المؤلفون: International Headache Genetics Consortium, HUNT All-in Headache, Danish Blood Donor Study Genomic Cohort

المساهمون: Faculty of Medicine, Other departments

مصطلحات موضوعية: Genarannsóknir, Taugasjúkdómafræði, Mígreni, Gen, Krabbameinslæknisfræði, Migraine Disorders, Genetic Predisposition to Disease, Genome-Wide Association Study, Humans, Migraine Disorders/genetics, Molecular Sequence Annotation, Genetic Loci, Case-Control Studies, Central Nervous System/metabolism, Migraine with Aura/genetics, Alleles, Polymorphism, Single Nucleotide, Cardiovascular System/metabolism, Quantitative Trait Loci, Genetics

وصف الملف: 152-160

العلاقة: Nature Genetics; 54(2); http://www.scopus.com/inward/record.url?scp=85124577579&partnerID=8YFLogxKTest; International Headache Genetics Consortium , HUNT All-in Headache & Danish Blood Donor Study Genomic Cohort 2022 , ' Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk alleles ' , Nature Genetics , vol. 54 , no. 2 , pp. 152-160 . https://doi.org/10.1038/s41588-021-00990-0Test; 422bc099-92e0-4953-8829-d0416008242e; 85124577579; unpaywall: 10.1038/s41588-021-00990-0; https://hdl.handle.net/20.500.11815/3029Test

الإتاحة: https://doi.org/20.500.11815/3029Test
https://doi.org/10.1038/s41588-021-00990-0Test
https://hdl.handle.net/20.500.11815/3029Test

المؤلفون: Hautakangas, Heidi, Winsvold, Bendik S, Ruotsalainen, Sanni E, Bjornsdottir, Gyda, Harder, Aster V E, Kogelman, Lisette J A, Thomas, Laurent F, Noordam, Raymond, Benner, Christian, Gormley, Padhraig, Artto, Ville, Banasik, Karina, Bjornsdottir, Anna, Boomsma, Dorret I, Brumpton, Ben M, Burgdorf, Kristoffer Sølvsten, Buring, Julie E, Chalmer, Mona Ameri, de Boer, Irene, Dichgans, Martin, Erikstrup, Christian, Färkkilä, Markus, Garbrielsen, Maiken Elvestad, Ghanbari, Mohsen, Hagen, Knut, Häppölä, Paavo, Hottenga, Jouke-Jan, Hrafnsdottir, Maria G, Hveem, Kristian, Johnsen, Marianne Bakke, Kähönen, Mika, Kristoffersen, Espen S, Kurth, Tobias, Lehtimäki, Terho, Lighart, Lannie, Magnusson, Sigurdur H, Malik, Rainer, Pedersen, Ole Birger, Pelzer, Nadine, Penninx, Brenda W J H, Ran, Caroline, Ridker, Paul M, Rosendaal, Frits R, Sigurdardottir, Gudrun R, Skogholt, Anne Heidi, Sveinsson, Olafur A, Thorgeirsson, Thorgeir E, Ullum, Henrik, Vijfhuizen, Lisanne S, Widén, Elisabeth, van Dijk, Ko Willems, Aromaa, Arpo, Belin, Andrea Carmine, Freilinger, Tobias, Ikram, M Arfan, Järvelin, Marjo-Riitta, Raitakari, Olli T, Terwindt, Gisela M, Kallela, Mikko, Wessman, Maija, Olesen, Jes, Chasman, Daniel I, Nyholt, Dale R, Stefánsson, Hreinn, Stefansson, Kari, van den Maagdenberg, Arn M J M, Hansen, Thomas Folkmann, Ripatti, Samuli, Zwart, John-Anker, Palotie, Aarno, Pirinen, Matti

