A citation-based method for searching scientific literature

Alfred K Yu, Lanying Song, Karl D Murray, Deborah van der List, Chao Sun, Yan Shen, Zhengui Xia, Gino A Cortopassi. Hum Mol Genet 2015
Times Cited: 28







List of co-cited articles
95 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Mice with mitochondrial complex I deficiency develop a fatal encephalomyopathy.
Shane E Kruse, William C Watt, David J Marcinek, Raj P Kapur, Kenneth A Schenkman, Richard D Palmiter. Cell Metab 2008
222
42

Bipolar cell reduction precedes retinal ganglion neuron loss in a complex 1 knockout mouse model.
Lanying Song, Alfred Yu, Karl Murray, Gino Cortopassi. Brain Res 2017
11
72

Complex I deficiency due to loss of Ndufs4 in the brain results in progressive encephalopathy resembling Leigh syndrome.
Albert Quintana, Shane E Kruse, Raj P Kapur, Elisenda Sanz, Richard D Palmiter. Proc Natl Acad Sci U S A 2010
134
21

mTOR inhibition alleviates mitochondrial disease in a mouse model of Leigh syndrome.
Simon C Johnson, Melana E Yanos, Ernst-Bernhard Kayser, Albert Quintana, Maya Sangesland, Anthony Castanza, Lauren Uhde, Jessica Hui, Valerie Z Wall, Arni Gagnidze,[...]. Science 2013
281
17

Mitochondrial dysfunction as a cause of optic neuropathies.
Valerio Carelli, Fred N Ross-Cisneros, Alfredo A Sadun. Prog Retin Eye Res 2004
510
17

Mouse mtDNA mutant model of Leber hereditary optic neuropathy.
Chun Shi Lin, Mark S Sharpley, Weiwei Fan, Katrina G Waymire, Alfredo A Sadun, Valerio Carelli, Fred N Ross-Cisneros, Peter Baciu, Eric Sung, Meagan J McManus,[...]. Proc Natl Acad Sci U S A 2012
115
17

Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy.
D C Wallace, G Singh, M T Lott, J A Hodge, T G Schurr, A M Lezza, L J Elsas, E K Nikoskelainen. Science 1988
17

Fatal breathing dysfunction in a mouse model of Leigh syndrome.
Albert Quintana, Sebastien Zanella, Henner Koch, Shane E Kruse, Donghoon Lee, Jan M Ramirez, Richard D Palmiter. J Clin Invest 2012
58
14

Retinal ganglion cell neurodegeneration in mitochondrial inherited disorders.
Valerio Carelli, Chiara La Morgia, Maria Lucia Valentino, Piero Barboni, Fred N Ross-Cisneros, Alfredo A Sadun. Biochim Biophys Acta 2009
141
14

OXPHOS mutations and neurodegeneration.
Werner J H Koopman, Felix Distelmaier, Jan A M Smeitink, Peter H G M Willems. EMBO J 2013
161
10

Glial lipid droplets and ROS induced by mitochondrial defects promote neurodegeneration.
Lucy Liu, Ke Zhang, Hector Sandoval, Shinya Yamamoto, Manish Jaiswal, Elisenda Sanz, Zhihong Li, Jessica Hui, Brett H Graham, Albert Quintana,[...]. Cell 2015
319
10

Cells bearing mutations causing Leber's hereditary optic neuropathy are sensitized to Fas-Induced apoptosis.
Steven R Danielson, Alice Wong, Valerio Carelli, Andrea Martinuzzi, Anthony H V Schapira, Gino A Cortopassi. J Biol Chem 2002
97
10

Efficient mitochondrial biogenesis drives incomplete penetrance in Leber's hereditary optic neuropathy.
Carla Giordano, Luisa Iommarini, Luca Giordano, Alessandra Maresca, Annalinda Pisano, Maria Lucia Valentino, Leonardo Caporali, Rocco Liguori, Stefania Deceglie, Marina Roberti,[...]. Brain 2014
156
10

Hypoxia as a therapy for mitochondrial disease.
Isha H Jain, Luca Zazzeron, Rahul Goli, Kristen Alexa, Stephanie Schatzman-Bone, Harveen Dhillon, Olga Goldberger, Jun Peng, Ophir Shalem, Neville E Sanjana,[...]. Science 2016
206
10

Leigh syndrome: One disorder, more than 75 monogenic causes.
Nicole J Lake, Alison G Compton, Shamima Rahman, David R Thorburn. Ann Neurol 2016
186
10

