缅北禁地

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Staff Profile

Professor Sir John Burn

Professor of Clinical Genetics

  • Personal Website:
  • Address: Translational and Clinical Research Institute
    International Centre for Life
    Times Square
    缅北禁地 upon Tyne
    NE1 3BZ
Background

Professor of Clinical Genetics, 缅北禁地 1991-

Consultant Clinical Geneticist, Northern Genetics Service 1984-1996, Honorary from 96-2017 and 2023-

Chairman, 缅北禁地 Hospitals NHS Foundation Trust 2017 - 2023

Knighted for services to Medicine and Healthcare in 2010

Chief Investigator of the International 

Co-Chair of the International Scientific Advisory Committee to the  and Executive Chairman/ Director/ Company Board Member of the non-for profit holding company, Global Variome Ltd (缅北禁地, UK). HVP/GV is a recognised NGO of UNESCO.

Co-chair to the  of the Global Alliance for Genomics and Health (GA4GH)

Vice President, Human Genome Organisation. Trustee HUGO London

Member to Genomics England Scientific Advisory Committee, Bowel Cancer UK Scientific Advisory Committee Committee. Trustee and board member, European Hereditary Tumour Group.


Chairman of  -  


Patron charity Veterans at Ease.

 

PA: Karen Ritchie

Karen.Ritchie@ncl.ac.uk or 0191 241 8794

 

Research

I now have two major areas of research: The CAPP programme has now succeeded in establishing that aspirin significantly reduces the risk of cancer in people with Lynch syndrome, the major form of hereditary colorectal cancer. We are now poised to transform the clinical management of cancer in all people with a family history. I am Chief Investigator of the CaPP3 trial, a dose non-inferiority study to determine the optimal dose of aspirin for cancer chemoprevention in Lynch Syndrome, will reach last Patient Last Visit in June 2024. 1879 carriers of Lynch Syndrome have been randomised in the UK, Finland, Spain, Israel and Australia. CAPP2 also demonstrated a major reduction of non-colorectal cancers in those randomised to resistant starch (high fibre) supplements.


Our Cancer Prevention Group has developed a patented multiplex PCR assay, the 缅北禁地 MSI-Plus Assay, which is being deployed to screen colorectal and other tumours for evidence of sporadic or germline MisMatch Repair deficiency, the underlying molecular basis of Lynch syndrome and a target for Immune Checkpoint Inhibitors. We have shown the assay to be able to detect Microsatellite Instability in cell free DNA from urine of people with Lynch syndrome who have a urinary tract cancer.



