Bendik S. Winsvold

  • Group leader, Senior researcher; PhD

Background

Bendik S Winsvold has a medical degree from Royal College of Surgeons in Ireland (2006), and started specializing in neurology at Oslo University Hospital in 2008. His PhD (2014) was on the genetic basis of migraine, and the relationship between migraine and cardiovascular disease. He has worked as visiting scientist at the department of Human Genetics, Wellcome Trust Sanger Institute (Cambridge, UK) for two years (2011-2012), and at the Broad Institute of MIT and Harvard (Boston, USA) for six months (2014-2015). His main research focus has since been on the genetics of neurological and psychiatric disorders. He organizes the neuropsychiatric arm of a large genetic study (HUNT-MI/All-In) of 70,000 participants in the HUNT Study (https://www.ntnu.edu/huntgenes/research). Former secretary, and active member, of the International Headache Genetics Consortium. Alongside his research activity, he takes a special interest in the follow-up of patients with headache at the department of Neurology.

Research Projects

Supervision of PhD candidates

  • Main supervisor for Sigrid Børte (MD)
  • Co-supervisor for Marie Udnesseter Lie (MSc) and Ioannis Kitsos (MD)

Methodology and interests

  • Population genetics of neurological and psychiatric disorders. Epigenetics. Epidemiological studies of chronic pain disorders and headache. Organizes the neuropsychiatric arm of the HUNT-MI (All-In) study (https://www.ntnu.edu/huntgenes/research).

Publications

  1. Lane JM, Jones S, Dashti HS, Wood AR, Aragam KG, van Hees VT, Brumpton B, Winsvold BS, Wang H, Bowden J, Song Y, Patel K, Anderson SG, Beaumont R, Bechtold DA, Cade B, Haas M, Kathiresan S, Little MA, Luik AI, Loudon AS, Purcell S, Richmond RC, Scheer FAJL, Schormair B, Tyrrell J, Winkelman J, Winkelmann J, HUNT All In Sleep, Strand LB, Zhao C, Nielsen JB, Willer CJ, Redline S, Spiegelhalder K, Kyle SD, Ray DW, Zwart J-A, Hveem K, Frayling TM, Lawlor DA, Rutter MK, Weedon MN, Saxena R. Biological and clinical insights from genetics of insomnia symptoms. Nature Genetics 2018 (accepted).
  1. Åsberg AN, Hagen K, Stovner LJ, Heuch I, Zwart JA, Winsvold BS. Do incident musculoskeletal complaints influence mortality? The Nord-Trøndelag Health study. Plos One 2018 Sep 28;13(9):e0203925. doi: 10.1371/journal.pone.0203925.
  1. Liu M, Jiang Y, Wedow R, Li Y, Brazel DM, Chen F, Datta G, Davila-Velderrain I, McGuire D, Tian C [... ] Winsvold BSal. Association studies of up to 1.2 million individuals yield new insights in the genetic etiology of tobacco and alcohol use. Nature Genetics 2018 (accepted)
  1. Yang Y, Zhao H, Boomsma DI, Ligthart L, Belin AC, Smith GD, Esko T, Freilinger TM, Hansen TF, Ikram MA, Kallela M, Kubisch C, Paraskevi C, Strachan DP, Wessman M; International Headache Genetics Consortium [Winsvold B.S.], van den Maagdenberg AMJM, Terwindt GM, Nyholt DR.Molecular genetic overlap between migraine and major depressive disorder. Eur J Hum Genet 2018 [Epub ahead of print]
  1. Anttila V., Bulik-Sullivan B., Finucane H.K., Walters R.K., Bras J., Duncan L., Escott-Price V., Falcone G.J., [...] Winsvold B.al. Analysis of shared heritability in common disorders of the brain. Science 2018 Jun 22;360(6395).
  1. Johnsen M.B, Winsvold B.S., Børte S., Vie G.Å., Pedersen L.M., Storheim K., Skorpen F., Hagen K., Bjørngaard J.H., Åsvold B.O., Zwart J.-A. The causal role of smoking on the risk of headache. A Mendelian randomization analysis in the HUNT Study. Eur J Neurology 2018 (Epub ahead of print).
  1. Gormley P, Kurki MI, Hiekkala ME, Veerapen K, Häppölä P, Mitchell AA, Lal D, Palta P, Surakka I, Kaunisto MA, Hämäläinen E, Vepsäläinen S, Havanka H, Harno H, Ilmavirta M, Nissilä M, Säkö E, Sumelahti ML, Liukkonen J, Sillanpää M, Metsähonkala L, Koskinen S, Lehtimäki T, Raitakari O, Männikkö M, Ran C, Belin AC, Jousilahti P, Anttila V, Salomaa V, Artto V, Färkkilä M; 23andMe Research Team; International Headache Genetics Consortium (IHGC) [Winsvold B.S.], Runz H, Daly MJ, Neale BM, Ripatti S, Kallela M, Wessman M, Palotie A. Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families. Neuron 2018 May 16;98(4):743-753.e4.
  1. Hagen K., Kristoffersen E.S., Winsvold B.S., Stovner L., Zwart J.-A. Remission of chronic headache: an 11-year follow-up study. Data from the Nord-Trøndelag Health Surveys 1995-1997 and 2006-2008. Cephalalgia 2018 (Epub ahead of print).
  1. Kambur O., Kaunisto M.A., Winsvold B.S., Wilsgaard T., Stubhaug A., Zwart J.A., Kalso E., Nielsen C.S.. Genetic Variation in P2rx7 and Pain Tolerance. Pain 2018 Feb 20 (Epub ahead of print). 
  1. Hagen K., Åsberg A.N., Stovner L., Linde M., Zwart J.-A., Winsvold B.S., Heuch I. Lifestyle factors and risk of migraine and tension-type headache. Follow-up data from the Nord-Trøndelag Health Surveys 1995-1997 and 2006-2008. Cephalalgia 2018 (Epub ahead of print). 
  1. Winsvold B.S., Marvik A., Zwart J.A., Aamodt A.H. Migraine and stroke. Tidsskr Nor Laegeforen. 2018 Feb 19 (Epub ahead of print). 
  1. Winsvold B.S., Bettella F., Witoelar A., Anttila V., Gormley P., Kurth T., Terwindt G.M., Freilinger T.M., Frei O., Shadrin A., Wang Y., Dale A.M., van den Maagdenberg A., Chasman D.I., Nyholt D.R., Palotie A., Andreassen O.A., Zwart J.A., International Headache Genetics C. Shared genetic risk between migraine and coronary artery disease: A genome-wide analysis of common variants. PLoS One 2017: Sep 28;12(9):e0185663. 
  1. Børte S., Winsvold B.S., Stensland S.Ø., Småstuen M.C., Zwart J.A. The effect of foetal growth restriction on the development of migraine and tension-type headache in adulthood. The HUNT Study. PLoS One 2017:12(4):e0175908.
  1. Winsvold B.S., Palta P., Eising E., Page C.M., International Headache Genetics C., van den Maagdenberg A.M., Palotie A., Zwart J.A. Epigenetic DNA methylation changes associated with headache chronification: A retrospective case-control study. Cephalalgia 2017: doi: 10.1177/0333102417690111 (Epub ahead of print).
  1. Johnsen M.B., Vie G.A., Winsvold B.S., Bjorngaard J.H., Asvold B.O., Gabrielsen M.E., Pedersen L.M., Hellevik A.I., Langhammer A., Furnes O., Flugsrud G.B., Skorpen F., Romundstad P.R., Storheim K., Nordsletten L., Zwart J.A. The causal role of smoking on the risk of hip or knee replacement due to primary osteoarthritis: a Mendelian randomisation analysis of the HUNT study. Osteoarthritis Cartilage 2017 (Epub ahead of print). 
  1. Gustavsen, M.W., Celius, E.G., Winsvold, B.S., Moen, S.M., Nygaard, G.O., Berg-Hansen, P., Lie, B.A., Zwart, J.-A., Harbo, H.F. Migraine and frequent tension-type headache are not associated with multiple sclerosis in a Norwegian case-control study. Multiple Sclerosis Journal – Experimental, Translational and Clinical 2016: 10.1177/2055217316682976.
  1. Gormley P., Winsvold B.S., Nyholt D.R., Kallela M., Chasman D.I., Palotie A. Migraine genetics: from genome-wide association studies to translational insights. Genome Medicine 2016;8:86.
  1. Gormley P., Anttila V., Winsvold B.S., Palta P., Esko T., Pers T.H., Farh K.H., Cuenca-Leon E., Muona M., Furlotte N.A., Kurth T., Ingason A., McMahon G., Ligthart L., Terwindt G.M., Kallela M., Freilinger T.M., Ran C., Gordon S.G., Stam A.H., Steinberg S., Borck G., Koiranen M., Quaye L., Adams H.H., Lehtimaki T., Sarin A.P., Wedenoja J., Hinds D.A., Buring J.E., Schurks M., Ridker P.M., Hrafnsdottir M.G., Stefansson H., Ring S.M., Hottenga J.J., Penninx B.W., Farkkila M., Artto V., Kaunisto M., Vepsalainen S., Malik R., Heath A.C., Madden P.A., Martin N.G., Montgomery G.W., Kurki M.I., Kals M., Magi R., Parn K., Hamalainen E., Huang H., Byrnes A.E., Franke L., Huang J., Stergiakouli E., Lee P.H., Sandor C., Webber C., Cader Z., Muller-Myhsok B., Schreiber S., Meitinger T., Eriksson J.G., Salomaa V., Heikkila K., Loehrer E., Uitterlinden A.G., Hofman A., van Duijn C.M., Cherkas L., Pedersen L.M., Stubhaug A., Nielsen C.S., Mannikko M., Mihailov E., Milani L., Gobel H., Esserlind A.L., Christensen A.F., Hansen T.F., Werge T., International Headache Genetics C., Kaprio J., Aromaa A.J., Raitakari O., Ikram M.A., Spector T., Jarvelin M.R., Metspalu A., Kubisch C., Strachan D.P., Ferrari M.D., Belin A.C., Dichgans M., Wessman M., van den Maagdenberg A.M., Zwart J.A., Boomsma D.I., Smith G.D., Stefansson K., Eriksson N., Daly M.J., Neale B.M., Olesen J., Chasman D.I., Nyholt D.R., Palotie A. Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine. Nature Genetics 2016;48(8): 856-866.
  1. Eising E., Huisman S.M., Mahfouz A., Vijfhuizen L.S., Anttila V., Winsvold B.S., Kurth T., Ikram M.A., Freilinger T., Kaprio J., Boomsma D.I., van Duijn C.M., Jarvelin M.R., Zwart J.A., Quaye L., Strachan D.P., Kubisch C., Dichgans M., Davey Smith G., Stefansson K., Palotie A., Chasman D.I., Ferrari M.D., Terwindt G.M., de Vries B., Nyholt D.R., Lelieveldt B.P., van den Maagdenberg A.M., Reinders M.J. Gene co-expression analysis identifies brain regions and cell types involved in migraine pathophysiology: a GWAS-based study using the Allen Human Brain Atlas. Human Genetics 2016;135(4):425-439.
  1. Åsberg A.N., Stovner L., Zwart J.A., Winsvold B.S., Heuch I., Hagen K. Chronic musculoskeletal complaints as a predictor of mortality. The HUNT study. Pain 2016;157:1443-1447.
  1. Malik R., Winsvold B.S., Auffenberg E., Dichgans M., Freilinger T. The migraine–stroke connection: A genetic perspective. Cephalalgia 2016;36(7):658-668.
  1. Srinivasan S., Bettella F., Mattingsdal M., Wang Y., Witoelar A., Schork A.J., Thompson W.K., Zuber V., The Schizophrenia Working Group of the Psychiatric Genomics Consortium, International Headache Genetics Consortium, Winsvold B.S., Zwart J.A., Collier D.A. Desikan R.S., Melle I., Werge T., Dale A.M., Djurovic S., Andreassen O.A. Genetic markers of human evolution are enriched in schizophrenia.Biological Psychiatry 2015;80(4):284-92.
  1. Zhao H., Eising E., de Vries B., Anttila V., Winsvold B.S., Kurth T., Stefansson H., Kallela M., Malik R., Stam A.H., Ikram M.A., Ligthart L., Freilinger T., Alexander M., Muller-Myhsok B., Schreiber S., Meitinger T., Aromaa A., Eriksson J.G., Boomsma D.I., van Duijn C.M., Zwart J.-A., Quaye L., Kubisch C., Dichgans M., Wessman M., Stefansson K., Chasman D.I., Palotie A., Martin N.G., Montgomery G.W., Ferrari M.D., Terwindt G.M., van den Maagdenberg A.M.J.M., Nyholt D.R. Gene-based pleiotropy across migraine with aura and migraine without aura. Cephalalgia2016;36(7):648-657.
  2. Winsvold B.S., Nelson C.P., Malik R., Gormley P., Anttila V., Vander Heiden J., Elliott K.S., Jacobsen L.M., Palta P., Amin N., de Vries B., Hämäläinen E., Freilinger T., Ikram M.A., Kessler T., Koiranen M., Ligthart L., McMahon G., Pedersen L.M., Willenborg C., Won H.-H., Olesen J., Artto V., Assimes T.L., Blankenberg S., Boomsma D.I., Cherkas L., Smith G.D., Epstein S.E., Erdmann J., Ferrari M.D., Göbel H., Hall A.S., Jarvelin M.-R., Kallela M., Kaprio J., Kathiresan S., Lehtimäki T., McPherson R., März W., Nyholt D., O’Donnell C.J., Quaye L., Rader D.J., Raitakari O., Roberts R., Schunkert H., Schürks M., Stewart A.F.R., Terwindt G.M., Thorsteinsdottir U., van den Maagdenberg A.M.J.M, van Duijn C., Wessman M., Kurth T., Kubisch C., Dichgans M., Chasman D.I., Cotsapas C., Zwart J.-A., Samani N.J., Palotie A. for the CARDIoGRAM Consortium and the International Headache Genetics Consortium. Genetic analysis for a shared biological basis between migraine and coronary artery disease. Neurology: Genetics 2015; 1(1);doi:http:/​/​dx.​doi.​org/​10.​1212/​NXG.​ 00000000000010.

