A citation-based method for searching scientific literature

Rocio Rius, Mark J Cowley, Lisa Riley, Clare Puttick, David R Thorburn, John Christodoulou. Genet Med 2019
Times Cited: 19







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



Times Cited
  Times     Co-cited
Similarity


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
141
73

Paternal inheritance of mitochondrial DNA.
Marianne Schwartz, John Vissing. N Engl J Med 2002
342
26

No further evidence for paternal leakage of mitochondrial DNA in humans yet.
Sabine Lutz-Bonengel, Walther Parson. Proc Natl Acad Sci U S A 2019
28
26

Germline selection shapes human mitochondrial DNA diversity.
Wei Wei, Salih Tuna, Michael J Keogh, Katherine R Smith, Timothy J Aitman, Phil L Beales, David L Bennett, Daniel P Gale, Maria A K Bitner-Glindzicz, Graeme C Black,[...]. Science 2019
67
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
80
21

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
21

Maternal inheritance of human mitochondrial DNA.
R E Giles, H Blanc, H M Cann, D C Wallace. Proc Natl Acad Sci U S A 1980
872
21

Nuclear-mitochondrial DNA segments resemble paternally inherited mitochondrial DNA in humans.
Wei Wei, Alistair T Pagnamenta, Nicholas Gleadall, Alba Sanchis-Juan, Jonathan Stephens, John Broxholme, Salih Tuna, Christopher A Odhams, Carl Fratter, Ernest Turro,[...]. Nat Commun 2020
25
21

Mitochondrial DNA can be inherited from fathers, not just mothers.
Thomas G McWilliams, Anu Suomalainen. Nature 2019
12
33


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
431
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
15


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
15

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
123
15

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
15


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
88
15

Mitochondrial fragmentation drives selective removal of deleterious mtDNA in the germline.
Toby Lieber, Swathi P Jeedigunta, Jonathan M Palozzi, Ruth Lehmann, Thomas R Hurd. Nature 2019
65
10

Mutation-specific effects in germline transmission of pathogenic mtDNA variants.
Auke B C Otten, Suzanne C E H Sallevelt, Phillippa J Carling, Joseph C F M Dreesen, Marion Drüsedau, Sabine Spierts, Aimee D C Paulussen, Christine E M de Die-Smulders, Mary Herbert, Patrick F Chinnery,[...]. Hum Reprod 2018
17
11


Mitochondrial threshold effects.
Rodrigue Rossignol, Benjamin Faustin, Christophe Rocher, Monique Malgat, Jean-Pierre Mazat, Thierry Letellier. Biochem J 2003
452
10

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
10


Nucleotide sequence evidence for rapid genotypic shifts in the bovine mitochondrial DNA D-loop.
P D Olivo, M J Van de Walle, P J Laipis, W W Hauswirth. Nature 1983
159
10

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
10

CRISPR/Cas9 and mitochondrial gene replacement therapy: promising techniques and ethical considerations.
Sarah Fogleman, Casey Santana, Casey Bishop, Alyssa Miller, David G Capco. Am J Stem Cells 2016
22
10

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
215
10

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
233
10

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
133
10

Maternal inheritance of mammalian mitochondrial DNA.
C A Hutchison, J E Newbold, S S Potter, M H Edgell. Nature 1974
247
10

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
161
10

HaploGrep 2: mitochondrial haplogroup classification in the era of high-throughput sequencing.
Hansi Weissensteiner, Dominic Pacher, Anita Kloss-Brandstätter, Lukas Forer, Günther Specht, Hans-Jürgen Bandelt, Florian Kronenberg, Antonio Salas, Sebastian Schönherr. Nucleic Acids Res 2016
300
10

Mitochondrial genetic medicine.
Douglas C Wallace. Nat Genet 2018
95
10


Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA.
R M Andrews, I Kubacka, P F Chinnery, R N Lightowlers, D M Turnbull, N Howell. Nat Genet 1999
10

A "Copernican" reassessment of the human mitochondrial DNA tree from its root.
Doron M Behar, Mannis van Oven, Saharon Rosset, Mait Metspalu, Eva-Liis Loogväli, Nuno M Silva, Toomas Kivisild, Antonio Torroni, Richard Villems. Am J Hum Genet 2012
260
10



Mitochondrial dysfunction: the missing link between aging and sporadic Alzheimer's disease.
Amandine Grimm, Kristina Friedland, Anne Eckert. Biogerontology 2016
87
10

Mitochondria: a central target for sex differences in pathologies.
Renée Ventura-Clapier, Maryline Moulin, Jérôme Piquereau, Christophe Lemaire, Mathias Mericskay, Vladimir Veksler, Anne Garnier. Clin Sci (Lond) 2017
115
10

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
105
10

Mitochondrial Genome Engineering: The Revolution May Not Be CRISPR-Ized.
Payam A Gammage, Carlos T Moraes, Michal Minczuk. Trends Genet 2018
103
10

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
85
10

TALEN-mediated shift of mitochondrial DNA heteroplasmy in MELAS-iPSCs with m.13513G>A mutation.
Naoki Yahata, Yuji Matsumoto, Minoru Omi, Naoki Yamamoto, Ryuji Hata. Sci Rep 2017
26
10

Extreme-Depth Re-sequencing of Mitochondrial DNA Finds No Evidence of Paternal Transmission in Humans.
Angela Pyle, Gavin Hudson, Ian J Wilson, Jonathan Coxhead, Tania Smertenko, Mary Herbert, Mauro Santibanez-Koref, Patrick F Chinnery. PLoS Genet 2015
45
10


Mitochondrial DNA deletions in progressive external ophthalmoplegia and Kearns-Sayre syndrome.
C T Moraes, S DiMauro, M Zeviani, A Lombes, S Shanske, A F Miranda, H Nakase, E Bonilla, L C Werneck, S Servidei. N Engl J Med 1989
855
10

No recombination of mtDNA after heteroplasmy for 50 generations in the mouse maternal germline.
Erik Hagström, Christoph Freyer, Brendan J Battersby, James B Stewart, Nils-Göran Larsson. Nucleic Acids Res 2014
57
10

A Phenotype-Driven Approach to Generate Mouse Models with Pathogenic mtDNA Mutations Causing Mitochondrial Disease.
Johanna H K Kauppila, Holly L Baines, Ana Bratic, Marie-Lune Simard, Christoph Freyer, Arnaud Mourier, Craig Stamp, Roberta Filograna, Nils-Göran Larsson, Laura C Greaves,[...]. Cell Rep 2016
56
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.