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Plos One|September 8, 2011
Quantification of age-dependent somatic CAG repeat instability in Hdh CAG knock-in mice reveals different expansion dynamics in striatum and liverJong-Min Lee, Ricardo Mouro Pinto, Tammy Gillis, et al.European Journal of Human Genetics : EJHG|June 23, 2016
A novel neurodevelopmental disorder associated with compound heterozygous variants in the huntingtin geneLance H Rodan, Julie Cohen, Ali Fatemi, et al.BMC Neuroscience|September 9, 2006
Genetic analysis of the GRIK2 modifier effect in Huntington's diseaseWenqi Zeng, Tammy Gillis, Michael Hakky, et al.Human Molecular Genetics|May 26, 2009
Somatic expansion of the Huntington's disease CAG repeat in the brain is associated with an earlier age of disease onsetMeera Swami, Audrey E Hendricks, Tammy Gillis, et al.American Journal of Human Genetics|May 5, 2005
Biotin-responsive basal ganglia disease maps to 2q36.3 and is due to mutations in SLC19A3Wen-Qi Zeng, Eiman Al-Yamani, James S Acierno, et al.Human Molecular Genetics|May 12, 2006
Genetic background modifies nuclear mutant huntingtin accumulation and HD CAG repeat instability in Huntington's disease knock-in miceAlejandro Lloret, Ella Dragileva, Allison Teed, et al.Neurobiology of Disease|September 12, 2006
Brain-derived neurotrophic factor does not influence age at neurologic onset of Huntington's diseaseShotaro Kishikawa, Jian-Liang Li, Tammy Gillis, et al.Human Molecular Genetics|February 8, 2017
Permanent inactivation of Huntington's disease mutation by personalized allele-specific CRISPR/Cas9Jun Wan Shin, Kyung-Hee Kim, Michael J Chao, et al.Genetics|December 4, 2016
Genetic Contributors to Intergenerational CAG Repeat Instability in Huntington's Disease Knock-In MiceJoão Luís Neto, Jong-Min Lee, Ali Afridi, et al.Mammalian Genome : Official Journal of the International Mammalian Genome Society|February 4, 2015
Chromosome substitution strain assessment of a Huntington's disease modifier locusEliana Marisa Ramos, Marina Kovalenko, Jolene R Guide, et al.Pageof 7