Abstract 419: The development of BRPF1 degraders as a potential treatment for acute myeloid leukemia by Glynn, Daniel Joseph, Crampton, Rosie, Pesnot, Thomas, Scott, Andrew, Nassoy, Anne-Chloe, Kirk, Ralph, Narducci, Daniele, Nelson, Gary, Ongiri, Lynette, Begum, Habiba, Rao, Vincent, Bingham, Matilda, McPherson, Rhoanne, Turner, Darryl

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Ultra-rare genetic variation in common epilepsies: a case-control sequencing study by Allen, Andrew S, Bellows, Susannah T, Berkovic, Samuel F, Bridgers, Joshua, Burgess, Rosemary, Cavalleri, Gianpiero, Chung, Seo-Kyung, Cossette, Patrick, Delanty, Norman, Dlugos, Dennis, Epstein, Michael P, Freyer, Catharine, Goldstein, David B, Heinzen, Erin L, Hildebrand, Michael S, Johnson, Michael R, Kuzniecky, Ruben, Lowenstein, Daniel H, Marson, Anthony G, Mayeux, Richard, Mebane, Caroline, Mefford, Heather C, O'Brien, Terence J, Ottman, Ruth, Petrou, Steven, Petrovski, Slavgé, Pickrell, William O, Poduri, Annapurna, Radtke, Rodney A, Rees, Mark I, Regan, Brigid M, Ren, Zhong, Scheffer, Ingrid E, Sills, Graeme J, Thomas, Rhys H, Wang, Quanli, Abou-Khalil, Bassel, Alldredge, Brian K, Amrom, Dina, Andermann, Eva, Andermann, Frederick, Bautista, Jocelyn F., Bluvstein, Judith, Boro, Alex, Cascino, Gregory D, Consalvo, Damian, Crumrine, Patricia, Devinsky, Orrin, Fiol, Miguel, Fountain, Nathan B, French, Jacqueline, Friedman, Daniel, Geller, Eric B, Glauser, Tracy, Glynn, Simon, Haas, Kevin, Haut, Sheryl R, Hayward, Jean, Helmers, Sandra L, Joshi, Sucheta, Kanner, Andres, Kirsch, Heidi E, Knowlton, Robert C, Kossoff, Eric H, Kuperman, Rachel, Motika, Paul V, Novotny, Edward J, Paolicchi, Juliann M, Parent, Jack M, Park, Kristen, Sadleir, Lynette G, Shellhaas, Renée A., Sherr, Elliott H, Shih, Jerry J., Shinnar, Shlomo, Singh, Rani K, Sirven, Joseph, Smith, Michael C, Sullivan, Joseph, Thio, Liu Lin, Venkat, Anu, Vining, Eileen P.G, Von Allmen, Gretchen K, Weisenberg, Judith L, Widdess-Walsh, Peter, Winawer, Melodie R

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De novo mutations in epileptic encephalopathies by Allen, Andrew S, Berkovic, Samuel F, Cossette, Patrick, Delanty, Norman, Dlugos, Dennis, Eichler, Evan E, Epstein, Michael P, Glauser, Tracy, Goldstein, David B, Han, Yujun, Heinzen, Erin L, Hitomi, Yuki, Howell, Katherine B, Johnson, Michael R, Kuzniecky, Ruben, Lowenstein, Daniel H, Lu, Yi-Fan, Madou, Maura R Z, Marson, Anthony G, Mefford, Heather C, Esmaeeli Nieh, Sahar, O'Brien, Terence J, Ottman, Ruth, Petrovski, Slavé, Poduri, Annapurna, Ruzzo, Elizabeth K, Scheffer, Ingrid E, Sherr, Elliott H, Yuskaitis, Christopher J, Abou-Khalil, Bassel, Alldredge, Brian K, Bautista, Jocelyn F, Boro, Alex, Cascino, Gregory D, Consalvo, Damian, Crumrine, Patricia, Devinsky, Orrin, Fiol, Miguel, Fountain, Nathan B, French, Jacqueline, Friedman, Daniel, Geller, Eric B, Glynn, Simon, Haut, Sheryl R, Hayward, Jean, Helmers, Sandra L, Joshi, Sucheta, Kanner, Andres, Kirsch, Heidi E, Knowlton, Robert C, Kossoff, Eric H, Kuperman, Rachel, McGuire, Shannon M, Motika, Paul V, Novotny, Edward J, Paolicchi, Juliann M, Parent, Jack M, Park, Kristen, Shellhaas, Renée A, Shih, Jerry J, Singh, Rani, Sirven, Joseph, Smith, Michael C, Sullivan, Joseph, Lin Thio, Liu, Venkat, Anu, Vining, Eileen P G, Von Allmen, Gretchen K, Weisenberg, Judith L, Widdess-Walsh, Peter, Winawer, Melodie R

