نتائج البحث - "Genetics cardiovascular diseases"

1

Associations of genetically predicted IL-6 signaling with cardiovascular disease risk across population subgroups

المؤلفون: Marios K. Georgakis, Rainer Malik, Tom G. Richardson, Joanna M. M. Howson, Christopher D. Anderson, Stephen Burgess, G. Kees Hovingh, Martin Dichgans, Dipender Gill

المساهمون: Burgess, Stephen [0000-0001-5365-8760], Apollo - University of Cambridge Repository, Experimental Vascular Medicine, Vascular Medicine, ACS - Atherosclerosis & ischemic syndromes, ACS - Amsterdam Cardiovascular Sciences

المصدر: BMC medicine, 20(1):245. BioMed Central
BMC medicine 20(1), 245 (2022). doi:10.1186/s12916-022-02446-6

وصف الملف: application/octet-stream; application/pdf; text/xml; application/zip

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::390bdab43f2b70d7b1cac331631a7418Test
https://doi.org/10.1186/s12916-022-02446-6Test

2

Additive Effects of Genetic Interleukin-6 Signaling Downregulation and Low-Density Lipoprotein Cholesterol Lowering on Cardiovascular Disease: A 2×2 Factorial Mendelian Randomization Analysis

المؤلفون: Marios K. Georgakis, Rainer Malik, Stephen Burgess, Martin Dichgans

المساهمون: Georgakis, Marios K [0000-0003-3507-3659], Malik, Rainer [0000-0001-9212-2520], Burgess, Stephen [0000-0001-5365-8760], Dichgans, Martin [0000-0002-0654-387X], Apollo - University of Cambridge Repository

المصدر: Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 11, Iss 1 (2022)
J Am Heart Assoc
Journal of the American Heart Association 11(1), e023277 (2022). doi:10.1161/JAHA.121.023277

وصف الملف: application/vnd.openxmlformats-officedocument.wordprocessingml.document

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ed2efa66c72a1d30a18776f6d770557eTest
https://pubmed.ncbi.nlm.nih.gov/34927447Test

3

Genetically Proxied Inhibition of Coagulation Factors and Risk of Cardiovascular Disease: A Mendelian Randomization Study

المؤلفون: Dipender Gill, Michael Laffan, Amy M. Mason, Martin Dichgans, Susanna C. Larsson, Shuai Yuan, Stephen Burgess

المساهمون: Burgess, Stephen [0000-0001-5365-8760], Mason, Amy [0000-0002-8019-0777], Apollo - University of Cambridge Repository

المصدر: Journal of the American Heart Association 10(8), e019644 (2021). doi:10.1161/JAHA.120.019644
Journal of the American Heart Association
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease

مصطلحات موضوعية: Cardiac & Cardiovascular Systems, Neurologi, Disease, 030204 cardiovascular system & hematology, Bioinformatics, methods [Genome-Wide Association Study], 0302 clinical medicine, Japan, methods [Mendelian Randomization Analysis], cardiovascular disease, Risk Factors, Medicine, Cardiac and Cardiovascular Systems, metabolism [Blood Coagulation Factors], 030212 general & internal medicine, 1102 Cardiorespiratory Medicine and Haematology, Stroke, Original Research, ORAL ANTICOAGULANTS, Kardiologi, DABIGATRAN, Mendelian Randomization Analysis, genetics [Cardiovascular Diseases], stroke, epidemiology [Cardiovascular Diseases], Blood Coagulation Factors, Neurology, Coagulation, Cardiovascular Diseases, epidemiology [Japan], Cardiology and Cardiovascular Medicine, Life Sciences & Biomedicine, Mendelian randomization analysis, venous thromboembolism, genetics [Blood Coagulation Factors], Polymorphism, Single Nucleotide, 03 medical and health sciences, Mendelian randomization, Genetics, Humans, Genetic Predisposition to Disease, ddc:610, coagulation, METAANALYSIS, Ischemic Stroke, FIBRINOGEN, Science & Technology, business.industry, RIVAROXABAN, medicine.disease, PREVENTION, ASPIRIN, THROMBOSIS, ATRIAL-FIBRILLATION, Cardiovascular System & Cardiology, business, Venous thromboembolism, Genome-Wide Association Study

وصف الملف: application/pdf; application/vnd.openxmlformats-officedocument.wordprocessingml.document

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f69faf3378ba780cb432d7fd9b2c7518Test

