Index | PMID | Date | Reference |
---|---|---|---|
1 | 12618962 | 2003 | van der Walt, J. M., Nicodemus, K. K., Martin, E. R., Scott, W. K., Nance, M. A., Watts, R. L., Hubble, J. P., Haines, J. L., Koller, W. C., Lyons, K., Pahwa, R., Stern, M. B., Colcher, A., Hiner, B. C., Jankovic, J., Ondo, W. G., Allen, F. H., Jr., Goetz, C. G., Small, G. W., Mastaglia, F., Stajich, J. M., McLaurin, A. C., Middleton, L. T., Scott, B. L., Schmechel, D. E., Pericak-Vance, M. A., Vance, J. M. (2003) Mitochondrial polymorphisms significantly reduce the risk of Parkinson disease American Journal of Human Genetics . 72 (4): 804-811 . |
2 | 12670626 | 2003 | Ross, O. A., McCormack, R., Maxwell, L. D., Duguid, R. A., Quinn, D. J., Barnett, Y. A., Rea, I. M., El-Agnaf, O. M., Gibson, J. M., Wallace, A., Middleton, D., Curran, M. D. (2003) mt4216C variant in linkage with the mtDNA TJ cluster may confer a susceptibility to mitochondrial dysfunction resulting in an increased risk of Parkinson's disease in the Irish Experimental Gerontology . 38 (4): 397-405 . |
3 | 15488317 | 2004 | Otaegui, D., Paisan, C., Saenz, A., Marti, I., Ribate, M., Marti-Masso, J. F., Perez-Tur, J., Lopez de Munain, A. (2004) Mitochondrial polymporphisms in Parkinson's Disease Neuroscience Letters . 370 (40577): 171-174 . |
4 | 15483642 | 2005 | Niemi, A. K., Moilanen, J. S., Tanaka, M., Hervonen, A., Hurme, M., Lehtimaki, T., Arai, Y., Hirose, N., Majamaa, K. (2005) A combination of three common inherited mitochondrial DNA polymorphisms promotes longevity in Finnish and Japanese subjects European Journal of Human Genetics . 13 (2): 166-170 . |
5 | 15786469 | 2005 | Pyle, A., Foltynie, T., Tiangyou, W., Lambert, C., Keers, S. M., Allcock, L. M., Davison, J., Lewis, S. J., Perry, R. H., Barker, R., Burn, D. J., Chinnery, P. F. (2005) Mitochondrial DNA haplogroup cluster UKJT reduces the risk of PD Annals of Neurology . 57 (4): 564-567 . |
6 | 15827561 | 2005 | Ghezzi, D., Marelli, C., Achilli, A., Goldwurm, S., Pezzoli, G., Barone, P., Pellecchia, M. T., Stanzione, P., Brusa, L., Bentivoglio, A. R., Bonuccelli, U., Petrozzi, L., Abbruzzese, G., Marchese, R., Cortelli, P., Grimaldi, D., Martinelli, P., Ferrarese, C., Garavaglia, B., Sangiorgi, S., Carelli, V., Torroni, A., Albanese, A., Zeviani, M. (2005) Mitochondrial DNA haplogroup K is associated with a lower risk of Parkinson's disease in Italians European Journal of Human Genetics . 13 (6): 748-752 . |
7 | 15975594 | 2005 | Huerta, C., Castro, M. G., Coto, E., Blazquez, M., Ribacoba, R., Guisasola, L. M., Salvador, C., Martinez, C., Lahoz, C. H., Alvarez, V. (2005) Mitochondrial DNA polymorphisms and risk of Parkinson's disease in Spanish population Journal of the Neurological Sciences . 236 (40545): 49-54 . |
8 | 16140977 | 2005 | Canter, J. A., Kallianpur, A. R., Parl, F. F., Millikan, R. C. (2005) Mitochondrial DNA G10398A polymorphism and invasive breast cancer in African-American women Cancer Research . 65 (17): 8028-8033 . |
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10 | 16895436 | 2006 | Kazuno, A. A., Munakata, K., Nagai, T., Shimozono, S., Tanaka, M., Yoneda, M., Kato, N., Miyawaki, A., Kato, T. (2006) Identification of mitochondrial DNA polymorphisms that alter mitochondrial matrix pH and intracellular calcium dynamics PLoS Genetics . 2 (8): e128 . |
