المؤلفون: Cannie, Douglas E, Protonotarios, Alexandros, Bakalakos, Athanasios, Syrris, Petros, Lorenzini, Massimiliano, De Stavola, Bianca, Bjerregaard, Louise, Dybro, Anne M, Hey, Thomas M, Hansen, Frederikke G, Navarro Penalver, Marina, Crespo-Leiro, Maria G, Larrañaga-Moreira, Jose M, de Frutos, Fernando, Johnson, Renee, Slater, Thomas A, Monserrat, Lorenzo, Sengupta, Anshuman, Mestroni, Luisa, Taylor, Matthew R G, Sinagra, Gianfranco, Bilinska, Zofia, Solla-Ruiz, Itziar, Arana Achaga, Xabier, Barriales-Villa, Roberto, Garcia-Pavia, Pablo, Gimeno, Juan R, Dal Ferro, Matteo, Merlo, Marco, Wahbi, Karim, Fatkin, Diane, Mogensen, Jens, Rasmussen, Torsten B, Elliott, Perry M

المصدر: Cannie , D E , Protonotarios , A , Bakalakos , A , Syrris , P , Lorenzini , M , De Stavola , B , Bjerregaard , L , Dybro , A M , Hey , T M , Hansen , F G , Navarro Penalver , M , Crespo-Leiro , M G , Larrañaga-Moreira , J M , de Frutos , F , Johnson , R , Slater , T A , Monserrat , L , Sengupta , A , Mestroni , L , Taylor , M R G , Sinagra , G , Bilinska , Z ....

مصطلحات موضوعية: dilated cardiomyopathy, heart failure, sudden cardiac death, Ventricular Function, Left, Heart Failure/genetics, Humans, Male, Arrhythmias, Cardiac, Ventricular Dysfunction, Left/genetics, Stroke Volume, Adult, Female, Retrospective Studies

العلاقة: https://pure.au.dk/portal/da/publications/risks-of-ventricular-arrhythmia-and-heart-failure-in-carriers-of-rbm20-variantsTest(b1d96c92-5d1d-4c71-a8ec-c923a39a7500).html

الإتاحة: https://doi.org/10.1161/CIRCGEN.123.004059Test
https://pure.au.dk/portal/da/publications/risks-of-ventricular-arrhythmia-and-heart-failure-in-carriers-of-rbm20-variantsTest(b1d96c92-5d1d-4c71-a8ec-c923a39a7500).html
http://www.scopus.com/inward/record.url?scp=85174865768&partnerID=8YFLogxKTest

المؤلفون: Tadros, Rafik, Francis, Catherine, Xu, Xiao, Vermeer, Alexa M. C., Harper, Andrew R., Huurman, Roy, Bisabu, Ken Kelu, Walsh, Roddy, Hoorntje, Edgar T., te Rijdt, Wouter P., Buchan, Rachel J., van Velzen, Hannah G., van Slegtenhorst, Marjon A., Vermeulen, Jentien M., Offerhaus, Joost Allard, Bai, Wenjia, de Marvao, Antonio, Lahrouchi, Najim, Beekman, Leander, Karper, Jacco C., Veldink, Jan H., Kayvanpour, Elham, Pantazis, Antonis, Baksi, A. John, Whiffin, Nicola, Mazzarotto, Francesco, Sloane, Geraldine, Suzuki, Hideaki, Schneider-Luftman, Deborah, Elliott, Paul, Richard, Pascale, Ader, Flavie, Villard, Eric, Lichtner, Peter, Meitinger, Thomas, Tanck, Michael W. T., van Tintelen, J. Peter, Thain, Andrew, McCarty, David, Hegele, Robert A., Roberts, Jason D., Amyot, Julie, Dube, Marie-Pierre, Cadrin-Tourigny, Julia, Giraldeau, Genevieve, L'Allier, Philippe L., Garceau, Patrick, Tardif, Jean-Claude, Boekholdt, S. Matthijs, Lumbers, R. Thomas, Asselbergs, Folkert W., Barton, Paul J. R., Cook, Stuart A., Prasad, Sanjay K., O'Regan, Declan P., van der Velden, Jolanda, Verweij, Karin J. H., Talajic, Mario, Lettre, Guillaume, Pinto, Yigal M., Meder, Benjamin, Charron, Philippe, de Boer, Rudolf A., Christiaans, Imke, Michels, Michelle, Wilde, Arthur A. M., Watkins, Hugh, Matthews, Paul M., Ware, James S., Bezzina, Connie R.