Publications

  • Articles

    • Huntley C, Loong L, Mallinson C, Bethell R, Rahman T, Alhaddad N, Tulloch O, Zhou X, Lee J, Eves P, Cook J, Armstrong R, Ahmed M, McVeigh T, DeSouza B, Kulkarni A, Bezuidenhout H, Martin R, Holliday D, Hart R, Lalloo F, Donaldson A, Cleaver R, Willis C, Kiesel V, O'Reilly M-A, Halliday D, Solomons J, Ong KR, McRonald F, Torr B, Burn J, Shaw A, Morris EJA, Monahan K, Hardy S, Turnbull C. . eClinicalMedicine 2024, 69, 102465.
    • Lincoln AG, Benton SC, Piggott C, Sheikh SR, Beggs AD, Buckley L, Desouza B, East JE, Sanders P, Lim M, Sheehan D, Snape K, Hanson H, Greenaway JR, Burn J, Nylander D, Hawkins M, Lalloo F, Green K, Lee TJ, Walker J, Matthews G, Rutherford T, Sasieni P, Monahan KJ. . BJS Open 2023, 7(5), zrad079.
    • Rasmussen M, Sowter P, Gallon R, Durhuus JA, Hayes C, Andersen O, Nilbert M, Schejbel L, Hogdall E, Santibanez-Koref M, Jackson MS, Burn J, Therkildsen C. . Frontiers in Oncology 2023, 13, 1147591.
    • Gallon R, Phelps R, Hayes C, Brugieres L, Guerrini-Rousseau L, Colas C, Muleris M, Ryan NAJ, Evans DG, Grice H, Jessop E, Kunzemann-Martinez A, Marshall L, Schamschula E, Oberhuber K, Azizi AA, Baris Feldman H, Beilken A, Brauer N, Brozou N, Dahan K, Demirsoy U, Florkin B, Foulkes W, Januszkiewicz-Lewandowska D, Jones KJ, Kratz CP, Lobitz S, Meade J, Nathrath M, Pander HJ, Perne C, Ragab I, Ripperger T, Rosenbaum T, Rueda D, Sarosiek T, Sehested A, Spier I, Suerink M, Zimmermann SY, Zschocke J, Borthwick GM, Wimmer K, Burn J, Jackson MS, Santibanez-Koref M. . Gastroenterology 2023, 164(4), 579-592.e8.
    • Bohaumilitzky L, Kluck K, Huneburg R, Gallon R, Nattermann J, Kirchner M, Kristiansen G, Hommerding O, Pfuderer PL, Wagner L, Echterdiek F, Kosegi S, Muller N, Fischer K, Nelius N, Hartog B, Borthwick G, Busch E, Haag GM, Blaker H, Moslein G, von Knebel Doeberitz M, Seppala TT, Ahtiainen M, Mecklin J-P, Bishop DT, Burn J, Stenzinger A, Budczies J, Kloor M, Ahadova A. . Gastroenterology 2022, 162(3), 907-919.e10.
    • Phelps R, Gallon R, Hayes C, Glover E, Gibson P, Edidi I, Lee T, Mills S, Shaw A, Heer R, Ralte A, McAnulty C, Santibanez-Koref M, Burn J, Jackson MS. . Cancers 2022, 14(15), 3838.
    • Moller P, Seppala T, Dowty JG, Haupt S, Dominguez-Valentin M, Sunde L, Bernstein I, Engel C, Aretz S, Nielsen M, Capella G, Evans DG, Burn J, Holinski-Feder E, Bertario L, Bonanni B, Lindblom A, Levi Z, Macrae F, Winship I, Plazzer J-P, Sijmons R, Laghi L, Valle AD, Heinimann K, Half E, Lopez-Koestner F, Alvarez-Valenzuela K, Scott RJ, Katz L, Laish I, Vainer E, Vaccaro CA, Carraro DM, Gluck N, Abu-Freha N, Stakelum A, Kennelly R, Winter D, Rossi BM, Greenblatt M, Bohorquez M, Sheth H, Tibiletti MG, Lino-Silva LS, Horisberger K, Portenkirchner C, Nascimento I, Rossi NT, da Silva LA, Thomas H, Zarand A, Mecklin J-P, Pylvanainen K, Renkonen-Sinisalo L, Lepisto A, Peltomaki P, Therkildsen C, Lindberg LJ, Thorlacius-Ussing O, von Knebel Doeberitz M, Loeffler M, Rahner N, Steinke-Lange V, Schmiegel W, Vangala D, Perne C, Huneburg R, de Vargas AF, Latchford A, Gerdes A-M, Backman A-S, Guillen-Ponce C, Snyder C, Lautrup CK, Amor D, Palmero E, Stoffel E, Duijkers F, Hall MJ, Hampel H, Williams H, Okkels H, Lubinski J, Reece J, Ngeow J, Guillem JG, Arnold J, Wadt K, Monahan K, Senter L, Rasmussen LJ, van Hest LP, Ricciardiello L, Kohonen-Corish MRJ, Ligtenberg MJL, Southey M, Aronson M, Zahary MN, Samadder NJ, Poplawski N, Hoogerbrugge N, Morrison PJ, James P, Lee G, Chen-Shtoyerman R, Ankathil R, Pai R, Ward R, Parry S, Debniak T, John T, van Overeem Hansen T, Caldes T, Yamaguchi T, Barca-Tierno V, Garre P, Cavestro GM, Weitz J, Redler S, Buttner R, Heuveline V, Hopper JL, Win AK, Lindor N, Gallinger S, Le Marchand L, Newcomb PA, Figueiredo J, Buchanan DD, Thibodeau SN, ten Broeke SW, Hovig E, Nakken S, Pineda M, Duenas N, Brunet J, Green K, Lalloo F, Newton K, Crosbie EJ, Mints M, Tjandra D, Neffa F, Esperon P, Kariv R, Rosner G, Pavicic WH, Kalfayan P, Torrezan GT, Bassaneze T, Martin C, Moslein G, Ahadova A, Kloor M, Sampson JR, Jenkins MA. . Hereditary Cancer in Clinical Practice 2022, 20(1), 36.
    • Mathers JC, Elliott F, Macrae F, Mecklin J-P, Moslein G, McRonald FE, Bertario L, Evans DG, Gerdes A-M, Ho JWC, Lindblom A, Morrison PJ, Rashbass J, Ramesar RS, Seppala TT, Thomas HJW, Sheth HJ, Pylvanainen K, Reed L, Borthwick GM, Bishop DT, Burn J. . Cancer Prevention Research 2022, 15(9), 623-634.
    • Martin HC, Gardner EJ, Samocha KE, Kaplanis J, Akawi N, Sifrim A, Eberhardt RY, Tavares ALT, Neville MDC, Niemi MEK, Gallone G, McRae J, Borras S, Clark C, Dean J, Miedzybrodzka Z, Ross A, Tennant S, Dabir T, Donnelly D, Humphreys M, Magee A, McConnell V, McKee S, McNerlan S, Morrison PJ, Rea G, Stewart F, Cole T, Cooper N, Cooper-Charles L, Cox H, Islam L, Jarvis J, Keelagher R, Lim D, McMullan D, Morton J, Naik S, O'Driscoll M, Ong K-R, Osio D, Ragge N, Turton S, Vogt J, Williams D, Bodek S, Donaldson A, Hills A, Low K, Newbury-Ecob R, Norman AM, Roberts E, Scurr I, Smithson S, Tooley M, Abbs S, Armstrong R, Dunn C, Holden S, Park S-M, Paterson J, Raymond L, Reid E, Sandford R, Simonic I, Tischkowitz M, Woods G, Bradley L, Comerford J, Green A, Lynch S, McQuaid S, Mullaney B, Berg J, Goudie D, Mavrak E, McLean J, McWilliam C, Reavey E, Azam T, Cleary E, Jackson A, Lam W, Lampe A, Moore D, Porteous M, Baple E, Baptista J, Brewer C, Castle B, Kivuva E, Owens M, Rankin J, Shaw-Smith C, Turner C, Turnpenny P, Tysoe C, Bradley T, Davidson R, Gardiner C, Joss S, Kinning E, Longman C, McGowan R, Murday V, Pilz D, Tobias E, Whiteford M, Williams N, Barnicoat A, Clement E, Faravelli F, Hurst J, Jenkins L, Jones W, Kumar VKA, Lees M, Loughlin S, Male A, Morrogh D, Rosser E, Scott R, Wilson L, Beleza A, Deshpande C, Flinter F, Holder M, Irving M, Izatt L, Josifova D, Mohammed S, Molenda A, Robert L, Roworth W, Ruddy D, Ryten M, Yau S, Bennett C, Blyth M, Campbell J, Coates A, Dobbie A, Hewitt S, Hobson E, Jackson E, Jewell R, Kraus A, Prescott K, Sheridan E, Thomson J, Bradshaw K, Dixit A, Eason J, Haines R, Harrison R, Mutch S, Sarkar A, Searle C, Shannon N, Sharif A, Suri M, Vasudevan P, Canham N, Ellis I, Greenhalgh L, Howard E, Stinton V, Swale A, Weber A, Banka S, Breen C, Briggs T, Burkitt-Wright E, Chandler K, Clayton-Smith J, Donnai D, Douzgou S, Gaunt L, Jones E, Kerr B, Langley C, Metcalfe K, Smith A, Wright R, Bourn D, Burn J, Fisher R, Hellens S, Henderson A, Montgomery T, Splitt M, Straub V, Wright M, Zwolinski S, Allen Z, Bernhard B, Brady A, Brooks C, Busby L, Clowes V, Ghali N, Holder S, Ibitoye R, Wakeling E, Blair E, Carmichael J, Cilliers D, Clasper S, Gibbons R, Kini U, Lester T, Nemeth A, Poulton J, Price S, Shears D, Stewart H, Wilkie A, Albaba S, Baker D, Balasubramanian M, Johnson D, Parker M, Quarrell O, Stewart A, Willoughby J, Crosby C, Elmslie F, Homfray T, Jin H, Lahiri N, Mansour S, Marks K, McEntagart M, Saggar A, Tatton-Brown K, Butler R, Clarke A, Corrin S, Fry A, Kamath A, McCann E, Mugalaasi H, Pottinger C, Procter A, Sampson J, Sansbury F, Varghese V, Baralle D, Callaway A, Cassidy EJ, Daniels S, Douglas A, Foulds N, Hunt D, Kharbanda M, Lachlan K, Mercer C, Side L, Temple IK, Wellesley D, Wright CF, FitzPatrick DR, Firth HV, Hurles ME. . Nature Communications 2021, 12(1), 627.
    • Gallon R, Kibbi N, Cook S, Santibanez-Koref M, Jackson MS, Burn J, Rajan N. . British Journal of Dermatology 2021, 185(5), 1045-1046.
    • Dominguez-Valentin M, Plazzer J-P, Sampson JR, Engel C, Aretz S, Jenkins MA, Sunde L, Bernstein I, Capella G, Balaguer F, Macrae F, Winship IM, Thomas H, Evans DG, Burn J, Greenblatt M, de Vos tot Nederveen Cappel WH, Sijmons RH, Nielsen M, Bertario L, Bonanni B, Tibiletti MG, Cavestro GM, Lindblom A, Della Valle A, Lopez-Kostner F, Alvarez K, Gluck N, Katz L, Heinimann K, Vaccaro CA, Nakken S, Hovig E, Green K, Lalloo F, Hill J, Vasen HFA, Perne C, Buttner R, Gorgens H, Holinski-Feder E, Morak M, Holzapfel S, Huneburg R, Doeberitz MVK, Loeffler M, Rahner N, Weitz J, Steinke-Lange V, Schmiegel W, Vangala D, Crosbie EJ, Pineda M, Navarro M, Brunet J, Moreira L, Sanchez A, Serra-Burriel M, Mints M, Kariv R, Rosner G, Pinero TA, Pavicic WH, Kalfayan P, Ten Broeke SW, Mecklin J-P, Pylvanainen K, Renkonen-Sinisalo L, Lepisto A, Peltomaki P, Hopper JL, Win AK, Buchanan DD, Lindor NM, Gallinger S, Marchand LL, Newcomb PA, Figueiredo JC, Thibodeau SN, Therkildsen C, Hansen TVO, Lindberg L, Rodland EA, Neffa F, Esperon P, Tjandra D, Moslein G, Seppala TT, Moller P. . Journal of Clinical Medicine 2021, 10(13), 2856.
