Warburton PE - Search Results

1

Formation of novel CENP-A domains on tandem repetitive DNA and across chromosome breakpoints on human chromosome 8q21 neocentromeres.

Hasson D, Alonso A, Cheung F, Tepperberg JH, Papenhausen PR, Engelen JJ, Warburton PE. Hasson D, et al. Among authors: warburton pe. Chromosoma. 2011 Dec;120(6):621-32. doi: 10.1007/s00412-011-0337-6. Epub 2011 Aug 9. Chromosoma. 2011. PMID: 21826412

2

Genomic microarray analysis reveals distinct locations for the CENP-A binding domains in three human chromosome 13q32 neocentromeres.

Alonso A, Mahmood R, Li S, Cheung F, Yoda K, Warburton PE. Alonso A, et al. Among authors: warburton pe. Hum Mol Genet. 2003 Oct 15;12(20):2711-21. doi: 10.1093/hmg/ddg282. Epub 2003 Aug 19. Hum Mol Genet. 2003. PMID: 12928482

3

Co-localization of CENP-C and CENP-H to discontinuous domains of CENP-A chromatin at human neocentromeres.

Alonso A, Fritz B, Hasson D, Abrusan G, Cheung F, Yoda K, Radlwimmer B, Ladurner AG, Warburton PE. Alonso A, et al. Among authors: warburton pe. Genome Biol. 2007;8(7):R148. doi: 10.1186/gb-2007-8-7-r148. Genome Biol. 2007. PMID: 17651496 Free PMC article.

4

A paucity of heterochromatin at functional human neocentromeres.

Alonso A, Hasson D, Cheung F, Warburton PE. Alonso A, et al. Among authors: warburton pe. Epigenetics Chromatin. 2010 Mar 8;3(1):6. doi: 10.1186/1756-8935-3-6. Epigenetics Chromatin. 2010. PMID: 20210998 Free PMC article.

5

The octamer is the major form of CENP-A nucleosomes at human centromeres.

Hasson D, Panchenko T, Salimian KJ, Salman MU, Sekulic N, Alonso A, Warburton PE, Black BE. Hasson D, et al. Among authors: warburton pe. Nat Struct Mol Biol. 2013 Jun;20(6):687-95. doi: 10.1038/nsmb.2562. Epub 2013 May 5. Nat Struct Mol Biol. 2013. PMID: 23644596 Free PMC article.

6

Tetrasomy 15q26: a distinct syndrome or Shprintzen-Goldberg syndrome phenocopy?

Levy B, Tegay D, Papenhausen P, Tepperberg J, Nahum O, Tsuchida T, Pletcher BA, Ala-Kokko L, Baker S, Frederick B, Hirschhorn K, Warburton P, Shanske A. Levy B, et al. Genet Med. 2012 Sep;14(9):811-8. doi: 10.1038/gim.2012.54. Epub 2012 May 31. Genet Med. 2012. PMID: 22653535 Free article.

7

Analysis of the largest tandemly repeated DNA families in the human genome.

Warburton PE, Hasson D, Guillem F, Lescale C, Jin X, Abrusan G. Warburton PE, et al. BMC Genomics. 2008 Nov 7;9:533. doi: 10.1186/1471-2164-9-533. BMC Genomics. 2008. PMID: 18992157 Free PMC article.

8

Prenatal molecular cytogenetic diagnosis of partial tetrasomy 10p due to neocentromere formation in an inversion duplication analphoid marker chromosome.

Levy B, Papenhausen P, Tepperberg J, Dunn T, Fallet S, Magid M, Kardon N, Hirschhorn K, Warburton P. Levy B, et al. Cytogenet Cell Genet. 2000;91(1-4):165-70. doi: 10.1159/000056839. Cytogenet Cell Genet. 2000. PMID: 11173851

9

Inverted repeat structure of the human genome: the X-chromosome contains a preponderance of large, highly homologous inverted repeats that contain testes genes.

Warburton PE, Giordano J, Cheung F, Gelfand Y, Benson G. Warburton PE, et al. Genome Res. 2004 Oct;14(10A):1861-9. doi: 10.1101/gr.2542904. Genome Res. 2004. PMID: 15466286 Free PMC article.

10

Prenatal diagnosis of a karyotypically normal pregnancy in a mother with a supernumerary neocentric 13q21 -->13q22 chromosome and balancing reciprocal deletion.

Knegt AC, Li S, Engelen JJ, Bijlsma EK, Warburton PE. Knegt AC, et al. Among authors: warburton pe. Prenat Diagn. 2003 Mar;23(3):215-20. doi: 10.1002/pd.559. Prenat Diagn. 2003. PMID: 12627422

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