المساهمون: Ji-Young Kang, Dasom Mun, Hyoeun Kim, Nuri Yun, Boyoung Joung, Joung, Bo Young

مصطلحات موضوعية: Atrial Fibrillation* / diagnosis, Atrial Fibrillation* / genetics, Atrial Fibrillation* / metabolism, Biomarkers / metabolism, Exosomes* / genetics, Exosomes* / metabolism, Humans, RNA, Long Noncoding* / genetics, Long Noncoding* / metabolism, Atrial fibrillation, Biomarker, Diagnosis, Exosome, Long noncoding RNAs

العلاقة: HEART RHYTHM; J00980; OAK-2022-07712; https://ir.ymlib.yonsei.ac.kr/handle/22282913/192028Test; https://www.sciencedirect.com/science/article/pii/S1547527122020495?via%3DihubTest; T202204252; HEART RHYTHM, Vol.19(9) : 1450-1458, 2022-09

الإتاحة: https://doi.org/10.1016/j.hrthm.2022.05.033Test
https://ir.ymlib.yonsei.ac.kr/handle/22282913/192028Test
https://www.sciencedirect.com/science/article/pii/S1547527122020495?via%3DihubTest

المساهمون: Dasom Mun, Hyoeun Kim, Ji-Young Kang, Nuri Yun, Young-Nam Youn, Boyoung Joung, Youn, Young Nam

مصطلحات موضوعية: Atrial Fibrillation* / genetics, Atrial Fibrillation* / metabolism, Calcium / metabolism, Calcium-Calmodulin-Dependent Protein Kinase Type 2 / genetics, Calcium-Calmodulin-Dependent Protein Kinase Type 2 / metabolism, Extracellular Vesicles* / metabolism, Humans, MicroRNAs* / genetics, MicroRNAs* / metabolism, atrial fibrillation, microRNA, small extracellular vesicles

العلاقة: CLINICAL SCIENCE; J00613; OAK-2022-05865; OAK-2022-05866; https://ir.ymlib.yonsei.ac.kr/handle/22282913/191343Test; https://portlandpress.com/clinsci/article/136/8/621/231137/Small-extracellular-vesicles-derived-from-patientsTest; T202204474; CLINICAL SCIENCE, Vol.136(8) : 621-637, 2022-04

الإتاحة: https://doi.org/10.1042/CS20211141Test
https://ir.ymlib.yonsei.ac.kr/handle/22282913/191343Test
https://portlandpress.com/clinsci/article/136/8/621/231137/Small-extracellular-vesicles-derived-from-patientsTest

المساهمون: Oh-Seok Kwon, Myunghee Hong, Tae-Hoon Kim, Inseok Hwang, Jaemin Shim, Eue-Keun Choi, Hong Euy Lim, Hee Tae Yu, Jae-Sun Uhm, Boyoung Joung, Seil Oh, Moon-Hyoung Lee, Young-Hoon Kim, Hui-Nam Pak, Kim, Tae-Hoon

مصطلحات موضوعية: Artificial Intelligence, Atrial Fibrillation / diagnosis, Atrial Fibrillation / epidemiology, Atrial Fibrillation / genetics, DNA / genetics, Female, Genetic Predisposition to Disease, Genome-Wide Association Study, Homeodomain Proteins / genetics, Homeodomain Proteins / metabolism, Humans, Male, Middle Aged, Morbidity / trends, Polymorphism, Single Nucleotide, Republic of Korea / epidemiology, Transcription Factors / genetics, Transcription Factors / metabolism, atrial fibrillation, genetics

وصف الملف: application/pdf

العلاقة: OPEN HEART; J04205; OAK-2022-01428; https://ir.ymlib.yonsei.ac.kr/handle/22282913/188710Test; T202201859; OPEN HEART, Vol.9(1) : e001898, 2022-01

الإتاحة: https://doi.org/10.1136/openhrt-2021-001898Test
https://ir.ymlib.yonsei.ac.kr/handle/22282913/188710Test

المؤلفون: Frerich, Simon, Malik, Rainer, Georgakis, Marios K, Sinner, Moritz F, Kittner, Steven J, Mitchell, Braxton D, Dichgans, Martin

