Increased stress right ventricular activity on dual isotope perfusion SPECT: A sign of multivessel and/or left main coronary artery disease von WILLIAMS, K. A, SCHNEIDER, C. M

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Correct spatial normalization of myocardial perfusion SPECT improves detection of multivessel coronary artery disease von Williams, Kim A, Schuster, Robert A, Williams, Kim A, Schneider, Candace M, Pokharna, Hemlata K

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Increased stress right ventricular activity on dual isotope perfusion SPECT von Williams, Kim A, Schneider, Candace M

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Outcome prediction from simultaneous stress SPECT and first-pass radionuclide angiography von Williams, Kim A, Schneider, Candace M, Bryant, Todd A, Rajjoub, Hassan

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Estimated life-history traits and movements of the Caribbean reef shark (Carcharhinus perezi) in The Bahamas based on tag-recapture data von Talwar, Brendan S., Bradley, Darcy, Berry, Christopher, Bond, Mark E., Bouyoucos, Ian A., Brooks, Annabelle M. L., Fields, Candace Y. A., Gallagher, Austin J., Guttridge, Tristan L., Guttridge, Annie E., Hammerschlag, Neil, Hamilton, Ian, Keller, Bryan A., Kessel, Steven T., Matich, Philip, O’Shea, Owen R., Papastamatiou, Yannis P., Raguse, Cameron, Schneider, Eric V. C., Shipley, Oliver N., Smukall, Matthew J., van Zinnicq Bergmann, Maurits P. M., Brooks, Edward J.

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Parental Mosaicism in “De Novo” Epileptic Encephalopathies von Myers, Candace T, Hollingsworth, Georgina, Muir, Alison M, Schneider, Amy L, Thuesmunn, Zoe, Knupp, Allison, King, Chontelle, Lacroix, Amy, Mehaffey, Michele G, Berkovic, Samuel F, Carvill, Gemma L, Sadleir, Lynette G, Scheffer, Ingrid E, Mefford, Heather C

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Insights into the Relative Abundance, Life History, and Ecology of Oceanic Sharks in the Eastern Bahamas von Talwar, Brendan S, Brooks, Edward J, Abercrombie, Debra L, Anderson, Brenda, Bond, Mark E, Brooks, Annabelle M. L, Chapman, Demian D, Clementi, Gina M, Fields, Candace Y. A, Gelsleichter, Jim, Grubbs, R. Dean, Howey, Lucy A, Jordan, Lance K. B, Kiszka, Jeremy J, Knotek, Ryan J, Papastamatiou, Yannis P, Peterson, Cheston T, Schneider, Eric V. C, Shipley, Oliver N, Williams, Sean, Winchester, Maggie M, Heithaus, Michael R

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Germline De Novo Mutations in GNB1 Cause Severe Neurodevelopmental Disability, Hypotonia, and Seizures von Petrovski, Slavé, Küry, Sébastien, Myers, Candace T., Anyane-Yeboa, Kwame, Cogné, Benjamin, Bialer, Martin, Xia, Fan, Hemati, Parisa, Riviello, James, Mehaffey, Michele, Besnard, Thomas, Becraft, Emily, Wadley, Alexandrea, Politi, Anya Revah, Colombo, Sophie, Zhu, Xiaolin, Ren, Zhong, Andrews, Ian, Dudding-Byth, Tracy, Schneider, Amy L., Wallace, Geoffrey, Rosen, Aaron B.I., Schelley, Susan, Enns, Gregory M., Corre, Pierre, Dalton, Joline, Mercier, Sandra, Latypova, Xénia, Schmitt, Sébastien, Guzman, Edwin, Moore, Christine, Bier, Louise, Heinzen, Erin L., Karachunski, Peter, Shur, Natasha, Grebe, Theresa, Basinger, Alice, Nguyen, Joanne M., Bézieau, Stéphane, Wierenga, Klaas, Bernstein, Jonathan A., Scheffer, Ingrid E., Rosenfeld, Jill A., Mefford, Heather C., Isidor, Bertrand, Goldstein, David B.

