Published in Chromosoma on October 09, 2002
Recurrent sites for new centromere seeding. Genome Res (2004) 1.54
Primate chromosome evolution: ancestral karyotypes, marker order and neocentromeres. Chromosome Res (2008) 1.24
New insights into centromere organization and evolution from the white-cheeked gibbon and marmoset. Mol Biol Evol (2009) 1.10
Hominoid chromosomal rearrangements on 17q map to complex regions of segmental duplication. Genome Biol (2008) 1.04
Human chromosome 16 conservation in primates. Chromosome Res (2003) 0.83
Chromosomal evolution of the PKD1 gene family in primates. BMC Evol Biol (2008) 0.82
Evolutionary descent of a human chromosome 6 neocentromere: a jump back to 17 million years ago. Genome Res (2009) 0.80
Evolutionary and biomedical insights from the rhesus macaque genome. Science (2007) 16.21
Ancestral reconstruction of segmental duplications reveals punctuated cores of human genome evolution. Nat Genet (2007) 10.38
A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures. Nat Genet (2008) 8.44
A genome-wide comparison of recent chimpanzee and human segmental duplications. Nature (2005) 5.51
Characterization of missing human genome sequences and copy-number polymorphic insertions. Nat Methods (2010) 5.44
Noninvasive whole-genome sequencing of a human fetus. Sci Transl Med (2012) 3.94
Comparative and demographic analysis of orang-utan genomes. Nature (2011) 3.83
A burst of segmental duplications in the genome of the African great ape ancestor. Nature (2009) 3.63
Evolutionary toggling of the MAPT 17q21.31 inversion region. Nat Genet (2008) 3.42
Heterozygous submicroscopic inversions involving olfactory receptor-gene clusters mediate the recurrent t(4;8)(p16;p23) translocation. Am J Hum Genet (2002) 3.09
Great ape genetic diversity and population history. Nature (2013) 2.95
The structure and evolution of centromeric transition regions within the human genome. Nature (2004) 2.78
A genome-wide survey of structural variation between human and chimpanzee. Genome Res (2005) 2.61
A large and complex structural polymorphism at 16p12.1 underlies microdeletion disease risk. Nat Genet (2010) 2.57
Recurrent reciprocal genomic rearrangements of 17q12 are associated with renal disease, diabetes, and epilepsy. Am J Hum Genet (2007) 2.54
The bonobo genome compared with the chimpanzee and human genomes. Nature (2012) 2.49
The genomic architecture of segmental duplications and associated copy number variants in dogs. Genome Res (2009) 2.44
Large-scale variation among human and great ape genomes determined by array comparative genomic hybridization. Genome Res (2003) 2.41
Analysis of copy number variations among diverse cattle breeds. Genome Res (2010) 2.02
Characterization of six human disease-associated inversion polymorphisms. Hum Mol Genet (2009) 2.00
Human-specific duplication and mosaic transcripts: the recent paralogous structure of chromosome 22. Am J Hum Genet (2001) 1.95
Analysis of segmental duplications and genome assembly in the mouse. Genome Res (2004) 1.89
Death and resurrection of the human IRGM gene. PLoS Genet (2009) 1.72
A preliminary comparative analysis of primate segmental duplications shows elevated substitution rates and a great-ape expansion of intrachromosomal duplications. Genome Res (2006) 1.69
Evolutionary formation of new centromeres in macaque. Science (2007) 1.67
Refinement of a chimpanzee pericentric inversion breakpoint to a segmental duplication cluster. Genome Biol (2003) 1.65
Gene amplification as double minutes or homogeneously staining regions in solid tumors: origin and structure. Genome Res (2010) 1.62
Copy number variation of individual cattle genomes using next-generation sequencing. Genome Res (2012) 1.62
Alu repeat discovery and characterization within human genomes. Genome Res (2010) 1.62
Recurrent sites for new centromere seeding. Genome Res (2004) 1.54
Concomitant tetrasomy 3q and trisomy 18 in CD5(-), CD13(+) chronic lymphocytic leukemia. Cancer Genet Cytogenet (2002) 1.50
Genomic characteristics of cattle copy number variations. BMC Genomics (2011) 1.48
Recurrent duplication-driven transposition of DNA during hominoid evolution. Proc Natl Acad Sci U S A (2006) 1.47
Gorilla genome structural variation reveals evolutionary parallelisms with chimpanzee. Genome Res (2011) 1.47
