Progressive increase in mtDNA 3243A>G heteroplasmy causes abrupt transcriptional reprogramming by Picard, Martin, Zhang, Jiangwen, Hancock, Saege, Derbeneva, Olga, Golhar, Ryan, Golik, Pawel, O'Hearn, Sean, Levy, Shawn, Potluri, Prasanth, Lvova, Maria, Davila, Antonio, Lin, Chun Shi, Perin, Juan Carlos, Rappaport, Eric F, Hakonarson, Hakon, Trounce, Ian A, Procaccio, Vincent, Wallace, Douglas C

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Mitochondrial energy deficiency leads to hyperproliferation of skeletal muscle mitochondria and enhanced insulin sensitivity by Morrow, Ryan M., Picard, Martin, Derbeneva, Olga, Leipzig, Jeremy, McManus, Meagan J., Gouspillou, Gilles, Barbat-Artigas, Sébastien, Dos Santos, Carlos, Hepple, Russell T., Murdock, Deborah G., Wallace, Douglas C.

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Mitochondrial DNA variant associated with Leber hereditary optic neuropathy and high-altitude Tibetans by Ji, Fuyun, Sharpley, Mark S, Derbeneva, Olga, Alves, Leonardo Scherer, Qian, Pin, Wang, Yaoli, Chalkia, Dimitra, Lvova, Maria, Xu, Jiancheng, Yao, Wei, Simon, Mariella, Platt, Julia, Xu, Shiqin, Angelin, Alessia, Davila, Antonio, Huang, Taosheng, Wang, Ping H, Chuang, Lee-Ming, Moore, Lorna G, Qian, Guisheng, Wallace, Douglas C

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Mitochondrial DNA Diversity in Indigenous Populations of the Southern Extent of Siberia, and the Origins of Native American Haplogroups by Starikovskaya, Elena B., Sukernik, Rem I., Derbeneva, Olga A., Volodko, Natalia V., Ruiz‐Pesini, Eduardo, Torroni, Antonio, Brown, Michael D., Lott, Marie T., Hosseini, Seyed H., Huoponen, Kirsi, Wallace, Douglas C.

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Traces of Early Eurasians in the Mansi of Northwest Siberia Revealed by Mitochondrial DNA Analysis by Derbeneva, Olga A., Starikovskaya, Elena B., Wallace, Douglas C., Sukernik, Rem I.

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Analysis of Mitochondrial DNA Diversity in the Aleuts of the Commander Islands and Its Implications for the Genetic History of Beringia by Derbeneva, Olga A., Sukernik, Rem I., Volodko, Natalia V., Hosseini, Seyed H., Lott, Marie T., Wallace, Douglas C.

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Mitochondrial DNA associations with East Asian metabolic syndrome by Chalkia, Dimitra, Chang, Yi-Cheng, Derbeneva, Olga, Lvova, Maria, Wang, Ping, Mishmar, Dan, Liu, Xiaogang, Singh, Larry N., Chuang, Lee-Ming, Wallace, Douglas C.

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A Mitochondrial Etiology of Neurodegenerative Diseases: Evidence from Parkinson's Disease by Khusnutdinova, Elza, Gilyazova, Irina, Ruiz-Pesini, Eduardo, Derbeneva, Olga, Khusainova, Rita, Khidiyatova, Irina, Magzhanov, Rim, Wallace, Douglas C.

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Association between mitochondrial DNA variations and Alzheimer's disease in the ADNI cohort by Lakatos, Anita, Derbeneva, Olga, Younes, Danny, Keator, David, Bakken, Trygve, Lvova, Maria, Brandon, Marty, Guffanti, Guia, Reglodi, Dora, Saykin, Andrew, Weiner, Michael, Macciardi, Fabio, Schork, Nicholas, Wallace, Douglas C, Potkin, Steven G

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A mitochondrial bioenergetic hypothesis for autism spectrum disorder (570.3) by Chalkia, Dimitra, Derbeneva, Olga, Lvova, Maria, Lakatos, Anita, Leipzig, Jeremy, Hadley, Dexter, Hakonarson, Hakon, Wallace, Douglas

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Cytoskeletal mitochondrial interactions in collagen VI related disorders by Angelin, Alessia, Potluri, Prasanth, Lvova, Maria, Keller, Kierstin, Sweeney, Katelyn, Berardinelli, Danielle, Lin, Chun Shi, Derbeneva, Olga, Sharpley, Mark, Bonaldo, Paolo, Bernardi, Paolo, Wallace, Douglas C.

