A citation-based method for searching scientific literature

Daniela Strobbe, Leonardo Caporali, Luisa Iommarini, Alessandra Maresca, Monica Montopoli, Andrea Martinuzzi, Alessandro Achilli, Anna Olivieri, Antonio Torroni, Valerio Carelli, Anna Ghelli. Neurobiol Dis 2018
Times Cited: 15







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



Times Cited
  Times     Co-cited
Similarity


Clinical expression of Leber hereditary optic neuropathy is affected by the mitochondrial DNA-haplogroup background.
Gavin Hudson, Valerio Carelli, Liesbeth Spruijt, Mike Gerards, Catherine Mowbray, Alessandro Achilli, Angela Pyle, Joanna Elson, Neil Howell, Chiara La Morgia,[...]. Am J Hum Genet 2007
260
33

Unmasking the causes of multifactorial disorders: OXPHOS differences between mitochondrial haplogroups.
Aurora Gómez-Durán, David Pacheu-Grau, Ester López-Gallardo, Carmen Díez-Sánchez, Julio Montoya, Manuel J López-Pérez, Eduardo Ruiz-Pesini. Hum Mol Genet 2010
194
33

The background of mitochondrial DNA haplogroup J increases the sensitivity of Leber's hereditary optic neuropathy cells to 2,5-hexanedione toxicity.
Anna Ghelli, Anna Maria Porcelli, Claudia Zanna, Sara Vidoni, Stefano Mattioli, Anna Barbieri, Luisa Iommarini, Maria Pala, Alessandro Achilli, Antonio Torroni,[...]. PLoS One 2009
62
33

Mitochondrial antibiograms in personalized medicine.
David Pacheu-Grau, Aurora Gómez-Durán, Eldris Iglesias, Ester López-Gallardo, Julio Montoya, Eduardo Ruiz-Pesini. Hum Mol Genet 2013
31
26

MToolBox: a highly automated pipeline for heteroplasmy annotation and prioritization analysis of human mitochondrial variants in high-throughput sequencing.
Claudia Calabrese, Domenico Simone, Maria Angela Diroma, Mariangela Santorsola, Cristiano Guttà, Giuseppe Gasparre, Ernesto Picardi, Graziano Pesole, Marcella Attimonelli. Bioinformatics 2014
108
26

Mitochondrial genetics.
Patrick Francis Chinnery, Gavin Hudson. Br Med Bull 2013
183
26

Cytoplasmic hybrid (cybrid) cell lines as a practical model for mitochondriopathies.
Heather M Wilkins, Steven M Carl, Russell H Swerdlow. Redox Biol 2014
65
26

Oxidative phosphorylation differences between mitochondrial DNA haplogroups modify the risk of Leber's hereditary optic neuropathy.
Aurora Gómez-Durán, David Pacheu-Grau, Iñigo Martínez-Romero, Ester López-Gallardo, Manuel J López-Pérez, Julio Montoya, Eduardo Ruiz-Pesini. Biochim Biophys Acta 2012
71
26

Oestrogens ameliorate mitochondrial dysfunction in Leber's hereditary optic neuropathy.
Carla Giordano, Monica Montopoli, Elena Perli, Maurizia Orlandi, Marianna Fantin, Fred N Ross-Cisneros, Laura Caparrotta, Andrea Martinuzzi, Eugenio Ragazzi, Anna Ghelli,[...]. Brain 2011
146
20


Two-stage association study and meta-analysis of mitochondrial DNA variants in Parkinson disease.
Gavin Hudson, Mike Nalls, Jonathan R Evans, David P Breen, Sophie Winder-Rhodes, Karen E Morrison, Huw R Morris, Caroline H Williams-Gray, Roger A Barker, Andrew B Singleton,[...]. Neurology 2013
86
20



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
547
20

Development and implementation of standardized respiratory chain spectrophotometric assays for clinical diagnosis.
F Medja, S Allouche, P Frachon, C Jardel, M Malgat, B Mousson de Camaret, A Slama, J Lunardi, J P Mazat, A Lombès. Mitochondrion 2009
138
20

Recent Advances in Mitochondrial Disease.
Lyndsey Craven, Charlotte L Alston, Robert W Taylor, Doug M Turnbull. Annu Rev Genomics Hum Genet 2017
114
20

