A citation-based method for searching scientific literature

Meghan M Slean, Gagan B Panigrahi, Laura P Ranum, Christopher E Pearson. DNA Repair (Amst) 2008
Times Cited: 37







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



Times Cited
  Times     Co-cited
Similarity



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
40

Repeat instability: mechanisms of dynamic mutations.
Christopher E Pearson, Kerrie Nichol Edamura, John D Cleary. Nat Rev Genet 2005
608
37

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
37

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
37

Repeat instability as the basis for human diseases and as a potential target for therapy.
Arturo López Castel, John D Cleary, Christopher E Pearson. Nat Rev Mol Cell Biol 2010
293
37

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
35

Mismatch repair gene Msh2 modifies the timing of early disease in Hdh(Q111) striatum.
Vanessa C Wheeler, Lori-Anne Lebel, Vladimir Vrbanac, Allison Teed, Hein te Riele, Marcy E MacDonald. Hum Mol Genet 2003
158
35

(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
32

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
32

OGG1 initiates age-dependent CAG trinucleotide expansion in somatic cells.
Irina V Kovtun, Yuan Liu, Magnar Bjoras, Arne Klungland, Samuel H Wilson, Cynthia T McMurray. Nature 2007
324
29

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
29

Stoichiometry of base excision repair proteins correlates with increased somatic CAG instability in striatum over cerebellum in Huntington's disease transgenic mice.
Agathi-Vassiliki Goula, Brian R Berquist, David M Wilson, Vanessa C Wheeler, Yvon Trottier, Karine Merienne. PLoS Genet 2009
102
29

MSH2-dependent germinal CTG repeat expansions are produced continuously in spermatogonia from DM1 transgenic mice.
Cédric Savouret, Corinne Garcia-Cordier, Jérôme Megret, Hein te Riele, Claudine Junien, Geneviève Gourdon. Mol Cell Biol 2004
78
27

Slipped (CTG)*(CAG) repeats can be correctly repaired, escape repair or undergo error-prone repair.
Gagan B Panigrahi, Rachel Lau, S Erin Montgomery, Michelle R Leonard, Christopher E Pearson. Nat Struct Mol Biol 2005
114
27

Intergenerational and striatal CAG repeat instability in Huntington's disease knock-in mice involve different DNA repair genes.
Ella Dragileva, Audrey Hendricks, Allison Teed, Tammy Gillis, Edith T Lopez, Errol C Friedberg, Raju Kucherlapati, Winfried Edelmann, Kathryn L Lunetta, Marcy E MacDonald,[...]. Neurobiol Dis 2009
135
27

Transcription promotes contraction of CAG repeat tracts in human cells.
Yunfu Lin, Vincent Dion, John H Wilson. Nat Struct Mol Biol 2006
121
27


DNA instability in postmitotic neurons.
Roman Gonitel, Hilary Moffitt, Kirupa Sathasivam, Ben Woodman, Peter J Detloff, Richard L M Faull, Gillian P Bates. Proc Natl Acad Sci U S A 2008
132
24

Triplet repeat mutation length gains correlate with cell-type specific vulnerability in Huntington disease brain.
Peggy F Shelbourne, Christine Keller-McGandy, Wenya Linda Bi, Song-Ro Yoon, Louis Dubeau, Nicola J Veitch, Jean Paul Vonsattel, Nancy S Wexler, Norman Arnheim, Sarah J Augood. Hum Mol Genet 2007
125
24


CTCF cis-regulates trinucleotide repeat instability in an epigenetic manner: a novel basis for mutational hot spot determination.
Randell T Libby, Katharine A Hagerman, Victor V Pineda, Rachel Lau, Diane H Cho, Sandy L Baccam, Michelle M Axford, John D Cleary, James M Moore, Bryce L Sopher,[...]. PLoS Genet 2008
99
21

The multifaceted mismatch-repair system.
Josef Jiricny. Nat Rev Mol Cell Biol 2006
799
21

