| Celecoxib for the prevention of sporadic colorectal adenomas MM Bertagnolli, CJ Eagle, AG Zauber, M Redston, SD Solomon, KM Kim, ... New England Journal of Medicine 355 (9), 873-884, 2006 | 1259 | 2006 |
| A prospective study of acute cerebrovascular disease in the community: the Oxfordshire Community Stroke Project--1981-86. 2. Incidence, case fatality rates and overall outcome … JM Bamford, PAG Sandercock, MS Dennis, JPS Burn, CP Warlow Journal of Neurology, Neurosurgery & Psychiatry 53 (1), 16-22, 1990 | 1156 | 1990 |
| Long-term effect of aspirin on cancer risk in carriers of hereditary colorectal cancer: an analysis from the CAPP2 randomised controlled trial J Burn, AM Gerdes, F Macrae, JP Mecklin, G Moeslein, S Olschwang, ... The Lancet 378 (9809), 2081-2087, 2011 | 1133 | 2011 |
| Peutz–Jeghers syndrome: a systematic review and recommendations for management AD Beggs, AR Latchford, HFA Vasen, G Moslein, A Alonso, S Aretz, ... Gut 59 (7), 975-986, 2010 | 953 | 2010 |
| Prevalence and architecture of de novo mutations in developmental disorders Nature 542 (7642), 433-438, 2017 | 874 | 2017 |
| Aspirin and non-steroidal anti-inflammatory drugs for cancer prevention: an international consensus statement J Cuzick, F Otto, JA Baron, PH Brown, J Burn, P Greenwald, J Jankowski, ... The lancet oncology 10 (5), 501-507, 2009 | 869 | 2009 |
| Cancer risk associated with germline DNA mismatch repair gene mutations MG Dunlop, SM Farrington, AD Carothers, AH Wyllie, L Sharp, J Burn, ... Human molecular genetics 6 (1), 105-110, 1997 | 849 | 1997 |
| Revised guidelines for the clinical management of Lynch syndrome (HNPCC): recommendations by a group of European experts HFA Vasen, I Blanco, K Aktan-Collan, JP Gopie, A Alonso, S Aretz, ... Gut 62 (6), 812-823, 2013 | 840 | 2013 |
| Identification of the familial cylindromatosis tumour-suppressor gene GR Bignell, W Warren, S Seal, M Takahashi, E Rapley, R Barfoot, ... Nature genetics 25 (2), 160-165, 2000 | 838 | 2000 |
| Guidelines for the clinical management of familial adenomatous polyposis (FAP) HFA Vasen, G Moeslein, A Alonso, S Aretz, I Bernstein, L Bertario, ... Gut 57 (5), 704-713, 2008 | 831 | 2008 |
| Long-term risk of recurrent stroke after a first-ever stroke. The Oxfordshire Community Stroke Project. J Burn, M Dennis, J Bamford, P Sandercock, D Wade, C Warlow Stroke 25 (2), 333-337, 1994 | 790 | 1994 |
| Guidelines for the clinical management of Lynch syndrome (hereditary non-polyposis cancer) HFA Vasen, G Möslein, A Alonso, I Bernstein, L Bertario, I Blanco, J Burn, ... Journal of medical genetics 44 (6), 353-362, 2007 | 752 | 2007 |
| Large-scale discovery of novel genetic causes of developmental disorders Nature 519 (7542), 223-228, 2015 | 742 | 2015 |
| DiGeorge syndrome: part of CATCH 22. DI Wilson, J Burn, P Scambler, J Goodship Journal of medical genetics 30 (10), 852-856, 1993 | 663 | 1993 |
| Endoglin, an ancillary TGFβ receptor, is required for extraembryonic angiogenesis and plays a key role in heart development HM Arthur, J Ure, AJH Smith, G Renforth, DI Wilson, E Torsney, ... Developmental biology 217 (1), 42-53, 2000 | 615 | 2000 |
| Mutation in the gene encoding ferritin light polypeptide causes dominant adult-onset basal ganglia disease ARJ Curtis, C Fey, CM Morris, LA Bindoff, PG Ince, PF Chinnery, ... Nature genetics 28 (4), 350-354, 2001 | 600 | 2001 |
| Epileptic seizures after a first stroke: the Oxfordshire Community Stroke Project J Burn, M Dennis, J Bamford, P Sandercock, D Wade, C Warlow Bmj 315 (7122), 1582-1587, 1997 | 570 | 1997 |
| Cancer risk and survival in path_MMR carriers by gene and gender up to 75 years of age: a report from the Prospective Lynch Syndrome Database P Møller, TT Seppälä, I Bernstein, E Holinski-Feder, P Sala, DG Evans, ... Gut 67 (7), 1306-1316, 2018 | 539 | 2018 |
| Cancer incidence and survival in Lynch syndrome patients receiving colonoscopic and gynaecological surveillance: first report from the prospective Lynch syndrome database P Møller, T Seppälä, I Bernstein, E Holinski-Feder, P Sala, DG Evans, ... Gut 66 (3), 464-472, 2017 | 539 | 2017 |
| Velo-cardio-facial syndrome associated with chromosome 22 deletions encompassing the DiGeorge locus PJ Scambler, D Kelly, E Lindsay, R Williamson, R Goldberg, R Shprintzen, ... The Lancet 339 (8802), 1138-1139, 1992 | 505 | 1992 |
Peter ScamblerEmeritus Professor of Molecular MedicineVerified email at ich.ucl.ac.uk