    • Kurzawa-Akanbi M, Keogh M, Tsefou E, Ramsay L, Johnson M, Keers S, Ochieng LW, McNair A, Singh P, Khan A, Pyle A, Hudson G, Ince PG, Attems J, Burn J, Chinnery PF, Morris CM. . Neuropathology and Applied Neurobiology 2021, 47(1), 26-42.
    • Turro E, Astle WJ, Graf S, Greene D, Allen HL, Frontini M, Stephens J, Downes K, Tuna S, Deevi SVV, Aitman TJ, Bennett DL, Calleja P, Caulfield MJ, Chinnery PF, Dixon PH, James R, Laffan MA, Levine AP, Maher ER, Markus HS, Morales J, Morrell NW, Mumford AD, Rankin S, Rendon A, Richardson S, Roberts I, Roy NBA, Saleem MA, Smith KGC, Tan RYY, Thrasher AJ, Watkins H, Webster AR, Wilkins MR, Williamson C, Whitworth J, Humphray S, Abbs S, Abulhoul L, Adlard J, Ahmed M, Aitman TJ, Alachkar H, Allsup DJ, Almeida-King J, Ancliff P, Antrobus R, Armstrong R, Arno G, Ashford S, Astle WJ, Attwood A, Aurora P, Babbs C, Bacchelli C, Bakchoul T, Banka S, Bariana T, Barwell J, Batista J, Baxendale HE, Beales PL, Bennett DL, Bentley DR, Bentley DR, Bierzynska A, Biss T, Bitner-Glindzicz MAK, Black GC, Bleda M, Blesneac I, Bockenhauer D, Bogaard H, Bourne CJ, Boyce S, Bradley JR, Bragin E, Breen G, Brennan P, Brewer C, Brown M, Browning AC, Browning MJ, Buchan RJ, Buckland MS, Bueser T, Diz CB, Burn J, Burns SO, Burren OS, Burren OS, Burrows N, Calleja P, Campbell C, Carr-White G, Carss K, Carss K, Casey R, Caulfield MJ, Chambers J, Chambers J, Chan MMY, Cheah C, Cheng F, Chinnery PF, Chitre M, Christian MT, Church C, Clayton-Smith J, Cleary M, Brod NC, Coghlan G, Colby E, Cole TRP, Collins J, Collins PW, Colombo C, Compton CJ, Condliffe R, Cook S, Cook HT, Cooper N, Corris PA, Furnell A, Cunningham F, Curry NS, Cutler AJ, Daniels MJ, Dattani M, Daugherty LC, Davis J, De Soyza A, Deevi SVV, Dent T, Deshpande C, Dewhurst EF, Dixon PH, Douzgou S, Downes K, Drazyk AM, Drewe E, Duarte D, Dutt T, Edgar JDM, Edwards K, Egner W, Ekani MN, Elliott P, Erber WN, Erwood M, Estiu MC, Evans DG, Evans G, Everington T, Eyries M, Fassihi H, Favier R, Findhammer J, Fletcher D, Flinter FA, Floto RA, Fowler T, Fox J, Frary AJ, French CE, Freson K, Frontini M, Gale DP, Gale DP, Gall H, Ganesan V, Gattens M, Geoghegan C, Gerighty TSA, Gharavi AG, Ghio S, Ghofrani H-A, Gibbs JSR, Gibson K, Gilmour KC, Girerd B, Gleadall NS, Goddard S, Goldstein DB, Gomez K, Gordins P, Gosal D, Graf S, Graham J, Grassi L, Greene D, Greenhalgh L, Greinacher A, Gresele P, Griffiths P, Grigoriadou S, Grocock RJ, Grozeva D, Gurnell M, Hackett S, Hadinnapola C, Hague WM, Hague R, Haimel M, Haimel M, Hall M, Hanson HL, Haque E, Harkness K, Harper AR, Harris CL, Hart D, Hassan A, Hayman G, Henderson A, Herwadkar A, Hoffman J, Holden S, Horvath R, Houlden H, Houweling AC, Howard LS, Hu F, Hudson G, Hughes J, Huissoon AP, Humbert M, Humphray S, Hunter S, Hurles M, Irving M, Izatt L, James R, Johnson SA, Jolles S, Jolley J, Josifova D, Jurkute N, Karten T, Karten J, Kasanicki MA, Kazkaz H, Kazmi R, Kelleher P, Kelly AM, Kelsall W, Kempster C, Kiely DG, Kingston N, Klima R, Koelling N, Kostadima M, Kovacs G, Koziell A, Koziell A, Kreuzhuber R, Kuijpers TW, Kumar A, Kumararatne D, Kurian MA, Laffan MA, Lalloo F, Lambert M, Allen HL, Lawrie A, Layton DM, Lench N, Lentaigne C, Lester T, Levine AP, Linger R, Longhurst H, Lorenzo LE, Louka E, Lyons PA, Machado RD, MacKenzie Ross RV, Madan B, Maher ER, Maimaris J, Malka S, Mangles S, Mapeta R, Mapeta R, Marchbank KJ, Marks S, Markus HS, Marschall H-U, Marshall A, Martin J, Mathias M, Matthews E, Maxwell H, McAlinden P, McCarthy MI, McKinney H, McMahon A, Meacham S, Mead AJ, Castello IM, Megy K, Megy K, Mehta SG, Michaelides M, Millar C, Mohammed SN, Moledina S, Montani D, Moore AT, Morales J, Morrell NW, Mozere M, Muir KW, Mumford AD, Nemeth AH, Newman WG, Newnham M, Noorani S, Nurden P, O'Sullivan J, Obaji S, Odhams C, Okoli S, Olschewski A, Olschewski H, Ong KR, Oram SH, Ormondroyd E, Ormondroyd E, Ouwehand WH, Palles C, Papadia S, Park S-M, Parry D, Patel S, Paterson J, Peacock A, Pearce SH, Peden J, Peerlinck K, Pepke-Zaba J, Petersen R, Pilkington C, Poole KES, Prathalingam R, Psaila B, Pyle A, Quinton R, Rahman S, Rankin S, Rao A, Raymond FL, Rayner-Matthews PJ, Rees C, Rendon A, Renton T, Rhodes CJ, Rice ASC, Richardson S, Richter A, Robert L, Roberts I, Rogers A, Rose SJ, Ross-Russell R, Roughley C, Roy NBA, Ruddy DM, Sadeghi-Alavijeh O, Saleem MA, Samani N, Samarghitean C, Sanchis-Juan A, Sanchis-Juan A, Sargur RB, Sarkany RN, Satchell S, Savic S, Sayer JA, Sayer G, Scelsi L, Schaefer AM, Schulman S, Scott R, Scully M, Searle C, Seeger W, Sen A, Sewell WAC, Seyres D, Shah N, Shamardina O, Shamardina O, Shapiro SE, Shaw AC, Short PJ, Sibson K, Side L, Simeoni I, Simpson MA, Sims MC, Sivapalaratnam S, Smedley D, Smith KR, Smith KGC, Snape K, Soranzo N, Soubrier F, Southgate L, Spasic-Boskovic O, Staines S, Staples E, Stark H, Stark H, Stephens J, Steward C, Stirrups KE, Stuckey A, Suntharalingam J, Swietlik EM, Syrris P, Tait RC, Talks K, Tan RYY, Tate K, Taylor JM, Taylor JC, Thaventhiran JE, Themistocleous AC, Themistocleous AC, Thomas E, Thomas D, Thomas MJ, Thomas P, Thomson K, Thrasher AJ, Threadgold G, Thys C, Thys C, Tilly T, Tischkowitz M, Titterton C, Todd JA, Toh C-H, Tolhuis B, Tomlinson IP, Toshner M, Traylor M, Treacy C, Treadaway P, Trembath R, Tuna S, Turek W, Turro E, Twiss P, Vale T, Geet CV, Zuydam N, Vandekuilen M, Vandersteen AM, Vazquez-Lopez M, von Ziegenweidt J, Noordegraaf AV, Wagner A, Waisfisz Q, Walker SM, Walker N, Walter K, Ware JS, Watkins H, Watt C, Webster AR, Wedderburn L, Wei W, Welch SB, Wessels J, Westbury SK, Westwood J-P, Wharton J, Whitehorn D, Whitworth J, Wilkie AOM, Wilkins MR, Williamson C, Wilson BT, Wong EKS, Wood N, Wood Y, Woods CG, Woodward ER, Wort SJ, Worth A, Wright M, Yates K, Yong PFK, Young T, Yu P, Yu-Wai-Man P, Zlamalova E, Kingston N, Walker N, Bradley JR, Ashford S, Penkett CJ, Penkett CJ, Freson K, Stirrups KE, Raymond FL, Ouwehand WH. . Nature 2020, 583, 96-102.
    • Gallon R, Sheth H, Hayes C, Redford L, Alhilal G, O'Brien O, Spiewak H, Waltham A, McAnulty C, Izuogu OG, Arends MJ, Oniscu A, Alonso AM, Laguna SM, Borthwick GM, Santibanez-Koref M, Jackson MS, Burn J. . Human Mutation 2020, 41(1), 332-341.
    • Dlay JK, Duncan GW, Khoo TK, Williams-Gray CH, Breen DP, Barker RA, Burn DJ, Lawson RA, Yarnall AJ. . Brain Sciences 2020, 10(2), 78.
    • Burn J. . Clinical Medicine 2020, 20(1), 8-20.
    • Burke CA, Dekker E, Lynch P, Samadder NJ, Balaguer F, Hüneburg R, Burn J, Castells A, Gallinger S, Lim R, Stoffel EM, Gupta S, Henderson A, Kallenberg FG, Kanth P, Roos VH, Ginsberg GG, Sinicrope FA, Strassburg CP, VanCutsem E, Church J, Lalloo F, Willingham FF, Wise PE, Grady WM, Ford M, Weiss JM, Gryfe R, Rustgi AK, Syngal S, Cohen A. . The New England Journal of Medicine 2020, 383(11), 1028-1039.
    • Dominguez-Valentin M, Sampson JR, Seppala TT, ten Broeke SW, Plazzer J-P, Nakken S, Engel C, Aretz S, Jenkins MA, Sunde L, Bernstein I, Capella G, Balaguer F, Thomas H, Evans DG, Burn J, Greenblatt M, Hovig E, de Vos tot Nederveen Cappel WH, Sijmons RH, Bertario L, Tibiletti MG, Cavestro GM, Lindblom A, Della Valle A, Lopez-Kostner F, Gluck N, Katz LH, Heinimann K, Vaccaro CA, Buttner R, Gorgens H, Holinski-Feder E, Morak M, Holzapfel S, Huneburg R, Knebel Doeberitz M, Loeffler M, Rahner N, Schackert HK, Steinke-Lange V, Schmiegel W, Vangala D, Pylvanainen K, Renkonen-Sinisalo L, Hopper JL, Win AK, Haile RW, Lindor NM, Gallinger S, Le Marchand L, Newcomb PA, Figueiredo JC, Thibodeau SN, Wadt K, Therkildsen C, Okkels H, Ketabi Z, Moreira L, Sanchez A, Serra-Burriel M, Pineda M, Navarro M, Blanco I, Green K, Lalloo F, Crosbie EJ, Hill J, Denton OG, Frayling IM, Rodland EA, Vasen H, Mints M, Neffa F, Esperon P, Alvarez K, Kariv R, Rosner G, Pinero TA, Gonzalez ML, Kalfayan P, Tjandra D, Winship IM, Macrae F, Moslein G, Mecklin J-P, Nielsen M, Moller P. . Genetics in Medicine 2020, 22, 15-25.
    • Burn J, Sheth H, Elliott F, Reed L, Macrae F, Mecklin J-P, Moslein G, McRonald FE, Bertario L, Evans DG, Gerdes A-M, Ho JWC, Lindblom A, Morrison PJ, Rashbass J, Ramesar R, Seppala T, Thomas HJW, Pylvanainen K, Borthwick GM, Mathers JC, Bishop DT, Boussioutas A, Brewer C, Cook J, Eccles D, Ellis A, Hodgson SV, Lubinski J, Maher ER, Porteous ME, Sampson J, Scott RJ, Side L. . The Lancet 2020, 395(10240), 1855-1863.
