A citation-based method for searching scientific literature

A T Rovio, D R Marchington, S Donat, H C Schuppe, J Abel, E Fritsche, D J Elliott, P Laippala, A L Ahola, D McNay, R F Harrison, B Hughes, T Barrett, D M Bailey, D Mehmet, A M Jequier, T B Hargreave, S H Kao, J M Cummins, D E Barton, H J Cooke, Y H Wei, L Wichmann, J Poulton, H T Jacobs. Nat Genet 2001
Times Cited: 136







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



Times Cited
  Times     Co-cited
Similarity


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
39

Frequent polymorphism of the mitochondrial DNA polymerase gamma gene (POLG) in patients with normal spermiograms and unexplained subfertility.
Martin Jensen, Henrik Leffers, Jørgen H Petersen, Anders Nyboe Andersen, Niels Jørgensen, Elisabeth Carlsen, Tina Kold Jensen, Niels E Skakkebaek, Ewa Rajpert-De Meyts. Hum Reprod 2004
64
59

The clinical significance of the POLG gene polymorphism in male infertility.
C Krausz, E Guarducci, L Becherini, S Degl'Innocenti, L Gerace, G Balercia, G Forti. J Clin Endocrinol Metab 2004
49
73

Is the CAG repeat of mitochondrial DNA polymerase gamma (POLG) associated with male infertility? A multi-centre French study.
I E Aknin-Seifer, R L Touraine, H Lejeune, C Jimenez, J Chouteau, J P Siffroi, K McElreavey, T Bienvenu, C Patrat, R Levy. Hum Reprod 2005
40
85


Parkinsonism, premature menopause, and mitochondrial DNA polymerase gamma mutations: clinical and molecular genetic study.
Petri Luoma, Atle Melberg, Juha O Rinne, Jyrki A Kaukonen, Nina N Nupponen, Richard M Chalmers, Anders Oldfors, Ilkka Rautakorpi, Leena Peltonen, Kari Majamaa,[...]. Lancet 2004
388
27

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
24


The polymorphic polyglutamine repeat in the mitochondrial DNA polymerase gamma gene is not associated with oligozoospermia.
A Brusco, C Michielotto, V Gatta, C Foresta, G Matullo, M Zeviani, G Ferrari, E Dragone, G Calabrese, M Rossato,[...]. J Endocrinol Invest 2006
23
82

Recessive POLG mutations presenting with sensory and ataxic neuropathy in compound heterozygote patients with progressive external ophthalmoplegia.
G Van Goethem, J J Martin, B Dermaut, A Löfgren, A Wibail, D Ververken, P Tack, I Dehaene, M Van Zandijcke, M Moonen,[...]. Neuromuscul Disord 2003
179
18

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
16

Can mitochondrial DNA mutations cause sperm dysfunction?
John Spiropoulos, Douglass M Turnbull, Patrick F Chinnery. Mol Hum Reprod 2002
111
16

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
16

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
15

Increased sperm mitochondrial DNA content in male infertility.
P May-Panloup, M-F Chrétien, F Savagner, C Vasseur, M Jean, Y Malthièry, P Reynier. Hum Reprod 2003
105
15

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
15

Analysis of the trinucleotide CAG repeat from the human mitochondrial DNA polymerase gene in healthy and diseased individuals.
A Rovio, V Tiranti, A L Bednarz, A Suomalainen, J N Spelbrink, N Lecrenier, A Melberg, M Zeviani, J Poulton, F Foury,[...]. Eur J Hum Genet 1999
28
50

In vivo functional analysis of the human mitochondrial DNA polymerase POLG expressed in cultured human cells.
J N Spelbrink, J M Toivonen, G A Hakkaart, J M Kurkela, H M Cooper, S K Lehtinen, N Lecrenier, J W Back, D Speijer, F Foury,[...]. J Biol Chem 2000
145
14

Structure-function defects of human mitochondrial DNA polymerase in autosomal dominant progressive external ophthalmoplegia.
Maria A Graziewicz, Matthew J Longley, Rachelle J Bienstock, Massimo Zeviani, William C Copeland. Nat Struct Mol Biol 2004
104
14

Mitochondrial disease and reduced sperm motility.
T Folgerø, K Bertheussen, S Lindal, T Torbergsen, P Oian. Hum Reprod 1993
133
14


