Thompson ER - Search Results

1

CONTRA: copy number analysis for targeted resequencing.

Li J, Lupat R, Amarasinghe KC, Thompson ER, Doyle MA, Ryland GL, Tothill RW, Halgamuge SK, Campbell IG, Gorringe KL. Li J, et al. Among authors: thompson er. Bioinformatics. 2012 May 15;28(10):1307-13. doi: 10.1093/bioinformatics/bts146. Epub 2012 Apr 2. Bioinformatics. 2012. PMID: 22474122 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. 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. Hum Mutat. 2005 Oct;26(4):384-9. doi: 10.1002/humu.20220. Hum Mutat. 2005. PMID: 16116623

4

Genome-wide, high-resolution detection of copy number, loss of heterozygosity, and genotypes from formalin-fixed, paraffin-embedded tumor tissue using microarrays.

Jacobs S, Thompson ER, Nannya Y, Yamamoto G, Pillai R, Ogawa S, Bailey DK, Campbell IG. Jacobs S, et al. Among authors: thompson er. Cancer Res. 2007 Mar 15;67(6):2544-51. doi: 10.1158/0008-5472.CAN-06-3597. Cancer Res. 2007. PMID: 17363572

5

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: thompson er. Clin Cancer Res. 2007 Aug 15;13(16):4731-9. doi: 10.1158/1078-0432.CCR-07-0502. Clin Cancer Res. 2007. PMID: 17699850

6

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: thompson er. 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.

7

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. Hum Mutat. 2012 Jan;33(1):95-9. doi: 10.1002/humu.21625. Epub 2011 Nov 4. Hum Mutat. 2012. PMID: 21990120 Free article.

8

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: thompson er. 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.

9

Analysis of KLLN as a high-penetrance breast cancer predisposition gene.

Thompson ER, Gorringe KL, Choong DY, Eccles DM; kConFab; Mitchell G, Campbell IG. Thompson ER, et al. Breast Cancer Res Treat. 2012 Jul;134(2):543-7. doi: 10.1007/s10549-012-2088-3. Epub 2012 May 13. Breast Cancer Res Treat. 2012. PMID: 22580995

10

Exome sequencing identifies rare deleterious mutations in DNA repair genes FANCC and BLM as potential breast cancer susceptibility alleles.

Thompson ER, Doyle MA, Ryland GL, Rowley SM, Choong DY, Tothill RW, Thorne H; kConFab; Barnes DR, Li J, Ellul J, Philip GK, Antill YC, James PA, Trainer AH, Mitchell G, Campbell IG. Thompson ER, et al. PLoS Genet. 2012 Sep;8(9):e1002894. doi: 10.1371/journal.pgen.1002894. Epub 2012 Sep 27. PLoS Genet. 2012. PMID: 23028338 Free PMC article.

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