Electrostatic ion cyclotron waves driven by a radial electric field von Niekerk, E G Van, Krumm, P H, Alport, M J

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The electrostatic ion-cyclotron instability-a two-dimensional potential relaxation instability von Popa, G, Schrittwieser, R, Rasmussen, J J, Krumm, P H

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Filamental quenching of the current-driven ion-cyclotron instability von Cartier, S. L., Dangelo, N., Merlino, R. L., Krumm, P. H.

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The role of the electron-collecting disc in the excitation of electrostatic ion-cyclotron waves von Krumm, P H, Alport, M J

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The light in Maxwell's wave equation von Krumm, H P, Scourfield, M W J

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Molecular Genetic Anatomy and Risk Profile of Hirschsprung’s Disease von Tilghman, Joseph M, Ling, Albee Y, Turner, Tychele N, Sosa, Maria X, Krumm, Niklas, Chatterjee, Sumantra, Kapoor, Ashish, Coe, Bradley P, Nguyen, Khanh-Dung H, Gupta, Namrata, Gabriel, Stacey, Eichler, Evan E, Berrios, Courtney, Chakravarti, Aravinda

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On the Filamental Quenching of the Current-Driven Ion-Cyclotron Instability von Cartier,S L, D'Angelo,N, Krumm,P H, Merlino,R L

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Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations von O’Roak, Brian J., Vives, Laura, Girirajan, Santhosh, Karakoc, Emre, Krumm, Niklas, Coe, Bradley P., Levy, Roie, Ko, Arthur, Lee, Choli, Smith, Joshua D., Turner, Emily H., Stanaway, Ian B., Vernot, Benjamin, Malig, Maika, Baker, Carl, Reilly, Beau, Akey, Joshua M., Borenstein, Elhanan, Rieder, Mark J., Nickerson, Deborah A., Bernier, Raphael, Shendure, Jay, Eichler, Evan E.

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Copy number variation detection and genotyping from exome sequence data von Krumm, Niklas, Sudmant, Peter H, Ko, Arthur, O'Roak, Brian J, Malig, Maika, Coe, Bradley P, Quinlan, Aaron R, Nickerson, Deborah A, Eichler, Evan E

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Precision therapeutic targets for COVID-19 von Krumm, Zachary A, Lloyd, Grace M, Francis, Connor P, Nasif, Lith H, Mitchell, Duane A, Golde, Todd E, Giasson, Benoit I, Xia, Yuxing

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Multiplex Targeted Sequencing Identifies Recurrently Mutated Genes in Autism Spectrum Disorders von O'Roak, Brian J., Vives, Laura, Fu, Wenqing, Egertson, Jarrett D., Stanaway, Ian B., Phelps, Ian G., Carvill, Gemma, Kumar, Akash, Lee, Choli, Ankenman, Katy, Munson, Jeff, Hiatt, Joseph B., Turner, Emily H., Levy, Roie, O'Day, Diana R., Krumm, Niklas, Coe, Bradley P., Martin, Beth K., Borenstein, Elhanan, Nickerson, Deborah A., Mefford, Heather C., Doherty, Dan, Akey, Joshua M., Bernier, Raphael, Eichler, Evan E., Shendure, Jay

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A Higher Mutational Burden in Females Supports a “Female Protective Model” in Neurodevelopmental Disorders von Jacquemont, Sébastien, Coe, Bradley P., Hersch, Micha, Duyzend, Michael H., Krumm, Niklas, Bergmann, Sven, Beckmann, Jacques S., Rosenfeld, Jill A., Eichler, Evan E.

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BNT162b vaccines protect rhesus macaques from SARS-CoV-2 von Vogel, Annette B., Kanevsky, Isis, Che, Ye, Swanson, Kena A., Muik, Alexander, Vormehr, Mathias, Kranz, Lena M., Walzer, Kerstin C., Hein, Stephanie, Güler, Alptekin, Loschko, Jakob, Maddur, Mohan S., Ota-Setlik, Ayuko, Tompkins, Kristin, Cole, Journey, Lui, Bonny G., Ziegenhals, Thomas, Plaschke, Arianne, Eisel, David, Dany, Sarah C., Fesser, Stephanie, Erbar, Stephanie, Bates, Ferdia, Schneider, Diana, Jesionek, Bernadette, Sänger, Bianca, Wallisch, Ann-Kathrin, Feuchter, Yvonne, Junginger, Hanna, Krumm, Stefanie A., Heinen, André P., Adams-Quack, Petra, Schlereth, Julia, Schille, Stefan, Kröner, Christoph, de la Caridad Güimil Garcia, Ramón, Hiller, Thomas, Fischer, Leyla, Sellers, Rani S., Choudhary, Shambhunath, Gonzalez, Olga, Vascotto, Fulvia, Gutman, Matthew R., Fontenot, Jane A., Hall-Ursone, Shannan, Brasky, Kathleen, Griffor, Matthew C., Han, Seungil, Su, Andreas A. H., Lees, Joshua A., Nedoma, Nicole L., Mashalidis, Ellene H., Sahasrabudhe, Parag V., Tan, Charles Y., Pavliakova, Danka, Singh, Guy, Fontes-Garfias, Camila, Pride, Michael, Scully, Ingrid L., Ciolino, Tara, Obregon, Jennifer, Gazi, Michal, Carrion, Ricardo, Alfson, Kendra J., Kalina, Warren V., Kaushal, Deepak, Shi, Pei-Yong, Klamp, Thorsten, Rosenbaum, Corinna, Kuhn, Andreas N., Türeci, Özlem, Dormitzer, Philip R., Jansen, Kathrin U., Sahin, Ugur