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A population‐based cost‐effectiveness study of early genetic testing in severe epilepsies of infancy von Howell, Katherine B., Eggers, Stefanie, Dalziel, Kim, Riseley, Jessica, Mandelstam, Simone, Myers, Candace T., McMahon, Jacinta M., Schneider, Amy, Carvill, Gemma L., Mefford, Heather C., Scheffer, Ingrid E., Harvey, A. Simon

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Mutations in the GABA transporter SLC6A1 cause epilepsy with myoclonic atonic seizures von Carvill, Gemma L., McMahon, Jacinta M., Schneider, Amy, Zemel, Matthew, Myers, Candace T., Saykally, Julia, Nguyen, John, Robbiano, Angela, Zara, Federico, Specchio, Nicola, Mecarelli, Oriano, Smith, Robert L., Leventer, Richard J., Møller, Rikke S., Nikanorova, Marina, Dimova, Petia, Jordanova, Albena, Petrou, Steven, Helbig, Ingo, Striano, Pasquale, Weckhuysen, Sarah, Berkovic, Samuel F., Scheffer, Ingrid E., Mefford, Heather C.

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De Novo Mutations in SLC1A2 and CACNA1A Are Important Causes of Epileptic Encephalopathies von Myers, Candace T., McMahon, Jacinta M., Schneider, Amy L., Petrovski, Slavé, Allen, Andrew S., Carvill, Gemma L., Zemel, Matthew, Saykally, Julia E., LaCroix, Amy J., Heinzen, Erin L., Hollingsworth, Georgina, Nikanorova, Marina, Corbett, Mark, Gecz, Jozef, Coman, David, Freeman, Jeremy, Calvert, Sophie, Gill, Deepak, Carney, Patrick, Lerman-Sagie, Tally, Sampaio, Hugo, Cossette, Patrick, Delanty, Norman, Dlugos, Dennis, Eichler, Evan E., Epstein, Michael P., Glauser, Tracy, Johnson, Michael R., Kuzniecky, Ruben, Marson, Anthony G., O’Brien, Terence J., Ottman, Ruth, Petrou, Stephen, Poduri, Annapurna, Pickrell, William O., Chung, Seo-Kyung, Rees, Mark I., Sherr, Elliott, Sadleir, Lynette G., Goldstein, David B., Lowenstein, Daniel H., Møller, Rikke S., Berkovic, Samuel F., Scheffer, Ingrid E., Mefford, Heather C.

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Solving the Etiology of Developmental and Epileptic Encephalopathy with Spike-Wave Activation in Sleep (D/EE-SWAS) von Viswanathan, Sindhu, Oliver, Karen L, Regan, Brigid M, Schneider, Amy L, Myers, Candace T, Mehaffey, Michele G, LaCroix, Amy J, Antony, Jayne, Webster, Richard, Cardamone, Michael, Subramanian, Gopinath M, Chiu, Annie T G, Roza, Eugenia, Teleanu, Raluca I, Malone, Stephen, Leventer, Richard J, Gill, Deepak, Berkovic, Samuel F, Hildebrand, Michael S, Goad, Beatrice S, Howell, Katherine B, Symonds, Joseph D, Brunklaus, Andreas, Sadleir, Lynette G, Zuberi, Sameer M, Mefford, Heather C, Scheffer, Ingrid E

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BRAT1 encephalopathy: a recessive cause of epilepsy of infancy with migrating focal seizures von Scheffer, Ingrid E, Boysen, Katja E, Schneider, Amy L, Myers, Candace T, Mehaffey, Michele G, Rochtus, Anne M, Yuen, Yuet‐Ping, Ronen, Gabriel M, Chak, Wai Km, Gill, Deepak, Poduri, Annapurna, Mefford, Heather C