المساهمون: 1Institute for Molecular Medicine Finland (FIMM), Helsinki Institute of Life Science (HiLIFE), University of Helsinki, Helsinki, Finland. 2Department of Research, Innovation and Education, Division of Clinical Neuroscience, Oslo University Hospital, Oslo, Norway. 3K. G. Jebsen Center for Genetic Epidemiology, Department of Public Health and Nursing, Faculty of Medicine and Health Sciences, Norwegian University of Science and Technology, Trondheim, Norway. 4Department of Neurology, Oslo University Hospital, Oslo, Norway. 5deCODE genetics/Amgen Inc., Reykjavik, Iceland. 6Department of Neurology, Leiden University Medical Center, Leiden, the Netherlands. 7Department of Human Genetics, Leiden University Medical Center, Leiden, the Netherlands. 8Danish Headache Center, Department of Neurology, Copenhagen University Hospital, Copenhagen, Denmark. 9Department of Clinical and Molecular Medicine, Norwegian University of Science and Technology, Trondheim, Norway. 10BioCore - Bioinformatics Core Facility, Norwegian University of Science and Technology, Trondheim, Norway. 11Clinic of Laboratory Medicine, St. Olavs Hospital, Trondheim University Hospital, Trondheim, Norway. 12Department of Internal Medicine, Section of Gerontology and Geriatrics, Leiden University Medical Center, Leiden, the Netherlands. 13GlaxoSmithKline, Cambridge, MA, USA. 14Department of Neurology, Helsinki University Central Hospital, Helsinki, Finland. 15Novo Nordic Foundation Center for Protein Research, Copenhagen University, Copenhagen, Denmark. 16Neurology Private Practice, Laeknasetrid, Reykjavik, Iceland. 17Netherlands Twin Register, Department of Biological Psychology, Vrije Universiteit, Amsterdam, the Netherlands. 18Department of Clinical Immunology, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark. 19Division of Preventive Medicine, Brigham and Women's Hospital, Boston, MA, USA. 20Harvard Medical School, Boston, MA, USA. 21Institute for Stroke and Dementia Research, University Hospital, LMU Munich, Munich, Germany. 22Munich Cluster for Systems Neurology (Synergy), Munich, Germany. 23Department of Clinical Immunology, Aarhus University Hospital, Aarhus, Denmark. 24Department of Epidemiology, Erasmus University Medical Center, Rotterdam, the Netherlands. 25Department of Neuromedicine and Movement Science, Faculty of Medicine and Health Sciences, Norwegian University of Science and Technology (NTNU), Trondheim, Norway. 26Clinical Research Unit Central Norway, St. Olavs University Hospital, Trondheim, Norway. 27Landspitali University Hospital, Reykjavik, Iceland. 28HUNT Research Center, Department of Public Health and Nursing, Faculty of Medicine and Health Sciences, Norwegian University of Science and Technology, Trondheim, Norway. 29Institute of Clinical Medicine, Faculty of Medicine, University of Oslo, Oslo, Norway. 30Research and Communication Unit for Musculoskeletal Health (FORMI), Department of Research, Innovation and Education, Division of Clinical Neuroscience, Oslo University Hospital, Oslo, Norway. 31Department of Clinical Physiology, Tampere University Hospital, and Finnish Cardiovascular Research Center - Tampere, Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland. 32Department of General Practice, Institute of Health and Society, University of Oslo, Oslo, Norway. 33Department of Neurology, Akershus University Hospital, Lørenskog, Norway. 34Institute of Public Health, Charité - Universitätsmedizin Berlin, Berlin, Germany. 35Department of Clinical Chemistry, Fimlab Laboratories, and Finnish Cardiovascular Research Center - Tampere, Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland. 36Department of Clinical Immunology, Zealand University Hospital, Køge, Denmark. 37Department of Psychiatry, Amsterdam UMC, Vrije Universiteit, Amsterdam Public Health Research Institute, Amsterdam, the Netherlands. 38GGZ inGeest Specialized Mental Health Care, Amsterdam, the Netherlands. 39Department of Neuroscience, Karolinska Institutet, Stockholm, Sweden. 40Department of Clinical Epidemiology, Leiden University Medical Center, Leiden, the Netherlands. 41Department of Internal Medicine, Division of Endocrinology, Leiden University Medical Center, Leiden, the Netherlands. 42National Public Health Institute (Finnish Institute for Health and Welfare - THL), Helsinki, Finland. 43Klinikum Passau, Department of Neurology, Passau, Germany. 44Centre of Neurology, Hertie Institute for Clinical Brain Research, Tuebingen, Germany. 45Department of Epidemiology and Biostatistics, MRC-PHE Centre for Environment and Health, School of Public Health, Imperial College London, London, UK. 46Center for Life Course Health Research, Faculty of Medicine, University of Oulu, Oulu, Finland. 47Unit of Primary Health Care, Oulu University Hospital, Oulu, Finland. 48Department of Life Sciences, College of Health and Life Sciences, Brunel University London, London, UK. 49Centre for Population Health Research, University of Turku and Turku University Hospital, Turku, Finland. 50Research Centre of Applied and Preventive Cardiovascular Medicine, University of Turku, Turku, Finland. 51Department of Clinical Physiology and Nuclear Medicine, Turku University Hospital, Turku, Finland. 52Folkhälsan Research Center, Helsinki, Finland. 53School of Biomedical Sciences and Centre for Genomics and Personalised Health, Faculty of Health, Queensland University of Technology, Brisbane, QLD, Australia. 54Broad Institute of MIT and Harvard, Cambridge, MA, USA. 55Department of Public Health, University of Helsinki, Helsinki, Finland. 56Analytic and Translational Genetics Unit, Department of Medicine, Department of Neurology and Department of Psychiatry, Massachusetts General Hospital, Boston, MA, USA. 57The Stanley Center for Psychiatric Research and Program in Medical and Population Genetics, The Broad Institute of MIT and Harvard, Cambridge, MA, USA. 58Institute for Molecular Medicine Finland (FIMM), Helsinki Institute of Life Science (HiLIFE), University of Helsinki, Helsinki, Finland. matti.pirinen@helsinki.fi. 59Department of Public Health, University of Helsinki, Helsinki, Finland. matti.pirinen@helsinki.fi. 60Department of Mathematics and Statistics, University of Helsinki, Helsinki, Finland. matti.pirinen@helsinki.fi.

