A citation-based method for searching scientific literature

H T Jacobs. Trends Genet 2001
Times Cited: 15







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



Times Cited
  Times     Co-cited
Similarity


Generation of mice with mitochondrial dysfunction by introducing mouse mtDNA carrying a deletion into zygotes.
K Inoue, K Nakada, A Ogura, K Isobe, Y Goto, I Nonaka, J I Hayashi. Nat Genet 2000
293
26

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
26


Animal models for respiratory chain disease.
N G Larsson, P Rustin. Trends Mol Med 2001
37
26


Molecular genetic aspects of human mitochondrial disorders.
N G Larsson, D A Clayton. Annu Rev Genet 1995
365
20




Human mitochondrial DNA diseases.
T Pulkes, M G Hanna. Adv Drug Deliv Rev 2001
47
20

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
20

Mitochondrial DNA mutations and pathogenesis.
E A Schon, E Bonilla, S DiMauro. J Bioenerg Biomembr 1997
354
20


The inheritance of mitochondrial DNA heteroplasmy: random drift, selection or both?
P F Chinnery, D R Thorburn, D C Samuels, S L White, H M Dahl, D M Turnbull, R N Lightowlers, N Howell. Trends Genet 2000
170
20



Mitochondrial DNA mutations in the pathogenesis of human disease.
P F Chinnery, D M Turnbull. Mol Med Today 2000
64
20

Detecting heteroplasmy from high-throughput sequencing of complete human mitochondrial DNA genomes.
Mingkun Li, Anna Schönberg, Michael Schaefer, Roland Schroeder, Ivane Nasidze, Mark Stoneking. Am J Hum Genet 2010
199
20


Elimination of paternal mitochondrial DNA in intraspecific crosses during early mouse embryogenesis.
H Kaneda, J Hayashi, S Takahama, C Taya, K F Lindahl, H Yonekawa. Proc Natl Acad Sci U S A 1995
328
13


Maternal germ-line transmission of mutant mtDNAs from embryonic stem cell-derived chimeric mice.
J E Sligh, S E Levy, K G Waymire, P Allard, D L Dillehay, S Nusinowitz, J R Heckenlively, G R MacGregor, D C Wallace. Proc Natl Acad Sci U S A 2000
102
13

Paternal inheritance of mitochondrial DNA in mice.
U Gyllensten, D Wharton, A Josefsson, A C Wilson. Nature 1991
378
13

Mouse models for mitochondrial disease.
D C Wallace. Am J Med Genet 2001
126
13

Tissue-specific selection for different mtDNA genotypes in heteroplasmic mice.
J P Jenuth, A C Peterson, E A Shoubridge. Nat Genet 1997
287
13


Cloning of neuronal mtDNA variants in cultured cells by synaptosome fusion with mtDNA-less cells.
I Trounce, J Schmiedel, H C Yen, S Hosseini, M D Brown, J J Olson, D C Wallace. Nucleic Acids Res 2000
39
13

Mitochondrial dysfunction and neuromuscular disease.
R A Nardin, D R Johns. Muscle Nerve 2001
62
13


Decreased aminoacylation of mutant tRNAs in MELAS but not in MERRF patients.
G V Börner, M Zeviani, V Tiranti, F Carrara, S Hoffmann, K D Gerbitz, H Lochmüller, D Pongratz, T Klopstock, A Melberg,[...]. Hum Mol Genet 2000
65
13

Suppression of mutations in mitochondrial DNA by tRNAs imported from the cytoplasm.
O A Kolesnikova, N S Entelis, H Mireau, T D Fox, R P Martin, I A Tarassov. Science 2000
114
13


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
13

Mitochondrial genetics and disease.
E A Schon. Trends Biochem Sci 2000
134
13

A pathogenic point mutation reduces stability of mitochondrial mutant tRNA(Ile).
T Yasukawa, N Hino, T Suzuki, K Watanabe, T Ueda, S Ohta. Nucleic Acids Res 2000
46
13

Isolation of mitochondrial DNA-less mouse cell lines and their application for trapping mouse synaptosomal mitochondrial DNA with deletion mutations.
K Inoue, S Ito, D Takai, A Soejima, H Shisa, J B LePecq, E Segal-Bendirdjian, Y Kagawa, J I Hayashi. J Biol Chem 1997
59
13


Pathophysiology of the MELAS 3243 transition mutation.
A Flierl, H Reichmann, P Seibel. J Biol Chem 1997
71
13

Ubiquitinated sperm mitochondria, selective proteolysis, and the regulation of mitochondrial inheritance in mammalian embryos.
P Sutovsky, R D Moreno, J Ramalho-Santos, T Dominko, C Simerly, G Schatten. Biol Reprod 2000
271
13

Epidemiology and treatment of mitochondrial disorders.
P F Chinnery, D M Turnbull. Am J Med Genet 2001
131
13

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
13

Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation.
J M Shoffner, M T Lott, A M Lezza, P Seibel, S W Ballinger, D C Wallace. Cell 1990
13






Mitochondrial genome variation and the origin of modern humans.
M Ingman, H Kaessmann, S Pääbo, U Gyllensten. Nature 2000
779
13

Gene expression profiling: monitoring transcription and translation products using DNA microarrays and proteomics.
J E Celis, M Kruhøffer, I Gromova, C Frederiksen, M Ostergaard, T Thykjaer, P Gromov, J Yu, H Pálsdóttir, N Magnusson,[...]. FEBS Lett 2000
217
13

The large subunit of the mammalian mitochondrial ribosome. Analysis of the complement of ribosomal proteins present.
E C Koc, W Burkhart, K Blackburn, M B Moyer, D M Schlatzer, A Moseley, L L Spremulli. J Biol Chem 2001
196
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.