A citation-based method for searching scientific literature

Rosa Pello, Miguel A Martín, Valerio Carelli, Leo G Nijtmans, Alessandro Achilli, Maria Pala, Antonio Torroni, Aurora Gómez-Durán, Eduardo Ruiz-Pesini, Andrea Martinuzzi, Jan A Smeitink, Joaquín Arenas, Cristina Ugalde. Hum Mol Genet 2008
Times Cited: 122







List of co-cited articles
1192 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
259
23

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
192
23


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
244
20

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

Ancient mtDNA genetic variants modulate mtDNA transcription and replication.
Sarit Suissa, Zhibo Wang, Jason Poole, Sharine Wittkopp, Jeanette Feder, Timothy E Shutt, Douglas C Wallace, Gerald S Shadel, Dan Mishmar. PLoS Genet 2009
112
19


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
541
17



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
16

Gene-environment interactions in Leber hereditary optic neuropathy.
Matthew Anthony Kirkman, Patrick Yu-Wai-Man, Alex Korsten, Miriam Leonhardt, Konstantin Dimitriadis, Ireneaus F De Coo, Thomas Klopstock, Patrick Francis Chinnery. Brain 2009
201
15

An enhanced MITOMAP with a global mtDNA mutational phylogeny.
Eduardo Ruiz-Pesini, Marie T Lott, Vincent Procaccio, Jason C Poole, Marty C Brandon, Dan Mishmar, Christina Yi, James Kreuziger, Pierre Baldi, Douglas C Wallace. Nucleic Acids Res 2007
412
15

Identification of mitochondrial DNA polymorphisms that alter mitochondrial matrix pH and intracellular calcium dynamics.
An-a Kazuno, Kae Munakata, Takeharu Nagai, Satoshi Shimozono, Masashi Tanaka, Makoto Yoneda, Nobumasa Kato, Atsushi Miyawaki, Tadafumi Kato. PLoS Genet 2006
164
15

Updating the East Asian mtDNA phylogeny: a prerequisite for the identification of pathogenic mutations.
Qing-Peng Kong, Hans-Jürgen Bandelt, Chang Sun, Yong-Gang Yao, Antonio Salas, Alessandro Achilli, Cheng-Ye Wang, Li Zhong, Chun-Ling Zhu, Shi-Fang Wu,[...]. Hum Mol Genet 2006
305
14

Blue native PAGE.
Ilka Wittig, Hans-Peter Braun, Hermann Schägger. Nat Protoc 2006
13

Inherited mitochondrial optic neuropathies.
P Yu-Wai-Man, P G Griffiths, G Hudson, P F Chinnery. J Med Genet 2009
243
13

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
140
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
12

Respiratory function in cybrid cell lines carrying European mtDNA haplogroups: implications for Leber's hereditary optic neuropathy.
Valerio Carelli, Lodovica Vergani, Barbara Bernazzi, Claudia Zampieron, Laura Bucchi, Maria Valentino, Chiara Rengo, Antonio Torroni, Andrea Martinuzzi. Biochim Biophys Acta 2002
49
24

Leber's hereditary optic neuropathy (LHON) pathogenic mutations induce mitochondrial-dependent apoptotic death in transmitochondrial cells incubated with galactose medium.
Anna Ghelli, Claudia Zanna, Anna Maria Porcelli, Anthony H V Schapira, Andrea Martinuzzi, Valerio Carelli, Michela Rugolo. J Biol Chem 2003
142
12

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
12



Classification of European mtDNAs from an analysis of three European populations.
A Torroni, K Huoponen, P Francalacci, M Petrozzi, L Morelli, R Scozzari, D Obinu, M L Savontaus, D C Wallace. Genetics 1996
595
11


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
11

Natural selection shaped regional mtDNA variation in humans.
Dan Mishmar, Eduardo Ruiz-Pesini, Pawel Golik, Vincent Macaulay, Andrew G Clark, Seyed Hosseini, Martin Brandon, Kirk Easley, Estella Chen, Michael D Brown,[...]. Proc Natl Acad Sci U S A 2003
648
11