  3. Kvalheim S., Sandvik L., Winsvold B., Hagen K., Zwart J.A. (2016) Early menarche and chronic widespread musculoskeletal complaints- Results from the HUNT study.European Journal of Pain 2016: 20(3): 458-464.
  1. Asberg A.N., Stovner L.J., Zwart J.A., Winsvold B.S., Heuch I., Hagen K. Migraine as a predictor of mortality: The HUNT study. Cephalalgia 2016 36: 351-357.
  1. Malik R., Freilinger T., Winsvold B.S., Anttila V., Vander Heiden J., Traylor M., de Vries B., Holliday E.G., Terwindt G.M., Sturm J., Bis J.C., Hopewell J.C., Ferrari M.D., Rannikmae K., Wessman M., Kallela M., Kubisch C., Fornage M., Meschia J.F., Lehtimaki T., Sudlow C., Clarke R., Chasman D.I., Mitchell B.D., Maguire J., Kaprio J., Farrall M., Raitakari O.T., Kurth T., Ikram M.A., Reiner A.P., Longstreth W.T., Jr., Rothwell P.M., Strachan D.P., Sharma P., Seshadri S., Quaye L., Cherkas L., Schurks M., Rosand J., Ligthart L., Boncoraglio G.B., Davey Smith G., van Duijn C.M., Stefansson K., Worrall B.B., Nyholt D.R., Markus H.S., van den Maagdenberg A.M., Cotsapas C., Zwart J.A., Palotie A., Dichgans M. Shared genetic basis for migraine and ischemic stroke: A genome-wide analysis of common variants. Neurology 2015;84:2132-2145.
  1. Jacobsen K.K., Nievergelt C.M., Zayats T., Greenwood T.A., Anttila V., Akiskal H.S., Kelsoe J.R., Greenwood T.A., Nievergelt C.M., McKinney R., Shilling P.D., Smith E.N., Schork N.J., Bloss C.S., Nurnberger J.I.J., Edenberg H.J., Foroud T., Koller D.L., Gershon E.S., Badner J.A., Liu C., Scheftner W.A., Lawson W.B., Nwulia E.A., Hipolito M., Potash J., Coryell W., Rice J., Byerley W., McMahon F.J., Berrettini W.H., Zandi P.P., Mahon P.B., McInnis M.G., Zöllner S., Zhang P., Craig D.W., Szelinger S., Barrett T.B., Schulze T.G., Wedenoja J., Kaunisto M.A., Heikkilä K., Kaprio J., Wessman M., Kallela M., Färkkilä M., Artto V., Aromaa A., Eriksson J.G., Winsvold B.S., Zwart J., Gormley P., Palotie A., Kurth T., Rose L.M., Buring J.E., Ridker P.M., Chasman D.I., Bettella F., Steinberg S., Stefansson H., Stefansson K., McMahon G., Davey-Smith G., Malik R., Freilinger T., Wichmann H.E., Dichgans M., Muller-Myhsok B., Meitinger T., de Vries B., Terwindt G., Stam A.H., Frants R.R., Pelzer N., Weller C.M., Zielman R., Ferrari M.D., van den Maagdenberg A.M., Medland S.E., Montgomery G.W., Martin N.G., Nyholt D.R., Todt U., Borck G., Kubisch C., Quaye L., Williams F.M.K., Cherkas L., Koiranen M., Hartikainen A., Pouta A., Jarvelin M., Ikram M.A., van den Ende J., Uitterlinden A.G., Hofman A., Amin N., van Duijn C., Lehtimäki T., Ligthart L., Hottenga J., Vink J.M., Penninx B.W., Boomsma D.I., Schürks M., Jakobsson F., Schoenen J., Heath A.C., Madden P.A.F., Göbel H., Heinze A., Heinze-Kuhn K., Schreiber S., Anttila V., Daly M.J., Alexander M., Raitakari O., Strachan D.P., Haavik J., Fasmer O.B., Kelsoe J.R., Johansson S., Oedegaard K.J. Genome wide association study identifies variants in NBEA associated with migraine in bipolar disorder. J Affect Disord 2015;10: 453-461.
  1. Louter M.A.*, Fernandez-Morales J.*, de Vries B., Winsvold B., Anttila V., Fernandez-Cadenas I., Vila-Pueyo M., Sintas C., van Duijn C.M., Cormand B., Álvarez-Sabin J., Montaner J., Ferrari M.D., van den Maagdenberg M.J.M., Palotie A., Zwart J.A., Macaya A., Terwindt G.M., Pozo-Rosich P. Candidate gene association study searching for genetic factors involved in migraine chronification. Cephalalgia 2015;35:500-507.
  1. Nyholt D.R., Anttila V., Winsvold B.S., Kurth, T., Bettella F., Kallela MN., Malik R., de Vries B., Terwindt G., Ikram M.A., Stam A.H., Ligthart L., Freilinger T., Alexander M., Muller-Myhsok B., Schreiber S., Meitinger T., Aromaa A., Eriksson J.G., Kaprio J., Boomsma D.I., van Duijn C., Raitakari O., Jarvelin M.R., Zwart J.A., Cherkas L., Strachan D.P., Kubisch C., Ferrari M.D., van den Maagdenberg A.M., Dichgans M., Wessman M., Davey Smith G., Stefansson K., Chasman D.I. & Palotie A. Concordance of genetic risk across migraine subgroups: impact on current and future genetic association studies. Cephalalgia 2015;35:489-499.
  1. Fagernæs C.F., Heuch I., Zwart, J.A., Winsvold B., Linde M, Hagen K. Blood pressure as a risk factor for headache and migraine: A prospective population-based study. European Journal of Neurology 2015;22:156-162, e110-151.
     
