about
Molecular insights into arrhythmogenic right ventricular cardiomyopathy caused by plakophilin-2 missense mutationsNovel associations of CPS1, MUT, NOX4, and DPEP1 with plasma homocysteine in a healthy population: a genome-wide evaluation of 13 974 participants in the Women's Genome Health StudyChylomicronemia with low postheparin lipoprotein lipase levels in the setting of GPIHBP1 defectsMolecular genetic and functional characterization implicate muscle-restricted coiled-coil gene (MURC) as a causal gene for familial dilated cardiomyopathyHomozygous founder mutation in desmocollin-2 (DSC2) causes arrhythmogenic cardiomyopathy in the Hutterite populationNovel Abetalipoproteinemia Missense Mutation Highlights the Importance of the N-Terminal β-Barrel in Microsomal Triglyceride Transfer Protein FunctionHomozygosity mapping and exome sequencing reveal GATAD1 mutation in autosomal recessive dilated cardiomyopathyA genome-wide association study identifies LIPA as a susceptibility gene for coronary artery diseasePharmacogenetic predictors of statin-mediated low-density lipoprotein cholesterol reduction and dose responseInvestigation of variants identified in caucasian genome-wide association studies for plasma high-density lipoprotein cholesterol and triglycerides levels in Mexican dyslipidemic study samplesPolymorphism in the CETP gene region, HDL cholesterol, and risk of future myocardial infarction: Genomewide analysis among 18 245 initially healthy women from the Women's Genome Health StudyA genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN projectHypophosphatemia, hyperphosphaturia, and bisphosphonate treatment are associated with survival beyond infancy in generalized arterial calcification of infancyA clinical approach to inherited arrhythmiasChallenges of exercise recommendations and sports participation in genetic heart disease patientsUsing extracellular matrix proteomics to understand left ventricular remodelingQuantitative mass spectrometry-based approaches in cardiovascular researchGenome-wide meta-analyses of plasma renin activity and concentration reveal association with the kininogen 1 and prekallikrein genesGenetic basis of familial valvular heart diseaseSupravalvular aortic stenosis: elastin arteriopathyThe implications of inheritance for clinical managementSPARC-Dependent Cardiomyopathy in Drosophila.Loss of Function Mutations in NNT Are Associated With Left Ventricular NoncompactionThe impact of mechanical forces in heart morphogenesis.Top advances in functional genomics and translational biology for 2014The novel desmin mutant p.A120D impairs filament formation, prevents intercalated disk localization, and causes sudden cardiac deathSarcomere gene mutations in isolated left ventricular noncompaction cardiomyopathy do not predict clinical phenotypeSkin-heart connection: what can the epidermis tell us about the myocardium in arrhythmogenic cardiomyopathy?Haploinsufficiency of the NOTCH1 Receptor as a Cause of Adams-Oliver Syndrome With Variable Cardiac AnomaliesDesmoglein 2-Dependent Arrhythmogenic Cardiomyopathy Is Caused by a Loss of Adhesive FunctionA dream, a journey, and a promise: the inauguration of Circulation: Cardiovascular GeneticsClinical and functional characterization of TNNT2 mutations identified in patients with dilated cardiomyopathyComprehensive desmosome mutation analysis in north americans with arrhythmogenic right ventricular dysplasia/cardiomyopathyCoding sequence rare variants identified in MYBPC3, MYH6, TPM1, TNNC1, and TNNI3 from 312 patients with