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1
Sex Differences in the Genetic Causes of Dilated Cardiomyopathy

von M Mangino ; KA McGurk ; P Theotokis ; et al.

Schlagworte: Cardiovascular medicine and haematology; Health sciences; GO-DCM Investigators
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2
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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3
Exposure to Elevated Nitrogen Dioxide Concentrations and Cardiac Remodeling in Patients With Dilated Cardiomyopathy

von D Fecht ; MARC CHADEAU-HYAM ; RUTH OWEN ; et al.

Schlagworte: Uncategorised value
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4
Impact of Risk Factors on COVID-19 Outcomes in Unvaccinated People With Rheumatic Diseases: A Comparative Analysis of Pandemic Epochs Using the COVID-19 Global Rheumatology Alliance Registry

von Yazdany, J ; Ware, A ; Wallace, Z ; et al.

Schlagworte: COVID-19; COVID-19 Testing; COVID-19 Vaccine; Human; Male; Pandemic; Registrie; Rheumatic Disease; Rheumatology; Risk Factors; info:eu-repo/semantics/article
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5
Guidance for estimating penetrance of monogenic disease-causing variants in population cohorts

von CF Wright ; LN Sharp ; L Jackson ; et al.

Schlagworte: No keyword
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6
The Gene Curation Coalition: A global effort to harmonize gene–disease evidence resources

von DiStefano, MT ; Goehringer, S ; Babb, L ; et al.

Schlagworte: Journal Article
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7
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8
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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9
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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10
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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11
Implementing an Online Sexually Transmitted Infection Testing Service for Young People in Regional and Rural Victoria, Australia: Insights From Local Public Health Authorities

von Ware, L ; McGrath, M ; Walsh, O ; et al.
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12
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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13
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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14
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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15
Fibrosis Entropy Is Associated With Life‐Threatening Arrhythmia in Nonischemic Cardiomyopathy

von Hammersley, DJ ; Zaidi, HA ; Jones, RE ; et al.
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16
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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17
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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18
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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19
Power source, data retrieval method, and attachment type affect success of dorsally mounted tracking tag deployments in 37 species of shorebirds

von EL Weiser ; RB Lanctot ; DR Ruthrauff ; et al.

Schlagworte: Agricultural; veterinary and food sciences; Biological sciences; Ecology; Evolutionary biology; Zoology; 3 Good Health and Well Being
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20
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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21
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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22
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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23
Shape programming lines of concentrated Gaussian curvature

von Duffy, D ; Cmok, L ; Biggins, JS ; et al.

Schlagworte: cond-mat.soft; Article
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24
Metric mechanics with nontrivial topology: Actuating irises, cylinders, and evertors.

von Duffy, D ; Javed, M ; Abdelrahman, MK ; et al.

Schlagworte: cond-mat.soft; Article
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25
Clinical likelihood ratios and balanced accuracy for 44 in silico tools against multiple large-scale functional assays of cancer susceptibility genes.

von Cubuk, C ; Garrett, A ; Choi, S ; et al.

Schlagworte: Computer Simulation; Genetic Variation; Genomics; Humans; Mutation, Missense; Neoplasms; Article
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