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Supplementing claims data with outpatient laboratory test results to improve confounding adjustment in effectiveness studies of lipid-lowering treatments by Schneeweiss, Sebastian, Rassen, Jeremy A, Glynn, Robert J, Myers, Jessica, Daniel, Gregory W, Singer, Joseph, Solomon, Daniel H, Kim, Seoyoung, Rothman, Kenneth J, Liu, Jun, Avorn, Jerry

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De Novo Mutations in Synaptic Transmission Genes Including DNM1 Cause Epileptic Encephalopathies by Appenzeller, Silke, Balling, Rudi, Barisic, Nina, Baulac, Stéphanie, Caglayan, Hande, De Jonghe, Peter, Depienne, Christel, Dimova, Petia, Djémié, Tania, Gormley, Padhraig, Guerrini, Renzo, Helbig, Ingo, Hjalgrim, Helle, Jähn, Johanna, Klein, Karl Martin, Koeleman, Bobby, Komarek, Vladimir, Krause, Roland, Kuhlenbäumer, Gregor, Lemke, Johannes R., Lerche, Holger, Linnankivi, Tarja, Marini, Carla, May, Patrick, Møller, Rikke S., Muhle, Hiltrud, Palotie, Aarno, Pendziwiat, Manuela, Roelens, Filip, Rosenow, Felix, Selmer, Kaja, Serratosa, Jose M., Sisodiya, Sanjay, Stephani, Ulrich, Sterbova, Katalin, Striano, Pasquale, Suls, Arvid, Talvik, Tiina, von Spiczak, Sarah, Weckhuysen, Sarah, Abou-Khalil, Bassel, Alldredge, Brian K., Andermann, Eva, Andermann, Frederick, Amron, Dina, Bautista, Jocelyn F., Berkovic, Samuel F., Bluvstein, Judith, Boro, Alex, Consalvo, Damian, Crumrine, Patricia, Devinsky, Orrin, Dlugos, Dennis, Epstein, Michael P., Fiol, Miguel, French, Jacqueline, Friedman, Daniel, Geller, Eric B., Glauser, Tracy, Glynn, Simon, Haas, Kevin, Haut, Sheryl R., Hayward, Jean, Helmers, Sandra L., Joshi, Sucheta, Kanner, Andres, Knowlton, Robert C., Kossoff, Eric H., Kuperman, Rachel, Kuzniecky, Ruben, Lowenstein, Daniel H., Motika, Paul V., Novotny, Edward J., Ottman, Ruth, Paolicchi, Juliann M., Parent, Jack, Park, Kristen, Scheffer, Ingrid E., Shellhaas, Renée A., Sherr, Elliott, Singh, Rani, Smith, Michael C., Sullivan, Joe, Venkat, Anu, Vining, Eileen P.G., Von Allmen, Gretchen K., Weisenberg, Judith L., Winawer, Melodie R., Cossette, Patrick, Delanty, Norman, Eichler, Evan E., Goldstein, David B., Han, Yujun, Heinzen, Erin L., Marson, Anthony G., Nieh, Sahar Esmaeeli, O’Brien, Terence J., Petrou, Stephen, Petrovski, Slavé, Ruzzo, Elizabeth K.

