A citation-based method for searching scientific literature

Oliver M Russell, Gráinne S Gorman, Robert N Lightowlers, Doug M Turnbull. Cell 2020
Times Cited: 96







List of co-cited articles
1299 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Mitochondrial diseases.
Gráinne S Gorman, Patrick F Chinnery, Salvatore DiMauro, Michio Hirano, Yasutoshi Koga, Robert McFarland, Anu Suomalainen, David R Thorburn, Massimo Zeviani, Douglass M Turnbull. Nat Rev Dis Primers 2016
552
38

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
446
23

A bacterial cytidine deaminase toxin enables CRISPR-free mitochondrial base editing.
Beverly Y Mok, Marcos H de Moraes, Jun Zeng, Dustin E Bosch, Anna V Kotrys, Aditya Raguram, FoSheng Hsu, Matthew C Radey, S Brook Peterson, Vamsi K Mootha,[...]. Nature 2020
187
18

Recent advances in understanding the molecular genetic basis of mitochondrial disease.
Kyle Thompson, Jack J Collier, Ruth I C Glasgow, Fiona M Robertson, Angela Pyle, Emma L Blakely, Charlotte L Alston, Monika Oláhová, Robert McFarland, Robert W Taylor. J Inherit Metab Dis 2020
69
24

Mitochondrial diseases: the contribution of organelle stress responses to pathology.
Anu Suomalainen, Brendan J Battersby. Nat Rev Mol Cell Biol 2018
209
15

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
323
15


MitoTALEN reduces mutant mtDNA load and restores tRNAAla levels in a mouse model of heteroplasmic mtDNA mutation.
Sandra R Bacman, Johanna H K Kauppila, Claudia V Pereira, Nadee Nissanka, Maria Miranda, Milena Pinto, Sion L Williams, Nils-Göran Larsson, James B Stewart, Carlos T Moraes. Nat Med 2018
110
14

Genetics of mitochondrial diseases: Identifying mutations to help diagnosis.
Sarah L Stenton, Holger Prokisch. EBioMedicine 2020
52
25

mtDNA heteroplasmy level and copy number indicate disease burden in m.3243A>G mitochondrial disease.
John P Grady, Sarah J Pickett, Yi Shiau Ng, Charlotte L Alston, Emma L Blakely, Steven A Hardy, Catherine L Feeney, Alexandra A Bright, Andrew M Schaefer, Gráinne S Gorman,[...]. EMBO Mol Med 2018
115
13

Genome editing in mitochondria corrects a pathogenic mtDNA mutation in vivo.
Payam A Gammage, Carlo Viscomi, Marie-Lune Simard, Ana S H Costa, Edoardo Gaude, Christopher A Powell, Lindsey Van Haute, Beverly J McCann, Pedro Rebelo-Guiomar, Raffaele Cerutti,[...]. Nat Med 2018
125
12

Leigh syndrome: One disorder, more than 75 monogenic causes.
Nicole J Lake, Alison G Compton, Shamima Rahman, David R Thorburn. Ann Neurol 2016
233
12

Sequence and organization of the human mitochondrial genome.
S Anderson, A T Bankier, B G Barrell, M H de Bruijn, A R Coulson, J Drouin, I C Eperon, D P Nierlich, B A Roe, F Sanger,[...]. Nature 1981
12

Mitochondrial energy generation disorders: genes, mechanisms, and clues to pathology.
Ann E Frazier, David R Thorburn, Alison G Compton. J Biol Chem 2019
110
11


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
237
11


Alleviation of neuronal energy deficiency by mTOR inhibition as a treatment for mitochondria-related neurodegeneration.
Xinde Zheng, Leah Boyer, Mingji Jin, Yongsung Kim, Weiwei Fan, Cedric Bardy, Travis Berggren, Ronald M Evans, Fred H Gage, Tony Hunter. Elife 2016
78
12


