Setting the Stage for a New Prologue von Leko, Melinda M., Griffin, Cynthia C., Ulrich, Tracy G.

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Priming Mathematics Word Problem Structures in a Rural Elementary Classroom von Griffin, Cynthia C., Gagnon, Joseph C., Jossi, Maggie H., Ulrich, Tracy G., Myers, Jonté A.

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Medulloblastoma Can Be Initiated by Deletion of Patched in Lineage-Restricted Progenitors or Stem Cells von Yang, Zeng-Jie, Ellis, Tammy, Markant, Shirley L., Read, Tracy-Ann, Kessler, Jessica D., Bourboulas, Melissa, Schüller, Ulrich, Machold, Robert, Fishell, Gord, Rowitch, David H., Wainwright, Brandon J., Wechsler-Reya, Robert J.

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ZCCHC17 Modulates Neuronal RNA Splicing and Supports Cognitive Resilience in Alzheimer's Disease von Bartosch, Anne Marie W, Youth, Elliot H H, Hansen, Shania, Wu, Yiyang, Buchanan, Heather M, Kaufman, Maria E, Xiao, Harrison, Koo, So Yeon, Ashok, Archana, Sivakumar, Sharanya, Soni, Rajesh K, Dumitrescu, Logan C, Lam, Tiffany G, Ropri, Ali S, Lee, Annie J, Klein, Hans-Ulrich, Vardarajan, Badri N, Bennett, David A, Young-Pearse, Tracy L, De Jager, Philip L, Hohman, Timothy J, Sproul, Andrew A, Teich, Andrew F

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Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals von Howrigan, Daniel P., Abbott, Liam E., Tashman, Katherine, Singh, Tarjinder, Watts, Nick, Lal, Dennis, Hakonarson, Hakon, Weckhuysen, Sarah, Petrovski, Slavé, Cossette, Patrick, Cotsapas, Chris, De Jonghe, Peter, Guerrini, Renzo, Marson, Anthony G., Depondt, Chantal, Striano, Pasquale, Freyer, Catharine, Regan, Brigid M., Leu, Costin, Johns, Esther M.C., Macdonald, Alexandra, Bahlo, Melanie, Todaro, Marian, Stamberger, Hannah, Sadoway, Tara R., Kousiappa, Ioanna, Tanteles, George A., Štěrbová, Katalin, Kunz, Wolfram S., Zsurka, Gábor, Elger, Christian E., Rademacher, Michael, van Baalen, Andreas, von Spiczak, Sarah, Afawi, Zaid, Canavati, Christina, Kluger, Gerhard, Blatt, Ilan, Weber, Yvonne G., Wolking, Stefan, Rau, Sarah, Steinhoff, Bernhard J., Schulze-Bonhage, Andreas, Borggräfe, Ingo, Madeleyn, Rene, Kälviäinen, Reetta, Linnankivi, Tarja, Chung, Seo-Kyung, Balestrini, Simona, Braatz, Vera, Johnson, Michael R., Auce, Pauls, Sham, Pak C., Lui, Colin H.T., Doherty, Colin P., Shukralla, Arif, El-Naggar, Hany, Vari, Maria Stella, Salpietro, Vincenzo, Tinuper, Paolo, Gagliardi, Monica, Montomoli, Martino, Doccini, Viola, Inoue, Yushi, Yamakawa, Kazuhiro, Tumiene, Birute, Sadleir, Lynette G., Caglayan, S. Hande, Arslan, Mutluay, Yis, Uluc, Topaloglu, Pınar, Baykan, Betül, Salman, Barış, Haryanyan, Garen, Özkara, Çiğdem, Poduri, Annapurna, Shiedley, Beth R., Shain, Catherine, French, Jacqueline A., Kuzniecky, Ruben I., Hegde, Manu, Helbig, Katherine L., Piras, Federica, Reif, Andreas, McQuillin, Andrew, Johnstone, Mandy, Palotie, Aarno, Carvalho, Celia Barreto, Achtyes, Eric D., Azevedo, Maria Helena, Kotov, Roman, Lehrer, Douglas S., Marder, Stephen R., Medeiros, Helena, Morley, Christopher P., Rapaport, Mark H., Knowles, James A., McCarroll, Steven A., Lowenstein, Daniel H., Goldstein, David B.

