Tomlinson I - Search Results

1

Deciphering the genetics of hereditary non-syndromic colorectal cancer.

Papaemmanuil E, Carvajal-Carmona L, Sellick GS, Kemp Z, Webb E, Spain S, Sullivan K, Barclay E, Lubbe S, Jaeger E, Vijayakrishnan J, Broderick P, Gorman M, Martin L, Lucassen A, Bishop DT, Evans DG, Maher ER, Steinke V, Rahner N, Schackert HK, Goecke TO, Holinski-Feder E, Propping P, Van Wezel T, Wijnen J, Cazier JB, Thomas H, Houlston RS, Tomlinson I; CORGI Consortium. Papaemmanuil E, et al. Among authors: tomlinson i. Eur J Hum Genet. 2008 Dec;16(12):1477-86. doi: 10.1038/ejhg.2008.129. Epub 2008 Jul 16. Eur J Hum Genet. 2008. PMID: 18628789

2

Polyclonal origin of colonic adenomas in an XO/XY patient with FAP.

Novelli MR, Williamson JA, Tomlinson IP, Elia G, Hodgson SV, Talbot IC, Bodmer WF, Wright NA. Novelli MR, et al. Among authors: tomlinson ip. Science. 1996 May 24;272(5265):1187-90. doi: 10.1126/science.272.5265.1187. Science. 1996. PMID: 8638166

3

Genetic mapping of hereditary mixed polyposis syndrome to chromosome 6q.

Thomas HJ, Whitelaw SC, Cottrell SE, Murday VA, Tomlinson IP, Markie D, Jones T, Bishop DT, Hodgson SV, Sheer D, Northover JM, Talbot IC, Solomon E, Bodmer WF. Thomas HJ, et al. Among authors: tomlinson ip. Am J Hum Genet. 1996 Apr;58(4):770-6. Am J Hum Genet. 1996. PMID: 8644741 Free PMC article.

4

A pericentric inversion of chromosome six in a patient with Peutz-Jeghers' syndrome and the use of FISH to localise the breakpoints on a genetic map.

Markie D, Huson S, Maher E, Davies A, Tomlinson I, Bodmer WF. Markie D, et al. Among authors: tomlinson i. Hum Genet. 1996 Aug;98(2):125-8. doi: 10.1007/s004390050173. Hum Genet. 1996. PMID: 8698325

5

A modifying locus for familial adenomatous polyposis may be present on chromosome 1p35-p36.

Tomlinson IP, Neale K, Talbot IC, Spigelman AD, Williams CB, Phillips RK, Bodmer WF. Tomlinson IP, et al. J Med Genet. 1996 Apr;33(4):268-73. doi: 10.1136/jmg.33.4.268. J Med Genet. 1996. PMID: 8730279 Free PMC article.

6

Variants at the secretory phospholipase A2 (PLA2G2A) locus: analysis of associations with familial adenomatous polyposis and sporadic colorectal tumours.

Tomlinson IP, Beck NE, Neale K, Bodmer WF. Tomlinson IP, et al. Ann Hum Genet. 1996 Sep;60(5):369-76. doi: 10.1111/j.1469-1809.1996.tb00434.x. Ann Hum Genet. 1996. PMID: 8912789

7

Testing candidate loci on chromosomes 1 and 6 for genetic linkage to Peutz-Jeghers' disease.

Tomlinson IP, Olschwang S, Abelovitch D, Nakamura Y, Bodmer WF, Thomas G, Markie D. Tomlinson IP, et al. Ann Hum Genet. 1996 Sep;60(5):377-84. doi: 10.1111/j.1469-1809.1996.tb00435.x. Ann Hum Genet. 1996. PMID: 8912790

8

Clinical and molecular features of the hereditary mixed polyposis syndrome.

Whitelaw SC, Murday VA, Tomlinson IP, Thomas HJ, Cottrell S, Ginsberg A, Bukofzer S, Hodgson SV, Skudowitz RB, Jass JR, Talbot IC, Northover JM, Bodmer WF, Solomon E. Whitelaw SC, et al. Among authors: tomlinson ip. Gastroenterology. 1997 Feb;112(2):327-34. doi: 10.1053/gast.1997.v112.pm9024286. Gastroenterology. 1997. PMID: 9024286

9

Germline HNPCC gene variants have little influence on the risk for sporadic colorectal cancer.

Tomlinson IP, Beck NE, Homfray T, Harocopos CJ, Bodmer WF. Tomlinson IP, et al. J Med Genet. 1997 Jan;34(1):39-42. doi: 10.1136/jmg.34.1.39. J Med Genet. 1997. PMID: 9032648 Free PMC article.

10

Use of SSCP analysis to identify germline mutations in HNPCC families fulfilling the Amsterdam criteria.

Beck NE, Tomlinson IP, Homfray T, Frayling I, Hodgson SV, Harocopos C, Bodmer WF. Beck NE, et al. Among authors: tomlinson ip. Hum Genet. 1997 Feb;99(2):219-24. doi: 10.1007/s004390050343. Hum Genet. 1997. PMID: 9048925

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