A citation-based method for searching scientific literature

Maria Pilar Bayona-Bafaluy, Bas Blits, Brendan J Battersby, Eric A Shoubridge, Carlos T Moraes. Proc Natl Acad Sci U S A 2005
Times Cited: 104







List of co-cited articles
1414 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


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
230
43

Gene therapy for mitochondrial disease by delivering restriction endonuclease SmaI into mitochondria.
Masashi Tanaka, Harm-Jan Borgeld, Jin Zhang, Shin-ichi Muramatsu, Jian-Sheng Gong, Makoto Yoneda, Wakako Maruyama, Makoto Naoi, Tohru Ibi, Ko Sahashi,[...]. J Biomed Sci 2002
138
40


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
150
38


Development of a single-chain, quasi-dimeric zinc-finger nuclease for the selective degradation of mutated human mitochondrial DNA.
Michal Minczuk, Monika A Papworth, Jeffrey C Miller, Michael P Murphy, Aaron Klug. Nucleic Acids Res 2008
121
36


Sequence-specific modification of mitochondrial DNA using a chimeric zinc finger methylase.
Michal Minczuk, Monika A Papworth, Paulina Kolasinska, Michael P Murphy, Aaron Klug. Proc Natl Acad Sci U S A 2006
102
32

Selective elimination of mutant mitochondrial genomes as therapeutic strategy for the treatment of NARP and MILS syndromes.
M F Alexeyev, N Venediktova, V Pastukh, I Shokolenko, G Bonilla, G L Wilson. Gene Ther 2008
60
46


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
26

Selective elimination of mitochondrial mutations in the germline by genome editing.
Pradeep Reddy, Alejandro Ocampo, Keiichiro Suzuki, Jinping Luo, Sandra R Bacman, Sion L Williams, Atsushi Sugawara, Daiji Okamura, Yuji Tsunekawa, Jun Wu,[...]. Cell 2015
161
26

MitoTALEN: A General Approach to Reduce Mutant mtDNA Loads and Restore Oxidative Phosphorylation Function in Mitochondrial Diseases.
Masami Hashimoto, Sandra R Bacman, Susana Peralta, Marni J Falk, Anne Chomyn, David C Chan, Sion L Williams, Carlos T Moraes. Mol Ther 2015
92
27

Rescue of a deficiency in ATP synthesis by transfer of MTATP6, a mitochondrial DNA-encoded gene, to the nucleus.
Giovanni Manfredi, Jin Fu, Joseline Ojaimi, James E Sadlock, Jennifer Q Kwong, John Guy, Eric A Schon. Nat Genet 2002
189
20

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
440
20

Mitochondrial Genome Engineering: The Revolution May Not Be CRISPR-Ized.
Payam A Gammage, Carlos T Moraes, Michal Minczuk. Trends Genet 2018
122
20

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
123
19


Rescue of a mitochondrial deficiency causing Leber Hereditary Optic Neuropathy.
John Guy, Xiaoping Qi, Francesco Pallotti, Eric A Schon, Giovanni Manfredi, Valerio Carelli, Andrea Martinuzzi, William W Hauswirth, Alfred S Lewin. Ann Neurol 2002
180
18

Selective inhibition of mutant human mitochondrial DNA replication in vitro by peptide nucleic acids.
R W Taylor, P F Chinnery, D M Turnbull, R N Lightowlers. Nat Genet 1997
177
18

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
107
18

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
16

A new mitochondrial disease associated with mitochondrial DNA heteroplasmy.
I J Holt, A E Harding, R K Petty, J A Morgan-Hughes. Am J Hum Genet 1990
808
16

Optimized allotopic expression of the human mitochondrial ND4 prevents blindness in a rat model of mitochondrial dysfunction.
Sami Ellouze, Sébastien Augustin, Aicha Bouaita, Crystel Bonnet, Manuel Simonutti, Valérie Forster, Serge Picaud, Jose-Alain Sahel, Marisol Corral-Debrinski. Am J Hum Genet 2008
144
16

Premature ageing in mice expressing defective mitochondrial DNA polymerase.
Aleksandra Trifunovic, Anna Wredenberg, Maria Falkenberg, Johannes N Spelbrink, Anja T Rovio, Carl E Bruder, Mohammad Bohlooly-Y, Sebastian Gidlöf, Anders Oldfors, Rolf Wibom,[...]. Nature 2004
15

Efficient Mitochondrial Genome Editing by CRISPR/Cas9.
Areum Jo, Sangwoo Ham, Gum Hwa Lee, Yun-Il Lee, SangSeong Kim, Yun-Song Lee, Joo-Ho Shin, Yunjong Lee. Biomed Res Int 2015
107
15

