A citation-based method for searching scientific literature

Zhe Chen, Fan Zhang, Hong Xu. J Genet Genomics 2019
Times Cited: 2







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



Times Cited
  Times     Co-cited
Similarity


Manipulating the metazoan mitochondrial genome with targeted restriction enzymes.
Hong Xu, Steven Z DeLuca, Patrick H O'Farrell. Science 2008
73
100


Identification of novel mutations in five patients with mitochondrial encephalomyopathy.
Lucia Valente, Daniela Piga, Eleonora Lamantea, Franco Carrara, Graziella Uziel, Paola Cudia, Anna Zani, Laura Farina, Lucia Morandi, Marina Mora,[...]. Biochim Biophys Acta 2009
68
50

Mitochondrial threshold effects.
Rodrigue Rossignol, Benjamin Faustin, Christophe Rocher, Monique Malgat, Jean-Pierre Mazat, Thierry Letellier. Biochem J 2003
457
50

Sensory ataxic neuropathy in golden retriever dogs is caused by a deletion in the mitochondrial tRNATyr gene.
Izabella Baranowska, Karin Hultin Jäderlund, Inger Nennesmo, Erik Holmqvist, Nadja Heidrich, Nils-Göran Larsson, Göran Andersson, E Gerhart H Wagner, Ake Hedhammar, Rolf Wibom,[...]. PLoS Genet 2009
26
50


The mtDNA mutation spectrum of the progeroid Polg mutator mouse includes abundant control region multimers.
Siôn L Williams, Jia Huang, Yvonne J K Edwards, Rick H Ulloa, Lloye M Dillon, Tomas A Prolla, Jeffery M Vance, Carlos T Moraes, Stephan Züchner. Cell Metab 2010
61
50


Transferring isolated mitochondria into tissue culture cells.
Yi-Wei Yang, Michael D Koob. Nucleic Acids Res 2012
10
50

Maternal segmental disomy in Leigh syndrome with cytochrome c oxidase deficiency caused by homozygous SURF1 mutation.
A K J van Riesen, H Antonicka, A Ohlenbusch, E A Shoubridge, E K G Wilichowski. Neuropediatrics 2006
12
50

Concentration of mitochondrial DNA mutations by cytoplasmic transfer from platelets to cultured mouse cells.
Kaori Ishikawa, Kohei Kobayashi, Akihito Yamada, Moe Umehara, Toshihiko Oka, Kazuto Nakada. PLoS One 2019
1
100


Strikingly bacteria-like and gene-rich mitochondrial genomes throughout jakobid protists.
Gertraud Burger, Michael W Gray, Lise Forget, B Franz Lang. Genome Biol Evol 2013
135
50

Episodic weakness associated with exertional lactic acidosis and myopathy in Old English sheepdog littermates.
E B Breitschwerdt, J N Kornegay, S J Wheeler, J B Stevens, C J Baty. J Am Vet Med Assoc 1992
27
50


Strategies for fighting mitochondrial diseases.
C Viscomi, M Zeviani. J Intern Med 2020
19
50

Tree of life reveals clock-like speciation and diversification.
S Blair Hedges, Julie Marin, Michael Suleski, Madeline Paymer, Sudhir Kumar. Mol Biol Evol 2015
475
50

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
124
50

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
286
50

Structure and Function of the Mitochondrial Ribosome.
Basil J Greber, Nenad Ban. Annu Rev Biochem 2016
121
50

Mitonuclear Compensatory Coevolution.
Geoffrey E Hill. Trends Genet 2020
14
50

RNase P without RNA: identification and functional reconstitution of the human mitochondrial tRNA processing enzyme.
Johann Holzmann, Peter Frank, Esther Löffler, Keiryn L Bennett, Christopher Gerner, Walter Rossmanith. Cell 2008
370
50

Mitochondrial DNA exhibits resistance to induced point and deletion mutations.
William J Valente, Nolan G Ericson, Alexandra S Long, Paul A White, Francesco Marchetti, Jason H Bielas. Nucleic Acids Res 2016
26
50

Mamit-tRNA, a database of mammalian mitochondrial tRNA primary and secondary structures.
Joern Pütz, Bruno Dupuis, Marie Sissler, Catherine Florentz. RNA 2007
105
50

Rare creation of recombinant mtDNA haplotypes in mammalian tissues.
Akitsugu Sato, Kazuto Nakada, Miho Akimoto, Kaori Ishikawa, Tomoko Ono, Hiroshi Shitara, Hiromichi Yonekawa, Jun-Ichi Hayashi. Proc Natl Acad Sci U S A 2005
40
50

