Stability-Indicating Assay for Tolmetin Sodium in Solid Dosage Forms von Daly, Katherine F., Janicki, Casimir A.

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Closed-loop neuromodulation in an individual with treatment-resistant depression von Scangos, Katherine W., Khambhati, Ankit N., Daly, Patrick M., Makhoul, Ghassan S., Sugrue, Leo P., Zamanian, Hashem, Liu, Tony X., Rao, Vikram R., Sellers, Kristin K., Dawes, Heather E., Starr, Philip A., Krystal, Andrew D., Chang, Edward F.

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Schizophrenia risk from complex variation of complement component 4 von Sekar, Aswin, Bialas, Allison R., de Rivera, Heather, Davis, Avery, Hammond, Timothy R., Kamitaki, Nolan, Tooley, Katherine, Presumey, Jessy, Baum, Matthew, Van Doren, Vanessa, Genovese, Giulio, Rose, Samuel A., Handsaker, Robert E., Daly, Mark J., Carroll, Michael C., Stevens, Beth, McCarroll, Steven A.

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Depression pathophysiology, risk prediction of recurrence and comorbid psychiatric disorders using genome-wide analyses von Als, Thomas D., Kurki, Mitja I., Grove, Jakob, Voloudakis, Georgios, Therrien, Karen, Tasanko, Elisa, Nielsen, Trine Tollerup, Naamanka, Joonas, Veerapen, Kumar, Levey, Daniel F., Bendl, Jaroslav, Bybjerg-Grauholm, Jonas, Zeng, Biao, Demontis, Ditte, Rosengren, Anders, Athanasiadis, Georgios, Bækved-Hansen, Marie, Qvist, Per, Bragi Walters, G., Thorgeirsson, Thorgeir, Stefánsson, Hreinn, Musliner, Katherine L., Rajagopal, Veera M., Farajzadeh, Leila, Thirstrup, Janne, Vilhjálmsson, Bjarni J., McGrath, John J., Mattheisen, Manuel, Meier, Sandra, Agerbo, Esben, Stefánsson, Kári, Nordentoft, Merete, Werge, Thomas, Hougaard, David M., Mortensen, Preben B., Stein, Murray B., Gelernter, Joel, Hovatta, Iiris, Roussos, Panos, Daly, Mark J., Mors, Ole, Palotie, Aarno, Børglum, Anders D.

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Mislocalization of protein kinase A drives pathology in Cushing’s syndrome von Omar, Mitchell H., Byrne, Dominic P., Jones, Kiana N., Lakey, Tyler M., Collins, Kerrie B., Lee, Kyung-Soon, Daly, Leonard A., Forbush, Katherine A., Lau, Ho-Tak, Golkowski, Martin, McKnight, G. Stanley, Breault, David T., Lefrançois-Martinez, Anne-Marie, Martinez, Antoine, Eyers, Claire E., Baird, Geoffrey S., Ong, Shao-En, Smith, F. Donelson, Eyers, Patrick A., Scott, John D.

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A communal catalogue reveals Earth’s multiscale microbial diversity von Thompson, Luke R., Sanders, Jon G., McDonald, Daniel, Amir, Amnon, Ladau, Joshua, Locey, Kenneth J., Prill, Robert J., Tripathi, Anupriya, Gibbons, Sean M., Ackermann, Gail, Navas-Molina, Jose A., Janssen, Stefan, Kopylova, Evguenia, Vázquez-Baeza, Yoshiki, González, Antonio, Morton, James T., Mirarab, Siavash, Zech Xu, Zhenjiang, Jiang, Lingjing, Haroon, Mohamed F., Kanbar, Jad, Zhu, Qiyun, Jin Song, Se, Kosciolek, Tomasz, Bokulich, Nicholas A., Lefler, Joshua, Brislawn, Colin J., Humphrey, Gregory, Owens, Sarah M., Hampton-Marcell, Jarrad, Berg-Lyons, Donna, McKenzie, Valerie, Fierer, Noah, Fuhrman, Jed A., Clauset, Aaron, Stevens, Rick L., Shade, Ashley, Pollard, Katherine S., Goodwin, Kelly D., Jansson, Janet K., Gilbert, Jack A., Knight, Rob

