Role of titin in cardiomyopathy: From DNA variants to patient stratification

by Ware J.S., Cook S.A.
Published 2018

Integrative genomics in cardiovascular medicine

by Ware J.S., Petretto E., Cook S.A.
Published 2018

NECTAR: A database of codon-centric missense variant annotations

by Gong S., Ware J.S., Walsh R., Cook S.A.
Published 2018

Next generation sequencing for clinical diagnostics and personalised medicine: Implications for the next generation cardiologist

by Ware J.S., Roberts A.M., Cook S.A.
Published 2018

Republished review: Next generation sequencing for clinical diagnostics and personalised medicine: Implications for the next generation cardiologist

by Ware J.S., Roberts A.M., Cook S.A.
Published 2018

Paralogue annotation identifies novel pathogenic variants in patients with brugada syndrome and catecholaminergic polymorphic ventricular tachycardia

by Walsh R., Peters N.S., Cook S.A., Ware J.S.
Published 2018

Paralogous annotation of disease-causing variants in long QT syndrome genes

by Ware J.S., Walsh R., Cunningham F., Birney E., Cook S.A.
Published 2018

Bayesian models for syndrome- and gene-specific probabilities of novel variant pathogenicity

by Ruklisa D., Ware J.S., Walsh R., Balding D.J., Cook S.A.
Published 2018

Truncating Variants in Titin Independently Predict Early Arrhythmias in Patients With Dilated Cardiomyopathy

by Tayal U., Newsome S., Buchan R., Whiffin N., Walsh R., Barton P.J., Ware J.S., Cook S.A., Prasad S.K.
Published 2018

Recovery of cardiac function in cardiomyopathy caused by titin truncation

by Felkin L.E., Walsh R., Ware J.S., Yacoub M.H., Birks E.J., Barton P.J.R., Cook S.A.
Published 2018

Moderate physical activity in healthy adults is associated with cardiac remodeling

by Dawes T.J.W., Corden B., Cotter S., De Marvao A., Walsh R., Ware J.S., Cook S.A., O'Regan D.P.
Published 2018

Next generation diagnostics in inherited arrhythmia syndromes: A comparison of two approaches

by Ware J.S., John S., Roberts A.M., Buchan R., Gong S., Peters N.S., Robinson D.O., Lucassen A., Behr E.R., Cook S.A.
Published 2018

Towards Clinical Molecular Diagnosis of Inherited Cardiac Conditions: A Comparison of Bench-Top Genome DNA Sequencers

by Li X., Buckton A.J., Wilkinson S.L., John S., Walsh R., Novotny T., Valaskova I., Gupta M., Game L., Barton P.J.R., Cook S.A., Ware J.S.
Published 2019

Using high-resolution variant frequencies to empower clinical genome interpretation

by Whiffin N., Minikel E., Walsh R., O'Donnell-Luria A.H., Karczewski K., Ing A.Y., Barton P.J.R., Funke B., Cook S.A., Macarthur D., Ware J.S.
Published 2019

Cloning and expression of the ApaLI, NspI, NspHI, SacI, ScaI, and SapI restriction-modification systems in Escherichia coli

by Xu, S.-Y., Xiao, J.-P., Ettwiller, L., Dalton, M., Robinson, D.P., Petronzio, T.R., Moran, L., Ganatra, M., Ware, J., Slatko, B., Benner, J., Holden, M., Aliotta, J., Poh, C.L.
Published 2012

Detection of mutations in KLHL3 and CUL3 in families with fhht (familial hyperkalaemic hypertension or gordon's syndrome)

by Glover M., Ware J.S., Henry A., Wolley M., Walsh R., Wain L.V., Xu S., Hoff W.G.V., Tobin M.D., Hall I.P., Cook S., Gordon R.D., Stowasser M., O'shaughnessy K.M.
Published 2019

Defining the genetic architecture of hypertrophic cardiomyopathy: Re-evaluating the role of non-sarcomeric genes

by Walsh R., Buchan R., Wilk A., John S., Felkin L.E., Thomson K.L., Chiaw T.H., Loong C.C.W., Pua C.J., Raphael C., Prasad S., Barton P.J., Funke B., Watkins H., Ware J.S., Cook S.A.
Published 2019

Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples

by Walsh R., Thomson K.L., Ware J.S., Funke B.H., Woodley J., McGuire K.J., Mazzarotto F., Blair E., Seller A., Taylor J.C., Minikel E.V., MacArthur D.G., Farrall M., Cook S.A., Watkins H.
Published 2019

Development of a Comprehensive Sequencing Assay for Inherited Cardiac Condition Genes

by Pua C.J., Bhalshankar J., Miao K., Walsh R., John S., Lim S.Q., Chow K., Buchan R., Soh B.Y., Lio P.M., Lim J., Schafer S., Lim J.Q., Tan P., Whiffin N., Barton P.J., Ware J.S., Cook S.A.
Published 2019

Phenotypic and pharmacogenetic evaluation of patients with thiazide-induced hyponatremia

by Ware J.S., Wain L.V., Channavajjhala S.K., Jackson V.E., Edwards E., Lu R., Siew K., Jia W., Shrine N., Kinnear S., Jalland M., Henry A.P., Clayton J., O'Shaughnessy K.M., Tobin M.D., Schuster V.L., Cook S., Hall I.P., Glover M.
Published 2019