Catheter Ablation of Accessory Atrioventricular Pathways (Wolff–Parkinson–White Syndrome) by Radiofrequency Current von Jackman, Warren M, Wang, Xunzhang, Friday, Karen J, Roman, Carlos A, Moulton, Kriech P, Beckman, Karen J, McClelland, James H, Twidale, Nicholas, Hazlitt, H. Andrew, Prior, Michael I, Margolis, P. David, Calame, James D, Overholt, Edward D, Lazzara, Ralph

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Characterization of reentrant circuit in macroreentrant right atrial tachycardia after surgical repair of congenital heart disease : Isolated channels between scars allow focal abl... von NAKAGAWA, Hiroshi, SHAH, Nayyar, OTOMO, Kenichiro, ZULU WANG, LAZZARA, Ralph, JACKMAN, Warren M, MATSUDAIRA, Kagari, OVERHOLT, Edward, CHANDRASEKARAN, Krishnaswamy, BECKMAN, Karen J, SPECTOR, Peter, CALAME, James D, RAO, Arun, HASDEMIR, Can

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Role of the tricuspid annulus and the eustachian valve/ridge on atrial flutter. Relevance to catheter ablation of the septal isthmus and a new technique for rapid identification of... von Nakagawa, H, Lazzara, R, Khastgir, T, Beckman, K J, McClelland, J H, Imai, S, Pitha, J V, Becker, A E, Arruda, M, Gonzalez, M D, Widman, L E, Rome, M, Neuhauser, J, Wang, X, Calame, J D, Goudeau, M D, Jackman, W M

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Relation between pulmonary vein firing and extent of left atrial-pulmonary vein connection in patients with atrial fibrillation von NAKAGAWA, Hiroshi, AOYAMA, Hiroshi, HASDEMIR, Can, SINGH, Dalip, LAZZARA, Ralph, JACKMAN, Warren M, BECKMAN, Karen J, PO, Sunny S, WU, Richard, LOCKWOOD, Deborah, SPECTOR, Peter, CALAME, James D, LUSTGARTEN, Daniel L, HERRING, Lisa

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TLR7 gain-of-function genetic variation causes human lupus von Brown, Grant J., Cañete, Pablo F., Wang, Hao, Medhavy, Arti, Bones, Josiah, Roco, Jonathan A., He, Yuke, Qin, Yuting, Cappello, Jean, Ellyard, Julia I., Bassett, Katharine, Shen, Qian, Burgio, Gaetan, Zhang, Yaoyuan, Turnbull, Cynthia, Meng, Xiangpeng, Wu, Phil, Cho, Eun, Miosge, Lisa A., Andrews, T. Daniel, Field, Matt A., Tvorogov, Denis, Lopez, Angel F., Babon, Jeffrey J., López, Cristina Aparicio, Gónzalez-Murillo, África, Garulo, Daniel Clemente, Pascual, Virginia, Levy, Tess, Mallack, Eric J., Calame, Daniel G., Lotze, Timothy, Lupski, James R., Ding, Huihua, Ullah, Tomalika R., Walters, Giles D., Koina, Mark E., Cook, Matthew C., Shen, Nan, de Lucas Collantes, Carmen, Corry, Ben, Gantier, Michael P., Athanasopoulos, Vicki, Vinuesa, Carola G.

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PLS3 missense variants affecting the actin-binding domains cause X-linked congenital diaphragmatic hernia and body-wall defects von Petit, Florence, Longoni, Mauro, Wells, Julie, Maser, Richard S., Bogenschutz, Eric L., Dysart, Matthew J., Contreras, Hannah T.M., Frénois, Frederic, Pober, Barbara R., Clark, Robin D., Giampietro, Philip F., Ropers, Hilger H., Hu, Hao, Loscertales, Maria, Wagner, Richard, Ai, Xingbin, Brand, Harrison, Jourdain, Anne-Sophie, Delrue, Marie-Ange, Gilbert-Dussardier, Brigitte, Devisme, Louise, Keren, Boris, McCulley, David J., Qiao, Lu, Hernan, Rebecca, Wynn, Julia, Scott, Tiana M., Calame, Daniel G., Coban-Akdemir, Zeynep, Hernandez, Patricia, Hernandez-Garcia, Andres, Yonath, Hagith, Lupski, James R., Shen, Yufeng, Chung, Wendy K., Scott, Daryl A., Bult, Carol J., Donahoe, Patricia K., High, Frances A.

