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Genomic Insights into Cardiomyopathies: A Comparative Cross-Species Review

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Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1001/jama.2009.371openalex-snapshot

Clinical Outcome and Phenotypic Expression in LAMP2 Cardiomyopathy

inferredcites →https://doi.org/10.1001/jama.296.15.1867openalex-snapshot

Incidence, Causes, and Outcomes of Dilated Cardiomyopathy in Children

inferredcites →https://doi.org/10.1002/(sici)1522-2683(19990101)20:4/5<898::aid-elps898>3.0.co;2-bopenalex-snapshot

Bovine dilated cardiomyopathy: Proteomic analysis of an animal model of human dilated cardiomyopathy

inferredcites →https://doi.org/10.1002/1098-1004(200011)16:5<448::aid-humu19>3.0.co;2-dopenalex-snapshot

Genetic variants in the promoter (g983G>T) and coding region (A92T) of the human cardiotrophin-1 gene (CTF1) in patients with dilated cardiomyopathy

inferredcites →https://doi.org/10.1002/1531-8249(199911)46:5<684::aid-ana2>3.0.co;2-#openalex-snapshot

Autosomal dominant myofibrillar myopathy with arrhythmogenic right ventricular cardiomyopathy linked to chromosome 10q

inferredcites →https://doi.org/10.1002/ana.20973openalex-snapshot

Fukutin gene mutations cause dilated cardiomyopathy with minimal muscle weakness

inferredcites →https://doi.org/10.1002/humu.20250openalex-snapshot

Thymopoietin (lamina-associated polypeptide 2) gene mutation associated with dilated cardiomyopathy

inferredcites →https://doi.org/10.1002/humu.21603openalex-snapshot

Dilated cardiomyopathy-associatedBAG3mutations impair Z-disc assembly and enhance sensitivity to apoptosis in cardiomyocytes

inferredcites →https://doi.org/10.1002/humu.22765openalex-snapshot

The ARVD/C Genetic Variants Database: 2014 Update

inferredcites →https://doi.org/10.1002/humu.22942openalex-snapshot

Mutations in FLNC are Associated with Familial Restrictive Cardiomyopathy

inferredcites →https://doi.org/10.1002/mus.22228openalex-snapshot

Dilated cardiomyopathy with conduction defects in a patient with partial merosin deficiency due to mutations in the laminin‐α2‐chain gene: A chance association or a novel phenotype?

inferredcites →https://doi.org/10.1006/geno.1996.0031openalex-snapshot

A New Locus for Arrhythmogenic Right Ventricular Dysplasia on the Long Arm of Chromosome 14

inferredcites →https://doi.org/10.1006/geno.1997.4927openalex-snapshot

ARVD4, a New Locus for Arrhythmogenic Right Ventricular Cardiomyopathy, Maps to Chromosome 2 Long Arm

inferredcites →https://doi.org/10.1007/bf02828188openalex-snapshot

Possible association of HLA-DRB1 gene with the autoantibody against myocardial mitochondria ADP/ATP carrier in dilated cardiomyopathy

inferredcites →https://doi.org/10.1007/s001090050210openalex-snapshot

Identification of two novel mutations in the ventricular regulatory myosin light chain gene ( MYL2 ) associated with familial and classical forms of hypertrophic cardiomyopathy

inferredcites →https://doi.org/10.1007/s00246-014-1018-zopenalex-snapshot

Applicability of Published Guidelines for Assessment of Left Ventricular Diastolic Function in Adults to Children with Restrictive Cardiomyopathy: An Observational Study

inferredcites →https://doi.org/10.1007/s00439-010-0855-yopenalex-snapshot

Genome-wide association identifies a deletion in the 3′ untranslated region of Striatin in a canine model of arrhythmogenic right ventricular cardiomyopathy

inferredcites →https://doi.org/10.1007/s00439-012-1158-2openalex-snapshot

A splice site mutation in a gene encoding for PDK4, a mitochondrial protein, is associated with the development of dilated cardiomyopathy in the Doberman pinscher

inferredcites →https://doi.org/10.1007/s00439-016-1685-3openalex-snapshot

De novo RRAGC mutation activates mTORC1 signaling in syndromic fetal dilated cardiomyopathy

inferredcites →https://doi.org/10.1016/0092-8674(87)90579-4openalex-snapshot

Dystrophin: The protein product of the duchenne muscular dystrophy locus

inferredcites →https://doi.org/10.1016/0092-8674(90)90274-iopenalex-snapshot

A molecular basis for familial hypertrophic cardiomyopathy: A β cardiac myosin heavy chain gene missense mutation

inferredcites →https://doi.org/10.1016/0092-8674(94)90054-xopenalex-snapshot

α-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: A disease of the sarcomere

inferredcites →https://doi.org/10.1016/0092-8674(94)90136-8openalex-snapshot

Isolation of the gene for McLeod syndrome that encodes a novel membrane transport protein

inferredcites →https://doi.org/10.1016/j.ajhg.2008.01.010openalex-snapshot

Arrhythmogenic Right Ventricular Cardiomyopathy Type 5 Is a Fully Penetrant, Lethal Arrhythmic Disorder Caused by a Missense Mutation in the TMEM43 Gene

inferredcites →https://doi.org/10.1016/j.ajhg.2011.01.016openalex-snapshot

Genome-wide Studies of Copy Number Variation and Exome Sequencing Identify Rare Variants in BAG3 as a Cause of Dilated Cardiomyopathy

inferredcites →https://doi.org/10.1016/j.ajhg.2013.05.015openalex-snapshot

Fine Mapping of the 1p36 Deletion Syndrome Identifies Mutation of PRDM16 as a Cause of Cardiomyopathy

