A citation-based method for searching scientific literature

Petri Luoma, Atle Melberg, Juha O Rinne, Jyrki A Kaukonen, Nina N Nupponen, Richard M Chalmers, Anders Oldfors, Ilkka Rautakorpi, Leena Peltonen, Kari Majamaa, Hannu Somer, Anu Suomalainen. Lancet 2004
Times Cited: 388







List of co-cited articles
1526 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


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
972
26

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
22

Early-onset familial parkinsonism due to POLG mutations.
Guido Davidzon, Paul Greene, Michelangelo Mancuso, Kevin J Klos, J Eric Ahlskog, Michio Hirano, Salvatore DiMauro. Ann Neurol 2006
160
21

Dominant inheritance of premature ovarian failure associated with mutant mitochondrial DNA polymerase gamma.
Alistair T Pagnamenta, Jan-Willem Taanman, Callum J Wilson, Neil E Anderson, Rosetta Marotta, Andrew J Duncan, Maria Bitner-Glindzicz, Robert W Taylor, Adrienne Laskowski, David R Thorburn,[...]. Hum Reprod 2006
100
20

Mutation of POLG is associated with progressive external ophthalmoplegia characterized by mtDNA deletions.
G Van Goethem, B Dermaut, A Löfgren, J J Martin, C Van Broeckhoven. Nat Genet 2001
572
16

Severe nigrostriatal degeneration without clinical parkinsonism in patients with polymerase gamma mutations.
Charalampos Tzoulis, Gia Tuong Tran, Thomas Schwarzlmüller, Karsten Specht, Kristoffer Haugarvoll, Novin Balafkan, Peer K Lilleng, Hrvoje Miletic, Martin Biermann, Laurence A Bindoff. Brain 2013
55
29

Mitochondrial DNA deletions are abundant and cause functional impairment in aged human substantia nigra neurons.
Yevgenya Kraytsberg, Elena Kudryavtseva, Ann C McKee, Changiz Geula, Neil W Kowall, Konstantin Khrapko. Nat Genet 2006
617
16

Mitochondrial DNA polymerase W748S mutation: a common cause of autosomal recessive ataxia with ancient European origin.
Anna H Hakonen, Silja Heiskanen, Vesa Juvonen, Ilse Lappalainen, Petri T Luoma, Maria Rantamaki, Gert Van Goethem, Ann Lofgren, Peter Hackman, Anders Paetau,[...]. Am J Hum Genet 2005
217
14

The spectrum of clinical disease caused by the A467T and W748S POLG mutations: a study of 26 cases.
Charalampos Tzoulis, Bernt A Engelsen, Wenche Telstad, Jan Aasly, Massimo Zeviani, Synnøve Winterthun, Gianfrancesco Ferrari, Jan H Aarseth, Laurence A Bindoff. Brain 2006
224
13

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
12

A novel polymerase gamma mutation in a family with ophthalmoplegia, neuropathy, and Parkinsonism.
Michelangelo Mancuso, Massimiliano Filosto, Shin J Oh, Salvatore DiMauro. Arch Neurol 2004
79
15

Chronic Parkinsonism in humans due to a product of meperidine-analog synthesis.
J W Langston, P Ballard, J W Tetrud, I Irwin. Science 1983
12

POLG-related disorders and their neurological manifestations.
Shamima Rahman, William C Copeland. Nat Rev Neurol 2019
84
14

Phenotypic spectrum associated with mutations of the mitochondrial polymerase gamma gene.
Rita Horvath, Gavin Hudson, Gianfrancesco Ferrari, Nancy Fütterer, Sofia Ahola, Eleonora Lamantea, Holger Prokisch, Hanns Lochmüller, Robert McFarland, V Ramesh,[...]. Brain 2006
281
11

Human mitochondrial DNA deletions associated with mutations in the gene encoding Twinkle, a phage T7 gene 4-like protein localized in mitochondria.
J N Spelbrink, F Y Li, V Tiranti, K Nikali, Q P Yuan, M Tariq, S Wanrooij, N Garrido, G Comi, L Morandi,[...]. Nat Genet 2001
603
11