المصدر: Tadros , R , Francis , C , Xu , X , Vermeer , A M C , Harper , A R , Huurman , R , Bisabu , K K , Walsh , R , Hoorntje , E T , te Rijdt , W P , Buchan , R J , van Velzen , H G , van Slegtenhorst , M A , Vermeulen , J M , Offerhaus , J A , Bai , W , de Marvao , A , Lahrouchi , N , Beekman , L , Karper , J C , Veldink , J ....

مصطلحات موضوعية: Cardiomyopathy, Dilated/genetics, Hypertrophic/genetics, Case-Control Studies, Gene Frequency, Genetic Predisposition to Disease, Genome-Wide Association Study, Heart Ventricles/physiopathology, Humans, Kaplan-Meier Estimate, Linkage Disequilibrium, Polymorphism, Single Nucleotide, Quantitative Trait Loci, Ventricular Function, Left/genetics

وصف الملف: application/pdf

العلاقة: https://research.rug.nl/en/publications/d610e46c-d485-4799-a499-afc7c13bd101Test

الإتاحة: https://doi.org/10.1038/s41588-020-00762-2Test
https://hdl.handle.net/11370/d610e46c-d485-4799-a499-afc7c13bd101Test
https://research.rug.nl/en/publications/d610e46c-d485-4799-a499-afc7c13bd101Test
https://pure.rug.nl/ws/files/169770368/Shared_genetic_pathways_contribute_to_risk_of_hypertrophic_and_dilated_cardiomyopathies_with_opposite_directions_of_effect.pdfTest

المؤلفون: Kattih, Badder, Shirvani, Amir, Klement, Piroska, Garrido, Abel Martin, Gabdoulline, Razif, Liebich, Alessandro, Brandes, Maximilian, Chaturvedi, Anuhar, Seeger, Timon, Thol, Felicitas, Göhring, Gudrun, Schlegelberger, Brigitte, Geffers, Robert, John, David, Bavendiek, Udo, Bauersachs, Johann, Ganser, Arnold, Heineke, Joerg, Heuser, Michael

المصدر: http://lobid.org/resources/99370672770606441Test#!, 35(5):1301-1316.

مصطلحات موضوعية: Coronary Artery Disease/pathology [MeSH], Acute myeloid leukaemia, Aged, 80 and over [MeSH], Coronary Artery Disease/genetics [MeSH], Aged [MeSH], Male [MeSH], Leukemia, Myeloid, Acute/genetics [MeSH], Stroke Volume [MeSH], Propensity Score [MeSH], Mutation/genetics [MeSH], Adolescent [MeSH], Female [MeSH], Adult [MeSH], Humans [MeSH], Retrospective Studies [MeSH], Middle Aged [MeSH], Article, Coronary Artery Disease/etiology [MeSH], Cancer genetics, Biomarkers, Tumor/genetics [MeSH], Prognosis [MeSH], Young Adult [MeSH], Genotype [MeSH], Ventricular Function, Left/genetics [MeSH], Isocitrate Dehydrogenase/genetics [MeSH]

العلاقة: https://repository.publisso.de/resource/frl:6471010Test; https://doi.org/10.1038/s41375-020-01043-xTest; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8102189Test/

الإتاحة: https://doi.org/10.1038/s41375-020-01043-xTest
https://repository.publisso.de/resource/frl:6471010Test
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8102189Test/

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

المؤلفون: Florijn, Barend W., Valstar, Gideon B., Duijs, Jacques M.G.J., Menken, Roxana, Cramer, Maarten J., Teske, Arco J., Ghossein-Doha, Chahinda, Rutten, Frans H., Spaanderman, Marc E.A., den Ruijter, Hester M., Bijkerk, Roel, van Zonneveld, Anton Jan

المساهمون: Onderzoek Vrouw Hart & Vaatziekten, Team Medisch, Circulatory Health, HAG Hart- Vaatziekten, JC onderzoeksprogramma Cardiovasculaire Epidemiologie

مصطلحات موضوعية: Adult, Aged, Angiopoietin-2/analysis, Biomarkers/blood, Diabetes Complications/genetics, Diabetes Mellitus/genetics, Female, Heart Failure/genetics, Humans, Male, MicroRNAs/genetics, Middle Aged, Pilot Projects, Sex Characteristics, Stroke Volume/genetics, Ventricular Dysfunction, Left/genetics, Ventricular Function, Journal Article, Research Support, Non-U.S. Gov't