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Polygenic burden in focal and generalized epilepsies von Leu, Costin, Stevelink, Remi, Smith, Alexander W, Goleva, Slavina B, Kanai, Masahiro, Ferguson, Lisa, Campbell, Ciaran, Kamatani, Yoichiro, Okada, Yukinori, Sisodiya, Sanjay M, Cavalleri, Gianpiero L, Koeleman, Bobby P C, Lerche, Holger, Jehi, Lara, Davis, Lea K, Najm, Imad M, Palotie, Aarno, Daly, Mark J, Busch, Robyn M, Lal, Dennis

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Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease von Katz, Daniel H., Tahir, Usman A., Bick, Alexander G., Pampana, Akhil, Ngo, Debby, Benson, Mark D., Yu, Zhi, Robbins, Jeremy M., Chen, Zsu-Zsu, Cruz, Daniel E., Deng, Shuliang, Farrell, Laurie, Sinha, Sumita, Schmaier, Alec A., Shen, Dongxiao, Gao, Yan, Hall, Michael E., Correa, Adolfo, Tracy, Russell P., Durda, Peter, Taylor, Kent D., Liu, Yongmei, Johnson, W. Craig, Guo, Xiuqing, Yao, Jie, Ida Chen, Yii-Der, Manichaikul, Ani W., Jain, Deepti, Bouchard, Claude, Sarzynski, Mark A., Rich, Stephen S., Rotter, Jerome I., Wang, Thomas J., Wilson, James G., Natarajan, Pradeep, Gerszten, Robert E.

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Age-Related Gliosis Promotes Central Nervous System Lymphoma through CCL19-Mediated Tumor Cell Retention von O'Connor, Tracy, Zhou, Xiaolan, Kosla, Jan, Adili, Arlind, Garcia Beccaria, Maria, Kotsiliti, Elena, Pfister, Dominik, Johlke, Anna-Lena, Sinha, Ankit, Sankowski, Roman, Schick, Markus, Lewis, Richard, Dokalis, Nikolaos, Seubert, Bastian, Höchst, Bastian, Inverso, Donato, Heide, Danijela, Zhang, Wenlong, Weihrich, Petra, Manske, Katrin, Wohlleber, Dirk, Anton, Martina, Hoellein, Alexander, Seleznik, Gitta, Bremer, Juliane, Bleul, Sabine, Augustin, Hellmut G., Scherer, Florian, Koedel, Uwe, Weber, Achim, Protzer, Ulrike, Förster, Reinhold, Wirth, Thomas, Aguzzi, Adriano, Meissner, Felix, Prinz, Marco, Baumann, Bernd, Höpken, Uta E., Knolle, Percy A., von Baumgarten, Louisa, Keller, Ulrich, Heikenwalder, Mathias

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A Recurrent Missense Variant in AP2M1 Impairs Clathrin-Mediated Endocytosis and Causes Developmental and Epileptic Encephalopathy von Helbig, Ingo, Lopez-Hernandez, Tania, Shor, Oded, Galer, Peter, Ganesan, Shiva, Pendziwiat, Manuela, Rademacher, Annika, Ellis, Colin A., Hümpfer, Nadja, Schwarz, Niklas, Seiffert, Simone, Peeden, Joseph, Shen, Joseph, Štěrbová, Katalin, Hammer, Trine Bjørg, Møller, Rikke S., Shinde, Deepali N., Tang, Sha, Smith, Lacey, Poduri, Annapurna, Krause, Roland, Benninger, Felix, Helbig, Katherine L., Haucke, Volker, Weber, Yvonne G., Balling, Rudi, Barisic, Nina, Baulac, Stéphanie, Caglayan, Hande, Craiu, Dana, De Jonghe, Peter, Depienne, Christel, Guerrini, Renzo, Hjalgrim, Helle, Hoffman-Zacharska, Dorota, Jähn, Johanna, Klein, Karl Martin, Koeleman, Bobby P.C., Komarek, Vladimir, Leguern, Eric, Lehesjoki, Anna-Elina, Lemke, Johannes R., Lerche, Holger, Linnankivi, Tarja, Marini, Carla, May, Patrick, Muhle, Hiltrud, Pal, Deb K., Palotie, Aarno, Rosenow, Felix, Schubert-Bast, Susanne, Selmer, Kaja, Serratosa, Jose M., Sisodiya, Sanjay, Stephani, Ulrich, Striano, Pasquale, Suls, Arvid, Talvik, Tiina, von Spiczak, Sarah, Weckhuysen, Sarah, Zara, Federico, Avillach, Paul, Bartels, Anna, Biswas, Sawona, Bourgeois, Florence, Devkota, Batsal, Glauser, Tracy, Hallinan, Barbara, Heath, Allison, Hirschhorn, Joel, Kilbourn, Judson, Kong, Sek Won, Krantz, Ian, Lee, In-Hee, Mandl, Kenneth D., Marsh, Eric, Sund, Kristen, Taylor, Deanne, White, Peter

