De novo mutations in epileptic encephalopathies von 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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De Novo Mutations in Synaptic Transmission Genes Including DNM1 Cause Epileptic Encephalopathies von 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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The role of copy number variants in the genetic architecture of common familial epilepsies von 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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Copy number variant analysis from exome data in 349 patients with epileptic encephalopathy von 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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De Novo Mutations in Synaptic Transmission Genes Including DNM1 Cause Epileptic Encephalopathies von 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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Application of rare variant transmission disequilibrium tests to epileptic encephalopathy trio sequence data von Allen, Andrew S, Berkovic, Samuel F, Bridgers, Joshua, Cossette, Patrick, Dlugos, Dennis, Epstein, Michael P, Glauser, Tracy, Goldstein, David B, Heinzen, Erin L, Jiang, Yu, Johnson, Michael R, Kuzniecky, Ruben, Lowenstein, Daniel H, Marson, Anthony G, Mefford, Heather C, O'Brien, Terence J, Ottman, Ruth, Petrou, Steven, Petrovski, Slave, Poduri, Annapurna, Ren, Zhong, Scheffer, Ingrid E, Sherr, Elliott, Wang, Quanli, Balling, Rudi, Barisic, Nina, Baulac, Stephanie, Caglayan, Hande, Craiu, Dana, De Jonghe, Peter, Depienne, Christel, Guerrini, Renzo, Helbig, Ingo, Hjalgrim, Helle, Hoffman-Zacharska, Dorota, Jaehn, Johanna, Klein, Karl Martin, Koeleman, Bobby, Komarek, Vladimir, Krause, Roland, Leguern, Eric, Lehesjoki, Anna-Elina, Lemke, Johannes R, Lerche, Holger, Linnankivi, Tarja, Marini, Carla, May, Patrick, Moeller, Rikke S, Muhle, Hiltrud, Pal, Deb, et. al

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Terlipressin plus Albumin for the Treatment of Type 1 Hepatorenal Syndrome von Wong, Florence, Pappas, S. Chris, Curry, Michael P, Reddy, K. Rajender, Rubin, Raymond A, Porayko, Michael K, Gonzalez, Stevan A, Mumtaz, Khalid, Lim, Nicholas, Simonetto, Douglas A, Sharma, Pratima, Sanyal, Arun J, Mayo, Marlyn J, Frederick, R. Todd, Escalante, Shannon, Jamil, Khurram

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Neurotoxicity after CTL019 in a pediatric and young adult cohort von Gofshteyn, Jacqueline S., Shaw, Pamela A., Teachey, David T., Grupp, Stephan A., Maude, Shannon, Banwell, Brenda, Chen, Fang, Lacey, Simon F., Melenhorst, Jan J., Edmonson, MacKenzie J., Panzer, Jessica, Barrett, David M., McGuire, Jennifer L.

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Risk-Adapted Preemptive Tocilizumab to Prevent Severe Cytokine Release Syndrome After CTL019 for Pediatric B-Cell Acute Lymphoblastic Leukemia: A Prospective Clinical Trial von Kadauke, Stephan, Myers, Regina M., Li, Yimei, Aplenc, Richard, Baniewicz, Diane, Barrett, David M., Leahy, Allison Barz, Callahan, Colleen, Dolan, Joseph G., Fitzgerald, Julie C., Gladney, Whitney, Lacey, Simon F., Liu, Hongyan, Maude, Shannon L., McGuire, Regina, Motley, Laura S., Teachey, David T., Wertheim, Gerald B., Wray, Lisa, Di Nofia, Amanda M., Grupp, Stephan A.

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Metabolite-based dietary supplementation in human type 1 diabetes is associated with microbiota and immune modulation von Bell, Kirstine J, Saad, Sonia, Tillett, Bree J, McGuire, Helen M, Bordbar, Sara, Yap, Yu Anne, Nguyen, Long T, Wilkins, Marc R, Corley, Susan, Brodie, Shannon, Duong, Sussan, Wright, Courtney J, Twigg, Stephen, de St Groth, Barbara Fazekas, Harrison, Leonard C, Mackay, Charles R, Gurzov, Esteban N, Hamilton-Williams, Emma E, Mariño, Eliana

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Long-term Outcomes of Behavior Therapy for Youth With Tourette Disorder von Espil, Flint M., Woods, Douglas W., Specht, Matthew W., Bennett, Shannon M., Walkup, John T., Ricketts, Emily J., McGuire, Joseph F., Stiede, Jordan T., Schild, Jennifer S., Chang, Susanna W., Peterson, Alan L., Scahill, Lawrence, Wilhelm, Sabine, Piacentini, John C.

