Outcomes in CLL patients with NOTCH1 regulatory pathway mutations von Helbig, Daniel R., Abu‐Zeinah, Ghaith, Bhavsar, Erica, Christos, Paul J., Furman, Richard R., Allan, John N.

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Outcomes in chronic lymphocytic leukemia (CLL) patients with NOTCH1 signaling pathway mutations von Helbig, Daniel R., Abu Zeinah, Ghaith F, Bhavsar, Erica B., Allan, John N.

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Clinical spectrum of STX1B-related epileptic disorders von Wolking, Stefan, May, Patrick, Mei, Davide, Møller, Rikke S, Balestrini, Simona, Helbig, Katherine L, Altuzarra, Cecilia Desmettre, Chatron, Nicolas, Kaiwar, Charu, Stöhr, Katharina, Widdess-Walsh, Peter, Mendelsohn, Bryce A, Numis, Adam, Cilio, Maria R, Van Paesschen, Wim, Svendsen, Lene L, Oates, Stephanie, Hughes, Elaine, Goyal, Sushma, Brown, Kathleen, Sifuentes Saenz, Margarita, Dorn, Thomas, Muhle, Hiltrud, Pagnamenta, Alistair T, Vavoulis, Dimitris V, Knight, Samantha J.L, Taylor, Jenny C, Canevini, Maria Paola, Darra, Francesca, Gavrilova, Ralitza H, Powis, Zöe, Tang, Shan, Marquetand, Justus, Armstrong, Martin, McHale, Duncan, Klee, Eric W, Kluger, Gerhard J, Lowenstein, Daniel H, Weckhuysen, Sarah, Pal, Deb K, Helbig, Ingo, Guerrini, Renzo, Thomas, Rhys H, Rees, Mark I, Lesca, Gaetan, Sisodiya, Sanjay M, Weber, Yvonne G, Lal, Dennis, Marini, Carla, Lerche, Holger, Schubert, Julian

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Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders von Wolff, Markus, Johannesen, Katrine M, Hedrich, Ulrike B S, Masnada, Silvia, Rubboli, Guido, Gardella, Elena, Lesca, Gaetan, Ville, Dorothée, Milh, Mathieu, Villard, Laurent, Afenjar, Alexandra, Chantot-Bastaraud, Sandra, Mignot, Cyril, Lardennois, Caroline, Nava, Caroline, Schwarz, Niklas, Gérard, Marion, Perrin, Laurence, Doummar, Diane, Auvin, Stéphane, Miranda, Maria J, Hempel, Maja, Brilstra, Eva, Knoers, Nine, Verbeek, Nienke, van Kempen, Marjan, Braun, Kees P, Mancini, Grazia, Biskup, Saskia, Hörtnagel, Konstanze, Döcker, Miriam, Bast, Thomas, Loddenkemper, Tobias, Wong-Kisiel, Lily, Baumeister, Friedrich M, Fazeli, Walid, Striano, Pasquale, Dilena, Robertino, Fontana, Elena, Zara, Federico, Kurlemann, Gerhard, Klepper, Joerg, Thoene, Jess G, Arndt, Daniel H, Deconinck, Nicolas, Schmitt-Mechelke, Thomas, Maier, Oliver, Muhle, Hiltrud, Wical, Beverly, Finetti, Claudio, Brückner, Reinhard, Pietz, Joachim, Golla, Günther, Jillella, Dinesh, Linnet, Karen M, Charles, Perrine, Moog, Ute, Õiglane-Shlik, Eve, Mantovani, John F, Park, Kristen, Deprez, Marie, Lederer, Damien, Mary, Sandrine, Scalais, Emmanuel, Selim, Laila, Van Coster, Rudy, Lagae, Lieven, Nikanorova, Marina, Hjalgrim, Helle, Korenke, G Christoph, Trivisano, Marina, Specchio, Nicola, Ceulemans, Berten, Dorn, Thomas, Helbig, Katherine L, Hardies, Katia, Stamberger, Hannah, de Jonghe, Peter, Weckhuysen, Sarah, Lemke, Johannes R, Krägeloh-Mann, Ingeborg, Helbig, Ingo, Kluger, Gerhard, Lerche, Holger, Møller, Rikke S

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Molecular landscapes of human hippocampal immature neurons across lifespan von Zhou, Yi, Su, Yijing, Li, Shiying, Kennedy, Benjamin C., Zhang, Daniel Y., Bond, Allison M., Sun, Yusha, Jacob, Fadi, Lu, Lu, Hu, Peng, Viaene, Angela N., Helbig, Ingo, Kessler, Sudha K., Lucas, Timothy, Salinas, Ryan D., Gu, Xiaosong, Chen, H. Isaac, Wu, Hao, Kleinman, Joel E., Hyde, Thomas M., Nauen, David W., Weinberger, Daniel R., Ming, Guo-li, Song, Hongjun

