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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1989 1
1990 1
1991 1
1992 3
1993 4
1994 7
1995 2
1996 1
1998 1
1999 5
2000 3
2001 7
2002 1
2003 4
2004 8
2005 4
2006 11
2007 9
2008 4
2009 3
2010 5
2011 4
2012 4
2013 2
2014 2
2015 9
2016 6
2017 3
2018 6
2019 1
2020 1
2021 3
2022 4
2023 1
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120 results
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Page 1
Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk alleles.
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, Häppölä P, Hottenga JJ, Hrafnsdottir MG, Hveem K, Johnsen MB, Kähönen M, Kristoffersen ES, Kurth T, Lehtimäki T, Lighart L, Magnusson SH, Malik R, Pedersen OB, Pelzer N, Penninx BWJH, Ran C, Ridker PM, Rosendaal FR, Sigurdardottir GR, Skogholt AH, Sveinsson OA, Thorgeirsson TE, Ullum H, Vijfhuizen LS, Widén E, van Dijk KW; International Headache Genetics Consortium; HUNT All-in Headache; Danish Blood Donor Study Genomic Cohort; Aromaa A, Belin AC, Freilinger T, Ikram MA, Järvelin MR, Raitakari OT, Terwindt GM, Kallela M, Wessman M, Olesen J, Chasman DI, Nyholt DR, Stefánsson H, Stefansson K, van den Maagdenberg AMJM, Hansen TF, Ripatti S, Zwart JA, Palotie A, Pirinen M. Hautakangas H, et al. Among authors: wessman m. Nat Genet. 2022 Feb;54(2):152-160. doi: 10.1038/s41588-021-00990-0. Epub 2022 Feb 3. Nat Genet. 2022. PMID: 35115687 Free PMC article.
Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine.
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, Lehtimäki T, Sarin AP, Wedenoja J, Hinds DA, Buring JE, Schürks M, Ridker PM, Hrafnsdottir MG, Stefansson H, Ring SM, Hottenga JJ, Penninx BW, Färkkilä M, Artto V, Kaunisto M, Vepsäläinen S, Malik R, Heath AC, Madden PA, Martin NG, Montgomery GW, Kurki MI, Kals M, Mägi R, Pärn K, Hämäläinen E, Huang H, Byrnes AE, Franke L, Huang J, Stergiakouli E, Lee PH, Sandor C, Webber C, Cader Z, Muller-Myhsok B, Schreiber S, Meitinger T, Eriksson JG, Salomaa V, Heikkilä K, Loehrer E, Uitterlinden AG, Hofman A, van Duijn CM, Cherkas L, Pedersen LM, Stubhaug A, Nielsen CS, Männikkö M, Mihailov E, Milani L, Göbel H, Esserlind AL, Christensen AF, Hansen TF, Werge T; International Headache Genetics Consortium; Kaprio J, Aromaa AJ, Raitakari O, Ikram MA, Spector T, Järvelin MR, Metspalu A, Kubisch C, Strachan DP, Ferrari MD, Belin AC, Dichgans M, Wessman M, van den Maagdenberg AM, Zwart JA, Boomsma DI, Smith GD, Stefansson K, E… See abstract for full author list ➔ Gormley P, et al. Among authors: wessman m. Nat Genet. 2016 Aug;48(8):856-66. doi: 10.1038/ng.3598. Epub 2016 Jun 20. Nat Genet. 2016. PMID: 27322543 Free PMC article.
Genetics of migraine.
Anttila V, Wessman M, Kallela M, Palotie A. Anttila V, et al. Among authors: wessman m. Handb Clin Neurol. 2018;148:493-503. doi: 10.1016/B978-0-444-64076-5.00031-4. Handb Clin Neurol. 2018. PMID: 29478595 Review.
Migraine: a complex genetic disorder.
Wessman M, Terwindt GM, Kaunisto MA, Palotie A, Ophoff RA. Wessman M, et al. Lancet Neurol. 2007 Jun;6(6):521-32. doi: 10.1016/S1474-4422(07)70126-6. Lancet Neurol. 2007. PMID: 17509487 Review.
[The significance of HIV to bone mineral density].
Wessman M, Weis N, Katzenstein TL, Lebech AM, Thorsteinsson K, Hansen AE, Jensen JB. Wessman M, et al. Ugeskr Laeger. 2017 Sep 4;179(36):V05170420. Ugeskr Laeger. 2017. PMID: 28874254 Free article. Review. Danish.
NCOR2 is a novel candidate gene for migraine-epilepsy phenotype.
Nuottamo ME, Häppölä P, Artto V, Hautakangas H, Pirinen M, Hiekkalinna T, Ellonen P, Lepistö M, Hämäläinen E; International Headache Genetics Consortium (IHGC), FinnGenConsortium; Siren A, Lehesjoki AE, Kallela M, Palotie A, Kaunisto MA, Wessman M. Nuottamo ME, et al. Among authors: wessman m. Cephalalgia. 2022 Jun;42(7):631-644. doi: 10.1177/03331024211068065. Epub 2022 Feb 15. Cephalalgia. 2022. PMID: 35166138
The molecular genetics of migraine.
Wessman M, Kaunisto MA, Kallela M, Palotie A. Wessman M, et al. Ann Med. 2004;36(6):462-73. doi: 10.1080/07853890410018060. Ann Med. 2004. PMID: 15513297 Review.
High-throughput pedigree drawing.
Mäkinen VP, Parkkonen M, Wessman M, Groop PH, Kanninen T, Kaski K. Mäkinen VP, et al. Among authors: wessman m. Eur J Hum Genet. 2005 Aug;13(8):987-9. doi: 10.1038/sj.ejhg.5201430. Eur J Hum Genet. 2005. PMID: 15870825
HIV disclosure and stigma among women living with HIV in Denmark.
Wessman M, Thorsteinsson K, Storgaard M, Rönsholt FF, Johansen IS, Pedersen G, Nielsen LN, Wies N, Katzenstein TL, Lebech AM. Wessman M, et al. J Virus Erad. 2017 Jul 1;3(3):140-144. J Virus Erad. 2017. PMID: 28758021 Free PMC article.
120 results