  2. Chasman D.I., Anttila V., Buring J.E., Ridker P.M., Schurks M. Kurth, T., International Headache Genetics Consortium [including Winsvold, B.S.]. Selectivity in Genetic Association with Sub-classified Migraine in Women. PLoS Genet 2014;10:e1004366.
     
  3. Jacobsen L.M., Winsvold, B.S., Romundstad, S., Pripp, A.H., Holmen J., Zwart, J.A. Urinary albumin excretion as a marker of endothelial dysfunction in migraine sufferers: the HUNT study, Norway. BMJ Open 2013;3(8);doi:10.1136/bmjopen-2013-003268.
     
  4. Anttila, V.*, Winsvold, B.S.*, Gormley, P., Kurth, T., Bettella, F., McMahon, G., Kallela, M., Malik, R., de Vries, B., Terwindt, G., Medland, S.E., Todt, U., McArdle, W.L., Quaye, L., Koiranen, M., Ikram, M.A., Lehtimaki, T., Stam, A.H., Ligthart, L., Wedenoja, J., Dunham, I., Neale, B.M., Palta, P., Hamalainen, E., Schurks, M., Rose, L.M., Buring, J.E., Ridker, P.M., Steinberg, S., Stefansson, H., Jakobsson, F., Lawlor, D.A., Evans, D.M., Ring, S.M., Farkkila, M., Artto, V., Kaunisto, M.A., Freilinger, T., Schoenen, J., Frants, R.R., Pelzer, N., Weller, C.M., Zielman, R., Heath, A.C., Madden, P.A., Montgomery, G.W., Martin, N.G., Borck, G., Gobel, H., Heinze, A., Heinze-Kuhn, K., Williams, F.M., Hartikainen, A.L., Pouta, A., van den Ende, J., Uitterlinden, A.G., Hofman, A., Amin, N., Hottenga, J.J., Vink, J.M., Heikkila, K., Alexander, M., Muller-Myhsok, B., Schreiber, S., Meitinger, T., Wichmann, H.E., Aromaa, A., Eriksson, J.G., Traynor, B.J., Trabzuni, D., North American Brain Expression Consortium, UK Brain Expression Consortium, Rossin, E., Lage, K., Jacobs, S.B., Gibbs, J.R., Birney, E., Kaprio, J., Penninx, B.W., Boomsma, D.I., van Duijn, C., Raitakari, O., Jarvelin, M.R., Zwart, J.A., Cherkas, L., Strachan, D.P., Kubisch, C., Ferrari, M.D., van den Maagdenberg, A.M., Dichgans, M., Wessman, M., Smith, G.D., Stefansson, K., Daly, M.J., Nyholt, D.R., Chasman, D.I. & Palotie, A. , for the International Headache Genetics Consortium. Genome-wide meta-analysis identifies new susceptibility loci for migraine.Nature Genetics 2013;45(8):912-7.*The authors contributed equally.
     
  5. Winsvold B, Sandven I, Hagen K, Linde M, Midthjell K, Zwart J-A. Migraine, headache and development of metabolic syndrome: An 11 year follow-up in the HUNT Study. Pain 2013;154(8):1305-11.

  6. Freilinger T, Anttila V, de Vries B, Malik R, Kallela M, Terwindt GM, Pozo-Rosich P, Winsvold B, Nyholt D, van osterhout DPJ, Artto V, Todt U, Hämäläinen E, Fernandez-Morales J, Louter M, Kaunisto M, Schoenen J, Raitakari O, Lehtimäki T, Vila-Pueyo M, Göbel H, Wichmann E, Sintas C, Uitterlinden A, Hofman A, Rivadeneira F, Heinze A, Tronvik E, van Duijn C, Kaprio J, Cormand B, Wessman M, Frants R, Meitinger T, Müller-Myhsok B, Zwart JA, Färkkilä M, Macaya A, Ferrari M, Kubisch C, Palotie A, Dichgans M, van den Maagdenberg A for the International Headache Genetics Consortium. Genome-wide association analysis identifies susceptibility loci for migraine without aura. Nature Genetics 2012;44(7):777-82.

  7. Boraska V, Day-Williams A, Franklin C, Elliott K, Panoutsopoulou K, Tachmazidou I, Albrecht E, Bandinelli S, Beilin L, Bochud M, Cadby G, Ernst F, Evans D, Hayward C, Hicks A, Huffman J, Huth C, James A, Klopp N, Kolcic I, Kutalik Z, Lawlor D, Musk A, Pehlic M, Pennell C, Perry J, Peters A, Polasek O, Pourcain B, Ring S, Salvi E, Schipf S, Staessen J, Teumer A, Timpson N, Vitart V, Warrington N, Yaghootkar H, Zemunik T, Zgaga L, An P, Anttila V, Borecki I, Holmen J, Ntalla J, Palotie A, Pietiläinen K, Wedenoja J, Winsvold B, Dedoussis G, Kaprio J, Province M, Zwart JA, Burnier M, Campbell, Cusi D, Davey-Smith G, Frayling T, Gieger C, Palmer L, Pramstaller P, Rudan I, Völzke H, Wichmann HE, Wright A, Zeggini E. Genome-wide association study to identify common variants associated with brachial circumference: a meta-analysis of 14 cohorts. PLoS One 2012;7(3):e31369.

  8. Winsvold B, Hagen K, Aamodt AH, Stovner LJ, Holmen J, Zwart JA. Headache, migraine and cardiovascular risk factors. The HUNT study. Eur J Neurol 2011;18(3):504-11.

  9. Lian A, Karlsen PJ, Winsvold B. A re-evaluation of the phonological similarity effect in adults’ short-term memory of words and nonwords. Memory 2001;9:281-299.
 

Publications 2024

Argren MB, Engstrand H, Husøy AK, Zwart JA, Winsvold BS (2024)
The PopHEAD study: a population-based, cross-sectional study on headache burden in Norway: methods and validation of questionnaire-based diagnoses
J Headache Pain, 25 (1), 201
DOI 10.1186/s10194-024-01901-4, PubMed 39567888

Engstrand H, Revdal E, Argren MB, Hagen K, Zwart JA, Brodtkorb E, Winsvold BS (2024)
Relationship between migraine and epilepsy in a large population-based cohort: The HUNT Study
Eur J Neurol, 31 (12), e16496
DOI 10.1111/ene.16496, PubMed 39331386

Hagen K, Winsvold BS, Bjørk MH, Tronvik E, Mathiesen LB, Ofte HK, Lundqvist C, Sønnervik J, Bäcklund N (2024)
Room for improvement in the follow-up for unilateral headache with autonomic symptoms
Tidsskr Nor Laegeforen, 144 (7)
DOI 10.4045/tidsskr.24.0184, PubMed 38832616

Nievergelt CM, Maihofer AX, Atkinson EG, Chen CY, Choi KW, Coleman JRI, Daskalakis NP, Duncan LE, Polimanti R, Aaronson C, Amstadter AB, Andersen SB, Andreassen OA, Arbisi PA, Ashley-Koch AE, Austin SB, Avdibegoviç E, Babić D, Bacanu SA, Baker DG, Batzler A, Beckham JC, Belangero S, Benjet C, Bergner C et al. (2024)
Genome-wide association analyses identify 95 risk loci and provide insights into the neurobiology of post-traumatic stress disorder
Nat Genet, 56 (5), 792-808
DOI 10.1038/s41588-024-01707-9, PubMed 38637617

