Campbell IG - Search Results

1

Bioinformatics pipelines for targeted resequencing and whole-exome sequencing of human and mouse genomes: a virtual appliance approach for instant deployment.

Li J, Doyle MA, Saeed I, Wong SQ, Mar V, Goode DL, Caramia F, Doig K, Ryland GL, Thompson ER, Hunter SM, Halgamuge SK, Ellul J, Dobrovic A, Campbell IG, Papenfuss AT, McArthur GA, Tothill RW. Li J, et al. Among authors: campbell ig. PLoS One. 2014 Apr 21;9(4):e95217. doi: 10.1371/journal.pone.0095217. eCollection 2014. PLoS One. 2014. PMID: 24752294 Free PMC article.

2

A novel duplication polymorphism in the FANCA promoter and its association with breast and ovarian cancer.

Thompson E, Dragovic RL, Stephenson SA, Eccles DM, Campbell IG, Dobrovic A. Thompson E, et al. Among authors: campbell ig. BMC Cancer. 2005 Apr 29;5:43. doi: 10.1186/1471-2407-5-43. BMC Cancer. 2005. PMID: 15860134 Free PMC article.

3

Whole genome SNP arrays using DNA derived from formalin-fixed, paraffin-embedded ovarian tumor tissue.

Thompson ER, Herbert SC, Forrest SM, Campbell IG. Thompson ER, et al. Among authors: campbell ig. Hum Mutat. 2005 Oct;26(4):384-9. doi: 10.1002/humu.20220. Hum Mutat. 2005. PMID: 16116623

4

High-resolution single nucleotide polymorphism array analysis of epithelial ovarian cancer reveals numerous microdeletions and amplifications.

Gorringe KL, Jacobs S, Thompson ER, Sridhar A, Qiu W, Choong DY, Campbell IG. Gorringe KL, et al. Among authors: campbell ig. Clin Cancer Res. 2007 Aug 15;13(16):4731-9. doi: 10.1158/1078-0432.CCR-07-0502. Clin Cancer Res. 2007. PMID: 17699850

5

No evidence of clonal somatic genetic alterations in cancer-associated fibroblasts from human breast and ovarian carcinomas.

Qiu W, Hu M, Sridhar A, Opeskin K, Fox S, Shipitsin M, Trivett M, Thompson ER, Ramakrishna M, Gorringe KL, Polyak K, Haviv I, Campbell IG. Qiu W, et al. Among authors: campbell ig. Nat Genet. 2008 May;40(5):650-5. doi: 10.1038/ng.117. Epub 2008 Apr 13. Nat Genet. 2008. PMID: 18408720 Free PMC article.

6

Are there any more ovarian tumor suppressor genes? A new perspective using ultra high-resolution copy number and loss of heterozygosity analysis.

Gorringe KL, Ramakrishna M, Williams LH, Sridhar A, Boyle SE, Bearfoot JL, Li J, Anglesio MS, Campbell IG. Gorringe KL, et al. Among authors: campbell ig. Genes Chromosomes Cancer. 2009 Oct;48(10):931-42. doi: 10.1002/gcc.20694. Genes Chromosomes Cancer. 2009. PMID: 19603523

7

Analysis of the mitogen-activated protein kinase kinase 4 (MAP2K4) tumor suppressor gene in ovarian cancer.

Davis SJ, Choong DY, Ramakrishna M, Ryland GL, Campbell IG, Gorringe KL. Davis SJ, et al. Among authors: campbell ig. BMC Cancer. 2011 May 17;11:173. doi: 10.1186/1471-2407-11-173. BMC Cancer. 2011. PMID: 21575258 Free PMC article.

8

Copy number aberrations in benign serous ovarian tumors: a case for reclassification?

Hunter SM, Anglesio MS, Sharma R, Gilks CB, Melnyk N, Chiew YE, deFazio A; Australian Ovarian Cancer Study Group; Longacre TA, Huntsman DG, Gorringe KL, Campbell IG. Hunter SM, et al. Among authors: campbell ig. Clin Cancer Res. 2011 Dec 1;17(23):7273-82. doi: 10.1158/1078-0432.CCR-11-2080. Epub 2011 Oct 5. Clin Cancer Res. 2011. PMID: 21976534

9

Analysis of RAD51C germline mutations in high-risk breast and ovarian cancer families and ovarian cancer patients.

Thompson ER, Boyle SE, Johnson J, Ryland GL, Sawyer S, Choong DY, kConFab, Chenevix-Trench G, Trainer AH, Lindeman GJ, Mitchell G, James PA, Campbell IG. Thompson ER, et al. Among authors: campbell ig. Hum Mutat. 2012 Jan;33(1):95-9. doi: 10.1002/humu.21625. Epub 2011 Nov 4. Hum Mutat. 2012. PMID: 21990120 Free article.

10

Identification of copy number alterations associated with the progression of DCIS to invasive ductal carcinoma.

Johnson CE, Gorringe KL, Thompson ER, Opeskin K, Boyle SE, Wang Y, Hill P, Mann GB, Campbell IG. Johnson CE, et al. Among authors: campbell ig. Breast Cancer Res Treat. 2012 Jun;133(3):889-98. doi: 10.1007/s10549-011-1835-1. Epub 2011 Nov 4. Breast Cancer Res Treat. 2012. PMID: 22052326 Free article.

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