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Mitochondrial DNA as a Risk Factor for False Positives in Case-Control Association Studies

Antonio Salas Joanna L. Elson

Antonio Salas, Joanna L. Elson. Mitochondrial DNA as a Risk Factor for False Positives in Case-Control Association Studies[J]. Journal of Genetics and Genomics, 2015, 42(4): 169-172. doi: 10.1016/j.jgg.2015.03.002
Citation: Antonio Salas, Joanna L. Elson. Mitochondrial DNA as a Risk Factor for False Positives in Case-Control Association Studies[J]. Journal of Genetics and Genomics, 2015, 42(4): 169-172. doi: 10.1016/j.jgg.2015.03.002

doi: 10.1016/j.jgg.2015.03.002

Mitochondrial DNA as a Risk Factor for False Positives in Case-Control Association Studies

More Information
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    [2] Bandelt, H.-J., Salas, A. Contamination and sample mix-up can best explain some patterns of mtDNA instabilities in buccal cells and oral squamous cell carcinoma BMC Cancer, 9 (2009),p. 113
    [3] Bandelt, H.J., Salas, A., Lutz-Bonengel, S. Artificial recombination in forensic mtDNA population databases Int. J. Legal Med., 118 (2004),pp. 267-273
    [4] Bi, R., Zhang, W., Yu, D. et al. Mitochondrial DNA haplogroup B5 confers genetic susceptibility to Alzheimer's disease in Han Chinese Neurobiol. Aging (2014)
    [5] Canter, J.A., Kallianpur, A.R., Parl, F.F. et al. Mitochondrial DNA G10398A polymorphism and invasive breast cancer in African-American women Cancer Res., 65 (2005),pp. 8028-8033
    [6] Chinnery, P.F., Elliott, H.R., Syed, A. et al. Mitochondrial DNA haplogroups and risk of transient ischaemic attack and ischaemic stroke: a genetic association study Lancet Neurol., 9 (2010),pp. 498-503
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    [9] García-Magariños, M., López-de-Ullibarri, I., Cao, R. et al. Evaluating the ability of tree-based methods and logistic regression for the detection of SNP-SNP interaction Ann. Hum. Genet., 73 (2009),pp. 360-369
    [10] Herrnstadt, C., Howell, N. An evolutionary perspective on pathogenic mtDNA mutations: haplogroup associations of clinical disorders Mitochondrion, 4 (2004),pp. 791-798
    [11] Hudson, G., Carelli, V., Spruijt, L. et al. Clinical expression of Leber hereditary optic neuropathy is affected by the mitochondrial DNA-haplogroup background Am. J. Hum. Genet., 81 (2007),pp. 228-233
    [12] Ji, Y., Zhang, A.M., Jia, X. et al. Mitochondrial DNA haplogroups M7b1'2 and M8a affect clinical expression of Leber hereditary optic neuropathy in Chinese families with the m.11778G>A mutation Am. J. Hum. Genet., 83 (2008),pp. 760-768
    [13] Johnson, R.T., Dickersin, K. Publication bias against negative results from clinical trials: three of the seven deadly sins Nat. Clin. Pract. Neurol., 3 (2007),pp. 590-591
    [14] Køsel, S., Grasbon-Frodl, E.M., Mautsch, U. et al. Novel mutations of mitochondrial complex I in pathologically proven Parkinson disease Neurogenetics, 1 (1998),pp. 197-204
    [15] Man, P.Y., Howell, N., Mackey, D.A. et al. Mitochondrial DNA haplogroup distribution within Leber hereditary optic neuropathy pedigrees J. Med. Genet., 41 (2004),p. e41
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出版历程
  • 收稿日期:  2014-11-12
  • 录用日期:  2015-03-10
  • 修回日期:  2015-02-12
  • 网络出版日期:  2015-03-17
  • 刊出日期:  2015-04-20

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