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Author Details
Full Name
Devin Absher
Affiliation
Kaiser Permanente Research Bank
ORCID
Career Start Year
1994
Papers
167
H Index
67
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36803404
Distinct genome-wide DNA methylation and gene expression signatures in classical monocytes from African American patients with systemic sclerosis.
Clin Epigenetics
2023
36951251
Genetic associations with age at dementia onset in the PSEN1 E280A Colombian kindred.
Alzheimers Dement
2023
36803404
Distinct genome-wide DNA methylation and gene expression signatures in classical monocytes from African American patients with systemic sclerosis.
Clin Epigenetics
2023
36621880
Returning integrated genomic risk and clinical recommendations: The eMERGE study.
Genet Med
2023
37506491
Genome-wide DNA methylation analysis implicates enrichment of interferon pathway in African American patients with Systemic Lupus Erythematosus and European Americans with lupus nephritis.
J Autoimmun
2023
37506491
Genome-wide DNA methylation analysis implicates enrichment of interferon pathway in African American patients with Systemic Lupus Erythematosus and European Americans with lupus nephritis.
J Autoimmun
2023
36951251
Genetic associations with age at dementia onset in the PSEN1 E280A Colombian kindred.
Alzheimers Dement
2023
36621880
Returning integrated genomic risk and clinical recommendations: The eMERGE study.
Genet Med
2023
35188103
STAT3-mediated allelic imbalance of novel genetic variant Rs1047643 and B-cell-specific super-enhancer in association with systemic lupus erythematosus.
Elife
2022
35392283
Phase I Study of High-Dose L-methylfolate in Combination with Temozolomide and Bevacizumab in Recurrent IDH wild-type High-Grade Glioma.
Cancer Res Commun
2022
36292585
Differentially Methylated DNA Regions and Left Ventricular Hypertrophy in African Americans: A HyperGEN Study.
Genes (Basel)
2022
35576644
Longitudinal analysis of blood DNA methylation identifies mechanisms of response to tumor necrosis factor inhibitor therapy in rheumatoid arthritis.
EBioMedicine
2022
35551307
Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation.
Nat Genet
2022
35188103
STAT3-mediated allelic imbalance of novel genetic variant Rs1047643 and B-cell-specific super-enhancer in association with systemic lupus erythematosus.
Elife
2022
35551307
Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation.
Nat Genet
2022
35576644
Longitudinal analysis of blood DNA methylation identifies mechanisms of response to tumor necrosis factor inhibitor therapy in rheumatoid arthritis.
EBioMedicine
2022
35392283
Phase I Study of High-Dose L-methylfolate in Combination with Temozolomide and Bevacizumab in Recurrent IDH wild-type High-Grade Glioma.
Cancer Res Commun
2022
36292585
Differentially Methylated DNA Regions and Left Ventricular Hypertrophy in African Americans: A HyperGEN Study.
Genes (Basel)
2022
32989269
Identifying rare, medically relevant variation via population-based genomic screening in Alabama: opportunities and pitfalls.
Genet Med
2021
34121327
Evaluation of population-level pharmacogenetic actionability in Alabama.
Clin Transl Sci
2021
34230475
Publisher Correction: A multi-ethnic epigenome-wide association study of leukocyte DNA methylation and blood lipids.
Nat Commun
2021
34144992
Predicting future from past: The genomic basis of recurrent and rapid stickleback evolution.
Sci Adv
2021
33935738
Multifocal Analysis of Acute Pain After Third Molar Removal.
Front Pharmacol
2021
34183656
A multi-ethnic epigenome-wide association study of leukocyte DNA methylation and blood lipids.
Nat Commun
2021
33205280
CYP450 polymorphisms and clinical pharmacogenetics of ibuprofen after lower third molar extraction.
Eur J Clin Pharmacol
2021
32989269
Identifying rare, medically relevant variation via population-based genomic screening in Alabama: opportunities and pitfalls.
Genet Med
2021
34873174
Proximal and distal effects of genetic susceptibility to multiple sclerosis on the T cell epigenome.
Nat Commun
2021
34873174
Proximal and distal effects of genetic susceptibility to multiple sclerosis on the T cell epigenome.
Nat Commun
2021
34183656
A multi-ethnic epigenome-wide association study of leukocyte DNA methylation and blood lipids.
Nat Commun
2021
33935738
Multifocal Analysis of Acute Pain After Third Molar Removal.
Front Pharmacol
2021
34121327
Evaluation of population-level pharmacogenetic actionability in Alabama.
Clin Transl Sci
2021
34144992
Predicting future from past: The genomic basis of recurrent and rapid stickleback evolution.
Sci Adv
2021
34230475
Publisher Correction: A multi-ethnic epigenome-wide association study of leukocyte DNA methylation and blood lipids.
Nat Commun
2021
33205280
CYP450 polymorphisms and clinical pharmacogenetics of ibuprofen after lower third molar extraction.
Eur J Clin Pharmacol
2021
31430064
Population-Specific Patterns of Epigenetic Defects in the B Cell Lineage in Patients With Systemic Lupus Erythematosus.
Arthritis Rheumatol
2020
32930325
Carbohydrate and fat intake associated with risk of metabolic diseases through epigenetics of CPT1A.
Am J Clin Nutr
2020
32928875
Teleological role of L-2-hydroxyglutarate dehydrogenase in the kidney.
Dis Model Mech
2020
32697766
Blood DNA methylation sites predict death risk in a longitudinal study of 12, 300 individuals.
Aging (Albany NY)
2020
32628254
Skewed allelic expression on X chromosome associated with aberrant expression of XIST on systemic lupus erythematosus lymphocytes.
Hum Mol Genet
2020
31430064
Population-Specific Patterns of Epigenetic Defects in the B Cell Lineage in Patients With Systemic Lupus Erythematosus.
Arthritis Rheumatol
2020
32628254
Skewed allelic expression on X chromosome associated with aberrant expression of XIST on systemic lupus erythematosus lymphocytes.
Hum Mol Genet
2020
32930325
Carbohydrate and fat intake associated with risk of metabolic diseases through epigenetics of CPT1A.
Am J Clin Nutr
2020
32928875
Teleological role of L-2-hydroxyglutarate dehydrogenase in the kidney.
Dis Model Mech
2020
32697766
Blood DNA methylation sites predict death risk in a longitudinal study of 12, 300 individuals.
Aging (Albany NY)
2020
30541122
Corrigendum: Identification and validation of seven new loci showing differential DNA methylation related to serum lipid profile: an epigenome-wide approach. The REGICOR study.
Hum Mol Genet
2019
31921313
Exonic Variants in Aging-Related Genes Are Predictive of Phenotypic Aging Status.
Front Genet
2019
30552173
Genetic variation at the glycosaminoglycan metabolism pathway contributes to the risk of psoriatic arthritis but not psoriasis.
Ann Rheum Dis
2019
30541122
Corrigendum: Identification and validation of seven new loci showing differential DNA methylation related to serum lipid profile: an epigenome-wide approach. The REGICOR study.
Hum Mol Genet
2019
30423114
Genetic influences on susceptibility to rheumatoid arthritis in African-Americans.
Hum Mol Genet
2019
31491410
Exome-Derived Adiponectin-Associated Variants Implicate Obesity and Lipid Biology.
Am J Hum Genet
2019
1 - 50 of 334
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Jose M Ordovas
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Stefania Bandinelli
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Jerome I Rotter
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