Olofsson IA, Kristjansson RP, Callesen I, Davidsson O, Winsvold B, Hjalgrim H, Ostrowski SR, Erikstrup C, Bruun MT, Pedersen OB, Burgdorf KS, Banasik K, Sørensen E, Mikkelsen C, Didriksen M, Dinh KM, Mikkelsen S, International Headache Genetic Consortium, DBDS Genomic Consortium, Brunak S, Ullum H, Chalmer MA, Olesen J, Kogelman LJA, Hansen TF (2024)
Genome-wide association study reveals a locus in ADARB2 for complete freedom from headache in Danish Blood Donors
Commun Biol, 7 (1), 646
DOI 10.1038/s42003-024-06299-y, PubMed 38802570

Sargurupremraj M, Soumaré A, Bis JC, Surakka I, Jürgenson T, Joly P, Knol MJ, Wang R, Yang Q, Satizabal CL, Gudjonsson A, Mishra A, Bouteloup V, Phuah CL, van Duijn CM, Cruchaga C, Dufouil C, Chêne G, Lopez OL, Psaty BM, Tzourio C, Amouyel P, Adams HH, Jacqmin-Gadda H, Ikram MA et al. (2024)
Genetic Complexities of Cerebral Small Vessel Disease, Blood Pressure, and Dementia
JAMA Netw Open, 7 (5), e2412824
DOI 10.1001/jamanetworkopen.2024.12824, PubMed 38776079

Strom NI, Gerring ZF, Galimberti M, Yu D, Halvorsen MW, Abdellaoui A, Rodriguez-Fontenla C, Sealock JM, Bigdeli T, Coleman JR, Mahjani B, Thorp JG, Bey K, Burton CL, Luykx JJ, Zai G, Alemany S, Andre C, Askland KD, Banaj N, Barlassina C, Nissen JB, Bienvenu OJ, Black D, Bloch MH et al. (2024)
Genome-wide association study identifies 30 obsessive-compulsive disorder associated loci
medRxiv
DOI 10.1101/2024.03.13.24304161, PubMed 38712091

Strom NI, Verhulst B, Bacanu SA, Cheesman R, Purves KL, Gedik H, Mitchell BL, Kwong AS, Faucon AB, Singh K, Medland S, Colodro-Conde L, Krebs K, Hoffmann P, Herms S, Gehlen J, Ripke S, Awasthi S, Palviainen T, Tasanko EM, Peterson RE, Adkins DE, Shabalin AA, Adams MJ, Iveson MH et al. (2024)
Genome-wide association study of major anxiety disorders in 122,341 European-ancestry cases identifies 58 loci and highlights GABAergic signaling
medRxiv
DOI 10.1101/2024.07.03.24309466, PubMed 39006447

Publications 2023

Ao X, Parisien M, Zidan M, Grant AV, Martinsen AE, Winsvold BS, Diatchenko L (2023)
Rare variant analyses in large-scale cohorts identified SLC13A1 associated with chronic pain
Pain, 164 (8), 1841-1851
DOI 10.1097/j.pain.0000000000002882, PubMed 36943258

Bakker MK, Kanning JP, Abraham G, Martinsen AE, Winsvold BS, Zwart JA, Bourcier R, Sawada T, Koido M, Kamatani Y, Morel S, Amouyel P, Debette S, Bijlenga P, Berrandou T, Ganesh SK, Bouatia-Naji N, Jones G, Bown M, Rinkel GJE, Veldink JH, Ruigrok YM, HUNT All-In Stroke, CADISP group, International Consortium for Blood Pressure, International Headache Genetics Consortium, International Stroke Genetics Consortium (ISGC) Intracranial Aneurysm Working Group (2023)
Genetic Risk Score for Intracranial Aneurysms: Prediction of Subarachnoid Hemorrhage and Role in Clinical Heterogeneity
Stroke, 54 (3), 810-818
DOI 10.1161/STROKEAHA.122.040715, PubMed 36655558

Nievergelt CM, Maihofer AX, Atkinson EG, Chen CY, Choi KW, Coleman JR, Daskalakis NP, Duncan LE, Polimanti R, Aaronson C, Amstadter AB, Andersen SB, Andreassen OA, Arbisi PA, Ashley-Koch AE, Austin SB, Avdibegoviç E, Babic D, Bacanu SA, Baker DG, Batzler A, Beckham JC, Belangero S, Benjet C, Bergner C et al. (2023)
Discovery of 95 PTSD loci provides insight into genetic architecture and neurobiology of trauma and stress-related disorders
medRxiv
DOI 10.1101/2023.08.31.23294915, PubMed 37693460

Petersen AS, Barloese M, Lund N, Pedersen AF, Søborg MK, Chalmer MA, Callesen I, Winsvold BS, Zwart JA, DBDS Genomic Consortium, Ostrowski SR, Pedersen OB, Sellebjerg F, Søndergaard HB, Hansen MB, Jensen RH, Hansen TF (2023)
Cluster headache polygenetic risk and known functional variants of CYP3A4 are not associated with treatment response
Eur J Neurol, 30 (5), 1425-1434
DOI 10.1111/ene.15736, PubMed 36773010

Revdal E, Kolstad BP, Winsvold BS, Selmer KK, Morken G, Brodtkorb E (2023)
Psychiatric comorbidity in relation to clinical characteristics of epilepsy: A retrospective observational study
Seizure, 110, 136-143
DOI 10.1016/j.seizure.2023.06.011, PubMed 37379699

Sargurupremraj M, Soumare A, Bis JC, Surakka I, Jurgenson T, Joly P, Knol MJ, Wang R, Yang Q, Satizabal CL, Gudjonsson A, Mishra A, Bouteloup V, Phuah CL, van Duijn CM, Cruchaga C, Dufouil C, Chêne G, Lopez O, Psaty BM, Tzourio C, Amouyel P, Adams HH, Jacqmin-Gadda H, Ikram MA et al. (2023)
Complexities of cerebral small vessel disease, blood pressure, and dementia relationship: new insights from genetics
medRxiv
DOI 10.1101/2023.08.08.23293761, PubMed 37790435

Winsvold BS, Harder AVE, Ran C, Chalmer MA, Dalmasso MC, Ferkingstad E, Tripathi KP, Bacchelli E, Børte S, Fourier C, Petersen AS, Vijfhuizen LS, Magnusson SH, O'Connor E, Bjornsdottir G, Häppölä P, Wang YF, Callesen I, Kelderman T, Gallardo VJ, de Boer I, Olofsgård FJ, Heinze K, Lund N, Thomas LF et al. (2023)
Cluster Headache Genomewide Association Study and Meta-Analysis Identifies Eight Loci and Implicates Smoking as Causal Risk Factor
Ann Neurol, 94 (4), 713-726
DOI 10.1002/ana.26743, PubMed 37486023

Publications 2022

Bahrami S, Hindley G, Winsvold BS, O'Connell KS, Frei O, Shadrin A, Cheng W, Bettella F, Rødevand L, Odegaard KJ, Fan CC, Pirinen MJ, Hautakangas HM, HUNT All-In Headache, Dale AM, Djurovic S, Smeland OB, Andreassen OA (2022)
Dissecting the shared genetic basis of migraine and mental disorders using novel statistical tools
Brain, 145 (1), 142-153
DOI 10.1093/brain/awab267, PubMed 34273149

Bortsov AV, Parisien M, Khoury S, Martinsen AE, Lie MU, Heuch I, Hveem K, Zwart JA, Winsvold BS, Diatchenko L (2022)
Brain-specific genes contribute to chronic but not to acute back pain
Pain Rep, 7 (5), e1018
DOI 10.1097/PR9.0000000000001018, PubMed 35975136

Hautakangas H, Winsvold BS, Ruotsalainen SE, Bjornsdottir G, Harder AVE, Kogelman LJA, Thomas LF, Noordam R, Benner C, Gormley P, Artto V, Banasik K, Bjornsdottir A, Boomsma DI, Brumpton BM, Burgdorf KS, Buring JE, Chalmer MA, de Boer I, Dichgans M, Erikstrup C, Färkkilä M, Garbrielsen ME, Ghanbari M, Hagen K et al. (2022)
Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk alleles
Nat Genet, 54 (2), 152-160
DOI 10.1038/s41588-021-00990-0, PubMed 35115687

Khoury S, Parisien M, Thompson SJ, Vachon-Presseau E, Roy M, Martinsen AE, Winsvold BS, HUNT All-In Pain, Mundal IP, Zwart JA, Kania A, Mogil JS, Diatchenko L (2022)
Genome-wide analysis identifies impaired axonogenesis in chronic overlapping pain conditions
Brain, 145 (3), 1111-1123
DOI 10.1093/brain/awab359, PubMed 34788396

Lie MU, Pedersen LM, Heuch I, Winsvold B, Gjerstad J, Hasvik E, Nygaard ØP, Grotle M, Matre D, Zwart JA, Nilsen KB (2022)
Low Back Pain With Persistent Radiculopathy; the Clinical Role of Genetic Variants in the Genes SOX5, CCDC26/GSDMC and DCC
Front Genet, 12, 757632
DOI 10.3389/fgene.2021.757632, PubMed 35140737

