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Age-Related Somatic Structural Changes in the Nuclear Genome of Human Blood Cells

Forsberg, Lars A., Rasi, Chiara, Razzaghian, Hamid R., Pakalapati, Geeta, Waite, Lindsay, Thilbeault, Krista Stanton, Ronowicz, Anna, Wineinger, Nathan E., Tiwari, Hemant K., Boomsma, Dorret, Westerman, Maxwell P., Harris, Jennifer R., Lyle, Robert, Essand, Magnus, Eriksson, Fredrik, Assimes, Themistocles L., Iribarren, Carlos, Strachan, Eric, O'Hanlon, Terrance P., Rider, Lisa G., Miller, Frederick W., Giedraitis, Vilmantas, Lannfelt, Lars, Ingelsson, Martin, Piotrowski, Arkadiusz, Pedersen, Nancy L., Absher, Devin, Dumanski, Jan P.·2012·The American Journal of Human Genetics
DOI 10.1016/j.ajhg.2011.12.009
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Citations

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Research works printed but not linked: 34

  1. van Ommen, 2005, Frequency of new copy number variation in humans, Nat. Genet., 37, 333, 10.1038/ng0405-333 · DOI
  2. Lupski, 2007, Genomic rearrangements and sporadic disease, Nat. Genet., 39, S43, 10.1038/ng2084 · DOI
  3. Vaziri, 1993, Loss of telomeric DNA during aging of normal and trisomy 21 human lymphocytes, Am. J. Hum. Genet., 52, 661
  4. Lee, 1994, Differential accumulations of 4,977 bp deletion in mitochondrial DNA of various tissues in human ageing, Biochim. Biophys. Acta, 1226, 37, 10.1016/0925-4439(94)90056-6 · DOI
  5. Mohamed, 2006, Mitochondrial DNA deletions and the aging heart, Exp. Gerontol., 41, 508, 10.1016/j.exger.2006.03.014 · DOI
  6. Flores, 2007, Recurrent DNA inversion rearrangements in the human genome, Proc. Natl. Acad. Sci. USA, 104, 6099, 10.1073/pnas.0701631104 · DOI
  7. Sloter, 2007, Frequency of human sperm carrying structural aberrations of chromosome 1 increases with advancing age, Fertil. Steril., 87, 1077, 10.1016/j.fertnstert.2006.08.112 · DOI
  8. Frank, 2010, Evolution in health and medicine Sackler colloquium: Somatic evolutionary genomics: Mutations during development cause highly variable genetic mosaicism with risk of cancer and neurodegeneration, Proc. Natl. Acad. Sci. USA, 107, 1725, 10.1073/pnas.0909343106 · DOI
  9. Lynch, 2010, Evolution of the mutation rate, Trends Genet., 26, 345, 10.1016/j.tig.2010.05.003 · DOI
  10. Youssoufian, 2002, Mechanisms and consequences of somatic mosaicism in humans, Nat. Rev. Genet., 3, 748, 10.1038/nrg906 · DOI
  11. Erickson, 2010, Somatic gene mutation and human disease other than cancer: An update, Mutat. Res., 705, 96, 10.1016/j.mrrev.2010.04.002 · DOI
  12. De, 2011, Somatic mosaicism in healthy human tissues, Trends Genet., 27, 217, 10.1016/j.tig.2011.03.002 · DOI
  13. Rodríguez-Santiago, 2010, Mosaic uniparental disomies and aneuploidies as large structural variants of the human genome, Am. J. Hum. Genet., 87, 129, 10.1016/j.ajhg.2010.06.002 · DOI
  14. Piotrowski, 2008, Somatic mosaicism for copy number variation in differentiated human tissues, Hum. Mutat., 29, 1118, 10.1002/humu.20815 · DOI
  15. Bruder, 2008, Phenotypically concordant and discordant monozygotic twins display different DNA copy-number-variation profiles, Am. J. Hum. Genet., 82, 763, 10.1016/j.ajhg.2007.12.011 · DOI
  16. Steemers, 2006, Whole-genome genotyping with the single-base extension assay, Nat. Methods, 3, 31, 10.1038/nmeth842 · DOI
  17. Olshen, 2004, Circular binary segmentation for the analysis of array-based DNA copy number data, Biostatistics, 5, 557, 10.1093/biostatistics/kxh008 · DOI
  18. Conlin, 2010, Mechanisms of mosaicism, chimerism and uniparental disomy identified by single nucleotide polymorphism array analysis, Hum. Mol. Genet., 19, 1263, 10.1093/hmg/ddq003 · DOI
