The origins and impact of primate segmental duplications.
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[1] J. Lupski,et al. Mechanisms of change in gene copy number , 2009, Nature Reviews Genetics.
[2] Mira V. Han,et al. Adaptive evolution of young gene duplicates in mammals. , 2009, Genome research.
[3] Peter A. Meric,et al. Lineage-Specific Biology Revealed by a Finished Genome Assembly of the Mouse , 2009, PLoS biology.
[4] K. Worley,et al. The Genome Sequence of Taurine Cattle: A Window to Ruminant Biology and Evolution , 2009, Science.
[5] Can Alkan,et al. Death and Resurrection of the Human IRGM Gene , 2009, PLoS genetics.
[6] C. Baker,et al. A burst of segmental duplications in the genome of the African great ape ancestor , 2009, Nature.
[7] Jeremiah D. Degenhardt,et al. Copy Number Variation of CCL3-like Genes Affects Rate of Progression to Simian-AIDS in Rhesus Macaques (Macaca mulatta) , 2009, PLoS genetics.
[8] Thomas J. Nicholas,et al. The genomic architecture of segmental duplications and associated copy number variants in dogs. , 2008, Genome research.
[9] E. Eichler,et al. Sequencing human-gibbon breakpoints of synteny reveals mosaic new insertions at rearrangement sites. , 2009, Genome research.
[10] Danielle G. Lemay,et al. The bovine lactation genome: insights into the evolution of mammalian milk , 2009, Genome Biology.
[11] Hugo Y. K. Lam,et al. Analysis of copy number variants and segmental duplications in the human genome: Evidence for a change in the process of formation in recent evolutionary history. , 2008, Genome research.
[12] Kenneth H. Wolfe,et al. Turning a hobby into a job: How duplicated genes find new functions , 2008, Nature Reviews Genetics.
[13] Orsolya Symmons,et al. How segmental duplications shape our genome: recent evolution of ABCC6 and PKD1 Mendelian disease genes. , 2008, Molecular biology and evolution.
[14] C. Münch,et al. Evolutionary analysis of the highly dynamic CHEK2 duplicon in anthropoids , 2008, BMC Evolutionary Biology.
[15] Zhaoshi Jiang,et al. Evolutionary toggling of the MAPT 17q21.31 inversion region , 2008, Nature Genetics.
[16] Romain Koszul,et al. Segmental Duplications Arise from Pol32-Dependent Repair of Broken Forks through Two Alternative Replication-Based Mechanisms , 2008, PLoS genetics.
[17] Anthony T Papenfuss,et al. Defensins and the convergent evolution of platypus and reptile venom genes. , 2008, Genome research.
[18] E. Eichler,et al. Mouse segmental duplication and copy number variation , 2008, Nature Genetics.
[19] Ryan D. Hernandez,et al. Proportionally more deleterious genetic variation in European than in African populations , 2008, Nature.
[20] André Reis,et al. Psoriasis is associated with increased beta-defensin genomic copy number. , 2008, Nature genetics.
[21] André Reis,et al. Psoriasis is associated with increased β-defensin genomic copy number , 2008, Nature Genetics.
[22] P. Yen,et al. Evolution of the DAZ gene and the AZFc region on primate Y chromosomes , 2008, BMC Evolutionary Biology.
[23] J. Lupski,et al. A DNA Replication Mechanism for Generating Nonrecurrent Rearrangements Associated with Genomic Disorders , 2007, Cell.
[24] Mario Cáceres,et al. A recurrent inversion on the eutherian X chromosome , 2007, Proceedings of the National Academy of Sciences.
[25] E. Eichler,et al. Ancestral reconstruction of segmental duplications reveals punctuated cores of human genome evolution , 2007, Nature Genetics.
[26] P. Stankiewicz,et al. Hominoid lineage specific amplification of low-copy repeats on 22q11.2 (LCR22s) associated with velo-cardio-facial/digeorge syndrome. , 2007, Human molecular genetics.
[27] L. Armengol,et al. Characterization and evolution of the novel gene family FAM90A in primates originated by multiple duplication and rearrangement events. , 2007, Human molecular genetics.
[28] Jeffery P. Demuth,et al. Accelerated Rate of Gene Gain and Loss in Primates , 2007, Genetics.
[29] J. Sikela,et al. Gene copy number variation spanning 60 million years of human and primate evolution. , 2007, Genome research.
[30] Adrian Gherman,et al. Population Bottlenecks as a Potential Major Shaping Force of Human Genome Architecture , 2007, PLoS genetics.
