Peters GB - Search Results

1

Tumor protein D52 (TPD52) is overexpressed and a gene amplification target in ovarian cancer.

Byrne JA, Balleine RL, Schoenberg Fejzo M, Mercieca J, Chiew YE, Livnat Y, St Heaps L, Peters GB, Byth K, Karlan BY, Slamon DJ, Harnett P, Defazio A. Byrne JA, et al. Among authors: peters gb. Int J Cancer. 2005 Dec 20;117(6):1049-54. doi: 10.1002/ijc.21250. Int J Cancer. 2005. PMID: 15986428

2

Three patients with terminal deletions within the subtelomeric region of chromosome 9q.

Neas KR, Smith JM, Chia N, Huseyin S, St Heaps L, Peters G, Sholler G, Tzioumi D, Sillence DO, Mowat D. Neas KR, et al. Am J Med Genet A. 2005 Feb 1;132A(4):425-30. doi: 10.1002/ajmg.a.30496. Am J Med Genet A. 2005. PMID: 15633179 Review.

3

Axenfeld-Rieger malformation and distinctive facial features: Clues to a recognizable 6p25 microdeletion syndrome.

Maclean K, Smith J, St Heaps L, Chia N, Williams R, Peters GB, Onikul E, McCrossin T, Lehmann OJ, Adès LC. Maclean K, et al. Among authors: peters gb. Am J Med Genet A. 2005 Feb 1;132A(4):381-5. doi: 10.1002/ajmg.a.30274. Am J Med Genet A. 2005. PMID: 15654696 Review.

4

Deletion at 14q22-23 indicates a contiguous gene syndrome comprising anophthalmia, pituitary hypoplasia, and ear anomalies.

Nolen LD, Amor D, Haywood A, St Heaps L, Willcock C, Mihelec M, Tam P, Billson F, Grigg J, Peters G, Jamieson RV. Nolen LD, et al. Am J Med Genet A. 2006 Aug 15;140(16):1711-8. doi: 10.1002/ajmg.a.31335. Am J Med Genet A. 2006. PMID: 16835935

5

Paternally inherited submicroscopic duplication at 11p15.5 implicates insulin-like growth factor II in overgrowth and Wilms' tumorigenesis.

Algar EM, St Heaps L, Darmanian A, Dagar V, Prawitt D, Peters GB, Collins F. Algar EM, et al. Among authors: peters gb. Cancer Res. 2007 Mar 1;67(5):2360-5. doi: 10.1158/0008-5472.CAN-06-3383. Epub 2007 Feb 26. Cancer Res. 2007. PMID: 17325026

6

Two mosaic terminal inverted duplications arising post-zygotically: Evidence for possible formation of neo-telomeres.

Daniel A, St Heaps L, Sylvester D, Diaz S, Peters G. Daniel A, et al. Cell Chromosome. 2008 Mar 10;7:1. doi: 10.1186/1475-9268-7-1. Cell Chromosome. 2008. PMID: 18331649 Free PMC article.

7

Chromosomal rearrangements and novel genes in disorders of eye development, cataract and glaucoma.

Mihelec M, St Heaps L, Flaherty M, Billson F, Rudduck C, Tam PP, Grigg JR, Peters GB, Jamieson RV. Mihelec M, et al. Among authors: peters gb. Twin Res Hum Genet. 2008 Aug;11(4):412-21. doi: 10.1375/twin.11.4.412. Twin Res Hum Genet. 2008. PMID: 18637741 Review.

8

Challenges in identifying candidate amplification targets in human cancers: chromosome 8q21 as a case study.

Byrne JA, Chen Y, Martin La Rotta N, Peters GB. Byrne JA, et al. Among authors: peters gb. Genes Cancer. 2012 Feb;3(2):87-101. doi: 10.1177/1947601912456287. Genes Cancer. 2012. PMID: 23050042 Free PMC article.

9

A balanced paternal interchromosomal reciprocal insertion between 5q12.1q13.2 and 20p12.3p12.1 resulting in separate genetic conditions in two siblings.

Wallis MJ, Kelly AL, Peters GB, St Heaps L, Nandini A, McGaughran JM. Wallis MJ, et al. Among authors: peters gb. Am J Med Genet A. 2016 Jul;170(7):1930-3. doi: 10.1002/ajmg.a.37689. Epub 2016 May 9. Am J Med Genet A. 2016. PMID: 27159256 No abstract available.

10

An innocuous duplication of 11.2 Mb at 13q21 is gene poor: sub-bands of gene paucity and pervasive CNV characterize the chromosome anomalies.

Daniel A, Darmanian A, Peters G, Goodwin L, Hort JR. Daniel A, et al. Am J Med Genet A. 2007 Oct 15;143A(20):2452-9. doi: 10.1002/ajmg.a.31960. Am J Med Genet A. 2007. PMID: 17853472

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