familial or idiopathic dilated cardiomyopathyA comprehensive genetic study on left atrium size in Caribbean Hispanics identifies potential candidate genes in 17p10Coronary heart disease in systemic lupus erythematosus is associated with interferon regulatory factor-8 gene variantsThe role of CAV3 in long-QT syndrome: clinical and functional assessment of a caveolin-3/Kv11.1 double heterozygote versus caveolin-3 single heterozygoteCompound and digenic heterozygosity predicts lifetime arrhythmic outcome and sudden cardiac death in desmosomal gene-related arrhythmogenic right ventricular cardiomyopathyCorrelation of ventricular arrhythmias with genotype in arrhythmogenic right ventricular cardiomyopathyKcne2 deletion creates a multisystem syndrome predisposing to sudden cardiac death
P1433
Q24292940-8457B0BF-28E2-4774-8D6F-D1F21F0A15B4Q24293230-ABE9DE50-3DC9-42F9-BB26-E5CB2F41B44FQ24298184-6AD12A23-9886-473A-B2CC-3BB4B4E8AF00Q24305518-FC3A69AA-8C05-4CB0-A2CF-C04F45B1A77BQ24309579-75CED14B-2E9D-465B-BE69-1E17B99FE5B0Q24338622-B2D914B5-8447-4EC8-9D52-DE9192B217DDQ24339132-4D66A75A-702A-4510-95C0-24C2F7A37D58Q24615584-03E0E72D-A38F-405C-8022-512B7AE0876CQ24632568-6DF6C05E-2F0F-45C4-AB55-14EF3496B89DQ24642868-6B39D6FF-0779-4E5F-85EF-4BEAD71A697AQ24649155-668FC06D-FE30-4146-BDCE-38F1EEB05BC8Q24653943-AA679999-AA36-4356-A438-7FD58A6B2728Q24657630-69E4F943-469F-4F7B-B0E1-167777BFFFEBQ26851743-559F24BB-8D8C-4C2F-A095-D7C7B6803573Q26859962-01C7A3D1-10BB-4EE2-9B9C-735205785FCFQ26863127-D6EB1A28-20E7-4910-BBF6-5D7B6DD0D18AQ26864913-8874CAC5-1053-4B56-80CA-DA42A361DB1EQ26991686-2337B8C3-8AA0-460D-A0F8-C652505D18C8Q27004837-08EB72AD-85BF-4A49-8B2E-A02484DF3C7DQ27008817-E09D36DC-4912-4F76-9A01-8218AF38002BQ27027728-1C390B18-FCFC-46FD-A84D-3D7466E19D54Q27340405-2E18E804-567F-490C-B931-23215DB5F366Q27340446-7062E024-FD4F-42EB-A272-1BB9816BE20DQ27692679-C4AD78F1-56E0-4BB6-BBA6-08A959ABE1A0Q28084667-694F1BAF-86CA-4694-BE90-15201E98B6F7Q28114840-7D796C63-7B92-462E-A6C2-838C02A4D9CCQ28236991-427A1251-7E4C-4D4C-8742-4C94A13CA4B7Q28242515-A486FE8D-CFC5-47A9-AE8F-922717ADEEE8Q28261852-131AD427-8312-46E7-8A16-2483CAC72471Q28263644-B5A7E998-4E3F-4098-86D3-39B0774445A0Q28268618-DB780309-7969-47F7-B5F8-3E57F14FA336Q28268628-060A54A2-5D81-4097-97D3-FFEE4558E182Q28268639-57999CD0-EE8E-4C8E-AD6A-A73AE9C83CFCQ28275501-F9513326-2B50-4C5E-927B-F27E20E712FFQ28285734-91CC8644-39C6-4AFB-B5B6-BFC586BD916EQ28290376-D4DFDCA2-1C71-41D7-83FF-E8FC421C16DCQ28298218-108FA8A6-025F-4A3F-A76C-A012BCAA9B4EQ28299300-E1A1CD2F-43F3-4BD3-ACC2-F712BF8A9CF1Q28300243-893FC232-24A0-4D83-985F-D36CAE73B9A2Q28305511-C1DA5EAC-3EF6-470A-B835-00F6296ECD19
P1433
description
journal
@en
revista científica
@es
rivista scientifica
@it
wetenschappelijk tijdschrift van Lippincott Williams & Wilkins
@nl
wissenschaftliche Fachzeitschrift
@de
name
Circulation: Cardiovascular Genetics
@ast
Circulation: Cardiovascular Genetics
@en
Circulation: Cardiovascular Genetics
@es
Circulation: Cardiovascular Genetics
@it
Circulation: Cardiovascular Genetics
@nl
type
label
Circulation: Cardiovascular Genetics
@ast
Circulation: Cardiovascular Genetics
@en
Circulation: Cardiovascular Genetics
@es
Circulation: Cardiovascular Genetics
@it
Circulation: Cardiovascular Genetics
@nl
prefLabel
Circulation: Cardiovascular Genetics
@ast
Circulation: Cardiovascular Genetics
@en
Circulation: Cardiovascular Genetics
@es
Circulation: Cardiovascular Genetics
@it
Circulation: Cardiovascular Genetics
@nl
P3181
P4616
P1055
P1058
P1156
19600166306
P1250
P1476
Circulation: Cardiovascular Genetics
@und