Mitochondrial genetic medicine.
Douglas C Wallace. Nat Genet 2018
101
20


Haplogroup effects and recombination of mitochondrial DNA: novel clues from the analysis of Leber hereditary optic neuropathy pedigrees.
Valerio Carelli, Alessandro Achilli, Maria Lucia Valentino, Chiara Rengo, Ornella Semino, Maria Pala, Anna Olivieri, Marina Mattiazzi, Francesco Pallotti, Franco Carrara,[...]. Am J Hum Genet 2006
141
20

Functional Characterization of Three Concomitant MtDNA LHON Mutations Shows No Synergistic Effect on Mitochondrial Activity.
Alberto Cruz-Bermúdez, Ramiro J Vicente-Blanco, Rosana Hernández-Sierra, Mayte Montero, Javier Alvarez, Mar González Manrique, Alberto Blázquez, Miguel Angel Martín, Carmen Ayuso, Rafael Garesse,[...]. PLoS One 2016
12
16

Antioxidant defences in cybrids harboring mtDNA mutations associated with Leber's hereditary optic neuropathy.
Maura Floreani, Eleonora Napoli, Andrea Martinuzzi, Giorgia Pantano, Valentina De Riva, Roberta Trevisan, Elena Bisetto, Lucia Valente, Valerio Carelli, Federica Dabbeni-Sala. FEBS J 2005
77
13

Severe impairment of complex I-driven adenosine triphosphate synthesis in leber hereditary optic neuropathy cybrids.
Alessandra Baracca, Giancarlo Solaini, Gianluca Sgarbi, Giorgio Lenaz, Agostino Baruzzi, Anthony H V Schapira, Andrea Martinuzzi, Valerio Carelli. Arch Neurol 2005
118
13

Cells bearing mutations causing Leber's hereditary optic neuropathy are sensitized to Fas-Induced apoptosis.
Steven R Danielson, Alice Wong, Valerio Carelli, Andrea Martinuzzi, Anthony H V Schapira, Gino A Cortopassi. J Biol Chem 2002
97
13

Grand rounds: could occupational exposure to n-hexane and other solvents precipitate visual failure in leber hereditary optic neuropathy?
Valerio Carelli, Flavia Franceschini, Silvia Venturi, Piero Barboni, Giacomo Savini, Giuseppe Barbieri, Ettore Pirro, Chiara La Morgia, Maria L Valentino, Francesca Zanardi,[...]. Environ Health Perspect 2007
32
13

Mitochondrial DNA variants as genetic risk factors for Parkinson disease.
C W Liou, J H Chuang, J B Chen, M M Tiao, P W Wang, S T Huang, T L Huang, W C Lee, S W Weng, P H Huang,[...]. Eur J Neurol 2016
19
13

The Eye Drop Preservative Benzalkonium Chloride Potently Induces Mitochondrial Dysfunction and Preferentially Affects LHON Mutant Cells.
Sandipan Datta, Christophe Baudouin, Francoise Brignole-Baudouin, Alexandre Denoyer, Gino A Cortopassi. Invest Ophthalmol Vis Sci 2017
36
13

Machine learning classifier for identification of damaging missense mutations exclusive to human mitochondrial DNA-encoded polypeptides.
Antonio Martín-Navarro, Andrés Gaudioso-Simón, Jorge Álvarez-Jarreta, Julio Montoya, Elvira Mayordomo, Eduardo Ruiz-Pesini. BMC Bioinformatics 2017
14
14

Mitochondrially derived peptides as novel regulators of metabolism.
Su-Jeong Kim, Jialin Xiao, Junxiang Wan, Pinchas Cohen, Kelvin Yen. J Physiol 2017
77
13

Molecular and bioenergetic differences between cells with African versus European inherited mitochondrial DNA haplogroups: implications for population susceptibility to diseases.
M Cristina Kenney, Marilyn Chwa, Shari R Atilano, Payam Falatoonzadeh, Claudio Ramirez, Deepika Malik, Mohamed Tarek, Javier Cáceres Del Carpio, Anthony B Nesburn, David S Boyer,[...]. Biochim Biophys Acta 2014
93
13