وصف الملف: application/pdf

العلاقة: https://dspace.library.uu.nl/handle/1874/440474Test

الإتاحة: https://dspace.library.uu.nl/handle/1874/440474Test

المؤلفون: Miles, Chris, Finocchiaro, Gherardo, Papadakis, Michael, Gray, Belinda, Westaby, Joseph, Ensam, Bode, Basu, Joyee, Parry-Williams, Gemma, Papatheodorou, Efstathios, Paterson, Casey, Malhotra, Aneil, Robertus, Jan Lukas, Ware, James S, Cook, Stuart A, Asimaki, Angeliki, Witney, Adam, Ster, Irina Chis, Tome, Maite, Sharma, Sanjay, Behr, Elijah R, Sheppard, Mary N

المصدر: Miles , C , Finocchiaro , G , Papadakis , M , Gray , B , Westaby , J , Ensam , B , Basu , J , Parry-Williams , G , Papatheodorou , E , Paterson , C , Malhotra , A , Robertus , J L , Ware , J S , Cook , S A , Asimaki , A , Witney , A , Ster , I C , Tome , M , Sharma , S , Behr , E R & Sheppard , M N 2019 , ' Sudden Death and Left Ventricular Involvement in ....

مصطلحات موضوعية: Adult, Arrhythmogenic Right Ventricular Dysplasia/genetics, Cause of Death, Death, Sudden, Cardiac/etiology, Female, Genetic Predisposition to Disease, Heart Ventricles/pathology, Humans, Male, Middle Aged, Risk Assessment, Risk Factors, Ventricular Dysfunction, Left/genetics, Ventricular Function, Left, Young Adult

الإتاحة: https://doi.org/10.1161/CIRCULATIONAHA.118.037230Test
https://research.manchester.ac.uk/en/publications/c65d3836-91d3-49c4-a7b8-2414f4ef21a8Test

المؤلفون: Antonio de Marvao, Roddy Walsh, Jean-Claude Tardif, R. Thomas Lumbers, Eric Villard, Rafik Tadros, Peter Lichtner, Catherine Francis, Julie Amyot, Michelle Michels, Hugh Watkins, Julia Cadrin-Tourigny, Najim Lahrouchi, Rudolf A. de Boer, Patrick Garceau, Karin J. H. Verweij, Paul M. Matthews, Paul Elliott, S. Matthijs Boekholdt, Folkert W. Asselbergs, Declan P. O'Regan, Benjamin Meder, Joost A. Offerhaus, Nicola Whiffin, Jacco C. Karper, Jason D. Roberts, Marie-Pierre Dubé, Hideaki Suzuki, James S. Ware, Yigal M. Pinto, Thomas Meitinger, Guillaume Lettre, Hannah G. van Velzen, Arthur A.M. Wilde, Marjon van Slegtenhorst, Francesco Mazzarotto, Wouter P. te Rijdt, Paul J.R. Barton, Sanjay K Prasad, A. John Baksi, Michael W.T. Tanck, Mario Talajic, Roy Huurman, J. Peter van Tintelen, Connie R. Bezzina, Antonis Pantazis, Robert A. Hegele, Jentien M Vermeulen, Rachel Buchan, Imke Christiaans, Jan H. Veldink, Edgar T. Hoorntje, Elham Kayvanpour, Pascale Richard, Geneviève Giraldeau, Flavie Ader, Andrew Thain, Philippe L. L’Allier, Xiao Xu, Leander Beekman, David McCarty, Alexa M.C. Vermeer, Geraldine Sloane, Wenjia Bai, Andrew R. Harper, Jolanda van der Velden, Stuart A. Cook, Ken Kelu Bisabu, Philippe Charron, Deborah Schneider-Luftman

المساهمون: Human Genetics, ACS - Heart failure & arrhythmias, Cardiology, Adult Psychiatry, APH - Mental Health, ANS - Complex Trait Genetics, ANS - Compulsivity, Impulsivity & Attention, ANS - Mood, Anxiety, Psychosis, Stress & Sleep, ACS - Amsterdam Cardiovascular Sciences, Epidemiology and Data Science, APH - Methodology, ACS - Atherosclerosis & ischemic syndromes, Human genetics, Physiology, Cardiovascular Centre (CVC), Clinical Genetics, Wellcome Trust, Department of Health, British Heart Foundation, Engineering & Physical Science Research Council (EPSRC), UK DRI Ltd, The Academy of Medical Sciences, Imperial College Healthcare NHS Trust- BRC Funding