Mutation in the alpha-synuclein gene identified in families with Parkinson's disease.
M H Polymeropoulos, C Lavedan, E Leroy, S E Ide, A Dehejia, A Dutra, B Pike, H Root, J Rubenstein, R Boyer,[...]. Science 1997
11

Alpha-synuclein in Lewy bodies.
M G Spillantini, M L Schmidt, V M Lee, J Q Trojanowski, R Jakes, M Goedert. Nature 1997
11


Progressive parkinsonism in mice with respiratory-chain-deficient dopamine neurons.
Mats I Ekstrand, Mügen Terzioglu, Dagmar Galter, Shunwei Zhu, Christoph Hofstetter, Eva Lindqvist, Sebastian Thams, Anita Bergstrand, Fredrik Sterky Hansson, Aleksandra Trifunovic,[...]. Proc Natl Acad Sci U S A 2007
376
10


Mutation of the linker region of the polymerase gamma-1 (POLG1) gene associated with progressive external ophthalmoplegia and Parkinsonism.
Gavin Hudson, Andrew M Schaefer, Robert W Taylor, Watcharee Tiangyou, Andrew Gibson, Graham Venables, Philip Griffiths, David J Burn, Douglass M Turnbull, Patrick F Chinnery. Arch Neurol 2007
61
16

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
10

Mutations in LARS2, encoding mitochondrial leucyl-tRNA synthetase, lead to premature ovarian failure and hearing loss in Perrault syndrome.
Sarah B Pierce, Ksenija Gersak, Rachel Michaelson-Cohen, Tom Walsh, Ming K Lee, Daniel Malach, Rachel E Klevit, Mary-Claire King, Ephrat Levy-Lahad. Am J Hum Genet 2013
125
10

α-Synuclein is localized to mitochondria-associated ER membranes.
Cristina Guardia-Laguarta, Estela Area-Gomez, Cornelia Rüb, Yuhui Liu, Jordi Magrané, Dorothea Becker, Wolfgang Voos, Eric A Schon, Serge Przedborski. J Neurosci 2014
279
10

Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology.
Alexander Zimprich, Saskia Biskup, Petra Leitner, Peter Lichtner, Matthew Farrer, Sarah Lincoln, Jennifer Kachergus, Mary Hulihan, Ryan J Uitti, Donald B Calne,[...]. Neuron 2004
10

Mitochondrial complex I deficiency in Parkinson's disease.
A H Schapira, J M Cooper, D Dexter, P Jenner, J B Clark, C D Marsden. Lancet 1989
10

Hereditary early-onset Parkinson's disease caused by mutations in PINK1.
Enza Maria Valente, Patrick M Abou-Sleiman, Viviana Caputo, Miratul M K Muqit, Kirsten Harvey, Suzana Gispert, Zeeshan Ali, Domenico Del Turco, Anna Rita Bentivoglio, Daniel G Healy,[...]. Science 2004
10

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
109
10

Defective mitochondrial DNA homeostasis in the substantia nigra in Parkinson disease.
Christian Dölle, Irene Flønes, Gonzalo S Nido, Hrvoje Miletic, Nelson Osuagwu, Stine Kristoffersen, Peer K Lilleng, Jan Petter Larsen, Ole-Bjørn Tysnes, Kristoffer Haugarvoll,[...]. Nat Commun 2016
112
10

Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism.
T Kitada, S Asakawa, N Hattori, H Matsumine, Y Yamamura, S Minoshima, M Yokochi, Y Mizuno, N Shimizu. Nature 1998
10

Autosomal recessive mitochondrial ataxic syndrome due to mitochondrial polymerase gamma mutations.
S Winterthun, G Ferrari, L He, R W Taylor, M Zeviani, D M Turnbull, B A Engelsen, G Moen, L A Bindoff. Neurology 2005
179
9

Mutations of mitochondrial DNA polymerase gammaA are a frequent cause of autosomal dominant or recessive progressive external ophthalmoplegia.
Eleonora Lamantea, Valeria Tiranti, Andreina Bordoni, Antonio Toscano, Francesco Bono, Serena Servidei, Alex Papadimitriou, Hans Spelbrink, Laura Silvestri, Giorgio Casari,[...]. Ann Neurol 2002
200
9

