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References from Genotype–Phenotype Discordance in Cardiomyopathies: Pathophysiology, Clinical Expression, and Therapeutic Considerations. Local targets link to admitted publications; unresolved targets remain external evidence.
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2021 · External reference
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2020 · External reference
10.1038/nrcardio.2013.105
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10.1056/nejmoa1110186
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10.1038/gim.2014.205
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10.1093/eurheartj/ehx808
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10.3390/medicina59081424
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10.3390/ijms26094181
10.3390/ijms26094181 · External reference
10.3389/fgene.2025.1525941
10.3389/fgene.2025.1525941 · External reference
10.1155/crig/9517735
10.1155/crig/9517735 · External reference
10.3389/fcvm.2021.810291
10.3389/fcvm.2021.810291 · External reference
10.3390/genes14101864
10.3390/genes14101864 · External reference
10.1007/s11886-022-01727-z
10.1007/s11886-022-01727-z · External reference
10.1536/ihj.18-167
10.1536/ihj.18-167 · External reference
10.1016/j.amjcard.2025.01.034
10.1016/j.amjcard.2025.01.034 · External reference
10.3390/biom12101417
10.3390/biom12101417 · External reference
Abstract 15058: Critical Reappraisal of Genetic Variants in Hypertrophic Cardiomyopathy
2022 · External reference
10.3390/cardiogenetics14030010
10.3390/cardiogenetics14030010 · External reference
10.1038/s44161-023-00346-3
10.1038/s44161-023-00346-3 · External reference
10.1161/circulationaha.123.065987
10.1161/circulationaha.123.065987 · External reference
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10.1016/j.jacadv.2023.100767
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10.1016/j.hlc.2019.12.008 · External reference
10.3390/jcdd12050189
10.3390/jcdd12050189 · External reference
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10.1016/j.jacc.2021.12.002 · External reference
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10.1016/j.jcmg.2016.02.031 · External reference
10.1016/j.jcmg.2020.09.037
10.1016/j.jcmg.2020.09.037 · External reference
10.1161/circulationaha.113.007094
10.1161/circulationaha.113.007094 · External reference
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10.1186/s12968-016-0308-4 · External reference
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10.1093/cvr/cvae088.113
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10.1093/eurheartj/ehv529
10.1093/eurheartj/ehv529 · External reference
10.1093/eurheartj/ehae666.2062
10.1093/eurheartj/ehae666.2062 · External reference
10.1002/ejhf.3248
10.1002/ejhf.3248 · External reference
10.4081/cardiogenetics.2016.6306
10.4081/cardiogenetics.2016.6306 · External reference
10.1016/j.cardfail.2010.07.245
10.1016/j.cardfail.2010.07.245 · External reference
10.1002/clc.20622
10.1002/clc.20622 · External reference
10.1253/circj.cj-10-0782
10.1253/circj.cj-10-0782 · External reference
10.3390/ijms22062955
10.3390/ijms22062955 · External reference
10.3390/medicina60040543
10.3390/medicina60040543 · External reference
10.1161/circgen.122.003704
10.1161/circgen.122.003704 · External reference
10.1249/jsr.0000000000000037
10.1249/jsr.0000000000000037 · External reference
10.1161/circimaging.110.957563
10.1161/circimaging.110.957563 · External reference
Clinical Challenges of Genotype Positive–Phenotype Negative Family Members in Hypertrophic Cardiomyopathy
2010 · External reference
A Novel LMNA Nonsense Mutation Causes Two Distinct Phenotypes of Cardiomyopathy With High Risk of Sudden Cardiac Death in a Large Five‐Generation Family
2018 · External reference
10.2169/internalmedicine.1701-23
10.2169/internalmedicine.1701-23 · External reference
Clinical Phenotype, Genetics and Outcome of PLN Cardiomyopathy
2021 · External reference
10.1161/circgenetics.113.000374
10.1161/circgenetics.113.000374 · External reference
10.1016/j.jacc.2019.06.072
10.1016/j.jacc.2019.06.072 · External reference
10.3390/biomedicines12071602
10.3390/biomedicines12071602 · External reference
Deep Learning ECG Risk Score Predicts Cardiovascular Death
2023 · External reference
Artificial Intelligence‐Enabled ECG‐to‐CMR Translation for Myocardial Fibrosis Detection
2023 · External reference
10.1161/circgen.124.004558
10.1161/circgen.124.004558 · External reference
10.1007/s11886-025-02239-2
10.1007/s11886-025-02239-2 · External reference
10.1038/s41591-024-03243-9
10.1038/s41591-024-03243-9 · External reference
10.1161/circresaha.122.320496
10.1161/circresaha.122.320496 · External reference
10.3390/genes13040656
10.3390/genes13040656 · External reference
10.1056/nejmsa1507092
10.1056/nejmsa1507092 · External reference