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Diverse genetic causes of polymicrogyria with epilepsy by Allen, Andrew S, Aggarwal, Vimla, Berkovic, Samuel F, Cossette, Patrick, Delanty, Norman, Dlugos, Dennis, Eichler, Evan E, Epstein, Michael P, Freyer, Catharine, Goldstein, David B, Guerrini, Renzo, Glauser, Tracy, Heinzen, Erin L, Johnson, Michael R, Kuzniecky, Ruben, Lowenstein, Daniel H, Marson, Anthony G, Mefford, Heather C, O'Brien, Terence J, Ottman, Ruth, Poduri, Annapurna, Petrou, Stephen, Petrovski, Slavé, Ruzzo, Elizabeth K, Scheffer, Ingrid E, Sherr, Elliott H, Abou‐Khalil, Bassel, Amrom, Dina, Andermann, Eva, Andermann, Frederick, Berkovic, Samuel F., Bluvstein, Judith, Boro, Alexis, Cascino, Greg, Consalvo, Damian, Crumrine, Pat, Devinsky, Orrin, Dlugos, Dennis, Fountain, Nathan, Freyer, Catharine, Friedman, Dan, Geller, Eric, Glynn, Simon, Haas, Kevin, Haut, Sheryl, Joshi, Sucheta, Kirsch, Heidi, Knowlton, Robert, Kossoff, Eric, Kuzniecky, Ruben, Lowenstein, Daniel H., Motika, Paul V., Ottman, Ruth, Paolicchi, Juliann M., Parent, Jack M., Poduri, Annapurna, Scheffer, Ingrid, Shellhaas, Renée A., Sherr, Elliott H., Shih, Jerry J., Shinnar, Shlomo, Singh, Rani K., Sperling, Michael, Smith, Michael C., Sullivan, Joseph, Vining, Eileen P. G., Von Allmen, Gretchen K., Widdess‐Walsh, Peter, Winawer, Melodie R., Bautista, Jocelyn, Fiol, Miguel, Glauser, Tracy, Hayward, Jean, Helmers, Sandra, Park, Kristen, Sirven, Joseph, Lin Thio, Liu, Venkat, Anu, Weisenberg, Judith, Kuperman, Rachel, McGuire, Shannon, Novotny, Edward, Sadleir, Lynette

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Copy number variant analysis from exome data in 349 patients with epileptic encephalopathy by Allen, Andrew S., Berkovic, Samuel F., Coe, Bradley P., Cook, Joseph, Cossette, Patrick, Delanty, Norman, Dlugos, Dennis, Eichler, Evan E., Epstein, Michael P., Glauser, Tracy, Goldstein, David B., Heinzen, Erin L., Johnson, Michael R., Krumm, Nik, Kuzniecky, Ruben, Lowenstein, Daniel H., Marson, Anthony G., Mefford, Heather C., Nelson, Ben, Esmaeeli Nieh, Sahar, O'Brien, Terence J., Ottman, Ruth, Petrou, Stephen, Petrovski, Slavé, Poduri, Annapurna, Raja, Archana, Ruzzo, Elizabeth K., Scheffer, Ingrid E., Sherr, Elliott, Abou‐Khalil, Bassel, Alldredge, Brian K., Andermann, Eva, Andermann, Frederick, Amron, Dina, Bautista, Jocelyn F., Berkovic, Samuel F., Boro, Alex, Cascino, Gregory, Consalvo, Damian, Crumrine, Patricia, Devinsky, Orrin, Dlugos, Dennis, Epstein, Michael P., Fiol, Miguel, Fountain, Nathan B., French, Jacqueline, Friedman, Daniel, Geller, Eric B., Glauser, Tracy, Glynn, Simon, Haut, Sheryl R., Hayward, Jean, Helmers, Sandra L., Joshi, Sucheta, Kanner, Andres, Kirsch, Heidi E., Knowlton, Robert C., Kossoff, Eric H., Kuperman, Rachel, Kuzniecky, Ruben, Lowenstein, Daniel H., McGuire, Shannon M., Motika, Paul V., Novotny, Edward J., Ottman, Ruth, Paolicchi, Juliann M., Parent, Jack, Park, Kristen, Poduri, Annapurna, Scheffer, Ingrid E., Shellhaas, Renée A., Sherr, Elliott, Shih, Jerry J., Singh, Rani, Sirven, Joseph, Smith, Michael C., Sullivan, Joe, Thio, Liu Lin, Venkat, Anu, Vining, Eileen P.G., Von Allmen, Gretchen K., Weisenberg, Judith L., Widdess‐Walsh, Peter, Winawer, Melodie R.