Mitochondrial DNA haplogroup K is associated with a lower risk of Parkinson's disease in Italians.
Daniele Ghezzi, Cecilia Marelli, Alessandro Achilli, Stefano Goldwurm, Gianni Pezzoli, Paolo Barone, Maria Teresa Pellecchia, Paolo Stanzione, Livia Brusa, Anna Rita Bentivoglio,[...]. Eur J Hum Genet 2005
147
13

eKLIPse: a sensitive tool for the detection and quantification of mitochondrial DNA deletions from next-generation sequencing data.
David Goudenège, Celine Bris, Virginie Hoffmann, Valerie Desquiret-Dumas, Claude Jardel, Benoit Rucheton, Sylvie Bannwarth, Veronique Paquis-Flucklinger, Anne Sophie Lebre, Estelle Colin,[...]. Genet Med 2019
15
13

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
380
13

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
982
13

Mitochondrial polymorphisms significantly reduce the risk of Parkinson disease.
Joelle M van der Walt, Kristin K Nicodemus, Eden R Martin, William K Scott, Martha A Nance, Ray L Watts, Jean P Hubble, Jonathan L Haines, William C Koller, Kelly Lyons,[...]. Am J Hum Genet 2003
413
13

Precise determination of mitochondrial DNA copy number in human skeletal and cardiac muscle by a PCR-based assay: lack of change of copy number with age.
Francis J Miller, Franklin L Rosenfeldt, Chunfang Zhang, Anthony W Linnane, Phillip Nagley. Nucleic Acids Res 2003
218
13

High-throughput sequencing in mitochondrial DNA research.
Fei Ye, David C Samuels, Travis Clark, Yan Guo. Mitochondrion 2014
53
13

Mitochondrial Genomic Backgrounds Affect Nuclear DNA Methylation and Gene Expression.
Carolyn J Vivian, Amanda E Brinker, Stefan Graw, Devin C Koestler, Christophe Legendre, Gerald C Gooden, Bodour Salhia, Danny R Welch. Cancer Res 2017
34
13

Mitonuclear communication in homeostasis and stress.
Pedro M Quirós, Adrienne Mottis, Johan Auwerx. Nat Rev Mol Cell Biol 2016
327
13

Chronic systemic pesticide exposure reproduces features of Parkinson's disease.
R Betarbet, T B Sherer, G MacKenzie, M Garcia-Osuna, A V Panov, J T Greenamyre. Nat Neurosci 2000
13

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
145
13

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
13

Mitochondrial DNA Depletion in Respiratory Chain-Deficient Parkinson Disease Neurons.
Anne Grünewald, Karolina A Rygiel, Philippa D Hepplewhite, Christopher M Morris, Martin Picard, Doug M Turnbull. Ann Neurol 2016
111
13

DNA precursor asymmetries in mammalian tissue mitochondria and possible contribution to mutagenesis through reduced replication fidelity.
Shiwei Song, Zachary F Pursell, William C Copeland, Matthew J Longley, Thomas A Kunkel, Christopher K Mathews. Proc Natl Acad Sci U S A 2005
114
13

Mitochondrial DNA haplogroup cluster UKJT reduces the risk of PD.
Angela Pyle, Thomas Foltynie, Watcharee Tiangyou, Claire Lambert, Sharon M Keers, Liesl M Allcock, Jill Davison, Simon J Lewis, Robert H Perry, Roger Barker,[...]. Ann Neurol 2005
137
13

Distinct genomic copy number in mitochondria of different mammalian organs.
K L Veltri, M Espiritu, G Singh. J Cell Physiol 1990
148
13

Bioinformatics Tools and Databases to Assess the Pathogenicity of Mitochondrial DNA Variants in the Field of Next Generation Sequencing.
Céline Bris, David Goudenege, Valérie Desquiret-Dumas, Majida Charif, Estelle Colin, Dominique Bonneau, Patrizia Amati-Bonneau, Guy Lenaers, Pascal Reynier, Vincent Procaccio. Front Genet 2018
28
13

Somatic mtDNA variation is an important component of Parkinson's disease.
Jonathan Coxhead, Marzena Kurzawa-Akanbi, Rafiqul Hussain, Angela Pyle, Patrick Chinnery, Gavin Hudson. Neurobiol Aging 2016
40
13



A neurodegenerative perspective on mitochondrial optic neuropathies.
Patrick Yu-Wai-Man, Marcela Votruba, Florence Burté, Chiara La Morgia, Piero Barboni, Valerio Carelli. Acta Neuropathol 2016
77
13


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.