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Nature Biotechnology|January 22, 2013
Epigenome-wide association data implicate DNA methylation as an intermediary of genetic risk in rheumatoid arthritisYun Liu, Martin J Aryee, Leonid Padyukov, et al.Nature Communications|January 28, 2021
Endophilin A2 deficiency protects rodents from autoimmune arthritis by modulating T cell activationUlrika Norin, Carola Rintisch, Liesu Meng, et al.Molecular Medicine (Cambridge, Mass.)|August 18, 2016
Integration of known DNA, RNA and protein biomarkers provides prediction of anti-TNF response in rheumatoid arthritis: results from the COMBINE studyLasse Folkersen, Boel Brynedal, Lina Marcela Diaz-Gallo, et al.American Journal of Respiratory and Critical Care Medicine|December 15, 2015
High-Density Genetic Mapping Identifies New Susceptibility Variants in Sarcoidosis Phenotypes and Shows Genomic-driven Phenotypic DifferencesNatalia V Rivera, Marcus Ronninger, Klementy Shchetynsky, et al.Journal of Neurology|September 12, 2024
Pharmacogenomics of clinical response to Natalizumab in multiple sclerosis: a genome-wide multi-centric association studyFerdinando Clarelli, Andrea Corona, Kimmo Pääkkönen, et al.Annals of Neurology|September 27, 2023
A Genetic Risk Variant for Multiple Sclerosis Severity is Associated with Brain AtrophyChristiane Gasperi, Tun Wiltgen, Julian McGinnis, et al.Multiple Sclerosis (Houndmills, Basingstoke, England)|March 3, 2026
Pharmacogenomics of response to interferon-beta and glatiramer acetate in Multiple Sclerosis: A multi-centric studyAndrea Corona, Ferdinando Clarelli, Kimmo Pääkkönen, et al.Nature Communications|July 30, 2024
A genetic-epigenetic interplay at 1q21.1 locus underlies CHD1L-mediated vulnerability to primary progressive multiple sclerosisMajid Pahlevan Kakhki, Antonino Giordano, Chiara Starvaggi Cucuzza, et al.Annals of Neurology|August 7, 2025
Depression Polygenicity and Disease Activity and Disability Worsening in Multiple SclerosisAli Manouchehrinia, Kathryn C Fitzgerald, Amber Salter, et al.Acta Neuropathologica|February 4, 2026
A HIF1A variant impacts long-term disability and smoldering inflammation in multiple sclerosisAntonino Giordano, Pernilla Stridh, Paolo Preziosa, et al.Pageof 3