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Genetic therapies for cardiomyopathy: survey of attitudes of the patient community for the CureHeart project

Journal article

Ormondroyd E. et al, (2024), European Journal of Human Genetics

The genetic dissection of fetal haemoglobin persistence in sickle cell disease in Nigeria.

Journal article

Ojewunmi OO. et al, (2024), Human molecular genetics, 33, 919 - 929

Genetic Determinants of the Interventricular Septum Are Linked to Ventricular Septal Defects and Hypertrophic Cardiomyopathy

Journal article

Yu M. et al, (2023), Circulation: Genomic and Precision Medicine

Acknowledgment to reviewers of Journal of Translational Genetics and Genomics in 2022

Journal article

Wang N. et al, (2023), Journal of Translational Genetics and Genomics, 7, 1 - 2

A saturated map of common genetic variants associated with human height.

Journal article

Yengo L. et al, (2022), Nature, 610, 704 - 712

A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids.

Journal article

Ramdas S. et al, (2022), American journal of human genetics, 109, 1366 - 1387

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

Journal article

Graham SE. et al, (2021), Nature

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

Journal article

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

Genetic Predisposition to Coronary Artery Disease in Type 2 Diabetes Mellitus

Journal article

van Zuydam NR. et al, (2020), Circulation: Genomic and Precision Medicine, 13

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