Mishra A, Malik R, Hachiya T, Jürgenson T, Namba S, Posner DC, Kamanu FK, Koido M, Le Grand Q, Shi M, He Y, Georgakis MK, Caro I, Krebs K, Liaw YC, Vaura FC, Lin K, Winsvold BS, Srinivasasainagendra V, Parodi L, Bae HJ, Chauhan G, Chong MR, Tomppo L, Akinyemi R et al. (2022)
Stroke genetics informs drug discovery and risk prediction across ancestries
Nature, 611 (7934), 115-123
DOI 10.1038/s41586-022-05165-3, PubMed 36180795

Mishra A, Malik R, Hachiya T, Jürgenson T, Namba S, Posner DC, Kamanu FK, Koido M, Le Grand Q, Shi M, He Y, Georgakis MK, Caro I, Krebs K, Liaw YC, Vaura FC, Lin K, Winsvold BS, Srinivasasainagendra V, Parodi L, Bae HJ, Chauhan G, Chong MR, Tomppo L, Akinyemi R et al. (2022)
Publisher Correction: Stroke genetics informs drug discovery and risk prediction across ancestries
Nature, 612 (7938), E7
DOI 10.1038/s41586-022-05492-5, PubMed 36376532

Saunders GRB, Wang X, Chen F, Jang SK, Liu M, Wang C, Gao S, Jiang Y, Khunsriraksakul C, Otto JM, Addison C, Akiyama M, Albert CM, Aliev F, Alonso A, Arnett DK, Ashley-Koch AE, Ashrani AA, Barnes KC, Barr RG, Bartz TM, Becker DM, Bielak LF, Benjamin EJ, Bis JC et al. (2022)
Genetic diversity fuels gene discovery for tobacco and alcohol use
Nature, 612 (7941), 720-724
DOI 10.1038/s41586-022-05477-4, PubMed 36477530

Wightman DP, Jansen IE, Savage JE, Shadrin AA, Bahrami S, Holland D, Rongve A, Børte S, Winsvold BS, Drange OK, Martinsen AE, Skogholt AH, Willer C, Bråthen G, Bosnes I, Nielsen JB, Fritsche LG, Thomas LF, Pedersen LM, Gabrielsen ME, Johnsen MB, Meisingset TW, Zhou W, Proitsi P, Hodges A et al. (2022)
Author Correction: A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer's disease
Nat Genet, 54 (7), 1062
DOI 10.1038/s41588-022-01126-8, PubMed 35726068

Yengo L, Vedantam S, Marouli E, Sidorenko J, Bartell E, Sakaue S, Graff M, Eliasen AU, Jiang Y, Raghavan S, Miao J, Arias JD, Graham SE, Mukamel RE, Spracklen CN, Yin X, Chen SH, Ferreira T, Highland HH, Ji Y, Karaderi T, Lin K, Lüll K, Malden DE, Medina-Gomez C et al. (2022)
A saturated map of common genetic variants associated with human height
Nature, 610 (7933), 704-712
DOI 10.1038/s41586-022-05275-y, PubMed 36224396

Publications 2021

Bakker MK, van der Spek RAA, van Rheenen W, Morel S, Bourcier R, Hostettler IC, Alg VS, van Eijk KR, Koido M, Akiyama M, Terao C, Matsuda K, Walters RG, Lin K, Li L, Millwood IY, Chen Z, Rouleau GA, Zhou S, Rannikmäe K, Sudlow CLM, Houlden H, van den Berg LH, Dina C, Naggara O et al. (2021)
Author Correction: Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors
Nat Genet, 53 (2), 254
DOI 10.1038/s41588-020-00760-4, PubMed 33353957

Boer CG, Hatzikotoulas K, Southam L, Stefánsdóttir L, Zhang Y, Coutinho de Almeida R, Wu TT, Zheng J, Hartley A, Teder-Laving M, Skogholt AH, Terao C, Zengini E, Alexiadis G, Barysenka A, Bjornsdottir G, Gabrielsen ME, Gilly A, Ingvarsson T, Johnsen MB, Jonsson H, Kloppenburg M, Luetge A, Lund SH, Mägi R et al. (2021)
Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations
Cell, 184 (18), 4784-4818.e17
DOI 10.1016/j.cell.2021.07.038, PubMed 34450027

Boer CG, Hatzikotoulas K, Southam L, Stefánsdóttir L, Zhang Y, Coutinho de Almeida R, Wu TT, Zheng J, Hartley A, Teder-Laving M, Skogholt AH, Terao C, Zengini E, Alexiadis G, Barysenka A, Bjornsdottir G, Gabrielsen ME, Gilly A, Ingvarsson T, Johnsen MB, Jonsson H, Kloppenburg M, Luetge A, Lund SH, Mägi R et al. (2021)
Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations
Cell, 184 (24), 6003-6005
DOI 10.1016/j.cell.2021.11.003, PubMed 34822786

Burish MJ, Winsvold BS, Miao H (2021)
The current state of cluster headache genetics
Headache, 61 (7), 990-991
DOI 10.1111/head.14166, PubMed 34363404

Freidin MB, Tsepilov YA, Stanaway IB, Meng W, Hayward C, Smith BH, Khoury S, Parisien M, Bortsov A, Diatchenko L, Børte S, Winsvold BS, Brumpton BM, Zwart JA, Aulchenko YS, Suri P, Williams FMK, HUNT All-In Pain (2021)
Sex- and age-specific genetic analysis of chronic back pain
Pain, 162 (4), 1176-1187
DOI 10.1097/j.pain.0000000000002100, PubMed 33021770

Harder AVE, Winsvold BS, Noordam R, Vijfhuizen LS, Børte S, Kogelman LJA, de Boer I, Tronvik E, Rosendaal FR, Willems van Dijk K, O'Connor E, Fourier C, Thomas LF, Kristoffersen ES, Cluster Headache Genetics Working Group, Fronczek R, Pozo-Rosich P, Jensen RH, Ferrari MD, Hansen TF, Zwart JA, Terwindt GM, van den Maagdenberg AMJM (2021)
Genetic Susceptibility Loci in Genomewide Association Study of Cluster Headache
Ann Neurol, 90 (2), 203-216
DOI 10.1002/ana.26146, PubMed 34180076

Kristoffersen ES, Faiz KW, Hansen JM, Tronvik EA, Frich JC, Lundqvist C, Winsvold BS (2021)
The management and clinical knowledge of headache disorders among general practitioners in Norway: a questionnaire survey
J Headache Pain, 22 (1), 136
DOI 10.1186/s10194-021-01350-3, PubMed 34763647

Kristoffersen ES, Jahr SH, Faiz KW, Storstein AM, Winsvold BS, Sandset EC (2021)
Acute stroke care during the first phase of COVID-19 pandemic in Norway
Acta Neurol Scand, 143 (4), 349-354
DOI 10.1111/ane.13392, PubMed 33421104

Kristoffersen ES, Winsvold BS, Sandset EC, Storstein AM, Faiz KW (2021)
Experiences, distress and burden among neurologists in Norway during the COVID-19 pandemic
PLoS One, 16 (2), e0246567
DOI 10.1371/journal.pone.0246567, PubMed 33539418

Mullins N, Forstner AJ, O'Connell KS, Coombes B, Coleman JRI, Qiao Z, Als TD, Bigdeli TB, Børte S, Bryois J, Charney AW, Drange OK, Gandal MJ, Hagenaars SP, Ikeda M, Kamitaki N, Kim M, Krebs K, Panagiotaropoulou G, Schilder BM, Sloofman LG, Steinberg S, Trubetskoy V, Winsvold BS, Won HH et al. (2021)
Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology
Nat Genet, 53 (6), 817-829
DOI 10.1038/s41588-021-00857-4, PubMed 34002096

O'Connor E, Fourier C, Ran C, Sivakumar P, Liesecke F, Southgate L, Harder AVE, Vijfhuizen LS, Yip J, Giffin N, Silver N, Ahmed F, Hostettler IC, Davies B, Cader MZ, Simpson BS, Sullivan R, Efthymiou S, Adebimpe J, Quinn O, Campbell C, Cavalleri GL, Vikelis M, Kelderman T, Paemeleire K et al. (2021)
Genome-Wide Association Study Identifies Risk Loci for Cluster Headache
Ann Neurol, 90 (2), 193-202
DOI 10.1002/ana.26150, PubMed 34184781

Rahman MS, Winsvold BS, Chavez Chavez SO, Børte S, Tsepilov YA, Sharapov SZ, HUNT All-In Pain, Aulchenko YS, Hagen K, Fors EA, Hveem K, Zwart JA, van Meurs JB, Freidin MB, Williams FM (2021)
Genome-wide association study identifies RNF123 locus as associated with chronic widespread musculoskeletal pain
Ann Rheum Dis, 80 (9), 1227-1235
DOI 10.1136/annrheumdis-2020-219624, PubMed 33926923