inferredcites →https://doi.org/10.1016/j.amjcard.2012.10.017openalex-snapshot

Desmin Mutations and Arrhythmogenic Right Ventricular Cardiomyopathy

inferredcites →https://doi.org/10.1016/j.bbrc.2006.01.154openalex-snapshot

αB-crystallin mutation in dilated cardiomyopathy

inferredcites →https://doi.org/10.1016/j.bbrc.2006.04.151openalex-snapshot

A missense mutation in a ubiquitously expressed protein, vinculin, confers susceptibility to hypertrophic cardiomyopathy

inferredcites →https://doi.org/10.1016/j.bbrc.2007.03.128openalex-snapshot

Structural analysis of four and half LIM protein-2 in dilated cardiomyopathy

inferredcites →https://doi.org/10.1016/j.cardiores.2004.10.005openalex-snapshot

Regulatory mutations in transforming growth factor-?3 gene cause arrhythmogenic right ventricular cardiomyopathy type 1

inferredcites →https://doi.org/10.1016/j.carpath.2013.08.001openalex-snapshot

Spontaneously occurring restrictive nonhypertrophied cardiomyopathy in domestic cats: a new animal model of human disease

inferredcites →https://doi.org/10.1016/j.ejheart.2004.04.017openalex-snapshot

Two novel mutations in the β-Myosin Heavy Chain Gene Associated with Dilated Cardiomyopathy

inferredcites →https://doi.org/10.1016/j.gene.2013.09.022openalex-snapshot

The HLA class II allele DQB1*0309 is associated with dilated cardiomyopathy

inferredcites →https://doi.org/10.1016/j.hlc.2006.10.018openalex-snapshot

Guidelines for the Diagnosis and Management of Familial Dilated Cardiomyopathy

inferredcites →https://doi.org/10.1016/j.hrthm.2014.07.020openalex-snapshot

Prevalence and significance of rare RYR2 variants in arrhythmogenic right ventricular cardiomyopathy/dysplasia: Results of a systematic screening

inferredcites →https://doi.org/10.1016/j.ijcard.2004.05.060openalex-snapshot

Hypertrophic cardiomyopathy linked to homozygosity for a new mutation in the myosin-binding protein C gene (A627V) suggests a dosage effect

inferredcites →https://doi.org/10.1016/j.jacc.2004.08.058openalex-snapshot

Tcap gene mutations in hypertrophic cardiomyopathy and dilated cardiomyopathy

inferredcites →https://doi.org/10.1016/j.jacc.2007.02.061openalex-snapshot

Prevalence, Clinical Significance, and Genetic Basis of Hypertrophic Cardiomyopathy With Restrictive Phenotype

inferredcites →https://doi.org/10.1016/j.jacc.2008.12.082openalex-snapshot

Cardiac Ankyrin Repeat Protein Gene (ANKRD1) Mutations in Hypertrophic Cardiomyopathy

inferredcites →https://doi.org/10.1016/j.jacc.2009.02.076openalex-snapshot

ANKRD1, the Gene Encoding Cardiac Ankyrin Repeat Protein, Is a Novel Dilated Cardiomyopathy Gene

inferredcites →https://doi.org/10.1016/j.jacc.2009.05.038openalex-snapshot

Mutations in Ribonucleic Acid Binding Protein Gene Cause Familial Dilated Cardiomyopathy

inferredcites →https://doi.org/10.1016/j.jacc.2009.11.016openalex-snapshot

Mutations in Alpha-Actinin-2 Cause Hypertrophic Cardiomyopathy

inferredcites →https://doi.org/10.1016/j.jacc.2010.05.045openalex-snapshot

Nebulette Mutations Are Associated With Dilated Cardiomyopathy and Endocardial Fibroelastosis

inferredcites →https://doi.org/10.1016/j.jacc.2011.01.015openalex-snapshot

Update 2011: Clinical and Genetic Issues in Familial Dilated Cardiomyopathy

inferredcites →https://doi.org/10.1016/j.jacc.2012.02.068openalex-snapshot

Genetics of Hypertrophic Cardiomyopathy After 20 Years

inferredcites →https://doi.org/10.1016/j.jacc.2015.01.045openalex-snapshot

Exercise Triggers ARVC Phenotype in Mice Expressing a Disease-Causing Mutated Version of Human Plakophilin-2

inferredcites →https://doi.org/10.1016/j.jacc.2016.04.024openalex-snapshot

Idiopathic Restrictive Cardiomyopathy Is Primarily a Genetic Disease

inferredcites →https://doi.org/10.1016/j.jcmg.2015.05.013openalex-snapshot

Cardiomyopathy With Restrictive Physiology in Sickle Cell Disease

inferredcites →https://doi.org/10.1016/j.jcpa.2016.06.003openalex-snapshot

Pathological Features and Pathogenesis of the Endomyocardial Form of Restrictive Cardiomyopathy in Cats

inferredcites →https://doi.org/10.1016/j.jelectrocard.2015.06.005openalex-snapshot

Arrythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) and cathecholaminergic polymorphic ventricular tachycardia (CPVT): A phenotypic spectrum seen in same patient

inferredcites →https://doi.org/10.1016/j.jmb.2013.08.015openalex-snapshot

Type 2 Ryanodine Receptor Domain A Contains a Unique and Dynamic α-Helix That Transitions to a β-Strand in a Mutant Linked with a Heritable Cardiomyopathy

inferredcites →https://doi.org/10.1016/j.mgene.2016.03.006openalex-snapshot

Variants of resistin gene and the risk of idiopathic dilated cardiomyopathy in Pakistan

inferredcites →https://doi.org/10.1016/j.nmd.2005.02.004openalex-snapshot

Dilated cardiomyopathy may be an early sign of the C826A Fukutin-related protein mutation

inferredcites →https://doi.org/10.1016/j.nmd.2009.08.015openalex-snapshot

Rippling muscle disease and cardiomyopathy associated with a mutation in the CAV3 gene

inferredcites →https://doi.org/10.1016/j.pediatrneurol.2015.07.008openalex-snapshot

