John Burn
John Burn
Professor of Clinical Genetics
Verified email at ncl.ac.uk
Title
Cited by
Cited by
Year
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
11672006
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
10941990
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
9802011
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
8061997
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
7732009
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
7612000
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
7372010
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
7161994
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
6982013
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
6872007
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
6852008
DiGeorge syndrome: part of CATCH 22.
DI Wilson, J Burn, P Scambler, J Goodship
Journal of medical genetics 30 (10), 852-856, 1993
6191993
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
5632001
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
5502000
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
5051997
European Code Against Cancer and scientific justification: third version (2003)
P Boyle, P Autier, H Bartelink, J Baselga, P Boffetta, J Burn, HJG Burns, ...
Annals of oncology 14 (7), 973-1005, 2003
4812003
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
4751992
Prevalence and architecture of de novo mutations in developmental disorders
TDDD Study
Nature 542 (7642), 433, 2017
4482017
Recurrence risks in offspring of adults with major heart defects: results from first cohort of British collaborative study
J Burn, P Brennan, J Little, S Holloway, R Coffey, J Somerville, NR Dennis, ...
The Lancet 351 (9099), 311-316, 1998
4311998
Large-scale discovery of novel genetic causes of developmental disorders
TW Fitzgerald, SS Gerety, WD Jones, M Van Kogelenberg, DA King, ...
Nature 519 (7542), 223, 2015
4272015
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