INHERIT (INHibition of the renin angiotensin system in hypertrophic cardiomyopathy and the Effect on hypertrophy—a Randomised Intervention Trial with losartan)

Por Olivotto, Iacopo, Ashley, Euan A.
Publicado no Glob Cardiol Sci Pract (2015)

Taming the genome: towards better genetic test interpretation

Por Caleshu, Colleen, Ashley, Euan A.
Publicado no Genome Med (2016)

Next Generation Sequencing in Cardiovascular Disease: Present Clinical Applications and the Horizon of Precision Medicine

Por Parikh, Victoria N., Ashley, Euan A.
Publicado no Circulation (2017)

Personalized medicine: hope or hype?

Por Salari, Keyan, Watkins, Hugh, Ashley, Euan A.
Publicado em 2012

Nitric oxide control of cardiac function: is neuronal nitric oxide synthase a key component?

Por Sears, Claire E, Ashley, Euan A, Casadei, Barbara
Publicado em 2004

Cell-Intrinsic Functional Effects of the α-Cardiac Myosin Arg-403-Gln Mutation in Familial Hypertrophic Cardiomyopathy

Por Chuan, Peiying, Sivaramakrishnan, Sivaraj, Ashley, Euan A., Spudich, James A.
Publicado em 2012

Stable, Covalent Attachment of Laminin to Microposts Improves the Contractility of Mouse Neonatal Cardiomyocytes

Por Ribeiro, Alexandre J. S., Zaleta-Rivera, Kathia, Ashley, Euan A., Pruitt, Beth L.
Publicado em 2014

DNA sequencing: Clinical applications of new DNA sequencing technologies

Por Dewey, Frederick E., Pan, Stephen, Wheeler, Matthew T, Quake, Stephen R., Ashley, Euan A.
Publicado em 2012

A General Framework for Dose Optimization

Por Turcott, Robert G., Sagreiya, Hersh, Ashley, Euan A., Altman, Russ B., Das, Amar K.
Publicado em 2009

Cost effectiveness of pre-participation screening for prevention of sudden cardiac death in young athletes

Por Wheeler, Matthew T., Heidenreich, Paul A., Froelicher, Victor F., Hlatky, Mark A., Ashley, Euan A.
Publicado em 2010

A Clinical Approach to Inherited Hypertrophy: The use of family history in diagnosis, risk-assessment, and management

Por Dunn, Kyla E., Caleshu, Colleen, Cirino, Allison L., Ho, Carolyn Y., Ashley, Euan A.
Publicado em 2013

A Balanced Look at the Implications of Genomic (and Other “Omics”) Testing for Disease Diagnosis and Clinical Care

Por Boyd, Scott D., Galli, Stephen J., Schrijver, Iris, Zehnder, James L., Ashley, Euan A., Merker, Jason D.
Publicado em 2014

How does morphology impact on diastolic function in hypertrophic cardiomyopathy? A single centre experience

Por Finocchiaro, Gherardo, Haddad, Francois, Pavlovic, Aleksandra, Magavern, Emma, Sinagra, Gianfranco, Knowles, Joshua W, Myers, Jonathan, Ashley, Euan A
Publicado em 2014

Cardiac Structural and Sarcomere Genes Associated with Cardiomyopathy Exhibit Marked Intolerance of Genetic Variation

Por Pan, Stephen, Caleshu, Colleen A., Dunn, Kyla E., Foti, Marcia J., Moran, Maura K., Soyinka, Oretunlewa, Ashley, Euan A.
Publicado em 2012

In Situ Optical Mapping of Voltage and Calcium in the Heart

Por Lee, Peter, Taghavi, Fouad, Yan, Ping, Ewart, Paul, Ashley, Euan A., Loew, Leslie M., Kohl, Peter, Bollensdorff, Christian, Woods, Christopher E.
Publicado em 2012

Medical implications of technical accuracy in genome sequencing

Por Goldfeder, Rachel L., Priest, James R., Zook, Justin M., Grove, Megan E., Waggott, Daryl, Wheeler, Matthew T., Salit, Marc, Ashley, Euan A.
Publicado no Genome Med (2016)

Low-Dose Growth Hormone is Cardioprotective in Uremia

Por Rabkin, Ralph, Awwad, Ibrahim, Chen, Yu, Ashley, Euan A., Sun, Difei, Sood, Sumita, Clusin, William, Heidenreich, Paul, Piecha, Grzegorz, Gross, Marie-Luise
Publicado em 2008

Apelin prevents aortic aneurysm formation by inhibiting macrophage inflammation

Por Leeper, Nicholas J., Tedesco, Maureen M., Kojima, Yoko, Schultz, Geoffrey M., Kundu, Ramendra K., Ashley, Euan A., Tsao, Phillip S., Dalman, Ronald L., Quertermous, Thomas
Publicado em 2009

Gene Coexpression Network Topology of Cardiac Development, Hypertrophy, and Failure

Por Dewey, Frederick E., Perez, Marco V., Wheeler, Matthew T., Watt, Clifton, Spin, Joshua, Langfelder, Peter, Horvath, Stephen, Hannenhalli, Sridhar, Cappola, Thomas P., Ashley, Euan A.
Publicado em 2010

Establishing disease causality for a novel gene variant in familial dilated cardiomyopathy using a functional in-vitro assay of regulated thin filaments and human cardiac myosin

Por Pan, Stephen, Sommese, Ruth F., Sallam, Karim I., Nag, Suman, Sutton, Shirley, Miller, Susan M., Spudich, James A., Ruppel, Kathleen M., Ashley, Euan A.
Publicado no BMC Med Genet (2015)