    • Crosbie EJ, Ryan NAJ, Arends MJ, Bosse T, Burn J, Cornes JM, Crawford R, Eccles D, Frayling IM, Ghaem-Maghami S, Hampel H, Kauff ND, Kitchener HC, Kitson SJ, Manchanda R, McMahon RFT, Monahan KJ, Menon U, Moller P, Moslein G, Rosenthal A, Sasieni P, Seif MW, Singh N, Skarrott P, Snowsill TM, Steele R, Tischkowitz M, Evans DG. . Genetics in Medicine 2019, (ePub ahead of Print).
    • Dominguez-Valentin M, Seppälä TT, Sampson JR, Macrae F, Winship I, Evans DG, Scott RJ, Burn J, Möslein G, Bernstein I, Pylvänäinen K, Renkonen-Sinisalo L, Lepistö A, Lindblom A, Plazzer JP, Tjandra D, Thomas H, Green K, Lalloo F, Crosbie EJ, Hill J, Capella G, Pineda M, Navarro M, Vidal JB, Rønlund K, Nielsen RT, Yilmaz M, Elvang LL, Katz L, Nielsen M, ten Broeke SW, Nakken S, Hovig E, Sunde L, Kloor M, v Knebel Doeberitz M, Ahadova A, Lindor N, Steinke-Lange V, Holinski-Feder E, Mecklin JP, Møller P. . Hereditary Cancer in Clinical Practice 2019, 17, 28.
    • Gunter MJ, Alhomoud S, Arnold M, Brenner H, Burn J, Casey G, Chan AT, Cross AJ, Giovannucci E, Hoover R, Houlston R, Jenkins M, Laurent-Puig P, Peters U, Ransohoff D, Riboli E, Sinha R, Stadler ZK, Brennan P, Chanock SJ. . Annals of Oncology 2019, 30(4), 510-519.
    • Seppala TT, Ahadova A, Dominguez-Valentin M, Macrae F, Evans DG, Therkildsen C, Sampson J, Scott R, Burn J, Moslein G, Bernstein I, Holinski-Feder E, Pylvanainen K, Renkonen-Sinisalo L, Lepisto A, Lautrup CK, Lindblom A, Plazzer J-P, Winship I, Tjandra D, Katz LH, Aretz S, Huneburg R, Holzapfel S, Heinimann K, Valle AD, Neffa F, Gluck N, De Vos Tot Nederveen Cappel WH, Vasen H, Morak M, Steinke-Lange V, Engel C, Rahner N, Schmiegel W, Vangala D, Thomas H, Green K, Lalloo F, Crosbie EJ, Hill J, Capella G, Pineda M, Navarro M, Blanco I, Ten Broeke S, Nielsen M, Ljungmann K, Nakken S, Lindor N, Frayling I, Hovig E, Sunde L, Kloor M, Mecklin J-P, Kalager M, Moller P. . Hereditary Cancer in Clinical Practice 2019, 17, 8.
    • Arefi M, Wilson V, Muthiah S, Zwolinski S, Bajwa D, Brennan P, Blasdale K, Bourn D, Burn J, Santibanez-Koref M, Rajan N. . Journal of American Academy of Dermatology 2019, 81(6), 1300-1307.
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    • Burn J, Bishop DT, Mecklin JP, Macrae F, Moslein G, Olschwang S, Bisgaard ML, Ramesar R, Eccles D, Maher ER, Bertario L, Jarvinen HJ, Lindblom A, Evans DG, Lubinski J, Morrison PJ, Ho JWC, Vasen HFA, Side L, Thomas HJW, Scott RJ, Dunlop M, Barker G, Elliott F, Jass JR, Fodde R, Lynch HT, Mathers JC, for the CAPP2 Investigators. . New England Journal of Medicine 2008, 359(24), 2567-2578.
    • Burn J. . British Medical Journal 2008, 336(7653), 1132.
    • Hautot D, Pankhurst QA, Morris CM, Curtis A, Burn J, Dobson J. . Biochimica et Biophysica Acta - Molecular Basis of Disease 2007, 1772(1), 21-25.
    • Douglas J, Cilliers D, Coleman K, Tatton-Brown K, Barker K, Bernhard B, Burn J, Huson S, Josifova D, Lacombe D, Malik M, Mansour S, Reid E, Cormier-Daire V, Cole T, Rahman N. . Nature Genetics 2007, 39(8), 963-965.
    • Burn J. . British Medical Journal 2007, 334, s9.
    • Chinnery PF, Crompton DE, Birchall D, Jackson MJ, Coulthard A, Lombes A, Quinn N, Wills A, Fletcher N, Mottershead JP, Cooper P, Kellett M, Bates D, Burn J. . Brain 2007, 130(1), 110-119.
    • Borthwick GM, Johnson AS, Partington M, Burn J, Wilson R, Arthur HM. . The FASEB Journal 2006, 20(12), 2009-2016.
    • Park J-G, Kim D-W, Hong CW, Nam B-H, Shin Y-K, Hong S-H, Kim I-J, Lim S-B, Aronson M, Bisgaard ML, Brown GJ, Burn J, Chow E, Conrad P, Douglas F, Dunlop M, Ford J, Greenblatt MS, Heikki J, Heinimann K, Lynch EL, Macrae F, McKinnon WC, Moeslein G, Rossi BM, Rozen P, Schofield L, Vaccaro C, Vasen H, Velthuizen M, Viel A, Wijnen J. . Clinical Cancer Research 2006, 12(11), 3389-3393.
    • Burn J, Sims AJ, Ford GA, Murray A. . Physiological Measurement 2006, 27(6), 529-538.
    • Venables JP, Burn J. . Nucleic Acids Research 2006, 34(15), e103.
    • Bertagnolli MM, Eagle CJ, Zauber AG, Redston M, Solomon SD, Kim K, Tang J, Rosenstein RB, Wittes J, Corle D, Hess TM, Woloj GM, Boisserie F, Anderson WF, Viner JL, Bagheri D, Burn J, Chung DC, Dewar T, Foley TR, Hoffman N, Macrae F, Pruitt RE, Saltzman JR, Salzberg B, Sylwestrowicz T, Gordon GB, Hawk ET. . New England Journal of Medicine 2006, 355(9), 873-884.
    • Bian Y, Caldes T, Wijnen J, Franken P, Vasen H, Kaklamani V, Nafa K, Peterlongo P, Ellis N, Baron JA, Burn J, Moeslein G, Morrison PJ, Chen Y, Ahsan H, Watson P, Lynch HT, de la Chapelle A, Fodde R, Pasche B. . Journal of Clinical Oncology 2005, 23(13), 3074-3078.
    • Chow E, Macrae F, Burn J. . Hereditary Cancer in Clinical Practice 2005, 3(4), 137-146.
    • Crompton DE, Chinnery PF, Bates D, Walls TJ, Jackson MJ, Curtis AJ, Burn J. . Movement Disorders 2005, 20(1), 95-99.
    • Arun R, Khazim R, Webb JK, Burn J. . Spine 2005, 30(16), E471-E476.
    • Crossland DS, Jackson SP, Lyall R, Hamilton JRL, Hasan A, Burn J, O'Sullivan JJ. . Thoracic and Cardiovascular Surgeon 2005, 53(2), 93-95.
    • Van Der Klift H, Wijnen J, Wagner A, Verkuilen P, Tops C, Otway R, Kohonen-Corish M, Vasen H, Oliani C, Barana D, Moller P, DeLozier-Blanchet C, Hutter P, Foulkes W, Lynch H, Burn J, Moslein G, Fodde R. . Genes Chromosomes and Cancer 2005, 44(2), 123-138.
    • Hitchins M, Williams R, Cheong K, Halani N, Lin VAP, Packham D, Ku S, Buckle A, Hawkins N, Burn J, Gallinger S, Goldblatt J, Kirk J, Tomlinson I, Scott R, Spigelman A, Suter C, Martin D, Suthers G, Ward R. . Gastroenterology 2005, 129(5), 1392-1399.
    • Crossland DS, Jackson SP, Lyall R, Burn J, O'Sullivan JJ. . Cardiology in the Young 2005, 15(4), 391-395.
    • Relton CL, Pearce MS, Burn J, Parker L. . Paediatric and Perinatal Epidemiology 2005, 19(5), 360-367.
    • Burn J. . EJC Supplements 2005, 3(2), 9.
    • Wilding CS, Relton CL, Sutton MJ, Jonas PA, Lynch S-A, Tawn EJ, Burn J. . Birth Defects Research Part A - Clinical and Molecular Teratology 2004, 70(7), 483-485.
    • Relton CL, Wilding CS, Laffling AJ, Jonas PA, Burgess T, Binks K, Tawn EJ, Burn J. . Molecular Genetics and Metabolism 2004, 81(4), 273-281.
    • Crossland DS, Jackson SP, Lyall R, Hamilton JRL, Hasan A, Burn J, O'Sullivan JJ. . European Journal of Cardio-Thoracic Surgery 2004, 25(6), 931-934.
    • Relton CL, Wilding CS, Pearce MS, Laffling AJ, Jonas PA, Lynch SA, Tawn EJ, Burn J. . Journal of Medical Genetics 2004, 41(4), 256-260.
    • Relton CL, Daniel CP, Hammal DM, Parker L, Tawn EJ, Burn J. . Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis 2004, 545(1-2), 49-57.
    • Tonkin ET, Smith M, Eichhorn P, Jones S, Imamwerdi B, Lindsay S, Jackson M, Wang T-J, Ireland M, Burn J, Krantz ID, Carr P, Strachan T. . Human Genetics 2004, 115(2), 139-148.
    • Meijers-Heijboer H, Wijnen J, Vasen H, Wasielewski M, Wagner A, Hollestelle A, Elstrodt F, Van Den Bos R, De Snoo A, Fat GTA, Brekelmans C, Jagmohan S, Franken P, Verkuijlen P, Van Den Ouweland A, Chapman P, Tops C, Moslein G, Burn J, Lynch H, Klijn J, Fodde R, Schutte M. . American Journal of Human Genetics 2003, 72(5), 1308-1314.
    • Chinnery PF, Curtis ARJ, Fey C, Coulthard A, Crompton D, Curtis A, Lombes A, Burn J. . Journal of Medical Genetics 2003, 40(5), -.
    • Torsney E, Charlton R, Diamond AG, Burn J, Soames JV, Arthur HM. . Circulation 2003, 107(12), 1653-1657.
    • Wagner A, Barrows A, Wijnen JTh, Van Der Klift H, Franken PF, Verkuijlen P, Nakagawa H, Geugien M, Jaghmohan-Changur S, Breukel C, Meijers-Heijboer H, Morreau H, Van Puijenbroek M, Burn J, Coronel S, Kinarski Y, Okimoto R, Watson P, Lynch JF, De La Chapelle A, Lynch HT, Fodde R. . American Journal of Human Genetics 2003, 72(5), 1088-1100.
    • Ewart-Toland A, Briassouli P, De Koning JP, Mao J-H, Yuan J, Chan F, MacCarthy-Morrogh L, Ponder BAJ, Nagase H, Burn J, Ball S, Almeida M, Linardopoulos S, Balmain A. . Nature Genetics 2003, 34(4), 403-412.
    • Taylor CF, Charlton RS, Burn J, Sheridan E, Taylor GR. . Human Mutation 2003, 22(6), 428-433.
    • Boyle P, Autier P, Bartelink H, Baselga J, Boffetta P, Burn J, Burns HJG, Christensen L, Denis L, Dicato M, Diehl V, Doll R, Franceschi S, Gillis CR, Gray N, Griciute L, Hackshaw A, Kasler M, Kogevinas M, Kvinnsland S, La Vecchia C, Levi F, McVie JG, Maisonneuve P, Martin-Moreno JM, Newton Bishop J, Oleari F, Perrin P, Quinn M, Richards M, Ringborg U, Scully C, Siracka E, Storm H, Tubiana M, Tursz T, Veronesi U, Wald N, Weber W, Zaridze DG, Zatonski W, zur Hausen H. . Annals of Oncology 2003, 14(7), 973-1005.
