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Author Details

Minerva M Carrasquillo
Mayo Clinic
1997
107
44
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
37580163Association of Plasma Biomarkers of Alzheimer Disease With Cognition and Medical Comorbidities in a Biracial Cohort.Neurology2023
36999481APOE ε4 influences within and between network functional connectivity in posterior cortical atrophy and logopenic progressive aphasia.Alzheimers Dement2023
37327267The SERPINA5 coding variant E228Q does not contribute to clinicopathologic characteristics in Alzheimer's disease: A cross-sectional study.Medicine (Baltimore)2023
34813500Alzheimer's disease and progressive supranuclear palsy share similar transcriptomic changes in distinct brain regions.J Clin Invest2022
35691047APOE ε4 influences medial temporal atrophy and tau deposition in atypical Alzheimer's disease.Alzheimers Dement2022
35483899Investigating Heterogeneity and Neuroanatomic Correlates of Longitudinal Clinical Decline in Atypical Alzheimer Disease.Neurology2022
35307406Transcript levels in plasma contribute substantial predictive value as potential Alzheimer's disease biomarkers in African Americans.EBioMedicine2022
35199931Addressing the disparities in dementia risk, early detection and care in Latino populations: Highlights from the second Latinos &amp; Alzheimer's Symposium.Alzheimers Dement2022
33480174Integrative functional genomic analysis of intron retention in human and mouse brain with Alzheimer's disease.Alzheimers Dement2021
33875655Transcriptomic analysis to identify genes associated with selective hippocampal vulnerability in Alzheimer's disease.Nat Commun2021
33861770Impact of variant-level batch effects on identification of genetic risk factors in large sequencing studies.PLoS One2021
33635380Latent trait modeling of tau neuropathology in progressive supranuclear palsy.Acta Neuropathol2021
34020725Genome-wide analysis identifies a novel LINC-PINT splice variant associated with vascular amyloid pathology in Alzheimer's disease.Acta Neuropathol Commun2021
33957936Modulating innate immune activation states impacts the efficacy of specific Aβ immunotherapy.Mol Neurodegener2021
33252078Plasma Biomarkers of Alzheimer's Disease in African Americans.J Alzheimers Dis2021
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
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
33308163Comparative evaluation for the globin gene depletion methods for mRNA sequencing using the whole blood-derived total RNAs.BMC Genomics2020
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
31104630Systematic analysis of dark and camouflaged genes reveals disease-relevant genes hiding in plain sight.Genome Biol2019
31256143Evaluation of Associations of Alzheimer's Disease Risk Variants that Are Highly Expressed in Microglia with Neuropathological Outcome Measures.J Alzheimers Dis2019
30792090Ethnoracial differences in Alzheimer's disease from the FLorida Autopsied Multi-Ethnic (FLAME) cohort.Alzheimers Dement2019
30820047Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing.Nat Genet2019
29107053Conserved brain myelination networks are altered in Alzheimer's and other neurodegenerative diseases.Alzheimers Dement2018
29970152TMEM106B haplotypes have distinct gene expression patterns in aged brain.Mol Neurodegener2018
30201328Male-specific epistasis between WWC1 and TLN2 genes is associated with Alzheimer's disease.Neurobiol Aging2018
30136084Divergent brain gene expression patterns associate with distinct cell-specific tau neuropathology traits in progressive supranuclear palsy.Acta Neuropathol2018
30297099Electroencephalogram findings in patients with posterior cortical atrophy.Neurol Neurochir Pol2018
30326945ABI3 and PLCG2 missense variants as risk factors for neurodegenerative diseases in Caucasians and African Americans.Mol Neurodegener2018
29661148Identification of missing variants by combining multiple analytic pipelines.BMC Bioinformatics2018
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
28183528Transethnic genome-wide scan identifies novel Alzheimer's disease loci.Alzheimers Dement2017
28097223<i>ABCA7</i> loss-of-function variants, expression, and neurologic disease risk.Neurol Genet2017
28714976Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease.Nat Genet2017
27030769ABCA7 Deficiency Accelerates Amyloid-β Generation and Alzheimer's Neuronal Pathology.J Neurosci2016
28757004Corrigendum to "Genome-wide association interaction analysis for Alzheimer's disease." [Neurobiol. Aging 35 (2014) 2436-2443].Neurobiol Aging2016
26507310Evaluating pathogenic dementia variants in posterior cortical atrophy.Neurobiol Aging2016
27727239Human whole genome genotype and transcriptome data for Alzheimer's and other neurodegenerative diseases.Sci Data2016
27115769Gene expression, methylation and neuropathology correlations at progressive supranuclear palsy risk loci.Acta Neuropathol2016
26993346Genetic risk factors for the posterior cortical atrophy variant of Alzheimer's disease.Alzheimers Dement2016
25189118Late-onset Alzheimer's risk variants in memory decline, incident mild cognitive impairment, and Alzheimer's disease.Neurobiol Aging2015
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Collaborators

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Mayo Clinic Jacksonville
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Mayo Clinic Florida
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Mayo Clinic Rochester
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Center for Clinical and Translational Science, Mayo Clinic
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Mayo Clinic Florida
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Cincinnati Children's Hospital Medical Center
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Brigham Young University
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Mayo Clinic
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Icahn School of Medicine at Mount Sinai
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Mayo Clinic Rochester
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Mayo Clinic
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Mayo Clinic
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Cleveland Institute for Computational Biology, Case Western Reserve University
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University of Antwerp
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Boston University Chobanian & Avedisian School of Medicine
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Wien Center for Alzheimer's Disease and Memory Disorders, Mount Sinai Medical Center
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Columbia University Medical Center
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Washington University School of Medicine
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