Verma V, Drury GL, Parisien M, Özdağ Acarli AN, Al-Aubodah TA, Nijnik A, Wen X, Tugarinov N, Verner M, Klares R, Linton A, Krock E, Morado Urbina CE, Winsvold B, Fritsche LG, Fors EA, Piccirillo C, Khoutorsky A, Svensson CI, Fitzcharles MA, Ingelmo PM, Bernard NF, Dupuy FP, Üçeyler N, Sommer C et al. (2021)
Unbiased immune profiling reveals a natural killer cell-peripheral nerve axis in fibromyalgia
Pain, 163 (7), e821-e836
DOI 10.1097/j.pain.0000000000002498, PubMed 34913882

Wightman DP, Jansen IE, Savage JE, Shadrin AA, Bahrami S, Holland D, Rongve A, Børte S, Winsvold BS, Drange OK, Martinsen AE, Skogholt AH, Willer C, Bråthen G, Bosnes I, Nielsen JB, Fritsche LG, Thomas LF, Pedersen LM, Gabrielsen ME, Johnsen MB, Meisingset TW, Zhou W, Proitsi P, Hodges A et al. (2021)
A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer's disease
Nat Genet, 53 (9), 1276-1282
DOI 10.1038/s41588-021-00921-z, PubMed 34493870

Wightman DP, Jansen IE, Savage JE, Shadrin AA, Bahrami S, Holland D, Rongve A, Børte S, Winsvold BS, Drange OK, Martinsen AE, Skogholt AH, Willer C, Bråthen G, Bosnes I, Nielsen JB, Fritsche LG, Thomas LF, Pedersen LM, Gabrielsen ME, Johnsen MB, Meisingset TW, Zhou W, Proitsi P, Hodges A et al. (2021)
Author Correction: A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer's disease
Nat Genet, 53 (12), 1722
DOI 10.1038/s41588-021-00977-x, PubMed 34773122

Winsvold BS, Kitsos I, Thomas LF, Skogholt AH, Gabrielsen ME, Zwart JA, Nilsen KB (2021)
Genome-Wide Association Study of 2,093 Cases With Idiopathic Polyneuropathy and 445,256 Controls Identifies First Susceptibility Loci
Front Neurol, 12, 789093
DOI 10.3389/fneur.2021.789093, PubMed 34975738

Publications 2020

Bakker MK, van der Spek RAA, van Rheenen W, Morel S, Bourcier R, Hostettler IC, Alg VS, van Eijk KR, Koido M, Akiyama M, Terao C, Matsuda K, Walters RG, Lin K, Li L, Millwood IY, Chen Z, Rouleau GA, Zhou S, Rannikmäe K, Sudlow CLM, Houlden H, van den Berg LH, Dina C, Naggara O et al. (2020)
Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors
Nat Genet, 52 (12), 1303-1313
DOI 10.1038/s41588-020-00725-7, PubMed 33199917

Børte S, Zwart JA, Skogholt AH, Gabrielsen ME, Thomas LF, Fritsche LG, Surakka I, Nielsen JB, Zhou W, Wolford BN, Vigeland MD, Hagen K, Kristoffersen ES, Nyholt DR, Chasman DI, Brumpton BM, Willer CJ, Winsvold BS (2020)
Mitochondrial genome-wide association study of migraine - the HUNT Study
Cephalalgia, 40 (6), 625-634
DOI 10.1177/0333102420906835, PubMed 32056457

Johnsen MB, Magnusson K, Børte S, Gabrielsen ME, Winsvold BS, Skogholt AH, Thomas L, Storheim K, Hveem K, Zwart JA (2020)
Development and validation of a prediction model for incident hand osteoarthritis in the HUNT study
Osteoarthritis Cartilage, 28 (7), 932-940
DOI 10.1016/j.joca.2020.04.005, PubMed 32360252

Johnsen MB, Magnusson K, Børte S, Gabrielsen ME, Winsvold BS, Skogholt AH, Thomas L, Storheim K, Hveem K, Zwart JA (2020)
Response to Letter to the Editor: 'Comments on the paper presenting prediction models for incident hand OA in the HUNT study'
Osteoarthritis Cartilage, 29 (2), 292-293
DOI 10.1016/j.joca.2020.10.012, PubMed 33279719

Kristoffersen ES, Børte S, Hagen K, Zwart JA, Winsvold BS (2020)
Migraine, obesity and body fat distribution - a population-based study
J Headache Pain, 21 (1), 97
DOI 10.1186/s10194-020-01163-w, PubMed 32762643

Kristoffersen ES, Børte S, Hagen K, Zwart JA, Winsvold BS (2020)
Caesarean section and the association with migraine: a retrospective register-linked HUNT population cohort study
BMJ Open, 10 (11), e040685
DOI 10.1136/bmjopen-2020-040685, PubMed 33208331

Kristoffersen ES, Faiz KW, Sandset EC, Storstein AM, Stefansen S, Winsvold BS, Hansen JM (2020)
Hospital-based headache care during the Covid-19 pandemic in Denmark and Norway
J Headache Pain, 21 (1), 128
DOI 10.1186/s10194-020-01195-2, PubMed 33121445

Kristoffersen ES, Faiz KW, Sandset EC, Storstein AM, Stefansen S, Winsvold BS, Hansen JM (2020)
Correction to: Hospital-based headache care during the Covid-19 pandemic in Denmark and Norway
J Headache Pain, 21 (1), 132
DOI 10.1186/s10194-020-01199-y, PubMed 33198620

Kristoffersen ES, Sandset EC, Winsvold BS, Faiz KW, Storstein AM (2020)
Experiences of telemedicine in neurological out-patient clinics during the COVID-19 pandemic
Ann Clin Transl Neurol, 8 (2), 440-447
DOI 10.1002/acn3.51293, PubMed 33377609

Lie MU, Winsvold B, Gjerstad J, Matre D, Pedersen LM, Heuch I, Zwart JA, Nilsen KB (2020)
The association between selected genetic variants and individual differences in experimental pain
Scand J Pain, 21 (1), 163-173
DOI 10.1515/sjpain-2020-0091, PubMed 33108341

Publications 2019

Bråten LCH, Rolfsen MP, Espeland A, Wigemyr M, Aßmus J, Froholdt A, Haugen AJ, Marchand GH, Kristoffersen PM, Lutro O, Randen S, Wilhelmsen M, Winsvold BS, Kadar TI, Holmgard TE, Vigeland MD, Vetti N, Nygaard ØP, Lie BA, Hellum C, Anke A, Grotle M, Schistad EI, Skouen JS, Grøvle L et al. (2019)
Efficacy of antibiotic treatment in patients with chronic low back pain and Modic changes (the AIM study): double blind, randomised, placebo controlled, multicentre trial
BMJ, 367, l5654
DOI 10.1136/bmj.l5654, PubMed 31619437

Børte S, Zwart JA, Stensland SØ, Hagen K, Winsvold BS (2019)
Parental migraine in relation to migraine in offspring: Family linkage analyses from the HUNT Study
Cephalalgia, 39 (7), 854-862
DOI 10.1177/0333102419828989, PubMed 30714392

Hagen K, Stovner LJ, Nilsen KB, Kristoffersen ES, Winsvold BS (2019)
The impact of C-reactive protein levels on headache frequency in the HUNT study 2006-2008
BMC Neurol, 19 (1), 229
DOI 10.1186/s12883-019-1462-8, PubMed 31558164

Kogelman LJA, Esserlind AL, Christensen AF, Awasthi S, Ripke S, Ingason A, Davidsson OB, Erikstrup C, Hjalgrim H, Ullum H, Olesen J, Hansen TF, Gudbjartsson D, Gastafsson O, Stefansson K, Stefansson H, Porsteinsdottir U, Andersen S, Banasik K, Brunak S, Buil A, Burgdorf K, Gregor J, Jennum P, Nielsen KR et al. (2019)
Migraine polygenic risk score associates with efficacy of migraine-specific drugs
Neurol.-Genet., 5 (6), e364
DOI 10.1212/NXG.0000000000000364

Kristoffersen ES, Faiz KW, Winsvold BS (2019)
Neurology residents' knowledge of the management of headache
Cephalalgia, 39 (11), 1396-1406
DOI 10.1177/0333102419847973, PubMed 31067081

Kristoffersen ES, Winsvold BS, Faiz KW (2019)
Prestige of neurological disorders among future neurologists in Norway
Acta Neurol Scand, 139 (6), 555-558
DOI 10.1111/ane.13087, PubMed 30851195

Lane JM, Jones SE, Dashti HS, Wood AR, Aragam KG, van Hees VT, Strand LB, Winsvold BS, Wang H, Bowden J, Song Y, Patel K, Anderson SG, Beaumont RN, Bechtold DA, Cade BE, Haas M, Kathiresan S, Little MA, Luik AI, Loudon AS, Purcell S, Richmond RC, Scheer FAJL, Schormair B et al. (2019)
Biological and clinical insights from genetics of insomnia symptoms
Nat Genet, 51 (3), 387-393
DOI 10.1038/s41588-019-0361-7, PubMed 30804566

