Bonthron DT - Search Results

1

Extensive gene conversion at the PMS2 DNA mismatch repair locus.

Hayward BE, De Vos M, Valleley EM, Charlton RS, Taylor GR, Sheridan E, Bonthron DT. Hayward BE, et al. Among authors: bonthron dt. Hum Mutat. 2007 May;28(5):424-30. doi: 10.1002/humu.20457. Hum Mutat. 2007. PMID: 17253626

2

Novel PMS2 pseudogenes can conceal recessive mutations causing a distinctive childhood cancer syndrome.

De Vos M, Hayward BE, Picton S, Sheridan E, Bonthron DT. De Vos M, et al. Among authors: bonthron dt. Am J Hum Genet. 2004 May;74(5):954-64. doi: 10.1086/420796. Epub 2004 Apr 7. Am J Hum Genet. 2004. PMID: 15077197 Free PMC article.

3

PMS2 mutations in childhood cancer.

De Vos M, Hayward BE, Charlton R, Taylor GR, Glaser AW, Picton S, Cole TR, Maher ER, McKeown CM, Mann JR, Yates JR, Baralle D, Rankin J, Bonthron DT, Sheridan E. De Vos M, et al. Among authors: bonthron dt. J Natl Cancer Inst. 2006 Mar 1;98(5):358-61. doi: 10.1093/jnci/djj073. J Natl Cancer Inst. 2006. PMID: 16507833

4

Genetic and epigenetic analysis of recurrent hydatidiform mole.

Hayward BE, De Vos M, Talati N, Abdollahi MR, Taylor GR, Meyer E, Williams D, Maher ER, Setna F, Nazir K, Hussaini S, Jafri H, Rashid Y, Sheridan E, Bonthron DT. Hayward BE, et al. Among authors: bonthron dt. Hum Mutat. 2009 May;30(5):E629-39. doi: 10.1002/humu.20993. Hum Mutat. 2009. PMID: 19309689

5

Genetic diagnosis of familial breast cancer using clonal sequencing.

Morgan JE, Carr IM, Sheridan E, Chu CE, Hayward B, Camm N, Lindsay HA, Mattocks CJ, Markham AF, Bonthron DT, Taylor GR. Morgan JE, et al. Among authors: bonthron dt. Hum Mutat. 2010 Apr;31(4):484-91. doi: 10.1002/humu.21216. Hum Mutat. 2010. PMID: 20127978

6

Simple detection of germline microsatellite instability for diagnosis of constitutional mismatch repair cancer syndrome.

Ingham D, Diggle CP, Berry I, Bristow CA, Hayward BE, Rahman N, Markham AF, Sheridan EG, Bonthron DT, Carr IM. Ingham D, et al. Among authors: bonthron dt. Hum Mutat. 2013 Jun;34(6):847-52. doi: 10.1002/humu.22311. Epub 2013 Apr 2. Hum Mutat. 2013. PMID: 23483711

7

Phenotype associated with recessively inherited mutations in DNA mismatch repair (MMR) genes.

de Vos M, Hayward B, Bonthron DT, Sheridan E. de Vos M, et al. Among authors: bonthron dt. Biochem Soc Trans. 2005 Aug;33(Pt 4):718-20. doi: 10.1042/BST0330718. Biochem Soc Trans. 2005. PMID: 16042583 Review.

8

A global disorder of imprinting in the human female germ line.

Judson H, Hayward BE, Sheridan E, Bonthron DT. Judson H, et al. Among authors: bonthron dt. Nature. 2002 Apr 4;416(6880):539-42. doi: 10.1038/416539a. Nature. 2002. PMID: 11932746 Free article.

9

Interactive visual analysis of SNP data for rapid autozygosity mapping in consanguineous families.

Carr IM, Flintoff KJ, Taylor GR, Markham AF, Bonthron DT. Carr IM, et al. Among authors: bonthron dt. Hum Mutat. 2006 Oct;27(10):1041-6. doi: 10.1002/humu.20383. Hum Mutat. 2006. PMID: 16941472

10

Tissue-specific imprinting of the ZAC/PLAGL1 tumour suppressor gene results from variable utilization of monoallelic and biallelic promoters.

Valleley EM, Cordery SF, Bonthron DT. Valleley EM, et al. Among authors: bonthron dt. Hum Mol Genet. 2007 Apr 15;16(8):972-81. doi: 10.1093/hmg/ddm041. Epub 2007 Mar 6. Hum Mol Genet. 2007. PMID: 17341487

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