Publications 2025

Eriksson AM, Emini N, Harbo HF, Berge T (2025)
Is DEXI a Multiple Sclerosis Susceptibility Gene?
26 (3)
DOI 10.3390/ijms26031175, PubMed 39940946

Høgestøl EA, Rinker DA, Maximov I, Sowa P, Celius EG, Hope TR, Bjørnerud A, Sofia FM, de Las Heras EM, Solana E, Llufriu S, Gamez JFC, Farre JA, Pareto D, Collorone S, Pagani E, Gonzalez-Escamilla G, Groppa S, Sastre-Garriga J, Rovira À, Toosy A, Filippi M, Rocca MA, Westlye LT, Harbo HF et al. (2025)
A cross-sectional multicentre study of multishell diffusion MRI in multiple sclerosis
98, 106435
DOI 10.1016/j.msard.2025.106435, PubMed 40233645

Pontillo G, Prados F, Wink AM, Kanber B, Bisecco A, Broeders TAA, Brunetti A, Cagol A, Calabrese M, Castellaro M, Cocozza S, Colato E, Collorone S, Cortese R, De Stefano N, Douw L, Enzinger C, Filippi M, Foster MA, Gallo A, Gonzalez-Escamilla G, Granziera C, Groppa S, Harbo HF, Høgestøl EA et al. (2025)
More Than the Sum of Its Parts: Disrupted Core Periphery of Multiplex Brain Networks in Multiple Sclerosis
46 (1), e70107
DOI 10.1002/hbm.70107, PubMed 39740239

Skattebøl L, Lundby R, Øverås MH, Sowa P, Celius EG, Harbo HF, Nordhøy W, Høgestøl EA, Nygaard GO (2025)
Quantitative susceptibility mapping of paramagnetic rim lesions in early multiple sclerosis: A cross-sectional study of brain age and disability
5 (3), 100277
DOI 10.1016/j.ynirp.2025.100277, PubMed 41050950

Skattebøl L, Nygaard GO, Leonardsen EH, Kaufmann T, Moridi T, Stawiarz L, Ouellette R, Ineichen BV, Ferreira D, Muehlboeck JS, Beyer MK, Sowa P, Manouchehrinia A, Westman E, Olsson T, Celius EG, Hillert J, Kockum I, Harbo HF, Piehl F, Granberg T, Westlye LT, Høgestøl EA (2025)
Brain age in multiple sclerosis: a study with deep learning and traditional machine learning
7 (3), fcaf152
DOI 10.1093/braincomms/fcaf152, PubMed 40337466

Aamodt AH, Ueland T, Boldingh M, Bezgal BE, Argren MB, Dunne CA, Otterdal K, Gregersen I, Bjerkeli V, Michelsen AE, Husøy A, Morsund ÅH, Devik K, Poole AC, Gjendemsjø KB, Schlüter K, Mathisen SM, Aalstad-Johansen M, Skattør TH, Sønnervik J, Boye TB, Popperud TH, Høgestøl EA, Harbo HF, Lund-Johansen F et al. (2025)
Altered amyloid plasma profile in patients with disabling headaches after SARS-CoV-2 infection and vaccination
7 (2), e001013
DOI 10.1136/bmjno-2024-001013, PubMed 40881041

Publications 2024

Fleischer V, Gonzalez-Escamilla G, Pareto D, Rovira A, Sastre-Garriga J, Sowa P, Høgestøl EA, Harbo HF, Bellenberg B, Lukas C, Ruggieri S, Gasperini C, Uher T, Vaneckova M, Bittner S, Othman AE, Collorone S, Toosy AT, Meuth SG, Zipp F, Barkhof F, Ciccarelli O, Groppa S (2024)
Prognostic value of single-subject grey matter networks in early multiple sclerosis
147 (1), 135-146
DOI 10.1093/brain/awad288, PubMed 37642541

Kennedy KE, Kerlero de Rosbo N, Uccelli A, Cellerino M, Ivaldi F, Contini P, De Palma R, Harbo HF, Berge T, Bos SD, Høgestøl EA, Brune-Ingebretsen S, de Rodez Benavent SA, Paul F, Brandt AU, Bäcker-Koduah P, Behrens J, Kuchling J, Asseyer S, Scheel M, Chien C, Zimmermann H, Motamedi S, Kauer-Bonin J, Saez-Rodriguez J et al. (2024)
Multiscale networks in multiple sclerosis
20 (2), e1010980
DOI 10.1371/journal.pcbi.1010980, PubMed 38329927

Lindland ES, Røvang MS, Solheim AM, Andreassen S, Skarstein I, Dareez N, MacIntosh BJ, Eikeland R, Ljøstad U, Mygland Å, Bos SD, Ulvestad E, Reiso H, Lorentzen ÅR, Harbo HF, Bjørnerud A, Beyer MK (2024)
Are white matter hyperintensities associated with neuroborreliosis? The answer is twofold
67 (1), 37-48
DOI 10.1007/s00234-024-03482-0, PubMed 39422730

Martí-Juan G, Sastre-Garriga J, Vidal-Jordana A, Llufriu S, Martinez-Heras E, Groppa S, González-Escamilla G, Rocca MA, Filippi M, Høgestøl EA, Harbo HF, Foster MA, Collorone S, Toosy AT, Schoonheim MM, Strijbis E, Pontillo G, Petracca M, Deco G, Rovira À, Pareto D (2024)
Conservation of structural brain connectivity in people with multiple sclerosis
8 (4), 1545-1562
DOI 10.1162/netn_a_00404, PubMed 39735510

Pontillo G, Prados F, Colman J, Kanber B, Abdel-Mannan O, Al-Araji S, Bellenberg B, Bianchi A, Bisecco A, Brownlee WJ, Brunetti A, Cagol A, Calabrese M, Castellaro M, Christensen R, Cocozza S, Colato E, Collorone S, Cortese R, De Stefano N, Enzinger C, Filippi M, Foster MA, Gallo A, Gasperini C et al. (2024)
Disentangling Neurodegeneration From Aging in Multiple Sclerosis Using Deep Learning: The Brain-Predicted Disease Duration Gap
103 (10), e209976
DOI 10.1212/WNL.0000000000209976, PubMed 39496109

Publications 2023

Andorra M, Freire A, Zubizarreta I, de Rosbo NK, Bos SD, Rinas M, Høgestøl EA, de Rodez Benavent SA, Berge T, Brune-Ingebretse S, Ivaldi F, Cellerino M, Pardini M, Vila G, Pulido-Valdeolivas I, Martinez-Lapiscina EH, Llufriu S, Saiz A, Blanco Y, Martinez-Heras E, Solana E, Bäcker-Koduah P, Behrens J, Kuchling J, Asseyer S et al. (2023)
Predicting disease severity in multiple sclerosis using multimodal data and machine learning
271 (3), 1133-1149
DOI 10.1007/s00415-023-12132-z, PubMed 38133801

Brune-Ingebretsen S, Høgestøl EA, de Rosbo NK, Berg-Hansen P, Brunborg C, Blennow K, Zetterberg H, Paul F, Uccelli A, Villoslada P, Harbo HF, Berge T (2023)
Immune cell subpopulations and serum neurofilament light chain are associated with increased risk of disease worsening in multiple sclerosis
382, 578175
DOI 10.1016/j.jneuroim.2023.578175, PubMed 37573634

Feiring E, Løberg M, Bjaalie JG, Dyb GA, Harbo HF (2023)
[Gender and health, education and research]
143 (11)
DOI 10.4045/tidsskr.23.0408, PubMed 37589360

Lindland ES, Solheim AM, Andreassen S, Bugge R, Eikeland R, Reiso H, Lorentzen ÅR, Harbo HF, Beyer MK, Bjørnerud A (2023)
Dynamic contrast-enhanced MRI shows altered blood-brain barrier function of deep gray matter structures in neuroborreliosis: a case-control study
7 (1), 52
DOI 10.1186/s41747-023-00365-6, PubMed 37710058

Martí-Juan G, Sastre-Garriga J, Martinez-Heras E, Vidal-Jordana A, Llufriu S, Groppa S, Gonzalez-Escamilla G, Rocca MA, Filippi M, Høgestøl EA, Harbo HF, Foster MA, Toosy AT, Schoonheim MM, Tewarie P, Pontillo G, Petracca M, Rovira À, Deco G, Pareto D (2023)
Using The Virtual Brain to study the relationship between structural and functional connectivity in patients with multiple sclerosis: a multicenter study
33 (12), 7322-7334
DOI 10.1093/cercor/bhad041, PubMed 36813475

Wolf AS, Ravussin A, König M, Øverås MH, Solum G, Kjønstad IF, Chopra A, Holmøy T, Harbo HF, Syversen SW, Jørgensen KK, Høgestøl EA, Vaage JT, Celius EG, Lund-Johansen F, Munthe LA, Nygaard GO, Mjaaland S (2023)
T cell responses to SARS-CoV-2 vaccination differ by disease-modifying therapy for multiple sclerosis
8 (12)
DOI 10.1172/jci.insight.165111, PubMed 37159281

