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1) Warburton,PE, Dolled,M, Mahmood,R, Alonso,A, Li,S, Naritomi,K, Tohma,T., Nagai,T., Hasegawa,T., Ohashi,H., Govearts,LCP, Eussen,HJFMM, van Hemel,JO, Lozzio,C, Schwartz,S, Dowhanick-Morrissette,JJ, Spinner,N, Rivera, H, Crolla,JA, Yu,C, Warburton,D. Molecular cytogenetic analysis of eight inversion duplications of human chromosome 13q that each contain a neocentromere. Am. J. Hum. Genet., 66: 1794-1806, 2000. View PDF 2) Floridia,G, Gimelli,G, Zuffardi,O, Earnshaw,WC, Warburton,PE, Tyler-Smith,C. A neocentromere in the DAZ region of the human Y chromosome Chromosoma, 109: 318-327, 2000. View PDF 3) Sugata, N, Li, S, Earnshaw, WC, Yen, TJ, Yoda, K, Masumoto, H, Munekata, E, Warburton, PE and Todokoro, K. Human CENP-H multimers colocalize with CENP-A and CENP-C at active centromere-kinetochore complexes Hum. Mol. Genet., 9: 2919-2926, 2000. View PDF 4) Levy, B, Papenhausen, PR, Tepperberg, JH, Dunn, TM, Fallet, S, Magid, MS, Kardon, NB, Hirschhorn, K, Warburton, PE. Prenatal molecular cytogenetic diagnosis of partial tetrasomy 10p due to neocentromere formation in an inversion duplication analphoid marker chromosome Cyto. Cell Genet. 91: 165-170, 2000. View PDF 5) Warburton, P.E. Epigenetic analysis of kinetochore assembly at variant human centromeres. Trends Genet 17: 243-247, 2001. View PDF 6) Li, S., Malafiej, P., Levy, B, Mahmood, R., Field, M., Hughes, T., Lockhart, L.H., Wu, Z., Huang, M., Hirschhorn, K., Velagaleti, G.V.N., Daniel, A., and Warburton, P.E. Chromosome 13q neocentromeres: molecular cytogenetic characterization of three additional cases and clinical features. Am J. Med. Genet., 110: 258-267, 2002. View PDF 7) Assumpcao, JG, Berkofsky-Fessler, W., Campos, N.V., Maciel-Guerra, T., Melaragno, M.I., deMello, M.P. and Warburton, P.E. Identification of a neocentromere in a rearranged Y chromosome with no detectable DYZ3 centromeric sequence. Am. J. Med. Genet., 113: 263-267, 2002. View PDF 8) Grimes, BR, Warburton, PE and Farr, C. Chromosome engineering: prospects for gene therapy. Gene Therapy, 9, 713-718, 2002. View PDF 9) Knegt, A.C., Li, S., Biljsma, E.K. and Warburton, P.E. Prenatal diagnosis of a karyotypically normal pregnancy in a mother with a supernumerary neocentric ring 13q21/22 chromosome and balancing 13q21/22 deletion. Prenatal Diagnosiss. 23:215-220, 2003. View PDF 10) Narayanan, K. and Warburton, P.E. DNA modification and functional delivery into human cells using E. coli DH10B. Nucleic Acids Research. 31:e51 , 2003. View PDF 11) Alonso, A., Mahmood, R., Li, S., Cheung, F., Yoda, K., and Warburton, P.E. Genomic microarray analysis reveals distinct locations for the CENP-A binding domains in three human chromosome 13q32 neocentromeres. Hum. Mol. Genet. 12(20):2711-21, 2003. View PDF 12) Warburton, P.E. Chromosomal dynamics of human neocentromere formation. Chromo. Res. 12: 617-626, 2004. View PDF 13) Warburton, P.E., Giordano, J., Cheung, F., Gelfand, Y. and Benson, G. Inverted Repeat structure of the human genome: The X chromosome contains a preponderance of large highly homologous inverted repeats which contain testes genes. Gen. Res. 14: 1861-1869, 2004. View PDF 14) Warburton, P.E. Centromeric heterochromatin comes clean with DNA methylation. Nature Methods 1: 14-16, 2004. View PDF 15) Cardone, MF, Alonso A, Pazienza, M, Ventura, M, Montemurro, G, Cardone, L, de Jong, PJ, Stanyon, R, D’Addabbo, P, Archidiacono, N, She, X, Eichler, EE, Warburton, PE, Rocchi, M. Independent centromere formation in a capricious 7.2 Mbp domain of chromosome 13 in humans, Old World monkeys, and pigs. Genome Biol. 7:R91 2006. View PDF 16) Yu, S., Barbouth, D. Benke, PJ, Warburton, PE, and Fan, YS Characterization of a neocentric supernumerary marker chromosome originating from the Xp distal region by FISH, CENP-C staining, and array CGH. Cyto. Gen. Res. 116: 141-145, 2007. View PDF 17) Giordano, J, Ge, Y, Gelfand, Y, Abrusán, G, Benson, G and Warburton, PE Evolutionary History of Mammalian Transposons Determined by Genome-wide Defragmentation. PLoS Comp. Biol. 3:e137, 2007. View PDF |