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
11412006
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
9232011
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
7921997
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
7412000
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
7352009
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
6992010
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
6652008
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
6622007
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
6352013
DiGeorge syndrome: part of CATCH 22.
DI Wilson, J Burn, P Scambler, J Goodship
Journal of medical genetics 30 (10), 852-856, 1993
6031993
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
5492001
Is the stock exchange a casino?
T Arthur
Economic Affairs 20 (4), 42-45, 2000
5442000
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
4752003
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
4721997
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
4631992
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
4201998
X-linked situs abnormalities result from mutations in ZIC3
M Gebbia, GB Ferrero, G Pilia, MT Bassi, AS Aylsworth, M Penman-Splitt, ...
Nature genetics 17 (3), 305-308, 1997
4101997
Chromosome 9p21 SNPs associated with multiple disease phenotypes correlate with ANRIL expression
MS Cunnington, MS Koref, BM Mayosi, J Burn, B Keavney
PLoS Genet 6 (4), e1000899, 2010
3842010
Identification of Stk6/STK15 as a candidate low-penetrance tumor-susceptibility gene in mouse and human
A Ewart-Toland, P Briassouli, JP de Koning, JH Mao, J Yuan, F Chan, ...
Nature genetics 34 (4), 403-412, 2003
3632003
Prevalence and architecture of de novo mutations in developmental disorders
DDD Study, JF McRae, S Clayton, TW Fitzgerald, J Kaplanis, E Prigmore, ...
Nature 542 (7642), 433-438, 2017
3612017
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