A citation-based method for searching scientific literature

K Inoue, K Nakada, A Ogura, K Isobe, Y Goto, I Nonaka, J I Hayashi. Nat Genet 2000
Times Cited: 291







List of co-cited articles
1085 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


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
43

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
31

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
300
26


Mitochondrial DNA mutations in human disease.
Robert W Taylor, Doug M Turnbull. Nat Rev Genet 2005
21



Strong purifying selection in transmission of mammalian mitochondrial DNA.
James Bruce Stewart, Christoph Freyer, Joanna L Elson, Anna Wredenberg, Zekiye Cansu, Aleksandra Trifunovic, Nils-Göran Larsson. PLoS Biol 2008
323
18

Mutant mitochondrial helicase Twinkle causes multiple mtDNA deletions and a late-onset mitochondrial disease in mice.
Henna Tyynismaa, Katja Peltola Mjosund, Sjoerd Wanrooij, Ilse Lappalainen, Emil Ylikallio, Anu Jalanko, Johannes N Spelbrink, Anders Paetau, Anu Suomalainen. Proc Natl Acad Sci U S A 2005
219
17

Generation of trans-mitochondrial mice carrying homoplasmic mtDNAs with a missense mutation in a structural gene using ES cells.
Atsuko Kasahara, Kaori Ishikawa, Makiko Yamaoka, Masahito Ito, Naoki Watanabe, Miho Akimoto, Akitsugu Sato, Kazuto Nakada, Hitoshi Endo, Yoko Suda,[...]. Hum Mol Genet 2006
47
36

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
16


Transmitochondrial mice as models for primary prevention of diseases caused by mutation in the tRNA(Lys) gene.
Akinori Shimizu, Takayuki Mito, Chisato Hayashi, Emi Ogasawara, Ryusuke Koba, Issei Negishi, Keizo Takenaga, Kazuto Nakada, Jun-Ichi Hayashi. Proc Natl Acad Sci U S A 2014
29
55



Generation of trans-mitochondrial mito-mice by the introduction of a pathogenic G13997A mtDNA from highly metastatic lung carcinoma cells.
Mutsumi Yokota, Hiroshi Shitara, Osamu Hashizume, Kaori Ishikawa, Kazuto Nakada, Rie Ishii, Choji Taya, Keizo Takenaga, Hiromichi Yonekawa, Jun-Ichi Hayashi. FEBS Lett 2010
26
57

Specific mitochondrial DNA mutation in mice regulates diabetes and lymphoma development.
Osamu Hashizume, Akinori Shimizu, Mutsumi Yokota, Atsuko Sugiyama, Kazuto Nakada, Hiroyuki Miyoshi, Makiko Itami, Miki Ohira, Hiroki Nagase, Keizo Takenaga,[...]. Proc Natl Acad Sci U S A 2012
47
31

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
117
15

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
14

A reduction of mitochondrial DNA molecules during embryogenesis explains the rapid segregation of genotypes.
Lynsey M Cree, David C Samuels, Susana Chuva de Sousa Lopes, Harsha Karur Rajasimha, Passorn Wonnapinij, Jeffrey R Mann, Hans-Henrik M Dahl, Patrick F Chinnery. Nat Genet 2008
317
14

Somatic mtDNA mutations cause aging phenotypes without affecting reactive oxygen species production.
Aleksandra Trifunovic, Anna Hansson, Anna Wredenberg, Anja T Rovio, Eric Dufour, Ivan Khvorostov, Johannes N Spelbrink, Rolf Wibom, Howard T Jacobs, Nils-Göran Larsson. Proc Natl Acad Sci U S A 2005
379
14


Pronuclear transfer in human embryos to prevent transmission of mitochondrial DNA disease.
Lyndsey Craven, Helen A Tuppen, Gareth D Greggains, Stephen J Harbottle, Julie L Murphy, Lynsey M Cree, Alison P Murdoch, Patrick F Chinnery, Robert W Taylor, Robert N Lightowlers,[...]. Nature 2010
284
14

Gene therapy for progeny of mito-mice carrying pathogenic mtDNA by nuclear transplantation.
Akitsugu Sato, Tomohiro Kono, Kazuto Nakada, Kaori Ishikawa, Shin-Ichi Inoue, Hiromichi Yonekawa, Jun-Ichi Hayashi. Proc Natl Acad Sci U S A 2005
116
14

The mitochondrial bottleneck occurs without reduction of mtDNA content in female mouse germ cells.
Liqin Cao, Hiroshi Shitara, Takuro Horii, Yasumitsu Nagao, Hiroshi Imai, Kuniya Abe, Takahiko Hara, Jun-Ichi Hayashi, Hiromichi Yonekawa. Nat Genet 2007
216
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


Maternal germ-line transmission of mutant mtDNAs from embryonic stem cell-derived chimeric mice.
J E Sligh, S E Levy, K G Waymire, P Allard, D L Dillehay, S Nusinowitz, J R Heckenlively, G R MacGregor, D C Wallace. Proc Natl Acad Sci U S A 2000
102
13

