Volume measurements of zoisite at simultaneously elevated pressure and temperature von Pawley, A. R, Chinnery, N. J, Clark, S. M

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In situ observation of the formation of 10 Å phase from talc + H2O at mantle pressures and temperatures von CHINNERY, N. J, PAWLEY, A. R, CLARK, S. M

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In situ observation of the formation of 10 A phase from talc + H(2)O at mantle pressures and temperatures von Chinnery, NJ, Pawley, AR, Clark, SM

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A role for BCL2L13 and autophagy in germline purifying selection of mtDNA von Kremer, Laura S, Bozhilova, Lyuba V, Rubalcava-Gracia, Diana, Filograna, Roberta, Upadhyay, Mamta, Koolmeister, Camilla, Chinnery, Patrick F, Larsson, Nils-Göran

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Topoisomerase 3α Is Required for Decatenation and Segregation of Human mtDNA von Nicholls, Thomas J., Nadalutti, Cristina A., Motori, Elisa, Sommerville, Ewen W., Gorman, Gráinne S., Basu, Swaraj, Hoberg, Emily, Turnbull, Doug M., Chinnery, Patrick F., Larsson, Nils-Göran, Larsson, Erik, Falkenberg, Maria, Taylor, Robert W., Griffith, Jack D., Gustafsson, Claes M.

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Synaptotagmin 2 Mutations Cause an Autosomal-Dominant Form of Lambert-Eaton Myasthenic Syndrome and Nonprogressive Motor Neuropathy von Herrmann, David N., Horvath, Rita, Sowden, Janet E., Gonzales, Michael, Sanchez-Mejias, Avencia, Guan, Zhuo, Whittaker, Roger G., Almodovar, Jorge L., Lane, Maria, Bansagi, Boglarka, Pyle, Angela, Boczonadi, Veronika, Lochmüller, Hanns, Griffin, Helen, Chinnery, Patrick F., Lloyd, Thomas E., Littleton, J. Troy, Zuchner, Stephan

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Persistence of the treatment effect of idebenone in Leber's hereditary optic neuropathy von Klopstock, T, Metz, G, Yu-Wai-Man, P, Büchner, B, Gallenmüller, C, Bailie, M, Nwali, N, Griffiths, P G, von Livonius, B, Reznicek, L, Rouleau, J, Coppard, N, Meier, T, Chinnery, P F

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A founder mutation in Anoctamin 5 is a major cause of limb girdle muscular dystrophy von HICKS, Debbie, SARKOZY, Anna, BAILEY, Geraldine, MILLER, James, RADUNOVIC, Aleksander, HUGHES, Paul J, ROBERT, Richard, KRAUSE, Sabine, WALTER, Maggie C, LAVAL, Steven H, STRAUB, Volker, LOCHMÜLLER, Hanns, MUELAS, Nuria, BUSHBY, Kate, KÖEHLER, Katrin, HUEBNER, Angela, HUDSON, Gavin, CHINNERY, Patrick F, BARRESI, Rita, EAGLE, Michelle, POLVIKOSKI, Tuomo

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Variation in germline mtDNA heteroplasmy is determined prenatally but modified during subsequent transmission von Freyer, Christoph, Cree, Lynsey M, Mourier, Arnaud, Stewart, James B, Koolmeister, Camilla, Milenkovic, Dusanka, Wai, Timothy, Floros, Vasileios I, Hagström, Erik, Chatzidaki, Emmanouella E, Wiesner, Rudolf J, Samuels, David C, Larsson, Nils-Göran, Chinnery, Patrick F

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Pronuclear transfer in human embryos to prevent transmission of mitochondrial DNA disease von Herbert, Mary, Turnbull, Douglass M, Craven, Lyndsey, Tuppen, Helen A, Greggains, Gareth D, Harbottle, Stephen J, Murphy, Julie L, Cree, Lynsey M, Murdoch, Alison P, Chinnery, Patrick F, Taylor, Robert W, Lightowlers, Robert N

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What causes mitochondrial DNA deletions in human cells? von Krishnan, Kim J, Reeve, Amy K, Samuels, David C, Chinnery, Patrick F, Blackwood, John K, Taylor, Robert W, Wanrooij, Sjoerd, Spelbrink, Johannes N, Lightowlers, Robert N, Turnbull, Doug M

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Clearance and transport of amyloid β by peripheral monocytes correlate with Alzheimer’s disease progression von Huang, Xin, Fowler, Chris, Li, Yihan, Li, Qiao-Xin, Sun, Jiaqi, Pan, Yijun, Jin, Liang, Perez, Keyla A., Dubois, Céline, Lim, Yen Y., Drysdale, Candace, Rumble, Rebecca L., Chinnery, Holly R., Rowe, Christopher C., Martins, Ralph N., Maruff, Paul, Doecke, James D., Lin, Yong, Belaidi, Abdel A., Barnham, Kevin J., Masters, Colin L., Gu, Ben J.