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High Rate of Recurrent De Novo Mutations in Developmental and Epileptic Encephalopathies von Myers, Candace T., Cossette, Patrick, Lemay, Philippe, Spiegelman, Dan, Laporte, Alexandre Dionne, Nassif, Christina, Diallo, Ousmane, Monlong, Jean, Cadieux-Dion, Maxime, Dobrzeniecka, Sylvia, Meloche, Caroline, Retterer, Kyle, Cho, Megan T., Rosenfeld, Jill A., Bi, Weimin, Massicotte, Christine, Miguet, Marguerite, Brunga, Ledia, Regan, Brigid M., Mo, Kelly, Tam, Cory, Hollingsworth, Georgie, FitzPatrick, David R., Canham, Natalie, Blair, Edward, Kerr, Bronwyn, Fry, Andrew E., Thomas, Rhys H., Shelagh, Joss, Hurst, Jane A., Brittain, Helen, Blyth, Moira, Lebel, Robert Roger, Gerkes, Erica H., Davis-Keppen, Laura, Stein, Quinn, Dorison, Sara J., Benke, Paul J., Fassi, Emily, Corsten-Janssen, Nicole, Kamsteeg, Erik-Jan, Mau-Them, Frederic T., Bruel, Ange-Line, Verloes, Alain, Õunap, Katrin, Wojcik, Monica H., Albert, Dara V.F., Venkateswaran, Sunita, Ware, Tyson, Liu, Yu-Chi, Mohammad, Shekeeb S., Bizargity, Peyman, Bacino, Carlos A., Leuzzi, Vincenzo, Martinelli, Simone, Dallapiccola, Bruno, Tartaglia, Marco, Blumkin, Lubov, Wierenga, Klaas J., Purcarin, Gabriela, O’Byrne, James J., Stockler, Sylvia, Lehman, Anna, Keren, Boris, Nougues, Marie-Christine, Mignot, Cyril, Auvin, Stéphane, Nava, Caroline, Hiatt, Susan M., Bebin, Martina, Shao, Yunru, Scaglia, Fernando, Frye, Richard E., Jarjour, Imad T., Jacques, Stéphanie, Boucher, Renee-Myriam, Riou, Emilie, Srour, Myriam, Carmant, Lionel, Lortie, Anne, Major, Philippe, Diadori, Paola, Dubeau, François, D’Anjou, Guy, Bourque, Guillaume, Berkovic, Samuel F., Sadleir, Lynette G., Campeau, Philippe M., Kibar, Zoha, Lafrenière, Ronald G., Girard, Simon L., Mercimek-Mahmutoglu, Saadet, Boelman, Cyrus, Rouleau, Guy A., Scheffer, Ingrid E., Mefford, Heather C., Andrade, Danielle M., Rossignol, Elsa, Minassian, Berge A., Michaud, Jacques L.

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FBXO28 causes developmental and epileptic encephalopathy with profound intellectual disability von Schneider, Amy L., Myers, Candace T., Muir, Alison M., Calvert, Sophie, Basinger, Alice, Perry, M. Scott, Rodan, Lance, Helbig, Katherine L., Chambers, Chelsea, Gorman, Kathleen M., King, Mary D., Donkervoort, Sandra, Soldatos, Ariane, Bönnemann, Carsten G., Spataro, Nino, Gabau, Elisabeth, Arellano, Montserrat, Cappuccio, Gerarda, Brunetti‐Pierri, Nicola, Rossignol, Elsa, Hamdan, Fadi F., Michaud, Jacques L., Balak, Christopher, Mefford, Heather C., Scheffer, Ingrid E.

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Novel Benzoxazole Inhibitor of Dengue Virus Replication That Targets the NS3 Helicase von BYRD, Chelsea M, GROSENBACH, Douglas W, WINEINGER, Kristin A, PAGE, Jessica, STAVALE, Eric, STONE, Melialani A, FULLER, Kathleen P, LOVEJOY, Candace, LEEDS, Janet M, HRUBY, Dennis E, JORDAN, Robert, BERHANU, Aklile, DONGCHENG DAI, JONES, Kevin F, CARDWELL, Kara B, SCHNEIDER, Christine, GUANG YANG, TYAVANAGIMATT, Shanthakumar, HARVER, Chris

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The Genetic Landscape of Epilepsy of Infancy with Migrating Focal Seizures von Burgess, Rosemary, Wang, Shuyu, McTague, Amy, Boysen, Katja E., Yang, Xiaoling, Zeng, Qi, Myers, Kenneth A., Rochtus, Anne, Trivisano, Marina, Gill, Deepak, Sadleir, Lynette G., Specchio, Nicola, Guerrini, Renzo, Marini, Carla, Zhang, Yue‐Hua, Mefford, Heather C., Kurian, Manju A., Poduri, Annapurna H., Scheffer, Ingrid E.

