An international compendium of mutations in the SCN5A -encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testing von Kapplinger, Jamie D., BA, Tester, David J., BS, Alders, Marielle, PhD, Benito, Begoña, MD, Berthet, Myriam, BA, Brugada, Josep, MD, PhD, Brugada, Pedro, MD, PhD, Fressart, Véronique, MD, Guerchicoff, Alejandra, PhD, Harris-Kerr, Carole, PhD, Kamakura, Shiro, MD, PhD, Kyndt, Florence, PhD, Koopmann, Tamara T., PhD, Miyamoto, Yoshihiro, MD, Pfeiffer, Ryan, BS, Pollevick, Guido D., PhD, Probst, Vincent, MD, PhD, Zumhagen, Sven, MD, Vatta, Matteo, PhD, Towbin, Jeffrey A., MD, Shimizu, Wataru, MD, PhD, Schulze-Bahr, Eric, MD, Antzelevitch, Charles, PhD, Salisbury, Benjamin A., PhD, Guicheney, Pascale, PhD, Wilde, Arthur A.M., MD, PhD, Brugada, Ramon, MD, PhD, Schott, Jean-Jacques, PhD, Ackerman, Michael J., MD, PhD

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Spectrum and prevalence of mutations from the first 2,500 consecutive unrelated patients referred for the FAMILION® long QT syndrome genetic test von Kapplinger, Jamie D., BA, Tester, David J., BS, Salisbury, Benjamin A., PhD, Carr, Janet L., PhD, Harris-Kerr, Carole, PhD, Pollevick, Guido D., PhD, Wilde, Arthur A.M., MD, PhD, Ackerman, Michael J., MD, PhD

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Distinguishing Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia–Associated Mutations From Background Genetic Noise von Kapplinger, Jamie D., BA, Landstrom, Andrew P., BS, Salisbury, Benjamin A., PhD, Callis, Thomas E., PhD, Pollevick, Guido D., PhD, Tester, David J., BS, Cox, Moniek G.P.J., MD, Bhuiyan, Zahir, MD, PhD, Bikker, Hennie, PhD, Wiesfeld, Ans C.P., MD, PhD, Hauer, Richard N.W., MD, van Tintelen, J. Peter, MD, PhD, Jongbloed, Jan D.H., PhD, Calkins, Hugh, MD, Judge, Daniel P., MD, Wilde, Arthur A.M., MD, PhD, Ackerman, Michael J., MD, PhD

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Using the genome aggregation database, computational pathogenicity prediction tools, and patch clamp heterologous expression studies to demote previously published long QT syndrome... von Clemens, Daniel J., Lentino, Anne R., Kapplinger, Jamie D., Ye, Dan, Zhou, Wei, Tester, David J., Ackerman, Michael J.

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Genotype-Phenotype Correlation of SCN5A Mutation for the Clinical and Electrocardiographic Characteristics of Probands With Brugada Syndrome: A Japanese Multicenter Registry von Yamagata, Kenichiro, Horie, Minoru, Aiba, Takeshi, Ogawa, Satoshi, Aizawa, Yoshifusa, Ohe, Tohru, Yamagishi, Masakazu, Makita, Naomasa, Sakurada, Harumizu, Tanaka, Toshihiro, Shimizu, Akihiko, Hagiwara, Nobuhisa, Kishi, Ryoji, Nakano, Yukiko, Takagi, Masahiko, Makiyama, Takeru, Ohno, Seiko, Fukuda, Keiichi, Watanabe, Hiroshi, Morita, Hiroshi, Hayashi, Kenshi, Kusano, Kengo, Kamakura, Shiro, Yasuda, Satoshi, Ogawa, Hisao, Miyamoto, Yoshihiro, Kapplinger, Jamie D, Ackerman, Michael J, Shimizu, Wataru

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The Promise and Peril of Precision Medicine von Ackerman, Jaeger P., BA, Bartos, Daniel C., PhD, Kapplinger, Jamie D., BS, Tester, David J., BS, Delisle, Brian P., PhD, Ackerman, Michael J., MD, PhD

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The Promise and Peril of Precision Medicine: Phenotyping Still Matters Most von Ackerman, Jaeger P, Bartos, Daniel C, Kapplinger, Jamie D, Tester, David J, Delisle, Brian P, Ackerman, Michael J

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Enhancing the Predictive Power of Mutations in the C-Terminus of the KCNQ1-Encoded Kv7.1 Voltage-Gated Potassium Channel von Kapplinger, Jamie D., Tseng, Andrew S., Salisbury, Benjamin A., Tester, David J., Callis, Thomas E., Alders, Marielle, Wilde, Arthur A. M., Ackerman, Michael J.

