Author details

Full Name

Hong Quach

Affiliation

ORCID

Career Start Year

2003

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
36862625	Identification of SjÃ¶gren's syndrome patient subgroups by clustering of labial salivary gland DNA methylation profiles.		2023
36716083	Identification of Cell-Specific Differential DNA Methylation Associated With Methotrexate Treatment Response in Rheumatoid Arthritis.		2023
36755464	Rare and low-frequency coding genetic variants contribute to pediatric-onset multiple sclerosis.	Mult Scler	2023
36631270	Cross-Trait Mendelian Randomization Study to Investigate Whether Migraine Is a Risk Factor for Multiple Sclerosis.	Neurology	2023
36962725	Health inequities in SARS-CoV-2 infection, seroprevalence, and COVID-19 vaccination: Results from the East Bay COVID-19 study.	PLOS Glob Public Health	2022
35612315	Development and Implementation of Dried Blood Spot-Based COVID-19 Serological Assays for Epidemiologic Studies.	Microbiol Spectr	2022
34314426	Correction: Hypomethylation mediates genetic association with the major histocompatibility complex genes in SjÃ¶gren's syndrome.	PLoS ONE	2021
33886574	Hypomethylation mediates genetic association with the major histocompatibility complex genes in SjÃ¶gren's syndrome.	PLoS ONE	2021
31081484	Vitamin D genes influence MS relapses in children.	Mult Scler	2020
32231389	Global expression and CpG methylation analysis of primary endothelial cells before and after TNFa stimulation reveals gene modules enriched in inflammatory and infectious diseases and associated DMRs.	PLoS ONE	2020
30635658	Mother-child histocompatibility and risk of rheumatoid arthritis and systemic lupus erythematosus among mothers.	Genes Immun	2020
31211169	miRNA contributions to pediatric-onset multiple sclerosis inferred from GWAS.	Ann Clin Transl Neurol	2019
29495467	MS Sunshine Study: Sun Exposure But Not Vitamin D Is Associated with Multiple Sclerosis Risk in Blacks and Hispanics.	Nutrients	2018
28980494	Genetic risk factors for pediatric-onset multiple sclerosis.	Mult Scler	2018
30379917	Increased DNA methylation of SLFN12 in CD4+ and CD8+ T cells from multiple sclerosis patients.	PLoS ONE	2018
30044683	Comparison of DNA methylation measured by Illumina 450K and EPIC BeadChips in blood of newborns and 14-year-old children.	Epigenetics	2018
29287311	Hypomethylation of CYP2E1 and DUSP22 Promoters Associated With Disease Activity and Erosive Disease Among Rheumatoid Arthritis Patients.	Arthritis and Rheumatology	2018
29414925	Vitamin D-Binding Protein Polymorphisms, 25-Hydroxyvitamin D, Sunshine and Multiple Sclerosis.	Nutrients	2018
27723282	Rheumatoid Arthritis Naive T Cells Share Hypermethylation Sites With Synoviocytes.	Arthritis Rheumatol	2017
28391248	Increased risk of rheumatoid arthritis among mothers with children who carry <i>DRB1</i> risk-associated alleles.	Ann Rheum Dis	2017
28855411	Epstein-Barr virus, cytomegalovirus, and multiple sclerosis susceptibility: A multiethnic study.	Neurology	2017
28356466	Evidence for a causal relationship between low vitamin D, high BMI, and pediatric-onset MS.	Neurology	2017
28073764	Causal Effect of Genetic Variants Associated With Body Mass Index on Multiple Sclerosis Susceptibility.	Am J Epidemiol	2017
27652346	Mendelian randomization shows a causal effect of low vitamin D on multiple sclerosis risk.	Neurology: Genetics	2016
27388144	A Child's HLA-DRB1 genotype increases maternal risk of systemic lupus erythematosus.	J Autoimmun	2016
27332624	Epigenetic Signatures of Salivary Gland Inflammation in SjÃ¶gren's Syndrome.	Arthritis and Rheumatology	2016
26782299	Hypomethylation within gene promoter regions and type 1 diabetes in discordant monozygotic twins.	Journal of Autoimmunity	2016
26769066	Genetic predictors of relapse rate in pediatric MS.	Mult Scler	2016
28074145	Genome-wide profiling identifies associations between lupus nephritis and differential methylation of genes regulating tissue hypoxia and type 1 interferon responses.	Lupus Science and Medicine	2016
26192630	Genome-Wide Assessment of Differential DNA Methylation Associated with Autoantibody Production in Systemic Lupus Erythematosus.	PLoS ONE	2015
25734800	Genome-wide DNA methylation profiles indicate CD8+ T cell hypermethylation in multiple sclerosis.	PLoS ONE	2015
26332589	Estimation of blood cellular heterogeneity in newborns and children for epigenome-wide association studies.	Environmental and Molecular Mutagenesis	2015
25178362	Seroprevalence of aquaporin-4-IgG in a northern California population representative cohort of multiple sclerosis.	JAMA Neurology	2014
25263833	Obesity during childhood and adolescence increases susceptibility to multiple sclerosis after accounting for established genetic and environmental risk factors.	Obesity Research and Clinical Practice	2014
24625537	Smoking and risk of multiple sclerosis: evidence of modification by NAT1 variants.	Epidemiology	2014
24577137	Adverse socioeconomic position during the life course is associated with multiple sclerosis.	J Epidemiol Community Health	2014
23959097	Considerations for normalization of DNA methylation data by Illumina 450K BeadChip assay in population studies.	Epigenetics	2013
24076602	Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis.	Nat Genet	2013
21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Nature	2011
19851445	High-density SNP screening of the major histocompatibility complex in systemic lupus erythematosus demonstrates strong evidence for independent susceptibility regions.	PLoS Genet	2009
16284307	Functional genomic analysis of the AUXIN/INDOLE-3-ACETIC ACID gene family members in Arabidopsis thaliana.	Plant Cell	2005
15659631	Functional genomic analysis of the AUXIN RESPONSE FACTOR gene family members in Arabidopsis thaliana: unique and overlapping functions of ARF7 and ARF19.	Plant Cell	2005
15960614	AUXIN RESPONSE FACTOR 2 (ARF2): a pleiotropic developmental regulator.	Plant Journal	2005
14593172	Empirical analysis of transcriptional activity in the Arabidopsis genome.	Science	2003