Novel Rod Domain Duplication in Dystrophin Resulting in X-Linked Dilated Cardiomyopathy

inferredcites →https://doi.org/10.1016/j.ygeno.2007.04.007openalex-snapshot

A substitution mutation in the myosin binding protein C gene in ragdoll hypertrophic cardiomyopathy

inferredcites →https://doi.org/10.1016/j.ygeno.2008.03.007openalex-snapshot

A novel locus for dilated cardiomyopathy maps to canine chromosome 8

inferredcites →https://doi.org/10.1016/j.ygeno.2010.09.005openalex-snapshot

A nonsense mutation in the optic atrophy 3 gene (OPA3) causes dilated cardiomyopathy in Red Holstein cattle

inferredcites →https://doi.org/10.1016/j.yjmcc.2007.04.006openalex-snapshot

Mutations in JPH2-encoded junctophilin-2 associated with hypertrophic cardiomyopathy in humans

inferredcites →https://doi.org/10.1016/j.yjmcc.2007.06.009openalex-snapshot

Genetic screening of calcium regulation genes in familial hypertrophic cardiomyopathy

inferredcites →https://doi.org/10.1016/j.yjmcc.2012.05.018openalex-snapshot

Diastolic dysfunction and thin filament dysregulation resulting from excitation–contraction uncoupling in a mouse model of restrictive cardiomyopathy

inferredcites →https://doi.org/10.1016/j.yjmcc.2013.02.008openalex-snapshot

Global metabolomic analysis of heart tissue in a hamster model for dilated cardiomyopathy

inferredcites →https://doi.org/10.1016/j.ymgme.2005.10.008openalex-snapshot

Genotype–phenotype relationships involving hypertrophic cardiomyopathy-associated mutations in titin, muscle LIM protein, and telethonin

inferredcites →https://doi.org/10.1016/j.ymgme.2008.06.005openalex-snapshot

A missense variant in desmoglein-2 predisposes to dilated cardiomyopathy

inferredcites →https://doi.org/10.1016/s0006-291x(02)02374-4openalex-snapshot

Novel mutations in sarcomeric protein genes in dilated cardiomyopathy

inferredcites →https://doi.org/10.1016/s0006-291x(03)00526-6openalex-snapshot

Mutation of the phospholamban promoter associated with hypertrophic cardiomyopathy

inferredcites →https://doi.org/10.1016/s0006-2952(98)00305-0openalex-snapshot

Structural and functional impairment of mitochondria in adriamycin-induced cardiomyopathy in mice: suppression of cytochrome c oxidase II gene expression

inferredcites →https://doi.org/10.1016/s0022-5223(98)70221-1openalex-snapshot

A canine model of dilated cardiomyopathy induced by repetitive intracoronary doxorubicin administration

inferredcites →https://doi.org/10.1016/s0140-6736(00)02379-5openalex-snapshot

Identification of a deletion in plakoglobin in arrhythmogenic right ventricular cardiomyopathy with palmoplantar keratoderma and woolly hair (Naxos disease)

inferredcites →https://doi.org/10.1016/s0140-6736(04)15468-8openalex-snapshot

Novel mutation in cardiac troponin I in recessive idiopathic dilated cardiomyopathy

inferredcites →https://doi.org/10.1016/s0140-6736(09)60256-7openalex-snapshot

Arrhythmogenic right ventricular cardiomyopathy

inferredcites →https://doi.org/10.1016/s0960-8966(99)00011-5openalex-snapshot

Molecular analysis of a spontaneous dystrophin `knockout' dog

inferredcites →https://doi.org/10.1016/s1053-2498(02)00402-3openalex-snapshot

Adriamycin-induced cardiomyopathy in the dog—an appropriate model for research on partial left ventriculectomy?

inferredcites →https://doi.org/10.1016/s1096-7192(03)00142-2openalex-snapshot

Mutations in the muscle LIM protein and α-actinin-2 genes in dilated cardiomyopathy and endocardial fibroelastosis

inferredcites →https://doi.org/10.1016/s1098-612x(02)00133-xopenalex-snapshot

Feline idiopathic cardiomyopathy: A retrospective study of 106 cats (1994–2001)

inferredcites →https://doi.org/10.1016/s1760-2734(06)70047-9openalex-snapshot

Proposed Guidelines for the Diagnosis of Canine Idiopathic Dilated Cardiomyopathy

inferredcites →https://doi.org/10.1038/35022604openalex-snapshot

Primary LAMP-2 deficiency causes X-linked vacuolar cardiomyopathy and myopathy (Danon disease)

inferredcites →https://doi.org/10.1038/ejhg.2010.83openalex-snapshot

Familial neonatal isolated cardiomyopathy caused by a mutation in the flavoprotein subunit of succinate dehydrogenase

inferredcites →https://doi.org/10.1038/ejhg.2012.276openalex-snapshot

Clinical utility gene card for: Dilated Cardiomyopathy (CMD)

inferredcites →https://doi.org/10.1038/ng0496-385openalex-snapshot

A novel X-linked gene, G4.5. is responsible for Barth syndrome

inferredcites →https://doi.org/10.1038/ng0897-379openalex-snapshot

Mutations in the cardiac troponin I gene associated with hypertrophic cardiomyopathy

inferredcites →https://doi.org/10.1038/ng1294-323openalex-snapshot

Identification of a novel X-linked gene responsible for Emery-Dreifuss muscular dystrophy