Publications 2022

Andreassen S, Lindland EMS, Beyer MK, Solheim AM, Ljøstad U, Mygland Å, Lorentzen ÅR, Reiso H, Bjuland KJ, Pripp AH, Harbo HF, Løhaugen GCC, Eikeland R (2022)
Assessment of cognitive function, structural brain changes and fatigue 6 months after treatment of neuroborreliosis
270 (3), 1430-1438
DOI 10.1007/s00415-022-11463-7, PubMed 36380166

Andreassen S, Solheim AM, Ljøstad U, Mygland Å, Lorentzen ÅR, Reiso H, Beyer MK, Harbo HF, Løhaugen GCC, Eikeland R (2022)
Cognitive function in patients with neuroborreliosis: A prospective cohort study from the acute phase to 12 months post treatment
12 (6), e2608
DOI 10.1002/brb3.2608, PubMed 35593485

Brorson IS, Eriksson AM, Høgestøl E, Leikfoss IS, Harbo HF, Berge T, Vitelli V, Bos SD (2022)
Global DNA methylation changes in treated and untreated MS patients measured over time
364, 577808
DOI 10.1016/j.jneuroim.2022.577808, PubMed 35093762

Brune S, Høgestøl EA, de Rodez Benavent SA, Berg-Hansen P, Beyer MK, Leikfoss IS, Bos SD, Sowa P, Brunborg C, Andorra M, Pulido Valdeolivas I, Asseyer S, Brandt A, Chien C, Scheel M, Blennow K, Zetterberg H, Kerlero de Rosbo N, Paul F, Uccelli A, Villoslada P, Berge T, Harbo HF (2022)
Serum neurofilament light chain concentration predicts disease worsening in multiple sclerosis
28 (12), 1859-1870
DOI 10.1177/13524585221097296, PubMed 35658739

Cappelletti C, Eriksson A, Brorson IS, Leikfoss IS, Kråbøl O, Høgestøl EA, Vitelli V, Mjaavatten O, Harbo HF, Berven F, Bos SD, Berge T (2022)
Quantitative proteomics reveals protein dysregulation during T cell activation in multiple sclerosis patients compared to healthy controls
19 (1), 23
DOI 10.1186/s12014-022-09361-1, PubMed 35790914

Drobnjak Nes D, Berg-Hansen P, de Rodez Benavent SA, Høgestøl EA, Beyer MK, Rinker DA, Veiby N, Karabeg M, Petrovski BÉ, Celius EG, Harbo HF, Petrovski G (2022)
Exploring Retinal Blood Vessel Diameters as Biomarkers in Multiple Sclerosis
11 (11)
DOI 10.3390/jcm11113109, PubMed 35683496

Leonardsen EH, Peng H, Kaufmann T, Agartz I, Andreassen OA, Celius EG, Espeseth T, Harbo HF, Høgestøl EA, Lange AM, Marquand AF, Vidal-Piñeiro D, Roe JM, Selbæk G, Sørensen Ø, Smith SM, Westlye LT, Wolfers T, Wang Y (2022)
Deep neural networks learn general and clinically relevant representations of the ageing brain
256, 119210
DOI 10.1016/j.neuroimage.2022.119210, PubMed 35462035

Lie IA, Kaçar S, Wesnes K, Brouwer I, Kvistad SS, Wergeland S, Holmøy T, Midgard R, Bru A, Edland A, Eikeland R, Gosal S, Harbo HF, Kleveland G, Sørenes YS, Øksendal N, Varhaug KN, Vedeler CA, Barkhof F, Teunissen CE, Bø L, Torkildsen Ø, Myhr KM, Vrenken H (2022)
Serum neurofilament as a predictor of 10-year grey matter atrophy and clinical disability in multiple sclerosis: a longitudinal study
93 (8), 849-57 (in press)
DOI 10.1136/jnnp-2021-328568, PubMed 35649699

Lie IA, Wesnes K, Kvistad SS, Brouwer I, Wergeland S, Holmøy T, Midgard R, Bru A, Edland A, Eikeland R, Gosal S, Harbo HF, Kleveland G, Sørenes YS, Øksendal N, Barkhof F, Vrenken H, Myhr KM, Bø L, Torkildsen Ø (2022)
The Effect of Smoking on Long-term Gray Matter Atrophy and Clinical Disability in Patients with Relapsing-Remitting Multiple Sclerosis
9 (5)
DOI 10.1212/NXI.0000000000200008, PubMed 35738901

Lindland ES, Solheim AM, Dareez MN, Eikeland R, Ljøstad U, Mygland Å, Reiso H, Lorentzen ÅR, Harbo HF, Beyer MK (2022)
Enhancement of cranial nerves in Lyme neuroborreliosis: incidence and correlation with clinical symptoms and prognosis
64 (12), 2323-2333
DOI 10.1007/s00234-022-02957-2, PubMed 35608630

Rise HH, Brune S, Chien C, Berge T, Bos SD, Andorrà M, Valdeolivas IP, Beyer MK, Sowa P, Scheel M, Brandt AU, Asseyer S, Blennow K, Pedersen ML, Zetterberg H, de Schotten MT, Cellerino M, Uccelli A, Paul F, Villoslada P, Harbo HF, Westlye LT, Høgestøl EA (2022)
Brain disconnectome mapping derived from white matter lesions and serum neurofilament light levels in multiple sclerosis: A longitudinal multicenter study
35, 103099
DOI 10.1016/j.nicl.2022.103099, PubMed 35772194

Publications 2021

Andreassen S, Lindland EMS, Solheim AM, Beyer MK, Ljøstad U, Mygland Å, Lorentzen ÅR, Reiso H, Harbo HF, Løhaugen GCC, Eikeland R (2021)
Cognitive function, fatigue and Fazekas score in patients with acute neuroborreliosis
12 (3), 101678
DOI 10.1016/j.ttbdis.2021.101678, PubMed 33529985

Creary LE, Gangavarapu S, Caillier SJ, Cavalcante P, Frangiamore R, Lie BA, Bengtsson M, Harbo HF, Brauner S, Hollenbach JA, Oksenberg JR, Bernasconi P, Maniaol AH, Hammarström L, Mantegazza R, Fernández-Viña MA (2021)
Next-Generation Sequencing Identifies Extended HLA Class I and II Haplotypes Associated With Early-Onset and Late-Onset Myasthenia Gravis in Italian, Norwegian, and Swedish Populations
12, 667336
DOI 10.3389/fimmu.2021.667336, PubMed 34163474

Eriksson AM, Leikfoss IS, Abrahamsen G, Sundvold V, Isom MM, Keshari PK, Rognes T, Landsverk OJB, Bos SD, Harbo HF, Spurkland A, Berge T (2021)
Exploring the role of the multiple sclerosis susceptibility gene CLEC16A in T cells
94 (1), e13050
DOI 10.1111/sji.13050, PubMed 34643957

Høgestøl EA, Ghezzo S, Nygaard GO, Espeseth T, Sowa P, Beyer MK, Harbo HF, Westlye LT, Hulst HE, Alnæs D (2021)
Functional connectivity in multiple sclerosis modelled as connectome stability: A 5-year follow-up study
28 (4), 532-540
DOI 10.1177/13524585211030212, PubMed 34259578

König M, Lorentzen ÅR, Torgauten HM, Tran TT, Schikora-Rustad S, Vaage EB, Mygland Å, Wergeland S, Aarseth J, Aaberge IAS, Torkildsen Ø, Holmøy T, Berge T, Myhr KM, Harbo HF, Andersen JT, Munthe LA, Søraas A, Celius EG, Vaage JT, Lund-Johansen F, Nygaard GO (2021)
Humoral immunity to SARS-CoV-2 mRNA vaccination in multiple sclerosis: the relevance of time since last rituximab infusion and first experience from sporadic revaccinations
94 (1), 19-22
DOI 10.1136/jnnp-2021-327612, PubMed 34670844

Wesnes K, Myhr KM, Riise T, Kvistad SS, Torkildsen O, Wergeland S, Holmoy T, Midgard R, Bru A, Edland A, Eikeland R, Gosal S, Harbo HF, Kleveland G, Sorenes YS, Oksendal N, Bjornevik K (2021)
Low vitamin D, but not tobacco use or high BMI, is associated with long-term disability progression in multiple sclerosis
Mult. Scler. Relat. Disord., 50, 102801
DOI 10.1016/j.msard.2021.102801

Aamodt AH, Høgestøl EA, Popperud TH, Holter JC, Dyrhol-Riise AM, Tonby K, Stiksrud B, Quist-Paulsen E, Berge T, Barratt-Due A, Aukrust P, Heggelund L, Blennow K, Zetterberg H, Harbo HF (2021)
Blood neurofilament light concentration at admittance: a potential prognostic marker in COVID-19
268 (10), 3574-3583
DOI 10.1007/s00415-021-10517-6, PubMed 33743046

Publications 2020

Brorson IS, Eriksson AM, Leikfoss IS, Vitelli V, Celius EG, Lüders T, Berge T, Harbo HF, Nilsen H, Bos SD (2020)
CD8⁺ T cell gene expression analysis identifies differentially expressed genes between multiple sclerosis patients and healthy controls
6 (4), 2055217320978511
DOI 10.1177/2055217320978511, PubMed 33343920

Brune S, Høgestøl EA, Cengija V, Berg-Hansen P, Sowa P, Nygaard GO, Harbo HF, Beyer MK (2020)
LesionQuant for Assessment of MRI in Multiple Sclerosis-A Promising Supplement to the Visual Scan Inspection
11, 546744
DOI 10.3389/fneur.2020.546744, PubMed 33362682

