A citation-based method for searching scientific literature

Cinzia Cinesi, Bin Yang, Vincent Dion. Methods Mol Biol 2020
Times Cited: 1







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



Times Cited
  Times     Co-cited
Similarity


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
17
100

Oxidized dNTPs and the OGG1 and MUTYH DNA glycosylases combine to induce CAG/CTG repeat instability.
Piera Cilli, Ilenia Ventura, Anna Minoprio, Ettore Meccia, Alberto Martire, Samuel H Wilson, Margherita Bignami, Filomena Mazzei. Nucleic Acids Res 2016
14
100

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
56
100

Germline mutational dynamics in myotonic dystrophy type 1 males: allele length and age effects.
L Martorell, J Gámez, M L Cayuela, F K Gould, J P McAbney, T Ashizawa, D G Monckton, M Baiget. Neurology 2004
34
100

Environmental stress induces trinucleotide repeat mutagenesis in human cells.
Nimrat Chatterjee, Yunfu Lin, Beatriz A Santillan, Patricia Yotnda, John H Wilson. Proc Natl Acad Sci U S A 2015
29
100

HDAC3 deacetylates the DNA mismatch repair factor MutSβ to stimulate triplet repeat expansions.
Gregory M Williams, Vasileios Paschalis, Janice Ortega, Frederick W Muskett, James T Hodgkinson, Guo-Min Li, John W R Schwabe, Robert S Lahue. Proc Natl Acad Sci U S A 2020
5
100

Modifiers of Somatic Repeat Instability in Mouse Models of Friedreich Ataxia and the Fragile X-Related Disorders: Implications for the Mechanism of Somatic Expansion in Huntington's Disease.
Xiaonan Zhao, Daman Kumari, Carson J Miller, Geum-Yi Kim, Bruce Hayward, Antonia G Vitalo, Ricardo Mouro Pinto, Karen Usdin. J Huntingtons Dis 2021
5
100

Gametic and somatic tissue-specific heterogeneity of the expanded SCA1 CAG repeat in spinocerebellar ataxia type 1.
S S Chong, A E McCall, J Cota, S H Subramony, H T Orr, M R Hughes, H Y Zoghbi. Nat Genet 1995
153
100

A long CAG repeat in the mouse Sca1 locus replicates SCA1 features and reveals the impact of protein solubility on selective neurodegeneration.
Kei Watase, Edwin J Weeber, Bisong Xu, Barbara Antalffy, Lisa Yuva-Paylor, Kouichi Hashimoto, Masanobu Kano, Richard Atkinson, Yaling Sun, Dawna L Armstrong,[...]. Neuron 2002
214
100


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
100

DNA repair pathways underlie a common genetic mechanism modulating onset in polyglutamine diseases.
Conceição Bettencourt, Davina Hensman-Moss, Michael Flower, Sarah Wiethoff, Alexis Brice, Cyril Goizet, Giovanni Stevanin, Georgios Koutsis, Georgia Karadima, Marios Panas,[...]. Ann Neurol 2016
107
100

Large expansion of CTG•CAG repeats is exacerbated by MutSβ in human cells.
Rie Nakatani, Masayuki Nakamori, Harutoshi Fujimura, Hideki Mochizuki, Masanori P Takahashi. Sci Rep 2015
25
100

Genome-wide demethylation destabilizes CTG.CAG trinucleotide repeats in mammalian cells.
Vera Gorbunova, Andrei Seluanov, David Mittelman, John H Wilson. Hum Mol Genet 2004
58
100

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
100

Crosslinks and crosstalk: human cancer syndromes and DNA repair defects.
Mary A Risinger, Joanna Groden. Cancer Cell 2004
52
100


Chemotherapeutic deletion of CTG repeats in lymphoblast cells from DM1 patients.
Vera I Hashem, Malgorzata J Pytlos, Elzbieta A Klysik, Kuniko Tsuji, Mehrdad Khajavi, Tetsuo Ashizawa, Richard R Sinden. Nucleic Acids Res 2004
41
100

CTG trinucleotide repeat "big jumps": large expansions, small mice.
Mário Gomes-Pereira, Laurent Foiry, Annie Nicole, Aline Huguet, Claudine Junien, Arnold Munnich, Geneviève Gourdon. PLoS Genet 2007
73
100

On the wrong DNA track: Molecular mechanisms of repeat-mediated genome instability.
Alexandra N Khristich, Sergei M Mirkin. J Biol Chem 2020
30
100

RTEL1 inhibits trinucleotide repeat expansions and fragility.
Aisling Frizzell, Jennifer H G Nguyen, Mark I R Petalcorin, Katherine D Turner, Simon J Boulton, Catherine H Freudenreich, Robert S Lahue. Cell Rep 2014
23
100

Quantification of age-dependent somatic CAG repeat instability in Hdh CAG knock-in mice reveals different expansion dynamics in striatum and liver.
Jong-Min Lee, Ricardo Mouro Pinto, Tammy Gillis, Jason C St Claire, Vanessa C Wheeler. PLoS One 2011
39
100