inferredcites →https://doi.org/10.1038/ng1295-434openalex-snapshot

Mutations in the cardiac myosin binding protein–C gene on chromosome 11 cause familial hypertrophic cardiomyopathy

inferredcites →https://doi.org/10.1038/ng1295-438openalex-snapshot

Cardiac myosin binding protein–C gene splice acceptor site mutation is associated with familial hypertrophic cardiomyopathy

inferredcites →https://doi.org/10.1038/ng1329openalex-snapshot

ABCC9 mutations identified in human dilated cardiomyopathy disrupt catalytic KATP channel gating

inferredcites →https://doi.org/10.1038/ng1527openalex-snapshot

Mutation in the transcriptional coactivator EYA4 causes dilated cardiomyopathy and sensorineural hearing loss

inferredcites →https://doi.org/10.1038/ng815openalex-snapshot

Mutations of TTN, encoding the giant muscle filament titin, cause familial dilated cardiomyopathy

inferredcites →https://doi.org/10.1038/nm.2037openalex-snapshot

Nexilin mutations destabilize cardiac Z-disks and lead to dilated cardiomyopathy

inferredcites →https://doi.org/10.1056/nejm198911163212005openalex-snapshot

Mapping a Gene for Familial Hypertrophic Cardiomyopathy to Chromosome 14q1

inferredcites →https://doi.org/10.1056/nejm199309233291304openalex-snapshot

Deletion of the Dystrophin Muscle-Promoter Region Associated with X-Linked Dilated Cardiomyopathy

inferredcites →https://doi.org/10.1056/nejm199912023412302openalex-snapshot

Missense Mutations in the Rod Domain of the Lamin A/C Gene as Causes of Dilated Cardiomyopathy and Conduction-System Disease

inferredcites →https://doi.org/10.1056/nejm200012073432304openalex-snapshot

Mutations in Sarcomere Protein Genes as a Cause of Dilated Cardiomyopathy

inferredcites →https://doi.org/10.1056/nejmoa1110186openalex-snapshot

Truncations of Titin Causing Dilated Cardiomyopathy

inferredcites →https://doi.org/10.1056/nejmoa1505517openalex-snapshot

Shared Genetic Predisposition in Peripartum and Dilated Cardiomyopathies

inferredcites →https://doi.org/10.1073/pnas.1600311113openalex-snapshot

Sickle cell anemia mice develop a unique cardiomyopathy with restrictive physiology

inferredcites →https://doi.org/10.1073/pnas.90.9.3993openalex-snapshot

Missense mutations in the beta-myosin heavy-chain gene cause central core disease in hypertrophic cardiomyopathy.

inferredcites →https://doi.org/10.1073/pnas.94.25.13873openalex-snapshot

Both hypertrophic and dilated cardiomyopathies are caused by mutation of the same gene, δ-sarcoglycan, in hamster: An animal model of disrupted dystrophin-associated glycoprotein complex

inferredcites →https://doi.org/10.1074/jbc.m111.234336openalex-snapshot

Fetal Cardiac Troponin Isoforms Rescue the Increased Ca2+ Sensitivity Produced by a Novel Double Deletion in Cardiac Troponin T Linked to Restrictive Cardiomyopathy

inferredcites →https://doi.org/10.1074/jbc.m111.257436openalex-snapshot

Correlation of Molecular and Functional Effects of Mutations in Cardiac Troponin T Linked to Familial Hypertrophic Cardiomyopathy

inferredcites →https://doi.org/10.1074/jbc.m200788200openalex-snapshot

Exon Skipping in Cardiac Troponin T of Turkeys with Inherited Dilated Cardiomyopathy

inferredcites →https://doi.org/10.1074/jbc.m311849200openalex-snapshot

A Cypher/ZASP Mutation Associated with Dilated Cardiomyopathy Alters the Binding Affinity to Protein Kinase C

inferredcites →https://doi.org/10.1086/302713openalex-snapshot

The Locus of a Novel Gene Responsible for Arrhythmogenic Right-Ventricular Dysplasia Characterized by Early Onset and High Penetrance Maps to Chromosome 10p12-p14

inferredcites →https://doi.org/10.1086/344208openalex-snapshot

Mutation in Human Desmoplakin Domain Binding to Plakoglobin Causes a Dominant Form of Arrhythmogenic Right Ventricular Cardiomyopathy

inferredcites →https://doi.org/10.1086/504393openalex-snapshot

DSG2 Mutations Contribute to Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy

inferredcites →https://doi.org/10.1086/509900openalex-snapshot

Mutations of Presenilin Genes in Dilated Cardiomyopathy and Heart Failure

inferredcites →https://doi.org/10.1086/519530openalex-snapshot

Mutations in Cardiac T-Box Factor Gene TBX20 Are Associated with Diverse Cardiac Pathologies, Including Defects of Septation and Valvulogenesis and Cardiomyopathy

inferredcites →https://doi.org/10.1093/cvr/cvm015openalex-snapshot

Mutations in the Z-band protein myopalladin gene and idiopathic dilated cardiomyopathy

inferredcites →https://doi.org/10.1093/ejechocard/jep156openalex-snapshot

Restrictive cardiomyopathies

inferredcites →https://doi.org/10.1093/eurheartj/ehm342openalex-snapshot

Classification of the cardiomyopathies: a position statement from the european society of cardiology working group on myocardial and pericardial diseases

inferredcites →https://doi.org/10.1093/eurheartj/ehm429openalex-snapshot

Cardiac -myosin heavy chain defects in two families with non-compaction cardiomyopathy: linking non-compaction to hypertrophic, restrictive, and dilated cardiomyopathies

