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Vol. 10, Issue 5, 597-610, May 2000
REVIEW
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S. Kirsch, C. Munch, Z. Jiang, Z. Cheng, L. Chen, C. Batz, E. E. Eichler, and W. Schempp Evolutionary dynamics of segmental duplications from human Y-chromosomal euchromatin/heterochromatin transition regions Genome Res., July 1, 2008; 18(7): 1030 - 1042. [Abstract] [Full Text] [PDF] |
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J. Davidsson, A. Andersson, K. Paulsson, M. Heidenblad, M. Isaksson, A. Borg, J. Heldrup, M. Behrendtz, I. Panagopoulos, T. Fioretos, et al. Tiling resolution array comparative genomic hybridization, expression and methylation analyses of dup(1q) in Burkitt lymphomas and pediatric high hyperdiploid acute lymphoblastic leukemias reveal clustered near-centromeric breakpoints and overexpression of genes in 1q22-32.3 Hum. Mol. Genet., September 15, 2007; 16(18): 2215 - 2225. [Abstract] [Full Text] [PDF] |
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J. L. Freeman, G. H. Perry, L. Feuk, R. Redon, S. A. McCarroll, D. M. Altshuler, H. Aburatani, K. W. Jones, C. Tyler-Smith, M. E. Hurles, et al. Copy number variation: New insights in genome diversity Genome Res., August 1, 2006; 16(8): 949 - 961. [Abstract] [Full Text] [PDF] |
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V. Goidts, J. M. Szamalek, P. J. de Jong, D. N. Cooper, N. Chuzhanova, H. Hameister, and H. Kehrer-Sawatzki Independent intrachromosomal recombination events underlie the pericentric inversions of chimpanzee and gorilla chromosomes homologous to human chromosome 16 Genome Res., September 1, 2005; 15(9): 1232 - 1242. [Abstract] [Full Text] [PDF] |
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J C K Barber Directly transmitted unbalanced chromosome abnormalities and euchromatic variants J. Med. Genet., August 1, 2005; 42(8): 609 - 629. [Abstract] [Full Text] [PDF] |
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S. Caburet, C. Conti, C. Schurra, R. Lebofsky, S. J. Edelstein, and A. Bensimon Human ribosomal RNA gene arrays display a broad range of palindromic structures Genome Res., August 1, 2005; 15(8): 1079 - 1085. [Abstract] [Full Text] [PDF] |
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J. E. Horvath, C. L. Gulden, R. U. Vallente, M. Y. Eichler, M. Ventura, J. D. McPherson, T. A. Graves, R. K. Wilson, S. Schwartz, M. Rocchi, et al. Punctuated duplication seeding events during the evolution of human chromosome 2p11 Genome Res., July 1, 2005; 15(7): 914 - 927. [Abstract] [Full Text] [PDF] |
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A. M. Snijders, N. J. Nowak, B. Huey, J. Fridlyand, S. Law, J. Conroy, T. Tokuyasu, K. Demir, R. Chiu, J.-H. Mao, et al. Mapping segmental and sequence variations among laboratory mice using BAC array CGH Genome Res., February 1, 2005; 15(2): 302 - 311. [Abstract] [Full Text] [PDF] |
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S. Kirsch, B. Weiss, T. L. Miner, R. H. Waterston, R. A. Clark, E. E. Eichler, C. Munch, W. Schempp, and G. Rappold Interchromosomal segmental duplications of the pericentromeric region on the human Y chromosome Genome Res., February 1, 2005; 15(2): 195 - 204. [Abstract] [Full Text] [PDF] |
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C. T. Storlazzi, T. Fioretos, K. Paulsson, B. Strombeck, C. Lassen, T. Ahlgren, G. Juliusson, F. Mitelman, M. Rocchi, and B. Johansson Identification of a commonly amplified 4.3 Mb region with overexpression of C8FW, but not MYC in MYC-containing double minutes in myeloid malignancies Hum. Mol. Genet., July 15, 2004; 13(14): 1479 - 1485. [Abstract] [Full Text] [PDF] |
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M A Aldred, R O C Sanford, N S Thomas, M A Barrow, L C Wilson, L A Brueton, M C Bonaglia, R C M Hennekam, C Eng, N R Dennis, et al. Molecular analysis of 20 patients with 2q37.3 monosomy: definition of minimum deletion intervals for key phenotypes J. Med. Genet., June 1, 2004; 41(6): 433 - 439. [Full Text] [PDF] |
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J. A. Bailey, D. M. Church, M. Ventura, M. Rocchi, and E. E. Eichler Analysis of Segmental Duplications and Genome Assembly in the Mouse Genome Res., May 1, 2004; 14(5): 789 - 801. [Abstract] [Full Text] [PDF] |
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D P Locke, R Segraves, R D Nicholls, S Schwartz, D Pinkel, D G Albertson, and E E Eichler BAC microarray analysis of 15q11-q13 rearrangements and the impact of segmental duplications J. Med. Genet., March 1, 2004; 41(3): 175 - 182. [Abstract] [Full Text] [PDF] |