Cellerino M, Ivaldi F, Pardini M, Rotta G, Vila G, Bäcker-Koduah P, Berge T, Laroni A, Lapucci C, Novi G, Boffa G, Sbragia E, Palmeri S, Asseyer S, Høgestøl E, Campi C, Piana M, Inglese M, Paul F, Harbo HF, Villoslada P, Kerlero de Rosbo N, Uccelli A (2020)
Impact of treatment on cellular immunophenotype in MS: A cross-sectional study
7 (3)
DOI 10.1212/NXI.0000000000000693, PubMed 32139439

Elvsåshagen T, Bahrami S, van der Meer D, Agartz I, Alnæs D, Barch DM, Baur-Streubel R, Bertolino A, Beyer MK, Blasi G, Borgwardt S, Boye B, Buitelaar J, Bøen E, Celius EG, Cervenka S, Conzelmann A, Coynel D, Di Carlo P, Djurovic S, Eisenacher S, Espeseth T, Fatouros-Bergman H, Flyckt L, Franke B et al. (2020)
The genetic architecture of human brainstem structures and their involvement in common brain disorders
11 (1), 4016
DOI 10.1038/s41467-020-17376-1, PubMed 32782260

Kaufmann T, van der Meer D, Doan NT, Schwarz E, Lund MJ, Agartz I, Alnæs D, Barch DM, Baur-Streubel R, Bertolino A, Bettella F, Beyer MK, Bøen E, Borgwardt S, Brandt CL, Buitelaar J, Celius EG, Cervenka S, Conzelmann A, Córdova-Palomera A, Dale AM, de Quervain DJF, Di Carlo P, Djurovic S, Dørum ES et al. (2020)
Publisher Correction: Common brain disorders are associated with heritable patterns of apparent aging of the brain
23 (2), 295
DOI 10.1038/s41593-019-0553-6, PubMed 31848485

Publications 2019

Berge T, Eriksson A, Brorson IS, Høgestøl EA, Berg-Hansen P, Døskeland A, Mjaavatten O, Bos SD, Harbo HF, Berven F (2019)
Quantitative proteomic analyses of CD4⁺ and CD8⁺ T cells reveal differentially expressed proteins in multiple sclerosis patients and healthy controls
16, 19
DOI 10.1186/s12014-019-9241-5, PubMed 31080378

Brorson IS, Eriksson A, Leikfoss IS, Celius EG, Berg-Hansen P, Barcellos LF, Berge T, Harbo HF, Bos SD (2019)
No differential gene expression for CD4⁺ T cells of MS patients and healthy controls
5 (2), 2055217319856903
DOI 10.1177/2055217319856903, PubMed 31223483

de Rodez Benavent SA, Nygaard GO, Nilsen KB, Etholm L, Sowa P, Wendel-Haga M, Harbo HF, Drolsum L, Laeng B, Kerty E, Celius EG (2019)
Neurodegenerative Interplay of Cardiovascular Autonomic Dysregulation and the Retina in Early Multiple Sclerosis
10, 507
DOI 10.3389/fneur.2019.00507, PubMed 31156539

Høgestøl EA, Kaufmann T, Nygaard GO, Beyer MK, Sowa P, Nordvik JE, Kolskår K, Richard G, Andreassen OA, Harbo HF, Westlye LT (2019)
Cross-Sectional and Longitudinal MRI Brain Scans Reveal Accelerated Brain Aging in Multiple Sclerosis
10, 450
DOI 10.3389/fneur.2019.00450, PubMed 31114541

Høgestøl EA, Nygaard GO, Alnæs D, Beyer MK, Westlye LT, Harbo HF (2019)
Symptoms of fatigue and depression is reflected in altered default mode network connectivity in multiple sclerosis
14 (4), e0210375
DOI 10.1371/journal.pone.0210375, PubMed 30933977

Kaufmann T, van der Meer D, Doan NT, Schwarz E, Lund MJ, Agartz I, Alnæs D, Barch DM, Baur-Streubel R, Bertolino A, Bettella F, Beyer MK, Bøen E, Borgwardt S, Brandt CL, Buitelaar J, Celius EG, Cervenka S, Conzelmann A, Córdova-Palomera A, Dale AM, de Quervain DJF, Di Carlo P, Djurovic S, Dørum ES et al. (2019)
Common brain disorders are associated with heritable patterns of apparent aging of the brain
22 (10), 1617-1623
DOI 10.1038/s41593-019-0471-7, PubMed 31551603

Aamodt AH, Harbo HF (2019)
Hjernehelse
In Nevrologi og Nevrokirurgi: fra barn til voksen. (Harbo HF, Helseth E, Rootwelt T, eds.), Fagbokforlaget
PublikaID 430, ISBN 9788245024739

Publications 2018

Akhmadeev K, Houssein A, Moussaoui S, Hogestol EA, Tutturen I, Harbo HF, Bos-Haugen SD, Graves J, Laplaud DA, Gourraud PA (2018)
SVM-based Tool to Detect Patients with Multiple Sclerosis Using a Commercial EMG Sensor
PR IEEE SEN ARRAY, 376-379

Bajwa SK, Nilsen KB, Erichsen EAS, Berg-Hansen P, Harbo HF (2018)
A man in the 50s with dizziness, double vision and walking difficulties
Tidsskr. Nor. Laegeforen., 138 (3), 253-256

Kular L, Liu Y, Ruhrmann S, Zheleznyakova G, Marabita F, Gomez-Cabrero D, James T, Ewing E, Lindén M, Górnikiewicz B, Aeinehband S, Stridh P, Link J, Andlauer TFM, Gasperi C, Wiendl H, Zipp F, Gold R, Tackenberg B, Weber F, Hemmer B, Strauch K, Heilmann-Heimbach S, Rawal R, Schminke U et al. (2018)
DNA methylation as a mediator of HLA-DRB1*15:01 and a protective variant in multiple sclerosis
9 (1), 2397
DOI 10.1038/s41467-018-04732-5, PubMed 29921915

Lindland ES, Solheim AM, Andreassen S, Quist-Paulsen E, Eikeland R, Ljøstad U, Mygland Å, Elsais A, Nygaard GO, Lorentzen ÅR, Harbo HF, Beyer MK (2018)
Imaging in Lyme neuroborreliosis
9 (5), 833-844
DOI 10.1007/s13244-018-0646-x, PubMed 30187265

Page CM, Vos L, Rounge TB, Harbo HF, Andreassen BK (2018)
Assessing genome-wide significance for the detection of differentially methylated regions
17 (5)
DOI 10.1515/sagmb-2017-0050, PubMed 30231014

Rhead B, Brorson IS, Berge T, Adams C, Quach H, Moen SM, Berg-Hansen P, Celius EG, Sangurdekar DP, Bronson PG, Lea RA, Burnard S, Maltby VE, Scott RJ, Lechner-Scott J, Harbo HF, Bos SD, Barcellos LF (2018)
Increased DNA methylation of SLFN12 in CD4+ and CD8+ T cells from multiple sclerosis patients
13 (10), e0206511
DOI 10.1371/journal.pone.0206511, PubMed 30379917

Sowa P, Harbo HF, White NS, Celius EG, Bartsch H, Berg-Hansen P, Moen SM, Bjørnerud A, Westlye LT, Andreassen OA, Dale AM, Beyer MK (2018)
Restriction spectrum imaging of white matter and its relation to neurological disability in multiple sclerosis
25 (5), 687-698
DOI 10.1177/1352458518765671, PubMed 29542336

Publications 2017

de Rodez Benavent SA, Nygaard GO, Harbo HF, Tønnesen S, Sowa P, Landrø NI, Wendel-Haga M, Etholm L, Nilsen KB, Drolsum L, Kerty E, Celius EG, Laeng B (2017)
Fatigue and cognition: Pupillary responses to problem-solving in early multiple sclerosis patients
7 (7), e00717
DOI 10.1002/brb3.717, PubMed 28729927

Hedström AK, Katsoulis M, Hössjer O, Bomfim IL, Oturai A, Sondergaard HB, Sellebjerg F, Ullum H, Thørner LW, Gustavsen MW, Harbo HF, Obradovic D, Gianfrancesco MA, Barcellos LF, Schaefer CA, Hillert J, Kockum I, Olsson T, Alfredsson L (2017)
The interaction between smoking and HLA genes in multiple sclerosis: replication and refinement
32 (10), 909-919
DOI 10.1007/s10654-017-0250-2, PubMed 28597127

Olafsson S, Stridh P, Bos SD, Ingason A, Euesden J, Sulem P, Thorleifsson G, Gustafsson O, Johannesson A, Geirsson AJ, Thorsson AV, Sigurgeirsson B, Ludviksson BR, Olafsson E, Kristjansdottir H, Jonasson JG, Olafsson JH, Orvar KB, Benediktsson R, Bjarnason R, Kristjansdottir S, Gislason T, Valdimarsson T, Mikaelsdottir E, Sigurdsson S et al. (2017)
Fourteen sequence variants that associate with multiple sclerosis discovered by meta-analysis informed by genetic correlations
2, 24
DOI 10.1038/s41525-017-0027-2, PubMed 29263835

