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Times Cited: 46
Times Cited
Times Co-cited
Similarity
86
Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study.
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DNA repair pathways underlie a common genetic mechanism modulating onset in polyglutamine diseases.
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Mismatch repair genes Mlh1 and Mlh3 modify CAG instability in Huntington's disease mice: genome-wide and candidate approaches.
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MSH3 modifies somatic instability and disease severity in Huntington's and myotonic dystrophy type 1.
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MSH3 polymorphisms and protein levels affect CAG repeat instability in Huntington's disease mice.
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Somatic expansion of the Huntington's disease CAG repeat in the brain is associated with an earlier age of disease onset.
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A modifier of Huntington's disease onset at the MLH1 locus.
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Intergenerational and striatal CAG repeat instability in Huntington's disease knock-in mice involve different DNA repair genes.
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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.