Author details

Full Name

An Goris

Affiliation

ORCID

Career Start Year

1990

Papers

122

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37370875	Correction: Schroyen et al. Neuroinflammation and Its Association with Cognition, Neuronal Markers and Peripheral Inflammation after Chemotherapy for Breast Cancer. 2021, , 4198.		2023
37696578	A targeted sequencing extension for transcript genotyping in single-cell transcriptomics.		2023
36618380	Frequent somatic mosaicism in T lymphocyte subsets in individuals with and without multiple sclerosis.		2022
35464427	Natural Killer Cells in Multiple Sclerosis: Entering the Stage.	Frontiers in Immunology	2022
35393342	Effects of Vitamin D and Body Mass Index on Disease Risk and Relapse Hazard in Multiple Sclerosis: A Mendelian Randomization Study.	Neurology: Neuroimmunology and NeuroInflammation	2022
35963264	Genetics of multiple sclerosis: lessons from polygenicity.	Lancet Neurology, The	2022
35386698	Body Mass Index, Interleukin-6 Signaling and Multiple Sclerosis: A Mendelian Randomization Study.	Frontiers in Immunology	2022
35366084	Environmental risk factors in multiple sclerosis: bridging Mendelian randomization and observational studies.	Journal of Neurology	2022
34439351	Neuroinflammation and Its Association with Cognition, Neuronal Markers and Peripheral Inflammation after Chemotherapy for Breast Cancer.	Cancers	2021
33704824	Genetic Variation in WNT9B Increases Relapse Hazard in Multiple Sclerosis.	Ann Neurol	2021
34122439	Treatment-Induced BAFF Expression and B Cell Biology in Multiple Sclerosis.	Frontiers in Immunology	2021
33452402	Quantitative MRI phenotypes capture biological heterogeneity in multiple sclerosis patients.	Scientific Reports	2021
33239822	Author Correction: The cellular composition of the human immune system is shaped by age and cohabitation.	Nature Immunology	2021
34795445	Human immune diversity: from evolution to modernity.	Nature Immunology	2021
32529581	Smoking and multiple sclerosis risk: a Mendelian randomization study.	Journal of Neurology	2020
32242102	Transcript-specific regulation in T-cells in multiple sclerosis susceptibility.	European Journal of Human Genetics	2020
31997416	CHIT1 at Diagnosis Reflects Long-Term Multiple Sclerosis Disease Activity.	Annals of Neurology	2020
30894451	Leveraging human genetics to inform intervention strategies for multiple sclerosis.	Neurology	2019
30541027	A robust pipeline with high replication rate for detection of somatic variants in the adaptive immune system as a source of common genetic variation in autoimmune disease.	Human Molecular Genetics	2019
29908069	Serum neurofilament light chain levels as a marker of upper motor neuron degeneration in patients with Amyotrophic Lateral Sclerosis.	Neuropathology and Applied Neurobiology	2019
30918256	Myoglobinopathy is an adult-onset autosomal dominant myopathy with characteristic sarcoplasmic inclusions.	Nat Commun	2019
30862608	Machine learning identifies an immunological pattern associated with multiple juvenile idiopathic arthritis subtypes.	Annals of the Rheumatic Diseases	2019
29361022	Multiple sclerosis risk variants alter expression of co-stimulatory genes in B cells.	Brain	2018
30170791	LncRNAs expression profile in peripheral blood mononuclear cells from multiple sclerosis patients.	Journal of Neuroimmunology	2018
30004580	IFN-Î³ stimulates CpG-induced IL-10 production in BÂ cells via p38 and JNK signalling pathways.	European Journal of Immunology	2018
30332657	Genetic Architecture of Adaptive Immune System Identifies Key Immune Regulators.	Cell Reports	2018
29303040	Genetic basis for relapse rate in multiple sclerosis: Association with LRP2 genetic variation.	Multiple Sclerosis Journal	2018
29476185	The origins of diversity in human immunity.	Nature Immunology	2018
27696741	Inflammatory Gene Expression Profile and Defective Interferon-Î³ and Granzyme K in Natural Killer Cells From Systemic Juvenile Idiopathic Arthritis Patients.	Arthritis and Rheumatology	2017
28322246	Genetic correlation between amyotrophic lateral sclerosis and schizophrenia.	Nature Communications	2017
27455348	Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis.	Nat Genet	2016
27194806	Analysis of Plasminogen Genetic Variants in Multiple Sclerosis Patients.	G3: Genes, Genomes, Genetics	2016
27378687	Genetic ablation of IP3 receptor 2 increases cytokines and decreases survival of SOD1G93A mice.	Human Molecular Genetics	2016
27231713	Immunologic profiles of multiple sclerosis treatments reveal shared early B cell alterations.	Neurology: Neuroimmunology and NeuroInflammation	2016
26878114	The cellular composition of the human immune system is shaped by age and cohabitation.	Nature Immunology	2016
27039700	Power estimation for non-standardized multisite studies.	Neuroimage	2016
27030597	Familial autoinflammation with neutrophilic dermatosis reveals a regulatory mechanism of pyrin activation.	Science Translational Medicine	2016
26199351	Genetic burden mirrors epidemiology of multiple sclerosis.	Multiple Sclerosis Journal	2015
25616667	Genetic variants are major determinants of CSF antibody levels in multiple sclerosis.	Brain	2015
25948629	Burden of risk variants correlates with phenotype of multiple sclerosis.	Multiple Sclerosis Journal	2015
26343388	Class II HLA interactions modulate genetic risk for multiple sclerosis.	Nat Genet	2015
24838185	Analysis of the KIFAP3 gene in amyotrophic lateral sclerosis: a multicenter survival study.	Neurobiology of Aging	2014
24144875	HLA-E restricted CD8+ T cell subsets are phenotypically altered in multiple sclerosis patients.	Multiple Sclerosis Journal	2014
24234648	No evidence for shared genetic basis of common variants in multiple sclerosis and amyotrophic lateral sclerosis.	Hum Mol Genet	2014
25031287	Meta-analysis in more than 17,900 cases of ischemic stroke reveals a novel association at 12q24.12.	Neurology	2014
23065703	Novel COL4A1 mutations cause cerebral small vessel disease by haploinsufficiency.	Human Molecular Genetics	2013
23870417	Frequency of C9orf72 repeat expansions in amyotrophic lateral sclerosis: a Belgian cohort study.	Neurobiol Aging	2013
24076602	Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis.	Nat Genet	2013
23785401	Association of genetic markers with CSF oligoclonal bands in multiple sclerosis patients.	PLoS One	2013
23483640	No evidence for a role of rare CYP27B1 functional variations in multiple sclerosis.	Annals of Neurology	2013