The MAGPI survey: orbital distributions, intrinsic shapes, and mass profiles for MAGPI-like eagle galaxies using Schwarzschild dynamical models von Santucci, Giulia, Lagos, Claudia Del P, Harborne, Katherine E, Derkenne, Caro, Poci, Adriano, Thater, Sabine, McDermid, Richard M, Mendel, J Trevor, Wisnioski, Emily, Croom, Scott M, Ferré-Mateu, Anna, Muller, Eric G M, van de Sande, Jesse, Sharma, Gauri, Sweet, Sarah M, Tsukui, Takafumi, Valenzuela, Lucas M, van de Ven, Glenn, Zafar, Tayyaba

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TPCNet : Representation learning for H  i mapping von Nguyen, Hiep, Tang, Haiyang, Alger, Matthew, Marchal, Antoine, Muller, Eric G M, Ong, Cheng Soon, McClure-Griffiths, N M

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TPCNet: Representation learning for HI mapping von Nguyen, Hiep, Tang, Haiyang, Alger, Matthew, Marchal, Antoine, Muller, Eric G M, Ong, Cheng Soon, McClure-Griffiths, N M

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The MAGPI Survey: Orbital distributions, intrinsic shapes, and mass profiles for MAGPI-like Eagle galaxies using Schwarzschild dynamical models von Santucci, Giulia, Lagos, Claudia Del P, Harborne, Katherine E, Derkenne, Caro, Poci, Adriano, Thater, Sabine, McDermid, Richard M, Mendel, J. Trevor, Wisnioski, Emily, Croom, Scott M, Ferré-Mateu, Anna, Muller, Eric G. M, van de Sande, Jesse, Sharma, Gauri, Sweet, Sarah M, Tsukui, Takafumi, Valenzuela, Lucas M, van de Ven, Glenn, Zafar, Tayyaba

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The MAGPI Survey: Orbital distributions, intrinsic shapes, and mass profiles for MAGPI-like Eagle galaxies using Schwarzschild dynamical models von Santucci, Giulia, Claudia Del P Lagos, Harborne, Katherine E, Caro Derkenne, Poci, Adriano, Thater, Sabine, McDermid, Richard M, Mendel, J Trevor, Wisnioski, Emily, Croom, Scott M, Ferré-Mateu, Anna, Muller, Eric G M, van de Sande, Jesse, Sharma, Gauri, Sweet, Sarah M, Tsukui, Takafumi, Valenzuela, Lucas M, van de Ven, Glenn, Zafar, Tayyaba

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Frequent arousal from hibernation linked to severity of infection and mortality in bats with white-nose syndrome von Reeder, DeeAnn M, Frank, Craig L, Turner, Gregory G, Meteyer, Carol U, Kurta, Allen, Britzke, Eric R, Vodzak, Megan E, Darling, Scott R, Stihler, Craig W, Hicks, Alan C, Jacob, Roymon, Grieneisen, Laura E, Brownlee, Sarah A, Muller, Laura K, Blehert, David S

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Whole-genome and multisector exome sequencing of primary and post-treatment glioblastoma reveals patterns of tumor evolution von Kim, Hoon, Zheng, Siyuan, Amini, Seyed S, Virk, Selene M, Mikkelsen, Tom, Brat, Daniel J, Grimsby, Jonna, Sougnez, Carrie, Muller, Florian, Hu, Jian, Sloan, Andrew E, Cohen, Mark L, Van Meir, Erwin G, Scarpace, Lisa, Laird, Peter W, Weinstein, John N, Lander, Eric S, Gabriel, Stacey, Getz, Gad, Meyerson, Matthew, Chin, Lynda, Barnholtz-Sloan, Jill S, Verhaak, Roel G W

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De novo missense variants in exon 9 of SEPHS1 cause a neurodevelopmental condition with developmental delay, poor growth, hypotonia, and dysmorphic features von Mullegama, Sureni V., Kiernan, Kaitlyn A., Torti, Erin, Pavlovsky, Ethan, Tilton, Nicholas, Sekula, Austin, Gao, Hua, Alaimo, Joseph T., Engleman, Kendra, Rush, Eric T., Blocker, Karli, Dipple, Katrina M., Fettig, Veronica M., Hare, Heather, Glass, Ian, Grange, Dorothy K., Griffin, Michael, Phornphutkul, Chanika, Massingham, Lauren, Mehta, Lakshmi, Miller, Danny E., Thies, Jenny, Merritt, J Lawrence, Muller, Eric, Osmond, Matthew, Sawyer, Sarah L., Slaugh, Rachel, Hickey, Rachel E., Wolf, Barry, Choudhary, Sanjeev, Simonović, Miljan, Zhang, Yueqing, Palculict, Timothy Blake, Telegrafi, Aida, Carere, Deanna Alexis, Wentzensen, Ingrid M., Morrow, Michelle M., Monaghan, Kristin G., Yang, Jun, Juusola, Jane