11 | 17174475 | 2007 | Huerta, C., Sanchez-Ferrero, E., Coto, E., Blazquez, M., Ribacoba, R., Guisasola, L. M., Salvador, C., Alvarez, V. (2007) No association between Parkinson's disease and three polymorphisms in the eNOS, nNOS, and iNOS genes Neuroscience Letters . 413 (3): 202-205 . |
12 | 17510395 | 2007 | Bai, R. K., Leal, S. M., Covarrubias, D., Liu, A., Wong, L. J. (2007) Mitochondrial genetic background modifies breast cancer risk Cancer Research . 67 (10): 4687-4694 . |
13 | 17620498 | 2007 | Simon, D. K., Zheng, K., Velazquez, L., Santos, N., Almaguer, L., Figueroa, K. P., Pulst, S. M. (2007) Mitochondrial complex I gene variant associated with early age at onset in spinocerebellar ataxia type 2 Archives of Neurology . 64 (7): 1042-1044 . |
14 | 17627010 | 2007 | Wang, L., Bamlet, W. R., de Andrade, M., Boardman, L. A., Cunningham, J. M., Thibodeau, S. N., Petersen, G. M. (2007) Mitochondrial genetic polymorphisms and pancreatic cancer risk Cancer Epidemiology, Biomarkers and Prevention . 16 (7): 1455-1459 . |
15 | 17701054 | 2007 | Rai, E., Sharma, S., Koul, A., Bhat, A. K., Bhanwer, A. J., Bamezai, R. N. (2007) Interaction between the UCP2-866G/A, mtDNA 10398G/A and PGC1alpha p.Thr394Thr and p.Gly482Ser polymorphisms in type 2 diabetes susceptibility in North Indian population Human Genetics . 122 (5): 535-540 . |
16 | 17886251 | 2007 | Datta, S., Majumder, M., Biswas, N. K., Sikdar, N., Roy, B. (2007) Increased risk of oral cancer in relation to common Indian mitochondrial polymorphisms and Autosomal GSTP1 locus Cancer . 110 (9): 1991-1999 . |
17 | 17288645 | 2008 | Kazuno, A. A., Munakata, K., Kato, N., Kato, T. (2008) Mitochondrial DNA-dependent effects of valproate on mitochondrial calcium levels in transmitochondrial cybrids The International Journal of Neuropsychopharmacology . 11 (1): 71-78 . |
18 | 18177933 | 2008 | Kato, T. (2008) Role of mitochondrial DNA in calcium signaling abnormality in bipolar disorder Cell Calcium . 44 (1): 92-102 . |
19 | 18226984 | 2008 | Kazuno, A. A., Munakata, K., Tanaka, M., Kato, N., Kato, T. (2008) Relationships between mitochondrial DNA subhaplogroups and intracellular calcium dynamics Mitochondrion . 8 (2): 164-169 . |
20 | 18262047 | 2008 | Setiawan, V. W., Chu, L. H., John, E. M., Ding, Y. C., Ingles, S. A., Bernstein, L., Press, M. F., Ursin, G., Haiman, C. A., Neuhausen, S. L. (2008) Mitochondrial DNA G10398A variant is not associated with breast cancer in African-American women Cancer Genetics and Cytogenetics . 181 (1): 16-19 . |
21 | 18286226 | 2008 | Latsoudis, H., Spanaki, C., Chlouverakis, G., Plaitakis, A. (2008) Mitochondrial DNA polymorphisms and haplogroups in Parkinson's disease and control individuals with a similar genetic background Journal of Human Genetics . 53 (4): 349-356 . |
22 | 18679013 | 2008 | Liao, W. Q., Pang, Y., Yu, C. A., Wen, J. Y., Zhang, Y. G., Li, X. H. (2008) Novel mutations of mitochondrial DNA associated with type 2 diabetes in Chinese Han population The Tohoku Journal of Experimental Medicine . 215 (4): 377-384 . |
