A PRACTICABLE PROGRAM FOR THE ELIMINATION AND CONTROL OF CROSS CONNECTIONS by Mowry, C. W.

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2019 Annual Report of the American Association of Poison Control Centers' National Poison Data System (NPDS): 37th Annual Report by Gummin, David D, Mowry, James B, Beuhler, Michael C, Spyker, Daniel A, Brooks, Daniel E, Dibert, Katherine W, Rivers, Laura J, Pham, Nathaniel P T, Ryan, Mark L

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Genome-wide Association Studies in Ancestrally Diverse Populations: Opportunities, Methods, Pitfalls, and Recommendations by Peterson, Roseann E., Kuchenbaecker, Karoline, Walters, Raymond K., Chen, Chia-Yen, Popejoy, Alice B., Periyasamy, Sathish, Lam, Max, Iyegbe, Conrad, Strawbridge, Rona J., Brick, Leslie, Carey, Caitlin E., Martin, Alicia R., Meyers, Jacquelyn L., Su, Jinni, Chen, Junfang, Edwards, Alexis C., Kalungi, Allan, Koen, Nastassja, Majara, Lerato, Schwarz, Emanuel, Smoller, Jordan W., Stahl, Eli A., Sullivan, Patrick F., Vassos, Evangelos, Mowry, Bryan, Prieto, Miguel L., Cuellar-Barboza, Alfredo, Bigdeli, Tim B., Edenberg, Howard J., Huang, Hailiang, Duncan, Laramie E.

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Copy Number Variants in Schizophrenia: Confirmation of Five Previous Findings and New Evidence for 3q29 Microdeletions and VIPR2 Duplications by Levinson, Douglas F., Duan, Jubao, Oh, Sang, Wang, Kai, Sanders, Alan R., Shi, Jianxin, Zhang, Nancy, Mowry, Bryan J., Olincy, Ann, Amin, Farooq, Cloninger, C. Robert, Silverman, Jeremy M., Buccola, Nancy G., Byerley, William F., Black, Donald W., Kendler, Kenneth S., Freedman, Robert, Dudbridge, Frank, Pe'er, Itsik, Hakonarson, Hakon, Bergen, Sarah E., Fanous, Ayman H., Holmans, Peter A., Gejman, Pablo V.

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Additive Genetic Variation in Schizophrenia Risk Is Shared by Populations of African and European Descent by de Candia, Teresa R., Lee, S. Hong, Yang, Jian, Browning, Brian L., Gejman, Pablo V., Levinson, Douglas F., Mowry, Bryan J., Hewitt, John K., Goddard, Michael E., O’Donovan, Michael C., Purcell, Shaun M., Posthuma, Danielle, Visscher, Peter M., Wray, Naomi R., Keller, Matthew C.

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A PLAN FOR WATER WORKS BETTERMENT WORK AS A PART OF A NATIONAL WORK RELIEF CONSTRUCTION PROGRAM by Eddy, Harrison P., Maltbie, M. R., Booth, George W., Mowry, C. W., Brush, Wm. W., Oram, Hugh P., Wolman, Abel, Newsom, Reeves J., Sherrerd, Morris R., Sawyer, Donald H., Fuller, George W., Marshall, R. C., Pratt, Arthur H., Pirnie, Malcolm

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Common variants on chromosome 6p22.1 are associated with schizophrenia by Shi, Jianxin, Levinson, Douglas F., Duan, Jubao, Sanders, Alan R., Zheng, Yonglan, Pe’er, Itsik, Dudbridge, Frank, Holmans, Peter A., Whittemore, Alice S., Mowry, Bryan J., Olincy, Ann, Amin, Farooq, Cloninger, C. Robert, Silverman, Jeremy M., Buccola, Nancy G., Byerley, William F., Black, Donald W., Crowe, Raymond R., Oksenberg, Jorge R., Mirel, Daniel B., Kendler, Kenneth S., Freedman, Robert, Gejman, Pablo V.

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Harnessing Real-World Data to Inform Decision-Making: Multiple Sclerosis Partners Advancing Technology and Health Solutions (MS PATHS) by Mowry, Ellen M, Bermel, Robert A, Williams, James R, Benzinger, Tammie L S, de Moor, Carl, Fisher, Elizabeth, Hersh, Carrie M, Hyland, Megan H, Izbudak, Izlem, Jones, Stephen E, Kieseier, Bernd C, Kitzler, Hagen H, Krupp, Lauren, Lui, Yvonne W, Montalban, Xavier, Naismith, Robert T, Nicholas, Jacqueline A, Pellegrini, Fabio, Rovira, Alex, Schulze, Maximilian, Tackenberg, Björn, Tintore, Mar, Tivarus, Madalina E, Ziemssen, Tjalf, Rudick, Richard A

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Genome-Wide Association Study of Clinical Dimensions of Schizophrenia: Polygenic Effect on Disorganized Symptoms by Fanous, Ayman H., Zhou, Baiyu, Aggen, Steven H., Bergen, Sarah E., Amdur, Richard L., Duan, Jubao, Sanders, Alan R., Shi, Jianxin, Mowry, Bryan J., Olincy, Ann, Amin, Farooq, Cloninger, C. Robert, Silverman, Jeremy M., Buccola, Nancy G., Byerley, William F., Black, Donald W., Freedman, Robert, Dudbridge, Frank, Holmans, Peter A., Ripke, Stephan, Gejman, Pablo V., Kendler, Kenneth S., Levinson, Douglas F.