[31] Michael Ashburner,et al. Principles of Genome Evolution in the Drosophila melanogaster Species Group , 2007, PLoS biology.
[32] L. Symington,et al. Template switching during break-induced replication , 2007, Nature.
[33] David N. Messina,et al. Evolutionary and Biomedical Insights from the Rhesus Macaque Genome , 2007, Science.
[34] D. Cooper,et al. Structural divergence between the human and chimpanzee genomes , 2007, Human Genetics.
[35] Steven Scherer,et al. Recurrent duplication-driven transposition of DNA during hominoid evolution , 2006, Proceedings of the National Academy of Sciences.
[36] J. Rogers,et al. A High-Resolution Map of Synteny Disruptions in Gibbon and Human Genomes , 2006, PLoS genetics.
[37] R. Pfundt,et al. A new chromosome 17q21.31 microdeletion syndrome associated with a common inversion polymorphism , 2006, Nature Genetics.
[38] Andrew J Sharp,et al. Discovery of previously unidentified genomic disorders from the duplication architecture of the human genome , 2006, Nature Genetics.
[39] Andrew J Lees,et al. Microdeletion encompassing MAPT at chromosome 17q21.3 is associated with developmental delay and learning disability , 2006, Nature Genetics.
[40] Bernhard Radlwimmer,et al. A chromosome 8 gene-cluster polymorphism with low human beta-defensin 2 gene copy number predisposes to Crohn disease of the colon. , 2006, American journal of human genetics.
[41] Gerald J Wyckoff,et al. Human LineageSpecific Amplification, Selection, and Neuronal Expression of DUF1220 Domains , 2006, Science.
[42] E. Eichler,et al. A preliminary comparative analysis of primate segmental duplications shows elevated substitution rates and a great-ape expansion of intrachromosomal duplications. , 2006, Genome research.
[43] Enrico Petretto,et al. Copy number polymorphism in Fcgr3 predisposes to glomerulonephritis in rats and humans , 2006, Nature.
[44] E. Eichler,et al. Primate segmental duplications: crucibles of evolution, diversity and disease , 2006, Nature Reviews Genetics.
[45] James A. Cuff,et al. Genome sequence, comparative analysis and haplotype structure of the domestic dog , 2005, Nature.
[46] Pawel Stankiewicz,et al. Genomic Disorders: Molecular Mechanisms for Rearrangements and Conveyed Phenotypes , 2005, PLoS genetics.
[47] F. Speleman,et al. A novel gene family NBPF: intricate structure generated by gene duplications during primate evolution. , 2005, Molecular biology and evolution.
[48] Ton Feuth,et al. Diagnostic genome profiling in mental retardation. , 2005, American journal of human genetics.
[49] E. Eichler,et al. A genome-wide survey of structural variation between human and chimpanzee. , 2005, Genome research.
[50] Barbara J. Trask,et al. Human subtelomeres are hot spots of interchromosomal recombination and segmental duplication , 2005, Nature.
[51] Jean L. Chang,et al. Initial sequence of the chimpanzee genome and comparison with the human genome , 2005, Nature.
[52] E. Eichler,et al. A genome-wide comparison of recent chimpanzee and human segmental duplications , 2005, Nature.
[53] A. Kaur,et al. Interchromosomal segmental duplications explain the unusual structure of PRSS3, the gene for an inhibitor-resistant trypsinogen. , 2005, Molecular biology and evolution.
[54] P. Pevzner,et al. Dynamics of Mammalian Chromosome Evolution Inferred from Multispecies Comparative Maps , 2005, Science.
[55] E. Eichler,et al. Segmental duplications and copy-number variation in the human genome. , 2005, American journal of human genetics.
[56] J. Jurka,et al. RAG1 Core and V(D)J Recombination Signal Sequences Were Derived from Transib Transposons , 2005, PLoS biology.
[57] E. Eichler,et al. Fine-scale structural variation of the human genome , 2005, Nature Genetics.
[58] B. Rovin,et al. The Influence of CCL 3 L 1 Gene – Containing Segmental Duplications on HIV-1 / AIDS Susceptibility , 2009 .
[59] M. Suyama,et al. Complex genomic rearrangements lead to novel primate gene function. , 2005, Genome research.
[60] M. Lercher,et al. Explorer Evidence for Widespread Degradation of Gene Control Regions in Hominid Genomes , 2015 .
[61] H. Stefánsson,et al. A common inversion under selection in Europeans , 2005, Nature Genetics.
