Burgess T - Search Results

1

Methylation of novel markers of fragile X alleles is inversely correlated with FMRP expression and FMR1 activation ratio.

Godler DE, Tassone F, Loesch DZ, Taylor AK, Gehling F, Hagerman RJ, Burgess T, Ganesamoorthy D, Hennerich D, Gordon L, Evans A, Choo KH, Slater HR. Godler DE, et al. Among authors: burgess t. Hum Mol Genet. 2010 Apr 15;19(8):1618-32. doi: 10.1093/hmg/ddq037. Epub 2010 Jan 29. Hum Mol Genet. 2010. PMID: 20118148 Free PMC article.

2

Prenatal diagnosis of Prader-Willi syndrome using PW71 methylation analysis--uniparental disomy and the significance of residual trisomy 15.

Slater HR, Vaux C, Pertile M, Burgess T, Petrovic V. Slater HR, et al. Among authors: burgess t. Prenat Diagn. 1997 Feb;17(2):109-13. Prenat Diagn. 1997. PMID: 9061757

3

Identification of small FRAXA premutations.

Francis D, Burgess T, Mitchell J, Slater H. Francis D, et al. Among authors: burgess t. Mol Diagn. 2000 Sep;5(3):221-5. doi: 10.1054/modi.2000.9809. Mol Diagn. 2000. PMID: 11070156

4

Improved testing for CMT1A and HNPP using multiplex ligation-dependent probe amplification (MLPA) with rapid DNA preparations: comparison with the interphase FISH method.

Slater H, Bruno D, Ren H, La P, Burgess T, Hills L, Nouri S, Schouten J, Choo KH. Slater H, et al. Among authors: burgess t. Hum Mutat. 2004 Aug;24(2):164-71. doi: 10.1002/humu.20072. Hum Mutat. 2004. PMID: 15241798

5

FMR1 alleles in Tasmania: a screening study of the special educational needs population.

Mitchell RJ, Holden JJ, Zhang C, Curlis Y, Slater HR, Burgess T, Kirkby KC, Carmichael A, Heading KD, Loesch DZ. Mitchell RJ, et al. Among authors: burgess t. Clin Genet. 2005 Jan;67(1):38-46. doi: 10.1111/j.1399-0004.2004.00344.x. Clin Genet. 2005. PMID: 15617547

6

High-throughput analysis of chromosome abnormality in spontaneous miscarriage using an MLPA subtelomere assay with an ancillary FISH test for polyploidy.

Bruno DL, Burgess T, Ren H, Nouri S, Pertile MD, Francis DI, Norris F, Kenney BK, Schouten J, Andy Choo KH, Slater HR. Bruno DL, et al. Among authors: burgess t. Am J Med Genet A. 2006 Dec 15;140(24):2786-93. doi: 10.1002/ajmg.a.31552. Am J Med Genet A. 2006. PMID: 17106871

7

An improved Diagnostic PCR Assay for identification of Cryptic Heterozygosity for CGG Triplet Repeat Alleles in the Fragile X Gene (FMR1).

Khaniani MS, Kalitsis P, Burgess T, Slater HR. Khaniani MS, et al. Among authors: burgess t. Mol Cytogenet. 2008 Apr 8;1:5. doi: 10.1186/1755-8166-1-5. Mol Cytogenet. 2008. PMID: 18471319 Free PMC article.

8

A model for offering carrier screening for fragile X syndrome to nonpregnant women: results from a pilot study.

Metcalfe S, Jacques A, Archibald A, Burgess T, Collins V, Henry A, McNamee K, Sheffield L, Slater H, Wake S, Cohen J. Metcalfe S, et al. Among authors: burgess t. Genet Med. 2008 Jul;10(7):525-35. doi: 10.1097/gim.0b013e31817c036e. Genet Med. 2008. PMID: 18580686

9

Improved methodology for assessment of mRNA levels in blood of patients with FMR1 related disorders.

Godler DE, Loesch DZ, Huggins R, Gordon L, Slater HR, Gehling F, Burgess T, Choo KH. Godler DE, et al. Among authors: burgess t. BMC Clin Pathol. 2009 Jun 9;9:5. doi: 10.1186/1472-6890-9-5. BMC Clin Pathol. 2009. PMID: 19505339 Free PMC article.

10

Linking the FMR1 alleles with small CGG expansions with neurodevelopmental disorders: preliminary data suggest an involvement of epigenetic mechanisms.

Loesch DZ, Godler DE, Khaniani M, Gould E, Gehling F, Dissanayake C, Burgess T, Tassone F, Huggins R, Slater H, Choo KH. Loesch DZ, et al. Among authors: burgess t. Am J Med Genet A. 2009 Oct;149A(10):2306-10. doi: 10.1002/ajmg.a.32990. Am J Med Genet A. 2009. PMID: 19760650 Free PMC article. No abstract available.

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