Sowa P, Nygaard GO, Bjørnerud A, Celius EG, Harbo HF, Beyer MK (2017)
Magnetic resonance imaging perfusion is associated with disease severity and activity in multiple sclerosis
59 (7), 655-664
DOI 10.1007/s00234-017-1849-4, PubMed 28585082

Publications 2016

Berge T, Leikfoss IS, Brorson IS, Bos SD, Page CM, Gustavsen MW, Bjølgerud A, Holmøy T, Celius EG, Damoiseaux J, Smolders J, Harbo HF, Spurkland A (2016)
The multiple sclerosis susceptibility genes TAGAP and IL2RA are regulated by vitamin D in CD4+ T cells
17 (2), 118-27
DOI 10.1038/gene.2015.61, PubMed 26765264

Bos SD, Berge T, Celius EG, Harbo HF (2016)
From genetic associations to functional studies in multiple sclerosis
23 (5), 847-53
DOI 10.1111/ene.12981, PubMed 26948534

George MF, Briggs FB, Shao X, Gianfrancesco MA, Kockum I, Harbo HF, Celius EG, Bos SD, Hedström A, Shen L, Bernstein A, Alfredsson L, Hillert J, Olsson T, Patsopoulos NA, De Jager PL, Oturai AB, Søndergaard HB, Sellebjerg F, Sorensen PS, Gomez R, Caillier SJ, Cree BA, Oksenberg JR, Hauser SL et al. (2016)
Multiple sclerosis risk loci and disease severity in 7,125 individuals from 10 studies
2 (4), e87
DOI 10.1212/NXG.0000000000000087, PubMed 27540591

George MF, Briggs FBS, Shao X, Gianfrancesco MA, Kockum I, Harbo HF, Celius EG, Bos SD, Hedstrom A, Shen L, Bernstein A, Alfredsson L, Hiller J, Olsson T, Patsopoulos NA, De Jager PL, Oturai AB, Sondergaard HB, Sellebjerg F, Sorensen PS, Gomez R, Caillier SJ, Cree BAC, Oksenberg JR, Hauser SL et al. (2016)
Multiple sclerosis risk loci and disease severity in 7,125 individuals from 10 studies
Neurol.-Genet., 2 (4), eB7
DOI 10.1212/NXG.00000000000000B7

Gustavsen MW, Celius EG, Winsvold BS, Moen SM, Nygaard GO, Berg-Hansen P, Lie BA, Zwart JA, Harbo HF (2016)
Migraine and frequent tension-type headache are not associated with multiple sclerosis in a Norwegian case-control study
2, 2055217316682976
DOI 10.1177/2055217316682976, PubMed 28607748

Keshari PK, Harbo HF, Myhr KM, Aarseth JH, Bos SD, Berge T (2016)
Allelic imbalance of multiple sclerosis susceptibility genes IKZF3 and IQGAP1 in human peripheral blood
17, 59
DOI 10.1186/s12863-016-0367-4, PubMed 27080863

Keshavan A, Paul F, Beyer MK, Zhu AH, Papinutto N, Shinohara RT, Stern W, Amann M, Bakshi R, Bischof A, Carriero A, Comabella M, Crane JC, D'Alfonso S, Demaerel P, Dubois B, Filippi M, Fleischer V, Fontaine B, Gaetano L, Goris A, Graetz C, Gröger A, Groppa S, Hafler DA et al. (2016)
Power estimation for non-standardized multisite studies
134, 281-294
DOI 10.1016/j.neuroimage.2016.03.051, PubMed 27039700

Moen SM, Harbo HF, Celius EG, Sowa P, Nygaard GO, Beyer MK (2016)
S.M. Moen og medarbeidere svarer
136 (19), 1608
DOI 10.4045/tidsskr.16.0826, PubMed 27790879

Moen SM, Harbo HF, Celius EG, Sowa P, Nygaard GO, Beyer MK (2016)
S.M. Moen og medarbeidere svarer
136 (20), 1702
DOI 10.4045/tidsskr.16.0865, PubMed 27830899

Moen SM, Harbo HF, Sowa P, Celius EG, Nygaard GO, Beyer MK (2016)
[MRI in multiple sclerosis]
136 (16), 1373-6
DOI 10.4045/tidsskr.15.1361, PubMed 27637059

Moen SM, Harbo HF, Sowa P, Celius EG, Nygaard GO, Beyer MK (2016)
MRI- investigations in multiple sclerosis
Tidsskr. Nor. Laegeforen., 136 (16), 1373-1376

Wang Y, Bos SD, Harbo HF, Thompson WK, Schork AJ, Bettella F, Witoelar A, Lie BA, Li W, McEvoy LK, Djurovic S, Desikan RS, Dale AM, Andreassen OA (2016)
Genetic overlap between multiple sclerosis and several cardiovascular disease risk factors
22 (14), 1783-1793
DOI 10.1177/1352458516635873, PubMed 26920376

Publications 2015

Berg-Hansen P, Moen SM, Harbo HF, Celius EG (2015)
Comments on the review article 'Time trends in the incidence and prevalence of multiple sclerosis in Norway during eight decades'
132 (5), 364-7
DOI 10.1111/ane.12489, PubMed 26423981

Bos SD, Page CM, Andreassen BK, Elboudwarej E, Gustavsen MW, Briggs F, Quach H, Leikfoss IS, Bjølgerud A, Berge T, Harbo HF, Barcellos LF (2015)
Genome-wide DNA methylation profiles indicate CD8+ T cell hypermethylation in multiple sclerosis
10 (3), e0117403
DOI 10.1371/journal.pone.0117403, PubMed 25734800

Goris A, Pauwels I, Gustavsen MW, van Son B, Hilven K, Bos SD, Celius EG, Berg-Hansen P, Aarseth J, Myhr KM, D'Alfonso S, Barizzone N, Leone MA, Martinelli Boneschi F, Sorosina M, Liberatore G, Kockum I, Olsson T, Hillert J, Alfredsson L, Bedri SK, Hemmer B, Buck D, Berthele A, Knier B et al. (2015)
Genetic variants are major determinants of CSF antibody levels in multiple sclerosis
138 (Pt 3), 632-43
DOI 10.1093/brain/awu405, PubMed 25616667

Leikfoss IS, Keshari PK, Gustavsen MW, Bjølgerud A, Brorson IS, Celius EG, Spurkland A, Bos SD, Harbo HF, Berge T (2015)
Multiple Sclerosis Risk Allele in CLEC16A Acts as an Expression Quantitative Trait Locus for CLEC16A and SOCS1 in CD4+ T Cells
10 (7), e0132957
DOI 10.1371/journal.pone.0132957, PubMed 26203907

Moutsianas L, Jostins L, Beecham AH, Dilthey AT, Xifara DK, Ban M, Shah TS, Patsopoulos NA, Alfredsson L, Anderson CA, Attfield KE, Baranzini SE, Barrett J, Binder TMC, Booth D, Buck D, Celius EG, Cotsapas C, D'Alfonso S, Dendrou CA, Donnelly P, Dubois B, Fontaine B, Fugger L, Goris A et al. (2015)
Class II HLA interactions modulate genetic risk for multiple sclerosis
47 (10), 1107-1113
DOI 10.1038/ng.3395, PubMed 26343388

Nygaard GO, Celius EG, de Rodez Benavent SA, Sowa P, Gustavsen MW, Fjell AM, Landrø NI, Walhovd KB, Harbo HF (2015)
A Longitudinal Study of Disability, Cognition and Gray Matter Atrophy in Early Multiple Sclerosis Patients According to Evidence of Disease Activity
10 (8), e0135974
DOI 10.1371/journal.pone.0135974, PubMed 26280173

Nygaard GO, de Rodez Benavent SA, Harbo HF, Laeng B, Sowa P, Damangir S, Bernhard Nilsen K, Etholm L, Tønnesen S, Kerty E, Drolsum L, Inge Landrø N, Celius EG (2015)
Eye and hand motor interactions with the Symbol Digit Modalities Test in early multiple sclerosis
4 (6), 585-9
DOI 10.1016/j.msard.2015.08.003, PubMed 26590666

Page CM, Baranzini SE, Mevik BH, Bos SD, Harbo HF, Andreassen BK (2015)
Assessing the Power of Exome Chips
10 (10), e0139642
DOI 10.1371/journal.pone.0139642, PubMed 26437075

Seldin MF, Alkhairy OK, Lee AT, Lamb JA, Sussman J, Pirskanen-Matell R, Piehl F, Verschuuren JJGM, Kostera-Pruszczyk A, Szczudlik P, McKee D, Maniaol AH, Harbo HF, Lie BA, Melms A, Garchon HJ, Willcox N, Gregersen PK, Hammarstrom L (2015)
Genome-Wide Association Study of Late-Onset Myasthenia Gravis: Confirmation of TNFRSF11A and Identification of ZBTB10 and Three Distinct HLA Associations
21 (1), 769-781
DOI 10.2119/molmed.2015.00232, PubMed 26562150

Sowa P, Bjørnerud A, Nygaard GO, Damangir S, Spulber G, Celius EG, Due-Tønnessen P, Harbo HF, Beyer MK (2015)
Reduced perfusion in white matter lesions in multiple sclerosis
84 (12), 2605-12
DOI 10.1016/j.ejrad.2015.09.007, PubMed 26391230