المصدر: Stroke 53(4), e130-e135 (2022). doi:10.1161/STROKEAHA.121.036306

مصطلحات موضوعية: info:eu-repo/classification/ddc/610, Atrial Fibrillation: epidemiology, Atrial Fibrillation: genetics, Coronary Artery Disease, Genetic Predisposition to Disease, Genome-Wide Association Study, Humans, Mendelian Randomization Analysis, Polymorphism, Single Nucleotide, Risk Factors, Stroke: epidemiology, Stroke: genetics, atrial fibrillation, biomarker, cardiovascular disease, echocardiography

جغرافية الموضوع: DE

العلاقة: info:eu-repo/semantics/altIdentifier/issn/1524-4628; info:eu-repo/semantics/altIdentifier/issn/0039-2499; info:eu-repo/semantics/altIdentifier/pmid/pmid:34911345; https://pub.dzne.de/record/163723Test; https://pub.dzne.de/search?p=id:%22DZNE-2022-00462%22Test

الإتاحة: https://doi.org/10.1161/STROKEAHA.121.036306Test
https://pub.dzne.de/record/163723Test
https://pub.dzne.de/search?p=id:%22DZNE-2022-00462%22Test

المؤلفون: Thorolfsdottir, Rosa B, Sveinbjornsson, Gardar, Aegisdottir, Hildur M, Benonisdottir, Stefania, Stefansdottir, Lilja, Ivarsdottir, Erna V, Halldorsson, Gisli H, Sigurdsson, Jon K, Torp-Pedersen, Christian, Weeke, Peter E, Brunak, Søren, Westergaard, David, Pedersen, Ole B, Sorensen, Erik, Nielsen, Kaspar R, Burgdorf, Kristoffer S, Banasik, Karina, Brumpton, Ben, Zhou, Wei, Oddsson, Asmundur, Tragante, Vinicius, Hjorleifsson, Kristjan E, Davidsson, Olafur B, Rajamani, Sridharan, Jonsson, Stefan, Torfason, Bjarni, Valgardsson, Atli S, Thorgeirsson, Gudmundur, Frigge, Michael L, Thorleifsson, Gudmar, Norddahl, Gudmundur L, Helgadottir, Anna, Gretarsdottir, Solveig, Sulem, Patrick, Jonsdottir, Ingileif, Willer, Cristen J, Hveem, Kristian, Bundgaard, Henning, Ullum, Henrik, Arnar, David O, Thorsteinsdottir, Unnur, Gudbjartsson, Daniel F, Holm, Hilma, Stefansson, Kari, Bruun, Mie Topholm

المصدر: Thorolfsdottir , R B , Sveinbjornsson , G , Aegisdottir , H M , Benonisdottir , S , Stefansdottir , L , Ivarsdottir , E V , Halldorsson , G H , Sigurdsson , J K , Torp-Pedersen , C , Weeke , P E , Brunak , S , Westergaard , D , Pedersen , O B , Sorensen , E , Nielsen , K R , Burgdorf , K S , Banasik , K , Brumpton , B , Zhou , W , Oddsson , A , Tragante , V , Hjorleifsson , K E , Davidsson ....

مصطلحات موضوعية: Atrial Fibrillation/genetics, Diabetes Mellitus, Type 2, Genome-Wide Association Study, Humans, NAV1.8 Voltage-Gated Sodium Channel, Pacemaker, Artificial, Sick Sinus Syndrome/genetics

وصف الملف: application/pdf

العلاقة: https://portal.findresearcher.sdu.dk/da/publications/6ad450a7-e103-4ef6-81ed-0f9d2b17d80eTest

الإتاحة: https://doi.org/10.1093/eurheartj/ehaa1108Test
https://portal.findresearcher.sdu.dk/da/publications/6ad450a7-e103-4ef6-81ed-0f9d2b17d80eTest
https://findresearcher.sdu.dk/ws/files/197842265/ehaa1108.pdfTest

المؤلفون: DBDS Genomic Consortium

المساهمون: Faculty of Medicine, Office of Division of Diagnostic and Support Services, Faculty of Industrial Engineering, Mechanical Engineering and Computer Science, Clinical Laboratory Services, Diagnostics and Blood Bank, Health Sciences, Landspitali - The National University Hospital of Iceland