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
316
100


Heterozygosity for a hypomorphic Polβ mutation reduces the expansion frequency in a mouse model of the Fragile X-related disorders.
Rachel Adihe Lokanga, Alireza Ghodsi Senejani, Joann Balazs Sweasy, Karen Usdin. PLoS Genet 2015
26
100

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
100

Suppression of Somatic Expansion Delays the Onset of Pathophysiology in a Mouse Model of Huntington's Disease.
Helen Budworth, Faye R Harris, Paul Williams, Do Yup Lee, Amy Holt, Jens Pahnke, Bartosz Szczesny, Karina Acevedo-Torres, Sylvette Ayala-Peña, Cynthia T McMurray. PLoS Genet 2015
56
100

FAN1 protects against repeat expansions in a Fragile X mouse model.
Xiao-Nan Zhao, Karen Usdin. DNA Repair (Amst) 2018
28
100

Huntington disease.
Gillian P Bates, Ray Dorsey, James F Gusella, Michael R Hayden, Chris Kay, Blair R Leavitt, Martha Nance, Christopher A Ross, Rachael I Scahill, Ronald Wetzel,[...]. Nat Rev Dis Primers 2015
516
100

Approaches to Sequence the HTT CAG Repeat Expansion and Quantify Repeat Length Variation.
Marc Ciosi, Sarah A Cumming, Afroditi Chatzi, Eloise Larson, William Tottey, Vilija Lomeikaite, Graham Hamilton, Vanessa C Wheeler, Ricardo Mouro Pinto, Seung Kwak,[...]. J Huntingtons Dis 2021
5
100

HTT haplotypes contribute to differences in Huntington disease prevalence between Europe and East Asia.
Simon C Warby, Henk Visscher, Jennifer A Collins, Crystal N Doty, Catherine Carter, Stefanie L Butland, Anna R Hayden, Ichiro Kanazawa, Colin J Ross, Michael R Hayden. Eur J Hum Genet 2011
97
100


Milestones of Lynch syndrome: 1895-2015.
Henry T Lynch, Carrie L Snyder, Trudy G Shaw, Christopher D Heinen, Megan P Hitchins. Nat Rev Cancer 2015
323
100

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
47
100


In vitro repair of DNA hairpins containing various numbers of CAG/CTG trinucleotide repeats.
Tianyi Zhang, Jian Huang, Liya Gu, Guo-Min Li. DNA Repair (Amst) 2012
18
100


Fen1 does not control somatic hypermutability of the (CTG)(n)*(CAG)(n) repeat in a knock-in mouse model for DM1.
Walther J A A van den Broek, Marcel R Nelen, Godfried W van der Heijden, Derick G Wansink, Bé Wieringa. FEBS Lett 2006
29
100


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
119
100

Short motif sequences determine the targets of the prokaryotic CRISPR defence system.
F J M Mojica, C Díez-Villaseñor, J García-Martínez, C Almendros. Microbiology (Reading) 2009
789
100

NuA4 initiates dynamic histone H4 acetylation to promote high-fidelity sister chromatid recombination at postreplication gaps.
Nealia C M House, Jiahui H Yang, Stephen C Walsh, Jonathan M Moy, Catherine H Freudenreich. Mol Cell 2014
31
100

Inherited CAG.CTG allele length is a major modifier of somatic mutation length variability in Huntington disease.
Nicola J Veitch, Margaret Ennis, John P McAbney, Peggy F Shelbourne, Darren G Monckton. DNA Repair (Amst) 2007
34
100


Hypermutable myotonic dystrophy CTG repeats in transgenic mice.
D G Monckton, M I Coolbaugh, K T Ashizawa, M J Siciliano, C T Caskey. Nat Genet 1997
102
100

Trinucleotide expansion in haploid germ cells by gap repair.
I V Kovtun, C T McMurray. Nat Genet 2001
209
100


MSH3 modifies somatic instability and disease severity in Huntington's and myotonic dystrophy type 1.
Michael Flower, Vilija Lomeikaite, Marc Ciosi, Sarah Cumming, Fernando Morales, Kitty Lo, Davina Hensman Moss, Lesley Jones, Peter Holmans, Darren G Monckton,[...]. Brain 2019
39
100

An oxidized abasic lesion inhibits base excision repair leading to DNA strand breaks in a trinucleotide repeat tract.
Jill M Beaver, Yanhao Lai, Shantell J Rolle, Liwei Weng, Marc M Greenberg, Yuan Liu. PLoS One 2018
3
100

Patterns of CAG repeat instability in the central nervous system and periphery in Huntington's disease and in spinocerebellar ataxia type 1.
Ricardo Mouro Pinto, Larissa Arning, James V Giordano, Pedram Razghandi, Marissa A Andrew, Tammy Gillis, Kevin Correia, Jayalakshmi S Mysore, Debora-M Grote Urtubey, Constanze R Parwez,[...]. Hum Mol Genet 2020
19
100


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.