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The role of copy number variants in the genetic architecture of common familial epilepsies by Almanza Fuerte, Edith P., Nguyen, John, Mehaffey, Michelle, Sulovari, Arvis, Wang, Tianyun, Galey, Miranda, Miller, Danny E., Eichler, Evan E., Mefford, Heather C., Abou‐Khalil, Bassel, Afawi, Zaid Afawi, Allen, Andrew S., Amrom, Dina, Andermann, Eva, Bautista, Jocelyn F., Bellows, Susannah T., Berkovic, Samuel F., Bluvstein, Judith, Boro, Alexis, Burgess, Rosemary, Cascino, Gregory D., Chung, Seo‐Kyung, Consalvo, Damian, Cossette, Patrick, Crompton, Douglas E., Crumrine, Patricia, Curtis, Sarah W., Delanty, Norman, Devinsky, Orrin, Dlugos, Dennis, Ellis, Colin A., Epstein, Michael P., Fiol, Miguel, Fountain, Nathan B., Freyer, Catharine, Friedman, Dan, Geller, Eric B., Glauser, Tracy, Glynn, Simon, Goldstein, David B., Gravel, Micheline, Haas, Kevin, Harris, Rebekah V., Haut, Sheryl, Heinzen, Erin L., Helmers, Sandra, Henry, Olivia J., Joshi, Sucheta, Kirsch, Heidi E., Kivity, Sara, Knowlton, Robert C., Kossoff, Eric, Kuzniecky, Ruben, Loeb, Rebecca, Lowenstein, Daniel H., Marson, Anthony G., McCormack, Mark, McGuire, Shannon M., McKenna, Kevin, Motika, Paul V., Mullen, Saul A., Novotny, Edward J., O’Brien, Terence J., Oliver, Karen L., Ottman, Ruth, Paolicchi, Juliann M., Parent, Jack M., Park, Kristen L., Paterson, Sarah J., Petrovski, Slave, Pickrell, William O., Poduri, Annapurna, Rees, Mark I., Sadleir, Lynette G., Scheffer, Ingrid E., Shellhaas, Renee A., Sherr, Elliott H., Shih, Jerry J., Shinnar, Shlomo, Singh, Rani K., Sirven, Joseph, Smith, Michael C., Smith, Philip E. M., Sperling, Michael R., Sullivan, Joseph, Thio, Liu Lin, Thomas, Rhys H., Venkat, Anu, Vining, Eileen P. G., Von Allmen, Gretchen K., Weisenberg, Judith, Widdess‐Walsh, Peter, Winawer, Melodie R.