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Cell lineage-specific mitochondrial resilience during mammalian organogenesis von Burr, Stephen P., Klimm, Florian, Glynos, Angelos, Prater, Malwina, Sendon, Pamella, Nash, Pavel, Powell, Christopher A., Simard, Marie-Lune, Bonekamp, Nina A., Charl, Julia, Diaz, Hector, Bozhilova, Lyuba V., Nie, Yu, Zhang, Haixin, Frison, Michele, Falkenberg, Maria, Jones, Nick, Minczuk, Michal, Stewart, James B., Chinnery, Patrick F.

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Clinical features and natural history of neuroferritinopathy caused by the FTL1 460InsA mutation von Chinnery, Patrick F., Crompton, Douglas E., Birchall, Daniel, Jackson, Margaret J., Coulthard, Alan, Lombès, Anne, Quinn, Niall, Wills, Adrian, Fletcher, Nicholas, Mottershead, John P., Cooper, Paul, Kellett, Mark, Bates, David, Burn, John

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Clinical Expression of Leber Hereditary Optic Neuropathy Is Affected by the Mitochondrial DNA–Haplogroup Background von Hudson, Gavin, Carelli, Valerio, Spruijt, Liesbeth, Gerards, Mike, Mowbray, Catherine, Achilli, Alessandro, Pyle, Angela, Elson, Joanna, Howell, Neil, La Morgia, Chiara, Valentino, Maria Lucia, Huoponen, Kirsi, Savontaus, Marja-Liisa, Nikoskelainen, Eeva, Sadun, Alfredo A., Salomao, Solange R., Belfort, Rubens, Griffiths, Philip, Man, Patrick Yu Wai, de Coo, Rene F.M., Horvath, Rita, Zeviani, Massimo, Smeets, Hubert J.T., Torroni, Antonio, Chinnery, Patrick F.

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Intravital Imaging of the Human Cornea Reveals the Differential Effects of Season on Innate and Adaptive Immune Cell Morphodynamics von Wu, Mengliang, Zhang, Xinyuan, Karunaratne, Senuri, Lee, Ji-hyun, Lampugnani, Edwin R., Selva, Kevin J., Chung, Amy W., Mueller, Scott N., Chinnery, Holly R., Downie, Laura E.

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The Human Phenotype Ontology in 2017 von Köhler, Sebastian, Vasilevsky, Nicole A, Engelstad, Mark, Foster, Erin, McMurry, Julie, Aymé, Ségolène, Baynam, Gareth, Bello, Susan M, Boerkoel, Cornelius F, Boycott, Kym M, Brudno, Michael, Buske, Orion J, Chinnery, Patrick F, Cipriani, Valentina, Connell, Laureen E, Dawkins, Hugh J S, DeMare, Laura E, Devereau, Andrew D, de Vries, Bert B A, Firth, Helen V, Freson, Kathleen, Greene, Daniel, Hamosh, Ada, Helbig, Ingo, Hum, Courtney, Jähn, Johanna A, James, Roger, Krause, Roland, F Laulederkind, Stanley J, Lochmüller, Hanns, Lyon, Gholson J, Ogishima, Soichi, Olry, Annie, Ouwehand, Willem H, Pontikos, Nikolas, Rath, Ana, Schaefer, Franz, Scott, Richard H, Segal, Michael, Sergouniotis, Panagiotis I, Sever, Richard, Smith, Cynthia L, Straub, Volker, Thompson, Rachel, Turner, Catherine, Turro, Ernest, Veltman, Marijcke W M, Vulliamy, Tom, Yu, Jing, von Ziegenweidt, Julie, Zankl, Andreas, Züchner, Stephan, Zemojtel, Tomasz, Jacobsen, Julius O B, Groza, Tudor, Smedley, Damian, Mungall, Christopher J, Haendel, Melissa, Robinson, Peter N

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The relative contribution of neurocognition and social cognition to 6-month vocational outcomes following Individual Placement and Support in first-episode psychosis von Allott, Kelly A, Cotton, Susan M, Chinnery, Gina L, Baksheev, Gennady N, Massey, Jessica, Sun, Pamela, Collins, Zoe, Barlow, Emma, Broussard, Christina, Wahid, Tasha, Proffitt, Tina-Marie, Jackson, Henry J, Killackey, Eoin

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Mitochondrial DNA and survival after sepsis: a prospective study von Baudouin, Simon V, Saunders, David, Tiangyou, Watcharee, Elson, Joanna L, Poynter, Jayne, Pyle, Angela, Keers, Sharon, Turnbull, Douglass M, Howell, Neil, Chinnery, Patrick F

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Unbiased screen for interactors of leucine-rich repeat kinase 2 supports a common pathway for sporadic and familial Parkinson disease von Beilina, Alexandria, Rudenko, Iakov N., Kaganovich, Alice, Civiero, Laura, Chau, Hien, Kalia, Suneil K., Kalia, Lorraine V., Lobbestael, Evy, Chia, Ruth, Ndukwe, Kelechi, Ding, Jinhui, Nalls, Mike A., Olszewski, Maciej, Hauser, David N., Kumaran, Ravindran, Lozano, Andres M., Baekelandt, Veerle, Greene, Lois E., Taymans, Jean-Marc, Greggio, Elisa, Cookson, Mark R.

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