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AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders von Salpietro, Vincenzo, Dixon, Christine L., Guo, Hui, Bello, Oscar D., Vandrovcova, Jana, Efthymiou, Stephanie, Maroofian, Reza, Heimer, Gali, Burglen, Lydie, Valence, Stephanie, Torti, Erin, Hacke, Moritz, Rankin, Julia, Tariq, Huma, Colin, Estelle, Procaccio, Vincent, Striano, Pasquale, Mankad, Kshitij, Lieb, Andreas, Chen, Sharon, Pisani, Laura, Bettencourt, Conceicao, Männikkö, Roope, Manole, Andreea, Brusco, Alfredo, Grosso, Enrico, Ferrero, Giovanni Battista, Armstrong-Moron, Judith, Gueden, Sophie, Bar-Yosef, Omer, Tzadok, Michal, Monaghan, Kristin G., Santiago-Sim, Teresa, Person, Richard E., Cho, Megan T., Willaert, Rebecca, Yoo, Yongjin, Chae, Jong-Hee, Quan, Yingting, Wu, Huidan, Wang, Tianyun, Bernier, Raphael A., Xia, Kun, Blesson, Alyssa, Jain, Mahim, Motazacker, Mohammad M., Jaeger, Bregje, Schneider, Amy L., Boysen, Katja, Muir, Alison M., Myers, Candace T., Gavrilova, Ralitza H., Gunderson, Lauren, Schultz-Rogers, Laura, Klee, Eric W., Dyment, David, Osmond, Matthew, Parellada, Mara, Llorente, Cloe, Gonzalez-Peñas, Javier, Carracedo, Angel, Van Haeringen, Arie, Ruivenkamp, Claudia, Nava, Caroline, Heron, Delphine, Nardello, Rosaria, Iacomino, Michele, Minetti, Carlo, Skabar, Aldo, Fabretto, Antonella, Raspall-Chaure, Miquel, Chez, Michael, Tsai, Anne, Fassi, Emily, Shinawi, Marwan, Constantino, John N., De Zorzi, Rita, Fortuna, Sara, Kok, Fernando, Keren, Boris, Bonneau, Dominique, Choi, Murim, Benzeev, Bruria, Zara, Federico, Mefford, Heather C., Scheffer, Ingrid E., Clayton-Smith, Jill, Macaya, Alfons, Rothman, James E., Eichler, Evan E., Kullmann, Dimitri M., Houlden, Henry

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MoveApps: a serverless no-code analysis platform for animal tracking data von Kölzsch, Andrea, Davidson, Sarah C., Gauggel, Dominik, Hahn, Clemens, Hirt, Julian, Kays, Roland, Lang, Ilona, Lohr, Ashley, Russell, Benedict, Scharf, Anne K., Schneider, Gabriel, Vinciguerra, Candace M., Wikelski, Martin, Safi, Kamran

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Abatacept, Cenicriviroc, or Infliximab for Treatment of Adults Hospitalized With COVID-19 Pneumonia: A Randomized Clinical Trial von O’Halloran, Jane A, Ko, Emily R, Anstrom, Kevin J, Kedar, Eyal, McCarthy, Matthew W, Panettieri, Reynold A, Maillo, Martin, Nunez, Patricia Segura, Lachiewicz, Anne M, Gonzalez, Cynthia, Smith, P. Brian, de Tai, Sabina Mendivil-Tuchia, Khan, Akram, Lora, Alfredo J. Mena, Salathe, Matthias, Capo, Gerardo, Gonzalez, Daniel Rodríguez, Patterson, Thomas F, Palma, Christopher, Ariza, Horacio, Lima, Maria Patelli, Blamoun, John, Nannini, Esteban C, Sprinz, Eduardo, Mykietiuk, Analia, Alicic, Radica, Rauseo, Adriana M, Wolfe, Cameron R, Witting, Britta, Wang, Jennifer P, Parra-Rodriguez, Luis, Der, Tatyana, Willsey, Kate, Wen, Jun, Silverstein, Adam, O’Brien, Sean M, Al-Khalidi, Hussein R, Maldonado, Michael A, Melsheimer, Richard, Ferguson, William G, McNulty, Steven E, Zakroysky, Pearl, Halabi, Susan, Benjamin, Daniel K, Butler, Sandra, Atkinson, Jane C, Adam, Stacey J, Chang, Soju, LaVange, Lisa, Proschan, Michael, Bozzette, Samuel A, Powderly, William G

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