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Refining analyses of copy number variation identifies specific genes associated with developmental delay von Coe, Bradley P, Witherspoon, Kali, Rosenfeld, Jill A, van Bon, Bregje W M, Vulto-van Silfhout, Anneke T, Bosco, Paolo, Friend, Kathryn L, Baker, Carl, Buono, Serafino, Vissers, Lisenka E L M, Schuurs-Hoeijmakers, Janneke H, Hoischen, Alex, Pfundt, Rolph, Krumm, Nik, Carvill, Gemma L, Li, Deana, Amaral, David, Brown, Natasha, Lockhart, Paul J, Scheffer, Ingrid E, Alberti, Antonino, Shaw, Marie, Pettinato, Rosa, Tervo, Raymond, de Leeuw, Nicole, Reijnders, Margot R F, Torchia, Beth S, Peeters, Hilde, Thompson, Elizabeth, O'Roak, Brian J, Fichera, Marco, Hehir-Kwa, Jayne Y, Shendure, Jay, Mefford, Heather C, Haan, Eric, Gécz, Jozef, de Vries, Bert B A, Romano, Corrado, Eichler, Evan E

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Assessing the Effect of Class I Histone Deacetylase Activity on DNA Double-Strand Break Repair by Homologous Recombination von Krumm, Andrea, Roos, Wynand P.

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MicroRNA 33A controls SREBP-2 and LXR dependent regulation of the LDL receptor pathway von Ramachandran, V., Modder, M., Zhang, L., Krumm, C., In Het Panhuis, W., Schönke, M., Lu, Y.-C., Hla, T., Lee, A.-H., Rensen, P., Tontonoz, P., Kooijman, S., Najafi-Shoushtari, H.

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Design and operation of FACT – the first G-APD Cherenkov telescope von Anderhub, H, Backes, M, Biland, A, Boccone, V, Braun, I, Bretz, T, Buß, J, Cadoux, F, Commichau, V, Djambazov, L, Dorner, D, Einecke, S, Eisenacher, D, Gendotti, A, Grimm, O, Gunten, H von, Haller, C, Hildebrand, D, Horisberger, U, Huber, B, Kim, K -S, Knoetig, M L, Köhne, J -H, Krähenbühl, T, Krumm, B, Lee, M, Lorenz, E, Lustermann, W, Lyard, E, Mannheim, K, Meharga, M, Meier, K, Montaruli, T, Neise, D, Nessi-Tedaldi, F, Overkemping, A -K, Paravac, A, Pauss, F, Renker, D, Rhode, W, Ribordy, M, Röser, U, Stucki, J -P, Schneider, J, Steinbring, T, Temme, F, Thaele, J, Tobler, S, Viertel, G, Vogler, P, Walter, R, Warda, K, Weitzel, Q, Zänglein, M

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Mechanisms underlying the health benefits of intermittent hypoxia conditioning von Burtscher, J, Citherlet, T, Camacho-Cardenosa, A, Camacho-Cardenosa, M, Raberin, A, Krumm, B, Hohenauer, E, Egg, M, Lichtblau, M, Müller, J, Rybnikova, EA, Gatterer, H, Debevec, T, Baillieul, S, Manferdelli, G, Behrendt, T, Schega, L, Ehrenreich, H, Millet, GP, Gassmann, M, Schwarzer, C, Glazachev, O, Girard, O, Lalande, S, Hamlin, Michael, Samaja, M, Hüfner, K, Burtscher, M, Panza, G, Mallet, RT

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MORC1 exhibits cross-species differential methylation in association with early life stress as well as genome-wide association with MDD von Nieratschker, V, Massart, R, Gilles, M, Luoni, A, Suderman, M J, Krumm, B, Meier, S, Witt, S H, Nöthen, M M, Suomi, S J, Peus, V, Scharnholz, B, Dukal, H, Hohmeyer, C, Wolf, I A-C, Cirulli, F, Gass, P, Sütterlin, M W, Filsinger, B, Laucht, M, Riva, M A, Rietschel, M, Deuschle, M, Szyf, M

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Exome Sequencing and Genome-Wide Linkage Analysis in 17 Families Illustrate the Complex Contribution of TTN Truncating Variants to Dilated Cardiomyopathy von Norton, Nadine, Li, Duanxiang, Rampersaud, Evadnie, Morales, Ana, Martin, Eden R, Zuchner, Stephan, Guo, Shengru, Gonzalez, Michael, Hedges, Dale J, Robertson, Peggy D, Krumm, Niklas, Nickerson, Deborah A, Hershberger, Ray E

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