Publisher:
Impact Factor:
Years in Print:
Journal Website:

Articles of Interest

• Underhill, P. A.; Passarino, G.; Lin, A. A.; Marzuki, S.; Oefner, P. J.; Cavalli-Sforza, L. L. & Chambers, G. K. (2001). Maori origins, Y-chromosome haplotypes and implications for human history in the Pacific. Human mutation, 17(4), 271-280.
• Ballana, E., Govea, N., De Cid, R., Garcia, C., Arribas, C., Rosell, J. and Estivill, X. (2008). Detection of unrecognized low-level mtDNA heteroplasmy may explain the variable phenotypic expressivity of apparently homoplasmic mtDNA mutations. Human mutation, 29(2), 248-257.
• Behar, D.M., Blue‐Smith, J., Soria‐Hernanz, D.F., Tzur, S., Hadid, Y., Bormans, C., Moen, A., Tyler‐Smith, C., Quintana‐Murci, L. and Wells, R.S. (2008). A novel 154‐bp deletion in the human mitochondrial DNA control region in healthy individuals. Human mutation, 29(12), 1387-1391.
• Bi, R., Zhang, A.M., Zhang, W., Kong, Q.P., Wu, B.L., Yang, X.H., Wang, D., Zou, Y., Zhang, Y.P. and Yao, Y.G. (2010). The acquisition of an inheritable 50‐bp deletion in the human mtDNA control region does not affect the mtDNA copy number in peripheral blood cells. Human mutation, 31(5), 538-543.
• Hartmann, A., Thieme, M., Nanduri, L.K., Stempfl, T., Moehle, C., Kivisild, T. and Oefner, P.J. (2008). Validation of microarray-based resequencing of 93 worldwide mitochondrial genomes. Human mutation, 30(1), 115-122.
• Shen, P., Lavi, T., Kivisild, T., Chou, V., Sengun, D., Gefel, D., Shpirer, I., Woolf, E., Hillel, J., Feldman, M.W. and Oefner, P.J. (2004). Reconstruction of patrilineages and matrilineages of Samaritans and other Israeli populations from Y-Chromosome and mitochondrial DNA sequence Variation. Human mutation, 24(3), 248-260.
• Van Oven, M., & Kayser, M. (2009). Updated comprehensive phylogenetic tree of global human mitochondrial DNA variation. Human mutation, 30(2), E386-E394.
1