CoCites: A citation-based method for searching scientific literature

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
Times Cited: 9

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, Lesley Jones, Douglas R Langbehn, Seung Kwak, Sarah J Tabrizi, Darren G Monckton. EBioMedicine 2019
Times Cited: 60

List of shared articles

Times cited

New developments in Huntington's disease and other triplet repeat diseases: DNA repair turns to the dark side.
Robert S Lahue. Neuronal Signal 2020

Identifying genetic modifiers of age-associated penetrance in X-linked dystonia-parkinsonism.
Björn-Hergen Laabs, Christine Klein, Jelena Pozojevic, Aloysius Domingo, Norbert Brüggemann, Karen Grütz, Raymond L Rosales, Roland Dominic Jamora, Gerard Saranza, Cid Czarina E Diesta,[...]. Nat Commun 2021

Structure-forming repeats and their impact on genome stability.
Rebecca E Brown, Catherine H Freudenreich. Curr Opin Genet Dev 2021

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