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J. Jurka, O. Kohany, A. Pavlicek, V. V. Kapitonov, and M. V. Jurka Duplication, coclustering, and selection of human Alu retrotransposons PNAS, February 3, 2004; 101(5): 1268 - 1272. [Abstract] [Full Text] [PDF] |
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D. G. Albertson and D. Pinkel Genomic microarrays in human genetic disease and cancer Hum. Mol. Genet., October 15, 2003; 12(90002): R145 - 152. [Abstract] [Full Text] [PDF] |
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X. J. de Mollerat, F. Gurrieri, C. T. Morgan, E. Sangiorgi, D. B. Everman, P. Gaspari, J. Amiel, M. J. Bamshad, R. Lyle, J.-L. Blouin, et al. A genomic rearrangement resulting in a tandem duplication is associated with split hand-split foot malformation 3 (SHFM3) at 10q24 Hum. Mol. Genet., August 15, 2003; 12(16): 1959 - 1971. [Abstract] [Full Text] [PDF] |
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E. Spiteri, M. Babcock, C. D. Kashork, K. Wakui, S. Gogineni, D. A. Lewis, K. M. Williams, S. Minoshima, T. Sasaki, N. Shimizu, et al. Frequent translocations occur between low copy repeats on chromosome 22q11.2 (LCR22s) and telomeric bands of partner chromosomes Hum. Mol. Genet., August 1, 2003; 12(15): 1823 - 1837. [Abstract] [Full Text] [PDF] |
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T. Newman and B. J. Trask Complex Evolution of 7E Olfactory Receptor Genes in Segmental Duplications Genome Res., May 1, 2003; 13(5): 781 - 793. [Abstract] [Full Text] [PDF] |
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D. P. Locke, R. Segraves, L. Carbone, N. Archidiacono, D. G. Albertson, D. Pinkel, and E. E. Eichler Large-Scale Variation Among Human and Great Ape Genomes Determined by Array Comparative Genomic Hybridization Genome Res., March 1, 2003; 13(3): 347 - 357. [Abstract] [Full Text] [PDF] |
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A. Courseaux, F. Richard, J. Grosgeorge, C. Ortola, A. Viale, C. Turc-Carel, B. Dutrillaux, P. Gaudray, and J.-L. Nahon Segmental Duplications in Euchromatic Regions of Human Chromosome 5: A Source of Evolutionary Instability and Transcriptional Innovation Genome Res., March 1, 2003; 13(3): 369 - 381. [Abstract] [Full Text] [PDF] |
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D. A. COLLIER FISH, flexible joints and panic: are anxiety disorders really expressions of instability in the human genome? The British Journal of Psychiatry, December 1, 2002; 181(6): 457 - 459. [Full Text] [PDF] |
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Y. Fan, T. Newman, E. Linardopoulou, and B. J. Trask Gene Content and Function of the Ancestral Chromosome Fusion Site in Human Chromosome 2q13-2q14.1 and Paralogous Regions Genome Res., November 1, 2002; 12(11): 1663 - 1672. [Abstract] [Full Text] [PDF] |
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G. Saglio, C. T. Storlazzi, E. Giugliano, C. Surace, L. Anelli, G. Rege-Cambrin, A. Zagaria, A. J. Velasco, A. Heiniger, P. Scaravaglio, et al. A 76-kb duplicon maps close to the BCR gene on chromosome 22 and the ABL gene on chromosome 9: Possible involvement in the genesis of the Philadelphia chromosome translocation PNAS, July 23, 2002; 99(15): 9882 - 9887. [Abstract] [Full Text] [PDF] |
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L. B.K. Herzing, E. H. Cook Jr, and D. H. Ledbetter Allele-specific expression analysis by RNA-FISH demonstrates preferential maternal expression of UBE3A and imprint maintenance within 15q11- q13 duplications Hum. Mol. Genet., July 15, 2002; 11(15): 1707 - 1718. [Abstract] [Full Text] [PDF] |
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S.-S. Park, P. Stankiewicz, W. Bi, C. Shaw, J. Lehoczky, K. Dewar, B. Birren, and J. R. Lupski Structure and Evolution of the Smith-Magenis Syndrome Repeat Gene Clusters, SMS-REPs Genome Res., May 1, 2002; 12(5): 729 - 738. [Abstract] [Full Text] [PDF] |
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M. L. Farman Meiotic Deletion at the BUF1 Locus of the Fungus Magnaporthe grisea Is Controlled by Interaction With the Homologous Chromosome Genetics, January 1, 2002; 160(1): 137 - 148. [Abstract] [Full Text] [PDF] |
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R. D. Bagnall, N. Waseem, P. M. Green, and F. Giannelli Recurrent inversion breaking intron 1 of the factor VIII gene is a frequent cause of severe hemophilia A Blood, January 1, 2002; 99(1): 168 - 174. [Abstract] [Full Text] [PDF] |