4

دورية أكاديمية

Time for education in cardiogenetics

المؤلفون: Philippe Charron, Perry Elliott

المصدر: Cardiogenetics, Vol 1, Iss 1, Pp e2-e2 (2011)

مصطلحات موضوعية: education, clinical cardiovascular genetics, cardiovascular diseases., Diseases of the circulatory (Cardiovascular) system, RC666-701

وصف الملف: electronic resource

العلاقة: http://www.pagepressjournals.org/index.php/cardiogen/article/view/96Test; https://doaj.org/toc/2035-8253Test; https://doaj.org/toc/2035-8148Test

الوصول الحر: https://doaj.org/article/6911a5cd040d4c2bb9457cdf2646974cTest

View record in DOAJ

5

دورية أكاديمية

PHARMACOGENETIC OF LIPID-LOWERING DRUGS ; FARMACOGENÉTICA DE FÁRMACOS HIPOLIPEMIANTES

المؤلفون: Fiegenbaum, Marilu, Hutz, Mara H.

المصدر: Medicina (Ribeirao Preto); Vol. 39 No. 4 (2006); 543-553 ; Medicina (Ribeirao Preto); Vol. 39 Núm. 4 (2006); 543-553 ; Medicina (Ribeirão Preto); v. 39 n. 4 (2006); 543-553 ; 2176-7262 ; 0076-6046

مصطلحات موضوعية: Lipid Lowering Drugs. Pharmacogenetics. Variation (Genetics). Cardiovascular Diseases, Hipolipemiantes. Farmacogenética. Variação (Genética). Doenças Cardiovasculares

وصف الملف: application/pdf

العلاقة: https://www.revistas.usp.br/rmrp/article/view/405/406Test; https://www.revistas.usp.br/rmrp/article/view/405Test

الإتاحة: https://www.revistas.usp.br/rmrp/article/view/405Test

View record in BASE

6

MicroRNAs in age-related diseases

المؤلفون: Stefanie Dimmeler, Pierluigi Nicotera

المصدر: EMBO Molecular Medicine
EMBO molecular medicine 5(2), 180-190 (2013). doi:10.1002/emmm.201201986

مصطلحات موضوعية: Senescence, Aging, senescence, cardiac, Disease, Review, Biology, metabolism [Neurodegenerative Diseases], Bioinformatics, 03 medical and health sciences, 0302 clinical medicine, Immune system, vascular, metabolism [MicroRNAs], microRNA, Gene expression, medicine, Gene silencing, Animals, Humans, ddc:610, metabolism [Aging], genetics [MicroRNAs], 030304 developmental biology, 0303 health sciences, Neurodegeneration, neurodegeneration, Translation (biology), Neurodegenerative Diseases, genetics [Cardiovascular Diseases], medicine.disease, MicroRNAs, Cardiovascular Diseases, genetics [Aging], genetics [Neurodegenerative Diseases], Molecular Medicine, 030217 neurology & neurosurgery, metabolism [Cardiovascular Diseases]

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::726ffa69f1ee3452126e0899715d2f3fTest
http://europepmc.org/articles/PMC3569636Test

7

Update of the effect estimates for common variants associated with carotid intima media thickness within four independent samples: The Bonn IMT Family Study, the Heinz Nixdorf Recall Study, the SAPHIR Study and the Bruneck Study

المصدر: Atherosclerosis / Supplements 249, 83-87 (2016). doi:10.1016/j.atherosclerosis.2016.03.042

مصطلحات موضوعية: 0301 basic medicine, Adult, Male, Genotype, Medizin, Single-nucleotide polymorphism, Genome-wide association study, genetics [Atherosclerosis], Biology, Carotid Intima-Media Thickness, Polymorphism, Single Nucleotide, 03 medical and health sciences, Statistics, Independent samples, SNP, Humans, ddc:610, Prospective Studies, Genetic association, Aged, Aged, 80 and over, Family Health, Chromosome Mapping, genetics [Cardiovascular Diseases], Genomics, Middle Aged, Atherosclerosis, Observational Studies as Topic, 030104 developmental biology, Pooled analysis, Intima-media thickness, Cardiovascular Diseases, Research Design, Subclinical atherosclerosis, Data Interpretation, Statistical, Female, Cardiology and Cardiovascular Medicine, Genome-Wide Association Study

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::20d6aea9a6941f6fe45595400c7b388dTest
https://pubmed.ncbi.nlm.nih.gov/27085157Test

8

دورية أكاديمية

The role of molecular biology in the diagnosis and treatment of cardiovascular diseases.