Liu M, Jiang Y, Wedow R, Li Y, Brazel DM, Chen F, Datta G, Davila-Velderrain J, McGuire D, Tian C, Zhan X, 23andMe Research Team, HUNT All-In Psychiatry, Choquet H, Docherty AR, Faul JD, Foerster JR, Fritsche LG, Gabrielsen ME, Gordon SD, Haessler J, Hottenga JJ, Huang H, Jang SK, Jansen PR et al. (2019)
Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use
Nat Genet, 51 (2), 237-244
DOI 10.1038/s41588-018-0307-5, PubMed 30643251

Wang H, Lane JM, Jones SE, Dashti HS, Ollila HM, Wood AR, van Hees VT, Brumpton B, Winsvold BS, Kantojärvi K, Palviainen T, Cade BE, Sofer T, Song Y, Patel K, Anderson SG, Bechtold DA, Bowden J, Emsley R, Kyle SD, Little MA, Loudon AS, Scheer FAJL, Purcell SM, Richmond RC et al. (2019)
Genome-wide association analysis of self-reported daytime sleepiness identifies 42 loci that suggest biological subtypes
Nat Commun, 10 (1), 3503
DOI 10.1038/s41467-019-11456-7, PubMed 31409809

Aamodt AH, Bjork MH, Alstadhaug KB, Eldoen G, Dueland AN, Poole T, Hagen K, Vetvik KG, Ofte HK, Sonnervik J, Kristoffersen ES, Winsvold BS, Lundqvist C, Sagabraten SO (2019)
Practical management of headache
Tidsskr. Nor. Laegeforen., 139 (7), 617-620

Aamodt AH, Bjørk MH, Alstadhaug KB, Eldøen G, Dueland AN, Poole T, Hagen K, Vetvik KG, Ofte HK, Sønnervik J, Kristoffersen ES, Winsvold BS, Lundqvist C, Sagabråten SO (2019)
Practical management of headache
Tidsskr Nor Laegeforen, 139 (7)
DOI 10.4045/tidsskr.18.0837, PubMed 30969051

Publications 2018

Brainstorm Consortium, Anttila V, Bulik-Sullivan B, Finucane HK, Walters RK, Bras J, Duncan L, Escott-Price V, Falcone GJ, Gormley P, Malik R, Patsopoulos NA, Ripke S, Wei Z, Yu D, Lee PH, Turley P, Grenier-Boley B, Chouraki V, Kamatani Y, Berr C, Letenneur L, Hannequin D, Amouyel P, Boland A et al. (2018)
Analysis of shared heritability in common disorders of the brain
Science, 360 (6395)
DOI 10.1126/science.aap8757, PubMed 29930110

Hagen K, Kristoffersen ES, Winsvold BS, Stovner LJ, Zwart JA (2018)
Remission of chronic headache: An 11-year follow-up study. Data from the Nord-Trøndelag Health Surveys 1995-1997 and 2006-2008
Cephalalgia, 38 (14), 2026-2034
DOI 10.1177/0333102418769940, PubMed 29629599

Hagen K, Åsberg AN, Stovner L, Linde M, Zwart JA, Winsvold BS, Heuch I (2018)
Lifestyle factors and risk of migraine and tension-type headache. Follow-up data from the Nord-Trøndelag Health Surveys 1995-1997 and 2006-2008
Cephalalgia, 38 (13), 1919-1926
DOI 10.1177/0333102418764888, PubMed 29517305

Johnsen MB, Winsvold BS, Børte S, Vie GÅ, Pedersen LM, Storheim K, Skorpen F, Hagen K, Bjørngaard JH, Åsvold BO, Zwart JA (2018)
The causal role of smoking on the risk of headache. A Mendelian randomization analysis in the HUNT study
Eur J Neurol, 25 (9), 1148-e102
DOI 10.1111/ene.13675, PubMed 29747220

Kambur O, Kaunisto MA, Winsvold BS, Wilsgaard T, Stubhaug A, Zwart JA, Kalso E, Nielsen CS (2018)
Genetic variation in P2RX7 and pain tolerance
Pain, 159 (6), 1064-1073
DOI 10.1097/j.pain.0000000000001188, PubMed 29470314

Winsvold BS, Marvik A, Zwart JA, Aamodt AH (2018)
Migraine and stroke
Tidsskr Nor Laegeforen, 138 (4)
DOI 10.4045/tidsskr.17.0347, PubMed 29460580

Åsberg AN, Hagen K, Stovner LJ, Heuch I, Zwart JA, Winsvold BS (2018)
Do incident musculoskeletal complaints influence mortality? The Nord-Trøndelag Health study
PLoS One, 13 (9), e0203925
DOI 10.1371/journal.pone.0203925, PubMed 30265708

Publications 2017

Børte S, Winsvold BS, Stensland SØ, Småstuen MC, Zwart JA (2017)
The effect of foetal growth restriction on the development of migraine and tension-type headache in adulthood. The HUNT Study
PLoS One, 12 (4), e0175908
DOI 10.1371/journal.pone.0175908, PubMed 28410431

Johnsen MB, Vie GÅ, Winsvold BS, Bjørngaard JH, Åsvold BO, Gabrielsen ME, Pedersen LM, Hellevik AI, Langhammer A, Furnes O, Flugsrud GB, Skorpen F, Romundstad PR, Storheim K, Nordsletten L, Zwart JA (2017)
The causal role of smoking on the risk of hip or knee replacement due to primary osteoarthritis: a Mendelian randomisation analysis of the HUNT study
Osteoarthritis Cartilage, 25 (6), 817-823
DOI 10.1016/j.joca.2016.12.021, PubMed 28049019

Winsvold BS, Bettella F, Witoelar A, Anttila V, Gormley P, Kurth T, Terwindt GM, Freilinger TM, Frei O, Shadrin A, Wang Y, Dale AM, van den Maagdenberg AMJM, Chasman DI, Nyholt DR, Palotie A, Andreassen OA, Zwart JA, International Headache Genetics Consortium (2017)
Shared genetic risk between migraine and coronary artery disease: A genome-wide analysis of common variants
PLoS One, 12 (9), e0185663
DOI 10.1371/journal.pone.0185663, PubMed 28957430

Winsvold BS, Palta P, Eising E, Page CM, International Headache Genetics Consortium, van den Maagdenberg AM, Palotie A, Zwart JA (2017)
Epigenetic DNA methylation changes associated with headache chronification: A retrospective case-control study
Cephalalgia, 38 (2), 312-322
DOI 10.1177/0333102417690111, PubMed 28103696

Publications 2016

Eising E, Huisman SMH, Mahfouz A, Vijfhuizen LS, Anttila V, Winsvold BS, Kurth T, Ikram MA, Freilinger T, Kaprio J, Boomsma DI, van Duijn CM, Järvelin MR, Zwart JA, Quaye L, Strachan DP, Kubisch C, Dichgans M, Davey Smith G, Stefansson K, Palotie A, Chasman DI, Ferrari MD, Terwindt GM, de Vries B et al. (2016)
Gene co-expression analysis identifies brain regions and cell types involved in migraine pathophysiology: a GWAS-based study using the Allen Human Brain Atlas
Hum Genet, 135 (4), 425-439
DOI 10.1007/s00439-016-1638-x, PubMed 26899160

Gormley P, Anttila V, Winsvold BS, Palta P, Esko T, Pers TH, Farh KH, Cuenca-Leon E, Muona M, Furlotte NA, Kurth T, Ingason A, McMahon G, Ligthart L, Terwindt GM, Kallela M, Freilinger TM, Ran C, Gordon SG, Stam AH, Steinberg S, Borck G, Koiranen M, Quaye L, Adams HH et al. (2016)
Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine
Nat Genet, 48 (8), 856-66
DOI 10.1038/ng.3598, PubMed 27322543

Gormley P, Anttila V, Winsvold BS, Palta P, Esko T, Pers TH, Farh KH, Cuenca-Leon E, Muona M, Furlotte NA, Kurth T, Ingason A, McMahon G, Ligthart L, Terwindt GM, Kallela M, Freilinger TM, Ran C, Gordon SG, Stam AH, Steinberg S, Borck G, Koiranen M, Quaye L, Adams HH et al. (2016)
Corrigendum: Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine
Nat Genet, 48 (10), 1296
DOI 10.1038/ng1016-1296c, PubMed 27681292

Gormley P, Winsvold BS, Nyholt DR, Kallela M, Chasman DI, Palotie A (2016)
Migraine genetics: from genome-wide association studies to translational insights
Genome Med, 8 (1), 86
DOI 10.1186/s13073-016-0346-4, PubMed 27543003

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
Mult Scler J Exp Transl Clin, 2, 2055217316682976
DOI 10.1177/2055217316682976, PubMed 28607748

Åsberg AN, Stovner LJ, Zwart JA, Winsvold BS, Heuch I, Hagen K (2016)
Chronic musculoskeletal complaints as a predictor of mortality-The HUNT study
Pain, 157 (7), 1443-1447
DOI 10.1097/j.pain.0000000000000537, PubMed 26919487