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Safety and Efficacy of CT-Guided Percutaneous Biopsy of Suspicious Subcentimeter Pelvic and Retroperitoneal Lymph Nodes Detected by 11C-Choline PET in Patients With Prostate Cancer von Kapplinger, Jamie D, Lima, Livia M Frota, Packard, Annie T, Nathan, Mark A, Young, Jason R, Stish, Bradley J, Hough, David M

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Safety and Efficacy of CT-Guided Percutaneous Biopsy of Suspicious Subcentimeter Pelvic and Retroperitoneal Lymph Nodes Detected by 11 C-Choline PET in Patients With Prostate Cance... von Kapplinger, Jamie D, Lima, Livia M Frota, Packard, Annie T, Nathan, Mark A, Young, Jason R, Stish, Bradley J, Hough, David M

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Sudden infant death syndrome and inherited cardiac conditions von Baruteau, Alban-Elouen, Tester, David J., Kapplinger, Jamie D., Ackerman, Michael J., Behr, Elijah R.

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Sublobar Resection, Stereotactic Body Radiation Therapy, and Percutaneous Ablation Provide Comparable Outcomes for Lung Metastasis-Directed Therapy von Gits, Hunter C., Khosravi Flanigan, Mitra A., Kapplinger, Jamie D., Reisenauer, Janani S., Eiken, Patrick W., Breen, William G., Vu, Linh H., Welch, Brian T., Harmsen, William S., Day, Courtney N., Olivier, Kenneth R., Park, Sean S., Garces, Yolanda I., Hallemeier, Christopher L., Merrell, Kenneth W., Ashman, Jonathan B., Schild, Steven E., Grams, Michael P., Lucido, J. John, Shen, K. Robert, Cassivi, Stephen D., Wigle, Dennis, Nichols, Francis C., Blackmon, Shanda, Tapias, Luis F., Callstrom, Matthew R., Owen, Dawn

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Enhanced Classification of Brugada Syndrome-Associated and Long-QT Syndrome-Associated Genetic Variants in the SCN5A-Encoded Na(v)1.5 Cardiac Sodium Channel von Kapplinger, Jamie D, Giudicessi, John R, Ye, Dan, Tester, David J, Callis, Thomas E, Valdivia, Carmen R, Makielski, Jonathan C, Wilde, Arthur A, Ackerman, Michael J

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Variants in the 3' untranslated region of the KCNQ1-encoded Kv7.1 potassium channel modify disease severity in patients with type 1 long QT syndrome in an allele-specific manner von AMIN, Ahmad S, GIUDICESSI, John R, MÜLLER, Martina, WIJNEN, Wino J, TAN, Hanno L, BEZZINA, Connie R, CREEMERS, Esther E, WILDE, Arthur A. M, ACKERMAN, Michael J, PINTO, Yigal M, TIJSEN, Anke J, SPANJAART, Anne M, RECKMAN, Yolan J, KLEMENS, Christine A, TANCK, Michael W, KAPPLINGER, Jamie D, HOFMAN, Nynke, SINNER, Moritz F

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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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Response by Kapplinger et al to Letter Regarding Article, "Yield of the RYR2 Genetic Test in Suspected Catecholaminergic Polymorphic Ventricular Tachycardia and Implications for Te... von Kapplinger, Jamie D, Tester, David J, Ackerman, Michael J

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Lidocaine Attenuation Testing: An In Vivo Investigation of Putative LQT3-Associated Variants in the SCN5A- Encoded Sodium Channel von Heather N. Anderson, M.D, Bos, J. Martijn, MD PhD, Kapplinger, Jamie D, Meskill, Jana M., RN, Ye, Dan, MD, Ackerman, Michael J., MD PhD

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Evaluation of the Mayo Clinic Phenotype-Based Genotype Predictor Score in Patients with Clinically Diagnosed Hypertrophic Cardiomyopathy von Murphy, Sinead L., Anderson, Jason H., Kapplinger, Jamie D., Kruisselbrink, Teresa M., Gersh, Bernard J., Ommen, Steve R., Ackerman, Michael J., Bos, J. Martijn

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Founder Mutation Genotyping and Sudden Cardiac Arrest: The Promise of Precision Medicine Fulfilled or the Next Step Into Precise Uncertainty von Kapplinger, Jamie D, Ackerman, Michael J

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Distinguishing Hypertrophic Cardiomyopathy-Associated Mutations from Background Genetic Noise von Kapplinger, Jamie D., Landstrom, Andrew P., Bos, J. Martijn, Salisbury, Benjamin A., Callis, Thomas E., Ackerman, Michael J.

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