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Salt-responsive gut commensal modulates TH17 axis and disease von Wilck, Nicola, Matus, Mariana G., Kearney, Sean M., Olesen, Scott W., Forslund, Kristoffer, Bartolomaeus, Hendrik, Haase, Stefanie, Mähler, Anja, Balogh, András, Markó, Lajos, Vvedenskaya, Olga, Kleiner, Friedrich H., Tsvetkov, Dmitry, Klug, Lars, Costea, Paul I., Sunagawa, Shinichi, Maier, Lisa, Rakova, Natalia, Schatz, Valentin, Neubert, Patrick, Frätzer, Christian, Krannich, Alexander, Gollasch, Maik, Grohme, Diana A., Côrte-Real, Beatriz F., Gerlach, Roman G., Basic, Marijana, Typas, Athanasios, Wu, Chuan, Titze, Jens M., Jantsch, Jonathan, Boschmann, Michael, Dechend, Ralf, Kleinewietfeld, Markus, Kempa, Stefan, Bork, Peer, Linker, Ralf A., Alm, Eric J., Müller, Dominik N.

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Integrative phenomics reveals insight into the structure of phenotypic diversity in budding yeast von Skelly, Daniel A, Merrihew, Gennifer E, Riffle, Michael, Connelly, Caitlin F, Kerr, Emily O, Johansson, Marnie, Jaschob, Daniel, Graczyk, Beth, Shulman, Nicholas J, Wakefield, Jon, Cooper, Sara J, Fields, Stanley, Noble, William S, Muller, Eric G D, Davis, Trisha N, Dunham, Maitreya J, Maccoss, Michael J, Akey, Joshua M

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Adverse Events Associated With PCSK9 Inhibitors: A Real‐World Experience von Gürgöze, Muhammed T., Muller‐Hansma, Annemarie H.G., Schreuder, Michelle M., Galema‐Boers, Annette M.H., Boersma, Eric, Roeters van Lennep, Jeanine E.

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Hydrocortisone plus Fludrocortisone for Adults with Septic Shock von Annane, Djillali, Renault, Alain, Brun-Buisson, Christian, Megarbane, Bruno, Quenot, Jean-Pierre, Siami, Shidasp, Cariou, Alain, Forceville, Xavier, Schwebel, Carole, Martin, Claude, Timsit, Jean-François, Misset, Benoît, Ali Benali, Mohamed, Colin, Gwenhael, Souweine, Bertrand, Asehnoune, Karim, Mercier, Emmanuelle, Chimot, Loïc, Charpentier, Claire, François, Bruno, Boulain, Thierry, Petitpas, Franck, Constantin, Jean-Michel, Dhonneur, Gilles, Baudin, François, Combes, Alain, Bohé, Julien, Loriferne, Jean-François, Amathieu, Roland, Cook, Fabrice, Slama, Michel, Leroy, Olivier, Capellier, Gilles, Dargent, Auguste, Hissem, Tarik, Maxime, Virginie, Bellissant, Eric

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ALG11‐CDG syndrome: Expanding the phenotype von Haanpää, Maria K., Ng, Bobby G., Gallant, Natalie M., Singh, Kathryn E., Brown, Candida, Kimonis, Virginia, Freeze, Hudson H., Muller, Eric A.

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Percutaneous Coronary Intervention versus Coronary-Artery Bypass Grafting for Severe Coronary Artery Disease von Serruys, Patrick W, Morice, Marie-Claude, Kappetein, A. Pieter, Colombo, Antonio, Holmes, David R, Mack, Michael J, Ståhle, Elisabeth, Feldman, Ted E, van den Brand, Marcel, Bass, Eric J, Van Dyck, Nic, Leadley, Katrin, Dawkins, Keith D, Mohr, Friedrich W

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Translational and HIF-1α-Dependent Metabolic Reprogramming Underpin Metabolic Plasticity and Responses to Kinase Inhibitors and Biguanides von Hulea, Laura, Gravel, Simon-Pierre, Morita, Masahiro, Cargnello, Marie, Uchenunu, Oro, Im, Young Kyuen, Lehuédé, Camille, Ma, Eric H., Leibovitch, Matthew, McLaughlan, Shannon, Blouin, Marie-José, Parisotto, Maxime, Papavasiliou, Vasilios, Lavoie, Cynthia, Larsson, Ola, Ohh, Michael, Ferreira, Tiago, Greenwood, Celia, Bridon, Gaëlle, Avizonis, Daina, Ferbeyre, Gerardo, Siegel, Peter, Jones, Russell G., Muller, William, Ursini-Siegel, Josie, St-Pierre, Julie, Pollak, Michael, Topisirovic, Ivan

