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| Open AccessCardiac desmosomal adhesion relies on ideal-, slip- and catch bonds
- Manuel Göz
- , Sylvia M. Steinecker
- & Dario Anselmetti
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| Open AccessFetuin-A and its genetic association with cardiometabolic disease
- Lawien Al Ali
- , Yordi J. van de Vegte
- & Pim van der Harst
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| Open AccessFresh and frozen cardiac tissue are comparable in DNA methylation array β-values, but formalin-fixed, paraffin-embedded tissue may overestimate DNA methylation levels
- Mikkel Eriksen Dupont
- , Stine Bøttcher Jacobsen
- & Niels Morling
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| Open AccessSex-specific differences in the genetic and environmental effects on cardiac phenotypic variation assessed by echocardiography
- Honghuang Lin
- , Alan C. Kwan
- & Susan Cheng
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| Open AccessDNA quality evaluation of formalin-fixed paraffin-embedded heart tissue for DNA methylation array analysis
- Mikkel E. Dupont
- , Steffan N. Christiansen
- & Jeppe D. Andersen
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| Open AccessDeep learning-derived cardiovascular age shares a genetic basis with other cardiac phenotypes
- Julian Libiseller-Egger
- , Jody E. Phelan
- & Taane G. Clark
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| Open AccessLinking single nucleotide polymorphisms to signaling blueprints in abdominal aortic aneurysms
- Chrysania Lim
- , Muhammad Yogi Pratama
- & Bhama Ramkhelawon
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| Open AccessA pro-inflammatory and fibrous cap thinning transcriptome profile accompanies carotid plaque rupture leading to stroke
- Hernan A. Bazan
- , Ashton J. Brooks
- & T. Cooper Woods
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| Open AccessAn Myh11 single lysine deletion causes aortic dissection by reducing aortic structural integrity and contractility
- Keita Negishi
- , Kenichi Aizawa
- & Yasushi Imai
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| Open AccessPiezo2 is not an indispensable mechanosensor in murine cardiomyocytes
- Benjamin Kloth
- , Giulia Mearini
- & Marc N. Hirt
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| Open AccessExpression of cardiovascular-related microRNAs is altered in L-arginine:glycine amidinotransferase deficient mice
- Märit Jensen
- , Christian Müller
- & Tanja Zeller
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| Open AccessImpact of genetic risk score on the association between male childlessness and cardiovascular disease and mortality
- Angel Elenkov
- , Olle Melander
- & Aleksander Giwercman
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| Open AccessMapping gene and gene pathways associated with coronary artery disease: a CARDIoGRAM exome and multi-ancestry UK biobank analysis
- Praveen Hariharan
- & Josée Dupuis
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| Open AccessGenetic contributions to the expression of acquired causes of cardiac hypertrophy in non-ischemic sudden cardiac death victims
- Lauri Holmström
- , Katri Pylkäs
- & Juhani Junttila
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| Open AccessStress-induced differential gene expression in cardiac tissue
- Ana Elisa T. S. de Carvalho
- , Marco A. Cordeiro
- & Regina C. Spadari
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Article
| Open AccessAtrial fibrillation and left atrial size and function: a Mendelian randomization study
- Yordi J. van de Vegte
- , Joylene E. Siland
- & Pim van der Harst
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| Open AccessAltered metabolic and inflammatory transcriptomics after cardiac surgery in neonates with congenital heart disease
- Parag N. Jain
- , Matthew Robertson
- & Cristian Coarfa
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| Open AccessTRPM2 promotes autophagic degradation in vascular smooth muscle cells
- Qiannan Zhao
- , Jingxuan Li
- & Xiaoqiang Yao
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| Open AccessIdentifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndrome
- Cristina E. Trevino
- , Aaron M. Holleman
- & Michael E. Zwick
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Article
| Open AccessHuman essential hypertension: no significant association of polygenic risk scores with antihypertensive drug responses
- Heini Sánez Tähtisalo
- , Sanni Ruotsalainen
- & Timo P. Hiltunen
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| Open AccessVariation in RARG increases susceptibility to doxorubicin-induced cardiotoxicity in patient specific induced pluripotent stem cell-derived cardiomyocytes
- Effimia Christidi
- , Haojun Huang
- & Liam R. Brunham
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| Open AccessAssociation of the methylene-tetrahydrofolate reductase gene rs1801133 C677T variant with serum homocysteine levels, and the severity of coronary artery disease
- Nadia Bouzidi
- , Majed Hassine
- & Salima Ferchichi
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Article
| Open AccessEarly-onset atrial fibrillation patients show reduced left ventricular ejection fraction and increased atrial fibrosis
- Laura Andreasen
- , Litten Bertelsen
- & Morten S. Olesen
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| Open AccessCYP17A1 deficient XY mice display susceptibility to atherosclerosis, altered lipidomic profile and atypical sex development
- Redouane Aherrahrou
- , Alexandra E. Kulle
- & Zouhair Aherrahrou
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| Open AccessAnalysis of L-arginine:glycine amidinotransferase-, creatine- and homoarginine-dependent gene regulation in the murine heart