Retinal ganglion cell neurodegeneration in mitochondrial inherited disorders.
Valerio Carelli, Chiara La Morgia, Maria Lucia Valentino, Piero Barboni, Fred N Ross-Cisneros, Alfredo A Sadun. Biochim Biophys Acta 2009
144
11

Primary pathogenic mtDNA mutations in multigeneration pedigrees with Leber hereditary optic neuropathy.
D A Mackey, R J Oostra, T Rosenberg, E Nikoskelainen, J Bronte-Stewart, J Poulton, A E Harding, G Govan, P A Bolhuis, S Norby. Am J Hum Genet 1996
245
11

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
76
13

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
16

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
10

Differentiation-specific effects of LHON mutations introduced into neuronal NT2 cells.
Alice Wong, Lucia Cavelier, Heather E Collins-Schramm, Michael F Seldin, Michael McGrogan, Marja-Liisa Savontaus, Gino A Cortopassi. Hum Mol Genet 2002
144
10

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
70
14

Human mtDNA haplogroups associated with high or reduced spermatozoa motility.
E Ruiz-Pesini, A C Lapeña, C Díez-Sánchez, A Pérez-Martos, J Montoya, E Alvarez, M Díaz, A Urriés, L Montoro, M J López-Pérez,[...]. Am J Hum Genet 2000
337
9

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
9

Mitochondrial dysfunction as a cause of optic neuropathies.
Valerio Carelli, Fred N Ross-Cisneros, Alfredo A Sadun. Prog Retin Eye Res 2004
516
9

Identification of an X-chromosomal locus and haplotype modulating the phenotype of a mitochondrial DNA disorder.
Gavin Hudson, Sharon Keers, Patrick Yu-Wai-Man, Philip Griffiths, Kirsi Huoponen, Marja-Liisa Savontaus, Eeva Nikoskelainen, Massimo Zeviani, Franco Carrara, Rita Horvath,[...]. Am J Hum Genet 2005
135
9


Mitochondrial DNA haplogroups M7b1'2 and M8a affect clinical expression of leber hereditary optic neuropathy in Chinese families with the m.11778G-->a mutation.
Yanli Ji, A-Mei Zhang, Xiaoyun Jia, Ya-Ping Zhang, Xueshan Xiao, Shiqiang Li, Xiangming Guo, Hans-Jürgen Bandelt, Qingjiong Zhang, Yong-Gang Yao. Am J Hum Genet 2008
109
9

Cancer type-specific modulation of mitochondrial haplogroups in breast, colorectal and thyroid cancer.
Hezhi Fang, Lijun Shen, Tao Chen, Jing He, Zhinan Ding, Jia Wei, Jianchun Qu, Guorong Chen, Jianxin Lu, Yidong Bai. BMC Cancer 2010
76
11


Human mitochondrial DNA: roles of inherited and somatic mutations.
Eric A Schon, Salvatore DiMauro, Michio Hirano. Nat Rev Genet 2012
409
9

Progressive increase in mtDNA 3243A>G heteroplasmy causes abrupt transcriptional reprogramming.
Martin Picard, Jiangwen Zhang, Saege Hancock, Olga Derbeneva, Ryan Golhar, Pawel Golik, Sean O'Hearn, Shawn Levy, Prasanth Potluri, Maria Lvova,[...]. Proc Natl Acad Sci U S A 2014
160
9

Phylogeographic differentiation of mitochondrial DNA in Han Chinese.
Yong-Gang Yao, Qing-Peng Kong, Hans-Jürgen Bandelt, Toomas Kivisild, Ya-Ping Zhang. Am J Hum Genet 2002
367
8

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
8

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
8

Analysis of European mitochondrial haplogroups with Alzheimer disease risk.
Joelle M van der Walt, Yulia A Dementieva, Eden R Martin, William K Scott, Kristin K Nicodemus, Charles C Kroner, Kathleen A Welsh-Bohmer, Ann M Saunders, Allen D Roses, Gary W Small,[...]. Neurosci Lett 2004
216
8


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.