Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Kristoffer S. Burgdorf"'
Autor:
Isa Amalie Olofsson, Ragnar P. Kristjansson, Ida Callesen, Olafur Davidsson, Bendik Winsvold, Henrik Hjalgrim, Sisse R. Ostrowski, Christian Erikstrup, Mie Topholm Bruun, Ole Birger Pedersen, Kristoffer S. Burgdorf, Karina Banasik, Erik Sørensen, Christina Mikkelsen, Maria Didriksen, Khoa Manh Dinh, Susan Mikkelsen, International Headache Genetic Consortium, DBDS Genomic Consortium, Søren Brunak, Henrik Ullum, Mona Ameri Chalmer, Jes Olesen, Lisette J. A. Kogelman, Thomas Folkmann Hansen
Publikováno v:
Communications Biology, Vol 7, Iss 1, Pp 1-7 (2024)
Abstract Headache disorders are the most common disorders of the nervous system. The lifetime prevalence of headache disorders show that some individuals never experience headache. The etiology of complete freedom from headache is not known. To asses
Externí odkaz:
https://doaj.org/article/6ebd151e5db14c23a2d72ad9be537a6a
Autor:
Steven Bell, Andreas S. Rigas, Magnus K. Magnusson, Egil Ferkingstad, Elias Allara, Gyda Bjornsdottir, Anna Ramond, Erik Sørensen, Gisli H. Halldorsson, Dirk S. Paul, Kristoffer S. Burgdorf, Hannes P. Eggertsson, Joanna M. M. Howson, Lise W. Thørner, Snaedis Kristmundsdottir, William J. Astle, Christian Erikstrup, Jon K. Sigurdsson, Dragana Vuckovic, Khoa M. Dinh, Vinicius Tragante, Praveen Surendran, Ole B. Pedersen, Brynjar Vidarsson, Tao Jiang, Helene M. Paarup, Pall T. Onundarson, Parsa Akbari, Kaspar R. Nielsen, Sigrun H. Lund, Kristinn Juliusson, Magnus I. Magnusson, Michael L. Frigge, Asmundur Oddsson, Isleifur Olafsson, Stephen Kaptoge, Henrik Hjalgrim, Gudmundur Runarsson, Angela M. Wood, Ingileif Jonsdottir, Thomas F. Hansen, Olof Sigurdardottir, Hreinn Stefansson, David Rye, DBDS Genomic Consortium, James E. Peters, David Westergaard, Hilma Holm, Nicole Soranzo, Karina Banasik, Gudmar Thorleifsson, Willem H. Ouwehand, Unnur Thorsteinsdottir, David J. Roberts, Patrick Sulem, Adam S. Butterworth, Daniel F. Gudbjartsson, John Danesh, Søren Brunak, Emanuele Di Angelantonio, Henrik Ullum, Kari Stefansson
Publikováno v:
Communications Biology, Vol 4, Iss 1, Pp 1-14 (2021)
Bell et al. report 46 new loci associated with biomarkers of iron homeostasis, including ferritin levels, iron binding capacity, and iron saturation, in the Icelandic, Danish and UK populations. The associated loci point to new iron-regulating protei
Externí odkaz:
https://doaj.org/article/35ea0870b7404ce2af991707d7676fe3
Autor:
Astros Th. Skuladottir, Gyda Bjornsdottir, Gudmar Thorleifsson, G. Bragi Walters, Muhammad Sulaman Nawaz, Kristjan Helgi Swerford Moore, Pall I. Olason, Thorgeir E. Thorgeirsson, Brynja Sigurpalsdottir, Gardar Sveinbjornsson, Hannes P. Eggertsson, Sigurdur H. Magnusson, Asmundur Oddsson, Anna Bjornsdottir, Arnor Vikingsson, Olafur A. Sveinsson, Maria G. Hrafnsdottir, Gudrun R. Sigurdardottir, Bjarni V. Halldorsson, Thomas Folkmann Hansen, Helene Paarup, Christian Erikstrup, Kaspar Nielsen, Mads Klokker, Mie Topholm Bruun, Erik Sorensen, Karina Banasik, Kristoffer S. Burgdorf, Ole Birger Pedersen, Henrik Ullum, Ingileif Jonsdottir, Hreinn Stefansson, Kari Stefansson
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-8 (2021)
