A citation-based method for searching scientific literature

K Manley, T L Shirley, L Flaherty, A Messer. Nat Genet 1999
Times Cited: 281



Ella Dragileva, Audrey Hendricks, Allison Teed, Tammy Gillis, Edith T Lopez, Errol C Friedberg, Raju Kucherlapati, Winfried Edelmann, Kathryn L Lunetta, Marcy E MacDonald, Vanessa C Wheeler. Neurobiol Dis 2009
Times Cited: 134




List of shared articles



Times cited

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
6

Modifiers of CAG/CTG Repeat Instability: Insights from Mammalian Models.
Vanessa C Wheeler, Vincent Dion. J Huntingtons Dis 2021
12


DNA Mismatch Repair and its Role in Huntington's Disease.
Ravi R Iyer, Anna Pluciennik. J Huntingtons Dis 2021
8

Coordinated roles of SLX4 and MutSβ in DNA repair and the maintenance of genome stability.
Sarah J Young, Stephen C West. Crit Rev Biochem Mol Biol 2021
0


Huntington's disease: nearly four decades of human molecular genetics.
James F Gusella, Jong-Min Lee, Marcy E MacDonald. Hum Mol Genet 2021
0

Mitochondrial Abnormalities and Synaptic Damage in Huntington's Disease: a Focus on Defective Mitophagy and Mitochondria-Targeted Therapeutics.
Neha Sawant, Hallie Morton, Sudhir Kshirsagar, Arubala P Reddy, P Hemachandra Reddy. Mol Neurobiol 2021
0

On the wrong DNA track: Molecular mechanisms of repeat-mediated genome instability.
Alexandra N Khristich, Sergei M Mirkin. J Biol Chem 2020
43

Longitudinal increases in somatic mosaicism of the expanded CTG repeat in myotonic dystrophy type 1 are associated with variation in age-at-onset.
Fernando Morales, Melissa Vásquez, Eyleen Corrales, Rebeca Vindas-Smith, Carolina Santamaría-Ulloa, Baili Zhang, Mario Sirito, Marcos R Estecio, Ralf Krahe, Darren G Monckton. Hum Mol Genet 2020
5

Cell Type-Specific Transcriptomics Reveals that Mutant Huntingtin Leads to Mitochondrial RNA Release and Neuronal Innate Immune Activation.
Hyeseung Lee, Robert J Fenster, S Sebastian Pineda, Whitney S Gibbs, Shahin Mohammadi, Jose Davila-Velderrain, Francisco J Garcia, Martine Therrien, Hailey S Novis, Fan Gao,[...]. Neuron 2020
22

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



Methods for Assessing DNA Repair and Repeat Expansion in Huntington's Disease.
Thomas Massey, Branduff McAllister, Lesley Jones. Methods Mol Biol 2018
5

Age-related length variability of polymorphic CAG repeats.
Monica Sanchez-Contreras, Fernando Cardozo-Pelaez. DNA Repair (Amst) 2017
1



MutSβ abundance and Msh3 ATP hydrolysis activity are important drivers of CTG•CAG repeat expansions.
Norma Keogh, Kara Y Chan, Guo-Min Li, Robert S Lahue. Nucleic Acids Res 2017
14

DNA mismatch repair in trinucleotide repeat instability.
Jinzhen Guo, Luping Chen, Guo-Min Li. Sci China Life Sci 2017
2

Disease-associated repeat instability and mismatch repair.
Monika H M Schmidt, Christopher E Pearson. DNA Repair (Amst) 2016
117

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


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

Crosstalk between MSH2-MSH3 and polβ promotes trinucleotide repeat expansion during base excision repair.
Yanhao Lai, Helen Budworth, Jill M Beaver, Nelson L S Chan, Zunzhen Zhang, Cynthia T McMurray, Yuan Liu. Nat Commun 2016
31


DNA triplet repeat expansion and mismatch repair.
Ravi R Iyer, Anna Pluciennik, Marek Napierala, Robert D Wells. Annu Rev Biochem 2015
72

Repeat instability during DNA repair: Insights from model systems.
Karen Usdin, Nealia C M House, Catherine H Freudenreich. Crit Rev Biochem Mol Biol 2015
99


The Repeat Expansion Diseases: The dark side of DNA repair.
Xiao-Nan Zhao, Karen Usdin. DNA Repair (Amst) 2015
41

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

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
58


Expression levels of DNA replication and repair genes predict regional somatic repeat instability in the brain but are not altered by polyglutamine disease protein expression or age.
Amanda G Mason, Stephanie Tomé, Jodie P Simard, Randell T Libby, Theodor K Bammler, Richard P Beyer, A Jennifer Morton, Christopher E Pearson, Albert R La Spada. Hum Mol Genet 2014
33



The dual nature of mismatch repair as antimutator and mutator: for better or for worse.
Sara Thornby Bak, Despoina Sakellariou, Javier Pena-Diaz. Front Genet 2014
30

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


A brief history of triplet repeat diseases.
Helen Budworth, Cynthia T McMurray. Methods Mol Biol 2013
43