المصدر: Nature genetics ; 54 ; 2 ; 152 ; 160 ; United States

مصطلحات موضوعية: Mígreni, Genarannsóknir, Gen, Migraine Disorders, Genetic Predisposition to Disease, Genome-Wide Association Study

العلاقة: https://www.nature.com/articles/s41588-021-00990-0Test; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8837554Test/; Hautakangas H, Winsvold BS, Ruotsalainen SE, et al. Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk alleles. Nat Genet. 2022;54(2):152-160. doi:10.1038/s41588-021-00990-0; http://hdl.handle.net/2336/622124Test; Nature genetics

الإتاحة: https://doi.org/10.1038/s41588-021-00990-0Test
http://hdl.handle.net/2336/622124Test

المؤلفون: Bjornsdottir, Gyda, Stefansdottir, Lilja, Thorleifsson, Gudmar, Sulem, Patrick, Norland, Kristjan, Ferkingstad, Egil, Oddsson, Asmundur, Zink, Florian, Lund, Sigrun H, Nawaz, Muhammad S, Bragi Walters, G, Skuladottir, Astros Th, Gudjonsson, Sigurjon A, Einarsson, Gudmundur, Halldorsson, Gisli H, Bjarnadottir, Valgerdur, Sveinbjornsson, Gardar, Helgadottir, Anna, Styrkarsdottir, Unnur, Gudmundsson, Larus J, Pedersen, Ole B, Hansen, Thomas Folkmann, Werge, Thomas, Banasik, Karina, Troelsen, Anders, Skou, Soren T, Thørner, Lise Wegner, Erikstrup, Christian, Nielsen, Kaspar Rene, Mikkelsen, Susan, Jonsdottir, Ingileif, Bjornsson, Aron, Olafsson, Ingvar H, Ulfarsson, Elfar, Blondal, Josep, Vikingsson, Arnor, Brunak, Soren, Ostrowski, Sisse R, Ullum, Henrik, Thorsteinsdottir, Unnur, Stefansson, Hreinn, Gudbjartsson, Daniel F, Thorgeirsson, Thorgeir E, Stefansson, Kari