    • Mathers JC, Mickleburgh I, Chapman PC, Bishop DT, Burn J. . Proceedings of the Nutrition Society 2003, 62(1), 51-72.
    • Adams JM, White M, Barker G, Mathers JC, Burn J. . Familial Cancer 2003, 2(3-4), 169-173.
    • Toutain A, Dessay B, Ronce N, Ferrante MI, Tranchemontagne J, Newbury-Ecob R, Wallgren-Pettersson C, Burn J, Kaplan J, Rossi A, Russo S, Walpole I, Hartsfield JK, Oyen N, Nemeth A, Bitoun P, Trump D, Moraine C, Franco B. . European Journal of Human Genetics 2002, 10(9), 516-520.
    • Relton CL, Daniel CP, Fisher A, Chase DS, Burn J, Tawn EJ. . Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis 2002, 502(1-2), 61-68.
    • Chinnery PF, Curtis AR, Fey C, Jackson MJ, Bates D, Morris CM, Bindoff LA, Coulthard A, Ince PG, Curtis A, Burn J. . Journal of Neurology, Neurosurgery and Psychiatry 2002, 73(2), 213-213.
    • Chinnery PF, Reading PJ, McCarthy EL, Curtis A, Burn J. . Movement Disorders 2002, 17(1), 196-198.
    • Hutter P, Wijnen J, Rey-Berthod C, Thiffault I, Verkuijlen P, Farber D, Hamel N, Bapat B, Thibodeau SN, Burn J, Wu J, MacNamara E, Heinimann K, Chong G, Foulkes WD. . Journal of Medical Genetics 2002, 39(5), 323-327.
    • Klauck SM, Lindsay S, Beyer KS, Splitt M, Burn J, Poustka A. . American Journal of Human Genetics 2002, 70(4), 1034-1037.
    • Curtis ARJ, Fey C, Morris CM, Bindoff LA, Ince PG, Chinnery PF, Coulthard A, Jackson MJ, Jackson AP, McHale DP, Hay D, Barker WA, Markham AF, Bates D, Curtis A, Burn J. . Nature Genetics 2001, 28(4), 350-354.
    • Curtis ARJ, Fey C, Morris CM, Bindoff LA, Ince PG, Chinnery PF, Coulthard A, Jackson MJ, Jackson AP, McHale DP, Hay D, Barker WA, Markham AF, Bates D, Curtis A, Burn J. . Nature Genetics 2001, 28(4), 350-354.
    • Witsch-Baumgartner M, Ciara E, Loffler J, Menzel HJ, Seedorf U, Burn J, Gillessen-Kaesbach G, Hoffmann GF, Fitzky BU, Mundy H, Clayton P, Kelley RI, Krajewska-Walasek M, Utermann G. . European Journal of Human Genetics 2001, 9(1), 45-50.
    • Mills SJ, Mathers JC, Chapman PD, Burn J, Gunn A. . Gut 2001, 48(1), 41-46.
    • Fey C, Curtis ARJ, Chinnery PF, Morris CM, Ince PG, Coulthard A, Jackson MJ, Barker WA, Curtis A, Burn J. A dominant FTL mutation causes a novel and pleiotropic basal ganglia disorder that can mimic torsion-dystonia, Huntington's Disease and parkinsonism. American Journal of Human Genetics 2001, 69(4), 97.
    • Fairgrieve SD, Jackson M, Jonas P, Walshaw D, White K, Montgomery TL, Burn J, Lynch SA. . British Medical Journal 2000, 321(7262), 674-675.
    • Vigen T, Haites N, Burn J, Moller P, Steel M. . British Journal of General Practice 2000, 50(453), 337.
    • Satoda M, Zhao F, Diaz GA, Burn J, Goodship J, Davidson HR, Pierpont MEM, Gelb BD. . Nature Genetics 2000, 25(1), 42-46.
    • Takahashi M, Rapley E, Biggs PJ, Lakhani SR, Cooke D, Hansen J, Blair E, Hofmann B, Siebert R, Turner G, Evans DG, Schrander-Stumpel C, Beemer FA, Van Vloten WA, Breuning MH, Van Den Ouweland A, Halley D, Delpech B, Cleveland M, Leigh I, Chapman P, Burn J, Hohl D, Gorog J-P, Seal S, Mangion J, Warren W, Bignell G, Stratton MR. . Human Genetics 2000, 106(1), 58-65.
    • Daniel CP, Fisher A, Parker L, Burn J, Tawn EJ. . Mutation Research - Genetic Toxicology and Environmental Mutagenesis 2000, 467(2), 153-159.
    • Bignell GR, Warren W, Seal S, Takahashi M, Rapley E, Barfoot R, Green H, Brown C, Biggs PJ, Lakhani SR, Jones C, Hansen J, Blair E, Hofmann B, Siebert R, Turner G, Gareth Evans D, Schrander-Stumpel C, Beemer FA, Van Den Ouweland A, Halley D, Delpech B, Cleveland MG, Leigh I, Leisti J, Rasmussen S, Wallace MR, Fenske C, Banerjee P, Oiso N, Chaggar R, Merrett S, Leonard N, Huber M, Hohl D, Chapman P, Burn J, Swift S, Smith A, Ashworth A, Stratton MR. . Nature Genetics 2000, 25(2), 160-165.
    • Fidalgo P, Almeida MR, West S, Gaspar C, Maia L, Wijnen J, Albuquerque C, Curtis A, Cravo M, Fodde R, Leitao CN, Burn J. . European Journal of Human Genetics 2000, 8(1), 49-53.
    • Lynch SA, Wang Y, Strachan T, Burn J, Lindsay S. . Journal of Medical Genetics 2000, 37(8), 561-566.
    • Burn J, Curtis AR, Bindoff L, Ince P, Coulthard A, Jackson A, Jackson M, Fey C, Hay D, Shepherd D, Bates D, Curtis A. . American Journal of Human Genetics 2000, 67(4), 371-371.
    • Ryan A, Burn J, Court S, Jackson T, Smith JC, Barwick D. . Clinical Dysmorphology 1999, 8(1), 15-18.
    • Aitken DA, Ireland M, Berry E, Crossley JA, Macri JN, Burn J, Connor JM. . Prenatal Diagnosis 1999, 19(8), 706-710.
    • Denison CK, Barnes R, Gibson B, Hunt A, Hart I, Steel M, Casismir C, Liu D, Nevin NC, Anionwu E, Burn J, Dayan A, Denison K, Johnston P, Marteau T, Neil J, Pinching A, Platt E, Richards B, Steel CM, Train I. . Human Gene Therapy 1999, 10(4), 689-692.
    • Chu C, Sheridan E, Turner G, Robson F, Mason G, Thornton J, Burn J. Prenatal testing for cancer predisposition syndromes. Journal of Medical Genetics 1999, 36, S35-S35.
    • Williamson SLH, Kartheuser A, Coaker J, Kooshkghazi MD, Fodde R, Burn J, Mathers JC. . Carcinogenesis 1999, 20(5), 805-810.
    • Chapman PD, Burn J. . Cytogenetics and Cell Genetics 1999, 86(2), 118-124.
    • Kartheuser A, Walon C, West S, Breukel C, Detry R, Gribomont AC, Hamzehloei T, Hoang P, Maiter D, Pringot J, Rahier J, Khan PM, Curtis A, Burn J, Fodde R, Verellen-Dumoulin C. . Journal of Medical Genetics 1999, 36(1), 65-67.
    • Berney TP, Ireland M, Burn J. . Archives of Disease in Childhood 1999, 81(4), 333-336.
    • Chase DS, Tawn EJ, Parker L, Jonas P, Parker CO, Burn J. . Journal of Medical Genetics 1998, 35(5), 413-416.
    • Chase DS, Tawn EJ, Parker L, Jonas P, Parker CO, Burn J. The North Cumbria Community Genetics Project. JOURNAL OF MEDICAL GENETICS 1998, 35(5), 413-416.
    • K. Morrison, C. Papapetrou, F. A. Hol, E. C. M. Mariman, S. A. Lynch, J. Burn and Y. H. Edwards. Susceptibility to spina bifida; an association study of five candidate genes. Annals of Human Genetics 1998, 62, 379-396.
    • A. K. Ryan, K. Bartlett, P. Clayton, S. Eaton, L. Mills, D. Donnai, R. M. Winter and J. Burn. Smith-Lemli-Opitz syndrome: a variable clinical and biochemical phenotype. Journal of Medical Genetics 1998, 35, 558-565.
    • J. Burn, P. Brennan, J. Little, S. Holloway, R. Coffey, J. Somerville, N. R. Dennis, L. Allan, R. Arnold, J. E. Deanfield, M. Godman, A. Houston, B. Keeton, C. Oakley, O. Scott, E. Silove, J. Wilkinson, M. Pembrey and A. S. Hunter. Recurrence risks in offspring of adults with major heart defects: results from first cohort of British collaborative study. Lancet 1998, 351, 311-316.
    • D. G. R. Evans, J. Hill, T. Dudding, J. Burn and E. R. Maher. Molecular genetic tests in surgical management of familial adenomatous polyposis - reply. Lancet 1998, 351, 1131-1132.
    • Green SE, Bradburn DM, Varma JS, Burn J. . International Journal of Colorectal Disease 1998, 13(1), 3-12.
    • J. M. Varley, P. Chapman, G. McGown, M. Thorncroft, G. R. M. White, M. J. Greaves, D. Scott, A. Spreadborough, K. J. Tricker, J. M. Birch, D. G. R. Evans, R. Reddel, R. S. Camplejohn, J. Burn and J. M. Boyle. Genetic and functional studies of a germline TP53 splicing mutation in a Li-Fraumeni-like family. Oncogene 1998, 16, 3291-3298.
    • J. Burn, P. D. Chapman, D. T. Bishop and J. Mathers. Diet and cancer prevention: the Concerted Action Polyp Prevention (CAPP) Studies. Proceedings of the Nutrition Society 1998, 57, 183-186.
    • S. J. Mills, J. C. Mathers, P. D. Chapman, J. Burn and A. Gunn. Crypt cell proliferation state in the human colon. Validation of results obtained by whole crypt microdissection and the findings in patients with familial adenomatous polyposis, sporadic adenomas and colorectal cancer. British Journal of Surgery 1998, 85, 84-84.
    • Green SE, Chapman P, Burn J, Burt AD, Bennett M, Appleton DR, Varma JS, Mathers JC. . Gut 1998, 43(1), 85-92.
    • Douglas F. and Burn J. Cancer genetics: a summary. Cleveland Medical Journal 1998, 1998, 4-5.
    • Mills SJ, Mathers JC, Chapman PD, Burn J, Gunn A. Aspirin, sulindac and the rectum in familial adenomatous polyposis. British Journal of Surgery 1998, 85, 55-56.
    • Gebbia M, Ferrero GB, Pilia G, Bassi MT, Aylsworth AS, PenmanSplitt M, Bird LM, Bamforth JS, Burn J, Schlessinger D, Nelson DL, Casey B. . Nature Genetics 1997, 17, 305-308.
