Coghlan, Gerry

2015 ESC/ERS Guidelines for the diagnosis and treatment of pulmonary hypertension

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Whole-genome sequencing of patients with rare diseases in a national health system

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Identification of rare sequence variation underlying heritable pulmonary arterial hypertension

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Endothelial to mesenchymal transition contributes to endothelial dysfunction in pulmonary arterial hypertension

Good, R. B., Gilbane, A. J., Trinder, S. L., Denton, C. P., Coghlan, G., Abraham, D. J., & Holmes, A. M. (2015) · The American Journal of Pathology

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De Novo Truncating Mutations in WASF1 Cause Intellectual Disability with Seizures

Ito, Y., Carss, K. J., Duarte, S. T., Hartley, T., Keren, B., Kurian, M. A., Marey, I., Charles, P., Mendonça, C., Nava, C., et al. (2018) · The American Journal of Human Genetics

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