Publications 2014

Andreassen OA, Harbo HF, Wang Y, Thompson WK, Schork AJ, Mattingsdal M, Zuber V, Bettella F, Ripke S, Kelsoe JR, Kendler KS, O'Donovan MC, Sklar P, Psychiatric Genomics Consortium (PGC) Bipolar Disorder and Schizophrenia Work Groups, International Multiple Sclerosis Genetics Consortium (IMSGC), McEvoy LK, Desikan RS, Lie BA, Djurovic S, Dale AM (2014)
Genetic pleiotropy between multiple sclerosis and schizophrenia but not bipolar disorder: differential involvement of immune-related gene loci
20 (2), 207-14
DOI 10.1038/mp.2013.195, PubMed 24468824

Avidan N, Le Panse R, Harbo HF, Bernasconi P, Poulas K, Ginzburg E, Cavalcante P, Colleoni L, Baggi F, Antozzi C, Truffault F, Horn-Saban S, Pöschel S, Zagoriti Z, Maniaol A, Lie BA, Bernard I, Saoudi A, Illes Z, Casasnovas Pons C, Melms A, Tzartos S, Willcox N, Kostera-Pruszczyk A, Tallaksen C et al. (2014)
VAV1 and BAFF, via NFκB pathway, are genetic risk factors for myasthenia gravis
1 (5), 329-39
DOI 10.1002/acn3.51, PubMed 25356403

Berg-Hansen P, Moen SM, Harbo HF, Celius EG (2014)
High prevalence and no latitude gradient of multiple sclerosis in Norway
20 (13), 1780-2
DOI 10.1177/1352458514525871, PubMed 24603884

Berg-Hansen P, Moen SM, Sandvik L, Harbo HF, Bakken IJ, Stoltenberg C, Celius EG (2014)
Prevalence of multiple sclerosis among immigrants in Norway
21 (6), 695-702
DOI 10.1177/1352458514554055, PubMed 25344371

Eriksen AB, Berge T, Gustavsen MW, Leikfoss IS, Bos SD, Spurkland A, Harbo HF, Blomhoff HK (2014)
Retinoic acid enhances the levels of IL-10 in TLR-stimulated B cells from patients with relapsing-remitting multiple sclerosis
278, 11-8
DOI 10.1016/j.jneuroim.2014.11.019, PubMed 25595247

Gustavsen MW, Celius EG, Moen SM, Bjølgerud A, Berg-Hansen P, Nygaard GO, Sandvik L, Lie BA, Harbo HF (2014)
No association between multiple sclerosis and periodontitis after adjusting for smoking habits
22 (3), 588-90
DOI 10.1111/ene.12520, PubMed 25041906

Gustavsen MW, Page CM, Moen SM, Bjølgerud A, Berg-Hansen P, Nygaard GO, Sandvik L, Lie BA, Celius EG, Harbo HF (2014)
Environmental exposures and the risk of multiple sclerosis investigated in a Norwegian case-control study
14, 196
DOI 10.1186/s12883-014-0196-x, PubMed 25274070

Gustavsen MW, Viken MK, Celius EG, Berge T, Mero IL, Berg-Hansen P, Aarseth JH, Myhr KM, Søndergaard HB, Sellebjerg F, Oturai AB, Hillert J, Alfredsson L, Olsson T, Kockum I, Lie BA, Harbo HF (2014)
Oligoclonal band phenotypes in MS differ in their HLA class II association, while specific KIR ligands at HLA class I show association to MS in general
274 (1-2), 174-9
DOI 10.1016/j.jneuroim.2014.06.024, PubMed 25037176

Nygaard GO, Walhovd KB, Sowa P, Chepkoech JL, Bjørnerud A, Due-Tønnessen P, Landrø NI, Damangir S, Spulber G, Storsve AB, Beyer MK, Fjell AM, Celius EG, Harbo HF (2014)
Cortical thickness and surface area relate to specific symptoms in early relapsing-remitting multiple sclerosis
21 (4), 402-14
DOI 10.1177/1352458514543811, PubMed 25139946

Sundal C, Baker M, Karrenbauer V, Gustavsen M, Bedri S, Glaser A, Myhr KM, Haugarvoll K, Zetterberg H, Harbo H, Kockum I, Hillert J, Wszolek Z, Rademakers R, Andersen O (2014)
Hereditary diffuse leukoencephalopathy with spheroids with phenotype of primary progressive multiple sclerosis
22 (2), 328-333
DOI 10.1111/ene.12572, PubMed 25311247

Westerlind H, Imrell K, Ramanujam R, Myhr KM, Celius EG, Harbo HF, Oturai AB, Hamsten A, Alfredsson L, Olsson T, Kockum I, Koski T, Hillert J (2014)
Identity-by-descent mapping in a Scandinavian multiple sclerosis cohort
23 (5), 688-92
DOI 10.1038/ejhg.2014.155, PubMed 25159868

Publications 2013

Ban M, Caillier S, Mero IL, Myhr KM, Celius EG, Aarseth J, Torkildsen Ø, Harbo HF, Oksenberg J, Hauser SL, Sawcer S, Compston A (2013)
No evidence of association between mutant alleles of the CYP27B1 gene and multiple sclerosis
73 (3), 430-2
DOI 10.1002/ana.23833, PubMed 23444327

Berg-Hansen P, Smestad C, Sandvik L, Harbo HF, Celius EG (2013)
Increased disease severity in non-Western immigrants with multiple sclerosis in Oslo, Norway
20 (12), 1546-52
DOI 10.1111/ene.12227, PubMed 23834430

Berge T, Leikfoss IS, Harbo HF (2013)
From Identification to Characterization of the Multiple Sclerosis Susceptibility Gene CLEC16A
14 (3), 4476-97
DOI 10.3390/ijms14034476, PubMed 23439554

Harbo HF, Gold R, Tintoré M (2013)
Sex and gender issues in multiple sclerosis
6 (4), 237-48
DOI 10.1177/1756285613488434, PubMed 23858327

Harbo HF, Isobe N, Berg-Hansen P, Bos SD, Caillier SJ, Gustavsen MW, Mero IL, Celius EG, Hauser SL, Oksenberg JR, Gourraud PA (2013)
Oligoclonal bands and age at onset correlate with genetic risk score in multiple sclerosis
20 (6), 660-8
DOI 10.1177/1352458513506503, PubMed 24099750

Hoglund RA, Holmoy T, Harbo HF, Maghazachi AA (2013)
A One Year Follow-Up Study of Natural Killer and Dendritic Cells Activities in Multiple Sclerosis Patients Receiving Glatiramer Acetate (GA)
PLoS One, 8 (4), e62237
DOI 10.1371/journal.pone.0062237

International Multiple Sclerosis Genetics Consortium (IMSGC), Beecham AH, Patsopoulos NA, Xifara DK, Davis MF, Kemppinen A, Cotsapas C, Shah TS, Spencer C, Booth D, Goris A, Oturai A, Saarela J, Fontaine B, Hemmer B, Martin C, Zipp F, D'Alfonso S, Martinelli-Boneschi F, Taylor B, Harbo HF, Kockum I, Hillert J, Olsson T, Ban M et al. (2013)
Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis
45 (11), 1353-60
DOI 10.1038/ng.2770, PubMed 24076602

Isobe N, Gourraud PA, Harbo HF, Caillier SJ, Santaniello A, Khankhanian P, Maiers M, Spellman S, Cereb N, Yang SY, Pando MJ, Piccio L, Cross AH, De Jager PL, Cree BAC, Hauser SL, Oksenberg JR (2013)
Genetic risk variants in African Americans with multiple sclerosis
Neurology, 81 (3), 219-227
DOI 10.1212/WNL.0b013e31829bfe2f

Leone MA, Barizzone N, Esposito F, Lucenti A, Harbo HF, Goris A, Kockum I, Oturai AB, Celius EG, Mero IL, Dubois B, Olsson T, Søndergaard HB, Cusi D, Lupoli S, Andreassen BK, International Multiple Sclerosis Genetics Consortium, Wellcome Trust Case Control Consortium 2, Myhr KM, Guerini FR, PROGEMUS Group, PROGRESSO Group, Comi G, Martinelli-Boneschi F, D'Alfonso S (2013)
Association of genetic markers with CSF oligoclonal bands in multiple sclerosis patients
8 (6), e64408
DOI 10.1371/journal.pone.0064408, PubMed 23785401

Mero IL, Gustavsen MW, Sæther HS, Flåm ST, Berg-Hansen P, Søndergaard HB, Jensen PE, Berge T, Bjølgerud A, Muggerud A, Aarseth JH, International Multiple Sclerosis Genetics Consortium, Myhr KM, Celius EG, Sellebjerg F, Hillert J, Alfredsson L, Olsson T, Oturai AB, Kockum I, Lie BA, Andreassen BK, Harbo HF (2013)
Oligoclonal band status in Scandinavian multiple sclerosis patients is associated with specific genetic risk alleles
8 (3), e58352
DOI 10.1371/journal.pone.0058352, PubMed 23472185

