-
1دورية أكاديمية
المؤلفون: 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
المصدر: Communications Biology, Vol 3, Iss 1, Pp 1-9 (2020)
مصطلحات موضوعية: Biology (General), QH301-705.5
وصف الملف: electronic resource
العلاقة: https://doaj.org/toc/2399-3642Test
-
2
المؤلفون: Thordur Sigmundsson, Erik Sørensen, David B. Rye, Katja van den Hurk, Franke A. Quee, Poul Jennum, Muhammad Nawaz, Willem H. Ouwehand, Michael W.T. Tanck, Steven Bell, Sigurdur H. Magnusson, Hreinn Stefansson, Gudmar Thorleifsson, Nicole Soranzo, Prabhjyot Saini, Maria Didriksen, Joseph Dowsett, Emanuele Di Angelantonio, Lynn Marie Trotti, Henrik Ullum, Eric J. Earley, Alan E. Mast, Michael P. Busch, David J. Roberts, Christian Erikstrup, Kari Stefansson, Kristoffer Sølvsten Burgdorf, Albert P. Sigurdsson, Ole Birger Pedersen, John Danesh, Grier P. Page, Lilja Stefansdottir, Brendan Burchell, Adam S. Butterworth
المساهمون: Didriksen, Maria [0000-0002-4856-496X], Nawaz, Muhammad Sulaman [0000-0002-5576-9007], Dowsett, Joseph [0000-0001-5381-2633], Bell, Steven [0000-0001-6774-3149], Erikstrup, Christian [0000-0001-6551-6647], Pedersen, Ole B [0000-0003-2312-5976], Burchell, Brendan [0000-0002-8243-937X], Butterworth, Adam S [0000-0002-6915-9015], Tanck, Michael WT [0000-0001-9828-4459], Ouwehand, Willem H [0000-0002-7744-1790], Earley, Eric J [0000-0001-6576-1319], Busch, Michael P [0000-0002-1446-125X], Page, Grier P [0000-0003-2582-3786], Stefansson, Hreinn [0000-0002-9331-6666], Stefansson, Kari [0000-0003-1676-864X], Apollo - University of Cambridge Repository, Pedersen, Ole B. [0000-0003-2312-5976], Butterworth, Adam S. [0000-0002-6915-9015], Tanck, Michael W. T. [0000-0001-9828-4459], Ouwehand, Willem H. [0000-0002-7744-1790], Earley, Eric J. [0000-0001-6576-1319], Busch, Michael P. [0000-0002-1446-125X], Page, Grier P. [0000-0003-2582-3786], Epidemiology and Data Science, APH - Methodology, Public and occupational health
المصدر: Didriksen, M, Nawaz, M S, Dowsett, J, Bell, S, Erikstrup, C, Pedersen, O B, Sørensen, E, Jennum, P J, Burgdorf, K S, Burchell, B, Butterworth, A S, Soranzo, N, Rye, D B, Trotti, L M, Saini, P, Stefansdottir, L, Magnusson, S H, Thorleifsson, G, Sigmundsson, T, Sigurdsson, A P, Van Den Hurk, K, Quee, F, Tanck, M W T, Ouwehand, W H, Roberts, D J, Earley, E J, Busch, M P, Mast, A E, Page, G P, Danesh, J, Di Angelantonio, E, Stefansson, H, Ullum, H & Stefansson, K 2020, ' Large genome-wide association study identifies three novel risk variants for restless legs syndrome ', Communications Biology, vol. 3, no. 1, 703 . https://doi.org/10.1038/s42003-020-01430-1Test
Communications Biology, Vol 3, Iss 1, Pp 1-9 (2020)
Communications Biology
Communications Biology, 3(1):703. Springer Natureمصطلحات موضوعية: 0301 basic medicine, Adult, medicine.medical_specialty, Linkage disequilibrium, QH301-705.5, 692/617/375/1816, 631/208/205/2138, Medicine (miscellaneous), Genome-wide association study, Disease, Bioinformatics, Genome-wide association studies, Polymorphism, Single Nucleotide, General Biochemistry, Genetics and Molecular Biology, Linkage Disequilibrium, 38, 38/43, 03 medical and health sciences, 0302 clinical medicine, Restless Legs Syndrome, Epidemiology, 38/23, mental disorders, medicine, Humans, Genetic Predisposition to Disease, Restless legs syndrome, Biology (General), health care economics and organizations, Genetic association, Aged, business.industry, article, Sleep disorders, Middle Aged, medicine.disease, Obesity, 631/208/199, 030104 developmental biology, Meta-analysis, 38/39, Gene expression, General Agricultural and Biological Sciences, business, 030217 neurology & neurosurgery, Genome-Wide Association Study
وصف الملف: application/vnd.openxmlformats-officedocument.wordprocessingml.document; application/pdf; text/xml; application/zip
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cc86f673c5ba81e610b194e8bc3890dcTest
https://doi.org/10.1038/s42003-020-01430-1Test -
3