المساهمون: 1deCODE Genetics/Amgen, Inc., Reykjavik, Iceland. gyda.bjornsdottir@decode.is. 2deCODE Genetics/Amgen, Inc., Reykjavik, Iceland. 3Faculty of Medicine, School of Health Sciences, University of Iceland, Reykjavik, Iceland. 4School of Engineering and Natural Sciences, University of Iceland, Reykjavik, Iceland. 5Landspitali University Hospital, Reykjavik, Iceland. 6Department of Clinical Immunology, Zealand University Hospital, Køge, Denmark. 7Department of Clinical Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark. 8Danish Headache Center, Dept. Neurology, Rigshospitalet-Glostrup, Glostrup, Denmark. 9Novo Nordisk Foundation Center for Protein Research, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark. 10Institute of Biological Psychiatry, Mental Health Services, Copenhagen University Hospital, Copenhagen, Denmark. 11Lundbeck Foundation for GeoGenetics, GLOBE Institute, University of Copenhagen, Copenhagen, Denmark. 12Department of Orthopaedic Surgery, CAG ROAD-Research OsteoArthritis Denmark, Copenhagen University Hospital, Hvidovre, Denmark. 13Research Unit for Musculoskeletal Function and Physiotherapy, Department of Sports Science and Clinical Biomechanics, University of Southern Denmark, Odense, Denmark. 14The Research Unit PROgrez, Department of Physiotherapy and Occupational Therapy, Næstved-Slagelse-Ringsted Hospitals, Næstved, Denmark. 15Department of Clinical Immunology, Copenhagen University Hospital, Copenhagen, Denmark. 16Department of Clinical Immunology, Aarhus University Hospital, Aarhus, Denmark. 17Department of Clinical Immunology, Aalborg University Hospital, Aalborg, Denmark. 18Department of Neurosurgery, Landspitali University Hospital, Reykjavik, Iceland. 19Health Care Institution of West Iceland, Stykkisholmur, Iceland. 20Statens Serum Institut, Copenhagen, Copenhagen, Denmark. 21deCODE Genetics/Amgen, Inc., Reykjavik, Iceland. thorgeir.thorgeirsson@decode.is. 22deCODE Genetics/Amgen, Inc., Reykjavik, Iceland. kstefans@decode.is. 23Faculty of Medicine, School of Health Sciences, University of Iceland, Reykjavik, Iceland. kstefans@decode.is.

المصدر: Nature communications ; 13 ; 1 ; 634 ; England

مصطلحات موضوعية: Bakverkir, Genarannsóknir, Gen, Intervertebral Disc Degeneration, Intervertebral Disc Displacement, Intervertebral Disc, Genome-Wide Association Study, Back Pain, Bone and Bones, Pain

العلاقة: https://www.nature.com/articles/s41467-022-28167-1Test; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8810832Test/; Bjornsdottir G, Stefansdottir L, Thorleifsson G, et al. Rare SLC13A1 variants associate with intervertebral disc disorder highlighting role of sulfate in disc pathology. Nat Commun. 2022;13(1):634. Published 2022 Feb 2. doi:10.1038/s41467-022-28167-1; http://hdl.handle.net/2336/622123Test; Nature communications

الإتاحة: https://doi.org/10.1038/s41467-022-28167-1Test
http://hdl.handle.net/2336/622123Test

المؤلفون: Arnadottir, Gudny A, Oddsson, Asmundur, Jensson, Brynjar O, Gisladottir, Svanborg, Simon, Mariella T, Arnthorsson, Asgeir O, Katrinardottir, Hildigunnur, Fridriksdottir, Run, Ivarsdottir, Erna V, Jonasdottir, Adalbjorg, Jonasdottir, Aslaug, Barrick, Rebekah, Saemundsdottir, Jona, le Roux, Louise, Oskarsson, Gudjon R, Asmundsson, Jurate, Steffensen, Thora, Gudmundsson, Kjartan R, Ludvigsson, Petur, Jonsson, Jon J, Masson, Gisli, Jonsdottir, Ingileif, Holm, Hilma, Jonasson, Jon G, Magnusson, Olafur Th, Thorarensen, Olafur, Abdenur, Jose, Norddahl, Gudmundur L, Gudbjartsson, Daniel F, Bjornsson, Hans T, Thorsteinsdottir, Unnur, Sulem, Patrick, Stefansson, Kari