المؤلفون: Mariotti S., Capparuccia C., Ripa C., OLIVIERI, Fabiola, Lisa R., PROCOPIO, Antonio Domenico, Antonicelli R.

المساهمون: Mariotti, S., Capparuccia, C., Ripa, C., Olivieri, Fabiola, Lisa, R., Procopio, Antonio Domenico, Antonicelli, R.

مصطلحات موضوعية: Cardiovascular Diseases/diagnosis* Cardiovascular Diseases/genetics* Cardiovascular Diseases/therapy Gene Expression Profiling/methods Genetic Predisposition to Disease Genetic Testing Genotype Humans Mutation* Phenotype Polymorphism, Genetic* Prognosis Risk Factors

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/21246774; volume:11; issue:10; firstpage:730; lastpage:745; numberofpages:16; journal:GIORNALE ITALIANO DI CARDIOLOGIA; http://hdl.handle.net/11566/54146Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-77957946877

الإتاحة: http://hdl.handle.net/11566/54146Test

View record in BASE

9

Telomerer, åldrande och livsstil--forskning med motstridiga fynd

المؤلفون: Dahlman, Disa, Fyhrquist, Frej, Nilsson, Peter

المصدر: Läkartidningen; 107(48), pp 5-3053 (2010)

مصطلحات موضوعية: drug effects [Telomere], physiology [Telomere], metabolism [Telomerase], genetics [Aging], Other Clinical Medicine, genetics [Telomere], genetics [Cardiovascular Diseases], etiology [Cardiovascular Diseases], physiology [Aging]

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::020cef3cd8520122823293b29683f220Test
http://lup.lub.lu.se/record/1832361/file/1848707.pdfTest

10

Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants

المؤلفون: Myocardial Infarction Genetics, The complete list, Sekar, Kathiresan, Voight, Benjamin F., Shaun, Purcell, Kiran, Musunuru, Diego, Ardissino, Mannucci, Pier M., Sonia, Anand, Engert, James C., Samani, Nilesh J., Heribert, Schunkert, Jeanette, Erdmann, Reilly, Muredach P., Rader, Daniel J., Thomas, Morgan, Spertus, John A., Monika, Stoll, Girelli, Domenico, Mckeown, Pascal P., Patterson, Chris C., Siscovick, David S., O'Donnell, Christopher J., Roberto, Elosua, Leena, Peltonen, Veikko, Salomaa, Schwartz, Stephen M., Olle, Melander, David, Altshuler, Thrombosis Italian Atherosclerosis, Vascular Biology Study, Pier Angelica Merlini, Carlo, Berzuini, Luisa, Bernardinelli, Flora, Peyvandi, Marco, Tubaro, Patrizia, Celli, Maurizio, Ferrario, Raffaela, Fetiveau, Nicola, Marziliano, Giorgio, Casari, Michele, Galli, Ribichini, Flavio Luciano, Marco, Rossi, Francesco, Bernardi, Pietro, Zonzin, Alberto, Piazza, Heart Attack Risk, Jean, Yee, Yechiel, Friedlander, Registre Gironi del, Jaume, Marrugat, Gavin, Lucas, Isaac, Subirana, Joan, Sala, Rafael, Ramos, Massachusetts General Hospital, Meigs, James B., Gordon, Williams, Nathan, David M., Macrae, Calum A., F. I. N., Havulinna, Aki S., Malmo, Diet, Cancer, Study, Goran, Berglund, Stage, 1 data, Hirschhorn, Joel N., Rosanna, Asselta, Stefano, Duga, Marta, Spreafico, Daly, Mark J., Copy number variant, James, Nemesh, Korn, Joshua M., Mccarroll, Steven A., Stage, 1 phenotype, Stage, 1 genome wide, Aarti, Surti, Candace, Guiducci, Lauren, Gianniny, Daniel, Mirel, Melissa, Parkin, Noel, Burtt, Gabriel, Stacey B., Replication, Studies, Thompson, John R., Braund, Peter S., Wright, Benjamin J., Balmforth, Anthony J., Ball, Stephen G., Hall, Alistair S., Wellcome Trust Case, German MI Family, Patrick Linsel Nitschke, Wolfgang, Lieb, Andreas, Ziegler, König, Inke R., Christian, Hengstenberg, Marcus, Fischer, Klaus, Stark, Anika, Grosshennig, Michael, Preuss, Erich Wichmann, H., Stefan, Schreiber, Cardiogenics, Willem, Ouwehand, Panos, Deloukas, Michael, Scholz, Francois, Cambien, C. a. r. d. i. o. g. e. n. i. c. s., P. e. n. n. C. A. T., Mingyao, Li, Zhen, Chen, Robert, Wilensky, William, Matthai, Atif, Qasim, Hakonarson, Hakon H., Joe, Devaney, Mary Susan Burnett, Pichard, Augusto D., Kent, Kenneth M., Lowell, Satler, Lindsay, Joseph M., Ron, Waksman, Epstein, Stephen E., Acute Myocardial Infarction, Thomas, Scheffold, Klaus, Berger, Andreas, Huge, Verona Heart Study, Domenico, Girelli, Martinelli, Nicola, Olivieri, Oliviero, Corrocher, Roberto, Mid America Heart Institute, Irish Family Study, d. e. C. O. D., Hilma, Hólm, Gudmar, Thorleifsson, Unnur, Thorsteinsdottir, Kari, Stefansson, I. N. T., Ron, Do, Changchun, Xie, Gen, M. I., David, Siscovick

