| Index | PMID | Date | Reference |
|---|---|---|---|
| 1 | 11349229 | 2001 | Finnila, S., Lehtonen, M. S., Majamaa, K. (2001) Phylogenetic network for European mtDNA American Journal of Human Genetics . 68 (6): 1475-1484 . |
| 2 | 12464729 | 2002 | Howell, N., Miller, N. R., Mackey, D. A., Arnold, A., Herrnstadt, C., Williams, I. M., Kubacka, I. (2002) Lightning strikes twice: Leber hereditary optic neuropathy families with two pathogenic mtDNA mutations Journal of Neuro-ophthalmology . 22 (4): 262-269 . |
| 3 | 16404693 | 2006 | Behar, D. M., Metspalu, E., Kivisild, T., Achilli, A., Hadid, Y., Tzur, S., Pereira, L., Amorim, A., Quintana-Murci, L., Majamaa, K., Herrnstadt, C., Howell, N., Balanovsky, O., Kutuev, I., Pshenichnov, A., Gurwitz, D., Bonne-Tamir, B., Torroni, A., Villems, R., Skorecki, K. (2006) The matrilineal ancestry of Ashkenazi jewry: portrait of a recent founder event American Journal of Human Genetics . 78 (3): 487-497 . |
| 4 | 16714301 | 2006 | Kong, Q. P., Bandelt, H. J., Sun, C., Yao, Y. G., Salas, A., Achilli, A., Wang, C. Y., Zhong, L., Zhu, C. L., Wu, S. F., Torroni, A., Zhang, Y. P. (2006) Updating the East Asian mtDNA phylogeny: a prerequisite for the identification of pathogenic mutations Human Molecular Genetics . 15 (13): 2076-2086 . |
| 5 | 18691441 | 2008 | Kumar, S., Padmanabham, P. B., Ravuri, R. R., Uttaravalli, K., Koneru, P., Mukherjee, P. A., Das, B., Kotal, M., Xaviour, D., Saheb, S. Y., Rao, V. R. (2008) The earliest settlers' antiquity and evolutionary history of Indian populations: evidence from M2 mtDNA lineage BMC Evolutionary Biology . 8 (): 230 . |
| 6 | 18853457 | 2009 | van Oven, M., Kayser, M. (2009) Updated comprehensive phylogenetic tree of global human mitochondrial DNA variation Human Mutation (Online) . 29 (-): E386-E394 . |
| 7 | 19370763 | 2009 | Dobrowolski, S. F., Gray, J., Miller, T., Sears, M. (2009) Identifying sequence variants in the human mitochondrial genome using high-resolution melt (HRM) profiling Human Mutation (Online) . 30 (6): 891-898 . |
| 8 | 20454697 | 2010 | Kumar, M., Tanwar, M., Saxena, R., Sharma, P., Dada, R. (2010) Identification of novel mitochondrial mutations in Leber's hereditary optic neuropathy Molecular Vision . 16 (-): 782-792 . |
| 9 | 21978175 | 2011 | Kumar, S., Bellis, C., Zlojutro, M., Melton, P. E., Blangero, J., Curran, J. E. (2011) Large scale mitochondrial sequencing in Mexican Americans suggests a reappraisal of Native American origins BMC Evolutionary Biology . 11 (): 293 . |
| 10 | 22649055 | 2012 | Li, M., Schroeder, R., Ko, A., Stoneking, M. (2012) Fidelity of capture-enrichment for mtDNA genome sequencing: influence of NUMTs Nucleic Acids Research . 40 (18): e137 . |
| 11 | NA | 2014 | van Oven, M., Kayser, M. (2014) . http://www.phylotree.org . Variants appear in tree, sequence(s) available. Phylotree (Build 16): 19 Feb . |
| 12 | 24467713 | 2014 | Summerer, M., Horst, J., Erhart, G., Weissensteiner, H., Schonherr, S., Pacher, D., Forer, L., Horst, D., Manhart, A., Horst, B., Sanguansermsri, T., Kloss-Brandstatter, A. (2014) Large-scale mitochondrial DNA analysis in Southeast Asia reveals evolutionary effects of cultural isolation in the multi-ethnic population of Myanmar BMC Evolutionary Biology . 14 (): 184-192 . |
| 13 | 32949792 | 2020 | Cihlar, J. C., Strobl, C., Lagace, R., Muenzler, M., Parson, W., Budowle, B. (2020) Distinguishing mitochondrial DNA and NUMT sequences amplified with the precision ID mtDNA whole genome panel Mitochondrion . 55 (): 122-133 . |