inferredcites →https://doi.org/10.1093/eurheartj/ehq507openalex-snapshot

Mutations in the mitochondrial thioredoxin reductase gene TXNRD2 cause dilated cardiomyopathy

inferredcites →https://doi.org/10.1093/eurheartj/ehr105openalex-snapshot

A genome-wide association study identifies two loci associated with heart failure due to dilated cardiomyopathy

inferredcites →https://doi.org/10.1093/eurheartj/ehr451openalex-snapshot

Mutations in the Lamin A/C gene mimic arrhythmogenic right ventricular cardiomyopathy

inferredcites →https://doi.org/10.1093/eurheartj/ehs373openalex-snapshot

Mutations in the area composita protein αT-catenin are associated with arrhythmogenic right ventricular cardiomyopathy

inferredcites →https://doi.org/10.1093/eurheartj/ehu284openalex-snapshot

2014 ESC Guidelines on diagnosis and management of hypertrophic cardiomyopathy

inferredcites →https://doi.org/10.1093/eurheartj/ehv110openalex-snapshot

Association of competitive and recreational sport participation with cardiac events in patients with arrhythmogenic right ventricular cardiomyopathy: results from the North American multidisciplinary study of arrhythmogenic right ventricular cardiomyopathy

inferredcites →https://doi.org/10.1093/eurjhf/hfq120openalex-snapshot

Current State of Knowledge on Aetiology, Diagnosis, Management, and Therapy of Peripartum Cardiomyopathy: A Position Statement from the Heart Failure Association of the European Society of Cardiology Working Group on peripartum cardiomyopathy

inferredcites →https://doi.org/10.1093/eurjhf/hfr110openalex-snapshot

Genetic Basis of End-Stage Hypertrophic Cardiomyopathy

inferredcites →https://doi.org/10.1093/eurjhf/hfs119openalex-snapshot

Phospholamban R14del Mutation in Patients Diagnosed with Dilated Cardiomyopathy or Arrhythmogenic Right Ventricular Cardiomyopathy: Evidence Supporting the Concept of Arrhythmogenic Cardiomyopathy

inferredcites →https://doi.org/10.1093/hmg/10.3.189openalex-snapshot

Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2)

inferredcites →https://doi.org/10.1093/hmg/9.18.2761openalex-snapshot

Recessive mutation in desmoplakin disrupts desmoplakin-intermediate filament interactions and causes dilated cardiomyopathy, woolly hair and keratoderma

inferredcites →https://doi.org/10.1093/hmg/ddi386openalex-snapshot

A cardiac myosin binding protein C mutation in the Maine Coon cat with familial hypertrophic cardiomyopathy

inferredcites →https://doi.org/10.1093/hmg/ddm238openalex-snapshot

Nesprin-1 and -2 are involved in the pathogenesis of Emery–Dreifuss muscular dystrophy and are critical for nuclear envelope integrity

inferredcites →https://doi.org/10.1093/hmg/ddq315openalex-snapshot

α-Cardiac myosin heavy chain (MYH6) mutations affecting myofibril formation are associated with congenital heart defects

inferredcites →https://doi.org/10.1093/hmg/ddq387openalex-snapshot

De novo desmin-mutation N116S is associated with arrhythmogenic right ventricular cardiomyopathy

inferredcites →https://doi.org/10.1093/hmg/ddv423openalex-snapshot

PLEKHM2mutation leads to abnormal localization of lysosomes, impaired autophagy flux and associates with recessive dilated cardiomyopathy and left ventricular noncompaction

inferredcites →https://doi.org/10.1097/gim.0b013e3181f2481fopenalex-snapshot

Clinical and genetic issues in dilated cardiomyopathy: A review for genetics professionals

inferredcites →https://doi.org/10.1111/j.1365-2052.2008.01796.xopenalex-snapshot

A mutation in NFκB interacting protein 1 causes cardiomyopathy and woolly haircoat syndrome of Poll Hereford cattle

inferredcites →https://doi.org/10.1111/j.1469-7580.2009.01079.xopenalex-snapshot

Knockdown of alpha myosin heavy chain disrupts the cytoskeleton and leads to multiple defects during chick cardiogenesis

inferredcites →https://doi.org/10.1111/j.1939-1676.1993.tb01035.xopenalex-snapshot

Evidence for Genetic Involvement in Feline Dilated Cardiomyopathy

inferredcites →https://doi.org/10.1111/j.1939-1676.1999.tb02167.xopenalex-snapshot

Familial Dilated Cardiomyopathy of Young Portuguese Water Dogs

inferredcites →https://doi.org/10.1111/j.1939-1676.2006.tb01803.xopenalex-snapshot

Heart Disease as a Cause of Death in Insured Swedish Dogs Younger Than 10 Years of Age

inferredcites →https://doi.org/10.1111/j.1939-1676.2010.0514.xopenalex-snapshot

Association of A31P and A74T Polymorphisms in the Myosin Binding Protein C3 Gene and Hypertrophic Cardiomyopathy in Maine Coon and Other Breed Cats

inferredcites →https://doi.org/10.1111/jvim.12163openalex-snapshot

Association of Dilated Cardiomyopathy with the Striatin Mutation Genotype in Boxer Dogs

inferredcites →https://doi.org/10.1111/jvim.12459openalex-snapshot

Plasma Cardiac Troponin I Concentration and Cardiac Death in Cats with Hypertrophic Cardiomyopathy

inferredcites →https://doi.org/10.1126/science.280.5364.750openalex-snapshot

Actin Mutations in Dilated Cardiomyopathy, a Heritable Form of Heart Failure

inferredcites →https://doi.org/10.1126/science.3616607openalex-snapshot

Myocardial Failure in Cats Associated with Low Plasma Taurine: a Reversible Cardiomyopathy