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Association of ultra‐rare coding variants with genetic generalized epilepsy: A case–control whole exome sequencing study by Stanley, Kate E., Bobbili, Dheeraj R., Dhindsa, Ryan S., May, Patrick, Alldredge, Brian K., Allen, Andrew S., Altmüller, Janine, Amrom, Dina, Andermann, Eva, Auce, Pauls, Avbersek, Andreja, Bautista, Jocelyn F., Becker, Felicitas, Bellows, Susannah T., Berghuis, Bianca, Bluvstein, Judith, Boro, Alex, Burgess, Rosemary, Caglayan, Hande, Cascino, Gregory D., Chung, Seo‐Kyung, Cieuta‐Walti, Cécile, Consalvo, Damian, Cossette, Patrick, Crumrine, Patricia, Delanty, Norman, Depondt, Chantal, Desbiens, Richard, Dlugos, Dennis, Epstein, Michael P., Everett, Kate, Fountain, Nathan B., Francis, Ben, French, Jacqueline, Friedman, Daniel, Geller, Eric B., Girard, Simon, Glauser, Tracy, Glynn, Simon, Gravel, Micheline, Haas, Kevin, Haut, Sheryl R., Heinzen, Erin L., Helbig, Ingo, Hildebrand, Michael S., Jorgensen, Andrea, Joshi, Sucheta, Kirsch, Heidi E., Knowlton, Robert C., Koeleman, Bobby P. C., Kossoff, Eric H., Krause, Roland, Kunz, Wolfram S., Langley, Sarah R., LeGuern, Eric, Lerche, Holger, Leu, Costin, Lortie, Anne, Marson, Anthony G., Mebane, Caroline, Mefford, Heather C., Meloche, Caroline, Motika, Paul V., Muhle, Hiltrud, Nabbout, Rima, Nguyen, Dang K., Nikanorova, Marina, Novotny, Edward J., Ottman, Ruth, O’Brien, Terence J., Paolicchi, Juliann M., Parent, Jack M., Peter, Sarah, Petrou, Steven, Pickrell, William O., Poduri, Annapurna, Radtke, Rodney A., Rees, Mark I., Regan, Brigid M., Sadleir, Lynette G., Sander, Josemir W., Sander, Thomas, Scheffer, Ingrid E., Singh, Rani K., Sirven, Joseph, Sisodiya, Sanjay M., Smith, Michael C., Sonsma, Anja C. M., Sullivan, Joseph, Thio, Liu Lin, Thomas, Rhys H., Venkat, Anu, Von Allmen, Gretchen K., Wang, Quanli, Weber, Yvonne G., Weckhuysen, Sarah, Widdess‐Walsh, Peter, Winawer, Melodie R., Wolking, Stefan, Zimprich, Fritz

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Prognostic indicators and outcomes of hospitalised COVID-19 patients with neurological disease: An individual patient data meta-analysis by Bhagteshwar Singh, Suzannah Lant, Sofia Cividini, Jonathan W S Cattrall, Lynsey C Goodwin, Laura Benjamin, Benedict D Michael, Ayaz Khawaja, Aline de Moura Brasil Matos, Walid Alkeridy, Andrea Pilotto, Durjoy Lahiri, Rebecca Rawlinson, Sithembinkosi Mhlanga, Evelyn C Lopez, Brendan F Sargent, Anushri Somasundaran, Arina Tamborska, Glynn Webb, Komal Younas, Yaqub Al Sami, Heavenna Babu, Tristan Banks, Francesco Cavallieri, Matthew Cohen, Emma Davies, Shalley Dhar, Anna Fajardo Modol, Hamzah Farooq, Jeffrey Harte, Samuel Hey, Albert Joseph, Dileep Karthikappallil, Daniel Kassahun, Gareth Lipunga, Rachel Mason, Thomas Minton, Gabrielle Mond, Joseph Poxon, Sophie Rabas, Germander Soothill, Marialuisa Zedde, Konstantin Yenkoyan, Bruce Brew, Erika Contini, Lucette Cysique, Xin Zhang, Pietro Maggi, Vincent van Pesch, Jérome Lechien, Sven Saussez, Alex Heyse, Maria Lúcia Brito Ferreira, Cristiane N Soares, Isabel Elicer, Laura Eugenín-von Bernhardi, Waleng Ñancupil Reyes, Rong Yin, Mohammed A Azab, Foad Abd-Allah, Ahmed Elkady, Simon Escalard, Jean-Christophe Corvol, Cécile Delorme, Pierre Tattevin, Kévin Bigaut, Norbert Lorenz, Daniel Hornuss, Jonas Hosp, Siegbert Rieg, Dirk Wagner, Benjamin Knier, Paul Lingor, Andrea Sylvia Winkler, Athena Sharifi-Razavi, Shima T Moein, SeyedAhmad SeyedAlinaghi, Saeidreza JamaliMoghadamSiahkali, Mauro Morassi, Alessandro Padovani, Marcello Giunta, Ilenia Libri, Simone Beretta, Sabrina Ravaglia, Matteo Foschi, Paolo Calabresi, Guido Primiano, Serenella Servidei, Nicola Biagio Mercuri, Claudio Liguori, Mariangela Pierantozzi, Loredana Sarmati, Federica Boso, Silvia Garazzino, Sara Mariotto, Kimani N Patrick, Oana Costache, Alexander Pincherle, Frederikus A Klok, Roger Meza