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A single-cell transcriptome atlas of glial diversity in the human hippocampus across the postnatal lifespan von Su, Yijing, Zhou, Yi, Bennett, Mariko L., Li, Shiying, Carceles-Cordon, Marc, Lu, Lu, Huh, Sooyoung, Jimenez-Cyrus, Dennisse, Kennedy, Benjamin C., Kessler, Sudha K., Viaene, Angela N., Helbig, Ingo, Gu, Xiaosong, Kleinman, Joel E., Hyde, Thomas M., Weinberger, Daniel R., Nauen, David W., Song, Hongjun, Ming, Guo-li

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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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Current practice in diagnostic genetic testing of the epilepsies von Krey, Ilona, Platzer, Konrad, Esterhuizen, Alina, Berkovic, Samuel F., Helbig, Ingo, Hildebrand, Michael S., Lerche, Holger, Lowenstein, Daniel, Møller, Rikke S., Poduri, Annapurna, Sadleir, Lynette, Sisodiya, Sanjay M., Weckhuysen, Sarah, Wilmshurst, Jo M., Weber, Yvonne, Lemke, Johannes R.

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HCN1 mutation spectrum: from neonatal epileptic encephalopathy to benign generalized epilepsy and beyond von Marini, Carla, Porro, Alessandro, Rastetter, Agnès, Dalle, Carine, Rivolta, Ilaria, Bauer, Daniel, Oegema, Renske, Nava, Caroline, Parrini, Elena, Mei, Davide, Mercer, Catherine, Dhamija, Radhika, Chambers, Chelsea, Coubes, Christine, Thévenon, Julien, Kuentz, Paul, Julia, Sophie, Pasquier, Laurent, Dubourg, Christèle, Carré, Wilfrid, Rosati, Anna, Melani, Federico, Pisano, Tiziana, Giardino, Maria, Innes, A Micheil, Alembik, Yves, Scheidecker, Sophie, Santos, Manuela, Figueiroa, Sonia, Garrido, Cristina, Fusco, Carlo, Frattini, Daniele, Spagnoli, Carlotta, Binda, Anna, Granata, Tiziana, Ragona, Francesca, Freri, Elena, Franceschetti, Silvana, Canafoglia, Laura, Castellotti, Barbara, Gellera, Cinzia, Milanesi, Raffaella, Mancardi, Maria Margherita, Clark, Damien R, Kok, Fernando, Helbig, Katherine L, Ichikawa, Shoji, Sadler, Laurie, Neupauerová, Jana, Laššuthova, Petra, Štěrbová, Katalin, Laridon, Annick, Brilstra, Eva, Koeleman, Bobby, Lemke, Johannes R, Zara, Federico, Striano, Pasquale, Soblet, Julie, Smits, Guillaume, Deconinck, Nicolas, Barbuti, Andrea, DiFrancesco, Dario, LeGuern, Eric, Guerrini, Renzo, Santoro, Bina, Hamacher, Kay, Thiel, Gerhard, Moroni, Anna, DiFrancesco, Jacopo C, Depienne, Christel

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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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Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies von Abou-Khalil, Bassel, Auce, Pauls, Avbersek, Andreja, Bahlo, Melanie, Balding, David J., Bast, Thomas, Baum, Larry, Becker, Albert J., Becker, Felicitas, Berghuis, Bianca, Berkovic, Samuel F., Boysen, Katja E., Bradfield, Jonathan P., Brody, Lawrence C., Buono, Russell J., Campbell, Ellen, Cascino, Gregory D., Catarino, Claudia B., Cavalleri, Gianpiero L., Cherny, Stacey S., Chinthapalli, Krishna, Coffey, Alison J., Compston, Alastair, Coppola, Antonietta, Cossette, Patrick, Craig, John J., de Haan, Gerrit-Jan, De Jonghe, Peter, de Kovel, Carolien G. F., Delanty, Norman, Depondt, Chantal, Devinsky, Orrin, Dlugos, Dennis J., Doherty, Colin P., Elger, Christian E., Eriksson, Johan G., Ferraro, Thomas N., Feucht, Martha, Francis, Ben, Franke, Andre, French, Jacqueline A., Freytag, Saskia, Gaus, Verena, Geller, Eric B., Gieger, Christian, Glauser, Tracy, Glynn, Simon, Goldstein, David B., Gui, Hongsheng, Guo, Youling, Haas, Kevin F., Hakonarson, Hakon, Hallmann, Kerstin, Haut, Sheryl, Heinzen, Erin L., Helbig, Ingo, Hengsbach, Christian, Hjalgrim, Helle, Iacomino, Michele, Ingason, Andrés, Jamnadas-Khoda, Jennifer, Johnson, Michael R., Kälviäinen, Reetta, Kantanen, Anne-Mari, Kasperavičiūte, Dalia, Kasteleijn-Nolst Trenite, Dorothee, Kirsch, Heidi E., Knowlton, Robert C., Koeleman, Bobby P. C., Krause, Roland, Krenn, Martin, Kunz, Wolfram S., Kuzniecky, Ruben, Kwan, Patrick, Lal, Dennis, Lau, Yu-Lung, Lehesjoki, Anna-Elina, Lerche, Holger, Leu, Costin, Lieb, Wolfgang, Lindhout, Dick, Lo, Warren D., Lopes-Cendes, Iscia, Lowenstein, Daniel H., Malovini, Alberto, Marson, Anthony G., Mayer, Thomas, McCormack, Mark, Mills, James L., Mirza, Nasir, Moerzinger, Martina, Møller, Rikke S., Molloy, Anne M., Muhle, Hiltrud, Newton, Mark, Ng, Ping-Wing, Nöthen, Markus M., Nürnberg, Peter, O’Brien, Terence J., Oliver, Karen L.