- Märit Jensen
- , Christian Müller
- & Tanja Zeller
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Article
| Open AccessAutomated Quantitative Extraction and Analysis of 4D flow Patterns in the Ascending Aorta: An intraindividual comparison at 1.5 T and 3 T
- Sebastian Ebel
- , Josefin Dufke
- & Matthias Gutberlet
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| Open AccessGene expression in immortalized versus primary isolated cardiac endothelial cells
- Lisa Deng
- , Luisa Pollmeier
- & Achim Lother
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| Open AccessAssociation of the genetic ancestry with resistant hypertension in the ReHOT (Resistant Hypertension Optimal Treatment) randomized study
- Carolina Tosin Bueno
- , Alexandre Costa Pereira
- & Paulo Caleb Junior Lima Santos
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| Open AccessA Novel Loss-of-Function Variant in the Chloride Ion Channel Gene Clcn2 Associates with Atrial Fibrillation
- Thea Hyttel Hansen
- , Yannan Yan
- & Nicole Schmitt
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| Open AccessMIF gene rs755622 polymorphism positively associated with acute coronary syndrome in Chinese Han population: case–control study
- Guo-Li Du
- , Jun-Yi Luo
- & Yi-Ning Yang
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Article
| Open AccessThe CXCL12 SNPs and their haplotypes are associated with serum lipid traits
- Ling Qiu
- , Rui-Xing Yin
- & Fen-Han Zhang
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Article
| Open AccessLower risk of smoking-related cancer in individuals with familial hypercholesterolemia compared with controls: a prospective matched cohort study
- Henriette W. Krogh
- , Karianne Svendsen
- & Kjetil Retterstøl
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| Open AccessA novel circRNA-miRNA-mRNA network identifies circ-YOD1 as a biomarker for coronary artery disease
- Liu Miao
- , Rui-Xing Yin
- & Hui Li
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| Open AccessAssociation between the 4p16 genomic locus and different types of congenital heart disease: results from adult survivors in the UK Biobank
- Aldo Córdova-Palomera
- & James R. Priest
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| Open AccessLow mutation rate in the TTN gene in paediatric patients with dilated cardiomyopathy – a pilot study
- Elena Zaklyazminskaya
- , Vadim Mikhailov
- & Sergey Dzemeshkevich
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| Open AccessSex differences in risk factors for stroke in patients with hypertension and hyperhomocysteinemia
- Hui Pang
- , Qiang Fu
- & Zhenkun Zong
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| Open AccessHuman primary endothelial cells are impaired in nucleotide excision repair and sensitive to benzo[a]pyrene compared with smooth muscle cells and pericytes
- Joana M. Kress
- , Lorella Di Dio
- & Bernd Kaina
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| Open AccessMarked variation in heritability estimates of left ventricular mass depending on modality of measurement
- Richard M. Nethononda
- , Kathryn A. McGurk
- & Hugh Watkins
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| Open AccessAssociation among PlA1/A2 gene polymorphism, laboratory aspirin resistance and clinical outcomes in patients with coronary artery disease: An updated meta-analysis
- Jing Wang
- , Jie Liu
- & Chunjian Li
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Article
| Open AccessCETP, LIPC, and SCARB1 variants in individuals with extremely high high-density lipoprotein-cholesterol levels
- Chan Joo Lee
- , Mun Su Park
- & Sang-Hak Lee
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| Open AccessGenome-wide association study identifies loci for arterial stiffness index in 127,121 UK Biobank participants
- Kenneth Fung
- , Julia Ramírez
- & Patricia B. Munroe
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| Open AccessAnalysis of enriched rare variants in JPH2-encoded junctophilin-2 among Greater Middle Eastern individuals reveals a novel homozygous variant associated with neonatal dilated cardiomyopathy
- Edward G. Jones
- , Neda Mazaheri
- & Andrew P. Landstrom
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| Open AccessThe Effects of Regular Exercise on Circulating Cardiovascular-related MicroRNAs
- Jacob L. Barber
- , Kia N. Zellars
- & Mark A. Sarzynski
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| Open AccessEffect of a phosphodiesterase-5A (PDE5A) gene polymorphism on response to sildenafil therapy in canine pulmonary hypertension
- Yu Ueda
- , Lynelle R. Johnson
- & Joshua A. Stern
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| Open AccessDNAH11 variants and its association with congenital heart disease and heterotaxy syndrome
- Sida Liu
- , Weicheng Chen
- & Guoying Huang
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| Open AccessLewis and AB0 blood group-phenotypes in periodontitis, cardiovascular disease, obesity and stroke
- C. Enevold
- , C. H. Nielsen
- & P. Holmstrup
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| Open AccessA Multi-Trait Approach Identified Genetic Variants Including a Rare Mutation in RGS3 with Impact on Abnormalities of Cardiac Structure/Function
- Akram Yazdani
- , Azam Yazdani
- & Luca Sartore
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| Open AccessGenetic polymorphisms in MTR are associated with non-syndromic congenital heart disease from a family-based case-control study in the Chinese population
- Changfei Deng
- , Ying Deng
- & Li Dai
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| Open AccessRelevance of Titin Missense and Non-Frameshifting Insertions/Deletions Variants in Dilated Cardiomyopathy
- Oyediran Akinrinade
- , Tiina Heliö
- & Juha Koskenvuo