المصدر: Nature genetics, 53(2), 128-134. Nature Publishing Group
Nature genetics
Tadros, R, Francis, C, Xu, X, Vermeer, A M C, Harper, A R, Huurman, R, Kelu Bisabu, K, Walsh, R, Hoorntje, E T, te Rijdt, W P, Buchan, R J, van Velzen, H G, van Slegtenhorst, M A, Vermeulen, J M, Offerhaus, J A, Bai, W, de Marvao, A, Lahrouchi, N, Beekman, L, Karper, J C, Veldink, J H, Kayvanpour, E, Pantazis, A, Baksi, A J, Whiffin, N, Mazzarotto, F, Sloane, G, Suzuki, H, Schneider-Luftman, D, Elliott, P, Richard, P, Ader, F, Villard, E, Lichtner, P, Meitinger, T, Tanck, M W T, van Tintelen, J P, Thain, A, McCarty, D, Hegele, R A, Roberts, J D, Amyot, J, Dubé, M-P, Cadrin-Tourigny, J, Giraldeau, G, l’Allier, P L, Garceau, P, Tardif, J-C, Boekholdt, S M, Lumbers, R T, Asselbergs, F W, Barton, P J R, Cook, S A, Prasad, S K, O’Regan, D P, van der Velden, J, Verweij, K J H, Talajic, M, Lettre, G, Pinto, Y M, Meder, B, Charron, P, de Boer, R A, Christiaans, I, Michels, M, Wilde, A A M, Watkins, H, Matthews, P M, Ware, J S & Bezzina, C R 2021, ' Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect ', Nature Genetics, vol. 53, no. 2, pp. 128-134 . https://doi.org/10.1038/s41588-020-00762-2Test
Nature Genetics, 53(2), 128-134. Nature Publishing Group

مصطلحات موضوعية: Linkage disequilibrium, Cardiomyopathy, Dilated/genetics, Left, Cardiomyopathy, Genome-wide association study, Kaplan-Meier Estimate, VARIANTS, Ventricular Function, Left, Linkage Disequilibrium, 0302 clinical medicine, Gene Frequency, Dilated, Ventricular Function, 11 Medical and Health Sciences, Cardiomyopathy, Hypertrophic/genetics, Genetics & Heredity, 0303 health sciences, HERITABILITY, Single Nucleotide, MENDELIAN RANDOMIZATION, Cardiology, cardiovascular system, HEART, Life Sciences & Biomedicine, Ventricular Function, Left/genetics, Cardiomyopathy, Dilated, medicine.medical_specialty, Heart Ventricles, Quantitative Trait Loci, Biology, Quantitative trait locus, Sudden death, Polymorphism, Single Nucleotide, Article, Heart Ventricles/physiopathology, 03 medical and health sciences, Internal medicine, Mendelian randomization, Genetics, medicine, Humans, Genetic Predisposition to Disease, cardiovascular diseases, GENOME-WIDE ASSOCIATION, Polymorphism, 030304 developmental biology, Genetic association, Science & Technology, Hypertrophic/genetics, Left/genetics, Case-control study, CONTRACTILITY, 06 Biological Sciences, Cardiomyopathy, Hypertrophic, medicine.disease, Hypertrophic, Dilated/genetics, Case-Control Studies, Genome-Wide Association Study, 030217 neurology & neurosurgery, Developmental Biology

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cf7d23d192dff67828c4afc329009e0fTest
https://ora.ox.ac.uk/objects/uuid:c3ba02f5-a29f-4145-a8b8-d3e86d5db3f0Test

المؤلفون: Vissing, Christoffer Rasmus, Rasmussen, Torsten Bloch, Dybro, Anne Mette, Olesen, Morten Salling, Pedersen, Lisbeth Nørum, Jensen, Morten, Bundgaard, Henning, Christensen, Alex Hørby

المصدر: Vissing , C R , Rasmussen , T B , Dybro , A M , Olesen , M S , Pedersen , L N , Jensen , M , Bundgaard , H & Christensen , A H 2021 , ' Dilated cardiomyopathy caused by truncating titin variants : long-term outcomes, arrhythmias, response to treatment and sex differences ' , Journal of Medical Genetics , vol. 58 , no. 12 , pp. 832-841 . https://doi.org/10.1136/jmedgenet-2020-107178Test

مصطلحات موضوعية: arrhythmias, cardiac, cardiomyopathies, genetics, heart failure, medical, phenotype, Heart Failure/genetics, Cardiac/genetics, Humans, Middle Aged, Genetic Predisposition to Disease/genetics, Male, Ventricular Function, Left/genetics, Connectin/genetics, Adult, Female, Retrospective Studies, Cardiomyopathy, Dilated/genetics, Genetic Association Studies/methods, Sex Factors, Denmark, Aged, Outcome Assessment, Health Care/methods, Mutation, Longitudinal Studies

العلاقة: https://pure.au.dk/portal/en/publications/ef13479f-1559-4377-81d6-c7d2c8a39a4eTest