Publications 2012

Brambilla P, Esposito F, Lindstrom E, Sorosina M, Giacalone G, Clarelli F, Rodegher M, Colombo B, Moiola L, Ghezzi A, Capra R, Collimedaglia L, Coniglio G, Celius EG, Galimberti D, Sørensen PS, Martinelli V, Oturai AB, Harbo HF, Hillert J, Comi G, Martinelli-Boneschi F (2012)
Association between DPP6 polymorphism and the risk of progressive multiple sclerosis in Northern and Southern Europeans
530 (2), 155-60
DOI 10.1016/j.neulet.2012.10.008, PubMed 23069673

Gourraud PA, Harbo HF, Hauser SL, Baranzini SE (2012)
The genetics of multiple sclerosis: an up-to-date review
Immunol. Rev., 248, 87-103
DOI 10.1111/j.1600-065X.2012.01134.x

Gregersen PK, Kosoy R, Lee AT, Lamb J, Sussman J, McKee D, Simpfendorfer KR, Pirskanen-Matell R, Piehl F, Pan-Hammarstrom Q, Verschuuren JJ, Titulaer MJ, Niks EH, Marx A, Ströbel P, Tackenberg B, Pütz M, Maniaol A, Elsais A, Tallaksen C, Harbo HF, Lie BA, Raychaudhuri S, de Bakker PI, Melms A et al. (2012)
Risk for myasthenia gravis maps to a (151) Pro→Ala change in TNIP1 and to human leukocyte antigen-B*08
72 (6), 927-35
DOI 10.1002/ana.23691, PubMed 23055271

Harbo HF, Mero IL (2012)
From genes to characteristics of multiple sclerosis
(195), 76-83
DOI 10.1111/ane.12027, PubMed 23278661

Leikfoss IS, Mero IL, Dahle MK, Lie BA, Harbo HF, Spurkland A, Berge T (2012)
Multiple sclerosis-associated single-nucleotide polymorphisms in CLEC16A correlate with reduced SOCS1 and DEXI expression in the thymus
14 (1), 62-6
DOI 10.1038/gene.2012.52, PubMed 23151489

Link J, Kockum I, Lorentzen AR, Lie BA, Celius EG, Westerlind H, Schaffer M, Alfredsson L, Olsson T, Brynedal B, Harbo HF, Hillert J (2012)
Importance of human leukocyte antigen (HLA) class I and II alleles on the risk of multiple sclerosis
7 (5), e36779
DOI 10.1371/journal.pone.0036779, PubMed 22586495

Maniaol AH, Boldingh M, Brunborg C, Harbo HF, Tallaksen CME (2012)
Smoking and socio-economic status may affect myasthenia gravis
20 (3), 453-460
DOI 10.1111/j.1468-1331.2012.03843.x, PubMed 22934661

Maniaol AH, Elsais A, Lorentzen ÅR, Owe JF, Viken MK, Sæther H, Flåm ST, Bråthen G, Kampman MT, Midgard R, Christensen M, Rognerud A, Kerty E, Gilhus NE, Tallaksen CM, Lie BA, Harbo HF (2012)
Late onset myasthenia gravis is associated with HLA DRB1*15:01 in the Norwegian population
7 (5), e36603
DOI 10.1371/journal.pone.0036603, PubMed 22590574

Martinelli-Boneschi F, Esposito F, Brambilla P, Lindstrom E, Lavorgna G, Stankovich J, Rodegher M, Capra R, Ghezzi A, Coniglio G, Colombo B, Sorosina M, Martinelli V, Booth D, Oturai AB, Stewart G, Harbo HF, Kilpatrick TJ, Hillert J, Rubio JP, Abderrahim H, Wojcik J, Comi G (2012)
A genome-wide association study in progressive multiple sclerosis
Mult. Scler. J., 18 (10), 1384-1394
DOI 10.1177/1352458512439118

Mero IL, Smestad C, Lie BA, Lorentzen ÅR, Sandvik L, Landrø NI, Aarseth JH, Myhr KM, Celius EG, Harbo HF (2012)
Polymorphisms of the BDNF gene show neither association with multiple sclerosis susceptibility nor clinical course
244 (1-2), 107-10
DOI 10.1016/j.jneuroim.2012.01.011, PubMed 22341604

Publications 2011

Burgunder JM, Schöls L, Baets J, Andersen P, Gasser T, Szolnoki Z, Fontaine B, Van Broeckhoven C, Di Donato S, De Jonghe P, Lynch T, Mariotti C, Spinazzola A, Tabrizi SJ, Tallaksen C, Zeviani M, Harbo HF, Finsterer J (2011)
EFNS guidelines for the molecular diagnosis of neurogenetic disorders: motoneuron, peripheral nerve and muscle disorders
18 (2), 207-217
DOI 10.1111/j.1468-1331.2010.03069.x, PubMed 20500522

Hansen B, Oturai AB, Harbo HF, Celius EG, Nissen KK, Laska MJ, Søndergaard HB, Petersen T, Nexø BA (2011)
Genetic association of multiple sclerosis with the marker rs391745 near the endogenous retroviral locus HERV-Fc1: analysis of disease subtypes
6 (10), e26438
DOI 10.1371/journal.pone.0026438, PubMed 22039488

Harbo HF, Lorentzen AR, Lie BA, Celius EG, Spurkland A (2011)
[New gene map for multiple sclerosis]
131 (21), 2126-30
DOI 10.4045/tidsskr.10.0823, PubMed 22048209

International Multiple Sclerosis Genetics Consortium, Wellcome Trust Case Control Consortium 2, Sawcer S, Hellenthal G, Pirinen M, Spencer CC, Patsopoulos NA, Moutsianas L, Dilthey A, Su Z, Freeman C, Hunt SE, Edkins S, Gray E, Booth DR, Potter SC, Goris A, Band G, Oturai AB, Strange A, Saarela J, Bellenguez C, Fontaine B, Gillman M, Hemmer B et al. (2011)
Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis
476 (7359), 214-9
DOI 10.1038/nature10251, PubMed 21833088

Lundström W, Greiner E, Lundmark F, Westerlind H, Smestad C, Lorentzen AR, Kockum I, Link J, Brynedal B, Celius EG, Harbo HF, Masterman T, Hillert J (2011)
No influence on disease progression of non-HLA susceptibility genes in MS
237 (1-2), 98-100
DOI 10.1016/j.jneuroim.2011.05.003, PubMed 21742385

Pandya AD, Al-Jaderi Z, Hoglund RA, Holmoy T, Harbo HF, Norgauer J, Maghazachi AA (2011)
Identification of Human NK17/NK1 Cells
PLoS One, 6 (10), e26780
DOI 10.1371/journal.pone.0026780

Søndergaard HB, Sellebjerg F, Hillert J, Olsson T, Kockum I, Lindén M, Mero IL, Myhr KM, Celius EG, Harbo HF, Christensen JR, Börnsen L, Sørensen PS, Oturai AB (2011)
Alterations in KLRB1 gene expression and a Scandinavian multiple sclerosis association study of the KLRB1 SNP rs4763655
19 (10), 1100-3
DOI 10.1038/ejhg.2011.88, PubMed 21610746

Publications 2010

Beyeen AD, Adzemovic MZ, Ockinger J, Stridh P, Becanovic K, Laaksonen H, Lassmann H, Harris RA, Hillert J, Alfredsson L, Celius EG, Harbo HF, Kockum I, Jagodic M, Olsson T (2010)
IL-22RA2 associates with multiple sclerosis and macrophage effector mechanisms in experimental neuroinflammation
185 (11), 6883-90
DOI 10.4049/jimmunol.1001392, PubMed 21041731

Burgunder JM, Finsterer J, Szolnoki Z, Fontaine B, Baets J, Van Broeckhoven C, Di Donato S, De Jonghe P, Lynch T, Mariotti C, Schöls L, Spinazzola A, Tabrizi SJ, Tallaksen C, Zeviani M, Harbo HF, Gasser T, EFNS (2010)
EFNS guidelines on the molecular diagnosis of channelopathies, epilepsies, migraine, stroke, and dementias
17 (5), 641-8
DOI 10.1111/j.1468-1331.2010.02985.x, PubMed 20298421

Holmøy T, Harbo HF, Celius EG (2010)
[Treatment of multiple sclerosis]
130 (9), 923; author reply 923
DOI 10.4045/tidsskr.10.0346, PubMed 20453948

International Multiple Sclerosis Genetics Consortium (IMSGC), Booth DR, Heard RN, Stewart GJ, Cox M, Scott RJ, Lechner-Scott J, Goris A, Dobosi R, Dubois B, Saarela J, Leppä V, Peltonen L, Pirttila T, Cournu-Rebeix I, Fontaine B, Bergamaschi L, D'Alfonso S, Leone M, Lorentzen AR, Harbo HF, Celius EG, Spurkland A, Link J, Kockum I et al. (2010)
Lack of support for association between the KIF1B rs10492972[C] variant and multiple sclerosis
42 (6), 469-70; author reply 470-1
DOI 10.1038/ng0610-469, PubMed 20502484

Jakkula E, Leppa V, Sulonen AM, Varilo T, Kallio S, Kemppinen A, Purcell S, Koivisto K, Tienari P, Sumelahti ML, Elovaara I, Pirttila T, Reunanen M, Aromaa A, Oturai AB, Sondergaard HB, Harbo HF, Mero IL, Gabriel SB, Mirel DB, Hauser SL, Kappos L, Polman C, De Jager PL, Hafler DA et al. (2010)
Genome-wide Association Study in a High-Risk Isolate for Multiple Sclerosis Reveals Associated Variants in STAT3 Gene
Am. J. Hum. Genet., 86 (2), 285-291
DOI 10.1016/j.ajhg.2010.01.017