[62] E. Eichler,et al. Shotgun sequence assembly and recent segmental duplications within the human genome , 2004, Nature.
[63] L. Feuk,et al. Detection of large-scale variation in the human genome , 2004, Nature Genetics.
[64] D. Haussler,et al. The structure and evolution of centromeric transition regions within the human genome , 2004, Nature.
[65] J. Sikela,et al. Lineage-Specific Gene Duplication and Loss in Human and Great Ape Evolution , 2004, PLoS biology.
[66] E. Eichler,et al. Analysis of segmental duplications and genome assembly in the mouse. , 2004, Genome research.
[67] B. Dujon,et al. Eucaryotic genome evolution through the spontaneous duplication of large chromosomal segments , 2004, The EMBO journal.
[68] D. Haussler,et al. Hotspots of mammalian chromosomal evolution , 2004, Genome Biology.
[69] L. Shaffer,et al. Shuffling of genes within low-copy repeats on 22q11 (LCR22) by Alu-mediated recombination events during evolution. , 2003, Genome research.
[70] E. Eichler,et al. An Alu transposition model for the origin and expansion of human segmental duplications. , 2003, American journal of human genetics.
[71] S. Scherer,et al. Enrichment of segmental duplications in regions of breaks of synteny between the human and mouse genomes suggest their involvement in evolutionary rearrangements. , 2003, Human molecular genetics.
[72] P. Pevzner,et al. Human and mouse genomic sequences reveal extensive breakpoint reuse in mammalian evolution , 2003, Proceedings of the National Academy of Sciences of the United States of America.
[73] D. Haber,et al. The Tre2 (USP6) oncogene is a hominoid-specific gene , 2003, Proceedings of the National Academy of Sciences of the United States of America.
[74] Colin N. Dewey,et al. Initial sequencing and comparative analysis of the mouse genome. , 2002 .
[75] D. Nicolae,et al. Rapid divergence in expression between duplicate genes inferred from microarray data. , 2002, Trends in genetics : TIG.
[76] M. Adams,et al. Recent Segmental Duplications in the Human Genome , 2002, Science.
[77] Matthias Platzer,et al. Molecular characterization of the pericentric inversion that causes differences between chimpanzee chromosome 19 and human chromosome 17. , 2002, American journal of human genetics.
[78] B. Birren,et al. Structure and evolution of the Smith-Magenis syndrome repeat gene clusters, SMS-REPs. , 2002, Genome research.
[79] Richard Gibbs,et al. Bovine Genomic Sequencing Initiative Cattle-izing the Human Genome , 2002 .
[80] Evan E. Eichler,et al. Positive selection of a gene family during the emergence of humans and African apes , 2001, Nature.
[81] K. Osoegawa,et al. Construction of Bacterial Artificial Chromosome (BAC/PAC) Libraries , 2001, Current protocols in molecular biology.
[82] B. Trask,et al. Segmental duplications: organization and impact within the current human genome project assembly. , 2001, Genome research.
[83] N. Dominy,et al. Ecological importance of trichromatic vision to primates , 2001, Nature.
[84] N. Gilbert,et al. SMN gene duplication and the emergence of the SMN2 gene occurred in distinct hominids: SMN2 is unique to Homo sapiens , 2001, Human Genetics.
[85] J. V. Moran,et al. Initial sequencing and analysis of the human genome. , 2001, Nature.
[86] M. Lynch,et al. The evolutionary fate and consequences of duplicate genes. , 2000, Science.
[87] J. Lupski. Genomic disorders: structural features of the genome can lead to DNA rearrangements and human disease traits. , 1998, Trends in genetics : TIG.
[88] M. Nei,et al. Positive Darwinian selection after gene duplication in primate ribonuclease genes. , 1998, Proceedings of the National Academy of Sciences of the United States of America.
[89] J. Lupski,et al. The human COX10 gene is disrupted during homologous recombination between the 24 kb proximal and distal CMT1A-REPs. , 1997, Human molecular genetics.
[90] B. Dutrillaux,et al. Emergence and scattering of multiple neurofibromatosis (NF1)-related sequences during hominoid evolution suggest a process of pericentromeric interchromosomal transposition. , 1997, Human molecular genetics.
[91] K. Morrison. Advances in SMA research: Review of gene deletions , 1996, Neuromuscular Disorders.
[92] Jay Neitz,et al. Trichromatic colour vision in New World monkeys , 1996, Nature.
[93] S. Ohno,et al. Evolution from fish to mammals by gene duplication. , 2009, Hereditas.