5.9
CiteScore
5.9
Impact Factor
Volume 42 Issue 4
Apr.  2015
Turn off MathJax
Article Contents

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

doi: 10.1016/j.jgg.2015.03.002
More Information
  • Corresponding author: E-mail address: antonio.salas@usc.es (Antonio Salas)
  • Received Date: 2014-11-12
  • Accepted Date: 2015-03-10
  • Rev Recd Date: 2015-02-12
  • Available Online: 2015-03-17
  • Publish Date: 2015-04-20
  • loading
  • [1]
    Bandelt, H.-J., Achilli, A., Kong, Q.-P. et al. Low “penetrance” of phylogenetic knowledge in mitochondrial disease studies Biochem. Biophys. Res. Commun., 333 (2005),pp. 122-130
    [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
    [7]
    Elson, J.L., Andrews, R.M., Chinnery, P.F. et al. Analysis of European mtDNAs for recombination Am. J. Hum. Genet., 68 (2001),pp. 145-153
    [8]
    Fachal, L., Mosquera-Miguel, A., Pastor, P. et al. No evidence of association between common European mitochondrial DNA variants in Alzheimer, Parkinson and migraine in the Spanish population Am. J. Med. Genet. B Neuropsychiatr. Genet., 168 (2014),pp. 54-65
    [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
    [16]
    Mosquera-Miguel, A., Álvarez-Iglesias, V., Carracedo, Á. et al. Is mitochondrial DNA variation associated with sporadic breast cancer risk? Cancer Res., 68 (2008),pp. 623-625
    [17]
    Pardo-Seco, J., Amigo, J., González-Manteiga, W. et al. A generalized model to estimate the statistical power in mitochondrial disease studies involving 2 × k tables PLoS One, 8 (2013),p. e73567
    [18]
    Parson, W., Gusmão, L., Hares, D.R. et al. DNA commission of the international society for forensic genetics: revised and extended guidelines for mitochondrial DNA typing Forensic Sci. Int. Genet., 13 (2014),pp. 134-142
    [19]
    Raule, N., Sevini, F., Santoro, A. et al. Association studies on human mitochondrial DNA: methodological aspects and results in the most common age-related diseases Mitochondrion, 7 (2007),pp. 29-38
    [20]
    Salas, A., Bandelt, H.-J., Macaulay, V. et al. Phylogeographic investigations: the role of trees in forensic genetics Forensic Sci. Int., 168 (2007),pp. 1-13
    [21]
    Salas, A., Fachal, L., Marcos-Alonso, S. et al. Investigating the role of mitochondrial haplogroups in genetic predisposition to meningococcal disease PLoS One, 4 (2009),p. e8347
    [22]
    Salas, A., García-Magariños, M., Logan, I. et al. The saga of the misleading studies falsely associating mitochondrial DNA with breast cancer BMC Cancer, 14 (2014),p. 659
    [23]
    Salas, A., Yao, Y.-G., Macaulay, V. et al. A critical reassessment of the role of mitochondria in tumorigenesis PLoS Med., 2 (2005),p. e296
    [24]
    Samuels, D.C., Carothers, A.D., Horton, R. et al. The power to detect disease associations with mitochondrial DNA haplogroups Am. J. Hum. Genet., 78 (2006),pp. 713-720
    [25]
    Torroni, A., Achilli, A., Macaulay, V. et al. Harvesting the fruit of the human mtDNA tree Trends Genet., 22 (2006),pp. 339-345
    [26]
    van der Walt, J.M., Nicodemus, K.K., Martin, E.R. et al. Mitochondrial polymorphisms significantly reduce the risk of Parkinson disease Am. J. Hum. Genet., 72 (2003),pp. 804-811
    [27]
    Zhang, A.M., Jia, X., Bi, R. et al. Mitochondrial DNA haplogroup background affects LHON, but not suspected LHON, in Chinese patients PLoS One, 6 (2012),p. e27750
  • 加载中

Catalog

    通讯作者: 陈斌, bchen63@163.com
    • 1. 

      沈阳化工大学材料科学与工程学院 沈阳 110142

    1. 本站搜索
    2. 百度学术搜索
    3. 万方数据库搜索
    4. CNKI搜索

    Article Metrics

    Article views (55) PDF downloads (1) Cited by ()
    Proportional views
    Related

    /

    DownLoad:  Full-Size Img  PowerPoint
    Return
    Return