Near-complete elimination of mutant mtDNA by iterative or dynamic dose-controlled treatment with mtZFNs.
Payam A Gammage, Edoardo Gaude, Lindsey Van Haute, Pedro Rebelo-Guiomar, Christopher B Jackson, Joanna Rorbach, Marcin L Pekalski, Alan J Robinson, Marine Charpentier, Jean-Paul Concordet,[...]. Nucleic Acids Res 2016
56
26

Linear mitochondrial DNA is rapidly degraded by components of the replication machinery.
Viktoriya Peeva, Daniel Blei, Genevieve Trombly, Sarah Corsi, Maciej J Szukszto, Pedro Rebelo-Guiomar, Payam A Gammage, Alexei P Kudin, Christian Becker, Janine Altmüller,[...]. Nat Commun 2018
72
20

Generation of mice with mitochondrial dysfunction by introducing mouse mtDNA carrying a deletion into zygotes.
K Inoue, K Nakada, A Ogura, K Isobe, Y Goto, I Nonaka, J I Hayashi. Nat Genet 2000
298
14


Tissue-specific selection for different mtDNA genotypes in heteroplasmic mice.
J P Jenuth, A C Peterson, E A Shoubridge. Nat Genet 1997
290
14

Mitochondrial threshold effects.
Rodrigue Rossignol, Benjamin Faustin, Christophe Rocher, Monique Malgat, Jean-Pierre Mazat, Thierry Letellier. Biochem J 2003
484
14



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
543
14

Limitations of allotopic expression of mitochondrial genes in mammalian cells.
Jose Oca-Cossio, Lesley Kenyon, Huiling Hao, Carlos T Moraes. Genetics 2003
71
18

Mitochondrial DNA mutations, oxidative stress, and apoptosis in mammalian aging.
G C Kujoth, A Hiona, T D Pugh, S Someya, K Panzer, S E Wohlgemuth, T Hofer, A Y Seo, R Sullivan, W A Jobling,[...]. Science 2005
13

Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation.
J M Shoffner, M T Lott, A M Lezza, P Seibel, S W Ballinger, D C Wallace. Cell 1990
13


Mitochondrial DNA mutations in human disease.
Robert W Taylor, Doug M Turnbull. Nat Rev Genet 2005
13

A mouse model of mitochondrial disease reveals germline selection against severe mtDNA mutations.
Weiwei Fan, Katrina G Waymire, Navneet Narula, Peng Li, Christophe Rocher, Pinar E Coskun, Mani A Vannan, Jagat Narula, Grant R Macgregor, Douglas C Wallace. Science 2008
311
13

Ketogenic treatment reduces deleted mitochondrial DNAs in cultured human cells.
Sumana Santra, Robert W Gilkerson, Mercy Davidson, Eric A Schon. Ann Neurol 2004
104
13


Construction and testing of engineered zinc-finger proteins for sequence-specific modification of mtDNA.
Michal Minczuk, Paulina Kolasinska-Zwierz, Michael P Murphy, Monika A Papworth. Nat Protoc 2010
37
35

mitoTev-TALE: a monomeric DNA editing enzyme to reduce mutant mitochondrial DNA levels.
Claudia V Pereira, Sandra R Bacman, Tania Arguello, Ugne Zekonyte, Sion L Williams, David R Edgell, Carlos T Moraes. EMBO Mol Med 2018
37
35

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
177
13

High levels of mitochondrial DNA deletions in substantia nigra neurons in aging and Parkinson disease.
Andreas Bender, Kim J Krishnan, Christopher M Morris, Geoffrey A Taylor, Amy K Reeve, Robert H Perry, Evelyn Jaros, Joshua S Hersheson, Joanne Betts, Thomas Klopstock,[...]. Nat Genet 2006
12

A direct repeat is a hotspot for large-scale deletion of human mitochondrial DNA.
E A Schon, R Rizzuto, C T Moraes, H Nakase, M Zeviani, S DiMauro. Science 1989
498
12

Mitochondrial gene replacement in primate offspring and embryonic stem cells.
Masahito Tachibana, Michelle Sparman, Hathaitip Sritanaudomchai, Hong Ma, Lisa Clepper, Joy Woodward, Ying Li, Cathy Ramsey, Olena Kolotushkina, Shoukhrat Mitalipov. Nature 2009
343
12

Allotopic expression of mitochondrial-encoded genes in mammals: achieved goal, undemonstrated mechanism or impossible task?
Ester Perales-Clemente, Patricio Fernández-Silva, Rebeca Acín-Pérez, Acisclo Pérez-Martos, Jose Antonio Enríquez. Nucleic Acids Res 2011
159
12


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.