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J. E. Horvath, J. A. Bailey, D. P. Locke, and E. E. Eichler Lessons from the human genome: transitions between euchromatin and heterochromatin Hum. Mol. Genet., October 1, 2001; 10(20): 2215 - 2223. [Abstract] [Full Text] [PDF] |
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S. Aradhya, T. Bardaro, P. Galgoczy, T. Yamagata, T. Esposito, H. Patlan, A. Ciccodicola, A. Munnich, S. Kenwrick, M. Platzer, et al. Multiple pathogenic and benign genomic rearrangements occur at a 35 kb duplication involving the NEMO and LAGE2 genes Hum. Mol. Genet., October 1, 2001; 10(22): 2557 - 2567. [Abstract] [Full Text] [PDF] |
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S. Aradhya, H. Woffendin, T. Jakins, T. Bardaro, T. Esposito, A. Smahi, C. Shaw, M. Levy, A. Munnich, M. D'Urso, et al. A recurrent deletion in the ubiquitously expressed NEMO (IKK-{gamma}) gene accounts for the vast majority of incontinentia pigmenti mutations Hum. Mol. Genet., September 1, 2001; 10(19): 2171 - 2179. [Abstract] [Full Text] [PDF] |
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S. Banerjee-Basu and A. D. Baxevanis Molecular evolution of the homeodomain family of transcription factors Nucleic Acids Res., August 1, 2001; 29(15): 3258 - 3269. [Abstract] [Full Text] [PDF] |
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P. Dehal, P. Predki, A. S. Olsen, A. Kobayashi, P. Folta, S. Lucas, M. Land, A. Terry, C. L. Ecale Zhou, S. Rash, et al. Human Chromosome 19 and Related Regions in Mouse: Conservative and Lineage-Specific Evolution Science, July 6, 2001; 293(5527): 104 - 111. [Abstract] [Full Text] [PDF] |
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P. Stankiewicz, S.-S. Park, K. Inoue, and J. R. Lupski The Evolutionary Chromosome Translocation 4;19 in Gorilla gorilla is Associated with Microduplication of the Chromosome Fragment Syntenic to Sequences Surrounding the Human Proximal CMT1A-REP Genome Res., July 1, 2001; 11(7): 1205 - 1210. [Abstract] [Full Text] [PDF] |
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P. K. Rogan, P. M. Cazcarro, and J. H.M. Knoll Sequence-Based Design of Single-Copy Genomic DNA Probes for Fluorescence In Situ Hybridization Genome Res., June 1, 2001; 11(6): 1086 - 1094. [Abstract] [Full Text] [PDF] |
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E. Rossi, F. Piccini, M. Zollino, G. Neri, D. Caselli, R. Tenconi, C. Castellan, R. Carrozzo, C. Danesino, O. Zuffardi, et al. Cryptic telomeric rearrangements in subjects with mental retardation associated with dysmorphism and congenital malformations J. Med. Genet., June 1, 2001; 38(6): 417 - 420. [Full Text] |
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E. E. Eichler Segmental Duplications: What's Missing, Misassigned, and Misassembled---and Should We Care? Genome Res., May 1, 2001; 11(5): 653 - 656. [Full Text] |
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M. A. Pujana, M. Nadal, M. Gratacòs, B. Peral, K. Csiszar, R. González-Sarmiento, L. Sumoy, and X. Estivill Additional Complexity on Human Chromosome 15q: Identification of a Set of Newly Recognized Duplicons (LCR15) on 15q11-q13, 15q24, and 15q26 Genome Res., January 1, 2001; 11(1): 98 - 111. [Abstract] [Full Text] |
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H. Nakano and M. D. Gunn Gene Duplications at the Chemokine Locus on Mouse Chromosome 4: Multiple Strain-Specific Haplotypes and the Deletion of Secondary Lymphoid-Organ Chemokine and EBI-1 Ligand Chemokine Genes in the plt Mutation J. Immunol., January 1, 2001; 166(1): 361 - 369. [Abstract] [Full Text] [PDF] |
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C. Collins, S. Volik, D. Kowbel, D. Ginzinger, B. Ylstra, T. Cloutier, T. Hawkins, P. Predki, C. Martin, M. Wernick, et al. Comprehensive Genome Sequence Analysis of a Breast Cancer Amplicon Genome Res., June 1, 2001; 11(6): 1034 - 1042. [Abstract] [Full Text] [PDF] |
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W. J. Kent and D. Haussler Assembly of the Working Draft of the Human Genome with GigAssembler Genome Res., September 1, 2001; 11(9): 1541 - 1548. [Abstract] [Full Text] [PDF] |
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J. A. Bailey, A. M. Yavor, H. F. Massa, B. J. Trask, and E. E. Eichler Segmental Duplications: Organization and Impact Within the Current Human Genome Project Assembly Genome Res., June 1, 2001; 11(6): 1005 - 1017. [Abstract] [Full Text] [PDF] |
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