inferredcites →https://doi.org/10.1136/bmj.d6966openalex-snapshot

Inherited cardiomyopathies

inferredcites →https://doi.org/10.1136/heartjnl-2013-305420openalex-snapshot

Almanac 2014: cardiomyopathies

inferredcites →https://doi.org/10.1136/hrt.2003.023390openalex-snapshot

Multiple pathogenetic mechanisms in X linked dilated cardiomyopathy

inferredcites →https://doi.org/10.1136/jmg.2005.033886openalex-snapshot

Compound and double mutations in patients with hypertrophic cardiomyopathy: implications for genetic testing and counselling

inferredcites →https://doi.org/10.1136/jmg.2005.036657openalex-snapshot

Mutation of DNAJC19, a human homologue of yeast inner mitochondrial membrane co-chaperones, causes DCMA syndrome, a novel autosomal recessive Barth syndrome-like condition

inferredcites →https://doi.org/10.1136/vr.103549openalex-snapshot

Cardiac troponin I in three cat breeds with hypertrophic cardiomyopathy

inferredcites →https://doi.org/10.1136/vr.155.12.355openalex-snapshot

Clinical and pathological features of dilated cardiomyopathy in Holstein‐Friesian cattle

inferredcites →https://doi.org/10.1136/vr.c3000openalex-snapshot

Arrhythmogenic right ventricular cardiomyopathy as a cause of unexpected cardiac death in two horses

inferredcites →https://doi.org/10.1152/ajpheart.00530.2015openalex-snapshot

2-Deoxyadenosine triphosphate restores the contractile function of cardiac myofibril from adult dogs with naturally occurring dilated cardiomyopathy

inferredcites →https://doi.org/10.1155/2015/204823openalex-snapshot

Genetics of Human and Canine Dilated Cardiomyopathy

inferredcites →https://doi.org/10.1155/2016/6374082openalex-snapshot

Multiple Genetic Associations with Irish Wolfhound Dilated Cardiomyopathy

inferredcites →https://doi.org/10.1159/000369778openalex-snapshot

Aspirin plus Clopidogrel as Secondary Prevention after Stroke or Transient Ischemic Attack: A Systematic Review and Meta-Analysis

inferredcites →https://doi.org/10.1161/01.cir.0000118494.07530.65openalex-snapshot

Arrhythmogenic Right Ventricular Cardiomyopathy Causing Sudden Cardiac Death in Boxer Dogs

inferredcites →https://doi.org/10.1161/01.cir.0000139339.85840.ddopenalex-snapshot

Recombinant Glucagon-Like Peptide-1 Increases Myocardial Glucose Uptake and Improves Left Ventricular Performance in Conscious Dogs With Pacing-Induced Dilated Cardiomyopathy

inferredcites →https://doi.org/10.1161/01.cir.0000144458.58660.bbopenalex-snapshot

SCN5A Mutation Associated With Dilated Cardiomyopathy, Conduction Disorder, and Arrhythmia

inferredcites →https://doi.org/10.1161/01.cir.100.5.461openalex-snapshot

Desmin Mutation Responsible for Idiopathic Dilated Cardiomyopathy

inferredcites →https://doi.org/10.1161/01.cir.102.15.1863openalex-snapshot

Spontaneously Occurring Arrhythmogenic Right Ventricular Cardiomyopathy in the Domestic Cat

inferredcites →https://doi.org/10.1161/01.cir.80.3.564openalex-snapshot

Epidemiology of idiopathic dilated and hypertrophic cardiomyopathy. A population-based study in Olmsted County, Minnesota, 1975-1984.

inferredcites →https://doi.org/10.1161/01.cir.83.2.504openalex-snapshot

Impairment of the myocardial ultrastructure and changes of the cytoskeleton in dilated cardiomyopathy.

inferredcites →https://doi.org/10.1161/01.cir.92.9.2645openalex-snapshot

Echocardiographic Assessment of Spontaneously Occurring Feline Hypertrophic Cardiomyopathy

inferredcites →https://doi.org/10.1161/01.cir.95.10.2434openalex-snapshot

Evidence for a Dystrophin Missense Mutation as a Cause of X-Linked Dilated Cardiomyopathy

inferredcites →https://doi.org/10.1161/01.cir.99.24.3172openalex-snapshot

Familial Hypertrophic Cardiomyopathy in Maine Coon Cats

inferredcites →https://doi.org/10.1161/01.res.0000263008.66799.aaopenalex-snapshot

Myozenin 2 Is a Novel Gene for Human Hypertrophic Cardiomyopathy

inferredcites →https://doi.org/10.1161/01.res.0000435859.24609.b3openalex-snapshot

Organization and Sequence of Human Cardiac Myosin Binding Protein C Gene (MYBPC3) and Identification of Mutations Predicted to Produce Truncated Proteins in Familial Hypertrophic Cardiomyopathy

inferredcites →https://doi.org/10.1161/circgenetics.109.912345openalex-snapshot

Coding Sequence Rare Variants Identified in MYBPC3 , MYH6 , TPM1 , TNNC1 , and TNNI3 From 312 Patients With Familial or Idiopathic Dilated Cardiomyopathy

inferredcites →https://doi.org/10.1161/circgenetics.110.937805openalex-snapshot

Prevalence of Desmosomal Protein Gene Mutations in Patients With Dilated Cardiomyopathy

inferredcites →https://doi.org/10.1161/circgenetics.111.959866openalex-snapshot

Molecular Genetic and Functional Characterization Implicate Muscle-Restricted Coiled-Coil Gene ( MURC ) as a Causal Gene for Familial Dilated Cardiomyopathy

inferredcites →https://doi.org/10.1161/circgenetics.111.961052openalex-snapshot

Homozygosity Mapping and Exome Sequencing Reveal GATAD1 Mutation in Autosomal Recessive Dilated Cardiomyopathy

inferredcites →https://doi.org/10.1161/circresaha.107.167783openalex-snapshot

A Missense Mutation in the CHRM2 Gene Is Associated With Familial Dilated Cardiomyopathy

inferredcites →https://doi.org/10.1161/circulationaha.104.507699openalex-snapshot