Publications 2015

Kvalheim S, Sandvik L, Winsvold B, Hagen K, Zwart JA (2015)
Early menarche and chronic widespread musculoskeletal complaints--Results from the HUNT study
Eur J Pain, 20 (3), 458-64
DOI 10.1002/ejp.747, PubMed 26132558

Malik R, Freilinger T, Winsvold BS, Anttila V, Vander Heiden J, Traylor M, de Vries B, Holliday EG, Terwindt GM, Sturm J, Bis JC, Hopewell JC, Ferrari MD, Rannikmae K, Wessman M, Kallela M, Kubisch C, Fornage M, Meschia JF, Lehtimäki T, Sudlow C, Clarke R, Chasman DI, Mitchell BD, Maguire J et al. (2015)
Shared genetic basis for migraine and ischemic stroke: A genome-wide analysis of common variants
Neurology, 84 (21), 2132-45
DOI 10.1212/WNL.0000000000001606, PubMed 25934857

Malik R, Winsvold B, Auffenberg E, Dichgans M, Freilinger T (2015)
The migraine-stroke connection: A genetic perspective
Cephalalgia, 36 (7), 658-68
DOI 10.1177/0333102415621055, PubMed 26660850

Srinivasan S, Bettella F, Mattingsdal M, Wang Y, Witoelar A, Schork AJ, Thompson WK, Zuber V, Schizophrenia Working Group of the Psychiatric Genomics Consortium, The International Headache Genetics Consortium, Winsvold BS, Zwart JA, Collier DA, Desikan RS, Melle I, Werge T, Dale AM, Djurovic S, Andreassen OA (2015)
Genetic Markers of Human Evolution Are Enriched in Schizophrenia
Biol Psychiatry, 80 (4), 284-292
DOI 10.1016/j.biopsych.2015.10.009, PubMed 26681495

Winsvold BS, Nelson CP, Malik R, Gormley P, Anttila V, Vander Heiden J, Elliott KS, Jacobsen LM, Palta P, Amin N, de Vries B, Hämäläinen E, Freilinger T, Ikram MA, Kessler T, Koiranen M, Ligthart L, McMahon G, Pedersen LM, Willenborg C, Won HH, Olesen J, Artto V, Assimes TL, Blankenberg S et al. (2015)
Genetic analysis for a shared biological basis between migraine and coronary artery disease
Neurol Genet, 1 (1), e10
DOI 10.1212/NXG.0000000000000010, PubMed 27066539

Zhao H, Eising E, de Vries B, Vijfhuizen LS, International Headache Genetics Consortium, Anttila V, Winsvold BS, Kurth T, Stefansson H, Kallela M, Malik R, Stam AH, Ikram MA, Ligthart L, Freilinger T, Alexander M, Müller-Myhsok B, Schreiber S, Meitinger T, Aromas A, Eriksson JG, Boomsma DI, van Duijn CM, Zwart JA, Quaye L et al. (2015)
Gene-based pleiotropy across migraine with aura and migraine without aura patient groups
Cephalalgia, 36 (7), 648-57
DOI 10.1177/0333102415591497, PubMed 26660531

Åsberg AN, Stovner LJ, Zwart JA, Winsvold BS, Heuch I, Hagen K (2015)
Migraine as a predictor of mortality: The HUNT study
Cephalalgia, 36 (4), 351-7
DOI 10.1177/0333102415593090, PubMed 26115666

Publications 2014

Fagernæs CF, Heuch I, Zwart JA, Winsvold BS, Linde M, Hagen K (2014)
Blood pressure as a risk factor for headache and migraine: a prospective population-based study
Eur J Neurol, 22 (1), 156-62, e10-1
DOI 10.1111/ene.12547, PubMed 25155744

Louter MA, Fernandez-Morales J, de Vries B, Winsvold B, Anttila V, Fernandez-Cadenas I, Vila-Pueyo M, Sintas C, van Duijn CM, Cormand B, Álvarez-Sabin J, Montaner J, Ferrari MD, van den Maagdenberg A, Palotie A, Zwart JA, Macaya A, Terwindt GM, Pozo-Rosich P (2014)
Candidate-gene association study searching for genetic factors involved in migraine chronification
Cephalalgia, 35 (6), 500-7
DOI 10.1177/0333102414547141, PubMed 25169732

Nyholt DR, International Headache Genetics Consortium, Anttila V, Winsvold BS, Kurth T, Stefansson H, Kallela M, Malik R, Vries Bd, Terwindt GM, Ikram MA, Stam AH, Ligthart L, Freilinger T, Alexander M, Muller-Myhsok B, Schreiber S, Meitinger T, Aromaa A, Eriksson JG, Kaprio J, Boomsma DI, Duijn Cv, Raitakari O, Järvelin MR et al. (2014)
Concordance of genetic risk across migraine subgroups: Impact on current and future genetic association studies
Cephalalgia, 35 (6), 489-99
DOI 10.1177/0333102414547784, PubMed 25179292

Publications 2013

Anttila V, Winsvold BS, Gormley P, Kurth T, Bettella F, McMahon G, Kallela M, Malik R, de Vries B, Terwindt G, Medland SE, Todt U, McArdle WL, Quaye L, Koiranen M, Ikram MA, Lehtimäki T, Stam AH, Ligthart L, Wedenoja J, Dunham I, Neale BM, Palta P, Hamalainen E, Schürks M et al. (2013)
Genome-wide meta-analysis identifies new susceptibility loci for migraine
Nat Genet, 45 (8), 912-917
DOI 10.1038/ng.2676, PubMed 23793025

Jacobsen LM, Winsvold BS, Romundstad S, Pripp AH, Holmen J, Zwart JA (2013)
Urinary albumin excretion as a marker of endothelial dysfunction in migraine sufferers: the HUNT study, Norway
BMJ Open, 3 (8)
DOI 10.1136/bmjopen-2013-003268, PubMed 23943777

Winsvold BS, Sandven I, Hagen K, Linde M, Midthjell K, Zwart JA (2013)
Migraine, headache and development of metabolic syndrome: an 11-year follow-up in the Nord-Trøndelag Health Study (HUNT)
Pain, 154 (8), 1305-11
DOI 10.1016/j.pain.2013.04.007, PubMed 23726372

Publications 2012

Boraska V, Day-Williams A, Franklin CS, Elliott KS, Panoutsopoulou K, Tachmazidou I, Albrecht E, Bandinelli S, Beilin LJ, Bochud M, Cadby G, Ernst F, Evans DM, Hayward C, Hicks AA, Huffman J, Huth C, James AL, Klopp N, Kolcic I, Kutalik Z, Lawlor DA, Musk AW, Pehlic M, Pennell CE et al. (2012)
Genome-wide association study to identify common variants associated with brachial circumference: a meta-analysis of 14 cohorts
PLoS One, 7 (3), e31369
DOI 10.1371/journal.pone.0031369, PubMed 22479309

Freilinger T, Anttila V, de Vries B, Malik R, Kallela M, Terwindt GM, Pozo-Rosich P, Winsvold B, Nyholt DR, van Oosterhout WP, Artto V, Todt U, Hämäläinen E, Fernández-Morales J, Louter MA, Kaunisto MA, Schoenen J, Raitakari O, Lehtimäki T, Vila-Pueyo M, Göbel H, Wichmann E, Sintas C, Uitterlinden AG, Hofman A et al. (2012)
Genome-wide association analysis identifies susceptibility loci for migraine without aura
Nat Genet, 44 (7), 777-82
DOI 10.1038/ng.2307, PubMed 22683712

Johnson M, Brennecke S, Iversen AC, East C, Olsen G, Kent J, Dyer T, Said J, Roten L, Abraham L, Zwart JA, Winsvold B, Håberg A, Huentelman M, Krokan H, Gabrielsen M, Austgulen R, Blangero J, Moses E (2012)
OS046. Genome-wide association scans identify novel maternalsusceptibility loci for preeclampsia
Pregnancy Hypertens, 2 (3), 202
DOI 10.1016/j.preghy.2012.04.047, PubMed 26105260

Publications 2010

Winsvold BS, Hagen K, Aamodt AH, Stovner LJ, Holmen J, Zwart JA (2010)
Headache, migraine and cardiovascular risk factors: the HUNT study
Eur J Neurol, 18 (3), 504-11
DOI 10.1111/j.1468-1331.2010.03199.x, PubMed 20825470

Publications 2001

Lian A, Karisen PJ, Winsvold B (2001)
A re-evaluation of the phonological similarity effect in adults' short-term memory of words and nonwords
Memory, 9 (4-6), 281-99
DOI 10.1080/09658210143000074, PubMed 11594352

Lian A, Karlsen PJ, Winsvold B (2001)
A re-evaluation of the phonological similarity effect in adults' short-term memory of words and nonwords
Memory, 9 (4), 281-299
DOI 10.1080/09658210143000074, PubMed 11747583

Publications 1994

NIELSEN JL, WINSVOLD B (1994)
IMPLEMENTATION OF DIGITAL FILTERS FOR REVERBERATION ENHANCEMENT SYSTEMS
NAM '94 - NORDIC ACOUSTICAL MEETING, PROCEEDINGS, 143-148

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