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Right ventricular function declines prior to left ventricular ejection fraction in hypertrophic cardiomyopathy.

Journal article

Mahmod M. et al, (2022), Journal of cardiovascular magnetic resonance : official journal of the Society for Cardiovascular Magnetic Resonance, 24

Rare coding variants in 35 genes associate with circulating lipid levels-A multi-ancestry analysis of 170,000 exomes.

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Hindy G. et al, (2022), American journal of human genetics, 109, 81 - 96

Provocation Testing and Therapeutic Response in a Newly Described Channelopathy: RyR2 Calcium Release Deficiency Syndrome

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Ormerod JOM. et al, (2021), Circulation: Genomic and Precision Medicine

The power of genetic diversity in genome-wide association studies of lipids.

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Graham SE. et al, (2021), Nature

Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability

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Lagou V. et al, (2021), Nature Communications, 12

Incremental value of left atrial booster and reservoir strain in predicting atrial fibrillation in patients with hypertrophic cardiomyopathy: a cardiovascular magnetic resonance study.

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Raman B. et al, (2021), Journal of cardiovascular magnetic resonance : official journal of the Society for Cardiovascular Magnetic Resonance, 23

Predictors of Major Atrial Fibrillation Endpoints in the National Heart, Lung, and Blood Institute HCMR.

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Kramer CM. et al, (2021), JACC. Clinical electrophysiology

Time to Think Differently About Sarcomere-Negative Hypertrophic Cardiomyopathy

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Watkins H., (2021), Circulation, 143, 2415 - 2417

The trans-ancestral genomic architecture of glycemic traits.

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Chen J. et al, (2021), Nature genetics

CalTrack: High Throughput Automated Calcium Transient Analysis in Cardiomyocytes.

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Psaras Y. et al, (2021), Circulation research

A titan of Cardiovascular Research: Professor Peter Sleight (1929–2020)

Journal article

Channon KM. and Watkins H., (2021), Cardiovascular Research, 117, e64 - e66

Massively Parallel Sequencing of 43 Arrhythmia Genes in a Selected SUDI Cohort from Cape Town

Journal article

Heathfield LJ. et al, (2021), JOURNAL OF PEDIATRIC GENETICS

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