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903 results

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Page 1
MLH1 Differential allelic expression in mutation carriers and controls.
Santibanez Koref M, Wilson V, Cartwright N, Cunnington MS, Mathers JC, Bishop DT, Curtis A, Dunlop MG, Burn J. Santibanez Koref M, et al. Among authors: burn j. Ann Hum Genet. 2010 Nov;74(6):479-88. doi: 10.1111/j.1469-1809.2010.00603.x. Epub 2010 Sep 23. Ann Hum Genet. 2010. PMID: 20860725
Chemoprevention in Lynch syndrome.
Burn J, Mathers JC, Bishop DT. Burn J, et al. Fam Cancer. 2013 Dec;12(4):707-18. doi: 10.1007/s10689-013-9650-y. Fam Cancer. 2013. PMID: 23880960 Clinical Trial.
Point of care testing for improving risk- benefit ratio of aspirin and warfarin.
Sheth H, Northwood E, Elliott F, Jackson M, Koref MS, Tyson J, Daly A, O'Halloran J, Sheth J, Sheth F, Parikh K, Bishop DT, Burn J. Sheth H, et al. Among authors: burn j. Mol Cytogenet. 2014 Jan 21;7(Suppl 1 Proceedings of the International Conference on Human):I54. doi: 10.1186/1755-8166-7-S1-I54. eCollection 2014. Mol Cytogenet. 2014. PMID: 24949102 Free PMC article. No abstract available.
Three molecular pathways model colorectal carcinogenesis in Lynch syndrome.
Ahadova A, Gallon R, Gebert J, Ballhausen A, Endris V, Kirchner M, Stenzinger A, Burn J, von Knebel Doeberitz M, Bläker H, Kloor M. Ahadova A, et al. Among authors: burn j. Int J Cancer. 2018 Jul 1;143(1):139-150. doi: 10.1002/ijc.31300. Epub 2018 Feb 23. Int J Cancer. 2018. PMID: 29424427 Free article.
Interaction between polymorphisms in aspirin metabolic pathways, regular aspirin use and colorectal cancer risk: A case-control study in unselected white European populations.
Sheth H, Northwood E, Ulrich CM, Scherer D, Elliott F, Barrett JH, Forman D, Wolf CR, Smith G, Jackson MS, Santibanez-Koref M, Haile R, Casey G, Jenkins M, Win AK, Hopper JL, Marchand LL, Lindor NM, Thibodeau SN, Potter JD, Burn J, Bishop DT. Sheth H, et al. Among authors: burn j. PLoS One. 2018 Feb 9;13(2):e0192223. doi: 10.1371/journal.pone.0192223. eCollection 2018. PLoS One. 2018. PMID: 29425227 Free PMC article.
A novel panel of short mononucleotide repeats linked to informative polymorphisms enabling effective high volume low cost discrimination between mismatch repair deficient and proficient tumours.
Redford L, Alhilal G, Needham S, O'Brien O, Coaker J, Tyson J, Amorim LM, Middleton I, Izuogu O, Arends M, Oniscu A, Alonso ÁM, Laguna SM, Gallon R, Sheth H, Santibanez-Koref M, Jackson MS, Burn J. Redford L, et al. Among authors: burn j. PLoS One. 2018 Aug 29;13(8):e0203052. doi: 10.1371/journal.pone.0203052. eCollection 2018. PLoS One. 2018. PMID: 30157243 Free PMC article.
A sensitive and scalable microsatellite instability assay to diagnose constitutional mismatch repair deficiency by sequencing of peripheral blood leukocytes.
Gallon R, Mühlegger B, Wenzel SS, Sheth H, Hayes C, Aretz S, Dahan K, Foulkes W, Kratz CP, Ripperger T, Azizi AA, Baris Feldman H, Chong AL, Demirsoy U, Florkin B, Imschweiler T, Januszkiewicz-Lewandowska D, Lobitz S, Nathrath M, Pander HJ, Perez-Alonso V, Perne C, Ragab I, Rosenbaum T, Rueda D, Seidel MG, Suerink M, Taeubner J, Zimmermann SY, Zschocke J, Borthwick GM, Burn J, Jackson MS, Santibanez-Koref M, Wimmer K. Gallon R, et al. Among authors: burn j. Hum Mutat. 2019 May;40(5):649-655. doi: 10.1002/humu.23721. Epub 2019 Mar 6. Hum Mutat. 2019. PMID: 30740824 Free PMC article.
903 results