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Author Details

Karen N McFarland
Center for Translational Research in Neurodegenerative Disease, University of Florida
2005
47
20
Timothy Clark (CM4AI)
PMIDPaper TitleJournal TitlePublished Year
37337279Humanized APOE genotypes influence lifespan independently of tau aggregation in the P301S mouse model of tauopathy.Acta Neuropathol Commun2023
37602238Semantic intrusion errors are associated with plasma Ptau-181 among persons with amnestic mild cognitive impairment who are amyloid positive.Front Neurol2023
34825397Combinatorial model of amyloid β and tau reveals synergy between amyloid deposits and tangle formation.Neuropathol Appl Neurobiol2022
35440098Impact of APOE genotype on prion-type propagation of tauopathy.Acta Neuropathol Commun2022
35897751<i>MhcII</i> Regulates Transmission of α-Synuclein-Seeded Pathology in Mice.Int J Mol Sci2022
35897046Deletion of Abi3/Gngt2 influences age-progressive amyloid β and tau pathologies in distinctive ways.Alzheimers Res Ther2022
35286658Microglia in Alzheimer's Disease: a Key Player in the Transition Between Homeostasis and Pathogenesis.Neurotherapeutics2022
33480174Integrative functional genomic analysis of intron retention in human and mouse brain with Alzheimer's disease.Alzheimers Dement2021
33741985Il-10 signaling reduces survival in mouse models of synucleinopathy.NPJ Parkinsons Dis2021
34127518Microglia show differential transcriptomic response to Aβ peptide aggregates ex vivo and in vivo.Life Sci Alliance2021
33957936Modulating innate immune activation states impacts the efficacy of specific Aβ immunotherapy.Mol Neurodegener2021
33216030Utility of Plasma Neurofilament Light in the 1Florida Alzheimer's Disease Research Center (ADRC).J Alzheimers Dis2021
32160188Pulse-Field capillary electrophoresis of repeat-primed PCR amplicons for analysis of large repeats in Spinocerebellar Ataxia Type 10.PLoS One2020
32298361Correction: Pulse-Field capillary electrophoresis of repeat-primed PCR amplicons for analysis of large repeats in Spinocerebellar Ataxia Type 10.PLoS One2020
32164763Prominent amyloid plaque pathology and cerebral amyloid angiopathy in APP V717I (London) carrier - phenotypic variability in autosomal dominant Alzheimer's disease.Acta Neuropathol Commun2020
31477175Unique α-synuclein pathology within the amygdala in Lewy body dementia: implications for disease initiation and progression.Acta Neuropathol Commun2019
29922950Olfactory Function in SCA10.Cerebellum2019
29610297Intron retention induced by microsatellite expansions as a disease biomarker.Proc Natl Acad Sci U S A2018
27557734SPG7 and Impaired Emotional Communication.Cerebellum2017
28423040Inheritance patterns of ATCCT repeat interruptions in spinocerebellar ataxia type 10 (SCA10) expansions.PLoS One2017
29181771Correction to: SPG7 and Impaired Emotional Communication.Cerebellum2017
28586798Parkinson Disease and Autoimmune Disorders-What Can We Learn From Genome-wide Pleiotropy?JAMA Neurol2017
28890930Parkinson's disease associated with pure <i>ATXN10</i> repeat expansion.NPJ Parkinsons Dis2017
27256065A case report of SPG11 mutations in a Chinese ARHSP-TCC family.BMC Neurol2016
25349168ADAR2-dependent GluA2 editing regulates cocaine seeking.Mol Psychiatry2015
26295943SMRT Sequencing of Long Tandem Nucleotide Repeats in SCA10 Reveals Unique Insight of Repeat Expansion Structure.PLoS One2015
27066563Spinocerebellar ataxia type 10 in Chinese Han.Neurol Genet2015
24105466MeCP2: a novel Huntingtin interactor.Hum Mol Genet2014
24935856Spinocerebellar ataxia type 10 in Peru: the missing link in the Amerindian origin of the disease.J Neurol2014
24318420Repeat interruptions in spinocerebellar ataxia type 10 expansions are strongly associated with epileptic seizures.Neurogenetics2014
24307138Consensus paper: pathological mechanisms underlying neurodegeneration in spinocerebellar ataxias.Cerebellum2014
23443018Paradoxical effects of repeat interruptions on spinocerebellar ataxia type 10 expansions and repeat instability.Eur J Hum Genet2013
25062675Genome-wide increase in histone H2A ubiquitylation in a mouse model of Huntington's disease.J Huntingtons Dis2013
24278426Expansion of the Spinocerebellar ataxia type 10 (SCA10) repeat in a patient with Sioux Native American ancestry.PLoS One2013
23813740Purkinje cell loss is the major brain pathology of spinocerebellar ataxia type 10.J Neurol Neurosurg Psychiatry2013
22065565Transgenic mice with SCA10 pentanucleotide repeats show motor phenotype and susceptibility to seizure: a toxic RNA gain-of-function model.J Neurosci Res2012
24533179Transgenic models of spinocerebellar ataxia type 10: modeling a repeat expansion disorder.Genes (Basel)2012
22791905Olfactory impairment in familial ataxias.J Neurol Neurosurg Psychiatry2012
22848491Genome-wide histone acetylation is altered in a transgenic mouse model of Huntington's disease.PLoS One2012
21496570Molecular biology of Huntington's disease.Handb Clin Neurol2011
20146251Characterization of harpy/Rca1/emi1 mutants: patterning in the absence of cell division.Dev Dyn2010
18423594Hh and Wnt signaling regulate formation of olig2+ neurons in the zebrafish cerebellum.Dev Biol2008
18923047Huntingtin modulates transcription, occupies gene promoters in vivo, and binds directly to DNA in a polyglutamine-dependent manner.J Neurosci2008
17283059Bmp2 transcription in osteoblast progenitors is regulated by a distant 3' enhancer located 156.3 kilobases from the promoter.Mol Cell Biol2007
16870734Neural-specific inactivation of ShcA results in increased embryonic neural progenitor apoptosis and microencephaly.J Neurosci2006
15689372Mutations in half baked/E-cadherin block cell behaviors that are necessary for teleost epiboly.Development2005
15768401Genetic locus half baked is necessary for morphogenesis of the ectoderm.Dev Dyn2005
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Release 1.2