Abstract Bell’s palsy is the most common cause of unilateral facial paralysis and is defined as an idiopathic and acute inability to control movements of the facial muscles on the affected side. While the pathogenesis remains unknown, previous stud
Externí odkaz:
https://doaj.org/article/3d2fc42f3e4e427a80a49c09b7408bbb
Autor:
Maria Didriksen, Muhammad Sulaman Nawaz, Joseph Dowsett, Steven Bell, Christian Erikstrup, Ole B. Pedersen, Erik Sørensen, Poul J. Jennum, Kristoffer S. Burgdorf, Brendan Burchell, Adam S. Butterworth, Nicole Soranzo, David B. Rye, Lynn Marie Trotti, Prabhjyot Saini, Lilja Stefansdottir, Sigurdur H. Magnusson, Gudmar Thorleifsson, Thordur Sigmundsson, Albert P. Sigurdsson, Katja Van Den Hurk, Franke Quee, Michael W. T. Tanck, Willem H. Ouwehand, David J. Roberts, Eric J. Earley, Michael P. Busch, Alan E. Mast, Grier P. Page, John Danesh, Emanuele Di Angelantonio, Hreinn Stefansson, Henrik Ullum, Kari Stefansson
Publikováno v:
Communications Biology, Vol 3, Iss 1, Pp 1-9 (2020)
Didriksen, Nawaz, et al. identify three novel genetic risk variants for restless legs syndrome and confirm 19 out of 20 previously reported variants through a genome-wide association meta-analysis including nearly half a million individuals. Using ex
Externí odkaz:
https://doaj.org/article/b804eef352554c768c94ad94c5a8a74a
Autor:
Mattias A.S. Henning, Kristina S. Ibler, Isabella Loft, Henrik Ullum, Christian Erikstrup, Kaspar R. Nielsen, Mie Topholm Bruun, Henrik Hjalgrim, Erik Sørensen, Kristoffer S. Burgdorf, Susan Mikkelsen, Thomas F. Hansen, Ole B. Pedersen, Gregor B.E. Jemec
Publikováno v:
Acta Dermato-Venereologica, Vol 101, Iss 4, p adv00435 (2021)
The risk factors and disease implications of hyperhidrosis are unknown. The objectives of this retrospective cohort study were to estimate the prevalence of hyperhidrosis and to compare demographic, lifestyle, and socioeconomic parameters in bloo
Externí odkaz:
https://doaj.org/article/9373b88bcc344eee92cdae9a7a08c970
Autor:
Maria Didriksen, Thomas F Hansen, Lise W Thørner, Kristoffer S Burgdorf, Christian Erikstrup, Ole B Pedersen, Helene M Paarup, Kaspar R Nielsen, Henrik Hjalgrim, Erik Sørensen, Henrik Ullum
Publikováno v:
Cephalalgia Reports, Vol 1 (2018)
Migraine and restless legs syndrome (RLS) are common disorders that are associated with a high level of individual suffering and major comorbidities. The aetiologies of the disorders are largely unknown, although both migraine and RLS have been linke
Externí odkaz:
https://doaj.org/article/e5a79fdc46fd4bc3adbad27fbd3f4416
Autor:
Mona Ameri Chalmer, Ida Callesen, Lisette J.A. Kogelman, Charlotte Grønvold Christensen, Tanya Ramdal Techlo, Peter L. Møller, Olafur B. Davidsson, Isa A. Olofsson, Michael Schwinn, Susan Mikkelsen, Khoa Manh Dinh, Kaspar Nielsen, Mie Topholm, Christian Erikstrup, Sisse Rye Ostrowski, Ole Birger Pedersen, Henrik Hjalgrim, Karina Banasik, Kristoffer S. Burgdorf, Mette Nyegaard, Jes Olesen, Thomas Folkmann Hansen
Publikováno v:
SSRN Electronic Journal.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e8c59d10fb09ae37f5601ea7eb5c7ffd
https://doi.org/10.2139/ssrn.4031580
https://doi.org/10.2139/ssrn.4031580
Autor:
Erik, Sørensen, Andreas S, Rigas, Lise W, Thørner, Kristoffer S, Burgdorf, Ole B, Pedersen, Mikkel S, Petersen, Henrik, Hjalgrim, Christian, Erikstrup, Henrik, Ullum
Publikováno v:
Transfusion. 56(3)
Many biologic functions depend on sufficient iron levels, and iron deficiency is especially common among blood donors. Genetic variants associated with iron levels have been identified, but the impact of genetic variation on iron levels among blood d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f0b6fda55890872b7f4ea80a74c565b9
https://pubmed.ncbi.nlm.nih.gov/26597663
https://pubmed.ncbi.nlm.nih.gov/26597663
Autor:
Dorit P, Zobel, Camilla H, Andreasen, Kristoffer S, Burgdorf, Ehm A, Andersson, Annelli, Sandbaek, Torsten, Lauritzen, Knut, Borch-Johnsen, Torben, Jørgensen, Shiro, Maeda, Yusuke, Nakamura, Hans, Eiberg, Oluf, Pedersen, Oluf, Pederse, Torben, Hansen
Publikováno v:
Zobel, D, Andreasen, C, Burgdorf, K, Andersson, E, Sandbæk, A, Lauritzen, T, Borch-Johnsen, K, Jørgensen, T, Maeda, S, Nakamura, Y, Eiberg, H, Pedersen, O & Hansen, T 2009, ' Variation in the gene encoding Kruppel-like factor 7 influences body fat: studies of 14,818 Danes ', European Journal of Endocrinology . https://doi.org/10.1530/EJE-08-0688
Zobel, D P, Andreasen, C H, Burgdorf, K S, Andersson, E A, Sandbaek, A, Lauritzen, T, Borch-Johnsen, K, Jørgensen, T, Maeda, S, Nakamura, Y, Eiberg, H, Pederse, O & Hansen, T 2009, ' Variation in the gene encoding Krüppel-like factor 7 influences body fat: studies of 14 818 Danes ', European Journal of Endocrinology, vol. 160, no. 4, pp. 603-9 . https://doi.org/10.1530/EJE-08-0688
Zobel, D P, Andreasen, C H, Burgdorf, K S, Andersson, E A, Sandbaek, A, Lauritzen, T, Borch-Johnsen, K, Jørgensen, T, Maeda, S, Nakamura, Y, Eiberg, H, Pederse, O & Hansen, T 2009, ' Variation in the gene encoding Krüppel-like factor 7 influences body fat: studies of 14 818 Danes ', European Journal of Endocrinology, vol. 160, no. 4, pp. 603-9 . https://doi.org/10.1530/EJE-08-0688
ObjectiveKLF7encodes Krüppel-like factor (KLF) 7, a member of the KLF family of transcription factors, initially shown to play important roles in cellular development and differentiation, and reported to be specifically involved in adipogenesis. Sev
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5928692cf2b4ef8ccc492e97cad653a4
https://pure.au.dk/portal/da/publications/variation-in-the-gene-encoding-kruppellike-factor-7-influences-body-fat-studies-of-14818-danes(32919240-057f-11de-8317-000ea68e967b).html
https://pure.au.dk/portal/da/publications/variation-in-the-gene-encoding-kruppellike-factor-7-influences-body-fat-studies-of-14818-danes(32919240-057f-11de-8317-000ea68e967b).html
Autor:
Mattias A S Henning, Kristina S Ibler, Henrik Ullum, Christian Erikstrup, Mie T Bruun, Kristoffer S Burgdorf, Khoa M Dinh, Andreas Rigas, Lise W Thørner, Ole B Pedersen, Gregor B Jemec
Publikováno v:
PLoS ONE, Vol 16, Iss 6, p e0252462 (2021)
BackgroundThe pathophysiology of xerosis depends on extrinsic and intrinsic exposures. Residential hard water may constitute such an exposure.ObjectivesTo estimate the prevalence of xerosis and to compare water hardness exposure in blood donors with
Externí odkaz:
https://doaj.org/article/d35114992e0549a48dcbb9ba4b8a6ba0