الإتاحة: https://doi.org/10.1136/jmedgenet-2020-107178Test
https://pure.au.dk/portal/en/publications/ef13479f-1559-4377-81d6-c7d2c8a39a4eTest
http://www.scopus.com/inward/record.url?scp=85095427110&partnerID=8YFLogxKTest

المؤلفون: Miles, C, Finocchiaro, G, Papadakis, M, Gray, B, Westaby, J, Ensam, B, Basu, J, Parry-Williams, G, Papatheodorou, E, Paterson, C, Malhotra, A, Robertus, JL, Ware, JS, Cook, SA, Asimaki, A, Witney, A, Chis Ster, I, Tome, M, Sharma, S, Behr, ER, Sheppard, MN

المساهمون: Wellcome Trust, St Georges University of London

المصدر: Circulation
Miles, C, Finocchiaro, G, Papadakis, M, Gray, B, Westaby, J, Ensam, B, Basu, J, Parry-Williams, G, Papatheodorou, E, Paterson, C, Malhotra, A, Robertus, J L, Ware, J S, Cook, S A, Asimaki, A, Witney, A, Ster, I C, Tome, M, Sharma, S, Behr, E R & Sheppard, M N 2019, ' Sudden Death and Left Ventricular Involvement in Arrhythmogenic Cardiomyopathy ', Circulation, vol. 139, no. 15, pp. 1786-1797 . https://doi.org/10.1161/CIRCULATIONAHA.118.037230Test

مصطلحات موضوعية: arrhythmogenic right ventricular dysplasia, cardiomyopathies, Adult, Male, Cardiac & Cardiovascular Systems, Heart Ventricles, AMERICAN-COLLEGE, Heart Ventricles/pathology, DIAGNOSIS, Risk Assessment, SPORTS, Ventricular Function, Left, 1117 Public Health and Health Services, Ventricular Dysfunction, Left, Young Adult, SUBSTRATE, Ventricular Dysfunction, Left/genetics, Risk Factors, Original Research Articles, Cause of Death, Humans, left ventricular arrhythmogenic cardiomyopathy, Genetic Predisposition to Disease, DYSPLASIA, Death, Sudden, Cardiac/etiology, 1102 Cardiorespiratory Medicine and Haematology, Arrhythmogenic Right Ventricular Dysplasia/genetics, Science & Technology, MUTATIONS, STATEMENT, MISSENSE, death, sudden, cardiac, 1103 Clinical Sciences, ASSOCIATION, arrhythmogenic cardiomyopathy, Middle Aged, MANIFESTATIONS, Peripheral Vascular Disease, Cardiovascular System & Hematology, Cardiovascular System & Cardiology, ComputingMethodologies_DOCUMENTANDTEXTPROCESSING, Female, Life Sciences & Biomedicine

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::53209902499421b9ecbc932e0e81bc7cTest
http://europepmc.org/articles/PMC6467560Test

المساهمون: Kyoung Hwa Lee, Heae Surng Park, Chul Hwan Park, Ki-Hyun Kim, Hyemoon Chung, Tae Hoon Kim, Se-Joong Rim, Eui-Young Choi, Kim, Tae Hoon, Park, Chul Hwan, Park, Heae Surng, Rim, Se Joong, Chung, Hye Moon, Choi, Eui Young

مصطلحات موضوعية: Adult, Amyloidosis/diagnosis, Cardiomyopathies/diagnosis, Cardiomyopathies/genetics, DNA, Mitochondrial/genetics, Diabetes Mellitus, Type 2/genetics, Diagnosis, Differential, Extracellular Space, Fabry Disease/diagnosis, Female, Hearing Loss, Sensorineural/genetics, Humans, MELAS Syndrome/diagnosis, MELAS Syndrome/genetics, Magnetic Resonance Imaging, Mitochondria, Heart/pathology, Myocarditis/diagnosis, Point Mutation, Ultrasonography, Ventricular Dysfunction, Left/diagnosis, Left/diagnostic imaging, Left/genetics

العلاقة: CIRCULATION; J00533; OAK-2014-02385; https://ir.ymlib.yonsei.ac.kr/handle/22282913/100305Test; http://circ.ahajournals.org/content/130/20/1832.longTest; T201404039; CIRCULATION, Vol.130(20) : 1832-1834, 2014

الإتاحة: https://doi.org/10.1161/CIRCULATIONAHA.114.010779Test
https://ir.ymlib.yonsei.ac.kr/handle/22282913/100305Test
http://circ.ahajournals.org/content/130/20/1832.longTest