مصطلحات موضوعية: Gáttatif, Sykursýki, Sjúkur skiptahnútur, Atrial fibrillation, GWAS, KRT8, Mendelian randomization, Sick sinus syndrome, Genome-Wide Association Study, NAV1.8 Voltage-Gated Sodium Channel, Sick Sinus Syndrome/genetics, Humans, Diabetes Mellitus, Type 2, Atrial Fibrillation/genetics, Pacemaker, Artificial, Cardiology and Cardiovascular Medicine

وصف الملف: 1959-1971

العلاقة: European Heart Journal; 42(20); http://www.scopus.com/inward/record.url?scp=85107088568&partnerID=8YFLogxKTest; DBDS Genomic Consortium 2021 , ' Genetic insight into sick sinus syndrome ' , European Heart Journal , vol. 42 , no. 20 , pp. 1959-1971 . https://doi.org/10.1093/eurheartj/ehaa1108Test; dbf7594a-dffc-4c61-a84f-d6a6becc31d4; 85107088568; unpaywall: 10.1093/eurheartj/ehaa1108; https://hdl.handle.net/20.500.11815/3201Test

الإتاحة: https://doi.org/20.500.11815/3201Test
https://doi.org/10.1093/eurheartj/ehaa1108Test
https://hdl.handle.net/20.500.11815/3201Test

المؤلفون: Rahm, Ann-Kathrin, Lugenbiel, Patrick, Ochs, Marco, Meder, Benjamin, Thomas, Dierk, Katus, Hugo A., Scholz, Eberhard

المصدر: http://lobid.org/resources/99370674986806441Test#!, 109(8):1070-1075.

مصطلحات موضوعية: Pulmonary vein isolation, Female [MeSH], Lamin Type A/metabolism [MeSH], Mutation [MeSH], Ablation, Adult [MeSH], Humans [MeSH], Catheter Ablation/methods [MeSH], Atrial fibrillation, Pulmonary Veins/surgery [MeSH], DNA Mutational Analysis [MeSH], Atrial Fibrillation/genetics [MeSH], Atrial Fibrillation/surgery [MeSH], Lamin a/c, Laminopathy, DNA/genetics [MeSH], Letter to the Editors, Lamin Type A/genetics [MeSH]

العلاقة: https://repository.publisso.de/resource/frl:6469864Test; https://doi.org/10.1007/s00392-020-01616-xTest; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7376080Test/

الإتاحة: https://doi.org/10.1007/s00392-020-01616-xTest
https://repository.publisso.de/resource/frl:6469864Test
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7376080Test/

المؤلفون: Regeneron Genetics Center

المساهمون: Onderzoek Precision medicine, Team Medisch, Circulatory Health

مصطلحات موضوعية: Adaptor Proteins, Signal Transducing/genetics, Apoptosis Regulatory Proteins/genetics, Atrial Fibrillation/genetics, Cardiomyopathies/genetics, Carrier Proteins/genetics, Case-Control Studies, Coronary Artery Disease/genetics, Cyclin-Dependent Kinase Inhibitor p21/genetics, Genome-Wide Association Study, Heart Failure/genetics, Humans, Mendelian Randomization Analysis, Microfilament Proteins/genetics, Muscle Proteins/genetics, Risk Factors, Ventricular Function, Left/genetics, General Physics and Astronomy, General Chemistry, General Biochemistry,Genetics and Molecular Biology, Meta-Analysis, Journal Article

