T. Gillis

T. Gillis, J. Mysore, M. MacDonald, 2012, Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases.

Population stratification may bias analysis of PGC-1α as a modifier of age at Huntington disease motor onset

Samuel Frank, Karen Marder, Christopher A. Ross, 2012, Human Genetics.

Genetic Risk Underlying Psychiatric and Cognitive Symptoms in Huntington’s Disease

Jane S. Paulsen, P. Holmans, T. Gillis, 2019, Biological Psychiatry.

Patterns of CAG repeat instability in the central nervous system and periphery in Huntington’s disease and in spinocerebellar ataxia type 1

T. Gillis, J. Mysore, H. Orr, 2020, Human molecular genetics.

Somatic expansion of the Huntington's disease CAG repeat in the brain is associated with an earlier age of disease onset.

Audrey E Hendricks, Tammy Gillis, T. Gillis, 2009, Human molecular genetics.

Functionally defective germline variants of sialic acid acetylesterase in autoimmunity

Annette Lee, P. Gregersen, T. Gillis, 2010, Nature.

Mismatch Repair Genes Mlh1 and Mlh3 Modify CAG Instability in Huntington's Disease Mice: Genome-Wide and Candidate Approaches

Edith T. Lopez, M. Daly, T. Gillis, 2013, PLoS genetics.

CAG repeat expansion in Huntington disease determines age at onset in a fully dominant fashion

Jane S. Paulsen, R H Myers, C A Ross, 2012, Neurology.

Sequence-Level Analysis of the Major European Huntington Disease Haplotype.

L. Hood, J. Roach, T. Gillis, 2015, American journal of human genetics.

Haplotype analysis of the 4p16.3 region in Portuguese families with Huntington's disease

T. Gillis, J. Mysore, M. MacDonald, 2015, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Assessment of cortical and striatal involvement in 523 Huntington disease brains

Richard H. Myers, L. Adrienne Cupples, Kathryn L. Lunetta, 2012, Neurology.

Genetic modifiers of Huntington's disease differentially influence motor and cognitive domains

Jane S. Paulsen, P. Holmans, T. Gillis, 2022, medRxiv.

Genome-wide significance for a modifier of age at neurological onset in Huntington's Disease at 6q23-24: the HD MAPS study

Jane S. Paulsen, T. Gillis, J. Mysore, 2006, BMC Medical Genetics.

Novel allele-specific quantification methods reveal no effects of adult onset CAG repeats on HTT mRNA and protein levels

T. Gillis, M. MacDonald, J. Gusella, 2017, Human molecular genetics.

Chromosome substitution strain assessment of a Huntington’s disease modifier locus

T. Gillis, J. Mysore, M. MacDonald, 2015, Mammalian Genome.

A Broad Phenotypic Screen Identifies Novel Phenotypes Driven by a Single Mutant Allele in Huntington’s Disease CAG Knock-In Mice

Edith T. Lopez, H. Fuchs, T. Gillis, 2013, PloS one.

Genetic background modifies nuclear mutant huntingtin accumulation and HD CAG repeat instability in Huntington's disease knock-in mice.

Edith T. Lopez, T. Gillis, M. MacDonald, 2006, Human molecular genetics.

Genetic overlap between psychiatric disorders and neuropsychiatric symptoms in HD

Jane S. Paulsen, P. Holmans, T. Gillis, 2019 .

Correction to: Tissue-specific and repeat length-dependent somatic instability of the X-linked dystonia parkinsonism-associated CCCTCT repeat

Trisha J. Multhaupt-Buell, T. Gillis, L. Ozelius, 2022, Acta neuropathologica communications.

The HTT CAG-Expansion Mutation Determines Age at Death but Not Disease Duration in Huntington Disease.

Peter Holmans, Lesley Jones, Michael Orth, 2016, American journal of human genetics.

Prevalence of incompletely penetrant Huntington's disease alleles among individuals with major depressive disorder.

