Loong, L, Huntley, C, McRonald, F et al. (48 more authors) (2022) Germline mismatch repair (MMR) gene analyses from English NHS regional molecular genomics laboratories 1996–2020: development of a national resource of patient-level genomics laboratory records. Journal of Medical Genetics (JMG). ISSN 0022-2593

Seppälä, TT, Latchford, A, Negoi, I et al. (16 more authors) (2021) European guidelines from the EHTG and ESCP for Lynch syndrome: an updated third edition of the Mallorca guidelines based on gene and gender. British Journal of Surgery, 108 (5). pp. 484-498. ISSN 0007-1323

Burn, J, Sheth, H, Elliott, F et al. (20 more authors) (2020) Cancer prevention with aspirin in hereditary colorectal cancer (Lynch syndrome), 10-year follow-up and registry-based 20-year data in the CAPP2 study: a double-blind, randomised, placebo-controlled trial. The Lancet, 395 (10240). pp. 1855-1863. ISSN 0140-6736

Aitken, S, Firth, HV, McRae, J et al. (280 more authors) (2019) Finding diagnostically useful patterns in quantitative phenotypic data. The American Journal of Human Genetics, 105 (5). pp. 933-946. ISSN 0002-9297

Wei, W, Tuna, S, Keogh, MJ et al. (426 more authors) (2019) Germline selection shapes human mitochondrial DNA diversity. Science, 364 (6442). 749-+. ISSN 0036-8075

Danilenko, M, Stamp, E, Stocken, DD orcid.org/0000-0001-8031-1738 et al. (15 more authors) (2018) Targeting Tropomyosin Receptor Kinase in Cutaneous CYLD Defective Tumors With Pegcantratinib: The TRAC Randomized Clinical Trial. JAMA dermatology, 154 (8). pp. 913-921. ISSN 2168-6068

Sheth, H, Northwood, E, Ulrich, CM et al. (19 more authors) (2018) Interaction between polymorphisms in aspirin metabolic pathways, regular aspirin use and colorectal cancer risk: A case-control study in unselected white European populations. PLoS ONE, 13 (2). e0192223. ISSN 1932-6203

Cranston, A, Stocken, DD orcid.org/0000-0001-8031-1738, Stamp, E et al. (7 more authors) (2017) Tropomyosin Receptor Antagonism in Cylindromatosis (TRAC), an early phase trial of a topical tropomyosin kinase inhibitor as a treatment for inherited CYLD defective skin tumours: study protocol for a randomised controlled trial. Trials, 18. 111. ISSN 1745-6215

Smith, SG orcid.org/0000-0003-1983-4470, Foy, R orcid.org/0000-0003-0605-7713, McGowan, J et al. (5 more authors) (2017) General practitioner attitudes towards prescribing aspirin to carriers of Lynch Syndrome: findings from a national survey. Familial Cancer, 16 (4). pp. 509-516. ISSN 1389-9600

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

Smith, S, Foy, R orcid.org/0000-0003-0605-7713, McGowan, J et al. (5 more authors) (2016) General practitioner attitudes towards prescribing aspirin to carriers of Lynch Syndrome: Findings from a national survey. European Journal of Surgical Oncology, 42 (11). S233. ISSN 0748-7983

McRae, JF, Clayton, S, Fitzgerald, TW et al. (298 more authors) (2016) Prevalence, phenotype and architecture of developmental disorders caused by de novo mutation: The Deciphering Developmental Disorders Study. bioRxiv. (Submitted)