المؤلفون: Hans Guttormur Thormar, Bjarki Gudmundsson, Margret Steinarsdottir, Stephen Meyn, Jon J. Jonsson, Anna M Halldorsdottir, Albert P. Sigurdsson, David Olafsson, Wendy Dankers, Stefan Hermanowicz, Stefan B. Sigurdsson
المساهمون: Clinical Immunology and Rheumatology, Faculty of Medicine (UI), The Biomedical Center (BMC) (UI), Lífvísindasetur (HÍ), Læknadeild (HÍ), Heilbrigðisvísindasvið (HÍ), School of Health Sciences (UI), Háskóli Íslands, University of Iceland
المصدر: Nucleic acids research, 46(20). Oxford University Press
Nucleic Acids Researchمصطلحات موضوعية: 0301 basic medicine, Genome instability, Male, Nucleic acid quantitation, Single-Stranded/analysis, Genomic DNA, DNA, Single-Stranded/analysis, medicine.disease_cause, chemistry.chemical_compound, Double-Stranded, 0302 clinical medicine, Nucleic Acids, Electrophoresis, Gel, Two-Dimensional, DNA Breaks, Double-Stranded, Cells, Cultured, Cell DNA, Gel, Cultured, Biochemistry, 030220 oncology & carcinogenesis, Dna breaks, Cytogenetic Analysis, MCF-7 Cells, Methods Online, Electrophoresis, Electrophoresis, Gel, Two-Dimensional/methods, DNA damage, Cells, Two-Dimensional/methods, DNA, Single-Stranded, Biology, Sensitivity and Specificity, 03 medical and health sciences, Genetics, medicine, Human Umbilical Vein Endothelial Cells, Erfðafræði, Humans, Cytogenetic Analysis/methods, Nucleic Acids/analysis, Mutagenicity Tests, DNA Breaks, Infant, Newborn, Infant, DNA, Newborn, DNA-rannsóknir, genomic DNA, 030104 developmental biology, chemistry, Nucleic acid, Genotoxicity, DNA Damage
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e6393e87d748b947ed8ac0def5c88b71Test
https://pure.amc.nl/en/publications/northern-lights-assayTest(e3a60687-1ebf-4682-84d1-cfcae0a00a12).html -
4
المؤلفون: Albert P. Sigurdsson, Thordur Sigmundsson, Kristleifur Kristjansson, David B. Rye, Lisa M. Organisak, Sophia A. Greer, Donald L. Bliwise, Thor Sigthorsson, Lynn Marie Trotti, Thomas Wessel, Gudbjörg Birna Gudmundsdóttir
المصدر: Sleep Medicine. 10:668-671
مصطلحات موضوعية: Adult, Male, medicine.medical_specialty, Polysomnography, Individuality, Audiology, Mean difference, Young Adult, Sex Factors, Sex factors, Restless Legs Syndrome, mental disorders, medicine, Humans, Restless legs syndrome, Monitoring, Physiologic, Analysis of Variance, Likelihood Functions, medicine.diagnostic_test, Actigraphy, General Medicine, Middle Aged, medicine.disease, Nocturnal Myoclonus Syndrome, Mood, Physical therapy, Female, Functional status, Analysis of variance, Psychology
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2f29fee30e2908f6b8334f2299d7f045Test
https://doi.org/10.1016/j.sleep.2008.06.009Test -
5
المؤلفون: Thordur Sigmundsson, Larus J. Gudmundsson, Augustine Kong, Ingibjorg Eiriksdottir, Daniel F. Gudbjartsson, Thorgeir E. Thorgeirsson, Emilia Soebech, Salina P. Waddy, Madhav Thambisetty, Ami Rosen, Stefan T Palsson, David B. Rye, H. Petursson, Albert P. Sigurdsson, Joseph M. Beck, Andres Ingason, Unnur Thorsteinsdottir, Hreinn Stefansson, Jeffrey R. Gulcher, Kari Stefansson, Gudmundur A. Hardarson, Andrew A. Hicks, Kristleifur Kristjansson, Alex Iranzo, Donald L. Bliwise, Lynn Marie Trotti
المصدر: New England Journal of Medicine. 357:639-647
مصطلحات موضوعية: Genetic Markers, Male, medicine.medical_specialty, Genotype, Nerve Tissue Proteins, Polymorphism, Single Nucleotide, Linkage Disequilibrium, Nocturnal Myoclonus Syndrome, Physical medicine and rehabilitation, Risk Factors, Restless Legs Syndrome, mental disorders, medicine, Humans, Genetic Predisposition to Disease, Restless legs syndrome, Risk factor, Genome, Human, Genetic heterogeneity, business.industry, Case-control study, Iron Deficiencies, General Medicine, Odds ratio, medicine.disease, Sleep in non-human animals, Surgery, BTBD9, Case-Control Studies, Ferritins, Chromosomes, Human, Pair 6, Female, business, Transcription Factors
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6252151fbd095d730d8486fff0b58546Test
https://doi.org/10.1056/nejmoa072743Test