Compendium of cardiac channel mutations in 541 consecutive unrelated patients referred for long QT syndrome genetic testing von Tester, David J., Will, Melissa L., Haglund, Carla M., Ackerman, Michael J.

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Loss-of-Function of the Voltage-Gated Sodium Channel NaV1.5 (Channelopathies) in Patients With Irritable Bowel Syndrome von Beyder, Arthur, Mazzone, Amelia, Strege, Peter R., Tester, David J., Saito, Yuri A., Bernard, Cheryl E., Enders, Felicity T., Ek, Weronica E., Schmidt, Peter T., Dlugosz, Aldona, Lindberg, Greger, Karling, Pontus, Ohlsson, Bodil, Gazouli, Maria, Nardone, Gerardo, Cuomo, Rosario, Usai–Satta, Paolo, Galeazzi, Francesca, Neri, Matteo, Portincasa, Piero, Bellini, Massimo, Barbara, Giovanni, Camilleri, Michael, Locke, G. Richard, Talley, Nicholas J., D’Amato, Mauro, Ackerman, Michael J., Farrugia, Gianrico

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Effect of Clinical Phenotype on Yield of Long QT Syndrome Genetic Testing von Tester, David J., Will, Melissa L., Haglund, Carla M., Ackerman, Michael J.

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Spectrum and frequency of cardiac channel defects in swimming-triggered arrhythmia syndromes von CHOI, Grace, KOPPLIN, Laura J, TESTER, David J, WILL, Melissa L, HAGLUND, Carla M, ACKERMAN, Michael J

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Yield of the RYR2 Genetic Test in Suspected Catecholaminergic Polymorphic Ventricular Tachycardia and Implications for Test Interpretation von Kapplinger, Jamie D, Pundi, Krishna N, Larson, Nicholas B, Callis, Thomas E, Tester, David J, Bikker, Hennie, Wilde, Arthur A M, Ackerman, Michael J

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Ethnic Differences in Cardiac Potassium Channel Variants: Implications for Genetic Susceptibility to Sudden Cardiac Death and Genetic Testing for Congenital Long QT Syndrome von Ackerman, Michael J., Tester, David J., Jones, Gregg S., Will, Melissa L., Burrow, Christopher R., Curran, Mark E.

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Postmortem Molecular Analysis of SCN5A Defects in Sudden Infant Death Syndrome von Ackerman, Michael J, Siu, Benjamin L, Sturner, William Q, Tester, David J, Valdivia, Carmen R, Makielski, Jonathan C, Towbin, Jeffrey A

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A Ubiquitous Splice Variant and a Common Polymorphism Affect Heterologous Expression of Recombinant Human SCN5A Heart Sodium Channels von Makielski, Jonathan C, Ye, Bin, Valdivia, Carmen R, Pagel, Matthew D, Pu, Jielin, Tester, David J, Ackerman, Michael J

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Spectrum and prevalence of cardiac sodium channel variants among black, white, Asian, and Hispanic individuals: Implications for arrhythmogenic susceptibility and Brugada/long QT s... von Ackerman, Michael J., Splawski, Igor, Makielski, Jonathan C., Tester, David J., Will, Melissa L., Timothy, Katherine W., Keating, Mark T., Jones, Gregg, Chadha, Monica, Burrow, Christopher R., Stephens, J. Claiborne, Xu, Chuanbo, Judson, Richard, Curran, Mark E.

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Hypermethylation of the hMLH1 promoter in colon cancer with microsatellite instability von CUNNINGHAM, J. M, CHRISTENSEN, E. R, TESTER, D. J, KIM, C.-Y, ROCHE, P. C, BURGART, L. J, THIBODEAU, S. N

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Swimming, a Gene-Specific Arrhythmogenic Trigger for Inherited Long QT Syndrome von Ackerman, Michael J., Tester, David J., Porter, Co-Burn J.

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A trafficking defective, Brugada syndrome-causing SCN5A mutation rescued by drugs von VALDIVIA, Carmen R, TESTER, David J, ROK, Benjamin A, PORTER, Co-Burn J, MUNEER, Thomas M, JAHANGIR, Arshad, MAKIELSKI, Jonathan C, ACKERMAN, Michael J

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Common human SCN5A polymorphisms have altered electrophysiology when expressed in Q1077 splice variants von Tan, Bi-Hua, Valdivia, Carmen R., Rok, Benjamin A., Ye, Bin, Ruwaldt, Karen M., Tester, David J., Ackerman, Michael J., Makielski, Jonathan C.

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Identification of a common genetic substrate underlying postpartum cardiac events in congenital long QT syndrome von Khositseth, Anant, Tester, David J, Will, Melissa L, Bell, Carla M, Ackerman, Michael J

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Altered expression of hMSH2 and hMLH1 in tumors with microsatellite instability and genetic alterations in mismatch repair genes von Thibodeau, S N, French, A J, Roche, P C, Cunningham, J M, Tester, D J, Lindor, N M, Moslein, G, Baker, S M, Liskay, R M, Burgart, L J, Honchel, R, Halling, K C

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Targeted mutational analysis of ankyrin-B in 541 consecutive, unrelated patients referred for long QT syndrome genetic testing and 200 healthy subjects von Sherman, Jonathan, Tester, David J., Ackerman, Michael J.

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Molecular autopsy of sudden unexplained death in the young von Ackerman, M J, Tester, D J, Driscoll, D J

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Molecular Diagnosis of the Inherited Long-QT Syndrome in a Woman Who Died after Near-Drowning von Ackerman, Michael J, Tester, David J, Porter, Co-burn J, Edwards, William D

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Reduced COX-2 protein in colorectal cancer with defective mismatch repair von KARNES, W. E, SHATTUCK-BRANDT, R, BURGART, L. J, DUBOIS, R. N, TESTER, D. J, CUNNINGHAM, J. M, KIM, C.-Y, MCDONNELL, S. K, SCHAID, D. J, THIBODEAU, S. N

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Allelic imbalance and microsatellite instability in prostatic adenocarcinoma von CUNNINGHAM, J. M, SHAN, A, THIBODEAU, S. N, WICK, M. J, MDCONNELL, S. K, SCHAID, D. J, TESTER, D. J, QIAN, J, TAKAHASHI, S, JENKINS, R. B, BOSTWICK, D. G

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