Mariet Allen
Affiliations: | 2011- | Department of Neuroscience | Mayo Clinic Florida |
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Publications
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Min Y, Wang X, İş Ö, et al. (2023) Cross species systems biology discovers glial DDR2, STOM, and KANK2 as therapeutic targets in progressive supranuclear palsy. Nature Communications. 14: 6801 |
Batra R, Krumsiek J, Wang X, et al. (2023) Comparative brain metabolomics reveals shared and distinct metabolic alterations in Alzheimer's disease and progressive supranuclear palsy. Medrxiv : the Preprint Server For Health Sciences |
Rajabli F, Benchek P, Tosto G, et al. (2023) Multi-ancestry genome-wide meta-analysis of 56,241 individuals identifies and nominates ancestry-specific loci , , and as novel risk loci for Alzheimer's disease: the Alzheimer's Disease Genetics Consortium. Medrxiv : the Preprint Server For Health Sciences |
Siddiqui T, Cosacak MI, Popova S, et al. (2023) Nerve growth factor receptor (Ngfr) induces neurogenic plasticity by suppressing reactive astroglial Lcn2/Slc22a17 signaling in Alzheimer's disease. Npj Regenerative Medicine. 8: 33 |
Caride A, Jang JS, Shi GX, et al. (2023) Titration-based normalization of antibody amount improves consistency of ChIP-seq experiments. Bmc Genomics. 24: 171 |
Oatman SR, Reddy JS, Quicksall Z, et al. (2023) Genome-wide association study of brain biochemical phenotypes reveals distinct genetic architecture of Alzheimer's disease related proteins. Molecular Neurodegeneration. 18: 2 |
Ibanez KR, McFarland KN, Phillips J, et al. (2022) Deletion of Abi3/Gngt2 influences age-progressive amyloid β and tau pathologies in distinctive ways. Alzheimer's Research & Therapy. 14: 104 |
Batra R, Arnold M, Wörheide MA, et al. (2022) The landscape of metabolic brain alterations in Alzheimer's disease. Alzheimer's & Dementia : the Journal of the Alzheimer's Association |
Patel T, Carnwath TP, Wang X, et al. (2022) Transcriptional landscape of human microglia implicates age, sex, and APOE-related immunometabolic pathway perturbations. Aging Cell. e13606 |
Campbell AS, Ho CCG, Atık M, et al. (2022) Clinical Deep Phenotyping of Mutation Carriers. Neurology. Genetics. 8: e655 |