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
9

POLG mutations in neurodegenerative disorders with ataxia but no muscle involvement.
G Van Goethem, P Luoma, M Rantamäki, A Al Memar, S Kaakkola, P Hackman, R Krahe, A Löfgren, J J Martin, P De Jonghe,[...]. Neurology 2004
197
9

Perrault syndrome is caused by recessive mutations in CLPP, encoding a mitochondrial ATP-dependent chambered protease.
Emma M Jenkinson, Atteeq U Rehman, Tom Walsh, Jill Clayton-Smith, Kwanghyuk Lee, Robert J Morell, Meghan C Drummond, Shaheen N Khan, Muhammad Asif Naeem, Bushra Rauf,[...]. Am J Hum Genet 2013
129
9

Familial parkinsonism and ophthalmoplegia from a mutation in the mitochondrial DNA helicase twinkle.
Robert H Baloh, Ezequiel Salavaggione, Jeffrey Milbrandt, Alan Pestronk. Arch Neurol 2007
68
13

Parkinson's disease: mechanisms and models.
William Dauer, Serge Przedborski. Neuron 2003
9

Molecular and clinical genetics of mitochondrial diseases due to POLG mutations.
Lee-Jun C Wong, Robert K Naviaux, Nicola Brunetti-Pierri, Qing Zhang, Eric S Schmitt, Cavatina Truong, Margherita Milone, Bruce H Cohen, Beverly Wical, Jaya Ganesh,[...]. Hum Mutat 2008
187
9

The unfolding clinical spectrum of POLG mutations.
M J Blok, B J van den Bosch, E Jongen, A Hendrickx, C E de Die-Smulders, J E Hoogendijk, E Brusse, M de Visser, B T Poll-The, J Bierau,[...]. J Med Genet 2009
60
13

Molecular pathogenesis of polymerase γ-related neurodegeneration.
Charalampos Tzoulis, Gia Tuong Tran, Jonathan Coxhead, Bjørn Bertelsen, Peer K Lilleng, Novin Balafkan, Brendan Payne, Hrvoje Miletic, Patrick F Chinnery, Laurence A Bindoff. Ann Neurol 2014
43
18

MitoCarta2.0: an updated inventory of mammalian mitochondrial proteins.
Sarah E Calvo, Karl R Clauser, Vamsi K Mootha. Nucleic Acids Res 2016
734
8

PINK1 is selectively stabilized on impaired mitochondria to activate Parkin.
Derek P Narendra, Seok Min Jin, Atsushi Tanaka, Der-Fen Suen, Clement A Gautier, Jie Shen, Mark R Cookson, Richard J Youle. PLoS Biol 2010
8

Low platelet mitochondrial complex I and complex II/III activity in early untreated Parkinson's disease.
R H Haas, F Nasirian, K Nakano, D Ward, M Pay, R Hill, C W Shults. Ann Neurol 1995
321
8

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
8

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
8

The ubiquitin kinase PINK1 recruits autophagy receptors to induce mitophagy.
Michael Lazarou, Danielle A Sliter, Lesley A Kane, Shireen A Sarraf, Chunxin Wang, Jonathon L Burman, Dionisia P Sideris, Adam I Fogel, Richard J Youle. Nature 2015
8

Clinical, Genetic, and Radiological Features of Extrapyramidal Movement Disorders in Mitochondrial Disease.
Mika H Martikainen, Yi Shiau Ng, Gráinne S Gorman, Charlotte L Alston, Emma L Blakely, Andrew M Schaefer, Patrick F Chinnery, David J Burn, Robert W Taylor, Robert McFarland,[...]. JAMA Neurol 2016
40
20

Mitochondria: in sickness and in health.
Jodi Nunnari, Anu Suomalainen. Cell 2012
8

Clinical and molecular features of POLG-related mitochondrial disease.
Jeffrey D Stumpf, Russell P Saneto, William C Copeland. Cold Spring Harb Perspect Biol 2013
68
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.