Link J, Lorentzen AR, Kockum I, Duvefelt K, Lie BA, Celius EG, Harbo HF, Hillert J, Brynedal B (2010)
Two HLA class I genes independently associated with multiple sclerosis
226 (1-2), 172-6
DOI 10.1016/j.jneuroim.2010.07.006, PubMed 20678810

Lorentzen AR, Melum E, Ellinghaus E, Smestad C, Mero IL, Aarseth JH, Myhr KM, Celius EG, Lie BA, Karlsen TH, Franke A, Harbo HF (2010)
Association to the Glypican-5 gene in multiple sclerosis
226 (1-2), 194-7
DOI 10.1016/j.jneuroim.2010.07.003, PubMed 20692050

Mero IL, Ban M, Lorentzen ÅR, Smestad C, Celius EG, Sæther H, Saeedi H, Viken MK, Skinningsrud B, Undlien DE, Aarseth J, Myhr KM, Granum S, Spurkland A, Sawcer S, Compston A, Lie BA, Harbo HF (2010)
Exploring the CLEC16A gene reveals a MS-associated variant with correlation to the relative expression of CLEC16A isoforms in thymus
12 (3), 191-8
DOI 10.1038/gene.2010.59, PubMed 21179112

Nohra R, Beyeen AD, Guo JP, Khademi M, Sundqvist E, Hedreul MT, Sellebjerg F, Smestad C, Oturai AB, Harbo HF, Wallström E, Hillert J, Alfredsson L, Kockum I, Jagodic M, Lorentzen J, Olsson T (2010)
RGMA and IL21R show association with experimental inflammation and multiple sclerosis
11 (4), 279-93
DOI 10.1038/gene.2009.111, PubMed 20072140

Publications 2009

Ban M, Goris A, Lorentzen AR, Baker A, Mihalova T, Ingram G, Booth DR, Heard RN, Stewart GJ, Bogaert E, Dubois B, Harbo HF, Celius EG, Spurkland A, Strange R, Hawkins C, Robertson NP, Dudbridge F, Wason J, De Jager PL, Hafler D, Rioux JD, Ivinson AJ, McCauley JL, Pericak-Vance M et al. (2009)
Replication analysis identifies TYK2 as a multiple sclerosis susceptibility factor
17 (10), 1309-13
DOI 10.1038/ejhg.2009.41, PubMed 19293837

Finsterer J, Harbo HF, Baets J, Van Broeckhoven C, Di Donato S, Fontaine B, De Jonghe P, Lossos A, Lynch T, Mariotti C, Schöls L, Spinazzola A, Szolnoki Z, Tabrizi SJ, Tallaksen CM, Zeviani M, Burgunder JM, Gasser T, European Federation of Neurological Sciences (2009)
EFNS guidelines on the molecular diagnosis of mitochondrial disorders
16 (12), 1255-64
DOI 10.1111/j.1468-1331.2009.02811.x, PubMed 19950421

Gasser T, Finsterer J, Baets J, Van Broeckhoven C, Di Donato S, Fontaine B, De Jonghe P, Lossos A, Lynch T, Mariotti C, Schöls L, Spinazzola A, Szolnoki Z, Tabrizi SJ, Tallaksen CM, Zeviani M, Burgunder JM, Harbo HF, EFNS (2009)
EFNS guidelines on the molecular diagnosis of ataxias and spastic paraplegias
17 (2), 179-88
DOI 10.1111/j.1468-1331.2009.02873.x, PubMed 20050888

Harbo HF, Finsterer J, Baets J, Van Broeckhoven C, Di Donato S, Fontaine B, De Jonghe P, Lossos A, Lynch T, Mariotti C, Schöls L, Spinazzola A, Szolnoki Z, Tabrizi SJ, Tallaksen C, Zeviani M, Burgunder JM, Gasser T, EFNS (2009)
EFNS guidelines on the molecular diagnosis of neurogenetic disorders: general issues, Huntington's disease, Parkinson's disease and dystonias
16 (7), 777-85
DOI 10.1111/j.1468-1331.2009.02646.x, PubMed 19469830

Harbo HF, Riccio ME, Lorentzen AR, Utsi E, Myhr KM, Mellgren SI, Flåm ST, Thorsby E, Sanchez-Mazas A, Lie BA (2009)
Norwegian Sami differs significantly from other Norwegians according to their HLA profile
75 (3), 207-17
DOI 10.1111/j.1399-0039.2009.01425.x, PubMed 20047643

Holmoy T, Harbo H, Vartdal F, Spurkland A (2009)
Genetic and Molecular Approaches to the Immunopathogenesis of Multiple Sclerosis: An Update
Curr. Mol. Med., 9 (5), 591-611
DOI 10.2174/156652409788488793

Jagodic M, Colacios C, Nohra R, Dejean AS, Beyeen AD, Khademi M, Casemayou A, Lamouroux L, Duthoit C, Papapietro O, Sjoholm L, Bernard I, Lagrange D, Dahlman I, Lundmark F, Oturai AB, Soendergaard HB, Kemppinen A, Saarela J, Tienari PJ, Harbo HF, Spurkland A, Ramagopalan SV, Sadovnick DA, Ebers GC et al. (2009)
A Role for VAV1 in Experimental Autoimmune Encephalomyelitis and Multiple Sclerosis
Sci. Transl. Med., 1 (10), 10ra21
DOI 10.1126/scitranslmed.3000278

Kallio SP, Jakkula E, Purcell S, Suvela M, Koivisto K, Tienari PJ, Elovaara I, Pirttila T, Reunanen M, Bronnikov D, Viander M, Meri S, Hillert J, Lundmark F, Harbo HF, Lorentzen AR, De Jager PL, Daly MJ, Hafler DA, Palotie A, Peltonen L, Saarela J (2009)
Use of a genetic isolate to identify rare disease variants: C7 on 5p associated with MS
Hum. Mol. Genet., 18 (9), 1670-1683
DOI 10.1093/hmg/ddp073

Kemppinen A, Suvela M, Tienari PJ, Elovaara I, Koivisto K, Pirttilä T, Reunanen M, Rautakorpi I, Hillert J, Lundmark F, Oturai A, Ryder L, Harbo HF, Celius EG, Palotie A, Daly M, Peltonen L, Saarela J (2009)
MYO9B polymorphisms in multiple sclerosis
17 (6), 840-3
DOI 10.1038/ejhg.2008.251, PubMed 19142207

Lorentzen AR, Karlsen TH, Olsson M, Smestad C, Mero IL, Woldseth B, Sun JY, Senitzer D, Celius EG, Thorsby E, Spurkland A, Lie BA, Harbo HF (2009)
Killer immunoglobulin-like receptor ligand HLA-Bw4 protects against multiple sclerosis
65 (6), 658-66
DOI 10.1002/ana.21695, PubMed 19630074

Mero IL, Lorentzen AR, Ban M, Smestad C, Celius EG, Aarseth JH, Myhr KM, Link J, Hillert J, Olsson T, Kockum I, Masterman T, Oturai AB, Søndergaard HB, Sellebjerg F, Saarela J, Kemppinen A, Elovaara I, Spurkland A, Dudbridge F, Lie BA, Harbo HF (2009)
A rare variant of the TYK2 gene is confirmed to be associated with multiple sclerosis
18 (4), 502-4
DOI 10.1038/ejhg.2009.195, PubMed 19888296

Ramagopalan SV, Link J, Byrnes JK, Dyment DA, Giovannoni G, Hintzen RQ, Sundqvist E, Kockum I, Smestad C, Lie BA, Harbo HF, Padyukov L, Alfredsson L, Olsson T, Sadovnick AD, Hillert J, Ebers GC (2009)
HLA-DRB1 and month of birth in multiple sclerosis
73 (24), 2107-11
DOI 10.1212/WNL.0b013e3181c679f3, PubMed 20018638

Publications 2008

Lorentzen AR, Smestad C, Lie BA, Oturai AB, Akesson E, Saarela J, Myhr KM, Vartdal F, Celius EG, Sørensen PS, Hillert J, Spurkland A, Harbo HF (2008)
The SH2D2A gene and susceptibility to multiple sclerosis
197 (2), 152-8
DOI 10.1016/j.jneuroim.2008.04.037, PubMed 18554728

Publications 2007

Datta P, Harbo HF, Ryder LP, Akesson E, Benedikz J, Celius EG, Andersen O, Myhr KM, Sandberg-Wollheim M, Hillert J, Svejgaard A, Sorensen PS, Spurkland A, Oturai A (2007)
A follow-up study of Nordic multiple sclerosis candidate gene regions
13 (5), 584-9
DOI 10.1177/1352458506071790, PubMed 17548436

Harbo HF, Spurkland A (2007)
Genetics in multiple sclerosis: past and future perspectives
Acta Neurol. Scand., 115 187, 34-38
DOI 10.1111/j.1600-0404.2007.00843.x

Harbo HF, Utsi E, Lorentzen AR, Kampman MT, Celius EG, Myhr KM, Lie BA, Mellgren SI, Thorsby E (2007)
Low frequency of the disease-associated DRB1*15-DQB1*06 haplotype may contribute to the low prevalence of multiple sclerosis in Sami
69 (4), 299-304
DOI 10.1111/j.1399-0039.2007.00803.x, PubMed 17389012