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A Homozygous Mutation in KCTD7 Links Neuronal Ceroid Lipofuscinosis to the Ubiquitin-Proteasome System von Staropoli, John F., Karaa, Amel, Lim, Elaine T., Kirby, Andrew, Elbalalesy, Naser, Romansky, Stephen G., Leydiker, Karen B., Coppel, Scott H., Barone, Rosemary, Xin, Winnie, MacDonald, Marcy E., Abdenur, Jose E., Daly, Mark J., Sims, Katherine B., Cotman, Susan L.

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Sequencing Chromosomal Abnormalities Reveals Neurodevelopmental Loci that Confer Risk across Diagnostic Boundaries von Talkowski, Michael E., Rosenfeld, Jill A., Blumenthal, Ian, Pillalamarri, Vamsee, Chiang, Colby, Heilbut, Adrian, Ernst, Carl, Hanscom, Carrie, Rossin, Elizabeth, Lindgren, Amelia M., Pereira, Shahrin, Ruderfer, Douglas, Kirby, Andrew, Ripke, Stephan, Harris, David J., Lee, Ji-Hyun, Ha, Kyungsoo, Kim, Hyung-Goo, Solomon, Benjamin D., Gropman, Andrea L., Lucente, Diane, Sims, Katherine, Ohsumi, Toshiro K., Borowsky, Mark L., Loranger, Stephanie, Quade, Bradley, Lage, Kasper, Miles, Judith, Wu, Bai-Lin, Shen, Yiping, Neale, Benjamin, Shaffer, Lisa G., Daly, Mark J., Morton, Cynthia C., Gusella, James F.

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A Randomized Trial of Erythropoietin for Neuroprotection in Preterm Infants von Juul, Sandra E, Comstock, Bryan A, Wadhawan, Rajan, Mayock, Dennis E, Courtney, Sherry E, Robinson, Tonya, Ahmad, Kaashif A, Bendel-Stenzel, Ellen, Baserga, Mariana, LaGamma, Edmund F, Downey, L. Corbin, Rao, Raghavendra, Fahim, Nancy, Lampland, Andrea, Frantz III, Ivan D, Khan, Janine Y, Weiss, Michael, Gilmore, Maureen M, Ohls, Robin K, Srinivasan, Nishant, Perez, Jorge E, McKay, Victor, Vu, Phuong T, Lowe, Jean, Kuban, Karl, O’Shea, T. Michael, Hartman, Adam L, Heagerty, Patrick J

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Pervasive sharing of genetic effects in autoimmune disease von Cotsapas, Chris, Voight, Benjamin F, Rossin, Elizabeth, Lage, Kasper, Neale, Benjamin M, Wallace, Chris, Abecasis, Gonçalo R, Barrett, Jeffrey C, Behrens, Timothy, Cho, Judy, De Jager, Philip L, Elder, James T, Graham, Robert R, Gregersen, Peter, Klareskog, Lars, Siminovitch, Katherine A, van Heel, David A, Wijmenga, Cisca, Worthington, Jane, Todd, John A, Hafler, David A, Rich, Stephen S, Daly, Mark J

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Effects of clinical and environmental factors on bronchoalveolar antibody responses to Pneumocystis jirovecii: A prospective cohort study of HIV+ patients von Blount, Robert J, Daly, Kieran R, Fong, Serena, Chang, Emily, Grieco, Katherine, Greene, Meredith, Stone, Stephen, Balmes, John, Miller, Robert F, Walzer, Peter D, Huang, Laurence

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In vivo genotoxicity assessment of N‐(‐9 acridinyl)‐b‐alanine hydrochloride (S‐300) using a validated Pig‐a mutagenesis assay von North, Anne, Ling, Katherine, Ricaud, Guillaume, Stankowski, Leon F., Daly, Jennifer A., Bentow, Stanley, Corash, Laurence, Benjamin, Richard J., Mufti, Nina

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Distributed Subnetworks of Depression Defined by Direct Intracranial Neurophysiology von Scangos, Katherine Wilson, Khambhati, Ankit N., Daly, Patrick M., Owen, Lucy W., Manning, Jeremy R., Ambrose, Josiah B., Austin, Everett, Dawes, Heather E., Krystal, Andrew D., Chang, Edward F.