ROS-generating mitochondrial DNA mutations can regulate tumor cell metastasis.
Kaori Ishikawa, Keizo Takenaga, Miho Akimoto, Nobuko Koshikawa, Aya Yamaguchi, Hirotake Imanishi, Kazuto Nakada, Yoshio Honma, Jun-Ichi Hayashi. Science 2008
894
13

Mitochondrial transcription factor A is necessary for mtDNA maintenance and embryogenesis in mice.
N G Larsson, J Wang, H Wilhelmsson, A Oldfors, P Rustin, M Lewandoski, G S Barsh, D A Clayton. Nat Genet 1998
12

Towards germline gene therapy of inherited mitochondrial diseases.
Masahito Tachibana, Paula Amato, Michelle Sparman, Joy Woodward, Dario Melguizo Sanchis, Hong Ma, Nuria Marti Gutierrez, Rebecca Tippner-Hedges, Eunju Kang, Hyo-Sang Lee,[...]. Nature 2013
228
12

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
151
12

Pathogenic mitochondrial DNA mutations are common in the general population.
Hannah R Elliott, David C Samuels, James A Eden, Caroline L Relton, Patrick F Chinnery. Am J Hum Genet 2008
356
11

Mitochondrial DNA mutations and aging: devils in the details?
Konstantin Khrapko, Jan Vijg. Trends Genet 2009
81
13

Variation in germline mtDNA heteroplasmy is determined prenatally but modified during subsequent transmission.
Christoph Freyer, Lynsey M Cree, Arnaud Mourier, James B Stewart, Camilla Koolmeister, Dusanka Milenkovic, Timothy Wai, Vasileios I Floros, Erik Hagström, Emmanouella E Chatzidaki,[...]. Nat Genet 2012
90
12

Mitochondrial DNA deletions are abundant and cause functional impairment in aged human substantia nigra neurons.
Yevgenya Kraytsberg, Elena Kudryavtseva, Ann C McKee, Changiz Geula, Neil W Kowall, Konstantin Khrapko. Nat Genet 2006
619
10

DNA deletions and clonal mutations drive premature aging in mitochondrial mutator mice.
Marc Vermulst, Jonathan Wanagat, Gregory C Kujoth, Jason H Bielas, Peter S Rabinovitch, Tomas A Prolla, Lawrence A Loeb. Nat Genet 2008
272
10

Mitochondrial fusion is required for mtDNA stability in skeletal muscle and tolerance of mtDNA mutations.
Hsiuchen Chen, Marc Vermulst, Yun E Wang, Anne Chomyn, Tomas A Prolla, J Michael McCaffery, David C Chan. Cell 2010
694
10

Tissue-specific selection for different mtDNA genotypes in heteroplasmic mice.
J P Jenuth, A C Peterson, E A Shoubridge. Nat Genet 1997
282
10

Human mitochondrial DNA deletions associated with mutations in the gene encoding Twinkle, a phage T7 gene 4-like protein localized in mitochondria.
J N Spelbrink, F Y Li, V Tiranti, K Nikali, Q P Yuan, M Tariq, S Wanrooij, N Garrido, G Comi, L Morandi,[...]. Nat Genet 2001
603
10

Accumulation of pathogenic DeltamtDNA induced deafness but not diabetic phenotypes in mito-mice.
Kazuto Nakada, Akitsugu Sato, Hideyuki Sone, Atsuko Kasahara, Katsuhisa Ikeda, Yasuo Kagawa, Hiromichi Yonekawa, Jun-Ichi Hayashi. Biochem Biophys Res Commun 2004
32
31


Mitochondrial threshold effects.
Rodrigue Rossignol, Benjamin Faustin, Christophe Rocher, Monique Malgat, Jean-Pierre Mazat, Thierry Letellier. Biochem J 2003
455
10

Mitochondria: in sickness and in health.
Jodi Nunnari, Anu Suomalainen. Cell 2012
10

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
440
10

Fission and selective fusion govern mitochondrial segregation and elimination by autophagy.
Gilad Twig, Alvaro Elorza, Anthony J A Molina, Hibo Mohamed, Jakob D Wikstrom, Gil Walzer, Linsey Stiles, Sarah E Haigh, Steve Katz, Guy Las,[...]. EMBO J 2008
9

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
976
9

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
334
9

New evidence confirms that the mitochondrial bottleneck is generated without reduction of mitochondrial DNA content in early primordial germ cells of mice.
Liqin Cao, Hiroshi Shitara, Michihiko Sugimoto, Jun-Ichi Hayashi, Kuniya Abe, Hiromichi Yonekawa. PLoS Genet 2009
85
10

Molecular genetic aspects of human mitochondrial disorders.
N G Larsson, D A Clayton. Annu Rev Genet 1995
364
9


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.