    • J. Burn, J. Camm, M. J. Davies, L. Peltonen, P. J. Schwartz and H. Watkins. The phenotype/genotype relation and the current status of genetic screening in hypertrophic cardiomyopathy, Marfan syndrome, and the long QT syndrome. Heart 1997, 78, 110-116.
    • P. Brennan, S. Holloway, J. Little and J. Burn. Tetralogy of Fallot: a triad of susceptibility genes?. Journal of Medical Genetics 1997, 34, 701-701.
    • J. Burn and N. M. Fisk. Terathanasia, folic acid, and birth defects. Lancet 1997, 350, 1322-1323.
    • Fisk N.M. and Burn J. Terathanasia, folic acid and birth defects (letter). Lancet 1997, 350, 1322-1323.
    • Wyllie J.P., Madar R.J., Wright M. and Burn J. Strategies for antenatal detection of Down's syndrome. Arch Dis Child 1997, 76, F26-F30.
    • A. K. Ryan, K. Bartlett, P. Clayton, S. Eaton, K. Mills, J. Collins, D. Donnai, R. Winter and J. Burn. Smith-Lemli-Opitz syndrome: A variable phenotype caused by 7 dehydro cholesterol reductase deficiency. American Journal of Human Genetics 1997, 61, 10.
    • A. K. Ryan, K. Barlett, P. Clayton, S. Eaton, K. Mills, J. Collins, D. Donnai, R. Winter and J. Burn. Smith Lemli Opitz syndrome: a variable phenotype caused by 7 dehydro cholesterol reductase deficiency. Journal of Medical Genetics 1997, 34, SP39-SP39.
    • B. Casey, M. Gebbia, G. B. Ferrero, G. Pilia, M. Yamada, A. S. Aylsworth, M. Penman-Splitt, L. M. Bird, J. S. Bamforth, J. Burn, D. Schlessinger and D. L. Nelson. Sites inversus, heart defects, and other manifestations of X- linked heterotaxy caused by mutations in the zinc-finger transcription factor ZIC3. American Journal of Human Genetics 1997, 61, 90.
    • P. Jonas, D. S. Chase, C. Parker, E. J. Tawn, L. Parker and J. Burn. Setting up a DNA bank: Practical issues. Journal of Medical Genetics 1997, 34, 707-707.
    • D. G. R. Evans, J. Hill, T. Dudding, J. Burn and E. R. Maher. Molecular genetic tests in surgical management of familial adenomatous polyposis. Lancet 1997, 350, 1777-1777.
    • K. Morrison, Y. H. Edwards, S. A. Lynch, J. Burn, F. Hol and E. Mariman. Methionine synthase and neural tube defects. Journal of Medical Genetics 1997, 34, 958-958.
    • S. Fairgrieve, D. Magnay, I. White and J. Burn. Maternal serum screening for Down's syndrome: a survey of midwives' views. Public Health 1997, 111, 383-385.
    • S. Lindsay, M. Ireland, O. Obrien, J. ClaytonSmith, J. A. Hurst, J. Mann, T. Cole, J. Sampson, S. Slaney, D. Schlessinger, J. Burn and G. Pilia. Large scale deletions in the GPC3 gene may account for a minority of cases of Simpson-Golabi-Behmel syndrome. Journal of Medical Genetics 1997, 34, 480-483.
    • S. A. Lynch and J. Burn. Genetic counselling in families with hereditary sacral agenesis. Journal of Medical Genetics 1997, 34, SP16-SP16.
    • S. J. Mills, P. D. Chapman, J. Burn and A. Gunn. Endoscopic screening and surgery for familial adenomatous polyposis: Dangerous delays. British Journal of Surgery 1997, 84, 74-77.
    • M. P. Splitt, J. Burn and J. A. Goodship. Determination of left-right asymmetry. Journal of Medical Genetics 1997, 34, SP28-SP28.
    • Burn J. and Chapman P.D. Colon cancers: genes or environment?. Nutrition Abstracts and Reviews, Series A: Human and Experimental 1997, 67, 787-784.
    • Fairgrieve S., Magnay D., White I. and Burn J. Case report. Maternal serum screening: a team approach. British Journal of Midwifery 1997, 5, 152-153.
    • J. Burn, P. D. Chapman, J. Mathers, D. T. Bishop and H. Lynch. CAPP2: An international controlled trial of aspirin and resistant starch in carriers of HNPCC. Journal of Medical Genetics 1997, 34, 518-518.
    • M. G. Dunlop, S. M. Farrington, A. D. Carothers, A. H. Wyllie, L. Sharp, J. Burn, B. Liu, K. W. Kinzler and B. Vogelstein. Cancer risk associated with germline DNA mismatch repair gene mutations. Human Molecular Genetics 1997, 6, 105-110.
    • S. A. Lynch, D. GardnerMedwin, J. Burn and K. M. D. Bushby. Absent nails, kinesogenic choreoathetosis, epilepsy and developmental delay - A new autosomal dominant disorder?. Clinical Dysmorphology 1997, 6, 133-138.
    • M. P. Splitt, M. Y. Tsai, J. Burn and J. A. Goodship. Absence of mutations in the regulatory domain of the gap junction protein connexin 43 in patients with visceroatrial heterotaxy. Heart 1997, 77, 369-370.
    • J. Goodship, J. Carter and J. Burn. X-inactivation patterns in monozygotic and dizygotic female twins. American Journal of Medical Genetics 1996, 61, 205-208.
    • P. J. Biggs, P. Chapman, S. R. Lakhani, J. Burn and M. R. Stratton. The cylindromatosis gene (cyld1) on chromosome 16q may be the only tumour suppressor gene involved in the development of cylindromas. Oncogene 1996, 12, 1375-1377.
    • S. Chatkupt, T. Lehner, Q. Li, R. Sun, K. Tolba, S. Chaudhari, C. V. Torigian, E. S. Stenroos, M. Thomas, T. Strachan, J. Burn and W. G. Johnson. Sacral defect families with wide phenotypic variation map to the same chromosomal region. Neurology 1996, 46, 2006-2006.
    • S. Lindsay, M. Splitt, S. Edney, T. P. Berney, S. J. L. Knight, K. E. Davies, O. Obrien, M. Gale and J. Burn. PPM-X: A new X-linked mental retardation syndrome with psychosis, pyramidal signs, and macroorchidism maps to Xq28. American Journal of Human Genetics 1996, 58, 1120-1126.
    • N. D. Embleton, J. P. Wyllie, M. J. Wright, J. Burn and S. Hunter. Natural history of trisomy 18. Archives of Disease in Childhood 1996, 75, F38-F41.
    • T. Hamzehloei, S. P. West, P. Chapman, J. Burn and N. Curtis. Mutation detection in exons 1-14 of the adenomatous polyposis coli gene: Identification of an alternatively spliced transcript. Molecular and Cellular Probes 1996, 10, 379-385.
    • C. Papapetrou, S. A. Lynch, J. Burn and Y. H. Edwards. Methylenetetrahydrofolate reductase and neural tube defects. Lancet 1996, 348, 58-58.
    • D. M. Eccles, R. vanderLuijt, C. Breukel, H. Bullman, D. Bunyan, A. Fisher, J. Barber, C. duBoulay, J. Primrose, J. Burn and R. Fodde. Hereditary desmoid disease due to a frameshift mutation at codon 1924 of the APC gene. American Journal of Human Genetics 1996, 59, 1193-1201.
    • K. Morrison, C. Papapetrou, J. Attwood, F. Hol, S. A. Lynch, A. Sampath, B. Hamel, J. Burn, J. Sowden, D. Stott, E. Mariman and Y. H. Edwards. Genetic mapping of the human homologue (T) of mouse T(Brachyury) and a search for allele association between human T and spina bifida. Human Molecular Genetics 1996, 5, 669-674.
    • D. McHale, M. E. M. Porteous, J. Wentzel and J. Burn. Further evidence of genetic heterogeneity in hereditary hydronephrosis. Clinical Genetics 1996, 50, 491-493.
    • J. Burn and J. Goodship. Developmental genetics of the heart. Current Opinion in Genetics & Development 1996, 6, 322-325.
    • M. P. Splitt, J. Burn and J. Goodship. Defects in the determination of left-right asymmetry. Journal of Medical Genetics 1996, 33, 498-503.
    • P. Baxter, S. Connolly, A. Curtis, V. Spencer, C. Ravindranath, J. Burn and D. GardnerMedwin. Co-dominant inheritance of hyperekplexia and spastic paraparesis. Developmental Medicine and Child Neurology 1996, 38, 739-743.
    • J. Burn, S. Fairgrieve, P. Franks, I. White and D. Magnay. Audit of maternal serum screening: Strategies to augment counselling in response to women's views. European Journal of Human Genetics 1996, 4, 108-112.
    • Wright MJ, Newell JN, Charlton ME, Hey EN, Donaldson LJ, Burn J. . Journal of Epidemiology & Community Health 1995, 49(3), 305-308.
    • Burn J, Strachan T. . Nature Genetics 1995, 11(1), 3-6.
    • Green SE, Chapman PD, Burn J, Bishop DT, Varma JS. . British Journal of Surgery 1995, 82(10), 1338-1340.
    • Porteous ME, Curtis A, Williams O, Marchuk D, Bhattacharya SS & Burn J. Genetic heterogeneity in hereditary haemorrhagic telangiectasia. J Med Genet 31: 925-926 1993.
    • Goldman A, Martin RH, Johannisson R, Gould CP, Davison EV, Emslie JE, Burn J, Hulten MA. . Journal of Medical Genetics 1992, 29(7), 460-464.
    • Porteous MEM, Burn J, Proctor SJ. . Journal of Medical Genetics 1992, 29(8), 527-530.
    • Goodship J, Curtis A, Cross I, Brown J, Emslie J, Wolstenholme J, Bhattacharya S, Burn J. . Journal of Medical Genetics 1992, 29(7), 451-454.
    • Wilson DI, Cross IE, Goodship JA, Coulthard S, Carey AH, Scambler PJ, Bain HH, Hunter AS, Carter PE, Burn J. . British Heart Journal 1991, 66(4), 308-312.
    • Ireland M, English C, Cross I, Houlsby WT, Burn J. . Journal of Medical Genetics 1991, 28(9), 639-640.
    • Burn J, Gibbens D. . Journal of Medical Genetics 1979, 16(3), 210-214.

