MITOMAP References for 11696 G-A

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1 16364244 2006 Zhou, X., Wei, Q., Yang, L., Tong, Y., Zhao, F., Lu, C., Qian, Y., Sun, Y., Lu, F., Qu, J., Guan, M. X. (2006) Leber's hereditary optic neuropathy is associated with the mitochondrial ND4 G11696A mutation in five Chinese families Biochemical and Biophysical Research Communications . 340 (1): 69-75 .
2 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 .
3 17123466 2007 Bandelt, H. J., Yao, Y. G., Salas, A., Kivisild, T., Bravi, C. M. (2007) High penetrance of sequencing errors and interpretative shortcomings in mtDNA sequence analysis of LHON patients Biochemical and Biophysical Research Communications . 352 (2): 283-291 .
4 18223312 2008 Thangaraj, K., Chaubey, G., Kivisild, T., Selvi Rani, D., Singh, V. K., Ismail, T., Carvalho-Silva, D., Metspalu, M., Bhaskar, L. V., Reddy, A. G., Chandra, S., Pande, V., Prathap Naidu, B., Adarsh, N., Verma, A., Jyothi, I. A., Mallick, C. B., Shrivastava, N., Devasena, R., Kumari, B., Singh, A. K., Dwivedi, S. K., Singh, S., Rao, G., Gupta, P., Sonvane, V., Kumari, K., Basha, A., Bhargavi, K. R., Lalremruata, A., Gupta, A. K., Kaur, G., Reddy, K. K., Rao, A. P., Villems, R., Tyler-Smith, C., Singh, L. (2008) Maternal footprints of Southeast Asians in North India Human Heredity . 66 (1): 1-9 .
5 18639500 2008 Chen, J., Yuan, H., Lu, J., Liu, X., Wang, G., Zhu, Y., Cheng, J., Wang, X., Han, B., Yang, L., Yang, S., Yang, A., Sun, Q., Kang, D., Zhang, X., Dai, P., Zhai, S., Han, D., Young, W. Y., Guan, M. X. (2008) Mutations at position 7445 in the precursor of mitochondrial tRNA(Ser(UCN)) gene in three maternal Chinese pedigrees with sensorineural hearing loss Mitochondrion . 8 (4): 285-292 .
6 18676632 2008 Bosley, T. M., Brodsky, M., Glasier, C. M., Abu-Amero, K. K. (2008) Sporadic bilateral optic neuropathy in children: the role of mitochondrial abnormalities Investigative Ophthalmology and Visual Science . 49 (12): 5250-5256 .
7 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 .
8 22487888 2012 Sukernik, R. I., Volodko, N. V., Mazunin, I. O., Eltsov, N. P., Dryomov, S. V., Starikovskaya, E. B. (2012) Mitochondrial genome diversity in the Tubalar, Even, and Ulchi: contribution to prehistory of native Siberians and their affinities to Native Americans American Journal of Physical Anthropology . 148 (1): 123-138 .
9 24002810 2013 Kang, L., Zheng, H. X., Chen, F., Yan, S., Liu, K., Qin, Z., Liu, L., Zhao, Z., Li, L., Wang, X., He, Y., Jin, L. (2013) mtDNA lineage expansions in Sherpa population suggest adaptive evolution in Tibetan highlands. [Supplementary Materials online.] Molecular Biology and Evolution . 30 (12): 2579-2587 .
10 NA 2014 van Oven, M., Kayser, M. (2014) . http://www.phylotree.org . Variants appear in tree, sequence(s) available. Phylotree (Build 16): 19 Feb .
11 24062162 2014 Ji, K., Zheng, J., Sun, B., Liu, F., Shan, J., Li, D., Luo, Y. B., Zhao, Y., Yan, C. (2014) Novel mitochondrial C15620A variant may modulate the phenotype of mitochondrial G11778A mutation in a Chinese family with Leigh syndrome Neuromolecular Medicine . 16 (1): 119-126 .
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 35801081 2022 Jia, M., Li, Q., Zhang, T., Dong, B., Liang, X., Fu, S., Yu, J. (2022) Genetic diversity analysis of the Chinese Daur ethnic group in Heilongjiang Province by complete mitochondrial genome sequencing Frontiers in Genetics . 13 (): 919063 .