Keating, Mark T.

Genotype-Phenotype Correlation in the Long-QT Syndrome: Gene-Specific Triggers for Life-Threatening Arrhythmias

Schwartz, P. J., Priori, S. G., Spazzolini, C., Moss, A. J., Vincent, G. M., Napolitano, C., Denjoy, I., Guicheney, P., Breithardt, G., Keating, M. T., et al. (2001) · Circulation

Cardiac electrophysiology and arrhythmiasIon channel regulation and function

Cited by 1,779

CaV1.2 Calcium Channel Dysfunction Causes a Multisystem Disorder Including Arrhythmia and Autism

Splawski, I., Timothy, K. W., Sharpe, L. M., Decher, N., Kumar, P., Bloise, R., Napolitano, C., Schwartz, P. J., Joseph, R. M., Condouris, K., et al. (2004) · Cell

Cardiac electrophysiology and arrhythmiasIon channel regulation and function

Cited by 1,586

Hemizygosity at the elastin locus in a developmental disorder, Williams syndrome

Ewart, A. K., Morris, C. A., Atkinson, D., Jin, W., Sternes, K., Spallone, P., Stock, A. D., Leppert, M., & Keating, M. T. (1993) · Nature Genetics

Williams Syndrome ResearchConnective tissue disorders research

Cited by 1,138

Severe arrhythmia disorder caused by cardiac L-type calcium channel mutations

Splawski, I., Timothy, K. W., Decher, N., Kumar, P., Sachse, F. B., Beggs, A. H., Sanguinetti, M. C., & Keating, M. T. (2005) · Proceedings of the National Academy of Sciences

Cardiac electrophysiology and arrhythmiasIon channel regulation and function

Cited by 624

ECG T-wave patterns in genetically distinct forms of the hereditary long QT syndrome

Moss, A. J., Zareba, W., Benhorin, J., Locati, E. H., Hall, W. J., Robinson, J. L., Schwartz, P. J., Towbin, J. A., Vincent, G. M., Lehmann, M. H., et al. (1995) · Circulation

Cardiac electrophysiology and arrhythmiasIon channel regulation and function

Cited by 616

Metavinculin mutations alter actin interaction in dilated cardiomyopathy

Olson, T. M., Illenberger, S., Kishimoto, N. Y., Huttelmaier, S., Keating, M. T., & Jockusch, B. M. (2002) · Circulation

Cardiomyopathy and Myosin StudiesCardiac electrophysiology and arrhythmias

Cited by 278

Expanding RNAi therapeutics to extrahepatic tissues with lipophilic conjugates

Brown, K. M., Nair, J. K., Janas, M. M., Anglero-Rodriguez, Y. I., Dang, L. T. H., Peng, H., Theile, C. S., Castellanos-Rizaldos, E., Brown, C., Foster, D., et al. (2022) · Nature Biotechnology

RNA Interference and Gene DeliveryNanoparticle-Based Drug Delivery

Cited by 258

CACNA1H mutations in autism spectrum disorders

Splawski, I., Yoo, D. S., Stotz, S. C., Cherry, A., Clapham, D. E., & Keating, M. T. (2006) · Journal of Biological Chemistry

Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders

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