α-Myosin Heavy Chain

inferredcites →https://doi.org/10.1161/circulationaha.105.583674openalex-snapshot

Mutations in Desmoglein-2 Gene Are Associated With Arrhythmogenic Right Ventricular Cardiomyopathy

inferredcites →https://doi.org/10.1161/circulationaha.106.174287openalex-snapshot

Contemporary Definitions and Classification of the Cardiomyopathies

inferredcites →https://doi.org/10.1161/circulationaha.107.689984openalex-snapshot

Laminin-α4 and Integrin-Linked Kinase Mutations Cause Human Cardiomyopathy Via Simultaneous Defects in Cardiomyocytes and Endothelial Cells

inferredcites →https://doi.org/10.1161/circulationaha.107.711606openalex-snapshot

Expanding Spectrum of Human RYR2 -Related Disease

inferredcites →https://doi.org/10.1161/circulationaha.109.929646openalex-snapshot

Peripartum Cardiomyopathy as a Part of Familial Dilated Cardiomyopathy

inferredcites →https://doi.org/10.1161/circulationaha.110.005405openalex-snapshot

Genetic Variation in Titin in Arrhythmogenic Right Ventricular Cardiomyopathy–Overlap Syndromes

inferredcites →https://doi.org/10.1161/circulationaha.110.954446openalex-snapshot

Mutation Type Is Not Clinically Useful in Predicting Prognosis in Hypertrophic Cardiomyopathy

inferredcites →https://doi.org/10.1161/hc0402.102930openalex-snapshot

Metavinculin Mutations Alter Actin Interaction in Dilated Cardiomyopathy

inferredcites →https://doi.org/10.1161/hc0402.102990openalex-snapshot

Sarcomere Protein Gene Mutations in Hypertrophic Cardiomyopathy of the Elderly

inferredcites →https://doi.org/10.1161/res.0b013e3182582523openalex-snapshot

Animal Models of Heart Failure

inferredcites →https://doi.org/10.1172/jci16336openalex-snapshot

Idiopathic restrictive cardiomyopathy is part of the clinical expression of cardiac troponin I mutations

inferredcites →https://doi.org/10.1172/jci17892openalex-snapshot

Human phospholamban null results in lethal dilated cardiomyopathy revealing a critical difference between mouse and human

inferredcites →https://doi.org/10.1172/jci200316336openalex-snapshot

Idiopathic restrictive cardiomyopathy is part of the clinical expression of cardiac troponin I mutations

inferredcites →https://doi.org/10.1172/jci6067openalex-snapshot

Cardiac troponin T mutations result in allele-specific phenotypes in a mouse model for hypertrophic cardiomyopathy

inferredcites →https://doi.org/10.1172/jci62862openalex-snapshot

Genetic mutations and mechanisms in dilated cardiomyopathy

inferredcites →https://doi.org/10.1172/jci6460openalex-snapshot

α-cardiac actin is a novel disease gene in familial hypertrophic cardiomyopathy

inferredcites →https://doi.org/10.1172/jci7956openalex-snapshot

A transgenic rabbit model for human hypertrophic cardiomyopathy

inferredcites →https://doi.org/10.1172/jci9224openalex-snapshot

Mutations in the human δ-sarcoglycan gene in familial and sporadic dilated cardiomyopathy

inferredcites →https://doi.org/10.1177/0883073814549807openalex-snapshot

X-linked Recessive Distal Myopathy With Hypertrophic Cardiomyopathy Caused by a Novel Mutation in the FHL1 Gene

inferredcites →https://doi.org/10.1177/1098612x11429645openalex-snapshot

Effect of pimobendan on the clinical outcome and survival of cats with non-taurine responsive dilated cardiomyopathy

inferredcites →https://doi.org/10.1186/1471-2350-10-47openalex-snapshot

Functional polymorphism of the NFKB1 gene promoter is related to the risk of dilated cardiomyopathy

inferredcites →https://doi.org/10.1186/1471-2350-15-77openalex-snapshot

Whole exome sequencing identifies a novel EMDmutation in a Chinese family with dilated cardiomyopathy

inferredcites →https://doi.org/10.1186/1471-2350-7-29openalex-snapshot

Arrhythmogenic right ventricular cardiomyopathy type 6 (ARVC6): support for the locus assignment, narrowing of the critical region and mutation screening of three candidate genes

inferredcites →https://doi.org/10.1186/1471-2350-8-65openalex-snapshot

Missense mutations in Desmocollin-2 N-terminus, associated with arrhythmogenic right ventricular cardiomyopathy, affect intracellular localization of desmocollin-2 in vitro

inferredcites →https://doi.org/10.1186/2047-783x-18-10openalex-snapshot

Polymorphism of ZBTB17 gene is associated with idiopathic dilated cardiomyopathy: a case control study in a Han Chinese population

inferredcites →https://doi.org/10.1186/s13059-015-0861-4openalex-snapshot

FBXO32, encoding a member of the SCF complex, is mutated in dilated cardiomyopathy

inferredcites →https://doi.org/10.1186/s13104-016-2131-2openalex-snapshot

Compound heterozygous RMND1 gene variants associated with chronic kidney disease, dilated cardiomyopathy and neurological involvement: a case report

