A citation-based method for searching scientific literature

Anasheh Halabi, Scott Ditch, Jeffrey Wang, Ed Grabczyk. J Biol Chem 2012
Times Cited: 48







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



Times Cited
  Times     Co-cited
Similarity


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
56

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
45

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
45

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
134
41



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
111
39

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
39

The mismatch repair system protects against intergenerational GAA repeat instability in a Friedreich ataxia mouse model.
Vahid Ezzatizadeh, Ricardo Mouro Pinto, Chiranjeevi Sandi, Madhavi Sandi, Sahar Al-Mahdawi, Hein Te Riele, Mark A Pook. Neurobiol Dis 2012
44
40

Pms2 suppresses large expansions of the (GAA·TTC)n sequence in neuronal tissues.
Rebecka L Bourn, Irene De Biase, Ricardo Mouro Pinto, Chiranjeevi Sandi, Sahar Al-Mahdawi, Mark A Pook, Sanjay I Bidichandani. PLoS One 2012
30
60

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
322
37

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
35

MSH3 polymorphisms and protein levels affect CAG repeat instability in Huntington's disease mice.
Stéphanie Tomé, Kevin Manley, Jodie P Simard, Greg W Clark, Meghan M Slean, Meera Swami, Peggy F Shelbourne, Elisabeth R M Tillier, Darren G Monckton, Anne Messer,[...]. PLoS Genet 2013
81
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
35

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
48
35

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
292
33

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
33


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
31

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
29


R-loops associated with triplet repeat expansions promote gene silencing in Friedreich ataxia and fragile X syndrome.
Matthias Groh, Michele M P Lufino, Richard Wade-Martins, Natalia Gromak. PLoS Genet 2014
192
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
27

MutLα heterodimers modify the molecular phenotype of Friedreich ataxia.
Vahid Ezzatizadeh, Chiranjeevi Sandi, Madhavi Sandi, Sara Anjomani-Virmouni, Sahar Al-Mahdawi, Mark A Pook. PLoS One 2014
16
81

Length-dependent CTG·CAG triplet-repeat expansion in myotonic dystrophy patient-derived induced pluripotent stem cells.
Jintang Du, Erica Campau, Elisabetta Soragni, Christine Jespersen, Joel M Gottesfeld. Hum Mol Genet 2013
53
27

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
64
25


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
49
25

Somatic instability of the expanded GAA triplet-repeat sequence in Friedreich ataxia progresses throughout life.
Irene De Biase, Astrid Rasmussen, Antonella Monticelli, Sahar Al-Mahdawi, Mark Pook, Sergio Cocozza, Sanjay I Bidichandani. Genomics 2007
56
22

Progressive GAA expansions in dorsal root ganglia of Friedreich's ataxia patients.
Irene De Biase, Astrid Rasmussen, Dan Endres, Sahar Al-Mahdawi, Antonella Monticelli, Sergio Cocozza, Mark Pook, Sanjay I Bidichandani. Ann Neurol 2007
74
22

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
22

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
22

Somatic expansion in mouse and human carriers of fragile X premutation alleles.
Rachel Adihe Lokanga, Ali Entezam, Daman Kumari, Dmitry Yudkin, Mei Qin, Carolyn Beebe Smith, Karen Usdin. Hum Mutat 2013
53
22


Transcription-associated R-loop formation across the human FMR1 CGG-repeat region.
Erick W Loomis, Lionel A Sanz, Frédéric Chédin, Paul J Hagerman. PLoS Genet 2014
119
22

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
22

Msh2 acts in medium-spiny striatal neurons as an enhancer of CAG instability and mutant huntingtin phenotypes in Huntington's disease knock-in mice.
Marina Kovalenko, Ella Dragileva, Jason St Claire, Tammy Gillis, Jolene R Guide, Jaclyn New, Hualing Dong, Raju Kucherlapati, Melanie H Kucherlapati, Michelle E Ehrlich,[...]. PLoS One 2012
42
26

Mutsβ generates both expansions and contractions in a mouse model of the Fragile X-associated disorders.
Xiao-Nan Zhao, Daman Kumari, Shikha Gupta, Di Wu, Maya Evanitsky, Wei Yang, Karen Usdin. Hum Mol Genet 2015
35
31



Potassium bromate, a potent DNA oxidizing agent, exacerbates germline repeat expansion in a fragile X premutation mouse model.
Ali Entezam, Adihe Rachel Lokanga, Wei Le, Gloria Hoffman, Karen Usdin. Hum Mutat 2010
44
22

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
20

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
63
20

Endonucleolytic function of MutLalpha in human mismatch repair.
Farid A Kadyrov, Leonid Dzantiev, Nicoleta Constantin, Paul Modrich. Cell 2006
412
20


A genetic association study of glutamine-encoding DNA sequence structures, somatic CAG expansion, and DNA repair gene variants, with Huntington disease clinical outcomes.
Marc Ciosi, Alastair Maxwell, Sarah A Cumming, Davina J Hensman Moss, Asma M Alshammari, Michael D Flower, Alexandra Durr, Blair R Leavitt, Raymund A C Roos, Peter Holmans,[...]. EBioMedicine 2019
47
21


Chromosome fragility at GAA tracts in yeast depends on repeat orientation and requires mismatch repair.
Hyun-Min Kim, Vidhya Narayanan, Piotr A Mieczkowski, Thomas D Petes, Maria M Krasilnikova, Sergei M Mirkin, Kirill S Lobachev. EMBO J 2008
76
18




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.