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
13

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
13

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
13

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
13


Infantile hepatocerebral syndromes associated with mutations in the mitochondrial DNA polymerase-gammaA.
Gianfrancesco Ferrari, Eleonora Lamantea, Alice Donati, Massimiliano Filosto, Egill Briem, Franco Carrara, Rossella Parini, Alessandro Simonati, René Santer, Massimo Zeviani. Brain 2005
220
12


A prevalent POLG CAG microsatellite length allele in humans and African great apes.
Anja T Rovio, Josef Abel, Arja L Ahola, Aida M Andres, Jaume Bertranpetit, Antoine Blancher, Ronald E Bontrop, Leona G Chemnick, Howard J Cooke, James M Cummins,[...]. Mamm Genome 2004
19
57

Mitochondrial DNA content of human spermatozoa.
Carmen Díez-Sánchez, Eduardo Ruiz-Pesini, Ana Cristina Lapeña, Julio Montoya, Acisclo Pérez-Martos, José Antonio Enríquez, Manuel J López-Pérez. Biol Reprod 2003
62
17

Functional defects due to spacer-region mutations of human mitochondrial DNA polymerase in a family with an ataxia-myopathy syndrome.
Petri T Luoma, Ningguang Luo, Wolfgang N Löscher, Carol L Farr, Rita Horvath, Julia Wanschitz, Stefan Kiechl, Laurie S Kaguni, Anu Suomalainen. Hum Mol Genet 2005
84
13


Molecular analysis of polymerase gamma gene and mitochondrial polymorphism in fertile and subfertile men.
T P Harris, K P Gomas, F Weir, A J Holyoake, P McHugh, M Wu, Y Sin, I L Sin, F Y T Sin. Int J Androl 2006
13
84

Mitochondria-related male infertility.
Kazuto Nakada, Akitsugu Sato, Kayo Yoshida, Takashi Morita, Hiromitsu Tanaka, Shin-Ichi Inoue, Hiromichi Yonekawa, Jun-Ichi Hayashi. Proc Natl Acad Sci U S A 2006
153
11

Mitochondrial DNA polymerase-gamma and human disease.
Gavin Hudson, Patrick F Chinnery. Hum Mol Genet 2006
150
11

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
10


Sperm mitochondrial mutations as a cause of low sperm motility.
Kumarasamy Thangaraj, Manjunath B Joshi, Alla G Reddy, Avinash A Rasalkar, Lalji Singh. J Androl 2003
68
14

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
12

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
10

POLG mutations in sporadic mitochondrial disorders with multiple mtDNA deletions.
Alessio Di Fonzo, Andreina Bordoni, Marco Crimi, Galbiati Sara, Roberto Del Bo, Nereo Bresolin, Giacomo P Comi. Hum Mutat 2003
77
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
9


High incidence of single nucleotide substitutions in the mitochondrial genome is associated with poor semen parameters in men.
A J Holyoake, P McHugh, M Wu, S O'Carroll, P Benny, I L Sin, F Y Sin. Int J Androl 2001
86
10

Paternal inheritance of mitochondrial DNA.
Marianne Schwartz, John Vissing. N Engl J Med 2002
342
9

Mitochondrial DNA content affects the fertilizability of human oocytes.
P Reynier, P May-Panloup, M F Chrétien, C J Morgan, M Jean, F Savagner, P Barrière, Y Malthièry. Mol Hum Reprod 2001
315
9

Association of a single-nucleotide polymorphism of the deleted-in-azoospermia-like gene with susceptibility to spermatogenic failure.
Yen-Ni Teng, Yung-Ming Lin, Ying-Hung Lin, Shu-Yi Tsao, Chao-Chin Hsu, Shio-Jean Lin, Wan-Ching Tsai, Pao-Lin Kuo. J Clin Endocrinol Metab 2002
69
13

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
9

Mutant POLG2 disrupts DNA polymerase gamma subunits and causes progressive external ophthalmoplegia.
Matthew J Longley, Susanna Clark, Cynthia Yu Wai Man, Gavin Hudson, Steve E Durham, Robert W Taylor, Simon Nightingale, Douglass M Turnbull, William C Copeland, Patrick F Chinnery. Am J Hum Genet 2006
164
9



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.