NAD+ Regeneration Rescues Lifespan, but Not Ataxia, in a Mouse Model of Brain Mitochondrial Complex I Dysfunction.
Gregory S McElroy, Colleen R Reczek, Paul A Reyfman, Divakar S Mithal, Craig M Horbinski, Navdeep S Chandel. Cell Metab 2020
14
50


Mitochondrial import, health and mtDNA copy number variability seen when using type II and type V CRISPR effectors.
Zuriñe Antón, Grace Mullally, Holly C Ford, Marc W van der Kamp, Mark D Szczelkun, Jon D Lane. J Cell Sci 2020
5
50

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
273
50

Sequence and gene organization of mouse mitochondrial DNA.
M J Bibb, R A Van Etten, C T Wright, M W Walberg, D A Clayton. Cell 1981
50

Sporadic myopathy and exercise intolerance associated with the mitochondrial 8328G>A tRNALys mutation.
Emma L Blakely, Helen Swalwell, Richard K H Petty, Robert McFarland, Douglass M Turnbull, Robert W Taylor. J Neurol 2007
12
50

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
50

Similar patterns of clonally expanded somatic mtDNA mutations in the colon of heterozygous mtDNA mutator mice and ageing humans.
Holly L Baines, James B Stewart, Craig Stamp, Anze Zupanic, Thomas B L Kirkwood, Nils-Göran Larsson, Douglass M Turnbull, Laura C Greaves. Mech Ageing Dev 2014
23
50

The CoRR hypothesis for genes in organelles.
John F Allen. J Theor Biol 2017
16
50

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
50

Advances in genome editing through control of DNA repair pathways.
Charles D Yeh, Christopher D Richardson, Jacob E Corn. Nat Cell Biol 2019
93
50

Mitochondrial DNA mutations in mutator mice confer respiration defects and B-cell lymphoma development.
Takayuki Mito, Yoshiaki Kikkawa, Akinori Shimizu, Osamu Hashizume, Shun Katada, Hirotake Imanishi, Azusa Ota, Yukina Kato, Kazuto Nakada, Jun-Ichi Hayashi. PLoS One 2013
22
50

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
153
50

A Single Intravenous Injection of AAV-PHP.B-hNDUFS4 Ameliorates the Phenotype of Ndufs4 -/- Mice.
Pedro Silva-Pinheiro, Raffaele Cerutti, Marta Luna-Sanchez, Massimo Zeviani, Carlo Viscomi. Mol Ther Methods Clin Dev 2020
7
50

mtDNA lineage analysis of mouse L-cell lines reveals the accumulation of multiple mtDNA mutants and intermolecular recombination.
Weiwei Fan, Chun Shi Lin, Prasanth Potluri, Vincent Procaccio, Douglas C Wallace. Genes Dev 2012
26
50

RNA-Independent DNA Cleavage Activities of Cas9 and Cas12a.
Ramya Sundaresan, Hari Priya Parameshwaran, S D Yogesha, Mark Walter Keilbarth, Rakhi Rajan. Cell Rep 2017
37
50

The mitochondrial DNA polymerase gamma degrades linear DNA fragments precluding the formation of deletions.
Nadee Nissanka, Sandra R Bacman, Melanie J Plastini, Carlos T Moraes. Nat Commun 2018
43
50


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
50


A tRNA(Ala) mutation causing mitochondrial myopathy clinically resembling myotonic dystrophy.
R Horváth, H Lochmüller, C Scharfe, B H Do, P J Oefner, J Müller-Höcker, B G Schoser, D Pongratz, D P Auer, M Jaksch. J Med Genet 2003
11
50

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
59
50

Age-Related Accumulation of Somatic Mitochondrial DNA Mutations in Adult-Derived Human iPSCs.
Eunju Kang, Xinjian Wang, Rebecca Tippner-Hedges, Hong Ma, Clifford D L Folmes, Nuria Marti Gutierrez, Yeonmi Lee, Crystal Van Dyken, Riffat Ahmed, Ying Li,[...]. Cell Stem Cell 2016
135
50

Tfam Knockdown Results in Reduction of mtDNA Copy Number, OXPHOS Deficiency and Abnormalities in Zebrafish Embryos.
Auke B C Otten, Rick Kamps, Patrick Lindsey, Mike Gerards, Hélène Pendeville-Samain, Marc Muller, Florence H J van Tienen, Hubert J M Smeets. Front Cell Dev Biol 2020
3
50



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.