A citation-based method for searching scientific literature

Valentina Del Dotto, Valerio Carelli. Front Neurol 2021
Times Cited: 1







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



Times Cited
  Times     Co-cited
Similarity





The mitochondrial inner membrane protein MPV17 prevents uracil accumulation in mitochondrial DNA.
Judith R Alonzo, Chantel Venkataraman, Martha S Field, Patrick J Stover. J Biol Chem 2018
13
100

In vivo analysis of mtDNA replication defects in yeast.
Enrico Baruffini, Iliana Ferrero, Françoise Foury. Methods 2010
43
100




[ANT1, twinkle, POLG mutation].
Hirofumi Komaki, Yu-ichi Goto. Nihon Rinsho 2002
1
100


OPA1 mutations in patients with autosomal dominant optic atrophy and evidence for semi-dominant inheritance.
U E Pesch, B Leo-Kottler, S Mayer, B Jurklies, U Kellner, E Apfelstedt-Sylla, E Zrenner, C Alexander, B Wissinger. Hum Mol Genet 2001
148
100




Phenotypic and Genotypic Heterogeneity of RRM2B Variants.
Josef Finsterer, Sinda Zarrouk-Mahjoub. Neuropediatrics 2018
5
100

History of genome editing in yeast.
Marcin G Fraczek, Samina Naseeb, Daniela Delneri. Yeast 2018
17
100

Regulation by degradation, a cellular defense against deoxyribonucleotide pool imbalances.
Chiara Rampazzo, Cristina Miazzi, Elisa Franzolin, Giovanna Pontarin, Paola Ferraro, Miriam Frangini, Peter Reichard, Vera Bianchi. Mutat Res 2010
82
100

Validation of a MGM1/OPA1 chimeric gene for functional analysis in yeast of mutations associated with dominant optic atrophy.
Cecilia Nolli, Paola Goffrini, Mirca Lazzaretti, Claudia Zanna, Rita Vitale, Tiziana Lodi, Enrico Baruffini. Mitochondrion 2015
14
100

OPA1 processing in cell death and disease - the long and short of it.
Thomas MacVicar, Thomas Langer. J Cell Sci 2016
231
100

Kearns-Sayre syndrome caused by defective R1/p53R2 assembly.
Robert D S Pitceathly, Elisa Fassone, Jan-Willem Taanman, Michael Sadowski, Carl Fratter, Ese E Mudanohwo, Cathy E Woodward, Mary G Sweeney, Janice L Holton, Michael G Hanna,[...]. J Med Genet 2011
28
100

Strategies for fighting mitochondrial diseases.
C Viscomi, M Zeviani. J Intern Med 2020
19
100


mip1 containing mutations associated with mitochondrial disease causes mutagenesis and depletion of mtDNA in Saccharomyces cerevisiae.
Jeffrey D Stumpf, Christopher M Bailey, Diana Spell, Matthew Stillwagon, Karen S Anderson, William C Copeland. Hum Mol Genet 2010
34
100

The Human Mitochondrial DNA Depletion Syndrome Gene MPV17 Encodes a Non-selective Channel That Modulates Membrane Potential.
Vasily D Antonenkov, Antti Isomursu, Daniela Mennerich, Miia H Vapola, Hans Weiher, Thomas Kietzmann, J Kalervo Hiltunen. J Biol Chem 2015
32
100

DNA damage induction of ribonucleotide reductase.
S J Elledge, R W Davis. Mol Cell Biol 1989
116
100

Mammalian ribonucleotide reductase subunit p53R2 is required for mitochondrial DNA replication and DNA repair in quiescent cells.
Giovanna Pontarin, Paola Ferraro, Leonardo Bee, Peter Reichard, Vera Bianchi. Proc Natl Acad Sci U S A 2012
75
100



Mitochondrial and nuclear DNA defects in Saccharomyces cerevisiae with mutations in DNA polymerase gamma associated with progressive external ophthalmoplegia.
Gregory R Stuart, Janine H Santos, Micheline K Strand, Bennett Van Houten, William C Copeland. Hum Mol Genet 2006
54
100

DNA polymerase gamma, the mitochondrial replicase.
Laurie S Kaguni. Annu Rev Biochem 2004
291
100

Dominance of yeast aac2R96H and aac2R252G mutations, equivalent to pathological mutations in ant1, is due to gain of function.
Cristina Dallabona, Enrico Baruffini, Paola Goffrini, Tiziana Lodi. Biochem Biophys Res Commun 2017
5
100

A novel mutation of the RRM2B gene in an infant with early fatal encephalomyopathy, central hypomyelination, and tubulopathy.
Birgit Acham-Roschitz, Barbara Plecko, Franz Lindbichler, Reginald Bittner, Christoph J Mache, Wolfgang Sperl, Johannes A Mayr. Mol Genet Metab 2009
40
100