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Prevalence and Risk Factors of Neurologic Manifestations in Hospitalized Children Diagnosed with Acute SARS-CoV-2 or MIS-C von Fink, Ericka L., Robertson, Courtney L., Wainwright, Mark S., Roa, Juan D., Lovett, Marlina E., Stulce, Casey, Yacoub, Mais, Potera, Renee M., Zivick, Elizabeth, Holloway, Adrian, Nagpal, Ashish, Wellnitz, Kari, Czech, Theresa, Even, Katelyn M., Brunow de Carvalho, Werther, Rodriguez, Isadora Souza, Schwartz, Stephanie P., Walker, Tracie C., Campos-Miño, Santiago, Dervan, Leslie A., Geneslaw, Andrew S., Sewell, Taylor B., Pryce, Patrice, Silver, Wendy G., Lin, Jieru Egeria, Vargas, Wendy S., Topjian, Alexis, Alcamo, Alicia M., McGuire, Jennifer L., Domínguez Rojas, Jesus Angel, Muñoz, Jaime Tasayco, Hong, Sue J., Muller, William J., Doerfler, Matthew, Williams, Cydni N., Drury, Kurt, Bhagat, Dhristie, Nelson, Aaron, Price, Dana, Dapul, Heda, Santos, Laura, Kahoud, Robert, Francoeur, Conall, Appavu, Brian, Guilliams, Kristin P., Agner, Shannon C., Walson, Karen H., Rasmussen, Lindsey, Janas, Anna, Ferrazzano, Peter, Farias-Moeller, Raquel, Snooks, Kellie C., Chang, Chung-Chou H., Yun, James, Schober, Michelle E.

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Primary oxidative phosphorylation defects lead to perturbations in the human B cell repertoire von Gordon-Lipkin, Eliza M, Banerjee, Payal, Franco, Jose Luis Marin, Tarasenko, Tatiana, Kruk, Shannon, Thompson, Elizabeth, Gildea, Derek E, Zhang, Suiyuan, Wolfsberg, Tyra G, Flegel, Willy A, McGuire, Peter J

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Distinguishing and Managing Acute-Onset Complex Tic-like Behaviors in Adolescence von McGuire, Joseph F., Bennett, Shannon M., Conelea, Christine A., Himle, Michael B., Anderson, Seonaid, Ricketts, Emily J., Capriotti, Matthew R., Lewin, Adam B., McNulty, Devin C., Thompson, Laurie Gayes, Espil, Flint M., Nadeau, Sarah E., McConnell, Melanie, Woods, Douglas W., Walkup, John T., Piacentini, John

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Inflammatory and interferon gene expression signatures in patients with mitochondrial disease von Warren, Emily B, Gordon-Lipkin, Eliza M, Cheung, Foo, Chen, Jinguo, Mukherjee, Amrita, Apps, Richard, Tsang, John S, Jetmore, Jillian, Schlein, Melissa L, Kruk, Shannon, Lei, Yuanjiu, West, A Phillip, McGuire, Peter J

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Childhood Predictors of Long-Term Tic Severity and Tic Impairment in Tourette’s Disorder von Ricketts, Emily J., Woods, Douglas W., Espil, Flint M., McGuire, Joseph F., Stiede, Jordan T., Schild, Jennifer, Yadegar, Mina, Bennett, Shannon M., Specht, Matthew W., Chang, Susanna, Scahill, Lawrence, Wilhelm, Sabine, Peterson, Alan L., Walkup, John T., Piacentini, John

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An improvement to the volcano-scan algorithm for atmospheric correction of CRISM and OMEGA spectral data von McGuire, Patrick C., Bishop, Janice L., Brown, Adrian J., Fraeman, Abigail A., Marzo, Giuseppe A., Frank Morgan, M., Murchie, Scott L., Mustard, John F., Parente, Mario, Pelkey, Shannon M., Roush, Ted L., Seelos, Frank P., Smith, Michael D., Wendt, Lorenz, Wolff, Michael J.

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Tubal ligation and risk of ovarian cancer subtypes: a pooled analysis of case-control studies von SIEH, Weiva, SALVADOR, Shannon, DOHERTY, Jennifer A, FELBERG, Anna, MILLER, Dianne, JORDAN, Susan J, GOODMAN, Marc T, LURIE, Galina, CHANG-CLAUDE, Jenny, RUDOLPH, Anja, KJAER, Susanne Krüger, JENSEN, Allan, MCGUIRE, Valerie, HØGDALL, Estrid, BANDERA, Elisa V, OLSON, Sara H, KING, Melony G, RODRIGUEZ-RODRIGUEZ, Lorna, KIEMENEY, Lambertus A, MAREES, Tamara, MASSUGER, Leon F, VAN ALTENA, Anne M, NESS, Roberta B, PALMIERI WEBER, Rachel, CRAMER, Daniel W, PIKE, Malcolm C, PEARCE, Celeste Leigh, BERCHUCK, Andrew, SCHILDKRAUT, Joellen M, WHITTEMORE, Alice S, TERRY, Kathryn L, ROSSING, Mary Anne, RISCH, Harvey, WU, Anna H, WEBB, Penelope M, MOYSICH, Kirsten

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Epitope-level profiling in children with mitochondrial disease reveals limitations in the antibacterial antibody repertoire von Gordon-Lipkin, Eliza M., Banerjee, Payal, Thompson, Elizabeth, Kruk, Shannon, Franco, Jose Luis Marin, McGuire, Peter J.

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Perceived Negative Effects of Tic Management Strategies in Adults With Tic Disorders von Barber, Kathryn E., Pitts, Brandon X., Stiede, Jordan T., Espil, Flint M., Woods, Douglas W., Specht, Matthew W., Bennett, Shannon M., Walkup, John T., Ricketts, Emily J., McGuire, Joseph F., Peterson, Alan L., Compton, Scott N., Wilhelm, Sabine, Scahill, Lawrence, Piacentini, John C.

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