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Characterization of the mitochondrial function and genetics in the pathogenesis of collagen VI related disorders (958.1) by Angelin, Alessia, Lin, Chun Shi, Sharpley, Mark, Derbeneva, Olga, Potluri, Prasanth, Bonaldo, Paolo, Bernardi, Paolo, Wallace, Douglas

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The role of mtDNA background in disease expression: a new primary LHON mutation associated with Western Eurasian haplogroup J by BROWN, Michael D, STARIKOVSKAYA, Elena, DERBENEVA, Olga, HOSSEINI, Seyed, ALLEN, Jon C, MIKHAILOVSKAYA, Irina E, SUKERNIK, Rem I, WALLACE, Douglas C

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Progressive increase in mtDNA 3243A by Picard, Martin, Zhang, Jiangwen, Hancock, Saege, Derbeneva, Olga, Golhar, Ryan, Golik, Pawel, O'Hearn, Sean, Levy, Shawn, Potluri, Prasanth, Lvova, Maria, Davila, Antonio, Lin, Chun Shi, Perin, Juan Carlos, Rappaport, Eric F, Hakonarson, Hakon, Trounce, Ian A, Procaccio, Vincent, Wallace, Douglas C

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Progressive increase in mtDNA 3243A>G heteroplasmy causes abrupt transcriptional reprogramming by Picard, Martin, Zhang, Jiangwen, Hancock, Saege, Derbeneva, Olga, Golhar, Ryan, Golik, Pawel, O'Hearn, Sean, Levy, Shawn, Potluri, Prasanth, Lvova, Maria, Davila, Antonio, Lin, Chun Shi, Perin, Juan Carlos, Rappaport, Eric F., Hakonarson, Hakon, Trounce, Ian A., Procaccio, Vincent, Wallace, Douglas C.

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Preterm birth is associated with mitochondrial DNA variation by Chalkia, Dimitra, Lowery, Ray, Derbeneva, Olga, Lvova, Masha, Sing, Charles, Shimmin, Lawrence, Hixson, James, Simham, Hyagriv, Wadhwa, Pathik, Wallace, Douglas

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19-OR: TOWARDS ALLELE LEVEL HLA GENOTYPING: A COMPARISON OF NEXT-GENERATION SEQUENCING PLATFORMS – ION TORRENT PGM AND ILLUMINA MiSeq by Lind, Curt, Mackiewicz, Kate, Duke, Jamie, Sasson, Ariella, Mahoney, Stephen, Rappaport, Eric, Derbeneva, Olga, Wallace, Doug, Rozemuller, Erik, Penning, Maarten, Mulder, Wietse, Monos, Dimitri

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19-OR by Lind, Curt, Mackiewicz, Kate, Duke, Jamie, Sasson, Ariella, Mahoney, Stephen, Rappaport, Eric, Derbeneva, Olga, Wallace, Doug, Rozemuller, Erik, Penning, Maarten, Mulder, Wietse, Monos, Dimitri

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Leber Hereditary Optic Neuropathy (LHON) associated mutation 3394 is also a high-altitude adaptive polymorphism by Alves, Leonardo S., Ji, Fuyun, Sharpley, Mark S., Derbeneva, Olga, Chalkia, Dimitra, Lvova, Maria, Qian, Guisheng, Moore, Lorna G., Wallace, Douglas C.

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Association between mitochondrial DNA variations and Alzheimer's disease in the ADNI cohort: Alzheimer's Disease Neuroimaging Initiative (ADNI) Studies by LAKATOS, Anita, DERBENEVA, Olga, WEINER, Michael, MACCIARDI, Fabio, SCHORK, Nicholas, WALLACE, Douglas C, POTKIN, Steven G, YOUNES, Danny, KEATOR, David, BAKKEN, Trygve, LVOVA, Maria, BRANDON, Marty, GUFFANTI, Guia, REGLODI, Dora, SAYKIN, Andrew

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