A citation-based method for searching scientific literature

J P Jenuth, A C Peterson, E A Shoubridge. Nat Genet 1997
Times Cited: 282







List of co-cited articles
1291 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity



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
37


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
36

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
35

Heteroplasmy of mouse mtDNA is genetically unstable and results in altered behavior and cognition.
Mark S Sharpley, Christine Marciniak, Kristin Eckel-Mahan, Meagan McManus, Marco Crimi, Katrina Waymire, Chun Shi Lin, Satoru Masubuchi, Nicole Friend, Maya Koike,[...]. Cell 2012
219
30

Mitochondrial DNA genetics and the heteroplasmy conundrum in evolution and disease.
Douglas C Wallace, Dimitra Chalkia. Cold Spring Harb Perspect Biol 2013
329
28

Nuclear genetic control of mitochondrial DNA segregation.
Brendan J Battersby, J C Loredo-Osti, Eric A Shoubridge. Nat Genet 2003
101
24

MtDNA segregation in heteroplasmic tissues is common in vivo and modulated by haplotype differences and developmental stage.
Joerg Patrick Burgstaller, Iain G Johnston, Nick S Jones, Jana Albrechtová, Thomas Kolbe, Claus Vogl, Andreas Futschik, Corina Mayrhofer, Dieter Klein, Sonja Sabitzer,[...]. Cell Rep 2014
64
37

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
23

Universal heteroplasmy of human mitochondrial DNA.
Brendan A I Payne, Ian J Wilson, Patrick Yu-Wai-Man, Jonathan Coxhead, David Deehan, Rita Horvath, Robert W Taylor, David C Samuels, Mauro Santibanez-Koref, Patrick F Chinnery. Hum Mol Genet 2013
234
23

Gimap3 regulates tissue-specific mitochondrial DNA segregation.
Riikka Jokinen, Paula Marttinen, Helen Katarin Sandell, Tuula Manninen, Heli Teerenhovi, Timothy Wai, Daniella Teoli, J C Loredo-Osti, Eric A Shoubridge, Brendan J Battersby. PLoS Genet 2010
46
45

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
20

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
19

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
21


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
18


Differences in reactive oxygen species production explain the phenotypes associated with common mouse mitochondrial DNA variants.
Raquel Moreno-Loshuertos, Rebeca Acín-Pérez, Patricio Fernández-Silva, Nieves Movilla, Acisclo Pérez-Martos, Santiago Rodriguez de Cordoba, M Esther Gallardo, José Antonio Enríquez. Nat Genet 2006
245
18

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
17

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
16

Heteroplasmic mitochondrial DNA mutations in normal and tumour cells.
Yiping He, Jian Wu, Devin C Dressman, Christine Iacobuzio-Donahue, Sanford D Markowitz, Victor E Velculescu, Luis A Diaz, Kenneth W Kinzler, Bert Vogelstein, Nickolas Papadopoulos. Nature 2010
369
16

Purifying selection of mtDNA and its implications for understanding evolution and mitochondrial disease.
James Bruce Stewart, Christoph Freyer, Joanna L Elson, Nils-Göran Larsson. Nat Rev Genet 2008
114
16

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
15

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
17

Ubiquitin tag for sperm mitochondria.
P Sutovsky, R D Moreno, J Ramalho-Santos, T Dominko, C Simerly, G Schatten. Nature 1999
404
14

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
14

Rapid mitochondrial DNA segregation in primate preimplantation embryos precedes somatic and germline bottleneck.
Hyo-Sang Lee, Hong Ma, Rita Cervera Juanes, Masahito Tachibana, Michelle Sparman, Joy Woodward, Cathy Ramsey, Jing Xu, Eun-Ju Kang, Paula Amato,[...]. Cell Rep 2012
79
17



Effects of purifying and adaptive selection on regional variation in human mtDNA.
Eduardo Ruiz-Pesini, Dan Mishmar, Martin Brandon, Vincent Procaccio, Douglas C Wallace. Science 2004
542
13

Random genetic drift determines the level of mutant mtDNA in human primary oocytes.
D T Brown, D C Samuels, E M Michael, D M Turnbull, P F Chinnery. Am J Hum Genet 2001
107
13

Recurrent tissue-specific mtDNA mutations are common in humans.
David C Samuels, Chun Li, Bingshan Li, Zhuo Song, Eric Torstenson, Hayley Boyd Clay, Antonis Rokas, Tricia A Thornton-Wells, Jason H Moore, Tia M Hughes,[...]. PLoS Genet 2013
90
14

Mitochondrial DNA mutations in human disease.
Robert W Taylor, Doug M Turnbull. Nat Rev Genet 2005
12



Skewed segregation of the mtDNA nt 8993 (T-->G) mutation in human oocytes.
R B Blok, D A Gook, D R Thorburn, H H Dahl. Am J Hum Genet 1997
126
12

Mitochondrial DNA polymorphism in a maternal lineage of Holstein cows.
W W Hauswirth, P J Laipis. Proc Natl Acad Sci U S A 1982
286
12

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
12

Neutral mitochondrial heteroplasmy alters physiological function in mice.
B M Acton, I Lai, X Shang, A Jurisicova, R F Casper. Biol Reprod 2007
57
21

Segregation of mitochondrial DNA heteroplasmy through a developmental genetic bottleneck in human embryos.
Vasileios I Floros, Angela Pyle, Sabine Dietmann, Wei Wei, Walfred C W Tang, Naoko Irie, Brendan Payne, Antonio Capalbo, Laila Noli, Jonathan Coxhead,[...]. Nat Cell Biol 2018
81
14

Prevalence of mitochondrial DNA disease in adults.
Andrew M Schaefer, Robert McFarland, Emma L Blakely, Langping He, Roger G Whittaker, Robert W Taylor, Patrick F Chinnery, Douglass M Turnbull. Ann Neurol 2008
379
11

Parkin overexpression selects against a deleterious mtDNA mutation in heteroplasmic cybrid cells.
Der-Fen Suen, Derek P Narendra, Atsushi Tanaka, Giovanni Manfredi, Richard J Youle. Proc Natl Acad Sci U S A 2010
201
11


Random intracellular drift explains the clonal expansion of mitochondrial DNA mutations with age.
J L Elson, D C Samuels, D M Turnbull, P F Chinnery. Am J Hum Genet 2001
217
11

Segregation of mtDNA throughout human embryofetal development: m.3243A>G as a model system.
Sophie Monnot, Nadine Gigarel, David C Samuels, Philippe Burlet, Laetitia Hesters, Nelly Frydman, René Frydman, Violaine Kerbrat, Benoit Funalot, Jelena Martinovic,[...]. Hum Mutat 2011
74
14

Postfertilization autophagy of sperm organelles prevents paternal mitochondrial DNA transmission.
Sara Al Rawi, Sophie Louvet-Vallée, Abderazak Djeddi, Martin Sachse, Emmanuel Culetto, Connie Hajjar, Lynn Boyd, Renaud Legouis, Vincent Galy. Science 2011
303
11


Mitochondrial replacement in human oocytes carrying pathogenic mitochondrial DNA mutations.
Eunju Kang, Jun Wu, Nuria Marti Gutierrez, Amy Koski, Rebecca Tippner-Hedges, Karen Agaronyan, Aida Platero-Luengo, Paloma Martinez-Redondo, Hong Ma, Yeonmi Lee,[...]. Nature 2016
134
11

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
794
10


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.