المساهمون: 1deCODE Genetics/Amgen, Inc., Reykjavik, Iceland. 2Faculty of Medicine, University of Iceland, Reykjavik, Iceland. 3Department of Genetics and Molecular Medicine, The National University Hospital of Iceland, Reykjavik, Iceland. 4Division of Metabolic Disorders, Children's Hospital of Orange County, Orange, CA, USA. 5Department of Pathology, The National University Hospital of Iceland, Reykjavik, Iceland. 6Children's Hospital Iceland, The National University Hospital of Iceland, Reykjavik, Iceland. 7School of Engineering and Natural Sciences, University of Iceland, Reykjavik, Iceland. 8Department of Genetic Medicine, Johns Hopkins University, Baltimore, MD, USA. 9deCODE Genetics/Amgen, Inc., Reykjavik, Iceland. patrick.sulem@decode.is. 10deCODE Genetics/Amgen, Inc., Reykjavik, Iceland. kari.stefansson@decode.is. 11Faculty of Medicine, University of Iceland, Reykjavik, Iceland. kari.stefansson@decode.is.

المصدر: Nature communications ; 13 ; 1 ; 705 ; England

مصطلحات موضوعية: Greindarskerðing, Genarannsóknir, Gen, Intellectual Disability, Genetic Predisposition to Disease

العلاقة: https://www.nature.com/articles/s41467-022-28330-8Test; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8817032Test/; Arnadottir GA, Oddsson A, Jensson BO, et al. Population-level deficit of homozygosity unveils CPSF3 as an intellectual disability syndrome gene. Nat Commun. 2022;13(1):705. Published 2022 Feb 4. doi:10.1038/s41467-022-28330-8; http://hdl.handle.net/2336/622125Test; Nature communications

الإتاحة: https://doi.org/10.1038/s41467-022-28330-8Test
http://hdl.handle.net/2336/622125Test

المؤلفون: Skuladottir, Astros Th, Bjornsdottir, Gyda, Nawaz, Muhammad Sulaman, Petersen, Hannes, Rognvaldsson, Solvi, Moore, Kristjan Helgi Swerford, Olafsson, Pall I, Magnusson, Sigurður H, Bjornsdottir, Anna, Sveinsson, Olafur A, Sigurdardottir, Gudrun R, Saevarsdottir, Saedis, Ivarsdottir, Erna V, Stefansdottir, Lilja, Gunnarsson, Bjarni, Muhlestein, Joseph B, Knowlton, Kirk U, Jones, David A, Nadauld, Lincoln D, Hartmann, Annette M, Rujescu, Dan, Strupp, Michael, Walters, G Bragi, Thorgeirsson, Thorgeir E, Jonsdottir, Ingileif, Holm, Hilma, Thorleifsson, Gudmar, Gudbjartsson, Daniel F, Sulem, Patrick, Stefansson, Hreinn, Stefansson, Kari

المساهمون: 1deCODE genetics/Amgen Inc., Reykjavik, Iceland. astros.skuladottir@decode.is. 2deCODE genetics/Amgen Inc., Reykjavik, Iceland. 3Faculty of Medicine, University of Iceland, Reykjavik, Iceland. 4Akureyri Hospital, Akureyri, Iceland. 5Heilsuklasinn Clinic, Reykjavik, Iceland. 6Landspitali-The National University Hospital of Iceland, Reykjavik, Iceland. 7Laeknasetrid Clinic, Reykjavik, Iceland. 8Intermountain Medical Center, Intermountain Heart Institute, Salt Lake City, UT, USA. 9University of Utah, School of Medicine, Salt Lake City, UT, USA. 10Precision Genomics, Intermountain Healthcare, Saint George, UT, USA. 11Stanford University, School of Medicine, Stanford, CA, USA. 12Department of Psychiatry, Psychotherapy and Psychosomatics, Martin-Luther-University Halle-Wittenberg, Halle, Germany. 13Department of Neurology and German Center for Vertigo and Balance Disorders, Ludwig Maximilians University, Munich, Germany. 14deCODE genetics/Amgen Inc., Reykjavik, Iceland. kstefans@decode.is. 15Faculty of Medicine, University of Iceland, Reykjavik, Iceland. kstefans@decode.is.

