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1
A double-blind, randomized placebo-controlled trial examining the effect of MitoQ on myocardial energetics in patients with dilated cardiomyopathy

von Halliday, BP ; Owen, R ; Ragavan, A ; et al.
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2
Influence of age and sex on the diagnostic yield of inherited cardiac conditions in sudden arrhythmic death syndrome decedents.

von Gray, B ; Behr, ER ; Papatheodorou, E ; et al.
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3
Rare disease gene association discovery in the 100,000 Genomes Project

von Cipriani V ; Vestito L ; Magavern EF ; et al.

Nature, 2025
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4
Genome-wide association study meta-analysis provides insights into the etiology of heart failure and its subtypes

von Henry, A ; Mo, X ; Finan, C ; et al.
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5
Prognostic Role of Myocarditis-Like Episodes and Their Treatment in Patients With Pathogenic Desmoplakin Variants

von Gasperetti, A ; Muller, SA ; Peretto, G ; et al.

Circulation , 152 (14) pp. 978-989. (2025)

Schlagworte: arrhythmias; cardiac; cardiomyopathies; death; sudden; genetics; inflammation; myocarditis; risk assessment
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6
Rare disease gene association discovery in the 100,000 Genomes Project

von Cipriani, V ; Vestito, L ; Magavern, EF ; et al.

Nature (2025) (In press).
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7
Fibrosis Entropy Is Associated With Life‐Threatening Arrhythmia in Nonischemic Cardiomyopathy

von Hammersley, DJ ; Zaidi, HA ; Jones, RE ; et al.
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8
Large-scale genome-wide association analyses identify novel genetic loci and mechanisms in hypertrophic cardiomyopathy

von Tadros, R ; Zheng, SL ; Grace, C ; et al.
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9
Evaluation of polygenic scores for hypertrophic cardiomyopathy in the general population and across clinical settings

von Zheng, SL ; Jurgens, SJ ; Mcgurk, KA ; et al.
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10
Genes Associated With Hypertrophic Cardiomyopathy: A Reappraisal by the ClinGen Hereditary Cardiovascular Disease Gene Curation Expert Panel.

von Hespe, S ; Waddell, A ; Asatryan, B ; et al.
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11
14 Myocardial sheetlet abnormality as a marker of sarcomere dysfunction in carriers of rare HCM-causing sarcomere gene variants before phenotypic conversion

von Dwornik, Maria ; Khalique, Z ; Scott, AD ; et al.

Abstracts ; page A7.2-A9
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12
The Human Phenotype Ontology in 2024: phenotypes around the world

von Gargano MA ; Matentzoglu N ; Coleman B ; et al.

Nucleic Acids Research, 5 January 2024
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13
Genetic constraint at single amino acid resolution in protein domains improves missense variant prioritisation and gene discovery

von Zhang, X ; Theotokis, PI ; Li, N ; et al.
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14
Long-Term Arrhythmic Follow-Up and Risk Stratification of Patients With Desmoplakin-Associated Arrhythmogenic Right Ventricular Cardiomyopathy

von Gasperetti, A ; Carrick, R ; Protonotarios, A ; et al.

JACC: Advances , 3 (3) , Article 100832. (2024)

Schlagworte: ACM; ARVC; desmoplakin; risk stratification
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15
Precision prediction of heart failure events in patients with dilated cardiomyopathy and mildly reduced ejection fraction using multi‐parametric cardiovascular magnetic resonance

von Hammersley, DJ ; Mukhopadhyay, S ; Chen, X ; et al.
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16
Arrhythmic Risk Stratification by Cardiovascular Magnetic Resonance Imaging in Patients With Nonischemic Cardiomyopathy

von Hammersley, DJ ; Zegard, A ; Androulakis, E ; et al.
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17
Cardiomyopathies in 100,000 genomes project: interval evaluation improves diagnostic yield and informs strategies for ongoing gene discovery.

von Josephs, KS ; Seaby, EG ; May, P ; et al.
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18
Genome-wide association study reveals mechanisms underlying dilated cardiomyopathy and myocardial resilience.

von Jurgens, SJ ; Rämö, JT ; Kramarenko, DR ; et al.
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19
Promise and Peril of a Genotype-First Approach to Mendelian Cardiovascular Disease.

von Asatryan, B ; Murray, B ; Tadros, R ; et al.

Schlagworte: biobank; cardiac arrhythmia; cardiomyopathy; genetics; precision health; precision medicine sudden cardiac death; Humans; Cardiovascular Diseases; Genetic Testing; Genetic Predisposition to Disease; Precision Medicine; Genotype; Risk Assessment; Phenotype
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20
Genome-wide association analysis provides insights into the molecular etiology of dilated cardiomyopathy

von Zheng, SL ; Henry, A ; Cannie, D ; et al.
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21
Artificial intelligence-enabled electrocardiogram for mortality and cardiovascular risk estimation: a model development and validation study

von Sau, A ; Pastika, L ; Sieliwonczyk, E ; et al.

e802 ; e791
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22
Characterization and natural history of patients with LMNA-related dilated cardiomyopathy in the phase 3 REALM-DCM trial

von Garcia-Pavia, P ; Lakdawala, NK ; Sinagra, G ; et al.

Schlagworte: England
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23
Comparative prognostic importance of measures of left atrial structure and function in non-ischaemic dilated cardiomyopathy

von Hammersley, DJ ; Mukhopadhyay, S ; Chen, X ; et al.

1574 ; 1566
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24
A novel tool for arrhythmic risk stratification in desmoplakin gene variant carriers

von Carrick, RT ; Gasperetti, A ; Protonotarios, A ; et al.

2979 ; 2968

Schlagworte: England
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25
Titin-related familial dilated cardiomyopathy: factors associated with disease onset.

von Johnson, R ; Fletcher, RA ; Peters, S ; et al.

Schlagworte: 1102 Cardiorespiratory Medicine and Haematology, 1103 Clinical Sciences; Journal Article
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