Hypoxia treatment reverses neurodegenerative disease in a mouse model of Leigh syndrome.
Michele Ferrari, Isha H Jain, Olga Goldberger, Emanuele Rezoagli, Robrecht Thoonen, Kai-Hung Cheng, David E Sosnovik, Marielle Scherrer-Crosbie, Vamsi K Mootha, Warren M Zapol. Proc Natl Acad Sci U S A 2017
64
10

Prevalence of nuclear and mitochondrial DNA mutations related to adult mitochondrial disease.
Gráinne S Gorman, Andrew M Schaefer, Yi Ng, Nicholas Gomez, Emma L Blakely, Charlotte L Alston, Catherine Feeney, Rita Horvath, Patrick Yu-Wai-Man, Patrick F Chinnery,[...]. Ann Neurol 2015
375
10

Emerging Mitochondrial Therapeutic Targets in Optic Neuropathies.
M I G Lopez Sanchez, J G Crowston, D A Mackey, I A Trounce. Pharmacol Ther 2016
41
10

Oestrogens ameliorate mitochondrial dysfunction in Leber's hereditary optic neuropathy.
Carla Giordano, Monica Montopoli, Elena Perli, Maurizia Orlandi, Marianna Fantin, Fred N Ross-Cisneros, Laura Caparrotta, Andrea Martinuzzi, Eugenio Ragazzi, Anna Ghelli,[...]. Brain 2011
144
10

LHON: Mitochondrial Mutations and More.
E Kirches. Curr Genomics 2011
54
10

Leber hereditary optic neuropathy: current perspectives.
Cherise Meyerson, Greg Van Stavern, Collin McClelland. Clin Ophthalmol 2015
81
10


Rescue of cell death and inflammation of a mouse model of complex 1-mediated vision loss by repurposed drug molecules.
Alfred K Yu, Sandipan Datta, Marissa Z McMackin, Gino A Cortopassi. Hum Mol Genet 2017
9
33

Leber Hereditary Optic Neuropathy: Exemplar of an mtDNA Disease.
Douglas C Wallace, Marie T Lott. Handb Exp Pharmacol 2017
24
12

Biochemical diagnosis of mitochondrial disorders.
Richard J T Rodenburg. J Inherit Metab Dis 2011
124
7

Cellular and animal models for mitochondrial complex I deficiency: a focus on the NDUFS4 subunit.
Megan E Breuer, Peter H G M Willems, Jan A M Smeitink, Werner J H Koopman, Marco Nooteboom. IUBMB Life 2013
27
7

A guide to diagnosis and treatment of Leigh syndrome.
Fabian Baertling, Richard J Rodenburg, Jörg Schaper, Jan A Smeitink, Werner J H Koopman, Ertan Mayatepek, Eva Morava, Felix Distelmaier. J Neurol Neurosurg Psychiatry 2014
97
7

Leigh syndrome: clinical features and biochemical and DNA abnormalities.
S Rahman, R B Blok, H H Dahl, D M Danks, D M Kirby, C W Chow, J Christodoulou, D R Thorburn. Ann Neurol 1996
508
7

The genetics and pathology of oxidative phosphorylation.
J Smeitink, L van den Heuvel, S DiMauro. Nat Rev Genet 2001
467
7

Oxidized mitochondrial DNA activates the NLRP3 inflammasome during apoptosis.
Kenichi Shimada, Timothy R Crother, Justin Karlin, Jargalsaikhan Dagvadorj, Norika Chiba, Shuang Chen, V Krishnan Ramanujan, Andrea J Wolf, Laurent Vergnes, David M Ojcius,[...]. Immunity 2012
7


Mechanisms of NOD-like receptor-associated inflammasome activation.
Haitao Wen, Edward A Miao, Jenny P-Y Ting. Immunity 2013
250
7

Autophagy proteins regulate innate immune responses by inhibiting the release of mitochondrial DNA mediated by the NALP3 inflammasome.
Kiichi Nakahira, Jeffrey Adam Haspel, Vijay A K Rathinam, Seon-Jin Lee, Tamas Dolinay, Hilaire C Lam, Joshua A Englert, Marlene Rabinovitch, Manuela Cernadas, Hong Pyo Kim,[...]. Nat Immunol 2011
7

Necroptosis and its role in inflammation.
Manolis Pasparakis, Peter Vandenabeele. Nature 2015
855
7

The retina as a window to the brain-from eye research to CNS disorders.
Anat London, Inbal Benhar, Michal Schwartz. Nat Rev Neurol 2013
390
7

