A citation-based method for searching scientific literature

Stéphanie Tomé, Ian Holt, Winfried Edelmann, Glenn E Morris, Arnold Munnich, Christopher E Pearson, Geneviève Gourdon. PLoS Genet 2009
Times Cited: 64



Vanessa C Wheeler, Lori-Anne Lebel, Vladimir Vrbanac, Allison Teed, Hein te Riele, Marcy E MacDonald. Hum Mol Genet 2003
Times Cited: 158




List of shared articles



Times cited

The mouse mismatch repair protein, MSH3, is a nucleoplasmic protein that aggregates into denser nuclear bodies under conditions of stress.
Ian Holt, Le Thanh Lam, Stéphanie Tomé, Derick G Wansink, Hein Te Riele, Geneviève Gourdon, Glenn E Morris. J Cell Biochem 2011
9

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

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

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


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

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

Dynamic mutations: where are they now?
Clare L van Eyk, Robert I Richards. Adv Exp Med Biol 2012
5

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

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
23

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

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

Maternal germline-specific effect of DNA ligase I on CTG/CAG instability.
Stéphanie Tomé, Gagan B Panigrahi, Arturo López Castel, Laurent Foiry, David W Melton, Geneviève Gourdon, Christopher E Pearson. Hum Mol Genet 2011
27

The nucleotide sequence, DNA damage location, and protein stoichiometry influence the base excision repair outcome at CAG/CTG repeats.
Agathi-Vasiliki Goula, Christopher E Pearson, Julie Della Maria, Yvon Trottier, Alan E Tomkinson, David M Wilson, Karine Merienne. Biochemistry 2012
28

A polymorphism in the MSH3 mismatch repair gene is associated with the levels of somatic instability of the expanded CTG repeat in the blood DNA of myotonic dystrophy type 1 patients.
Fernando Morales, Melissa Vásquez, Carolina Santamaría, Patricia Cuenca, Eyleen Corrales, Darren G Monckton. DNA Repair (Amst) 2016
48

Trinucleotide repeat expansions catalyzed by human cell-free extracts.
Jennifer R Stevens, Elaine E Lahue, Guo-Min Li, Robert S Lahue. Cell Res 2013
12


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

A slipped-CAG DNA-binding small molecule induces trinucleotide-repeat contractions in vivo.
Masayuki Nakamori, Gagan B Panigrahi, Stella Lanni, Terence Gall-Duncan, Hideki Hayakawa, Hana Tanaka, Jennifer Luo, Takahiro Otabe, Jinxing Li, Akihiro Sakata,[...]. Nat Genet 2020
39



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

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


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

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

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

Onset and progression of behavioral and molecular phenotypes in a novel congenic R6/2 line exhibiting intergenerational CAG repeat stability.
Randi-Michelle Cowin, Nghiem Bui, Deanna Graham, Jennie R Green, Stephan Grueninger, Lisa A Yuva-Paylor, Arsalan U Syed, Andreas Weiss, Richard Paylor. PLoS One 2011
16

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