Fguirouche A, Ouahmani F, Brahim I, Hazime R, Louhab N, Kissani N
Clin Pract. 2025; 15(1).
PMID: 39851793
PMC: 11763420.
DOI: 10.3390/clinpract15010010.
Arshad S, Cameron B, Joglekar A
NPJ Syst Biol Appl. 2025; 11(1):10.
PMID: 39833247
PMC: 11747513.
DOI: 10.1038/s41540-024-00482-x.
Ulutekin C, Galli E, Schreiner B, Khademi M, Callegari I, Piehl F
Cell Rep Med. 2023; 5(1):101351.
PMID: 38134930
PMC: 10829729.
DOI: 10.1016/j.xcrm.2023.101351.
Beecham A, Amezcua L, Chinea A, Manrique C, Gomez L, Martinez A
PLoS One. 2022; 17(12):e0279132.
PMID: 36548255
PMC: 9778564.
DOI: 10.1371/journal.pone.0279132.
Guerini F, Agliardi C, Bolognesi E, Zanzottera M, Caputo D, Pasanisi M
Int J Mol Sci. 2022; 23(23).
PMID: 36499708
PMC: 9736555.
DOI: 10.3390/ijms232315381.
HLA-II Alleles Influence Physical and Behavioral Responses to a Whey Allergen in a Transgenic Mouse Model of Cow's Milk Allergy.
Germundson D, Nookala S, Smith N, Warda Y, Nagamoto-Combs K
Front Allergy. 2022; 3:870513.
PMID: 35769584
PMC: 9234862.
DOI: 10.3389/falgy.2022.870513.
Human Herpesvirus 6A Is a Risk Factor for Multiple Sclerosis.
Lundstrom W, Gustafsson R
Front Immunol. 2022; 13:840753.
PMID: 35222435
PMC: 8866567.
DOI: 10.3389/fimmu.2022.840753.
Genetics and functional genomics of multiple sclerosis.
Kim W, Patsopoulos N
Semin Immunopathol. 2022; 44(1):63-79.
PMID: 35022889
DOI: 10.1007/s00281-021-00907-3.
HLA-DR15 Molecules Jointly Shape an Autoreactive T Cell Repertoire in Multiple Sclerosis.
Wang J, Jelcic I, Muhlenbruch L, Haunerdinger V, Toussaint N, Zhao Y
Cell. 2020; 183(5):1264-1281.e20.
PMID: 33091337
PMC: 7707104.
DOI: 10.1016/j.cell.2020.09.054.
Increased Serological Response Against Human Herpesvirus 6A Is Associated With Risk for Multiple Sclerosis.
Engdahl E, Gustafsson R, Huang J, Bistrom M, Lima Bomfim I, Stridh P
Front Immunol. 2020; 10:2715.
PMID: 32038605
PMC: 6988796.
DOI: 10.3389/fimmu.2019.02715.
Multiple sclerosis and human leukocyte antigen genotypes: Focus on the Middle East and North Africa region.
Maghbooli Z, Sahraian M, Naser Moghadasi A
Mult Scler J Exp Transl Clin. 2020; 6(1):2055217319881775.
PMID: 31976083
PMC: 6956601.
DOI: 10.1177/2055217319881775.
Memory B Cells Activate Brain-Homing, Autoreactive CD4 T Cells in Multiple Sclerosis.
Jelcic I, Al Nimer F, Wang J, Lentsch V, Planas R, Jelcic I
Cell. 2018; 175(1):85-100.e23.
PMID: 30173916
PMC: 6191934.
DOI: 10.1016/j.cell.2018.08.011.
Blood Mononuclear Cell Mitochondrial Respiratory Chain Complex IV Activity Is Decreased in Multiple Sclerosis Patients: Effects of β-Interferon Treatment.
Hargreaves I, Mody N, Land J, Heales S
J Clin Med. 2018; 7(2).
PMID: 29461488
PMC: 5852452.
DOI: 10.3390/jcm7020036.
Genetics of Multiple Sclerosis: An Overview and New Directions.
Patsopoulos N
Cold Spring Harb Perspect Med. 2018; 8(7).
PMID: 29440325
PMC: 6027932.
DOI: 10.1101/cshperspect.a028951.
The immunogenetics of neurological disease.
Misra M, Damotte V, Hollenbach J
Immunology. 2017; 153(4):399-414.
PMID: 29159928
PMC: 5838423.
DOI: 10.1111/imm.12869.
Burden of genetic risk variants in multiple sclerosis families in the Netherlands.
Mescheriakova J, Broer L, Wahedi S, Uitterlinden A, Van Duijn C, Hintzen R
Mult Scler J Exp Transl Clin. 2017; 2:2055217316648721.
PMID: 28607725
PMC: 5433503.
DOI: 10.1177/2055217316648721.
Axonal transport deficits in multiple sclerosis: spiraling into the abyss.
van den Berg R, Hoogenraad C, Hintzen R
Acta Neuropathol. 2017; 134(1):1-14.
PMID: 28315956
PMC: 5486629.
DOI: 10.1007/s00401-017-1697-7.
Impact of MS genetic loci on familial aggregation, clinical phenotype, and disease prediction.
Esposito F, Guaschino C, Sorosina M, Clarelli F, Ferre L, Mascia E
Neurol Neuroimmunol Neuroinflamm. 2015; 2(4):e129.
PMID: 26185776
PMC: 4503410.
DOI: 10.1212/NXI.0000000000000129.
The immunogenetics of multiple sclerosis: A comprehensive review.
Hollenbach J, Oksenberg J
J Autoimmun. 2015; 64:13-25.
PMID: 26142251
PMC: 4687745.
DOI: 10.1016/j.jaut.2015.06.010.
An assessment of genetic counseling services for individuals with multiple sclerosis.
Skinner S, Guimond C, Butler R, Dwosh E, Traboulsee A, Sadovnick A
J Genet Couns. 2014; 24(1):46-57.
PMID: 24993688
DOI: 10.1007/s10897-014-9735-2.