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Epilepsy subtype-specific copy number burden observed in a genome-wide study of 17 458 subjects von Niestroj, Lisa-Marie, Perez-Palma, Eduardo, Howrigan, Daniel P, Zhou, Yadi, Cheng, Feixiong, Saarentaus, Elmo, Nürnberg, Peter, Stevelink, Remi, Daly, Mark J, Palotie, Aarno, Lal, Dennis

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Agreement between local and central anti-synthetase antibodies detection: results from the Classification Criteria of Anti-Synthetase Syndrome project biobank von Loganathan, Aravinthan, Zanframundo, Giovanni, Yoshida, Akira, Faghihi-Kashani, Sara, Bauer Ventura, Iazsmin, Dourado, Eduardo, Bozan, Francisca, Sambataro, Gianluca, Yamano, Yasuhiko, Bae, Sharon Sangmee, Lim, Darosa, Ceribelli, Angela, Isailovic, Natasa, Selmi, Carlo, Fertig, Noreen, Bravi, Elena, Kaneko, Yuko, Saraiva, André Pinto, Jovani, Vega, Bachiller-Corral, Javier, Cifrian, Jose, Mera-Varela, Antonio, Moghadam-Kia, Siamak, Wolff, Veronica, Campagne, Julien, Meyer, Alain, Giannini, Margherita, Triantafyllias, Konstantinos, Knitza, Johannes, Gupta, Latika, Molad, Yair, Iannone, Florenzo, Cavazzana, Ilaria, Piga, Matteo, De Luca, Giacomo, Tansley, Sarah, Bozzalla-Cassione, Emanuele, Bonella, Francesco, Corte, Tamera J, Doyle, Tracy J, Fiorentino, David, Gonzalez-Gay, Miguel Angel, Hudson, Marie, Kuwana, Masataka, Lundberg, Ingrid E, Mammen, Andrew L, McHugh, Neil John, Miller, Fredrick W, Montecucco, Carlomaurizio, Oddis, Chester V, Rojas-Serrano, Jorge, Schmidt, Jens, Scirè, Carlo Alberto, Selva-O'Callaghan, Albert, Werth, Victoria P, Alpini, Claudia, Bozzini, Sara, Cavagna, Lorenzo, Aggarwal, Rohit

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Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals von Montanucci, Ludovica, Lewis-Smith, David, Collins, Ryan L., Niestroj, Lisa-Marie, Parthasarathy, Shridhar, Xian, Julie, Ganesan, Shiva, Macnee, Marie, Brünger, Tobias, Thomas, Rhys H., Talkowski, Michael, Helbig, Ingo, Leu, Costin, Lal, Dennis

