A citation-based method for searching scientific literature

Mário Gomes-Pereira, M Teresa Fortune, Laura Ingram, John P McAbney, Darren G Monckton. Hum Mol Genet 2004
Times Cited: 129



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

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


Somatic CAG expansion in Huntington's disease is dependent on the MLH3 endonuclease domain, which can be excluded via splice redirection.
Jennie C L Roy, Antonia Vitalo, Marissa A Andrew, Eduarda Mota-Silva, Marina Kovalenko, Zoe Burch, Anh M Nhu, Paula E Cohen, Ed Grabczyk, Vanessa C Wheeler,[...]. Nucleic Acids Res 2021
1

Association Analysis of Chromosome X to Identify Genetic Modifiers of Huntington's Disease.
Eun Pyo Hong, Michael J Chao, Thomas Massey, Branduff McAllister, Sergey Lobanov, Lesley Jones, Peter Holmans, Seung Kwak, Michael Orth, Marc Ciosi,[...]. J Huntingtons Dis 2021
0

Human MutLγ, the MLH1-MLH3 heterodimer, is an endonuclease that promotes DNA expansion.
Lyudmila Y Kadyrova, Vaibhavi Gujar, Vickers Burdett, Paul L Modrich, Farid A Kadyrov. Proc Natl Acad Sci U S A 2020
24

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



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

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

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

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


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

The 26S proteasome drives trinucleotide repeat expansions.
Claire Concannon, Robert S Lahue. Nucleic Acids Res 2013
6

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

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

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


Searching for non-B DNA-forming motifs using nBMST (non-B DNA motif search tool).
R Z Cer, K H Bruce, D E Donohue, N A Temiz, U S Mudunuri, M Yi, N Volfovsky, A Bacolla, B T Luke, J R Collins,[...]. Curr Protoc Hum Genet 2012
16

Histone deacetylase complexes as caretakers of genome stability.
Robert S Lahue, Aisling Frizzell. Epigenetics 2012
21

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

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

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

Cockayne syndrome B protein antagonizes OGG1 in modulating CAG repeat length in vivo.
Irina V Kovtun, Kurt O Johnson, Cynthia T McMurray. Aging (Albany NY) 2011
38

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


A novel approach to investigate tissue-specific trinucleotide repeat instability.
Jong-Min Lee, Jie Zhang, Andrew I Su, John R Walker, Tim Wiltshire, Kihwa Kang, Ella Dragileva, Tammy Gillis, Edith T Lopez, Marie-Josee Boily,[...]. BMC Syst Biol 2010
65

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

Continuous and periodic expansion of CAG repeats in Huntington's disease R6/1 mice.
Linda Møllersen, Alexander D Rowe, Elisabeth Larsen, Torbjørn Rognes, Arne Klungland. PLoS Genet 2010
48

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

E. coli mismatch repair acts downstream of replication fork stalling to stabilize the expanded (GAA.TTC)(n) sequence.
Rebecka L Bourn, Paul M Rindler, Laura M Pollard, Sanjay I Bidichandani. Mutat Res 2009
4

Paradoxical delay in the onset of disease caused by super-long CAG repeat expansions in R6/2 mice.
A Jennifer Morton, Dervila Glynn, Wendy Leavens, Zhiguang Zheng, Richard L M Faull, Jeremy N Skepper, James M Wight. Neurobiol Dis 2009
95



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