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Identification of common genetic risk variants for autism spectrum disorder von Grove, Jakob, Ripke, Stephan, Als, Thomas D., Mattheisen, Manuel, Walters, Raymond K., Won, Hyejung, Pallesen, Jonatan, Agerbo, Esben, Andreassen, Ole A., Anney, Richard, Awashti, Swapnil, Belliveau, Rich, Bettella, Francesco, Buxbaum, Joseph D., Bybjerg-Grauholm, Jonas, Bækvad-Hansen, Marie, Cerrato, Felecia, Chambert, Kimberly, Christensen, Jane H., Churchhouse, Claire, Dellenvall, Karin, Demontis, Ditte, De Rubeis, Silvia, Devlin, Bernie, Djurovic, Srdjan, Dumont, Ashley L., Goldstein, Jacqueline I., Hansen, Christine S., Hauberg, Mads Engel, Hollegaard, Mads V., Hope, Sigrun, Howrigan, Daniel P., Huang, Hailiang, Hultman, Christina M., Klei, Lambertus, Maller, Julian, Martin, Joanna, Martin, Alicia R., Moran, Jennifer L., Nyegaard, Mette, Nærland, Terje, Palmer, Duncan S., Palotie, Aarno, Pedersen, Carsten Bøcker, Pedersen, Marianne Giørtz, dPoterba, Timothy, Poulsen, Jesper Buchhave, Pourcain, Beate St, Qvist, Per, Rehnström, Karola, Reichenberg, Abraham, Reichert, Jennifer, Robinson, Elise B., Roeder, Kathryn, Roussos, Panos, Saemundsen, Evald, Sandin, Sven, Satterstrom, F. Kyle, Davey Smith, George, Stefansson, Hreinn, Steinberg, Stacy, Stevens, Christine R., Sullivan, Patrick F., Turley, Patrick, Walters, G. Bragi, Xu, Xinyi, Stefansson, Kari, Geschwind, Daniel H., Nordentoft, Merete, Hougaard, David M., Werge, Thomas, Mors, Ole, Mortensen, Preben Bo, Neale, Benjamin M., Daly, Mark J., Børglum, Anders D.

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Global, Regional, and National Consumption of Sugar-Sweetened Beverages, Fruit Juices, and Milk: A Systematic Assessment of Beverage Intake in 187 Countries von Singh, Gitanjali M, Micha, Renata, Khatibzadeh, Shahab, Shi, Peilin, Lim, Stephen, Andrews, Kathryn G, Engell, Rebecca E, Ezzati, Majid, Mozaffarian, Dariush

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Recurrent FXYD2 p.Gly41Arg mutation in patients with isolated dominant hypomagnesaemia von de Baaij, Jeroen H F, Dorresteijn, Eiske M, Hennekam, Eric A M, Kamsteeg, Erik-Jan, Meijer, Rowdy, Dahan, Karin, Muller, Michelle, van den Dorpel, Marinus A, Bindels, René J M, Hoenderop, Joost G J, Devuyst, Olivier, Knoers, Nine V A M

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Quantum many-body interactions in digital oxide superlattices von Monkman, Eric J., Adamo, Carolina, Mundy, Julia A., Shai, Daniel E., Harter, John W., Shen, Dawei, Burganov, Bulat, Muller, David A., Schlom, Darrell G., Shen, Kyle M.

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De novo missense variants in exon 9 of SEPHS1 cause a neurodevelopmental condition with developmental delay, poor growth, hypotonia, and dysmorphic features von Mullegama, Sureni V., Kiernan, Kaitlyn A., Torti, Erin, Pavlovsky, Ethan, Tilton, Nicholas, Sekula, Austin, Gao, Hua, Alaimo, Joseph T., Engleman, Kendra, Rush, Eric T., Blocker, Karli, Dipple, Katrina M., Fettig, Veronica M., Hare, Heather, Glass, Ian, Grange, Dorothy K., Griffin, Michael, Phornphutkul, Chanika, Massingham, Lauren, Mehta, Lakshmi, Miller, Danny E., Thies, Jenny, Merritt, J Lawrence, Muller, Eric, Osmond, Matthew, Sawyer, Sarah L., Slaugh, Rachel, Hickey, Rachel E., Wolf, Barry, Choudhary, Sanjeev, Simonović, Miljan, Zhang, Yueqing, Palculict, Timothy Blake, Telegrafi, Aida, Carere, Deanna Alexis, Wentzensen, Ingrid M., Morrow, Michelle M., Monaghan, Kristin G., Juusola, Jane, Yang, Jun

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