المساهمون: Kathiresan, S, Altschuler, D, Anand, S, Ardissino, D, Asselta, R, Ball, Sg, Balmforth, Aj, Berger, K, Berglund, G, Bernardi, F, Bernardinelli, L, Berzuini, C, Braund, P, Burnett, M, Burtt, N, Cambien, F, Casari, GIORGIO NEVIO, Celli, P, Chen, Z, Corrocher, R, Daly, Mj, Deloukas, P, Devaney, J, Do, R, Duga, S, Elosua, R, Engert, Jc, Epstein, Se, Erdmann, J, Ferrario, M, Fetiveau, R, Fischer, M, Friedlander, Y, Gabriel, Sb, Galli, M, Gianniny, L, Girelli, D, Grosshennig, A, Guiducci, C, Hakonarson, Hh, Hall, A, Havulinna, A, Hengstenberg, C, Hirschhorn, Jn, Holm, H, Huge, A, Kent, Km, Konig, Ir, Korn, Jm, Li, M, Lieb, W, Lindsay, Jm, Linsel Nitschke, P, Lucas, G, Macrae, Ca, Mannucci, Pm, Marrugat, J, Martinelli, N, Marziliano, N, Matthai, W, Mccarroll, Sa, Mckeown, Pp, Meigs, Jb, Melander, O, Merlini, Pa, Mirel, D, Morgan, T, Musunuru, K, Nathan, Dm, Nemesh, J, O'Donnell, Cj, Olivieri, O, Ouwehand, W, Parkin, M, Patterson, Cc, Peltonen, L, Peyvandi, F, Piazza, A, Pichard, Ad, Preuss, M, Purcell, S, Qasim, A, Rader, Dj, Ramos, R, Reilly, Mp, Ribichini, F, Rossi, M, Sala, J, Salomaa, V, Samani, Nj, Satler, L, Scheffold, T, Scholz, M, Schreiber, S, Schunkert, H, Schwartz, Sm, Siscovick, D, Spertus, Ja, Spreafico, M, Stark, K, Stefansson, K, Stoll, M, Subirana, I, Surti, A, Thompson, Jr, Thorleifsson, G, Thorsteinsdottir, U, Tubaro, M, Voight, Bf, Waksman, R, Wichmann, He, Wilensky, R, Williams, G, Wright, Bj, Xie, C, Yee, J, Ziegler, A, Zonzin, P.

مصطلحات موضوعية: Adult, Male, copy number variants (CNVs), Gene Dosage, Myocardial Infarction, Locus (genetics), Single-nucleotide polymorphism, Genome-wide association study, 030204 cardiovascular system & hematology, Biology, Bioinformatics, association study, Polymorphism, Single Nucleotide, Article, 03 medical and health sciences, 0302 clinical medicine, myocardial infarction with single, Gene Frequency, Risk Factors, Genetics cardiovascular diseases, genome-wide association, single nucleotide polymorphisms (SNPs), association with early-onset myocardial infarction, Genetics, Humans, Genetic Predisposition to Disease, Copy-number variation, Age of Onset, Gene, Allele frequency, 030304 developmental biology, 0303 health sciences, myocardial infarction, SNPs, Genome-wide association, nucleotide polymorphisms, Middle Aged, Genetic epidemiology, Case-Control Studies, Mutation, Female, Age of onset, Algorithms, Genome-Wide Association Study

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::97ab621c3c18cb6b5786a39cb4ff3146Test
http://hdl.handle.net/2318/60709Test

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