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Author Details

Mariet Allen
Mayo Clinic
2004
68
27
PMIDPaper TitleJournal TitlePublished Year
37461624Multi-ancestry genome-wide meta-analysis of 56,241 individuals identifies <i>LRRC4C, LHX5-AS1</i> and nominates ancestry-specific loci <i>PTPRK</i> , <i>GRB14</i> , and <i>KIAA0825</i> as novel risk loci for Alzheimer's disease: the Alzheimer's Disease Genetics Consortium.medRxiv2023
37919278Cross species systems biology discovers glial DDR2, STOM, and KANK2 as therapeutic targets in progressive supranuclear palsy.Nat Commun2023
37546878Comparative brain metabolomics reveals shared and distinct metabolic alterations in Alzheimer's disease and progressive supranuclear palsy.medRxiv2023
37016279Titration-based normalization of antibody amount improves consistency of ChIP-seq experiments.BMC Genomics2023
37429840Nerve growth factor receptor (Ngfr) induces neurogenic plasticity by suppressing reactive astroglial Lcn2/Slc22a17 signaling in Alzheimer's disease.NPJ Regen Med2023
34482628Epigenomic features related to microglia are associated with attenuated effect of APOE ε4 on Alzheimer's disease risk in humans.Alzheimers Dement2022
35829654The landscape of metabolic brain alterations in Alzheimer's disease.Alzheimers Dement2022
35388616Transcriptional landscape of human microglia implicates age, sex, and APOE-related immunometabolic pathway perturbations.Aging Cell2022
35897046Deletion of Abi3/Gngt2 influences age-progressive amyloid β and tau pathologies in distinctive ways.Alzheimers Res Ther2022
34918867Whole genome sequencing-based copy number variations reveal novel pathways and targets in Alzheimer's disease.Alzheimers Dement2022
35047668Clinical Deep Phenotyping of <i>ABCA7</i> Mutation Carriers.Neurol Genet2022
34813500Alzheimer's disease and progressive supranuclear palsy share similar transcriptomic changes in distinct brain regions.J Clin Invest2022
33480174Integrative functional genomic analysis of intron retention in human and mouse brain with Alzheimer's disease.Alzheimers Dement2021
33765507Analysis of intraoperative human brain tissue transcriptome reveals putative risk genes and altered molecular pathways in glioma-related seizures.Epilepsy Res2021
33875655Transcriptomic analysis to identify genes associated with selective hippocampal vulnerability in Alzheimer's disease.Nat Commun2021
33726851Expression of an alternatively spliced variant of SORL1 in neuronal dendrites is decreased in patients with Alzheimer's disease.Acta Neuropathol Commun2021
33635380Latent trait modeling of tau neuropathology in progressive supranuclear palsy.Acta Neuropathol2021
34857756Atlas of RNA editing events affecting protein expression in aged and Alzheimer's disease human brain tissue.Nat Commun2021
34020725Genome-wide analysis identifies a novel LINC-PINT splice variant associated with vascular amyloid pathology in Alzheimer's disease.Acta Neuropathol Commun2021
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
33417599Identifying drug targets for neurological and psychiatric disease via genetics and the brain transcriptome.PLoS Genet2021
32400971MAPT haplotype-stratified GWAS reveals differential association for AD risk variants.Alzheimers Dement2020
34393677EPIGENOMIC FEATURES RELATED TO MICROGLIA ARE ASSOCIATED WITH ATTENUATED EFFECT OF APOE ε4 ON ALZHEIMER'S DISEASE RISK IN HUMANS.Alzheimers Dement2020
31955222Correction to: A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer's disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity.Acta Neuropathol2020
33046718Large eQTL meta-analysis reveals differing patterns between cerebral cortical and cerebellar brain regions.Sci Data2020
33092647Association of ABI3 and PLCG2 missense variants with disease risk and neuropathology in Lewy body disease and progressive supranuclear palsy.Acta Neuropathol Commun2020
32660529Deciphering cellular transcriptional alterations in Alzheimer's disease brains.Mol Neurodegener2020
32827351Tau and apolipoprotein E modulate cerebrovascular tight junction integrity independent of cerebral amyloid angiopathy in Alzheimer's disease.Alzheimers Dement2020
32928256Correction to: Deciphering cellular transcriptional alterations in Alzheimer's disease brains.Mol Neurodegener2020
32755048Genome-wide transcriptome analysis identifies novel dysregulated genes implicated in Alzheimer's pathology.Alzheimers Dement2020