  • Book Chapters

    • Bamforth SD, Burn J. . In: Stanley Maloy and Kelly Hughes, ed. Brenner's Encyclopedia of Genetics. Academic Press, 2013, pp.319-321.
    • Burn J, Chapman PD, Mathers J, Bishop DT. . In: Utsunomiya, J; Mulvihill, JJ; Weber, W, ed. Familial Cancer and Prevention: Molecular Epidemiology - A New Strategy Toward Cancer Control: UICC Symposium on Familial Cancer and Prevention. Kobe, Japan: Wiley-Liss, Inc, 1999, pp.279-284.

  • Conference Proceedings (inc. Abstracts)

    • Burn J. . In: Molecular Cytogenetics. 2014, Ahmedabad, India: BioMed Central Ltd.
    • Burn J. . In: Molecular Cytogenetics. 2014, Ahmedabad, India: BioMed Central Ltd.
    • Burn J. . In: Journal of Medical Genetics. 2012, Coventry, UK: BMJ Group.
    • Cowley L, Burn J. . In: Journal of Medical Genetics. 2012, London, UK: BMJ Publishing Group.
    • Rajan N, Burn J, Langtry J, Sieber-Blum M, Lord CJ, Ashworth A. Loss of organisation in CYLD defective tumours is associated with reduced DKK2 expression. In: BRITISH JOURNAL OF DERMATOLOGY. 2011, COMMERCE PLACE, 350 MAIN ST, MALDEN 02148, MA USA: WILEY-BLACKWELL.
    • Rajan N, Gillinder K, Lord C, Langtry JAA, Burn J, Ashworth A, Chaudhury B, Sieber-Blum M. . In: 90th Annual Meeting of the British Association of Dermatologists. 2010, Manchester, UK: Wiley-Blackwell Publishing, Inc.
    • Cunnington M, Koref MS, Mayosi B, Burn J, Keavney B. . In: 78th Congress of the European Atherosclerosis Society. 2010, Hamburg, Germany: Atherosclerosis Supplements, Elsevier.
    • Cunnington MS, Koref MS, Mayosi B, Burn J, Keavney B. . In: Annual Conference and Exhibition of the British Cardiovascular Society. 2010, Manchester: BMJ Publushing Group.
    • Rajan N, Lord CJ, Clewes O, Burn J, Sieber-Blum M, Ashworth A. . In: Annual Meeting of the British Society for Investigative Dermatology. 2010, Edinburgh, Scotland: British Journal of Dermatology.
    • Rajan N, Lord CJ, Clewes O, Burn J, Sieber-Blum M, Ashworth A. Dysregulated tropomyosin receptor kinase signalling in CYLDtrunc/trunc tumours. In: BRITISH JOURNAL OF DERMATOLOGY. 2010, COMMERCE PLACE, 350 MAIN ST, MALDEN 02148, MA USA: WILEY-BLACKWELL.
    • Rajan N, Lord CJ, Clewes O, Burn J, Sieber-Blum M, Ashworth A. Dysregulated tropomyosin receptor kinase signalling in CYLDtrunc/trunc tumours. In: BRITISH JOURNAL OF DERMATOLOGY. 2010, COMMERCE PLACE, 350 MAIN ST, MALDEN 02148, MA USA: WILEY-BLACKWELL.
    • Rajan N, Elliott R, Lord C, Clewes O, Burn J, Sieber-Blum M, Ashworth A. . In: 40th Annual Meeting of the European Society for Dermatological Research. 2010, Nature Publishing Group.
    • Burn J, Mathers JC, Gerdes AM, Bisgaard ML, Evans G, Eccles D, Lindblom A, Macrae F, Maher ER, Mecklin JP, Moslein G, Olschwang S, Ramesar R, Vasen HFA, Wijnen J, Barker G, Elliott F, Lynch H, Bishop DT, CAPP2 Consortium. . In: Annals of Oncology: European Multidisciplinary Colorectal Cancer Congress. 2010, Nice, France: Oxford University Press.
    • Rajan N, Elliott R, Lord CJ, Burn J, Sieber-Blum M, Ashworth A. . In: British Society of Human Genetics Annual Conference. 2010, London, UK: BMJ Group.
    • Rajan N, Elliott R, Lord CJ, Burn J, Blum MS, Ashworth A. . In: Journal of Medical Genetics. 2010, BMJ Publishing Group.
    • Rajan N, Powell H, Langtry JAA, Carmichael A, Bourn D, Burn J. . In: 89th Annual Meeting of the British Association of Dermatologists. 2009, Glasgow, UK: Wiley-Blackwell Publishing, Inc.
    • Cunnington MS, Santibanez Koref MS, Mayosi BM, Burn J, Keavney B. . In: 82nd Scientific Session of the American Heart Association. 2009, Orlando, Florida, USA: Lippincott Williams & Wilkins.
    • Henderson A, Jonas P, Burn J, Douglas P. Familial Cholangiocarcinoma: Case Report and Review. In: JOURNAL OF MEDICAL GENETICS. 2009, BRITISH MED ASSOC HOUSE, TAVISTOCK SQUARE, LONDON WC1H 9JR, ENGLAND: B M J PUBLISHING GROUP.
    • Griffin H, Eden J, Burn J, Curtis A. . In: Journal of Medical Genetics: British Human Genetics Conference. 2009, University of Warwick, UK: BMJ Group.
    • Burn J, Gerdes AM, Mathers J, Mecklin JP, Macrae F, Moeslein G, Bisgaard ML, Ramesar R, Eccles D, Maher ER, Evans G, Morrison P, Bishop DT. . In: British Human Genetics Conference. 2009, University of Warwick, UK: BMJ Group.
    • Burn J, Gerdes AM, Mecklin JP, Macrae F, Moeslein G, Bisgaard ML, Ramesar R, Eccles DT, Mathers JC, Bishop DT. . In: Joint ECCO 15 – 34th ESMO Multidisciplinary Congress. 2009, Berlin, Germany: Pergamon.
    • Griffin H, Brown R, Santibanez-Koref M, Burn J, Curtis A. . In: British Human Genetics Conference. 2009, University of Warwick, UK: BMJ Group.
    • Rajan N, Bourn D, Roberts C, Langtry JAA, Burn J. . In: 89th Annual Meeting of the British Association of Dermatologists. 2009, Glasgow, UK: Wiley-Blackwell Publishing, Inc.
    • Burn J, Bishop DT, Mecklin J, Macrae F, Moslein G, Olschwang S, Bisgaard M, Ramesar R, Elliott F, Mathers J. . In: 5th International Conference on Cancer Prevention. 2008, St Gallen, Switzerland: Pergamon.
    • Norum J, Hagen AI, Maehle L, Apold J, Burn J, Moller P. . In: EJC Supplements: 6th European Breast Cancer Conference. 2008, Berlin, Germany: Pergamon.
    • Vasen HFA, Moslein G, Alonso A, Aretz S, Bernstein I, Bertario L, Blanco I, Bulow S, Burn J, Capella G, Colas C, Engel C, Frayling I, Friedl W, Hes FJ, Hodgson S, Jarvinen H, Mecklin J-P, Moller P, Myrhoi T, Nagengast FM, Pare Y, Phillips R, Clark SK, Ponz De Leon M, Renkonen-Sinisalo L, Sampson JR, Stormorken A, Tejpar S, Thomas HJW, Wijnen J. . In: Gut: Workshop on Hereditary Gastrointestinal Cancer. 2008, Mallorca, Spain: BMJ Group.
    • Brown SJ, Relton CL, Liao H, Zhao Y, Sandilands A, Wilson IJ, Burn J, Reynolds NJ, McLean W, Cordell HJ. . In: International Investigative Dermatology Meeting. 2008, Kyoto, Japan: Journal of Investigative Dermatology: Nature Publishing Group.
    • Brown S, Relton C, Liao H, Zhao Y, Sandilands A, Burn J, Cordell H, McLean WHI, Reynolds N. . In: 88th Annual Meeting of the British Association of Dermatologists. 2008, Liverpool, UK: Wiley-Blackwell.
    • Rajan N, Langtry J, Chapman P, Trainer A, Burn J. . In: 2008 Annual Meeting. 2008, Nature Publishing Group.
    • Stanley L, Coxhead J, Burn J, Curtis A. . In: British Human Genetics Conference 2008. 2008, University of York, UK: Journal of Medical Genetics: BMJ Group.
    • Curtis A, Chinnery PF, Batey SJ, Curtis A, Burn J. . In: British Human Genetics Conference 2008. 2008, University of York, UK: Journal of Medical Genetics: BMJ Group.
    • Cilliers D, Douglas J, Tatton-Brown K, Bernhard B, Burn J, Huson S, Josifova D, Lacombe D, Malik M, Mansour S, Reid E, Cormiere-Daire V, Cole T, Rahman N. . In: British Human Genetics Conference. 2007, University of York: BMJ Publishing Group.
    • Burn J, Bishop DT, Mecklin JP, Macrae F, Moeslein G, Olschwang S, Bisgaard MLS, Ramesar R, Jass J, Lynch HT, Barker G, Elliott F, Mathers JCM. . In: British Human Genetics Conference. 2007, University of York: BMJ Group.
    • Wilson V, Santibanez-Koref M, Strain L, Eden J, Curtis A, Burn J. . In: British Human Genetics Conference. 2005, York, UK: BMJ Group.
    • Cockburn D, Dyson L, Emslie J, Ellwood S, Kennedy D, Williams K, Blair M, Shaw R, Burn J. . In: British Human Genetics Conference. 2005, University of York, UK: Journal of Medical Genetics, BMJ Group.
    • Burn J, Mathers J, Barker G, Bishop T. . In: 3rd Annual AACR International Conference. 2004, Seattle, Washington, USA: American Association for Cancer Research.
    • Liljegren A, Barker G, Mathers J, Lindblom A, Nilsson B, Rotstein S, Burn J, Bishop T, CAPP2 Study Grp. . In: 40th Annual Meeting of the American Society of Clinical Oncology. 2004, New Orleans, Lousiana, USA: American Society of Clinical Oncology.
    • Crompton DE, Griffiths TD. . In: Annual Meeting of the British Neuropsychiatry Association at the Institute of Child Health. 2004, London, UK: BMJ Group.
    • Johnson AS, Arthur HM, Burn J, Wilson RG. . In: Annual Meeting of the British Society of Gastroenterology. 2004, Glasgow, UK: BMJ Group.
    • Arthur H, Torsney E, Burn J. . In: 13th Genetics-Societys Mammalian Genetics and Development Workshop. 2003, London, UK: Cambridge University Press.
    • Burn J, Chapman PD, Bishop DT, Dixon R, Turner F, Coaker J, Dunlop MG, Eccles D, Ellis A, Fidalgo P, Vasen HF, Fodde R, Moslein G, Bulow S, Phillips RKS, Bertario L, Evans G, Mathers J. . In: Annual Meeting of the American Society of Human Genetics. 2003, Los Angeles, California, USA: Cell Press.
    • Johnson S, Arthur HM, Burn J, Wilson RG. . In: 2nd Annual AACR International Conference on Frontiers in Cancer Prevention Research. 2003, Phoenix, Arizona, USA: American Association for Cancer Research.
    • Mathers JC, Mickleburgh I, Chapman PC, Bishop DT, Burn J. . In: 7th International Vahouny Fibre Symposium. 2003, Royal College of Physicians, Edinburgh: Proceedings of the Nutrition Society: Cambridge University Press.
    • Hutter P, Wijnen J, Chong G, Ray-Berthod C, Thiffault I, Thibodeau S, Burn J, Wong N, Chappuis P. . In: 52nd Annual Meeting of the American Society of Human Genetics. 2002, Baltimore, Maryland, USA: Cell Press.
    • Crompton DE, Chinnery PF, Fey C, Curtis ARJ, Morris CM, Kierstan J, Burt A, Young F, Coulthard A, Curtis A, Ince PG, Bates D, Jackson MJ, Burn J. . In: Meeting on Molecular and Clinical Aspects of Human Iron Metabolism. 2002, Chiemesee, Germany: Academic Press.
    • Fey C, Curtis ARJ, Chinnery PF, Lombes A, Morris CM, Curtis A, Burn J. . In: European Human Genetics Conference in conjunction with the European Meeting on Psychosocial Aspects of Genetics 2002. 2002, Strasbourg, France: Nature Publishing Group.
    • Chase DS, Tawn EJ, Jonas P, Parker L, Killip J, Burn J. . In: Journal of Medical Genetics. 2001, BMJ Group.
    • Curtis A, Fey C, Morris CM, Ince PG, Bindoff LA, Jackson MJ, Coulthard A, Curtis A, Burn J. . In: Journal of Medical Genetics. 2001, BMJ Group.
    • Tonkin E, Smith M, Eichhorn P, Hagan DM, Herrell S, Lusher M, Ireland M, Burn J, Strachan T. . In: American Journal of Human Genetics. 2001, Cell Press.
    • Wonderling D, Hopwood P, Cull A, Douglas F, Watson M, Burn J, McPherson K. UK cancer genetics services - the response to a new need. In: Journal of Medical Genetics. 2000.
    • Pinkett R, Spencer V, Curtis A, Hamzehloei T, Cross I, Burn J, Douglas F, West S, Chapman P, Gunn A. Genetic testing for familiar adenomatous polyposis coli (FAP) in 缅北禁地: eight years on. In: Journal of Medical Genetics. 2000.
    • Hopwood P, Wonderling D, Cull A, Douglas F, Watson M, Burn J, McPherson K, Cole T, Eccles D, Gray J, Murday V, Steel M. Cancer genetics counselling - psychosocial outcomes one month after first consultation. In: Journal of Medical Genetics. 2000.
    • Healey C, Dunning AM, Teare DM, Chase D, Burn J, Chang-Claude J, Mannermaa A, Easton DF, Ponder BAJ, Parker L, Kataja V, Pharoah PDP, Luben RN. Association of a common variant in BRCA2 with breast cancer and pre-natal development. In: Journal of Medical Genetics. 2000.
    • Arthur HM, Wilson DI, Torsney E, Renforth G, Diamond AG, Burn J. . In: ASHG Annual Meeting. 1999, San Francisco, California: Cell Press.
    • Almelda M, Fidalgo P, Wijnen J, Fodde R, Burn J, Curtis A, West SP. Mutation detection strategy in hereditary nonpolyposis colon cancer families. In: Journal of Medical Genetics. 1999, BMJ Group.
    • Almeida M, Coaker J, Gunn A, Bradburn M, Curtis A, Burn J, Mathers JC, West SP. Hereditary nonpolyposis colorectal cancer (HNPCC) amongst patients with apparently sporadic colorectal cancer. In: Journal of Medical Genetics. 1999, BMJ Group.
    • Casey B, Gebbia M, Ferrero GB, Pilia G, Yamada M, Aylsworth AS, Penman-Splitt M, Bird LM, Bamforth JS, Burn J, Schlessinger D, Nelson DL. Sites inversus, heart defects, and other manifestations of X-linked heterotaxy caused by mutations in the zinc-finger transcription factor ZIC3. In: AMERICAN JOURNAL OF HUMAN GENETICS. 1997.
    • Burn J, Gibbons D. . In: Heredity. 1978.

  • Digital or Visual Media

    • Burn J. . Ground Floor, 46 – 52 Pentonville Road, London N1 9HF: Hey Buddy TV, 2011.

  • Editorials

    • Lawler M, Siu LL, Rehm HL, Chanock SJ, Alterovitz G, Burn J, Calvo F, Lacombe D, Teh BT, North KN, Sawyers CL, Global Alliance Genomics Hlth GA4G. . Cancer Discovery 2015, 5(11), 1133-1136.
    • Burn J. . Surgical Oncology Clinics of North America 2015, 24(4), 635-637.
    • Burn J. . BMJ 2013, 346, f3132.
    • Kohonen-Corish MRJ, Macrae F, Genuardi M, Aretz S, Bapat B, Bernstein IT, Burn J, Cotton RGH, den Dunnen JT, Frebourg T, Greenblatt MS, Hofstra R, Holinski-Feder E, Lappalainen I, Lindblom A, Maglott D, Moller P, Morreau H, Moslein G, Sijmons R, Spurdle AB, Tavtigian S, Tops CMJ, Weber TK, de Wind N, Woods MO, Contributors InSiGHT-HVP Workshop. . Human Mutation 2011, 32(4), 491-494.
    • Kohonen-Corish MRJ, Al-Aama JY, Auerbach AD, Axton M, Barash CI, Bernstein I, Beroud C, Burn J, Cunningham F, Cutting GR, den Dunnen JT, Greenblatt MS, Kaput J, Katz M, Lindblom A, Macrae F, Maglott D, Moslein G, Povey S, Ramesar R, Richards S, Seminara D, Sobrido MJ, Tavtigian S, Taylor G, Vihinen M, Winship I, Cotton RGH, Contributors Human Variome Project. . Human Mutation 2010, 31(12), 1374-1381.
    • Burn J. . Journal of Medical Genetics 1999, 36(10), 737-738.