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Sub-genic intolerance, ClinVar, and the epilepsies: A whole-exome sequencing study of 29,165 individuals von Povysil, Gundula, Allen, Andrew S., Howrigan, Daniel P., Tashman, Katherine, Cerrato, Felecia, Cusick, Caroline, Heyne, Henrike, Churchhouse, Claire, Watts, Nick, Lal, Dennis, Gupta, Namrata, Cavalleri, Gianpiero L., Hakonarson, Hakon, Marson, Anthony G., Petrovski, Slavé, Sisodiya, Sanjay M., Depondt, Chantal, Scheffer, Ingrid E., Krause, Roland, Regan, Brigid M., Leu, Costin, Leech, Stephanie L., Todaro, Marian, Stamberger, Hannah, Kousiappa, Ioanna, Tanteles, George A., Christou, Yiolanda, Laššuthová, Petra, Knake, Susanne, Kunz, Wolfram S., Zsurka, Gábor, Surges, Rainer, Rademacher, Annika, von Spiczak, Sarah, Kanaan, Moien, Canavati, Christina, Lemke, Johannes R., Krey, Ilona, Weber, Yvonne G., Wolking, Stefan, Kegele, Josua, Borggräfe, Ingo, Mayer, Thomas, Brockmann, Knut, Madeleyn, Rene, Saarela, Anni, Linnankivi, Tarja, Lehesjoki, Anna-Elina, Derambure, Philippe, Hirsch, Edouard, Chassoux, Francine, Chung, Seo-Kyung, Schneider, Natascha, Balestrini, Simona, Zagaglia, Sara, Johnson, Michael R., Auce, Pauls, Barišić, Nina, Canafoglia, Laura, Franceschetti, Silvana, Castellotti, Barbara, Granata, Tiziana, Ragona, Francesca, Iacomino, Michele, Riva, Antonella, Vari, Maria Stella, Salpietro, Vincenzo, Mancardi, Maria Margherita, Nobili, Lino, Bisulli, Francesca, Pippucci, Tommaso, Licchetta, Laura, Tinuper, Paolo, Gambardella, Antonio, Labate, Angelo, Annesi, Grazia, Manna, Lorella, Parrini, Elena, Bianchini, Claudia, Montomoli, Martino, Hirose, Shinichi, Yamakawa, Kazuhiro, Beydoun, Ahmad, Sadleir, Lynette G., Topaloglu, Pınar, Baykan, Betül, Özkara, YeşÇiğdem, Ho, Chen-Jui, Chou, I-Jun, Shain, Catherine, Goldman, Alicia, Busch, Robyn M., Jehi, Lara, Ferguson, Lisa, Clark, Peggy O., Privitera, Michael, Schachter, Steven, Cosico, Mahgenn, Lowenstein, Daniel H., Goldstein, David B.

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Risk and safety requirements for diagnostic and therapeutic procedures in allergology: World Allergy Organization Statement von Kowalski, Marek L., Ansotegui, Ignacio, Aberer, Werner, Al-Ahmad, Mona, Akdis, Mubeccel, Ballmer-Weber, Barbara K., Beyer, Kirsten, Blanca, Miguel, Brown, Simon, Bunnag, Chaweewan, Hulett, Arnaldo Capriles, Castells, Mariana, Chng, Hiok Hee, De Blay, Frederic, Ebisawa, Motohiro, Fineman, Stanley, Golden, David B.K., Haahtela, Tari, Kaliner, Michael, Katelaris, Connie, Lee, Bee Wah, Makowska, Joanna, Muller, Ulrich, Mullol, Joaquim, Oppenheimer, John, Park, Hae-Sim, Parkerson, James, Passalacqua, Giovanni, Pawankar, Ruby, Renz, Harald, Rueff, Franziska, Sanchez-Borges, Mario, Sastre, Joaquin, Scadding, Glenis, Sicherer, Scott, Tantilipikorn, Pongsakorn, Tracy, James, van Kempen, Vera, Bohle, Barbara, Canonica, G Walter, Caraballo, Luis, Gomez, Maximiliano, Ito, Komei, Jensen-Jarolim, Erika, Larche, Mark, Melioli, Giovanni, Poulsen, Lars K., Valenta, Rudolf, Zuberbier, Torsten