32668255Meta-Analysis of the Alzheimer's Disease Human Brain Transcriptome and Functional Dissection in Mouse Models.Cell Rep2020
30820047Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing.Nat Genet2019
29329552Correction to: Linkage, whole genome sequence, and biological data implicate variants in RAB10 in Alzheimer's disease resilience.Genome Med2018
30078640An alternative transcript of the Alzheimer's disease risk gene SORL1 encodes a truncated receptor.Neurobiol Aging2018
30158114TLR5 decoy receptor as a novel anti-amyloid therapeutic for Alzheimer's disease.J Exp Med2018
29970152TMEM106B haplotypes have distinct gene expression patterns in aged brain.Mol Neurodegener2018
30136084Divergent brain gene expression patterns associate with distinct cell-specific tau neuropathology traits in progressive supranuclear palsy.Acta Neuropathol2018
30326945ABI3 and PLCG2 missense variants as risk factors for neurodegenerative diseases in Caucasians and African Americans.Mol Neurodegener2018
29458411Genome-wide pleiotropy analysis of neuropathological traits related to Alzheimer's disease.Alzheimers Res Ther2018
29107053Conserved brain myelination networks are altered in Alzheimer's and other neurodegenerative diseases.Alzheimers Dement2018
27939925A candidate regulatory variant at the TREM gene cluster associates with decreased Alzheimer's disease risk and increased TREML1 and TREM2 brain gene expression.Alzheimers Dement2017
28106563Comprehensive Screening for Disease Risk Variants in Early-Onset Alzheimer's Disease Genes in African Americans Identifies Novel PSEN Variants.J Alzheimers Dis2017
28480329African American exome sequencing identifies potential risk variants at Alzheimer disease loci.Neurol Genet2017
28242297Systems biology approach to late-onset Alzheimer's disease genome-wide association study identifies novel candidate genes validated using brain expression data and Caenorhabditis elegans experiments.Alzheimers Dement2017
28097223<i>ABCA7</i> loss-of-function variants, expression, and neurologic disease risk.Neurol Genet2017
29183403Linkage, whole genome sequence, and biological data implicate variants in RAB10 in Alzheimer's disease resilience.Genome Med2017
28714976Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease.Nat Genet2017
27287057MAPT haplotype H1G is associated with increased risk of dementia with Lewy bodies.Alzheimers Dement2016
27727239Human whole genome genotype and transcriptome data for Alzheimer's and other neurodegenerative diseases.Sci Data2016
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Mayo Clinic
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Mayo Clinic Jacksonville
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Mayo Clinic
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Mayo Clinic
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Mayo Clinic Florida
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Mayo Clinic
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Mayo Clinic Rochester
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Mayo Clinic Florida
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Center for Clinical and Translational Science, Mayo Clinic
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Emory Center for Neurodegenerative Disease
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Institute for Systems Biology
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Mayo Clinic
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Cincinnati Children's Hospital Medical Center
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Institute for Systems Biology
Co-authored papers 11
Columbia University Medical Center
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Mayo Clinic
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Rush University Medical Center
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Emory University School of Medicine
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Brigham Young University
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Center for Translational Research in Neurodegenerative Disease, University of Florida
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Mayo Clinic Rochester
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Wien Center for Alzheimer's Disease and Memory Disorders, Mount Sinai Medical Center
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