  19. Razzaghian, 2010, Somatic mosaicism for chromosome X and Y aneuploidies in monozygotic twins heterozygous for sickle cell disease mutation, Am. J. Med. Genet. A., 152A, 2595, 10.1002/ajmg.a.33604 · DOI
  20. Workman, 2002, A new non-linear normalization method for reducing variability in DNA microarray experiments, Genome Biol., 3, 10.1186/gb-2002-3-9-research0048 · DOI
  21. Gunnarsson, 2008, Screening for copy-number alterations and loss of heterozygosity in chronic lymphocytic leukemia—a comparative study of four differently designed, high resolution microarray platforms, Genes Chromosomes Cancer, 47, 697, 10.1002/gcc.20575 · DOI
  22. Gunnarsson, 2010, Large but not small copy-number alterations correlate to high-risk genomic aberrations and survival in chronic lymphocytic leukemia: A high-resolution genomic screening of newly diagnosed patients, Leukemia, 24, 211, 10.1038/leu.2009.187 · DOI
  23. González, 2011, A fast and accurate method to detect allelic genomic imbalances underlying mosaic rearrangements using SNP array data, BMC Bioinformatics, 12, 166, 10.1186/1471-2105-12-166 · DOI
  24. Schunkert, 2011, Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease, Nat. Genet., 43, 333, 10.1038/ng.784 · DOI · Paper page
  25. Assimes, 2008, Susceptibility locus for clinical and subclinical coronary artery disease at chromosome 9p21 in the multi-ethnic ADVANCE study, Hum. Mol. Genet., 17, 2320, 10.1093/hmg/ddn132 · DOI
  26. Hagenkord, 2010, Array-based karyotyping for prognostic assessment in chronic lymphocytic leukemia: Performance comparison of Affymetrix 10K2.0, 250K Nsp, and SNP6.0 arrays, J. Mol. Diagn., 12, 184, 10.2353/jmoldx.2010.090118 · DOI
  27. Bernasconi, 2006, Clinical relevance of cytogenetics in myelodysplastic syndromes, Ann. N Y Acad. Sci., 1089, 395, 10.1196/annals.1386.034 · DOI
  28. Haase, 2008, Cytogenetic features in myelodysplastic syndromes, Ann. Hematol., 87, 515, 10.1007/s00277-008-0483-y · DOI
  29. Tiu, 2011, Prognostic impact of SNP array karyotyping in myelodysplastic syndromes and related myeloid malignancies, Blood, 117, 4552, 10.1182/blood-2010-07-295857 · DOI
  30. Braun, 2011, Characteristics and outcome of myelodysplastic syndromes (MDS) with isolated 20q deletion: A report on 62 cases, Leuk. Res., 35, 863, 10.1016/j.leukres.2011.02.008 · DOI
  31. Bejar, 2011, Unraveling the molecular pathophysiology of myelodysplastic syndromes, J. Clin. Oncol., 29, 504, 10.1200/JCO.2010.31.1175 · DOI
  32. Conrad, 2010, Mutation spectrum revealed by breakpoint sequencing of human germline CNVs, Nat. Genet., 42, 385, 10.1038/ng.564 · DOI
  33. Mori, 2002, Chromosome translocations and covert leukemic clones are generated during normal fetal development, Proc. Natl. Acad. Sci. USA, 99, 8242, 10.1073/pnas.112218799 · DOI
  34. Naylor, 2005, The influence of age on T cell generation and TCR diversity, J. Immunol., 174, 7446, 10.4049/jimmunol.174.11.7446 · DOI · Paper page

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Metadata

Authors
Forsberg, L. A., Rasi, C., Razzaghian, H. R., Pakalapati, G., Waite, L., Thilbeault, K. S., Ronowicz, A., Wineinger, N. E., Tiwari, H. K., Boomsma, D., Westerman, M. P., Harris, J. R., Lyle, R., Essand, M., Eriksson, F., Assimes, T. L., Iribarren, C., Strachan, E., O'Hanlon, T. P., Rider, L. G., Miller, F. W., Giedraitis, V., Lannfelt, L., Ingelsson, M., Piotrowski, A., Pedersen, N. L., Absher, D., & Dumanski, J. P.
Venue
The American Journal of Human Genetics
Publisher
Elsevier BV
Published
2012-02
Volume
90
Issue
2
Pages
217-228
ISSN
0002-9297
DOI
10.1016/j.ajhg.2011.12.009
Cited by
176
References
6
Language
en
Licence

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