المصدر: Communications biology ; 4 ; 1 ; 1148 ; United States ; England

مصطلحات موضوعية: Svimi, Genarannsóknir, Gen, Vertigo, Labyrinth Diseases, Genome-Wide Association Study, Genome, Human

العلاقة: https://www.nature.com/articles/s42003-021-02673-2Test; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8497462Test/; Skuladottir AT, Bjornsdottir G, Nawaz MS, et al. A genome-wide meta-analysis uncovers six sequence variants conferring risk of vertigo. Commun Biol. 2021;4(1):1148. Published 2021 Oct 7. doi:10.1038/s42003-021-02673-2; http://hdl.handle.net/2336/622025Test; Communications biology

الإتاحة: https://doi.org/10.1038/s42003-021-02673-2Test
http://hdl.handle.net/2336/622025Test

المؤلفون: de Wert, Guido, Dondorp, Wybo, Clarke, Angus, Dequeker, Elisabeth M C, Cordier, Christophe, Deans, Zandra, van El, Carla G, Fellmann, Florence, Hastings, Ros, Hentze, Sabine, Howard, Heidi, Macek, Milan, Mendes, Alvaro, Patch, Chris, Rial-Sebbag, Emmanuelle, Stefansdottir, Vigdis, Cornel, Martina C, Forzano, Francesca

المساهمون: 1Department of Health, Ethics and Society, CAPHRI Care and Public Health Research Institute, and Research School GROW for Oncology & Developmental Biology, Maastricht University, Maastricht, The Netherlands. g.dewert@maastrichtuniversity.nl. 2Department of Health, Ethics and Society, CAPHRI Care and Public Health Research Institute, and Research School GROW for Oncology & Developmental Biology, Maastricht University, Maastricht, The Netherlands. 3Institute of Medical Genetics, Division of Cancer & Genetics, School of Medicine, Cardiff University, Cardiff, UK. 4Biomedical Quality Assurance Research Unit, Department of Public Health and Primary Care, University of Leuven, Leuven, Belgium. 5Département de génétique, SYNLAB, Chemin d'Entre-Bois 21, 1018, Lausanne, Switzerland. 6UK National External Quality Assessment Service for Molecular Genetics/Genomics Quality Assessment, Department of Laboratory Medicine, Royal Infirmary of Edinburgh, Edinburgh, UK. 7Section Community Genetics, Department of Clinical Genetics and Amsterdam Public Health research institute, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands. 8The ColLaboratory, University of Lausanne, Lausanne, Switzerland. 9CEQAS/GenQA, John Radcliffe Hospital, Oxford University Hospitals NHS Foundation Trust, Oxford, UK. 10Praxis für Humangenetik, Mannheim, Germany. 11Medical Ethics, Lund Universitet, Lund, SE-221 00, Sweden. 12Division of Industrial Biotechnology, Department of Biology and Biological Engineering, Chalmers University of Technology, Gothenburg, 412 96, Sweden. 13Department of Biology and Medical Genetics, Charles University and Motol University Hospital, Prague, Czech Republic. 14UnIGENe and CGPP-Centre for Predictive and Preventive Genetics, IBMC-Institute for Molecular and Cell Biology, i3S-Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Porto, Portugal. 15Genomics England, Queen Mary University of London, London, UK. 16Society and Ethics Research Group, Connecting Science, Wellcome Genome Campus, Cambridge, CB10 1SA, UK. 17Laboratoire d'Épidémiologie et de Santé Publique, UMR 1027 INSERM, Université Paul-Sabatier, Toulouse, France. 18Department of Genetics and Molecular Medicine, Landspitali University Hospital, Reykjavik, Iceland. 19Clinical Genetics Department, Guy's & St Thomas' NHS Foundation Trust, London, UK.