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Electrical resynchronization induced by direct His-bundle pacing von Lustgarten, Daniel L., MD, PhD, Calame, Susan, RN, Crespo, Eric M., MD, Calame, James, RN, Lobel, Robert, MD, Spector, Peter S., MD

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The temporal variability of dominant frequency and complex fractionated atrial electrograms constrains the validity of sequential mapping in human atrial fibrillation von Habel, Nicole, Znojkiewicz, Pierre, MD, Thompson, Nathaniel, MD, Müller, Joachim G., MD, Mason, Bryan, BA, Calame, James, RN, BSN, Calame, Susan, RN, Sharma, Shruti, BS, Mirchandani, Gagan, PhD, Janks, Deborah, PhD, Bates, Jason, PhD, Noori, Arshia, MD, Karnbach, Andreas, Lustgarten, Daniel L., MD, PhD, Sobel, Burton E., MD, Spector, Peter, MD

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Loss of non-motor kinesin KIF26A causes congenital brain malformations via dysregulated neuronal migration and axonal growth as well as apoptosis von Qian, Xuyu, DeGennaro, Ellen M, Talukdar, Maya, Akula, Shyam K, Lai, Abbe, Shao, Diane D, Gonzalez, Dilenny, Marciano, Jack H, Smith, Richard S, Hylton, Norma K, Yang, Edward, Bazan, J Fernando, Barrett, Lee, Yeh, Rebecca C, Hill, R Sean, Beck, Samantha G, Otani, Aoi, Angad, Jolly, Mitani, Tadahiro, Posey, Jennifer E, Pehlivan, Davut, Calame, Daniel, Aydin, Hatip, Yesilbas, Osman, Parks, Kendall C, Argilli, Emanuela, England, Eleina, Im, Kiho, Taranath, Ajay, Scott, Hamish S, Barnett, Christopher P, Arts, Peer, Sherr, Elliott H, Lupski, James R, Walsh, Christopher A

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Biallelic variation in the choline and ethanolamine transporter FLVCR1 underlies a severe developmental disorder spectrum von Calame, Daniel G., Wong, Jovi Huixin, Panda, Puravi, Nguyen, Dat Tuan, Leong, Nancy C.P., Sangermano, Riccardo, Patankar, Sohil G., Abdel-Hamid, Mohamed S., AlAbdi, Lama, Safwat, Sylvia, Flannery, Kyle P., Dardas, Zain, Fatih, Jawid M., Murali, Chaya, Kannan, Varun, Lotze, Timothy E., Herman, Isabella, Ammouri, Farah, Rezich, Brianna, Efthymiou, Stephanie, Alavi, Shahryar, Murphy, David, Firoozfar, Zahra, Nasab, Mahya Ebrahimi, Bahreini, Amir, Ghasemi, Majid, Haridy, Nourelhoda A., Goldouzi, Hamid Reza, Eghbal, Fatemeh, Karimiani, Ehsan Ghayoor, Begtrup, Amber, Elloumi, Houda, Srinivasan, Varunvenkat M., Gowda, Vykuntaraju K., Du, Haowei, Jhangiani, Shalini N., Coban-Akdemir, Zeynep, Marafi, Dana, Rodan, Lance, Isikay, Sedat, Rosenfeld, Jill A., Ramanathan, Subhadra, Staton, Michael, Oberg, Kerby C., Clark, Robin D., Wenman, Catharina, Loughlin, Sam, Saad, Ramy, Ashraf, Tazeen, Male, Alison, Tadros, Shereen, Boostani, Reza, Abdel-Salam, Ghada M.H., Zaki, Maha, Mardi, Ali, Hashemi-Gorji, Farzad, Abdalla, Ebtesam, Manzini, M. Chiara, Pehlivan, Davut, Posey, Jennifer E., Gibbs, Richard A., Houlden, Henry, Alkuraya, Fowzan S., Bujakowska, Kinga, Maroofian, Reza, Lupski, James R., Nguyen, Long N.

