Linear programming for sizing, Vth and Vdd assignment von Chinnery, D. G., Keutzer, K.

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Closing the gap between ASIC and custom: an ASIC perspective von Chinnery, D G, Keutzer, K

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Closing the power gap between ASIC and custom: an ASIC perspective von Chinnery, D. G., Keutzer, K.

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Achieving 550 MHz in an ASIC methodology von Chinnery, D. G., Nikolic, B., Keutzer, K.

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A functional validation technique: biased-random simulation guided by observability-based coverage von Tasiran, S., Fallah, F., Chinnery, D.G., Weber, S.J., Keutzer, K.

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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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Voltage sensor charge loss accounts for most cases of hypokalemic periodic paralysis von MATTHEWS, E, LABRUM, R, HANNA, M. G, SWEENEY, M. G, SUD, R, HAWORTH, A, CHINNERY, P. F, MEOLA, G, SCHORGE, S, KULLMANN, D. M, DAVIS, M. B

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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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A randomized placebo-controlled trial of idebenone in Leber's hereditary optic neuropathy von Klopstock, Thomas, Yu-Wai-Man, Patrick, Dimitriadis, Konstantinos, Rouleau, Jacinthe, Heck, Suzette, Bailie, Maura, Atawan, Alaa, Chattopadhyay, Sandip, Schubert, Marion, Garip, Aylin, Kernt, Marcus, Petraki, Diana, Rummey, Christian, Leinonen, Mika, Metz, Günther, Griffiths, Philip G., Meier, Thomas, Chinnery, Patrick 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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The Epidemiology of Leber Hereditary Optic Neuropathy in the North East of England von Man, P.Y.W., Griffiths, P.G., Brown, D.T., Howell, N., Turnbull, D.M., Chinnery, P.F.

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LRPPRC and SLIRP synergize to maintain sufficient and orderly mammalian mitochondrial translation von Rubalcava-Gracia, Diana, Bubb, Kristina, Levander, Fredrik, Burr, Stephen P, August, Amelie V, Chinnery, Patrick F, Koolmeister, Camilla, Larsson, Nils-Göran

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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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On the HORYZON: Moderated online social therapy for long-term recovery in first episode psychosis von Alvarez-Jimenez, M, Bendall, S, Lederman, R, Wadley, G, Chinnery, G, Vargas, S, Larkin, M, Killackey, E, McGorry, P.D, Gleeson, J.F

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The human mitochondrial genome contains a second light strand promoter von Tan, Benedict G., Mutti, Christian D., Shi, Yonghong, Xie, Xie, Zhu, Xuefeng, Silva-Pinheiro, Pedro, Menger, Katja E., Díaz-Maldonado, Héctor, Wei, Wei, Nicholls, Thomas J., Chinnery, Patrick F., Minczuk, Michal, Falkenberg, Maria, Gustafsson, Claes M.

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Metabolic effects of bezafibrate in mitochondrial disease von Steele, Hannah, Gomez‐Duran, Aurora, Pyle, Angela, Hopton, Sila, Newman, Jane, Stefanetti, Renae J, Charman, Sarah J, Parikh, Jehill D, He, Langping, Viscomi, Carlo, Jakovljevic, Djordje G, Hollingsworth, Kieren G, Robinson, Alan J, Taylor, Robert W, Bottolo, Leonardo, Horvath, Rita, Chinnery, Patrick F

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Multi-system neurological disease is common in patients with OPA1 mutations von Yu-Wai-Man, P., Griffiths, P.G., Gorman, G.S., Lourenco, C.M., Wright, A.F., Auer-Grumbach, M., Toscano, A., Musumeci, O., Valentino, M.L., Caporali, L., Lamperti, C., Tallaksen, C.M., Duffey, P., Miller, J., Whittaker, R.G., Baker, M.R., Jackson, M.J., Clarke, M.P., Dhillon, B., Czermin, B., Stewart, J.D., Hudson, G., Reynier, P., Bonneau, D., Marques, W., Lenaers, G., McFarland, R., Taylor, R.W., Turnbull, D.M., Votruba, M., Zeviani, M., Carelli, V., Bindoff, L.A., Horvath, R., Amati-Bonneau, P., Chinnery, P.F.

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Mutation of OPA1 causes dominant optic atrophy with external ophthalmoplegia, ataxia, deafness and multiple mitochondrial DNA deletions: a novel disorder of mtDNA maintenance von Hudson, Gavin, Amati-Bonneau, Patrizia, Blakely, Emma L., Stewart, Joanna D., He, Langping, Schaefer, Andrew M., Griffiths, Philip G., Ahlqvist, Kati, Suomalainen, Anu, Reynier, Pascal, McFarland, Robert, Turnbull, Douglass M., Chinnery, Patrick F., Taylor, Robert W.

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Chronic pain is common in mitochondrial disease von van den Ameele, Jelle, Fuge, Joshua, Pitceathly, Robert D.S., Berry, Sarah, McIntyre, Zoe, Hanna, Michael G., Lee, Michael, Chinnery, Patrick F.

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THE MINIMUM PREVALENCE OF CADASIL IN NORTHEAST ENGLAND von NARAYAN, S. K, GORMAN, G, KALARIA, R. N, FORD, G. A, CHINNERY, P. F

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