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European Heart Journal|March 7, 2021
Genome-wide association analysis in dilated cardiomyopathy reveals two new players in systolic heart failure on chromosomes 3p25.1 and 22q11.23Sophie Garnier, Magdalena Harakalova, Stefan Weiss, et al.
Nature Genetics|April 30, 2008
Integrated genomic approaches implicate osteoglycin (Ogn) in the regulation of left ventricular massEnrico Petretto, Rizwan Sarwar, Ian Grieve, et al.
American Journal of Human Genetics|June 18, 2013
Fine mapping of the 1p36 deletion syndrome identifies mutation of PRDM16 as a cause of cardiomyopathyAnne-Karin Arndt, Sebastian Schafer, Jorg-Detlef Drenckhahn, et al.
Circulation|March 30, 2017
Association Between Midwall Late Gadolinium Enhancement and Sudden Cardiac Death in Patients With Dilated Cardiomyopathy and Mild and Moderate Left Ventricular Systolic DysfunctionBrian P Halliday, Ankur Gulati, Aamir Ali, et al.
Nature Communications|July 9, 2016
Wars2 is a determinant of angiogenesisMao Wang, Patrick Sips, Ester Khin, et al.
Molecular Cell|July 16, 2022
A high-resolution map of human RNA translationSonia P Chothani, Eleonora Adami, Anissa A Widjaja, et al.
The Biochemical Journal|February 11, 2022
Cardiomyocyte BRAF and type 1 RAF inhibitors promote cardiomyocyte and cardiac hypertrophy in mice in vivoAngela Clerk, Daniel N Meijles, Michelle A Hardyman, et al.
Lancet (London, England)|November 16, 2018
Withdrawal of pharmacological treatment for heart failure in patients with recovered dilated cardiomyopathy (TRED-HF): an open-label, pilot, randomised trialBrian P Halliday, Rebecca Wassall, Amrit S Lota, et al.
Nature|July 17, 2024
Inhibition of IL-11 signalling extends mammalian healthspan and lifespanAnissa A Widjaja, Wei-Wen Lim, Sivakumar Viswanathan, et al.
Genome Medicine|January 31, 2019
Quantitative approaches to variant classification increase the yield and precision of genetic testing in Mendelian diseases: the case of hypertrophic cardiomyopathyRoddy Walsh, Francesco Mazzarotto, Nicola Whiffin, et al.
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