ProfessorStuartCook

Faculty of Medicine, National Heart & Lung Institute

Professor of Clinical & Molecular Cardiology

Contact

+44 (0)20 3313 1346stuart.cook

Location

RF 16Sydney StreetRoyal Brompton Campus

Summary

Professor Stuart Cook is the head of the Cardiovascular Genetics and Genomics group within Genetics & Imaging at the National Heart and Lung Institute (NHLI).

Publications

Journals

Dawes TJW, de Marvao A, Shi W, et al.Dawes TJW, de Marvao A, Shi W, Rueckert D, Cook SA, O'Regan DP close, 2019, Identifying the optimal regional predictor of right ventricular global function: a high-resolution three-dimensional cardiac magnetic resonance study, Anaesthesia, Vol:74, ISSN:0003-2409, Pages:312-320

Mazzarotto F, Girolami F, Boschi B, et al.Mazzarotto F, Girolami F, Boschi B, Barlocco F, Tomberli A, Baldini K, Coppini R, Tanini I, Bardi S, Contini E, Cecchi F, Pelo E, Cook SA, Cerbai E, Poggesi C, Torricelli F, Walsh R, Olivotto I close, 2019, Defining the diagnostic effectiveness of genes for inclusion in panels: the experience of two decades of genetic testing for hypertrophic cardiomyopathy at a single center, Genetics in Medicine, Vol:21, ISSN:1098-3600, Pages:284-292

Halliday BP, Wassall R, Lota AS, et al.Halliday BP, Wassall R, Lota AS, Khalique Z, Gregson J, Newsome S, Jackson R, Rahneva T, Wage R, Smith G, Venneri L, Tayal U, Auger D, Midwinter W, Whiffin N, Rajani R, Dungu JN, Pantazis A, Cook SA, Ware JS, Baksi AJ, Pennell DJ, Rosen SD, Cowie MR, Cleland JGF, Prasad SK close, 2019, Withdrawal of pharmacological treatment for heart failure in patients with recovered dilated cardiomyopathy (TRED-HF): an open-label, pilot, randomised trial, Lancet, Vol:393, ISSN:0140-6736, Pages:61-73

Horvat C, Johnson R, Lam L, et al.Horvat C, Johnson R, Lam L, Munro J, Mazzarotto F, Roberts AM, Herman DS, Parfenov M, Haghighi A, McDonough B, DePalma SR, Keogh AM, Macdonald PS, Hayward CS, Roberts A, Barton PJR, Felkin LE, Giannoulatou E, Cook SA, Seidman JG, Seidman CE, Fatkin D close, 2019, A gene-centric strategy for identifying disease-causing rare variants in dilated cardiomyopathy, Genetics in Medicine, Vol:21, ISSN:1098-3600, Pages:133-143

Bylstra Y, Kuan JL, Lim WK, et al.Bylstra Y, Kuan JL, Lim WK, Bhalshankar JD, Teo JX, Davila S, Teh BT, Rozen S, Tan E-C, Liew WKM, Yeo KK, Tan P, SinGapore Incidental Finding (SGIF) study group, Saw SM, Cheng C-Y, Cook S, Foo R, Jamuar SS close, 2019, Population genomics in South East Asia captures unexpectedly high carrier frequency for treatable inherited disorders., Genet Med, Vol:21, Pages:207-212

More Publications