A fourth ADP/ATP carrier isoform in man: identification, bacterial expression, functional characterization and tissue distribution.
Vincenza Dolce, Pasquale Scarcia, Domenico Iacopetta, Ferdinando Palmieri. FEBS Lett 2005
157
100

MitoFates: improved prediction of mitochondrial targeting sequences and their cleavage sites.
Yoshinori Fukasawa, Junko Tsuji, Szu-Chin Fu, Kentaro Tomii, Paul Horton, Kenichiro Imai. Mol Cell Proteomics 2015
245
100


Amino and carboxy-terminal extensions of yeast mitochondrial DNA polymerase assemble both the polymerization and exonuclease active sites.
Carlos H Trasviña-Arenas, Nallely Hoyos-Gonzalez, Atzimba Y Castro-Lara, Annia Rodriguez-Hernandez, María E Sanchez-Sandoval, Pedro Jimenez-Sandoval, Víctor M Ayala-García, Corina Díaz-Quezada, Tiziana Lodi, Enrico Baruffini,[...]. Mitochondrion 2019
4
100

Yeast model analysis of novel polymerase gamma variants found in patients with autosomal recessive mitochondrial disease.
Magdalena Kaliszewska, Jakub Kruszewski, Biruta Kierdaszuk, Anna Kostera-Pruszczyk, Monika Nojszewska, Anna Łusakowska, Joel Vizueta, Dorota Sabat, Dorota Lutyk, Michał Lower,[...]. Hum Genet 2015
11
100

Fatal infantile mitochondrial encephalomyopathy, hypertrophic cardiomyopathy and optic atrophy associated with a homozygous OPA1 mutation.
Ronen Spiegel, Ann Saada, Padraig J Flannery, Florence Burté, Devorah Soiferman, Morad Khayat, Verónica Eisner, Eugene Vladovski, Robert W Taylor, Laurence A Bindoff,[...]. J Med Genet 2016
55
100

MELAS associated with mutations in the POLG1 gene.
M Deschauer, S Tennant, A Rokicka, L He, T Kraya, D M Turnbull, S Zierz, R W Taylor. Neurology 2007
61
100


Replication of mitochondrial DNA. Circular replicative intermediates in mouse L cells.
D L Robberson, H Kasamatsu, J Vinograd. Proc Natl Acad Sci U S A 1972
201
100

A novel ANT1 gene mutation with probable germline mosaicism in autosomal dominant progressive external ophthalmoplegia.
Marcus Deschauer, Gavin Hudson, Tobias Müller, Robert W Taylor, Patrick F Chinnery, Stephan Zierz. Neuromuscul Disord 2005
45
100

U2552 methylation at the ribosomal A-site is a negative modulator of translational accuracy.
Magdalena Widerak, Renée Kern, Abderrahim Malki, Gilbert Richarme. Gene 2005
27
100

Yeast mitochondrial ADP/ATP carriers are monomeric in detergents.
Lisa Bamber, Marilyn Harding, P Jonathan G Butler, Edmund R S Kunji. Proc Natl Acad Sci U S A 2006
66
100

Sym1, the yeast ortholog of the MPV17 human disease protein, is a stress-induced bioenergetic and morphogenetic mitochondrial modulator.
Cristina Dallabona, René Massimiliano Marsano, Paola Arzuffi, Daniele Ghezzi, Patrizia Mancini, Massimo Zeviani, Iliana Ferrero, Claudia Donnini. Hum Mol Genet 2010
53
100

SnapShot: Mitochondrial Nucleoid.
Nina A Bonekamp, Nils-Göran Larsson. Cell 2018
25
100

The Power of Yeast in Modelling Human Nuclear Mutations Associated with Mitochondrial Diseases.
Camilla Ceccatelli Berti, Giulia di Punzio, Cristina Dallabona, Enrico Baruffini, Paola Goffrini, Tiziana Lodi, Claudia Donnini. Genes (Basel) 2021
5
100

Defective mitochondrial rRNA methyltransferase MRM2 causes MELAS-like clinical syndrome.
Caterina Garone, Aaron R D'Souza, Cristina Dallabona, Tiziana Lodi, Pedro Rebelo-Guiomar, Joanna Rorbach, Maria Alice Donati, Elena Procopio, Martino Montomoli, Renzo Guerrini,[...]. Hum Mol Genet 2017
35
100

Modeling of pathogenic variants of mitochondrial DNA polymerase: insight into the replication defects and implication for human disease.
Nallely Hoyos-Gonzalez, Carlos H Trasviña-Arenas, Andrea Degiorgi, Atzimaba Y Castro-Lara, Antolín Peralta-Castro, Pedro Jimenez-Sandoval, Corina Diaz-Quezada, Tiziana Lodi, Enrico Baruffini, Luis G Brieba. Biochim Biophys Acta Gen Subj 2020
2
100



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.