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Clinical and functional heterogeneity associated with the disruption of retinoic acid receptor beta von Caron, Véronique, Chassaing, Nicolas, Ragge, Nicola, Boschann, Felix, Ngu, Angelina My-Hoa, Meloche, Elisabeth, Chorfi, Sarah, Lakhani, Saquib A., Ji, Weizhen, Steiner, Laurie, Marcadier, Julien, Jansen, Philip R., van de Pol, Laura A., van Hagen, Johanna M., Russi, Alvaro Serrano, Le Guyader, Gwenaël, Nordenskjöld, Magnus, Nordgren, Ann, Anderlid, Britt-Marie, Plaisancié, Julie, Stoltenburg, Corinna, Horn, Denise, Drenckhahn, Anne, Hamdan, Fadi F., Lefebvre, Mathilde, Attie-Bitach, Tania, Forey, Peggy, Smirnov, Vasily, Ernould, Françoise, Jacquemont, Marie-Line, Grotto, Sarah, Alcantud, Alberto, Coret, Alicia, Ferrer-Avargues, Rosario, Srivastava, Siddharth, Vincent-Delorme, Catherine, Romoser, Shelby, Safina, Nicole, Saade, Dimah, Lupski, James R., Calame, Daniel G., Geneviève, David, Chatron, Nicolas, Schluth-Bolard, Caroline, Myers, Kenneth A., Dobyns, William B., Calvas, Patrick, Salmon, Caroline, Holt, Richard, Elmslie, Frances, Allaire, Marc, Prigozhin, Daniil M., Tremblay, André, Michaud, Jacques L.

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Biallelic variants in the ectonucleotidase ENTPD1 cause a complex neurodevelopmental disorder with intellectual disability, hypomyelination, and spastic paraplegia von Calame, Daniel G., Herman, Isabella, Marshall, Aren E., Maroofian, Reza, Donis, Karina Carvalho, Fatih, Jawid M., Mitani, Tadahiro, Du, Haowei, Grochowski, Christopher M., Sousa, Sergio, Bakhtiari, Somayeh, Ito, Yoko A., Rocca, Clarissa, Hunter, Jill V., Sutton, V. Reid, Emrick, Lisa T., Boycott, Kym M., Lossos, Alexander, Fellig, Yakov, Prus, Eugenia, Kalish, Yosef, Meiner, Vardiella, Suerink, Manon, Ruivenkamp, Claudia, Muirhead, Kayla, Saadi, Nebal W., Zaki, Maha S., Skidmore, David L., Osmond, Matthew, Silva, Thiago Oliveira, Houlden, Henry, Murphy, David, Ghayoorarimiani, Ehsan, Jamshidi, Yalda, Jaddoa, Asaad Ghanim, Tajsharghi, Homa, Jin, Sheng Chih, Coban-Akdemir, Zeynep, Travaglini, Lorena, Nicita, Francesco, Jhangiani, Shalini N., Gibbs, Richard A., Posey, Jennifer E., Kruer, Michael C., Kernohan, Kristin D., Morales Saute, Jonas A., Vanderver, Adeline, Pehlivan, Davut, Marafi, Dana, Lupski, James R.

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Coronary sinus-ventricular accessory connections producing posteroseptal and left posterior accessory pathways: Incidence and electrophysiological identification von YINGXIAN SUN, ARRUDA, Mauricio, LAZZARA, Ralph, JACKMAN, Warren, OTOMO, Kenichiro, BECKMAN, Karen, NAKAGAWA, Hiroshi, CALAME, James, PO, Sunny, SPECTOR, Peter, LUSTGARTEN, Daniel, HERRING, Lisa

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Safety and efficacy of epicardial cryoablation in a canine model von Lustgarten, Daniel L., Bell, Stephen, Hardin, Nicholas, Calame, James, Spector, Peter S.