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Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing von Sifrim, Alejandro, Hitz, Marc-Phillip, Wilsdon, Anna, Breckpot, Jeroen, Turki, Saeed H Al, Thienpont, Bernard, McRae, Jeremy, Fitzgerald, Tomas W, Singh, Tarjinder, Swaminathan, Ganesh Jawahar, Prigmore, Elena, Rajan, Diana, Abdul-Khaliq, Hashim, Banka, Siddharth, Bauer, Ulrike M M, Bentham, Jamie, Berger, Felix, Bhattacharya, Shoumo, Bu'Lock, Frances, Canham, Natalie, Colgiu, Irina-Gabriela, Cosgrove, Catherine, Cox, Helen, Daehnert, Ingo, Daly, Allan, Danesh, John, Fryer, Alan, Gewillig, Marc, Hobson, Emma, Hoff, Kirstin, Homfray, Tessa, Kahlert, Anne-Karin, Ketley, Ami, Kramer, Hans-Heiner, Lachlan, Katherine, Lampe, Anne Katrin, Louw, Jacoba J, Manickara, Ashok Kumar, Manase, Dorin, McCarthy, Karen P, Metcalfe, Kay, Moore, Carmel, Newbury-Ecob, Ruth, Omer, Seham Osman, Ouwehand, Willem H, Park, Soo-Mi, Parker, Michael J, Pickardt, Thomas, Pollard, Martin O, Robert, Leema, Roberts, David J, Sambrook, Jennifer, Setchfield, Kerry, Stiller, Brigitte, Thornborough, Chris, Toka, Okan, Watkins, Hugh, Williams, Denise, Wright, Michael, Mital, Seema, Daubeney, Piers E F, Keavney, Bernard, Goodship, Judith, Abu-Sulaiman, Riyadh Mahdi, Klaassen, Sabine, Wright, Caroline F, Firth, Helen V, Barrett, Jeffrey C, Devriendt, Koenraad, FitzPatrick, David R, Brook, J David, Hurles, Matthew E

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Expansion of the global RNA virome reveals diverse clades of bacteriophages von Neri, Uri, Wolf, Yuri I., Roux, Simon, Camargo, Antonio Pedro, Lee, Benjamin, Kazlauskas, Darius, Chen, I. Min, Zeigler Allen, Lisa, Paez-Espino, David, Bryant, Donald A., Bhaya, Devaki, Narrowe, Adrienne B., Sczyrba, Alexander, Kohler, Annegret, Séguin, Armand, Shade, Ashley, Campbell, Barbara J., Lindahl, Björn D., Reese, Brandi Kiel, Roque, Breanna M., DeRito, Chris, Averill, Colin, Cullen, Daniel, Walsh, David A., Ward, David M., Wu, Dongying, Eloe-Fadrosh, Emiley, Brodie, Eoin L., Young, Erica B., Lilleskov, Erik A., Castillo, Federico J., Martin, Francis M., LeCleir, Gary R., Attwood, Graeme T., Cadillo-Quiroz, Hinsby, Simon, Holly M., Hewson, Ian, Grigoriev, Igor V., Tiedje, James M., Jansson, Janet K., Lee, Janey, VanderGheynst, Jean S., Bowman, Jeff S., Blanchard, Jeffrey L., Bowen, Jennifer L., Xu, Jiangbing, Banfield, Jillian F., Deming, Jody W., Kostka, Joel E., Gladden, John M., Sharpe, Joshua, McMahon, Katherine D., Bidle, Kay D., Wrighton, Kelly C., Thamatrakoln, Kimberlee, Nusslein, Klaus, Meredith, Laura K., Ramirez, Lucia, Buee, Marc, Huntemann, Marcel, Kalyuzhnaya, Marina G., Waldrop, Mark P., Sullivan, Matthew B., Vega, Michael A., O’Malley, Michelle A., Medina, Monica, Gilbert, Naomi E., Delherbe, Nathalie, Mason, Olivia U., Dijkstra, Paul, Chuckran, Peter F., Baldrian, Petr, Constant, Philippe, Stepanauskas, Ramunas, Daly, Rebecca A., Lamendella, Regina, Gruninger, Robert J., McKay, Robert M., Hylander, Samuel, Lebeis, Sarah L., Esser, Sarah P., Acinas, Silvia G., Wilhelm, Steven S., Singer, Steven W., Tringe, Susannah S., Woyke, Tanja, Bell, Terrence H., Mock, Thomas, McAllister, Tim, Thiel, Vera, Denef, Vincent J., Liu, Wen-Tso, Martens-Habbena, Willm, Cooper, Zachary S., Wang, Zhong, Krupovic, Mart, Dolja, Valerian V., Kyrpides, Nikos C., Koonin, Eugene V., Gophna, Uri