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Author Correction: Inherited causes of clonal haematopoiesis in 97,691 whole genomes von Weinstock, Joshua S., Nandakumar, Satish K., Bao, Erik L., Szeto, Mindy D., Liao, Xiaotian, Nasser, Joseph, Laurie, Cecelia, Burugula, Bala Bharathi, Gibson, Christopher J., Lin, Amy E., Aguet, Francois, Ardlie, Kristin, Mitchell, Braxton D., Barnes, Kathleen C., Moscati, Arden, Redline, Susan, Psaty, Bruce M., Silverman, Edwin K., Weiss, Scott T., Palmer, Nicholette D., Vasan, Ramachandran S., He, Jiang, Kaplan, Robert C., Smith, Nicholas L., Arnett, Donna K., Schwartz, David A., Guo, Xiuqing, Konkle, Barbara A., Custer, Brian, Peralta, Juan M., Gui, Hongsheng, Meyers, Deborah A., McGarvey, Stephen T., Chen, Ida Yii-Der, Shoemaker, M. Benjamin, Peyser, Patricia A., Broome, Jai G., Wang, Fei Fei, North, Kari E., Launer, Lenore J., Cade, Brian E., Bis, Joshua C., Cho, Michael H., Lasky-Su, Jessica, Bowden, Donald W., Cupples, L. Adrienne, Mak, Angel C. Y., Smith, Jennifer A., Kelly, Tanika N., Aslibekyan, Stella, Heckbert, Susan R., Tiwari, Hemant K., Yang, Ivana V., Heit, John A., Johnsen, Jill M., Curran, Joanne E., Wenzel, Sally E., Rao, Dabeeru C., Darbar, Dawood, Moon, Jee-Young, Tracy, Russell P., Buth, Erin J., Rafaels, Nicholas, Loos, Ruth J. F., Liu, Yongmei, Hou, Lifang, Lee, Jiwon, Kachroo, Priyadarshini, Freedman, Barry I., Levy, Daniel, Bielak, Lawrence F., Hixson, James E., Floyd, James S., Whitsel, Eric A., Ellinor, Patrick T., Irvin, Marguerite R., Fingerlin, Tasha E., Armasu, Sebastian M., Wheeler, Marsha M., Blangero, John, Williams, L. Keoki, Levy, Bruce D., Sheu, Wayne Huey-Herng, Roden, Dan M., Boerwinkle, Eric, Taylor, Kent D., Johnson, Andrew D., Auer, Paul L., Kooperberg, Charles, Laurie, Cathy C., Blackwell, Thomas W., Smith, Albert V., Lange, Ethan, Rotter, Jerome I., Kitzman, Jacob O., Lander, Eric S., Ebert, Benjamin L., Reiner, Alexander P., Jaiswal, Siddhartha, Kathiresan, Sekar

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Sub-genic intolerance, ClinVar, and the epilepsies: A whole-exome sequencing study of 29,165 individuals von Povysil, Gundula, Allen, Andrew S., Howrigan, Daniel P., Tashman, Katherine, Cerrato, Felecia, Cusick, Caroline, Heyne, Henrike, Churchhouse, Claire, Watts, Nick, Lal, Dennis, Gupta, Namrata, Cavalleri, Gianpiero L., Hakonarson, Hakon, Marson, Anthony G., Petrovski, Slavé, Sisodiya, Sanjay M., Depondt, Chantal, Scheffer, Ingrid E., Krause, Roland, Regan, Brigid M., Leu, Costin, Leech, Stephanie L., Todaro, Marian, Stamberger, Hannah, Kousiappa, Ioanna, Tanteles, George A., Christou, Yiolanda, Laššuthová, Petra, Knake, Susanne, Kunz, Wolfram S., Zsurka, Gábor, Surges, Rainer, Rademacher, Annika, von Spiczak, Sarah, Kanaan, Moien, Canavati, Christina, Lemke, Johannes R., Krey, Ilona, Weber, Yvonne G., Wolking, Stefan, Kegele, Josua, Borggräfe, Ingo, Mayer, Thomas, Brockmann, Knut, Madeleyn, Rene, Saarela, Anni, Linnankivi, Tarja, Lehesjoki, Anna-Elina, Derambure, Philippe, Hirsch, Edouard, Chassoux, Francine, Chung, Seo-Kyung, Schneider, Natascha, Balestrini, Simona, Zagaglia, Sara, Johnson, Michael R., Auce, Pauls, Barišić, Nina, Canafoglia, Laura, Franceschetti, Silvana, Castellotti, Barbara, Granata, Tiziana, Ragona, Francesca, Iacomino, Michele, Riva, Antonella, Vari, Maria Stella, Salpietro, Vincenzo, Mancardi, Maria Margherita, Nobili, Lino, Bisulli, Francesca, Pippucci, Tommaso, Licchetta, Laura, Tinuper, Paolo, Gambardella, Antonio, Labate, Angelo, Annesi, Grazia, Manna, Lorella, Parrini, Elena, Bianchini, Claudia, Montomoli, Martino, Hirose, Shinichi, Yamakawa, Kazuhiro, Beydoun, Ahmad, Sadleir, Lynette G., Topaloglu, Pınar, Baykan, Betül, Özkara, Çiğdem, Ho, Chen-Jui, Chou, I-Jun, Shain, Catherine, Goldman, Alicia, Busch, Robyn M., Jehi, Lara, Ferguson, Lisa, Clark, Peggy O., Privitera, Michael, Schachter, Steven, Cosico, Mahgenn, Lowenstein, Daniel H., Goldstein, David B.