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Development and demonstration of high-average power W-band gyro-amplifiers for radar applications von Blank, M., Felch, K., James, B.G., Borchard, P., Cahalan, P., Chu, T.S., Jory, H., Danly, B.G., Levush, B., Calame, J.P., Nguyen, K.T., Pershing, D.E.

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Development and testing of a high-average power, 94-GHz gyroklystron von Danly, B.G., Blank, M., Calame, J.P., Levush, B., Nguyen, K.T., Pershing, D.E., Parker, R.K., Felch, K.L., James, B.G., Borchard, P., Cahalan, P., Chu, T.S., Jory, H.R., Hargreaves, T.A., True, R.B., Lawson, W.G., Antonsen, T.M.

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Demonstration of a 10 kW average power 94 GHz gyroklystron amplifier von Blank, M., Danly, B. G., Levush, B., Calame, J. P., Nguyen, K., Pershing, D., Petillo, J., Hargreaves, T. A., True, R. B., Theiss, A. J., Good, G. R., Felch, K., James, B. G., Borchard, P., Cahalan, P., Chu, T. S., Jory, H., Lawson, W. G., Antonsen, T. M.

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Biallelic Variants in the Ectonucleotidase ENTPD1 Cause a Complex Neurodevelopmental Disorder with Intellectual Disability, Distinct White Matter Abnormalities, and Spastic Paraple... von Calame, Daniel G, Herman, Isabella, Maroofian, Reza, Marshall, Aren E, Donis, Karina Carvalho, Fatih, Jawid M, Mitani, Tadahiro, Du, Haowei, Grochowski, Christopher M, Sousa, Sergio B, Gijavanekar, Charul, Bakhtiari, Somayeh, Ito, Yoko A, Rocca, Clarissa, Hunter, Jill, Sutton, V Reid, Emrick, Lisa T, Boycott, Kym M, Lossos, Alexander, Fellig, Yakov, Prus, Eugenia, Kalish, Yosef, Meiner, Vardiella, Suerink, Manon, Ruivenkamp, Claudia, Muirhead, Kayla, Saadi, Nebal W, Zaki, Maha S, Bouman, Arjan, Barakat, Tahsin Stefan, Skidmore, David L, Osmond, Matthew, Silva, Thiago Oliveira, Murphy, David, Karimiani, Ehsan Ghayoor, Jamshidi, Yalda, Jaddoa, Asaad Ghanim, Tajsharghi, Homa, Jin, Sheng Chih, Abbaszadegan, Mohammad Reza, Ebrahimzadeh-Vesal, Reza, Hosseini, Susan, Alavi, Shahryar, Bahreini, Amir, Zarean, Elahe, Salehi, Mohammad Mehdi, Al-Sannaa, Nouriya Abbas, Zifarelli, Giovanni, Bauer, Peter, Robson, Simon C, Coban-Akdemir, Zeynep, Travaglini, Lorena, Nicita, Francesco, Jhangiani, Shalini N, Gibbs, Richard A, Posey, Jennifer E, Kruer, Michael C, Kernohan, Kristin D, Morales Saute, Jonas A, Houlden, Henry, Vanderver, Adeline, Elsea, Sarah H, Pehlivan, Davut, Marafi, Dana, Lupski, James R

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An immunoglobulin promoter region is unaltered by DNA rearrangement and somatic mutation during B-cell development von Clarke, Catherine, Berenson, James, Goverman, Joan, Boyer, Paul David, Crews, Stephen, Siu, Gerald, Calame, Kathryn

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Demonstration of a high power W-band gyroklystron amplifier for radar applications von Blank, M., Theiss, A.J., Good, G.R., Felch, K., James, B., Borchard, P., Chu, T.S., Jory, H., Lawson, W., Antonsen, T.M., Danly, B.G., Levush, B., Calame, J.P., Nguyen, K.T., Pershing, D.E., Petillo, J., Hargreaves, T.A., True, R.B.

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