Author details

Full Name

Lisa F Barcellos

Affiliation

ORCID

Career Start Year

1997

Papers

191

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
35253861	Polygenic risk score association with multiple sclerosis susceptibility and phenotype in Europeans.	Brain	2023
37808459	Adverse childhood experiences in early life increase the odds of depression among adults with multiple sclerosis.	Mult Scler J Exp Transl Clin	2023
38073021	Local ancestry at the MHC region is not a major contributor to disease heterogeneity in a multi-ethnic lupus cohort.		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
36862625	Identification of SjÃ¶gren's syndrome patient subgroups by clustering of labial salivary gland DNA methylation profiles.		2023
36725329	Gene-environment interactions increase the risk of paediatric-onset multiple sclerosis associated with household chemical exposures.	J Neurol Neurosurg Psychiatry	2023
34880094	Association Between Time Spent Outdoors and Risk of Multiple Sclerosis.	Neurology	2022
35840705	From the prodromal stage of multiple sclerosis to disease prevention.	Nat Rev Neurol	2022
35635730	Dynamics of Methylation of CpG Sites Associated With Systemic Lupus Erythematosus Subtypes in a Longitudinal Cohort.	Arthritis and Rheumatology	2022
35612315	Development and Implementation of Dried Blood Spot-Based COVID-19 Serological Assays for Epidemiologic Studies.	Microbiol Spectr	2022
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
35025951	Case-control study of adverse childhood experiences and multiple sclerosis risk and clinical outcomes.	PLoS ONE	2022
35000467	Gene-environment interactions increase the risk of pediatric-onset multiple sclerosis associated with ozone pollution.	Mult Scler	2022
34873174	Proximal and distal effects of genetic susceptibility to multiple sclerosis on the T cell epigenome.	Nat Commun	2021
33886574	Hypomethylation mediates genetic association with the major histocompatibility complex genes in SjÃ¶gren's syndrome.	PLoS ONE	2021
34314426	Correction: Hypomethylation mediates genetic association with the major histocompatibility complex genes in SjÃ¶gren's syndrome.	PLoS ONE	2021
32662747	A validation study for remote testing of cognitive function in multiple sclerosis.	Mult Scler	2021
34409759	Gut microbiome is associated with multiple sclerosis activity in children.	Ann Clin Transl Neurol	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
32109229	Author Correction: A phenotypic and genomics approach in a multi-ethnic cohort to subtype systemic lupus erythematosus.	Nature Communications	2020
33037103	Pregnancy does not modify the risk of MS in genetically susceptible women.	Neurology: Neuroimmunology and NeuroInflammation	2020
33063621	Seafood, fatty acid biosynthesis genes, and multiple sclerosis susceptibility.	Mult Scler	2020
30635658	Mother-child histocompatibility and risk of rheumatoid arthritis and systemic lupus erythematosus among mothers.	Genes Immun	2020
31296947	Heritable variation at the chromosome 21 gene ERG is associated with acute lymphoblastic leukemia risk in children with and without Down syndrome.	Leukemia	2019
30653506	Admixture mapping reveals evidence of differential multiple sclerosis risk by genetic ancestry.	PLoS Genet	2019
31223483	No differential gene expression for CD4 T cells of MS patients and healthy controls.	Multiple Sclerosis Journal - Experimental, Translational and Clinical	2019
31467281	A phenotypic and genomics approach in a multi-ethnic cohort to subtype systemic lupus erythematosus.	Nature Communications	2019
31211169	miRNA contributions to pediatric-onset multiple sclerosis inferred from GWAS.	Ann Clin Transl Neurol	2019
31366909	Cell-type-specific resolution epigenetics without the need for cell sorting or single-cell biology.	Nature Communications	2019
31350265	Inherited genetic susceptibility to acute lymphoblastic leukemia in Down syndrome.	Blood	2019
28273777	Remote assessment of verbal memory in MS patients using the California Verbal Learning Test.	Multiple Sclerosis Journal	2018
28993476	Contribution of dietary intake to relapse rate in early paediatric multiple sclerosis.	J Neurol Neurosurg Psychiatry	2018
28980494	Genetic risk factors for pediatric-onset multiple sclerosis.	Mult Scler	2018
29025908	A germ-line deletion of APOBEC3B does not contribute to subtype-specific childhood acute lymphoblastic leukemia etiology.	Haematologica	2018
30068517	Allergies and Childhood Acute Lymphoblastic Leukemia: A Case-Control Study and Meta-analysis.	Cancer Epidemiol Biomarkers Prev	2018
30305912	Increased alloreactive and autoreactive antihuman leucocyte antigen antibodies associated with systemic lupus erythematosus and rheumatoid arthritis.	Lupus Sci Med	2018
30154825	To ERV Is Human: A Phenotype-Wide Scan Linking Polymorphic Human Endogenous Retrovirus-K Insertions to Complex Phenotypes.	Front Genet	2018
29923177	BMI1 enhancer polymorphism underlies chromosome 10p12.31 association with childhood acute lymphoblastic leukemia.	Int J Cancer	2018
30349857	Heterogeneity in association of remote herpesvirus infections and pediatric MS.	Ann Clin Transl Neurol	2018
30005356	Incorporating machine learning approaches to assess putative environmental risk factors for multiple sclerosis.	Multiple Sclerosis and Related Disorders	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
30564618	Several household chemical exposures are associated with pediatric-onset multiple sclerosis.	Ann Clin Transl Neurol	2018
29348612	GWAS in childhood acute lymphoblastic leukemia reveals novel genetic associations at chromosomes 17q12 and 8q24.21.	Nat Commun	2018
29168253	Genomewide association study of HLA alloimmunization in previously pregnant blood donors.	Transfusion	2018
29695455	Alloreactive fetal T cells promote uterine contractility in preterm labor via IFN-Î³ and TNF-Î±.	Sci Transl Med	2018
29287311	Hypomethylation of CYP2E1 and DUSP22 Promoters Associated With Disease Activity and Erosive Disease Among Rheumatoid Arthritis Patients.	Arthritis and Rheumatology	2018