Concepedia

Author

Stephen C. Harmer

Queen Mary University of LondonORCID

Also Known As

Harmer, S, S C Harmer, S. C. Harmer, S. Harmer, S.C. Harmer, SC Harmer, Sir Sidxey F. Harmer, Stephen C Harmer, Stephen C. Harmer, Stephen Harmer

62

Publications

1K

Citations

19

H-Index

54

Concepts

All Affiliations

Queen Mary University of LondonWilliam Harvey Research InstituteUniversity College LondonUniversity of BristolImperial College London
SC

About

Stephen C. Harmer is an author at Queen Mary University of London specializing in medicine, genetics, and molecular physiology.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

8

8

312

2

Natural Sciences

3

3

100

3

Biochemistry

2

2

52

4

Engineering

1

1

48

5

Social Sciences

1

1

19

Stephen C. Harmer

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22

Publications

845

Citations

17

H-Index

YearCitations

CRISPR/Cas9 editing in human pluripotent stem cell-cardiomyocytes highlights arrhythmias, hypocontractility, and energy depletion as potential therapeutic targets for hypertrophic cardiomyopathy

Diogo Mosqueira, Ingra Mannhardt, Jamie R. Bhagwan,

European Heart Journal

2018

242

Hyperinsulinaemic hypoglycaemia and diabetes mellitus due to dominant ABCC8/KCNJ11 mutations

Ritika R. Kapoor, Sarah E. Flanagan, Chela James,

Diabetologia

2011

92

Mechanisms of disease pathogenesis in long QT syndrome type 5

Stephen C. Harmer, Andrew J. Wilson, Robert W Aldridge,

American Journal of Physiology-Cell Physiology

2009

49

Characterization of a Binding Site for Anionic Phospholipids on KCNQ1

Alison Thomas, Stephen C. Harmer, Tapsi Khambra,

Journal of Biological Chemistry

2010

48

Human-based approaches to pharmacology and cardiology: an interdisciplinary and intersectorial workshop

Blanca Rodríguez, Annamaria Carusi, Najah Abi‐Gerges,

EP Europace

2015

48

GFRA2 Identifies Cardiac Progenitors and Mediates Cardiomyocyte Differentiation in a RET-Independent Signaling Pathway

Hidekazu Ishida, Rie Saba, Ioannis Kokkinopoulos,

Cell Reports

2016

35

Retinoic acid signaling modulation guides in vitro specification of human heart field-specific progenitor pools

Dorota Zawada, Jessica Kornherr, Anna B. Meier,

Nature Communications

2023

34

Postmortem Genetic Testing for Cardiac Ion Channelopathies in Stillbirths

Patricia B. Munroe, S Addison, Dominic J. Abrams,

Circulation Genomic and Precision Medicine

2018

30

Molecular mechanisms of congenital hyperinsulinism due to autosomal dominant mutations in<i>ABCC8</i>

Azizun Nessa, Qadeer Aziz, Alison Thomas,

Human Molecular Genetics

2015

29

Readthrough of long-QT syndrome type 1 nonsense mutations rescues function but alters the biophysical properties of the channel

Stephen C. Harmer, Jagdeep S. Mohal, Duncan Kemp,

Biochemical Journal

2012

28

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