وصف الملف: application/pdf

العلاقة: https://dspace.library.uu.nl/handle/1874/442049Test

الإتاحة: https://dspace.library.uu.nl/handle/1874/442049Test

المساهمون: Carolina Roselli, Mark D Chaffin, Lu-Chen Weng, Stefanie Aeschbacher, Gustav Ahlberg, Christine M Albert, Peter Almgren, Alvaro Alonso, Christopher D Anderson, Krishna G Aragam, Dan E Arking, John Barnard, Traci M Bartz, Emelia J Benjamin, Nathan A Bihlmeyer, Joshua C Bis, Heather L Bloom, Eric Boerwinkle, Erwin B Bottinger, Jennifer A Brody, Hugh Calkins, Archie Campbell, Thomas P Cappola, John Carlquist, Daniel I Chasman, Lin Y Chen, Yii-Der Ida Chen, Eue-Keun Choi, Seung Hoan Choi, Ingrid E Christophersen, Mina K Chung, John W Cole, David Conen, James Cook, Harry J Crijns, Michael J Cutler, Scott M Damrauer, Brian R Daniels, Dawood Darbar, Graciela Delgado, Joshua C Denny, Martin Dichgans, Marcus Dörr, Elton A Dudink, Samuel C Dudley, Nada Esa, Tonu Esko, Markku Eskola, Diane Fatkin, Stephan B Felix, Ian Ford, Oscar H Franco, Bastiaan Geelhoed, Raji P Grewal, Vilmundur Gudnason, Xiuqing Guo, Namrata Gupta, Stefan Gustafsson, Rebecca Gutmann, Anders Hamsten, Tamara B Harris, Caroline Hayward, Susan R Heckbert, Jussi Hernesniemi, Lynne J Hocking, Albert Hofman, Andrea R V R Horimoto, Jie Huang, Paul L Huang, Jennifer Huffman, Erik Ingelsson, Esra Gucuk Ipek, Kaoru Ito, Jordi Jimenez-Conde, Renee Johnson, J Wouter Jukema, Stefan Kääb, Mika Kähönen, Yoichiro Kamatani, John P Kane, Adnan Kastrati, Sekar Kathiresan, Petra Katschnig-Winter, Maryam Kavousi, Thorsten Kessler, Bas L Kietselaer, Paulus Kirchhof, Marcus E Kleber, Stacey Knight, Jose E Krieger, Michiaki Kubo, Lenore J Launer, Jari Laurikka, Terho Lehtimäki, Kirsten Leineweber, Rozenn N Lemaitre, Man Li, Hong Euy Lim, Henry J Lin, Honghuang Lin

مصطلحات موضوعية: Atrial Fibrillation / ethnology, Atrial Fibrillation / genetics, Case-Control Studies, Ethnicity / genetics, Genetic Predisposition to Disease, Genome-Wide Association Study / methods, Humans, Quantitative Trait Loci, Transcriptome

العلاقة: NATURE GENETICS; J02294; OAK-2022-02122; https://ir.ymlib.yonsei.ac.kr/handle/22282913/188946Test; T999201822; NATURE GENETICS, Vol.50(9) : 1225-1233, 2018-06

الإتاحة: https://doi.org/10.1038/s41588-018-0133-9Test
https://ir.ymlib.yonsei.ac.kr/handle/22282913/188946Test

المساهمون: Hye Ok Kim, Ji Eun Lim, Myung Jun Kim, Ji-One Kang, Sung-Moon Kim, Jeong Min Nam, Jihoon Tak, Hiroaki Konishi, Tasuku Nishino, In Song Koh, Young-Ho Jin, Hyung Hwan Baik, Jin-Bae Kim, Mi Kyung Kim, Bo Youl Choi, Sang-Hak Lee, Yangsoo Jang, Jinho Shin, Bermseok Oh, Lee, Snag Hak

مصطلحات موضوعية: Adult, Aged, Alleles, Animals, Atrial Fibrillation / diagnosis, Atrial Fibrillation / genetics, Atrial Fibrillation / physiopathology, Cell Line, Disease Models, Animal, Electrocardiography, Female, GRB2 Adaptor Protein / genetics, GRB2 Adaptor Protein / metabolism, Gene Expression, Gene Silencing, Genetic Association Studies, Genetic Predisposition to Disease, Genetic Variation, Genotype, Heart Atria / cytology, Heart Atria / metabolism, Heart Atria / physiopathology, Heart Conduction System, Humans, Male, Mice, Middle Aged, Polymorphism, Single Nucleotide

العلاقة: JOURNAL OF HUMAN GENETICS; J01446; OAK-2022-02209; https://ir.ymlib.yonsei.ac.kr/handle/22282913/188935Test; https://www.nature.com/articles/s10038-017-0367-xTest; T999201864; JOURNAL OF HUMAN GENETICS, Vol.63(3) : 297-307, 2018-03

الإتاحة: https://doi.org/10.1038/s10038-017-0367-xTest
https://ir.ymlib.yonsei.ac.kr/handle/22282913/188935Test
https://www.nature.com/articles/s10038-017-0367-xTest