Sharon Jenkins

University of Siena — Italy

Medicine · Health Sciences

30h-index3.2kcitations57works0.02yr avg
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Research Topics

Retinal Diseases and Treatments(16), Retinal Development and Disorders(13), Cardiomyopathy and Myosin Studies(12), Retinal Imaging and Analysis(8), Cardiovascular Effects of Exercise(7)

Publications55 total

Principles and Practice of Genetic Counselling for Inherited Cardiac Conditions
2018· 1 cited
Response by Andrews et al to Letter Regarding Article, “Electrical and Structural Substrate of Arrhythmogenic Right Ventricular Cardiomyopathy Determined Using Noninvasive Electrocardiographic Imaging and Late Gadolinium Magnetic Resonance Imaging”
Circulation Arrhythmia and Electrophysiology·2017· 1 citedOpen Access
Highlights From the <i>Circulation</i> Family of Journals
Circulation·2017Open Access
Electrical and Structural Substrate of Arrhythmogenic Right Ventricular Cardiomyopathy Determined Using Noninvasive Electrocardiographic Imaging and Late Gadolinium Magnetic Resonance Imaging
Circulation Arrhythmia and Electrophysiology·2017· 75 citedOpen Access
Desmoplakin missense and non-missense mutations in arrhythmogenic right ventricular cardiomyopathy: Genotype-phenotype correlation
International Journal of Cardiology·2017· 91 cited
Abstract 16150: Desmoplakin Missense vs Non-missense Mutations: Genotype-phenotype Correlations in Arrhythmogenic Right Ventricular Cardiomyopathy
Circulation·2016
Abnormal septal convexity into the left ventricle occurs in subclinical hypertrophic cardiomyopathy
Journal of Cardiovascular Magnetic Resonance·2015· 28 citedOpen Access
Novel genotype–phenotype associations demonstrated by high-throughput sequencing in patients with hypertrophic cardiomyopathy
Heart·2014· 168 citedOpen Access
High-throughput genotyping and phenotyping reveals new genetic determinants of clinical phenotype in hypertrophic cardiomyopathy
European Heart Journal·2013Open Access
Genetic complexity in hypertrophic cardiomyopathy revealed by high-throughput sequencing
Journal of Medical Genetics·2013· 244 citedOpen Access
Gender-Specific Differences in Major Cardiac Events and Mortality in Lamin A/C Mutation Carriers
European Journal of Heart Failure·2012· 143 citedOpen Access
New genetic determinants of disease phenotype in hypertrophic cardiomyopathy: high-throughput sequencing reveals unexpected complexicity
UCL Discovery (University College London)·2012
Genome-wide association study of age-related macular degeneration identifies associated variants in the TNXB–FKBPL–NOTCH4 region of chromosome 6p21.3
Human Molecular Genetics·2012· 90 cited
Prevalence of Sequence Variants in the RAS-Mitogen Activated Protein Kinase Signaling Pathway in Pre-Adolescent Children With Hypertrophic Cardiomyopathy
Circulation Cardiovascular Genetics·2012· 26 citedOpen Access
GENETIC COMPLEXITY IN HYPERTROPHIC CARDIOMYOPATHY: PRELIMINARY FINDINGS WITH NEXT GENERATION SEQUENCING
Journal of the American College of Cardiology·2012
Complement factor H genetic variant and age-related macular degeneration: effect size, modifiers and relationship to disease subtype
International Journal of Epidemiology·2012· 88 citedOpen Access
Risk Factors for Malignant Ventricular Arrhythmias in Lamin A/C Mutation Carriers
Journal of the American College of Cardiology·2012· 507 cited
Mutations in the Lamin A/C gene mimic arrhythmogenic right ventricular cardiomyopathy
European Heart Journal·2011· 246 citedOpen Access
The symmetry of phenotype between eyes of patients with early and late bilateral age-related macular degeneration (AMD)
Graefe s Archive for Clinical and Experimental Ophthalmology·2010· 31 cited
Prevalence of Sarcomere Protein Gene Mutations in Preadolescent Children With Hypertrophic Cardiomyopathy
Circulation Cardiovascular Genetics·2009· 216 citedOpen Access
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Frequent Co-authors

Andrew R. Webster(17), Alan C. Bird(13), William J. McKenna(10), Perry Elliott(9), Graham E. Holder(9), Petros Syrris(8), Naushin Waseem(8), Michel Michaelides(6), Anthony T. Moore(5), Lendon G. Payne(5), Catey Bunce(5), A.C. Bird(5), Anthony G. Robson(4), Antonis Pantazis(4), Tünde Pető(4), James Moon(4), A. R. Webster(4), S.S. Bhattacharya(4), Luís R. Lopes(3), Michael Hubank(3)