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Tau and TDP-43 proteinopathies: kindred pathologic cascades and genetic pleiotropy

Laboratory investigation, 2019-07, Vol.99 (7), p.993-1007

2019

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Genetics of PICALM expression and Alzheimer's disease

PloS one, 2014-03, Vol.9 (3), p.e91242-e91242

2014

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Evaluation of CD33 as a genetic risk factor for Alzheimer’s disease

Acta neuropathologica, 2019-08, Vol.138 (2), p.187-199

2019

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CD33 Alzheimer's risk-altering polymorphism, CD33 expression, and exon 2 splicing

The Journal of neuroscience, 2013-08, Vol.33 (33), p.13320-13325

2013

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Patterns and predictors of chronic opioid use in older adults: A retrospective cohort study

PloS one, 2019-01, Vol.14 (1), p.e0210341-e0210341

2019

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The Amygdala as a Locus of Pathologic Misfolding in Neurodegenerative Diseases

Journal of neuropathology and experimental neurology, 2018-01, Vol.77 (1), p.2-20

2018

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Genetics ignite focus on microglial inflammation in Alzheimer's disease

Molecular neurodegeneration, 2015-10, Vol.10 (1), p.52-52, Article 52

2015

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Outcomes after diagnosis of mild cognitive impairment in a large autopsy series

Annals of neurology, 2017-04, Vol.81 (4), p.549-559

2017

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Sclerostin and Dickkopf-1 in Renal Osteodystrophy

Clinical journal of the American Society of Nephrology, 2011-04, Vol.6 (4), p.877-882

2011

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Genetic data and cognitively defined late-onset Alzheimer’s disease subgroups

Molecular psychiatry, 2020-11, Vol.25 (11), p.2942-2951

2020

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Age and sex are associated with the plasma lipidome: findings from the GOLDN study

Lipids in health and disease, 2021-04, Vol.20 (1), p.30-30, Article 30

2021

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Apolipoprotein E ε4/4 genotype limits response to dietary induction of hyperhomocysteinemia and resulting inflammatory signaling

Journal of cerebral blood flow and metabolism, 2022-05, Vol.42 (5), p.771-787

2022

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Quantitative phenotype scan statistic (QPSS) reveals rare variant associations with Alzheimer's disease endophenotypes

BMC medical genetics, 2020-05, Vol.21 (1), p.106-106, Article 106

2020

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Multiple gene variants linked to Alzheimer's-type clinical dementia via GWAS are also associated with non-Alzheimer's neuropathologic entities

Neurobiology of disease, 2022-11, Vol.174, p.105880-"105880", Article 105880

2022

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Genetics of clusterin isoform expression and Alzheimer's disease risk

PloS one, 2012-04, Vol.7 (4), p.e33923

2012

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The association of gabapentin initiation and neurocognitive changes in older adults with normal cognition

Frontiers in pharmacology, 2022-11, Vol.13, p.910719

2022

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TDP-43 proteinopathy in aging: Associations with risk-associated gene variants and with brain parenchymal thyroid hormone levels

Neurobiology of disease, 2019-05, Vol.125, p.67-76

2019

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Hippocampal sclerosis of aging, a prevalent and high-morbidity brain disease

Acta neuropathologica, 2013-08, Vol.126 (2), p.161-177

2013

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Atorvastatin rescues hyperhomocysteinemia-induced cognitive deficits and neuroinflammatory gene changes

Journal of neuroinflammation, 2023-09, Vol.20 (1), p.199-199, Article 199

2023

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Dichotomous scoring of TDP-43 proteinopathy from specific brain regions in 27 academic research centers: associations with Alzheimer's disease and cerebrovascular disease pathologies

Acta neuropathologica communications, 2018-12, Vol.6 (1), p.142-142, Article 142

2018

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ABCC9/SUR2 in the brain: Implications for hippocampal sclerosis of aging and a potential therapeutic target

Ageing research reviews, 2015-11, Vol.24 (Pt B), p.111-125

2015

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Low plasma leptin in cognitively impaired ADNI subjects: gender differences and diagnostic and therapeutic potential

Current Alzheimer research, 2014-02, Vol.11 (2), p.165-174

2014

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Delays in Diagnosis of Congenital Hearing Loss in Rural Children

The Journal of pediatrics, 2014-02, Vol.164 (2), p.393-397

2014

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Predictors of chronic opioid therapy in Medicaid beneficiaries with HIV who initiated antiretroviral therapy

Scientific reports, 2021-07, Vol.11 (1), p.15503-15503, Article 15503

2021

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Analysis of genes (TMEM106B, GRN, ABCC9, KCNMB2, and APOE) implicated in risk for LATE-NC and hippocampal sclerosis provides pathogenetic insights: a retrospective genetic association study

Acta neuropathologica communications, 2021-09, Vol.9 (1), p.152-152, Article 152

2021

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Tau and TDP-43 proteinopathies: kindred pathologic cascades and genetic pleiotropy

Genetics of PICALM expression and Alzheimer's disease

Evaluation of CD33 as a genetic risk factor for Alzheimer’s disease

CD33 Alzheimer's risk-altering polymorphism, CD33 expression, and exon 2 splicing

Patterns and predictors of chronic opioid use in older adults: A retrospective cohort study

The Amygdala as a Locus of Pathologic Misfolding in Neurodegenerative Diseases

Genetics ignite focus on microglial inflammation in Alzheimer's disease

Outcomes after diagnosis of mild cognitive impairment in a large autopsy series

Sclerostin and Dickkopf-1 in Renal Osteodystrophy

Genetic data and cognitively defined late-onset Alzheimer’s disease subgroups

Age and sex are associated with the plasma lipidome: findings from the GOLDN study

Apolipoprotein E ε4/4 genotype limits response to dietary induction of hyperhomocysteinemia and resulting inflammatory signaling

Quantitative phenotype scan statistic (QPSS) reveals rare variant associations with Alzheimer's disease endophenotypes

Multiple gene variants linked to Alzheimer's-type clinical dementia via GWAS are also associated with non-Alzheimer's neuropathologic entities

Genetics of clusterin isoform expression and Alzheimer's disease risk

The association of gabapentin initiation and neurocognitive changes in older adults with normal cognition

TDP-43 proteinopathy in aging: Associations with risk-associated gene variants and with brain parenchymal thyroid hormone levels

Hippocampal sclerosis of aging, a prevalent and high-morbidity brain disease

Atorvastatin rescues hyperhomocysteinemia-induced cognitive deficits and neuroinflammatory gene changes

Dichotomous scoring of TDP-43 proteinopathy from specific brain regions in 27 academic research centers: associations with Alzheimer's disease and cerebrovascular disease pathologies

ABCC9/SUR2 in the brain: Implications for hippocampal sclerosis of aging and a potential therapeutic target

Low plasma leptin in cognitively impaired ADNI subjects: gender differences and diagnostic and therapeutic potential

Delays in Diagnosis of Congenital Hearing Loss in Rural Children

Predictors of chronic opioid therapy in Medicaid beneficiaries with HIV who initiated antiretroviral therapy

Analysis of genes (TMEM106B, GRN, ABCC9, KCNMB2, and APOE) implicated in risk for LATE-NC and hippocampal sclerosis provides pathogenetic insights: a retrospective genetic association study

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