المصدر: European journal of human genetics : EJHG ; England

مصطلحات موضوعية: Opportunistic genomic screening, OGS, Genome sequencing, Genarannsóknir

العلاقة: https://www.nature.com/articles/s41431-020-00758-wTest; de Wert G, Dondorp W, Clarke A, Dequeker EMC, Cordier C, Deans Z, et al. Opportunistic genomic screening. Recommendations of the European Society of Human Genetics. European journal of human genetics : EJHG. 2020.doi:10.1038/s41431-020-00758-w.; http://hdl.handle.net/2336/621616Test; European journal of human genetics : EJHG

الإتاحة: https://doi.org/10.1038/s41431-020-00758-wTest
http://hdl.handle.net/2336/621616Test

المؤلفون: Magnadottir, Bergljot, Uysal-Onganer, Pinar, Kraev, Igor, Dodds, Alister W., Guðmundsdóttir, Sigríður, Lange, Sigrun

المساهمون: Tilraunastöð í meinafræði að Keldum (HÍ), Institute for Experimental Pathology, Keldur (UI), Háskóli Íslands, University of Iceland

مصطلحات موضوعية: Atlantic cod, Extracellular vesicles, miRNA-155, miRNA-206, miRNA-21, Peptidylarginine deiminase, Temperature, Þorskur, Genarannsóknir

العلاقة: Aquaculture Reports;16; https://www.sciencedirect.com/science/article/pii/S235251341930136X?via%3DihubTest; Magnadóttir, B., et al. (2020). "Extracellular vesicles, deiminated protein cargo and microRNAs are novel serum biomarkers for environmental rearing temperature in Atlantic cod (Gadus morhua L.)." Aquaculture Reports 16: 100245.; https://hdl.handle.net/20.500.11815/2431Test; Aquaculture Reports

الإتاحة: https://doi.org/20.500.11815/2431Test
https://doi.org/10.1016/j.aqrep.2019.100245Test
https://hdl.handle.net/20.500.11815/2431Test

المؤلفون: Allen, Richard J., Guillen-Guio, Beatriz, Oldham, Justin M., Ma, Shwu-Fan, Dressen, Amy, Paynton, Megan L., Kraven, Luke M., Obeidat, Ma'en, Li, Xuan, Ng, Michael, Braybrooke, Rebecca, Molina-Molina, Maria, Hobbs, Brian D., Putman, Rachel K., Sakornsakolpat, Phuwanat, Booth, Helen L., Fahy, William A., Hart, Simon P., Hill, Mike R., Hirani, Nik, Hubbard, Richard B., McAnulty, Robin J., Millar, Ann B., Navaratnam, Vidyia, Oballa, Eunice, Parfrey, Helen, Saini, Gauri, Whyte, Moira K. B., Zhang, Yingze, Kaminski, Naftali, Adegunsoye, Ayodeji, Strek, Mary E., Neighbors, Margaret, Sheng, Xuting R., Guðmundsson, Gunnar, Gudnason, Vilmundur, Hatabu, Hiroto, Lederer, David J., Manichaikul, Ani, Newell, John D., O’Connor, George T., Ortega, Victor E., Xu, Hanfei, Fingerlin, Tasha E., Bossé, Yohan, Hao, Ke, Joubert, Philippe, Nickle, David C., Sin, Don D., Timens, Wim, Furniss, Dominic, Morris, Andrew P., Zondervan, Krina T., Hall, Ian P., Sayers, Ian, Tobin, Martin D., Maher, Toby M., Cho, Michael H., Hunninghake, Gary M., Schwartz, David A., Yaspan, Brian L., Molyneaux, Philip L., Flores, Carlos, Noth, Imre, Jenkins, R. Gisli, Wain, Louise V.

المساهمون: Læknadeild (HÍ), Faculty of Medicine (UI), Heilbrigðisvísindasvið (HÍ), School of Health Sciences (UI), Háskóli Íslands, University of Iceland

مصطلحات موضوعية: DEPTOR, Epidemiology, Genetics, KIF15, MAD1L1, Erfðafræði, Genarannsóknir, Lungnasjúkdómar

وصف الملف: 564-574

العلاقة: American Journal of Respiratory and Critical Care Medicine;201(5); Allen, R. J., et al. (2019). "Genome-Wide Association Study of Susceptibility to Idiopathic Pulmonary Fibrosis." American Journal of Respiratory and Critical Care Medicine 201(5): 564-574.; 1535-4970 (eISSN); https://hdl.handle.net/20.500.11815/2428Test; American Journal of Respiratory and Critical Care Medicine

