A citation-based method for searching scientific literature

J J Miret, L Pessoa-Brandão, R S Lahue. Mol Cell Biol 1997
Times Cited: 76







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



Times Cited
  Times     Co-cited
Similarity


Expansion and length-dependent fragility of CTG repeats in yeast.
C H Freudenreich, S M Kantrow, V A Zakian. Science 1998
343
61




Trinucleotide repeats that expand in human disease form hairpin structures in vitro.
A M Gacy, G Goellner, N Juranić, S Macura, C T McMurray. Cell 1995
465
55


Orientation dependence of trinucleotide CAG repeat instability in Saccharomyces cerevisiae.
D J Maurer, B L O'Callaghan, D M Livingston. Mol Cell Biol 1996
102
48


Trinucleotide repeats affect DNA replication in vivo.
G M Samadashwily, G Raca, S M Mirkin. Nat Genet 1997
260
44

Repeat expansion--all in a flap?
D A Gordenin, T A Kunkel, M A Resnick. Nat Genet 1997
176
38


Mismatch repair in Escherichia coli enhances instability of (CTG)n triplet repeats from human hereditary diseases.
A Jaworski, W A Rosche, R Gellibolian, S Kang, M Shimizu, R P Bowater, R R Sinden, R D Wells. Proc Natl Acad Sci U S A 1995
138
36


Somatic expansion behaviour of the (CTG)n repeat in myotonic dystrophy knock-in mice is differentially affected by Msh3 and Msh6 mismatch-repair proteins.
Walther J A A van den Broek, Marcel R Nelen, Derick G Wansink, Marga M Coerwinkel, Hein te Riele, Patricia J T A Groenen, Bé Wieringa. Hum Mol Genet 2002
210
32

Triplet repeats form secondary structures that escape DNA repair in yeast.
H Moore, P W Greenwell, C P Liu, N Arnheim, T D Petes. Proc Natl Acad Sci U S A 1999
160
31

Inhibition of FEN-1 processing by DNA secondary structure at trinucleotide repeats.
C Spiro, R Pelletier, M L Rolfsmeier, M J Dixon, R S Lahue, G Gupta, M S Park, X Chen, S V Mariappan, C T McMurray. Mol Cell 1999
141
31



Human MSH2 binds to trinucleotide repeat DNA structures associated with neurodegenerative diseases.
C E Pearson, A Ewel, S Acharya, R A Fishel, R R Sinden. Hum Mol Genet 1997
118
27




CTG repeat instability and size variation timing in DNA repair-deficient mice.
Cédric Savouret, Edith Brisson, Jeroen Essers, Roland Kanaar, Albert Pastink, Hein te Riele, Claudine Junien, Geneviève Gourdon. EMBO J 2003
146
23

(CAG)(n)-hairpin DNA binds to Msh2-Msh3 and changes properties of mismatch recognition.
Barbara A L Owen, Zungyoon Yang, Maoyi Lai, Maciej Gajec, John D Badger, Jeffrey J Hayes, Winfried Edelmann, Raju Kucherlapati, Teresa M Wilson, Cynthia T McMurray. Nat Struct Mol Biol 2005
162
23


Hairpin properties of single-stranded DNA containing a GC-rich triplet repeat: (CTG)15.
M Mitas, A Yu, J Dill, T J Kamp, E J Chambers, I S Haworth. Nucleic Acids Res 1995
127
22

CTG repeats show bimodal amplification in E. coli.
P S Sarkar, H C Chang, F B Boudi, S Reddy. Cell 1998
57
29

Sticky DNA: self-association properties of long GAA.TTC repeats in R.R.Y triplex structures from Friedreich's ataxia.
N Sakamoto, P D Chastain, P Parniewski, K Ohshima, M Pandolfo, J D Griffith, R D Wells. Mol Cell 1999
233
22



Meiotic instability of CAG repeat tracts occurs by double-strand break repair in yeast.
C Jankowski, F Nasar, D K Nag. Proc Natl Acad Sci U S A 2000
92
22




GAA instability in Friedreich's Ataxia shares a common, DNA-directed and intraallelic mechanism with other trinucleotide diseases.
A M Gacy, G M Goellner, C Spiro, X Chen, G Gupta, E M Bradbury, R B Dyer, M J Mikesell, J Z Yao, A J Johnson,[...]. Mol Cell 1998
133
21

Transcription increases the deletion frequency of long CTG.CAG triplet repeats from plasmids in Escherichia coli.
R P Bowater, A Jaworski, J E Larson, P Parniewski, R D Wells. Nucleic Acids Res 1997
78
21


Trinucleotide repeats in neurogenetic disorders.
H L Paulson, K H Fischbeck. Annu Rev Neurosci 1996
273
19

Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion.
V Campuzano, L Montermini, M D Moltò, L Pianese, M Cossée, F Cavalcanti, E Monros, F Rodius, F Duclos, A Monticelli,[...]. Science 1996
19



Single sperm analysis of the trinucleotide repeats in the Huntington's disease gene: quantification of the mutation frequency spectrum.
E P Leeflang, L Zhang, S Tavaré, R Hubert, J Srinidhi, M E MacDonald, R H Myers, M de Young, N S Wexler, J F Gusella. Hum Mol Genet 1995
142
19


Evidence of cis-acting factors in replication-mediated trinucleotide repeat instability in primate cells.
John D Cleary, Kerrie Nichol, Yuh-Hwa Wang, Christopher E Pearson. Nat Genet 2002
148
19

Pms2 is a genetic enhancer of trinucleotide CAG.CTG repeat somatic mosaicism: implications for the mechanism of triplet repeat expansion.
Mário Gomes-Pereira, M Teresa Fortune, Laura Ingram, John P McAbney, Darren G Monckton. Hum Mol Genet 2004
129
19



Different mechanisms underlie DNA instability in Huntington disease and colorectal cancer.
G M Goellner, D Tester, S Thibodeau, E Almqvist, Y P Goldberg, M R Hayden, C T McMurray. Am J Hum Genet 1997
52
26




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.