A randomized placebo-controlled trial of idebenone in Leber's hereditary optic neuropathy.
Thomas Klopstock, Patrick Yu-Wai-Man, Konstantinos Dimitriadis, Jacinthe Rouleau, Suzette Heck, Maura Bailie, Alaa Atawan, Sandip Chattopadhyay, Marion Schubert, Aylin Garip,[...]. Brain 2011
275
10

Mitochondrially targeted ZFNs for selective degradation of pathogenic mitochondrial genomes bearing large-scale deletions or point mutations.
Payam A Gammage, Joanna Rorbach, Anna I Vincent, Edward J Rebar, Michal Minczuk. EMBO Mol Med 2014
154
10

Mitochondrial DNA mutations in human disease.
Robert W Taylor, Doug M Turnbull. Nat Rev Genet 2005
10

Specific elimination of mutant mitochondrial genomes in patient-derived cells by mitoTALENs.
Sandra R Bacman, Siôn L Williams, Milena Pinto, Susana Peralta, Carlos T Moraes. Nat Med 2013
234
10

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
10

MitoCarta3.0: an updated mitochondrial proteome now with sub-organelle localization and pathway annotations.
Sneha Rath, Rohit Sharma, Rahul Gupta, Tslil Ast, Connie Chan, Timothy J Durham, Russell P Goodman, Zenon Grabarek, Mary E Haas, Wendy H W Hung,[...]. Nucleic Acids Res 2021
157
10

Metabolic rescue in pluripotent cells from patients with mtDNA disease.
Hong Ma, Clifford D L Folmes, Jun Wu, Robert Morey, Sergio Mora-Castilla, Alejandro Ocampo, Li Ma, Joanna Poulton, Xinjian Wang, Riffat Ahmed,[...]. Nature 2015
120
9

Strategies for fighting mitochondrial diseases.
C Viscomi, M Zeviani. J Intern Med 2020
28
32

Mitochondrial disease in children.
S Rahman. J Intern Med 2020
35
25

The multifaceted contributions of mitochondria to cellular metabolism.
Jessica B Spinelli, Marcia C Haigis. Nat Cell Biol 2018
416
9

mTORC1 Regulates Mitochondrial Integrated Stress Response and Mitochondrial Myopathy Progression.
Nahid A Khan, Joni Nikkanen, Shuichi Yatsuga, Christopher Jackson, Liya Wang, Swagat Pradhan, Riikka Kivelä, Alberto Pessia, Vidya Velagapudi, Anu Suomalainen. Cell Metab 2017
181
9

Mitochondrial genetic medicine.
Douglas C Wallace. Nat Genet 2018
121
9

Maintenance and Expression of Mammalian Mitochondrial DNA.
Claes M Gustafsson, Maria Falkenberg, Nils-Göran Larsson. Annu Rev Biochem 2016
298
8

Mitochondrial Genome Engineering: The Revolution May Not Be CRISPR-Ized.
Payam A Gammage, Carlos T Moraes, Michal Minczuk. Trends Genet 2018
126
8

Recent Advances in Mitochondrial Disease.
Lyndsey Craven, Charlotte L Alston, Robert W Taylor, Doug M Turnbull. Annu Rev Genomics Hum Genet 2017
133
8

Leigh Syndrome Mouse Model Can Be Rescued by Interventions that Normalize Brain Hyperoxia, but Not HIF Activation.
Isha H Jain, Luca Zazzeron, Olga Goldberger, Eizo Marutani, Gregory R Wojtkiewicz, Tslil Ast, Hong Wang, Grigorij Schleifer, Anna Stepanova, Kathleen Brepoels,[...]. Cell Metab 2019
43
18

Rapamycin rescues mitochondrial myopathy via coordinated activation of autophagy and lysosomal biogenesis.
Gabriele Civiletto, Sukru Anil Dogan, Raffaele Cerutti, Gigliola Fagiolari, Maurizio Moggio, Costanza Lamperti, Cristiane Benincá, Carlo Viscomi, Massimo Zeviani. EMBO Mol Med 2018
49
16

