A citation-based method for searching scientific literature


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



Times Cited
  Times     Co-cited
Similarity





Reduction in size of the myotonic dystrophy trinucleotide repeat mutation during transmission.
K L O'Hoy, C Tsilfidis, M S Mahadevan, C E Neville, J Barceló, A G Hunter, R G Korneluk. Science 1993
122
23

MSH2 ATPase domain mutation affects CTG*CAG repeat instability in transgenic mice.
Stéphanie Tomé, Ian Holt, Winfried Edelmann, Glenn E Morris, Arnold Munnich, Christopher E Pearson, Geneviève Gourdon. PLoS Genet 2009
65
23

Absence of MutSβ leads to the formation of slipped-DNA for CTG/CAG contractions at primate replication forks.
Meghan M Slean, Gagan B Panigrahi, Arturo López Castel, August B Pearson, Alan E Tomkinson, Christopher E Pearson. DNA Repair (Amst) 2016
18
33

Repeat instability during DNA repair: Insights from model systems.
Karen Usdin, Nealia C M House, Catherine H Freudenreich. Crit Rev Biochem Mol Biol 2015
101
23

Contracting CAG/CTG repeats using the CRISPR-Cas9 nickase.
Cinzia Cinesi, Lorène Aeschbach, Bin Yang, Vincent Dion. Nat Commun 2016
43
23






Repeat expansion--all in a flap?
D A Gordenin, T A Kunkel, M A Resnick. Nat Genet 1997
176
19



Saccharomyces cerevisiae flap endonuclease 1 uses flap equilibration to maintain triplet repeat stability.
Yuan Liu, Haihua Zhang, Janaki Veeraraghavan, Robert A Bambara, Catherine H Freudenreich. Mol Cell Biol 2004
59
19


Long CTG tracts from the myotonic dystrophy gene induce deletions and rearrangements during recombination at the APRT locus in CHO cells.
James L Meservy, R Geoffrey Sargent, Ravi R Iyer, Fung Chan, Gregory J McKenzie, Robert D Wells, John H Wilson. Mol Cell Biol 2003
34
19

Myotonic dystrophy type 2 caused by a CCTG expansion in intron 1 of ZNF9.
C L Liquori, K Ricker, M L Moseley, J F Jacobsen, W Kress, S L Naylor, J W Day, L P Ranum. Science 2001
819
19

Replication stalling at Friedreich's ataxia (GAA)n repeats in vivo.
Maria M Krasilnikova, Sergei M Mirkin. Mol Cell Biol 2004
143
19


Structure-dependent recombination hot spot activity of GAA.TTC sequences from intron 1 of the Friedreich's ataxia gene.
Marek Napierala, Ruhee Dere, Alexandre Vetcher, Robert D Wells. J Biol Chem 2004
47
19



Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3' end of a transcript encoding a protein kinase family member.
J D Brook, M E McCurrach, H G Harley, A J Buckler, D Church, H Aburatani, K Hunter, V P Stanton, J P Thirion, T Hudson. Cell 1992
19

Initial sequencing and analysis of the human genome.
E S Lander, L M Linton, B Birren, C Nusbaum, M C Zody, J Baldwin, K Devon, K Dewar, M Doyle, W FitzHugh,[...]. Nature 2001
19

Features of trinucleotide repeat instability in vivo.
Irina V Kovtun, Cynthia T McMurray. Cell Res 2008
101
19

Tissue- and age-specific DNA replication patterns at the CTG/CAG-expanded human myotonic dystrophy type 1 locus.
John D Cleary, Stéphanie Tomé, Arturo López Castel, Gagan B Panigrahi, Laurent Foiry, Katharine A Hagerman, Hana Sroka, David Chitayat, Geneviève Gourdon, Christopher E Pearson. Nat Struct Mol Biol 2010
55
19

Extrahelical (CAG)/(CTG) triplet repeat elements support proliferating cell nuclear antigen loading and MutLα endonuclease activation.
Anna Pluciennik, Vickers Burdett, Celia Baitinger, Ravi R Iyer, Kevin Shi, Paul Modrich. Proc Natl Acad Sci U S A 2013
48
19

Isolated short CTG/CAG DNA slip-outs are repaired efficiently by hMutSbeta, but clustered slip-outs are poorly repaired.
Gagan B Panigrahi, Meghan M Slean, Jodie P Simard, Opher Gileadi, Christopher E Pearson. Proc Natl Acad Sci U S A 2010
64
19

Overcoming natural replication barriers: differential helicase requirements.
Ranjith P Anand, Kartik A Shah, Hengyao Niu, Patrick Sung, Sergei M Mirkin, Catherine H Freudenreich. Nucleic Acids Res 2012
60
19

Mismatch recognition protein MutSbeta does not hijack (CAG)n hairpin repair in vitro.
Lei Tian, Caixia Hou, Keli Tian, Nathaniel C Holcomb, Liya Gu, Guo-Min Li. J Biol Chem 2009
39
19

Detection of slipped-DNAs at the trinucleotide repeats of the myotonic dystrophy type I disease locus in patient tissues.
Michelle M Axford, Yuh-Hwa Wang, Masayuki Nakamori, Maria Zannis-Hadjopoulos, Charles A Thornton, Christopher E Pearson. PLoS Genet 2013
42
19

Mismatch repair genes Mlh1 and Mlh3 modify CAG instability in Huntington's disease mice: genome-wide and candidate approaches.
Ricardo Mouro Pinto, Ella Dragileva, Andrew Kirby, Alejandro Lloret, Edith Lopez, Jason St Claire, Gagan B Panigrahi, Caixia Hou, Kim Holloway, Tammy Gillis,[...]. PLoS Genet 2013
112
19

MSH3 Promotes Dynamic Behavior of Trinucleotide Repeat Tracts In Vivo.
Gregory M Williams, Jennifer A Surtees. Genetics 2015
22
22

Msh3 is a limiting factor in the formation of intergenerational CTG expansions in DM1 transgenic mice.
Laurent Foiry, Li Dong, Cédric Savouret, Laurence Hubert, Hein te Riele, Claudine Junien, Geneviève Gourdon. Hum Genet 2006
100
19

CRISPR/Cas9-Induced (CTG⋅CAG)n Repeat Instability in the Myotonic Dystrophy Type 1 Locus: Implications for Therapeutic Genome Editing.
Ellen L van Agtmaal, Laurène M André, Marieke Willemse, Sarah A Cumming, Ingeborg D G van Kessel, Walther J A A van den Broek, Geneviève Gourdon, Denis Furling, Vincent Mouly, Darren G Monckton,[...]. Mol Ther 2017
72
19




Long CTG.CAG repeats from myotonic dystrophy are preferred sites for intermolecular recombination.
Anna Pluciennik, Ravi R Iyer, Marek Napierala, Jacquelynn E Larson, Marcin Filutowicz, Robert D Wells. J Biol Chem 2002
37
15

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
15


Long CTG.CAG repeat sequences markedly stimulate intramolecular recombination.
Marek Napierala, Pawel Parniewski, Anna Pluciennik, Robert D Wells. J Biol Chem 2002
44
15

Cis-elements governing trinucleotide repeat instability in Saccharomyces cerevisiae.
M L Rolfsmeier, M J Dixon, L Pessoa-Brandão, R Pelletier, J J Miret, R S Lahue. Genetics 2001
44
15






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.