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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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Molecular landscapes of human hippocampal immature neurons across lifespan von Zhou, Yi, Su, Yijing, Li, Shiying, Kennedy, Benjamin C., Zhang, Daniel Y., Bond, Allison M., Sun, Yusha, Jacob, Fadi, Lu, Lu, Hu, Peng, Viaene, Angela N., Helbig, Ingo, Kessler, Sudha K., Lucas, Timothy, Salinas, Ryan D., Gu, Xiaosong, Chen, H. Isaac, Wu, Hao, Kleinman, Joel E., Hyde, Thomas M., Nauen, David W., Weinberger, Daniel R., Ming, Guo-li, Song, Hongjun

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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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Monthly gridded data product of northern wetland methane emissions based on upscaling eddy covariance observations von Peltola, Olli, Vesala, Timo, Gao, Yao, Räty, Olle, Alekseychik, Pavel, Aurela, Mika, Chojnicki, Bogdan, Desai, Ankur R, Dolman, Albertus J, Euskirchen, Eugenie S, Friborg, Thomas, Göckede, Mathias, Helbig, Manuel, Humphreys, Elyn, Jackson, Robert B, Jocher, Georg, Joos, Fortunat, Klatt, Janina, Knox, Sara H, Kowalska, Natalia, Kutzbach, Lars, Lienert, Sebastian, Lohila, Annalea, Mammarella, Ivan, Nadeau, Daniel F, Nilsson, Mats B, Oechel, Walter C, Peichl, Matthias, Pypker, Thomas, Quinton, William, Rinne, Janne, Sachs, Torsten, Samson, Mateusz, Schmid, Hans Peter, Sonnentag, Oliver, Wille, Christian, Zona, Donatella, Aalto, Tuula

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Zanubrutinib and Venetoclax As Initial Therapy for CLL/SLL with Obinutuzumab Triplet Consolidation in Patients with Minimal Residual Disease Positivity (BruVenG) von Allan, John N., Helbig, Daniel, Mulvey, Erin, Nazir, Sarah, Stewart, Sandra, Lapinta, Melissa L., Rutherford, Sarah C., Ruan, Jia, Leonard, John P., Martin, Peter, Furman, Richard R.

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SvAnna: efficient and accurate pathogenicity prediction of coding and regulatory structural variants in long-read genome sequencing von Danis, Daniel, Jacobsen, Julius O B, Balachandran, Parithi, Zhu, Qihui, Yilmaz, Feyza, Reese, Justin, Haimel, Matthias, Lyon, Gholson J, Helbig, Ingo, Mungall, Christopher J, Beck, Christine R, Lee, Charles, Smedley, Damian, Robinson, Peter N

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Increasing contribution of peatlands to boreal evapotranspiration in a warming climate von Helbig, Manuel, Waddington, James Michael, Alekseychik, Pavel, Amiro, Brian D., Aurela, Mika, Barr, Alan G., Black, T. Andrew, Blanken, Peter D., Carey, Sean K., Chen, Jiquan, Chi, Jinshu, Desai, Ankur R., Dunn, Allison, Euskirchen, Eugenie S., Flanagan, Lawrence B., Forbrich, Inke, Friborg, Thomas, Grelle, Achim, Harder, Silvie, Heliasz, Michal, Humphreys, Elyn R., Ikawa, Hiroki, Isabelle, Pierre-Erik, Iwata, Hiroki, Jassal, Rachhpal, Korkiakoski, Mika, Kurbatova, Juliya, Kutzbach, Lars, Lindroth, Anders, Löfvenius, Mikaell Ottosson, Lohila, Annalea, Mammarella, Ivan, Marsh, Philip, Maximov, Trofim, Melton, Joe R., Moore, Paul A., Nadeau, Daniel F., Nicholls, Erin M., Nilsson, Mats B., Ohta, Takeshi, Peichl, Matthias, Petrone, Richard M., Petrov, Roman, Prokushkin, Anatoly, Quinton, William L., Reed, David E., Roulet, Nigel T., Runkle, Benjamin R. K., Sonnentag, Oliver, Strachan, Ian B., Taillardat, Pierre, Tuittila, Eeva-Stiina, Tuovinen, Juha-Pekka, Turner, Jessica, Ueyama, Masahito, Varlagin, Andrej, Wilmking, Martin, Wofsy, Steven C., Zyrianov, Vyacheslav

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Genetic determinants of common epilepsies: a meta-analysis of genome-wide association studies von Anon

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Molecular Genetics and Prognosis in Younger Patients with Chronic Lymphocytic Leukemia (CLL) von Helbig, Daniel, Abu Zeinah, Ghaith, Bhavsar, Erica B, Furman, Richard R., Allan, John N.

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