A neurodegenerative perspective on mitochondrial optic neuropathies.
Patrick Yu-Wai-Man, Marcela Votruba, Florence Burté, Chiara La Morgia, Piero Barboni, Valerio Carelli. Acta Neuropathol 2016
71
7

The retina as an early biomarker of neurodegeneration in a rotenone-induced model of Parkinson's disease: evidence for a neuroprotective effect of rosiglitazone in the eye and brain.
Eduardo Maria Normando, Benjamin Michael Davis, Lies De Groef, Shereen Nizari, Lisa A Turner, Nivedita Ravindran, Milena Pahlitzsch, Jonathan Brenton, Giulia Malaguarnera, Li Guo,[...]. Acta Neuropathol Commun 2016
52
7

Antioxidant defences in cybrids harboring mtDNA mutations associated with Leber's hereditary optic neuropathy.
Maura Floreani, Eleonora Napoli, Andrea Martinuzzi, Giorgia Pantano, Valentina De Riva, Roberta Trevisan, Elena Bisetto, Lucia Valente, Valerio Carelli, Federica Dabbeni-Sala. FEBS J 2005
76
7

Long-term in vivo imaging and measurement of dendritic shrinkage of retinal ganglion cells.
Christopher Kai-shun Leung, Robert N Weinreb, Zhi Wei Li, Shu Liu, James D Lindsey, Nathan Choi, Lan Liu, Carol Yim-lui Cheung, Cong Ye, Kunliang Qiu,[...]. Invest Ophthalmol Vis Sci 2011
79
7

Leber hereditary optic neuropathy mtDNA mutations disrupt glutamate transport in cybrid cell lines.
Simone Beretta, Laura Mattavelli, Gessica Sala, Lucio Tremolizzo, Anthony H V Schapira, Andrea Martinuzzi, Valerio Carelli, Carlo Ferrarese. Brain 2004
91
7

Differentiation-specific effects of LHON mutations introduced into neuronal NT2 cells.
Alice Wong, Lucia Cavelier, Heather E Collins-Schramm, Michael F Seldin, Michael McGrogan, Marja-Liisa Savontaus, Gino A Cortopassi. Hum Mol Genet 2002
144
7


Opa1 overexpression ameliorates the phenotype of two mitochondrial disease mouse models.
Gabriele Civiletto, Tatiana Varanita, Raffaele Cerutti, Tatiana Gorletta, Serena Barbaro, Silvia Marchet, Costanza Lamperti, Carlo Viscomi, Luca Scorrano, Massimo Zeviani. Cell Metab 2015
134
7

Emerging concepts in the therapy of mitochondrial disease.
Carlo Viscomi, Emanuela Bottani, Massimo Zeviani. Biochim Biophys Acta 2015
65
7

NAD(+)-dependent activation of Sirt1 corrects the phenotype in a mouse model of mitochondrial disease.
Raffaele Cerutti, Eija Pirinen, Costanza Lamperti, Silvia Marchet, Anthony A Sauve, Wei Li, Valerio Leoni, Eric A Schon, Françoise Dantzer, Johan Auwerx,[...]. Cell Metab 2014
201
7

Dose-dependent effects of mTOR inhibition on weight and mitochondrial disease in mice.
Simon C Johnson, Melana E Yanos, Alessandro Bitto, Anthony Castanza, Arni Gagnidze, Brenda Gonzalez, Kanav Gupta, Jessica Hui, Conner Jarvie, Brittany M Johnson,[...]. Front Genet 2015
42
7

NIH Image to ImageJ: 25 years of image analysis.
Caroline A Schneider, Wayne S Rasband, Kevin W Eliceiri. Nat Methods 2012
7

OXPHOS gene expression and control in mitochondrial disorders.
Fimmie Reinecke, Jan A M Smeitink, Francois H van der Westhuizen. Biochim Biophys Acta 2009
84
7

Mutations causing mitochondrial disease: What is new and what challenges remain?
Robert N Lightowlers, Robert W Taylor, Doug M Turnbull. Science 2015
166
7

In vivo correction of COX deficiency by activation of the AMPK/PGC-1α axis.
Carlo Viscomi, Emanuela Bottani, Gabriele Civiletto, Raffaele Cerutti, Maurizio Moggio, Gigliola Fagiolari, Eric A Schon, Costanza Lamperti, Massimo Zeviani. Cell Metab 2011
192
7


Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.