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Time-resolved multi-omics reveals diverse metabolic strategies of Salmonella during diet-induced inflammation von Kokkinias, Katherine, Sabag-Daigle, Anice, Kim, Yongseok, Leleiwi, Ikaia, Shaffer, Michael, Kevorkian, Richard, Daly, Rebecca A, Wysocki, Vicki H, Borton, Mikayla A, Ahmer, Brian M M, Wrighton, Kelly C

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Exposing new taxonomic variation with inflammation - a murine model-specific genome database for gut microbiome researchers von Leleiwi, Ikaia, Rodriguez-Ramos, Josué, Shaffer, Michael, Sabag-Daigle, Anice, Kokkinias, Katherine, Flynn, Rory M, Daly, Rebecca A, Kop, Linnea F M, Solden, Lindsey M, Ahmer, Brian M M, Borton, Mikayla A, Wrighton, Kelly C

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Aortic valve replacement in patients with amyloidosis von Java, Amit P., Greason, Kevin L., Dispenzieri, Angela, Grogan, Martha, King, Katherine S., Maleszewski, Joseph J., Daly, Richard C., Eleid, Mackram F., Pochettino, Alberto, Schaff, Hartzell V.

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Common variants in WFS1 confer risk of type 2 diabetes von Sandhu, Manjinder S, Barroso, Inês, Weedon, Michael N, Fawcett, Katherine A, Wasson, Jon, Debenham, Sally L, Daly, Allan, Lango, Hana, Frayling, Timothy M, Neumann, Rosalind J, Sherva, Richard, Blech, Ilana, Pharoah, Paul D, Palmer, Colin N A, Kimber, Charlotte, Tavendale, Roger, Morris, Andrew D, McCarthy, Mark I, Walker, Mark, Hitman, Graham, Glaser, Benjamin, Permutt, M Alan, Hattersley, Andrew T, Wareham, Nicholas J

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Disruption of Neurexin 1 Associated with Autism Spectrum Disorder von Kim, Hyung-Goo, Kishikawa, Shotaro, Higgins, Anne W., Seong, Ihn-Sik, Donovan, Diana J., Shen, Yiping, Lally, Eric, Weiss, Lauren A., Najm, Juliane, Kutsche, Kerstin, Descartes, Maria, Holt, Lynn, Braddock, Stephen, Troxell, Robin, Kaplan, Lee, Volkmar, Fred, Klin, Ami, Tsatsanis, Katherine, Harris, David J., Noens, Ilse, Pauls, David L., Daly, Mark J., MacDonald, Marcy E., Morton, Cynthia C., Quade, Bradley J., Gusella, James F.

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