Hensiek AE, Seaman SR, Barcellos LF, Oturai A, Eraksoi M, Cocco E, Vecsei L, Stewart G, Dubois B, Bellman-Strobl J, Leone M, Andersen O, Bencsik K, Booth D, Celius EG, Harbo HF, Hauser SL, Heard R, Hillert J, Myhr KM, Marrosu MG, Oksenberg JR, Rajda C, Sawcer SJ, Sørensen PS et al. (2007)
Familial effects on the clinical course of multiple sclerosis
68 (5), 376-83
DOI 10.1212/01.wnl.0000252822.53506.46, PubMed 17261686

Knudsen GP, Harbo HF, Smestad C, Celius EG, Akesson E, Oturai A, Ryder LP, Spurkland A, Ørstavik KH (2007)
X chromosome inactivation in females with multiple sclerosis
14 (12), 1392-6
DOI 10.1111/j.1468-1331.2007.01987.x, PubMed 17970735

Lundmark F, Duvefelt K, Iacobaeus E, Kockum I, Wallström E, Khademi M, Oturai A, Ryder LP, Saarela J, Harbo HF, Celius EG, Salter H, Olsson T, Hillert J (2007)
Variation in interleukin 7 receptor alpha chain (IL7R) influences risk of multiple sclerosis
39 (9), 1108-13
DOI 10.1038/ng2106, PubMed 17660816

Smestad C, Brynedal B, Jonasdottir G, Lorentzen AR, Masterman T, Akesson E, Spurkland A, Lie BA, Palmgren J, Celius EG, Hillert J, Harbo HF (2007)
The impact of HLA-A and -DRB1 on age at onset, disease course and severity in Scandinavian multiple sclerosis patients
14 (8), 835-40
DOI 10.1111/j.1468-1331.2007.01825.x, PubMed 17662002

Smestad C, Sandvik L, Holmoy T, Harbo HF, Celius EG (2007)
Marked differences in prevalence of multiple sclerosis between ethnic groups in Oslo, Norway
255 (1), 49-55
DOI 10.1007/s00415-007-0659-8, PubMed 18080855

Publications 2006

Harbo HF, Ekstrøm PO, Lorentzen AR, Sundvold-Gjerstad V, Celius EG, Sawcer S, Spurkland A (2006)
Coding region polymorphisms in T cell signal transduction genes. Prevalence and association to development of multiple sclerosis
177 (1-2), 40-5
DOI 10.1016/j.jneuroim.2006.04.021, PubMed 16764945

Lundmark F, Harbo HF, Celius EG, Saarela J, Datta P, Oturai A, Lindgren CM, Masterman T, Salter H, Hillert J (2006)
Association analysis of the LAG3 and CD4 genes in multiple sclerosis in two independent populations
180 (1-2), 193-8
DOI 10.1016/j.jneuroim.2006.08.009, PubMed 17020785

Wiencke K, Boberg KM, Donaldson P, Harbo H, Ling V, Schrumpf E, Spurkland A (2006)
No major effect of the CD28/CTLA4/ICOS gene region on susceptibility to primary sclerosing cholangitis
41 (5), 586-91
DOI 10.1080/00365520500377870, PubMed 16638702

Publications 2005

Lorentzen AR, Celius EG, Ekstrøm PO, Wiencke K, Lie BA, Myhr KM, Ling V, Thorsby E, Vartdal F, Spurkland A, Harbo HF (2005)
Lack of association with the CD28/CTLA4/ICOS gene region among Norwegian multiple sclerosis patients
166 (1-2), 197-201
DOI 10.1016/j.jneuroim.2005.06.002, PubMed 16005527

Smerdel-Ramoya A, Finholt C, Lilleby V, Gilboe IM, Harbo HF, Maslinski S, Førre Ø, Thorsby E, Lie BA (2005)
Systemic lupus erythematosus and the extended major histocompatibility complex--evidence for several predisposing loci
44 (11), 1368-73
DOI 10.1093/rheumatology/kei015, PubMed 16174649

Torkildsen O, Utsi E, Harbo HF, Mellgren SI, Vedeler CA, Myhr KM (2005)
Ethnic variations of IL-10 polymorphisms in a Sami and Norwegian population
62 (1), 71-4
DOI 10.1111/j.1365-3083.2005.01635.x, PubMed 16091126

Torkildsen O, Utsi E, Mellgren SI, Harbo HF, Vedeler CA, Myhr KM (2005)
Ethnic variation of Fc gamma receptor polymorphism in Sami and Norwegian populations
115 (3), 416-21
DOI 10.1111/j.1365-2567.2005.02158.x, PubMed 15946259

Publications 2004

Harbo HF, Lie BA, Sawcer S, Celius EG, Dai KZ, Oturai A, Hillert J, Lorentzen AR, Laaksonen M, Myhr KM, Ryder LP, Fredrikson S, Nyland H, Sørensen PS, Sandberg-Wollheim M, Andersen O, Svejgaard A, Edland A, Mellgren SI, Compston A, Vartdal F, Spurkland A (2004)
Genes in the HLA class I region may contribute to the HLA class II-associated genetic susceptibility to multiple sclerosis
63 (3), 237-47
DOI 10.1111/j.0001-2815.2004.00173.x, PubMed 14989713

Oturai AB, Ryder LP, Fredrikson S, Myhr KM, Celius EG, Harbo HF, Andersen O, Akesson E, Hillert J, Madsen HO, Nyland H, Spurkland A, Datta P, Svejgaard A, Sorensen PS (2004)
Concordance for disease course and age of onset in Scandinavian multiple sclerosis coaffected sib pairs
10 (1), 5-8
DOI 10.1191/1352458504ms975oa, PubMed 14760946

Publications 2003

Akesson E, Coraddu F, Marrosu MG, Massacesi L, Hensiek A, Harbo HF, Oturai A, Trojano M, Momigliano-Richiardi P, Cocco E, Murru R, Hillert J, Compston A, Sawcer S (2003)
Refining the linkage analysis on chromosome 10 in 449 sib-pairs with multiple sclerosis
143 (1-2), 31-8
DOI 10.1016/j.jneuroim.2003.08.008, PubMed 14575911

Harbo HF, Datta P, Oturai A, Ryder LP, Sawcer S, Setakis E, Akesson E, Celius EG, Modin H, Sandberg-Wollheim M, Myhr KM, Andersen O, Hillert J, Sorensen PS, Svejgaard A, Compston A, Vartdal F, Spurkland A (2003)
Two genome-wide linkage disequilibrium screens in Scandinavian multiple sclerosis patients
143 (1-2), 101-6
DOI 10.1016/j.jneuroim.2003.08.021, PubMed 14575924

Publications 2002

Akesson E, Oturai A, Berg J, Fredrikson S, Andersen O, Harbo HF, Laaksonen M, Myhr KM, Nyland HI, Ryder LP, Sandberg-Wollheim M, Sorensen PS, Spurkland A, Svejgaard A, Holmans P, Compston A, Hillert J, Sawcer S (2002)
A genome-wide screen for linkage in Nordic sib-pairs with multiple sclerosis
3 (5), 279-85
DOI 10.1038/sj.gene.6363866, PubMed 12140746

Publications 2001

Dai KZ, Harbo HF, Celius EG, Oturai A, Sørensen PS, Ryder LP, Datta P, Svejgaard A, Hillert J, Fredrikson S, Sandberg-Wollheim M, Laaksonen M, Myhr KM, Nyland H, Vartdal F, Spurkland A (2001)
The T cell regulator gene SH2D2A contributes to the genetic susceptibility of multiple sclerosis
2 (5), 263-8
DOI 10.1038/sj.gene.6363774, PubMed 11528519

Dai Y, Masterman T, Huang WX, Sandberg-Wollheim M, Laaksonen M, Harbo HF, Oturai A, Ryder LP, Soelberg-Sørensen P, Svejgaard A, Hillert J (2001)
Analysis of an interferon-gamma gene dinucleotide-repeat polymorphism in Nordic multiple sclerosis patients
7 (3), 157-63
DOI 10.1177/135245850100700304, PubMed 11475438

Isojärvi JI, Taubøll E, Pakarinen AJ, van Parys J, Rättyä J, Harbo HF, Dale PO, Fauser BC, Gjerstad L, Koivunen R, Knip M, Tapanainen JS (2001)
Altered ovarian function and cardiovascular risk factors in valproate-treated women
111 (4), 290-6
DOI 10.1016/s0002-9343(01)00806-3, PubMed 11566460

Publications 2000

Celius EG, Harbo HF, Egeland T, Vartdal F, Vandvik B, Spurkiand A (2000)
Sex and age at diagnosis are correlated with the HLA-DR2, DQ6 haplotype in multiple sclerosis
178 (2), 132-5
DOI 10.1016/s0022-510x(00)00389-0, PubMed 11018705

Publications 1999

Harbo HF, Celius EG, Vartdal F, Spurkland A (1999)
CTLA4 promoter and exon 1 dimorphisms in multiple sclerosis
53 (1), 106-10
DOI 10.1034/j.1399-0039.1999.530112.x, PubMed 10082437