Replication inhibitors modulate instability of an expanded trinucleotide repeat at the myotonic dystrophy type 1 disease locus in human cells.
Zhi Yang, Rachel Lau, Julien L Marcadier, David Chitayat, Christopher E Pearson. Am J Hum Genet 2003
59
21


Dramatic tissue-specific mutation length increases are an early molecular event in Huntington disease pathogenesis.
Laura Kennedy, Elizabeth Evans, Chiung-Mei Chen, Lyndsey Craven, Peter J Detloff, Margaret Ennis, Peggy F Shelbourne. Hum Mol Genet 2003
207
21

Huntington's and myotonic dystrophy hESCs: down-regulated trinucleotide repeat instability and mismatch repair machinery expression upon differentiation.
Anna Seriola, Claudia Spits, Jodie P Simard, Pierre Hilven, Patrick Haentjens, Christopher E Pearson, Karen Sermon. Hum Mol Genet 2011
67
21

Human mismatch repair protein hMutLα is required to repair short slipped-DNAs of trinucleotide repeats.
Gagan B Panigrahi, Meghan M Slean, Jodie P Simard, Christopher E Pearson. J Biol Chem 2012
24
33

Mechanisms in eukaryotic mismatch repair.
Paul Modrich. J Biol Chem 2006
285
18

Somatic expansion of the Huntington's disease CAG repeat in the brain is associated with an earlier age of disease onset.
Meera Swami, Audrey E Hendricks, Tammy Gillis, Tiffany Massood, Jayalakshmi Mysore, Richard H Myers, Vanessa C Wheeler. Hum Mol Genet 2009
159
18

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
18



Tissue-specific mismatch repair protein expression: MSH3 is higher than MSH6 in multiple mouse tissues.
Stéphanie Tomé, Jodie P Simard, Meghan M Slean, Ian Holt, Glenn E Morris, Kamila Wojciechowicz, Hein te Riele, Christopher E Pearson. DNA Repair (Amst) 2013
27
25

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
16

Expandable DNA repeats and human disease.
Sergei M Mirkin. Nature 2007
589
16

DNA mismatch repair: functions and mechanisms.
Ravi R Iyer, Anna Pluciennik, Vickers Burdett, Paul L Modrich. Chem Rev 2006
603
16

DNA mismatch repair.
Thomas A Kunkel, Dorothy A Erie. Annu Rev Biochem 2005
889
16

Length-dependent gametic CAG repeat instability in the Huntington's disease knock-in mouse.
V C Wheeler, W Auerbach, J K White, J Srinidhi, A Auerbach, A Ryan, M P Duyao, V Vrbanac, M Weaver, J F Gusella,[...]. Hum Mol Genet 1999
276
16

Xpa deficiency reduces CAG trinucleotide repeat instability in neuronal tissues in a mouse model of SCA1.
Leroy Hubert, Yunfu Lin, Vincent Dion, John H Wilson. Hum Mol Genet 2011
57
16



Steady-state regulation of the human DNA mismatch repair system.
D K Chang, L Ricciardiello, A Goel, C L Chang, C R Boland. J Biol Chem 2000
157
13

Trinucleotide repeat disorders.
Harry T Orr, Huda Y Zoghbi. Annu Rev Neurosci 2007
972
13

DNA mismatch repair: molecular mechanism, cancer, and ageing.
Peggy Hsieh, Kazuhiko Yamane. Mech Ageing Dev 2008
269
13



Saccharomyces cerevisiae Msh2-Msh3 acts in repair of base-base mispairs.
Jill M Harrington, Richard D Kolodner. Mol Cell Biol 2007
69
13


Mismatch repair deficiency associated with overexpression of the MSH3 gene.
G Marra, I Iaccarino, T Lettieri, G Roscilli, P Delmastro, J Jiricny. Proc Natl Acad Sci U S A 1998
168
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.