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Evidence for a shared genetic susceptibility to migraine and epilepsy by Winawer, Melodie R., Connors, Robert

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Phenotypic analysis of 303 multiplex families with common epilepsies

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Polymicrogyria‐associated epilepsy: A multicenter phenotypic study from the Epilepsy Phenome/Genome Project by Shain, Catherine, Ramgopal, Sriram, Fallil, Zianka, Parulkar, Isha, Alongi, Richard, Knowlton, Robert, Poduri, Annapurna

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Quantitative analysis of phenotypic elements augments traditional electroclinical classification of common familial epilepsies by Abou‐Khalil, Bassel, Afawi, Zaid, Allen, Andrew S., Bautista, Jocelyn F., Bellows, Susannah T., Berkovic, Samuel F., Bluvstein, Judith, Burgess, Rosemary, Cascino, Gregory, Cossette, Patrick, Cristofaro, Sabrina, Crompton, Douglas E., Delanty, Norman, Devinsky, Orrin, Dlugos, Dennis, Ellis, Colin A., Epstein, Michael P., Fountain, Nathan B., Freyer, Catharine, Geller, Eric B., Glauser, Tracy, Glynn, Simon, Goldberg‐Stern, Hadassa, Goldstein, David B., Gravel, Micheline, Haas, Kevin, Haut, Sheryl, Heinzen, Erin L., Kirsch, Heidi E., Kivity, Sara, Knowlton, Robert, Korczyn, Amos D., Kossoff, Eric, Kuzniecky, Ruben, Loeb, Rebecca, Lowenstein, Daniel H., Marson, Anthony G., McCormack, Mark, McKenna, Kevin, Mefford, Heather C., Motika, Paul, Mullen, Saul A., J. O'Brien, Terence, Ottman, Ruth, Paolicchi, Juliann, Parent, Jack M., Paterson, Sarah, Petrou, Steven, Petrovski, Slavé, Owen Pickrell, William, Poduri, Annapurna, Rees, Mark I., Sadleir, Lynette G., Scheffer, Ingrid E., Shih, Jerry, Singh, Rani, Sirven, Joseph, Smith, Michael, Smith, Phil E. M., Thio, Liu Lin, Thomas, Rhys H., Venkat, Anu, Vining, Eileen, Von Allmen, Gretchen, Weisenberg, Judith, Widdess‐Walsh, Peter, Winawer, Melodie R.

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De Novo Mutations in Synaptic Transmission Genes Including DNM1 Cause Epileptic Encephalopathies by Appenzeller, Silke, Balling, Rudi, Barisic, Nina, Baulac, Stéphanie, Caglayan, Hande, De Jonghe, Peter, Depienne, Christel, Dimova, Petia, Djémié, Tania, Gormley, Padhraig, Guerrini, Renzo, Helbig, Ingo, Hjalgrim, Helle, Jähn, Johanna, Klein, Karl Martin, Koeleman, Bobby, Komarek, Vladimir, Krause, Roland, Kuhlenbäumer, Gregor, Lerche, Holger, Marini, Carla, May, Patrick, Møller, Rikke S., Muhle, Hiltrud, Palotie, Aarno, Pendziwiat, Manuela, Roelens, Filip, Rosenow, Felix, Selmer, Kaja, Serratosa, Jose M., Sisodiya, Sanjay, Stephani, Ulrich, Sterbova, Katalin, Striano, Pasquale, Suls, Arvid, Talvik, Tiina, von Spiczak, Sarah, Weckhuysen, Sarah, Abou-Khalil, Bassel, Andermann, Eva, Andermann, Frederick, Amrom, Dina, Bautista, Jocelyn F., Berkovic, Samuel F., Bluvstein, Judith, Boro, Alex, Consalvo, Damian, Crumrine, Patricia, Devinsky, Orrin, Dlugos, Dennis, Epstein, Michael P., Fiol, Miguel, French, Jacqueline, Friedman, Daniel, Geller, Eric B., Glauser, Tracy, Glynn, Simon, Haas, Kevin, Haut, Sheryl R., Hayward, Jean, Helmers, Sandra L., Joshi, Sucheta, Kanner, Andres, Kirsch, Heidi E., Kossoff, Eric H., Kuperman, Rachel, Kuzniecky, Ruben, Lowenstein, Daniel H., McGuire, Shannon M., Motika, Paul V., Novotny, Edward J., Ottman, Ruth, Paolicchi, Juliann M., Parent, Jack, Park, Kristen, Scheffer, Ingrid E., Shellhaas, Renée A., Sherr, Elliott, Shih, Jerry J., Singh, Rani, Sullivan, Joe, Venkat, Anu, Vining, Eileen P.G., Von Allmen, Gretchen K., Weisenberg, Judith L., Winawer, Melodie R., Allen, Andrew S., Cossette, Patrick, Delanty, Norman, Eichler, Evan E., Goldstein, David B., Han, Yujun, Heinzen, Erin L., Johnson, Michael R., Marson, Anthony G., Mefford, Heather C., Nieh, Sahar Esmaeeli, O’Brien, Terence J., Petrovski, Slavé, Ruzzo, Elizabeth K.