Towards clinical application of pronuclear transfer to prevent mitochondrial DNA disease.
Louise A Hyslop, Paul Blakeley, Lyndsey Craven, Jessica Richardson, Norah M E Fogarty, Elpida Fragouli, Mahdi Lamb, Sissy E Wamaitha, Nilendran Prathalingam, Qi Zhang,[...]. Nature 2016
171
8

Bilateral visual improvement with unilateral gene therapy injection for Leber hereditary optic neuropathy.
Patrick Yu-Wai-Man, Nancy J Newman, Valerio Carelli, Mark L Moster, Valerie Biousse, Alfredo A Sadun, Thomas Klopstock, Catherine Vignal-Clermont, Robert C Sergott, Günther Rudolph,[...]. Sci Transl Med 2020
47
17

Biparental Inheritance of Mitochondrial DNA in Humans.
Shiyu Luo, C Alexander Valencia, Jinglan Zhang, Ni-Chung Lee, Jesse Slone, Baoheng Gui, Xinjian Wang, Zhuo Li, Sarah Dell, Jenice Brown,[...]. Proc Natl Acad Sci U S A 2018
159
8

Phenotypic heterogeneity in m.3243A>G mitochondrial disease: The role of nuclear factors.
Sarah J Pickett, John P Grady, Yi Shiau Ng, Gráinne S Gorman, Andrew M Schaefer, Ian J Wilson, Heather J Cordell, Doug M Turnbull, Robert W Taylor, Robert McFarland. Ann Clin Transl Neurol 2018
55
14

Maintenance and propagation of a deleterious mitochondrial genome by the mitochondrial unfolded protein response.
Yi-Fan Lin, Anna M Schulz, Mark W Pellegrino, Yun Lu, Shai Shaham, Cole M Haynes. Nature 2016
156
8

Tissue- and cell-type-specific manifestations of heteroplasmic mtDNA 3243A>G mutation in human induced pluripotent stem cell-derived disease model.
Riikka H Hämäläinen, Tuula Manninen, Hanna Koivumäki, Mikhail Kislin, Timo Otonkoski, Anu Suomalainen. Proc Natl Acad Sci U S A 2013
137
7

The Origin and Diversification of Mitochondria.
Andrew J Roger, Sergio A Muñoz-Gómez, Ryoma Kamikawa. Curr Biol 2017
341
7

Treatment for mitochondrial disorders.
Gerald Pfeffer, Kari Majamaa, Douglass M Turnbull, David Thorburn, Patrick F Chinnery. Cochrane Database Syst Rev 2012
224
7


De novo mtDNA point mutations are common and have a low recurrence risk.
Suzanne C E H Sallevelt, Christine E M de Die-Smulders, Alexandra T M Hendrickx, Debby M E I Hellebrekers, Irenaeus F M de Coo, Charlotte L Alston, Charlotte Knowles, Robert W Taylor, Robert McFarland, Hubert J M Smeets. J Med Genet 2017
36
19

Mitochondrial medicine in the omics era.
Joyeeta Rahman, Shamima Rahman. Lancet 2018
111
7

Live birth derived from oocyte spindle transfer to prevent mitochondrial disease.
John Zhang, Hui Liu, Shiyu Luo, Zhuo Lu, Alejandro Chávez-Badiola, Zitao Liu, Mingxue Yang, Zaher Merhi, Sherman J Silber, Santiago Munné,[...]. Reprod Biomed Online 2017
135
7

Deoxynucleoside Therapy for Thymidine Kinase 2-Deficient Myopathy.
Cristina Domínguez-González, Marcos Madruga-Garrido, Fabiola Mavillard, Caterina Garone, Francisco Javier Aguirre-Rodríguez, M Alice Donati, Karin Kleinsteuber, Itxaso Martí, Elena Martín-Hernández, Juan P Morealejo-Aycinena,[...]. Ann Neurol 2019
44
15

Mitochondrial donation: from test tube to clinic.
Gráinne S Gorman, Robert McFarland, Jane Stewart, Catherine Feeney, Doug M Turnbull. Lancet 2018
16
43


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.