inferredcites →https://doi.org/10.1186/s13620-015-0052-3openalex-snapshot

Arrhythmogenic right ventricular cardiomyopathy secondary to adipose infiltration as a cause of episodic collapse in a horse

inferredcites →https://doi.org/10.1212/00132979-199300030-00013openalex-snapshot

MITOCHONDRIAL DISEASES

inferredcites →https://doi.org/10.1242/dev.059063openalex-snapshot

Knockdown of embryonic myosin heavy chain reveals an essential role in the morphology and function of the developing heart

inferredcites →https://doi.org/10.1253/jcj.65.691openalex-snapshot

A Case of Cardiomyopathy Showing Progression From the Hypertrophic to the Dilated Form

inferredcites →https://doi.org/10.1292/jvms.65.753openalex-snapshot

Hypertrophic Cardiomyopathy in an Aged Dog

showing the first 200 of 223

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.3914970openalex-extracted

Heart Failure Across the Tree of Life: Insights for Human Cardiovascular Medicine

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Chickens, Quail, Turkeys, Pheasants, Peafowl, and Other Galliformes

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Myocardial and Valvular Diseases

inferred← citeshttps://doi.org/10.1016/j.micpath.2021.105207openalex-snapshot

Association of parvovirus B19 and myocarditis/dilated cardiomyopathy: A systematic review and meta-analysis

inferred← citeshttps://doi.org/10.1053/j.jvca.2021.03.040openalex-snapshot

Hypertrophic Cardiomyopathy: A Species-Spanning Pathology

inferred← citeshttps://doi.org/10.1186/s12917-022-03264-xopenalex-snapshot

Responses in randomised groups of healthy, adult Labrador retrievers fed grain-free diets with high legume inclusion for 30 days display commonalities with dogs with suspected dilated cardiomyopathy

inferred← citeshttps://doi.org/10.14202/vetworld.2019.1491-1498openalex-snapshot

Immune-inflammatory concept of the pathogenesis of chronic heart failure in dogs with dilated cardiomyopathy

inferred← citeshttps://doi.org/10.22159/ijap.2021v13i542488openalex-snapshot

NEW STABILITY INDICATING METHOD DEVELOPMENT AND VALIDATION OF CAPECITABINE AND DOCETAXEL IN BULK AND PHARMACEUTICAL DOSAGE FORM BY USING RP-HPLC

inferred← citeshttps://doi.org/10.22159/ijap.2024v16i4.50125openalex-snapshot

BIO ANALYTICAL METHOD FOR SIMULTANEOUS ESTIMATION OF CAPECITABINE AND DOCETAXEL AND ITS APPLICATION TO PHARMACOKINETIC STUDIES USING LC-MS/MS

inferred← citeshttps://doi.org/10.31579/2641-0419/219openalex-snapshot

A Missense Mutation (R723H) in the Head Motor Domain of β-MYH7 gene in an Indian HCM Patient and Phenotypic Plasticity

inferred← citeshttps://doi.org/10.32598/ijvm.17.3.1005173openalex-snapshot

Postmortem Diagnostic Imaging to Evaluate Idiopathic Hypertrophic Cardiomyopathy in a Roborovski Hamster

inferred← citeshttps://doi.org/10.32782/bsnau.vet.2023.4.22openalex-snapshot

МОНІТОРИНГ ЗАХВОРЮВАНЬ СОБАК І КОТІВ НА БАЗІ ЗВЦ «10 ДРУЗІВ» М. СУМИ

inferred← citeshttps://doi.org/10.3389/frym.2018.00019openalex-snapshot

Mending a Broken Heart—The Genetics of Heart Disease

inferred← citeshttps://doi.org/10.3389/frym.2020.00087openalex-snapshot

Can Toothache Cause Heartbreak?

inferred← citeshttps://doi.org/10.3389/frym.2020.540440openalex-snapshot

Hearts, and the Heartless, in the Animal Kingdom

inferred← citeshttps://doi.org/10.3389/fsci.2023.997136openalex-snapshot

The future of evolutionary medicine: sparking innovation in biomedicine and public health

inferred← citeshttps://doi.org/10.3390/ani12131679openalex-snapshot

Genetic Basis of Dilated Cardiomyopathy in Dogs and Its Potential as a Bidirectional Model

inferred← citeshttps://doi.org/10.3390/jcdd4030008openalex-snapshot

Multiple Species Comparison of Cardiac Troponin T and Dystrophin: Unravelling the DNA behind Dilated Cardiomyopathy

inferred← citeshttps://doi.org/10.3390/vetsci11050214openalex-snapshot

Influence of Clinical Aspects and Genetic Factors on Feline HCM Severity and Development

inferred← citeshttps://doi.org/10.47278/book.ahp/2022.29openalex-snapshot

METABOLIC DISORDERS OF POULTRY

inferred← citeshttps://doi.org/10.5772/intechopen.78005openalex-snapshot

Avian Cardiovascular Disease Characteristics, Causes and Genomics

inferred← citeshttps://doi.org/10.5772/intechopen.92513openalex-snapshot

Canine Genetics, Health and Medicine

inferred← citeshttps://doi.org/10.5772/intechopen.97682openalex-snapshot

Diagnosis, Prognosis, Management, Treatment, Research and Advances in Canine Dilated Cardiomyopathy

inferred← citeshttps://doi.org/10.58354/jvc.86.2019.1157openalex-snapshot

Ứng dụng giải trình tự gen toàn bộ vùng mã hoá (exome) phát hiện biến thể mới trên gen acyl-CoA dehydrogenase chuỗi rất dài (ACADVL) ở bệnh nhân bệnh cơ tim

Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.