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Association of Initial SARS-CoV-2 Test Positivity With Patient-Reported Well-being 3 Months After a Symptomatic Illness von Wisk, Lauren E, Gottlieb, Michael A, Spatz, Erica S, Yu, Huihui, Wang, Ralph C, Slovis, Benjamin H, Saydah, Sharon, Plumb, Ian D, O'Laughlin, Kelli N, Montoy, Juan Carlos C, McDonald, Samuel A, Lin, Zhenqiu, Lin, Jin-Mann S, Koo, Katherine, Idris, Ahamed H, Huebinger, Ryan M, Hill, Mandy J, Gentile, Nicole L, Chang, Anna Marie, Anderson, Jill, Hota, Bala, Venkatesh, Arjun K, Weinstein, Robert A, Elmore, Joann G, Nichol, Graham

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Interaction of ARC and Daxx: A Novel Endogenous Target to Preserve Motor Function and Cell Loss after Focal Brain Ischemia in Mice von Donath, Stefan, An, Junfeng, Lee, Sabrina Lin Lin, Gertz, Karen, Datwyler, Anna Lena, Harms, Ulrike, Müller, Susanne, Farr, Tracy Deanne, Füchtemeier, Martina, Lättig-Tünnemann, Gisela, Lips, Janet, Foddis, Marco, Mosch, Larissa, Bernard, René, Grittner, Ulrike, Balkaya, Mustafa, Kronenberg, Golo, Dirnagl, Ulrich, Endres, Matthias, Harms, Christoph

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Long COVID Clinical Phenotypes up to 6 Months After Infection Identified by Latent Class Analysis of Self-Reported Symptoms von Gottlieb, Michael, Spatz, Erica S, Yu, Huihui, Wisk, Lauren E, Elmore, Joann G, Gentile, Nicole L, Hill, Mandy, Huebinger, Ryan M, Idris, Ahamed H, Kean, Efrat R, Koo, Katherine, Li, Shu-Xia, McDonald, Samuel, Montoy, Juan Carlos C, Nichol, Graham, O’Laughlin, Kelli N, Plumb, Ian D, Rising, Kristin L, Santangelo, Michelle, Saydah, Sharon, Wang, Ralph C, Venkatesh, Arjun, Stephens, Kari A, Weinstein, Robert A

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Association Between SARS-CoV-2 Variants and Frequency of Acute Symptoms: Analysis of a Multi-institutional Prospective Cohort Study—December 20, 2020—June 20, 2022 von Wang, Ralph C, Gottlieb, Michael, Montoy, Juan Carlos C, Rodriguez, Robert M, Yu, Huihui, Spatz, Erica S, Chandler, Christopher W, Elmore, Joann G, Hannikainen, Paavali A, Chang, Anna Marie, Hill, Mandy, Huebinger, Ryan M, Idris, Ahamed H, Koo, Katherine, Li, Shu-Xia, McDonald, Samuel, Nichol, Graham, O’Laughlin, Kelli N, Plumb, Ian D, Santangelo, Michelle, Saydah, Sharon, Stephens, Kari A, Venkatesh, Arjun K, Weinstein, Robert A

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