23 | 18709563 | 2008 | Covarrubias, D., Bai, R. K., Wong, L. J., Leal, S. M. (2008) Mitochondrial DNA variant interactions modify breast cancer risk Journal of Human Genetics . 53 (10): 924-928 . |
24 | 19390621 | 2009 | Pezzotti, A., Kraft, P., Hankinson, S. E., Hunter, D. J., Buring, J., Cox, D. G. (2009) The mitochondrial A10398G polymorphism, interaction with alcohol consumption, and breast cancer risk PLoS One . 4 (4): e5356 . |
25 | 20043118 | 2010 | Czarnecka, A. M., Klemba, A., Krawczyk, T., Zdrozny, M., Arnold, R. S., Bartnik, E., Petros, J. A. (2010) Mitochondrial NADH-dehydrogenase polymorphisms as sporadic breast cancer risk factor Oncology Reports . 23 (2): 531-535 . |
26 | 20067846 | 2010 | Juo, S. H., Lu, M. Y., Bai, R. K., Liao, Y. C., Trieu, R. B., Yu, M. L., Wong, L. J. (2010) A common mitochondrial polymorphism 10398A>G is associated metabolic syndrome in a Chinese population Mitochondrion . 10 (3): 294-299 . |
27 | 21457906 | 2011 | Pereira, L., Soares, P., Radivojac, P., Li, B., Samuels, D. C. (2011) Comparing phylogeny and the predicted pathogenicity of protein variations reveals equal purifying selection across the global human mtDNA diversity American Journal of Human Genetics . 88 (4): 433-439 . |
28 | 23111160 | 2013 | Hao, X. D., Yang, Y. L., Tang, N. L., Kong, Q. P., Wu, S. F., Zhang, Y. P. (2013) Mitochondrial DNA haplogroup Y is associated to Leigh syndrome in Chinese population Gene . 512 (2): 460-463 . |
29 | 25199876 | 2014 | Salas, A., Garcia-Magarinos, M., Logan, I., Bandelt, H. J. (2014) The saga of the many studies wrongly associating mitochondrial DNA with breast cancer BMC Cancer . 14 (): 659 . |
30 | 27217714 | 2016 | Collins, D. W., Gudiseva, H. V., Trachtman, B., Bowman, A. S., Sagaser, A., Sankar, P., Miller-Ellis, E., Lehman, A., Addis, V., O'Brien, J. M. (2016) Association of primary open-angle glaucoma with mitochondrial variants and haplogroups common in African Americans Molecular Vision . 22 (): 454-471 . |
31 | 28648514 | 2017 | Monte, T. L., Pereira, F. S., Reckziegel, E. D. R., Augustin, M. C., Locks-Coelho, L. D., Santos, A. S. P., Pedroso, J. L., Barsottini, O., Vargas, F. R., Saraiva-Pereira, M. L., Jardim, L. B., Rede, N. (2017) Neurological phenotypes in spinocerebellar ataxia type 2: Role of mitochondrial polymorphism A10398G and other risk factors Parkinsonism and Related Disorders . 42 (): 54-60 . |
32 | 28793231 | 2017 | Hwang, I. W., Hong, J. H., Kwon, B. N., Kim, H. J., Lee, N. R., Lim, M. H., Kwon, H. J., Jin, H. J. (2017) Association of mitochondrial DNA 10398 A/G polymorphism with attention deficit and hyperactivity disorder in Korean children Gene . 630 (): 8-12 . |
33 | 29987491 | 2018 | O'Keefe, H., Queen, R. A., Meldau, S., Lord, P., Elson, J. L. (2018) Haplogroup context is less important in the penetrance of mitochondrial DNA complex I mutations compared to mt-tRNA mutations Journal of Molecular Evolution . 86 (6): 395-403 . |
34 | 31797714 | 2019 | Jahani, M. M., Azimi Meibody, A., Karimi, T., Banoei, M. M., Houshmand, M. (2019) An A10398G mitochondrial DNA alteration is related to increased risk of breast cancer, and associates with Her2 positive receptor Mitochondrial DNA. Part A, DNA Mapping, Sequencing, and Analysis . (): 1-6 . |