Author details

Full Name

Nikolaos A Patsopoulos

Affiliation

ORCID

Career Start Year

2005

Papers

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
36448302	Not all roads lead to the immune system: the genetic basis of multiple sclerosis severity.	Brain	2023
37183562	The CYP24A1 gene variant rs2762943 is associated with low serum 1,25-dihydroxyvitamin D levels in multiple sclerosis patients.		2023
35022889	Genetics and functional genomics of multiple sclerosis.	Seminars in Immunopathology	2022
36032128	Characterization of CD41<sup>+</sup> cells in the lymph node.	Front Immunol	2022
35672799	Dissection of multiple sclerosis genetics identifies B and CD4+ T cells as driver cell subsets.		2022
36553660	A Whole-Genome Sequencing Study Implicates GRAMD1B in Multiple Sclerosis Susceptibility.	Genes (Basel)	2022
36548255	Ancestral risk modification for multiple sclerosis susceptibility detected across the Major Histocompatibility Complex in a multi-ethnic population.	PLoS One	2022
34873174	Proximal and distal effects of genetic susceptibility to multiple sclerosis on the T cell epigenome.	Nat Commun	2021
31368393	The genetic diversity of multiple sclerosis risk among Hispanic and African American populations living in the United States.	Mult Scler	2020
31965883	Genetic and gene expression signatures in multiple sclerosis.	Mult Scler	2020
32196808	Targeted resequencing reveals rare variants enrichment in multiple sclerosis susceptibility genes.	Hum Mutat	2020
32470373	Non-parametric Polygenic Risk Prediction via Partitioned GWAS Summary Statistics.	Am J Hum Genet	2020
32763913	Integrated Skin Transcriptomics and Serum Multiplex Assays Reveal Novel Mechanisms of Wound Healing in Diabetic Foot Ulcers.	Diabetes	2020
33037294	Two genetic variants explain the association of European ancestry with multiple sclerosis risk in African-Americans.	Sci Rep	2020
30635658	Mother-child histocompatibility and risk of rheumatoid arthritis and systemic lupus erythematosus among mothers.	Genes Immun	2020
31440141	Time-Dependent Changes in Microglia Transcriptional Networks Following Traumatic Brain Injury.	Front Cell Neurosci	2019
31222336	Corrigendum: Loss of LDAH associated with prostate cancer and hearing loss.	Hum Mol Genet	2019
29317701	A genome-wide association study identifies only two ancestry specific variants associated with spontaneous preterm birth.	Sci Rep	2018
30169630	Loss of LDAH associated with prostate cancer and hearing loss.	Hum Mol Genet	2018
29930110	Analysis of shared heritability in common disorders of the brain.	Science	2018
30131872	An integrated clinical program and crowdsourcing strategy for genomic sequencing and Mendelian disease gene discovery.	NPJ Genom Med	2018
30041668	Polygenic analysis of inflammatory disease variants and effects on microglia in the aging brain.	Mol Neurodegener	2018
29440325	Genetics of Multiple Sclerosis: An Overview and New Directions.	Cold Spring Harbor Perspectives in Medicine	2018
28218759	Limited statistical evidence for shared genetic effects of eQTLs and autoimmune-disease-associated loci in three major immune-cell types.	Nat Genet	2017
28391248	Increased risk of rheumatoid arthritis among mothers with children who carry <i>DRB1</i> risk-associated alleles.	Ann Rheum Dis	2017
29379820	MS <i>AHI1</i> genetic risk promotes IFNÎ³<sup>+</sup> CD4<sup>+</sup> T cells.	Neurol Neuroimmunol Neuroinflamm	2017
27540591	Multiple sclerosis risk loci and disease severity in 7,125 individuals from 10 studies.	Neurol Genet	2016
27388144	A Child's HLA-DRB1 genotype increases maternal risk of systemic lupus erythematosus.	J Autoimmun	2016
27182951	Local Joint Testing Improves Power and Identifies Hidden Heritability in Association Studies.	Genetics	2016
27228176	WITHDRAWN: Immediate-release methylphenidate for attention deficit hyperactivity disorder (ADHD) in adults.		2016
26819262	Genetic loci for Epstein-Barr virus nuclear antigen-1 are associated with risk of multiple sclerosis.	Multiple Sclerosis Journal	2016
26343388	Class II HLA interactions modulate genetic risk for multiple sclerosis.	Nat Genet	2015
25363779	Genetic and epigenetic fine mapping of causal autoimmune disease variants.	Nature	2015
25914168	A pharmacogenetic study implicates SLC9a9 in multiple sclerosis disease activity.	Ann Neurol	2015
25948629	Burden of risk variants correlates with phenotype of multiple sclerosis.	Multiple Sclerosis Journal	2015
26433934	A non-synonymous single-nucleotide polymorphism associated with multiple sclerosis risk affects the EVI5 interactome.	Hum Mol Genet	2015
26430803	Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores.	Am J Hum Genet	2015
25080502	Functional variations modulating PRKCA expression and alternative splicing predispose to multiple sclerosis.	Hum Mol Genet	2014
24430173	A gene pathway analysis highlights the role of cellular adhesion molecules in multiple sclerosis susceptibility.	Genes Immun	2014
24234648	No evidence for shared genetic basis of common variants in multiple sclerosis and amyotrophic lateral sclerosis.	Hum Mol Genet	2014
25230710	Immediate-release methylphenidate for attention deficit hyperactivity disorder (ADHD) in adults.		2014
24786080	Polarization of the effects of autoimmune and neurodegenerative risk alleles in leukocytes.	Science	2014
24278027	Fine-mapping the genetic association of the major histocompatibility complex in multiple sclerosis: HLA and non-HLA effects.	PLoS Genet	2013
26053541	Reconstructing 2â¿¿xâ¿¿2 contingency tables from odds ratios using the Di Pietrantonj method: difficulties, constraints and impact in meta-analysis results.	Research Synthesis Methods	2013
24076602	Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis.	Nat Genet	2013
24183452	Association of Parkinson disease with structural and regulatory variants in the HLA region.	Am J Hum Genet	2013
23836404	Genetic susceptibility for Alzheimer disease neuritic plaque pathology.	JAMA Neurol	2013
23041981	Effect of genetic variants, especially CYP2C9 and VKORC1, on the pharmacology of warfarin.	Semin Thromb Hemost	2012
22718199	Fine-mapping classical HLA variation associated with durable host control of HIV-1 infection in African Americans.	Hum Mol Genet	2012