M. Rietschel, P. Sullivan, M. Fava, 2010, The American journal of psychiatry.

Promotion of somatic CAG repeat expansion by Fan1 knock-out in Huntington’s disease knock-in mice is blocked by Mlh1 knock-out

T. Gillis, J. Mysore, M. MacDonald, 2020, Human molecular genetics.

Haplotype-based stratification of Huntington's disease

P. Holmans, T. Gillis, J. Mysore, 2017, European Journal of Human Genetics.

Mutations causing Lopes-Maciel-Rodan Syndrome are huntingtin hypomorphs.

Ryan L. Collins, T. Gillis, J. Mysore, 2021, Human molecular genetics.

Common SNP-based haplotype analysis of the 4p16.3 Huntington disease gene region.

T. Gillis, J. Mysore, M. MacDonald, 2012, American journal of human genetics.

Candidate glutamatergic and dopaminergic pathway gene variants do not influence Huntington’s disease motor onset

T. Gillis, J. Mysore, M. MacDonald, 2013, neurogenetics.

Dominant effects of the Huntington's disease HTT CAG repeat length are captured in gene-expression data sets by a continuous analysis mathematical modeling strategy.

Bin Zhang, T. Gillis, M. MacDonald, 2013, Human molecular genetics.

Huntington CAG repeat size does not modify onset age in familial Parkinson's disease: The GenePD study

T. Gillis, J. Mysore, M. MacDonald, 2008, Movement disorders : official journal of the Movement Disorder Society.

Brain-derived neurotrophic factor does not influence age at neurologic onset of Huntington’s disease

T. Gillis, M. MacDonald, J. Gusella, 2006, Neurobiology of Disease.

Genetic analysis of the GRIK2 modifier effect in Huntington's disease

T. Gillis, M. MacDonald, J. Gusella, 2006, BMC Neuroscience.

CAG Repeat Not Polyglutamine Length Determines Timing of Huntington’s Disease Onset

Jane S. Paulsen, P. Holmans, T. Gillis, 2019, Cell.

TAA repeat variation in the GRIK2 gene does not influence age at onset in Huntington's disease.

T. Gillis, J. Mysore, M. MacDonald, 2012, Biochemical and biophysical research communications.

CAG Repeat Not Polyglutamine Length Determines Timing of Huntington’s Disease Onset

Jane S. Paulsen, P. Holmans, T. Gillis, 2019, Cell.

PMS1 as a target for splice modulation to prevent somatic CAG repeat expansion in Huntington’s disease

T. Gillis, M. MacDonald, J. Gusella, 2023, bioRxiv.

Genetic Modification of Huntington Disease Acts Early in the Prediagnosis Phase.

Jane S. Paulsen, T. Gillis, J. Mysore, 2018, American journal of human genetics.

High resolution time‐course mapping of early transcriptomic, molecular and cellular phenotypes in Huntington's disease CAG knock‐in mice across multiple genetic backgrounds

John C. Earls, L. Hood, D. Geman, 2017, Human molecular genetics.

The HTT CAG-Expansion Mutation Determines Age at Death but Not Disease Duration in Huntington Disease.

P. Holmans, T. Gillis, J. Mysore, 2016, American journal of human genetics.

Dominant effects of the Huntington's disease HTT CAG repeat length are captured in gene-expression data sets by a continuous analysis mathematical modeling strategy.

Bin Zhang, T. Gillis, M. MacDonald, 2013, Human molecular genetics.

Prevalence of incompletely penetrant Huntington's disease alleles among individuals with major depressive disorder.

M. Rietschel, P. Sullivan, M. Fava, 2010, The American journal of psychiatry.

Genetic modifiers of Huntington disease differentially influence motor and cognitive domains.

T. Gillis, J. Mysore, M. MacDonald, 2022, American journal of human genetics.

Somatic CAG Repeat Stability in a Transgenic Sheep Model of Huntington’s Disease

T. Gillis, M. MacDonald, V. Wheeler, 2024, Journal of Huntington's disease.

Modification of Huntington’s disease by short tandem repeats

T. Gillis, M. MacDonald, J. Gusella, 2024, Brain communications.