Concepedia

Author

Sharon Jenkins

University College London

Also Known As

S A Jenkins, S Jenkins, S. A. Jenkins, S. Jenkins, S. Patch, Sharon A Jenkins, Sharon A. Jenkins, Sharon Jenkins

57

Publications

3.2K

Citations

30

H-Index

43

Concepts

All Affiliations

University College LondonMoorfields Eye HospitalMoorfields Eye Hospital NHS Foundation TrustUniversity College Hospital at Westmoreland StreetSorbonne Université
SJ

About

Sharon Jenkins is an author at University College London specializing in medicine, immunology, and vaccination.

Top Concepts

#ConceptH-IndexPublicationsCitations

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Medicine

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1.1K

2

Engineering

1

1

30

3

Biomolecular Engineering

1

1

30

4

Cell Biology

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58

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Clinical Immunology

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Sharon Jenkins

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30

Publications

3K

Citations

28

H-Index

YearCitations

Risk Factors for Malignant Ventricular Arrhythmias in Lamin A/C Mutation Carriers

Ingrid A.W. van Rijsingen, Eloisa Arbustini, Perry Elliott,

Journal of the American College of Cardiology

2012

507

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

Giovanni Quarta, Petros Syrris, Michael T. Ashworth,

European Heart Journal

2011

246

Genetic complexity in hypertrophic cardiomyopathy revealed by high-throughput sequencing

Luís R. Lopes, Anna Zekavati, Petros Syrris,

Journal of Medical Genetics

2013

244

Prevalence of Sarcomere Protein Gene Mutations in Preadolescent Children With Hypertrophic Cardiomyopathy

Juan Pablo Kaski, Petros Syrris, Sharon Jenkins,

Circulation Cardiovascular Genetics

2009

216

Novel genotype–phenotype associations demonstrated by high-throughput sequencing in patients with hypertrophic cardiomyopathy

Luís R. Lopes, Petros Syrris, Oliver Guttmann,

Heart

2014

168

Gender-Specific Differences in Major Cardiac Events and Mortality in Lamin A/C Mutation Carriers

Ingrid A.W. van Rijsingen, Eline A. Nannenberg, Eloisa Arbustini,

European Journal of Heart Failure

2012

143

Mutations in the Gene KCNV2 Encoding a Voltage-Gated Potassium Channel Subunit Cause “Cone Dystrophy with Supernormal Rod Electroretinogram” in Humans

Huimin Wu, Jill A. Cowing, Michel Michaelides,

The American Journal of Human Genetics

2006

134

Identification of Novel<i>RPGR</i>ORF15 Mutations in X-linked Progressive Cone-Rod Dystrophy (XLCORD) Families

Neil D. Ebenezer, Michel Michaelides, Sharon Jenkins,

Investigative Ophthalmology & Visual Science

2005

112

Poly[di(carboxylatophenoxy)phosphazene] (PCPP) is a potent immunoadjuvant for an influenza vaccine

Lendon G. Payne, Sharon Jenkins, Angela Woods,

Vaccine

1998

107

Desmoplakin missense and non-missense mutations in arrhythmogenic right ventricular cardiomyopathy: Genotype-phenotype correlation

Silvia Castelletti, Annina S. Vischer, Petros Syrris,

International Journal of Cardiology

2017

91

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