William J. McKenna
0000-0001-7994-2460
Publication & Citation Trends
Publications
0 total
Emerging Themes in Genetics of Hypertrophic Cardiomyopathy. Current status and clinical application. OA
Cited by 15
Semantic Scholar
Feasibility and Significance of Preclinical Diagnosis in Hypertrophic Cardiomyopathy
Cited by 1
Semantic Scholar
Thin Filament Mutations : Developing an Integrative Approach to a Complex Disorder
Cited by 146
Semantic Scholar
Idiopathic restrictive cardiomyopathy in children is caused by mutations in cardiac sarcomere protein genes
Cited by 214
Semantic Scholar
Genotype-phenotype assessment in autosomal recessive arrhythmogenic right ventricular cardiomyopathy (Naxos disease) caused by a deletion in plakoglobin. OA
Cited by 189
Semantic Scholar
Experience from clinical genetics in hypertrophic cardiomyopathy: proposal for new diagnostic criteria in adult members of affected families. OA
Cited by 318
Semantic Scholar
Hypertrophic cardiomyopathy — pathology and pathogenesis
Cited by 164
Semantic Scholar
Independent origin of identical beta cardiac myosin heavy-chain mutations in hypertrophic cardiomyopathy.
Cited by 61
Semantic Scholar
Research Topics
Cardiomyopathy and Myosin Studies
(621)
Cardiovascular Effects of Exercise
(403)
Cardiovascular Function and Risk Factors
(215)
Health, Medicine and Society
(199)
Hermeneutics and Narrative Identity
(199)
Affiliations
Statens Serum Institut
Medical Council of Canada
Claremont McKenna College
Kagoshima University
University of Pisa