الإتاحة: https://doi.org/20.500.11815/2428Test
https://doi.org/10.1164/rccm.201905-1017OCTest
https://hdl.handle.net/20.500.11815/2428Test

المؤلفون: Ballesteros Alvarez, Josue, Dilshat, Ramile, Fock, Valerie, Möller, Katrin, Karl, Ludwig, LARUE, Lionel, Ogmundsdottir, Margret H, Steingrimsson, Eirikur

المساهمون: Læknadeild (HÍ), Faculty of Medicine (UI), Lífvísindasetur (HÍ), Biomedical Center (UI), Heilbrigðisvísindasvið (HÍ), School of Health Sciences (UI), Háskóli Íslands, University of Iceland

مصطلحات موضوعية: MITF, TFEB, Melanoma cells, Erfðarannsóknir, Genarannsóknir

وصف الملف: e0238546

العلاقة: PLOS ONE;15(9); https://dx.plos.org/10.1371/journal.pone.0238546Test; Citation: Ballesteros-Álvarez J, Dilshat R, Fock V, Möller K, Karl L, Larue L, et al. (2020) MITF and TFEB cross-regulation in melanoma cells. PLoS ONE 15(9): e0238546. https://doi.org/10.1371/journal.pone.0238546Test; https://hdl.handle.net/20.500.11815/2210Test; Plos One

الإتاحة: https://doi.org/20.500.11815/2210Test
https://doi.org/10.1371/journal.pone.0238546Test
https://hdl.handle.net/20.500.11815/2210Test

المؤلفون: Ólafsdóttir, Þórunn Ásta, Theódórs, Fannar, Bjarnadóttir, Kristbjörg, Björnsdóttir, Unnur Steina, Agustsdottir, Arna B., Stefánsson, Ólafur A., Ivarsdottir, Erna, Sigurðsson, Jón K., Benónísdóttir, Stefanía, Eyjólfsson, Guðmundur I., Gíslason, Davíð, Gislason, Thorarinn, Guðmundsdóttir, Steinunn, Gylfason, Arnaldur, Halldórsson, Bjarni, Halldorsson, Gisli, Júlíusdóttir, Þórhildur, Kristinsdottir, Anna M., Lúðvíksdóttir, Dóra, Ludviksson, Bjorn, Másson, Gísli, Norland, Kristjan, Onundarson, Pall, Olafsson, Isleifur, Sigurdardottir, Olof, Stefánsdóttir, Lilja, Sveinbjörnsson, Garðar, Tragante do O, Vinicius, Gudbjartsson, Daniel, Þorleifsson, Guðmar, sulem, patrick, Thorsteinsdottir, Unnur, Norddahl, Guðmundur L., Jonsdottir, Ingileif, Stefansson, Kari

المساهمون: Læknadeild (HÍ), Faculty of Medicine (UI), Verkfræðideild (HR), Department of Engineering (RU), Heilbrigðisvísindasvið (HÍ), School of Health Sciences (UI), Verkfræði- og náttúruvísindasvið (HÍ), School of Engineering and Natural Sciences (UI), Tæknisvið (HR), School of Technology (RU), Háskóli Íslands, University of Iceland, Háskólinn í Reykjavík, Reykjavik University

مصطلحات موضوعية: Asthma, Gene expression, Meta-analysis, Astmi, Genarannsóknir, Gen, Erfðarannsóknir

العلاقة: Nature Communications;11(1); https://www.nature.com/articles/s41467-019-14144-8Test; Olafsdottir, T.A., Theodors, F., Bjarnadottir, K. et al. Eighty-eight variants highlight the role of T cell regulation and airway remodeling in asthma pathogenesis. Nature Communications 11, 393 (2020). https://doi.org/10.1038/s41467-019-14144-8Test; https://hdl.handle.net/20.500.11815/2447Test; Nature Communications

الإتاحة: https://doi.org/20.500.11815/2447Test
https://doi.org/10.1038/s41467-019-14144-8Test
https://hdl.handle.net/20.500.11815/2447Test