Neocentromeres in 15q24-26 map to duplicons which flanked an ancestral centromere in 15q25. Genome Res (2003) 1.44
Copy number variation of CCL3-like genes affects rate of progression to simian-AIDS in Rhesus Macaques (Macaca mulatta). PLoS Genet (2009) 1.43
Analysis of recent segmental duplications in the bovine genome. BMC Genomics (2009) 1.36
MLL3, a new human member of the TRX/MLL gene family, maps to 7q36, a chromosome region frequently deleted in myeloid leukaemia. Gene (2002) 1.36
Evolutionary movement of centromeres in horse, donkey, and zebra. Genomics (2006) 1.34
Copy number variation analysis in the great apes reveals species-specific patterns of structural variation. Genome Res (2011) 1.33
Tracking the complex flow of chromosome rearrangements from the Hominoidea Ancestor to extant Hylobates and Nomascus Gibbons by high-resolution synteny mapping. Genome Res (2008) 1.29
Evolution and diversity of copy number variation in the great ape lineage. Genome Res (2013) 1.29
Progressive proximal expansion of the primate X chromosome centromere. Proc Natl Acad Sci U S A (2005) 1.27
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. Proc Natl Acad Sci U S A (2002) 1.25
Human chromosomes 9, 12, and 15 contain the nucleation sites of stress-induced nuclear bodies. Mol Biol Cell (2002) 1.23
Sequencing human-gibbon breakpoints of synteny reveals mosaic new insertions at rearrangement sites. Genome Res (2008) 1.21
Molecular refinement of gibbon genome rearrangements. Genome Res (2006) 1.16
Insertion of telomeric repeats at intrachromosomal break sites during primate evolution. Genome Res (2004) 1.15
Two classes of low-copy repeats comediate a new recurrent rearrangement consisting of duplication at 8p23.1 and triplication at 8p23.2. Hum Mutat (2007) 1.14
Independent centromere formation in a capricious, gene-free domain of chromosome 13q21 in Old World monkeys and pigs. Genome Biol (2006) 1.13
Chromosome 6 phylogeny in primates and centromere repositioning. Mol Biol Evol (2003) 1.13
MYC-containing double minutes in hematologic malignancies: evidence in favor of the episome model and exclusion of MYC as the target gene. Hum Mol Genet (2006) 1.13
Organization and evolution of primate centromeric DNA from whole-genome shotgun sequence data. PLoS Comput Biol (2007) 1.13
Genome-wide characterization of centromeric satellites from multiple mammalian genomes. Genome Res (2010) 1.12
Reciprocal translocations: a trap for cytogenetists? Hum Genet (2005) 1.12
Human paralogs of KIAA0187 were created through independent pericentromeric-directed and chromosome-specific duplication mechanisms. Genome Res (2002) 1.10
Translocation-excision-deletion-amplification mechanism leading to nonsyntenic coamplification of MYC and ATBF1. Genes Chromosomes Cancer (2006) 1.08
Hominoid chromosomal rearrangements on 17q map to complex regions of segmental duplication. Genome Biol (2008) 1.04
Evolutionary-new centromeres preferentially emerge within gene deserts. Genome Biol (2008) 1.04
Centromere remodeling in Hoolock leuconedys (Hylobatidae) by a new transposable element unique to the gibbons. Genome Biol Evol (2012) 1.02
Evolution of human IgH3'EC duplicated structures: both enhancers HS1,2 are polymorphic with variation of transcription factor's consensus sites. Gene (2004) 1.02
Refinement of macaque synteny arrangement with respect to the official rheMac2 macaque sequence assembly. Chromosome Res (2008) 1.01
Ancestral genomes reconstruction: an integrated, multi-disciplinary approach is needed. Genome Res (2006) 1.00
A double cryptic chromosome imbalance is an important factor to explain phenotypic variability in Wolf-Hirschhorn syndrome. Eur J Hum Genet (2004) 0.99
Evidence for widespread reticulate evolution within human duplicons. Am J Hum Genet (2005) 0.98
Non-invasive fetal genome sequencing: opportunities and challenges. Am J Med Genet A (2012) 0.98
Heterogeneous pattern of chromosomal breakpoints involving the MYC locus in multiple myeloma. Genes Chromosomes Cancer (2003) 0.97
Punctuated duplication seeding events during the evolution of human chromosome 2p11. Genome Res (2005) 0.97
Non random distribution of genomic features in breakpoint regions involved in chronic myeloid leukemia cases with variant t(9;22) or additional chromosomal rearrangements. Mol Cancer (2010) 0.97
Evolutionary history of chromosome 10 in primates. Chromosoma (2002) 0.97