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Lennox‐Gastaut syndrome of unknown cause: Phenotypic characteristics of patients in the Epilepsy Phenome/Genome Project by Widdess‐Walsh, Peter, Dlugos, Dennis, Fahlstrom, Robyn, Joshi, Sucheta, Shellhaas, Renée, Boro, Alex, Sullivan, Joseph, Geller, Eric

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Phenotypic and imaging features of FLNA -negative patients with bilateral periventricular nodular heterotopia and epilepsy by Fallil, Zianka, Pardoe, Heath, Bachman, Robert, Cunningham, Benjamin, Parulkar, Isha, Shain, Catherine, Poduri, Annapurna, Knowlton, Robert, Kuzniecky, Ruben

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The Epilepsy Phenome/Genome Project (EPGP) informatics platform by Nesbitt, Gerry, McKenna, Kevin, Mays, Vickie, Carpenter, Alan, Miller, Kevin, Williams, Michael

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2020-21 Annual Reports of COMMITTEES of The Florida Bar by Valdes, Michelle Otero, Meister, Tonya J, Kaplan, Ellen Michele, Adams, Jackson Wolfe, Bresky, Robin, Berman, Andrew S, Ray, Stephanie W, Owens, L. Forrest, Bauer, Galen, Biehl, Sheila, Lesser, Steven B, Greenlee, Paige, Dirose, Dean R, Berman, Ceci Culpepper, McLuskey, John W, Robbins, Russell M, Bodnar, Melisa L, Sockel-Stone, Bonnie, Dill, Joe, Palermo, Anthony J, Dawson, Patricia, McClenathen, Chad M, Koller, Pamela, Dempsey, Angela C, Syprett, Charlie Ann, Adams, Nathan A, Carland, J. Paul, Ohall, Laurie E, Brandfon, Cory A, Visconti, Melissa Damian, Mcconnell, Patricia, McElroy, R. Lee, High, Cary A, Valenti, Margo T, Pratt, Kenneth D, Squires-Binford, Grey, Rogers, Adam J, Ratzan, Jacob Lawrence, Arscott, Loreal, Wilson, Matthew Charles, Glynn, Gerry, Wiggins, Allison, Talenfeld, Howard M, Ficarrotta, Jennifer A, Steele, Alison M, Suarez, Michelle, Schwait, Carl, Vallandingham, Christopher, Joseph, John Paul, McEwen, Catherine Peek, McLeroy, Kathleen S, Gelfand, Michael J, Neymotin, Ita M, Hinden, Michelle Gomez, Korn, Michael J, Stein, Leslie Reicin, Rimes, John, Patel, Brijesh, Martinez, Daniel, Senne, Christine, McCabe, Susanne, Hodz, Vivian Cortes, Touby, Mark A, Fee, James F, Callahan, Charles W

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Racial and ethnic differences in epilepsy classification among probands in the Epilepsy Phenome/Genome Project (EPGP) by Friedman, Daniel, Fahlstrom, Robyn

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