  • Letters

    • Gallon R, Phelps R, Betts L, Hayes C, Masic D, Irving JAE, McAnulty C, Saha V, Vora A, Wimmer K, Motwani J, Macartney C, Burn J, Jackson MS, Moorman AV, Santibanez-Koref M. . Leukemia and Lymphoma 2023, 64(1), 217-220.
    • Monahan KJ, Lincoln A, East JE, Benton S, Burn J, DeSouza B, Hanson H, Lalloo F, McVeigh T, Rutter MD, Snape K, Thomas HJW, Sasieni P. . Gut 2021, 70(3), 624-626.
    • Moller P, Sampson J, Dominguez-Valentin M, Burn J, Sunde L, Moslein G, Mecklin J-P, Seppala T. Recent advances in Lynch syndrome. Familial Cancer 2020, -.
    • Cook S, Wilson V, Ness J, Burn J, Husain A, Rajan N. . British Journal of Dermatology 2020, 183(5), 949-950.
    • Monahan KJ, Alsina D, Bach S, Buchanan J, Burn J, Clark S, Dawson P, DeSouza B, Din FV, Dolwani S, Dunlop MG, East J, Evans DG, Fearnhead N, Frayling IM, GlynneJones R, Hill J, Houlston R, Hull M, Lalloo F, Latchford A, Lishman S, Quirke P, Rees C, Rutter M, Sasieni P, Senapati A, Speake D, Thomas H, Tomlinson I. . BMJ 2017, 356, j1388.
    • Sheth H, Jackson MS, Koref MS, Parikh K, Sheth J, Sheth F, Tyson J, Daly AK, Burn J. . Blood 2015, 126(4).
    • Deciphering Developmental Disorders Study. . Nature 2015, 519(7542), 223-228.
    • Burn J, Mathers JC, Bishop DT. . Lancet 2012, 379(9826), 1587-1587.
    • Batey S, Vuillaume I, Devos D, Destee A, Curtis AJ, Lombes A, Curtis A, Burn J, Chinnery PF. . Journal of Medical Genetics 2010, 47(1), 71-72.
    • Bishop D, Burn J, Mathers J. . New England Journal of Medicine 2009, 360(14), 1462-1463.
    • Bishop DT, Burn J, Mathers JC. . New England Journal of Medicine 2009, 360(14), 1462-1463.
    • Devos D, Tchofo PJ, Vuillaume I, Destée A, Batey S, Burn J, Chinnery PF. . Brain 2009, 132(6), e109.
    • Relton CL, Pearce MS, Ness A, Burn J. . Nature Genetics 2005.
    • Goodship JA, Burn J. . Molecular Medicine Today 2000, 6(1), 14.
    • Healey CS, Dunning AM, Teare MD, Chase D, Parker L, Burn J, Chang-Claude J, Mannermaa A, Kataja V, Huntsman DG, Pharoah PDP, Luben RN, Easton DF, Ponder BAJ. . Nature Genetics 2000, 26(3), 362-364.
    • Liling J, Cross I, Burn J, Daniel CP, Tawn EJ, Parker L. . Journal of Medical Genetics 1999, 36(10), 794-795.
    • Chinnery PF, Cartlidge N, Burn DJ, Cleland PG, McKeith I. . Journal of Neurology, Neurosurgery and Psychiatry 1997, 62(5), 542-542.
    • Clarke AJ, Burn J. . Lancet 1987, 1(8533), 626-626.

  • Notes

    • Burn J. . European Journal of Human Genetics 2018, 25, S50.
    • Burn J. . Familial Cancer 2006, 5(3), 295-296.
    • Opitz JM, Burn J. . American Journal of Medical Genetics, Part A 2006, 140(21), 2385.
    • Finnell RH, Burn J. . Lancet 2000, 356(9241), 1537-1538.

  • Online Publications

    • Burn J. . The Conversation Trust (UK) Limited, 2015. Available at: .
    • Wang J, Carvajal-Carmona LG, Chu JH, Zauber AG, APC-Trial Collaborators, Kubo M, Matsuda K, Dunlop M, Houlston RS, Sieber O, Lipton L, Gibbs P, Martin NG, Montgomery GW, Young J, Baird PN, Ratain MJ, Nakamura Y, Weiss ST, Tomlinson I, Bertagnolli MM. Germline variants and advanced colorectal adenomas: adenoma prevention with celecoxib trial genome-wide association study. 2013. In Preparation.

  • Reviews

    • Moller P, Seppala TT, Ahadova A, Crosbie EJ, Holinski-Feder E, Scott R, Haupt S, Moslein G, Winship I, Broeke SWB-T, Kohut KE, Ryan N, Bauerfeind P, Thomas LE, Evans DG, Aretz S, Sijmons RH, Half E, Heinimann K, Horisberger K, Monahan K, Engel C, Cavestro GM, Fruscio R, Abu-Freha N, Zohar L, Laghi L, Bertario L, Bonanni B, Tibiletti MG, Lino-Silva LS, Vaccaro C, Valle AD, Rossi BM, da Silva LA, de Oliveira Nascimento IL, Rossi NT, Debniak T, Mecklin J-P, Bernstein I, Lindblom A, Sunde L, Nakken S, Heuveline V, Burn J, Hovig E, Kloor M, Sampson JR, Dominguez-Valentin M. . Hereditary Cancer in Clinical Practice 2023, 21(1), 19.
    • Ahadova A, Seppala TT, Engel C, Gallon R, Burn J, Holinski-Feder E, Steinke-Lange V, Moslein G, Nielsen M, ten Broeke SW, Laghi L, Dominguez-Valentin M, Capella G, Macrae F, Scott R, Huneburg R, Nattermann J, Hoffmeister M, Brenner H, Blaker H, von Knebel Doeberitz M, Sampson JR, Vasen H, Mecklin J-P, Moller P, Kloor M. . International Journal of Cancer 2021, 148(4), 800-811.
    • Seppala TT, Latchford A, Negoi I, Sampaio Soares A, Jimenez-Rodriguez R, Sanchez-Guillen L, Evans DG, Ryan N, Crosbie EJ, Dominguez-Valentin M, Burn J, Kloor M, von Knebel Doeberitz M, van Duijnhoven FJB, Quirke P, Sampson JR, Moller P, Moslein G. . British Journal of Surgery 2021, 108(5), 484-498.
    • Sheth H, McNally D, Santibanez-Koref M, Burn J. . PLoS ONE 2019, 14(6), e0218878.
    • Cuzick J, Thorat MA, Bosetti C, Brown PH, Burn J, Cook NR, Ford LG, Jacobs EJ, Jankowski JA, La Vecchia C, Law M, Meyskens F, Rothwell PM, Senn HJ, Umar A. . Annals of Oncology 2015, 26(1), 47-57.
    • Vasen HFA, Blanco I, Aktan-Collan K, Gopie JP, Alonso A, Aretz S, Bernstein I, Bertario L, Burn J, Capella G, Colas C, Engel C, Frayling IM, Genuardi M, Heinimann K, Hes FJ, Hodgson SV, Karagiannis JA, Lalloo F, Lindblom A, Mecklin JP, Moller P, Myrhoj T, Nagengast FM, Parc Y, de Leon MP, Renkonen-Sinisalo L, Sampson JR, Stormorken A, Sijmons RH, Tejpar S, Thomas HJW, Rahner N, Wijnen JT, Jarvinen HJ, Moslein G, the Mallorca Group. . Gut 2013, 62(6), 812-823.
    • Chan AT, Arber N, Burn J, Chia WK, Elwood P, Hull MA, Logan RF, Rothwell PM, Schror K, Baron JA. . Cancer Prevention Research 2012, 5(2), 164-178.
    • Beggs A, Latchford A, Vasen H, Moslein G, Alonso A, Aretz S, Bertario L, Blanco I, Bülow S, Burn J, Capella G, Colas C, Friedl W, Møller P, Hes F, Järvinen H, Mecklin J, Nagengast F, Parc Y, Phillips R, Hyer W, Ponz De Leon M, Renkonen-Sinisalo L, Sampson J, Stormorken A, Tejpar S, Thomas H, Wijnen J, Clark S, Hodgson S. . Gut 2010, 59(7), 975-986.
    • Kaput J, Cotton RGH, Hardman L, Watson M, Al Aqeel AI, Al-Aama JY, Al-Mulla F, Alonso S, Aretz S, Auerbach AD, Bapat B, Bernstein IT, Bhak J, Bleoo SL, Blocker H, Brenner SE, Burn J, Bustamante M, Calone R, Cambon-Thomsen A, Cargill M, Carrera P, Cavedon L, Cho YS, Chung YJ, Claustres M, Cutting G, Dalgleish R, den Dunnen JT, Diaz C, Dobrowolski S, dos Santos MRN, Ekong R, Flanagan SB, Flicek P, Furukawa Y, Genuardi M, Ghang H, Golubenko MV, Greenblatt MS, Hamosh A, Hancock JM, Hardison R, Harrison TM, Hoffmann R, Horaitis R, Howard HJ, Barash CI, Izagirre N, Jung J, Kojima T, Laradi S, Lee YS, Lee JY, Gil-da-Silva-Lopes VL, Macrae FA, Maglott D, Marafie MJ, Marsh SGE, Matsubara Y, Messiaen LM, Moslein G, Netea MG, Norton ML, Oefner PJ, Oetting WS, O'Leary JC, de Ramirez AMO, Paalman MH, Parboosingh J, Patrinos GP, Perozzi G, Phillips IR, Povey S, Prasad S, Qi M, Quin DJ, Ramesar RS, Richards CS, Savige J, Scheible DG, Scott RJ, Seminara D, Shephard EA, Sijmons RH, Smith TD, Sobrido MJ, Tanaka T, Tavtigian SV, Taylor GR, Teague J, Topel T, Ullman-Cullere M, Utsunomiya J, van Kranen HJ, Vihinen M, Webb E, Weber TK, Yeager M, Yeom YI, Yim SH, Yoo HS, Human Variome Project Planning. . Human Mutation 2009, 30(4), 496-510.
    • Cuzick J, Otto F, Baron JA, Brown PH, Burn J, Greenwald P, Jankowski J, La Vecchia C, Meyskens F, Senn HJ, Thun M. . Lancet Oncology 2009, 10(5), 501-507.
    • Vasen HFA, Moslein G, Alonso A, Aretz S, Bernstein I, Bertario L, Blanco I, Bulow S, Burn J, Capella G, Colas C, Engel C, Frayling I, Friedl W, Hes FJ, Hodgson S, Jarvinen H, Mecklin JP, Moller P, Myrhoi T, Nagengast FM, Parc Y, Phillips R, Clark SK, de Leon MP, Renkonen-Sinisalo L, Sampson JR, Stormorken A, Tejpar S, Thomas HJW, Wijnen J. Guidelines for the clinical management of familial adenomatous polyposis (FAP). GUT 2008, 57(5).
    • Vasen HFA, Moslein G, Alonso A, Bernstein I, Bertario L, Blanco I, Burn J, Capella G, Engel C, Frayling I, Friedl W, Hes FJ, Hodgson S, Mecklin J-P, Moller P, Nagengast F, Parc Y, Renkonen-Sinisalo L, Sampson JR, Stormorken A, Wijnen J. . Journal of Medical Genetics 2007, 44(6), 353-362.
    • Burn J, Chinnery PF. . Seminars in Pediatric Neurology 2006, 13(3), 176-181.
    • Mathers JC, Nutr D, Burn J. . Current Opinion in Oncology 1999, 11(5), 402-407.