A citation-based method for searching scientific literature

Ian Holt, Le Thanh Lam, Stéphanie Tomé, Derick G Wansink, Hein Te Riele, Geneviève Gourdon, Glenn E Morris. J Cell Biochem 2011
Times Cited: 9







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



Times Cited
  Times     Co-cited
Similarity


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
55

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
55

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
55

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
44

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
44


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
44

Histone deacetylase complexes promote trinucleotide repeat expansions.
Kim Debacker, Aisling Frizzell, Olive Gleeson, Lucy Kirkham-McCarthy, Tony Mertz, Robert S Lahue. PLoS Biol 2012
47
44

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
44

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
44

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
44

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
33

Expandable DNA repeats and human disease.
Sergei M Mirkin. Nature 2007
589
33

Conformational trapping of mismatch recognition complex MSH2/MSH3 on repair-resistant DNA loops.
Walter H Lang, Julie E Coats, Jerzy Majka, Greg L Hura, Yuyen Lin, Ivan Rasnik, Cynthia T McMurray. Proc Natl Acad Sci U S A 2011
48
33

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
33

Mutagenic roles of DNA "repair" proteins in antibody diversity and disease-associated trinucleotide repeat instability.
Meghan M Slean, Gagan B Panigrahi, Laura P Ranum, Christopher E Pearson. DNA Repair (Amst) 2008
37
33

Repeat instability: mechanisms of dynamic mutations.
Christopher E Pearson, Kerrie Nichol Edamura, John D Cleary. Nat Rev Genet 2005
608
33


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
33

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
33

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
33


Genomic context drives SCA7 CAG repeat instability, while expressed SCA7 cDNAs are intergenerationally and somatically stable in transgenic mice.
Randell T Libby, Darren G Monckton, Ying-Hui Fu, Refugio A Martinez, John P McAbney, R Lau, David D Einum, K Nichol, Carol B Ware, Louis J Ptacek,[...]. Hum Mol Genet 2003
55
33

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
33

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
33

Genetic instability caused by loss of MutS homologue 3 in human colorectal cancer.
Astrid C Haugen, Ajay Goel, Kanae Yamada, Giancarlo Marra, Thuy-Phuong Nguyen, Takeshi Nagasaka, Shinsaku Kanazawa, Junichi Koike, Yoshinori Kikuchi, Xiaoling Zhong,[...]. Cancer Res 2008
108
33

Expansions of CAG.CTG repeats in immortalized human astrocytes.
David A Claassen, Robert S Lahue. Hum Mol Genet 2007
26
22

Lysine acetylation targets protein complexes and co-regulates major cellular functions.
Chunaram Choudhary, Chanchal Kumar, Florian Gnad, Michael L Nielsen, Michael Rehman, Tobias C Walther, Jesper V Olsen, Matthias Mann. Science 2009
22

(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
22

Distribution of histone deacetylases 1-11 in the rat brain.
Ron S Broide, Jeff M Redwine, Najla Aftahi, Warren Young, Floyd E Bloom, Christopher J Winrow. J Mol Neurosci 2007
242
22


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
22

Histone deacetylase activity is retained in primary neurons expressing mutant huntingtin protein.
Masataka Hoshino, Kazuhiko Tagawa, Tomohiro Okuda, Miho Murata, Kiyomitsu Oyanagi, Nobutaka Arai, Toshio Mizutani, Ichiro Kanazawa, Erich E Wanker, Hitoshi Okazawa. J Neurochem 2003
43
22

Trinucleotide repeats in neurogenetic disorders.
H L Paulson, K H Fischbeck. Annu Rev Neurosci 1996
273
22

Evaluation of histone deacetylases as drug targets in Huntington's disease models. Study of HDACs in brain tissues from R6/2 and CAG140 knock-in HD mouse models and human patients and in a neuronal HD cell model.
Luisa Quinti, Vanita Chopra, Dante Rotili, Sergio Valente, Allison Amore, Gianluigi Franci, Sarah Meade, Marta Valenza, Lucia Altucci, Michele M Maxwell,[...]. PLoS Curr 2010
29
22

Friedreich's ataxia induced pluripotent stem cells model intergenerational GAA⋅TTC triplet repeat instability.
Sherman Ku, Elisabetta Soragni, Erica Campau, Elizabeth A Thomas, Gulsah Altun, Louise C Laurent, Jeanne F Loring, Marek Napierala, Joel M Gottesfeld. Cell Stem Cell 2010
157
22

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
22

Saccharomyces cerevisiae Msh2-Msh3 acts in repair of base-base mispairs.
Jill M Harrington, Richard D Kolodner. Mol Cell Biol 2007
69
22

Steady-state regulation of the human DNA mismatch repair system
Chang, Ricciardiello, Goel, Chang, Boland. J Biol Chem 2000
35
22

HNPCC-like cancer predisposition in mice through simultaneous loss of Msh3 and Msh6 mismatch-repair protein functions.
N de Wind, M Dekker, N Claij, L Jansen, Y van Klink, M Radman, G Riggins, M van der Valk, K van't Wout, H te Riele. Nat Genet 1999
166
22

The multifaceted mismatch-repair system.
Josef Jiricny. Nat Rev Mol Cell Biol 2006
799
22



MutSβ and histone deacetylase complexes promote expansions of trinucleotide repeats in human cells.
Anne-Marie M Gannon, Aisling Frizzell, Evan Healy, Robert S Lahue. Nucleic Acids Res 2012
50
22


Role of mismatch repair enzymes in GAA·TTC triplet-repeat expansion in Friedreich ataxia induced pluripotent stem cells.
Jintang Du, Erica Campau, Elisabetta Soragni, Sherman Ku, James W Puckett, Peter B Dervan, Joel M Gottesfeld. J Biol Chem 2012
76
22

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
22

Microsatellite instability in cancer of the proximal colon.
S N Thibodeau, G Bren, D Schaid. Science 1993
22


Neil1 is a genetic modifier of somatic and germline CAG trinucleotide repeat instability in R6/1 mice.
Linda Møllersen, Alexander D Rowe, Jennifer L Illuzzi, Gunn A Hildrestrand, Katharina J Gerhold, Linda Tveterås, Anja Bjølgerud, David M Wilson, Magnar Bjørås, Arne Klungland. Hum Mol Genet 2012
51
22


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.