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Uncovering the Hidden Risk Architecture of the Schizophrenias: Confirmation in Three Independent Genome-Wide Association Studies by Arnedo, Javier, Svrakic, Dragan M., del Val, Coral, Romero-Zaliz, Rocío, Hernández-Cuervo, Helena, Fanous, Ayman H., Pato, Michele T., Pato, Carlos N., de Erausquin, Gabriel A., Cloninger, C. Robert, Zwir, Igor

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The genetic architecture of the human cerebral cortex by Grasby, Katrina L, Jahanshad, Neda, Painter, Jodie N, Colodro-Conde, Lucía, Bralten, Janita, Hibar, Derrek P, Lind, Penelope A, Pizzagalli, Fabrizio, Ching, Christopher R K, McMahon, Mary Agnes B, Shatokhina, Natalia, Zsembik, Leo C P, Thomopoulos, Sophia I, Zhu, Alyssa H, Strike, Lachlan T, Agartz, Ingrid, Alhusaini, Saud, Almeida, Marcio A A, Alnæs, Dag, Amlien, Inge K, Andersson, Micael, Ard, Tyler, Armstrong, Nicola J, Ashley-Koch, Allison, Atkins, Joshua R, Bernard, Manon, Brouwer, Rachel M, Buimer, Elizabeth E L, Bülow, Robin, Bürger, Christian, Cannon, Dara M, Chakravarty, Mallar, Chen, Qiang, Cheung, Joshua W, Couvy-Duchesne, Baptiste, Dale, Anders M, Dalvie, Shareefa, de Araujo, Tânia K, de Zubicaray, Greig I, de Zwarte, Sonja M C, den Braber, Anouk, Doan, Nhat Trung, Dohm, Katharina, Ehrlich, Stefan, Engelbrecht, Hannah-Ruth, Erk, Susanne, Fan, Chun Chieh, Fedko, Iryna O, Foley, Sonya F, Ford, Judith M, Fukunaga, Masaki, Garrett, Melanie E, Ge, Tian, Giddaluru, Sudheer, Goldman, Aaron L, Green, Melissa J, Groenewold, Nynke A, Grotegerd, Dominik, Gurholt, Tiril P, Gutman, Boris A, Hansell, Narelle K, Harris, Mathew A, Harrison, Marc B, Haswell, Courtney C, Hauser, Michael, Herms, Stefan, Heslenfeld, Dirk J, Ho, New Fei, Hoehn, David, Hoffmann, Per, Holleran, Laurena, Hoogman, Martine, Hottenga, Jouke-Jan, Ikeda, Masashi, Janowitz, Deborah, Jansen, Iris E, Jia, Tianye, Jockwitz, Christiane, Kanai, Ryota, Karama, Sherif, Kasperaviciute, Dalia, Kaufmann, Tobias, Kelly, Sinead, Kikuchi, Masataka, Klein, Marieke, Knapp, Michael, Knodt, Annchen R, Krämer, Bernd, Lam, Max, Lancaster, Thomas M, Lee, Phil H, Lett, Tristram A, Lewis, Lindsay B, Lopes-Cendes, Iscia, Luciano, Michelle, Macciardi, Fabio, Marquand, Andre F, Mathias, Samuel R, Melzer, Tracy R, Milaneschi, Yuri

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SummaryAUC: a tool for evaluating the performance of polygenic risk prediction models in validation datasets with only summary level statistics by Song, Lei, Liu, Aiyi, Shi, Jianxin

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A case for toggle-aware compression for GPU systems by Pekhimenko, Gennady, Bolotin, Evgeny, Vijaykumar, Nandita, Mutlu, Onur, Mowry, Todd C., Keckler, Stephen W.

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Dissecting the Shared Genetic Architecture of Suicide Attempt, Psychiatric Disorders, and Known Risk Factors by Mullins, Niamh, Campos, Adrian I., Shabalin, Andrey, Hafferty, Jonathan D., Okazaki, Satoshi, Bohus, Martin, Johnson, Craig, Li, Dong, Magistretti, Pierre J., Van der Auwera, Sandra, Byrne, Enda M., Casas, Miguel, Jonsson, Lina, O’Donovan, Michael C., Pato, Carlos, Ramos-Quiroga, Josep Antoni, Sánchez-Mora, Cristina, Smeland, Olav B., Shannon Weickert, Cynthia, Hauser, Elizabeth R., Andlauer, Till F.M., Colodro-Conde, Lucía, Craddock, Nick, Derks, Eske M., Escott-Price, Valentina, Gordon, Scott D., Wu, Yang, Xi, Hualin S., Esko, Tõnu, Kohane, Isaac S., McGrath, Patrick, McGuffin, Peter, Middeldorp, Christel M., Milaneschi, Yuri, Nauck, Matthias, Nyholt, Dale R., Nöthen, Markus M., Pedersen, Nancy L., Pedersen, Carsten Bøcker, Steinberg, Stacy, Potash, James B., Schaefer, Catherine, Smoller, Jordan W., Völzke, Henry, Drange, Ole Kristian, Ikeda, Masashi, Panagiotaropoulou, Georgia, Sloofman, Laura G., Casas, Miquel, Ferrier, I. Nicol, Guzman-Parra, José, Kogevinas, Manolis, Lee, Phil H., Magnusson, Sigurdur H., Mühleisen, Thomas W., Sirignano, Lea, Adolfsson, Rolf, Alda, Martin, Catts, Stanley, Corvin, Aiden, Craddock, Nicholas, Fullerton, Janice M., Iwata, Nakao, Mayoral, Fermin, Mowry, Bryan, McQuillin, Andrew, Bulik, Cynthia M., Courtet, Philippe, Dina, Christian, Fichter, Manfred M., Föcker, Manuel, Hinney, Anke, Hübel, Christopher, Purves, Kirstin L., Rujescu, Dan, Scherer, Stephen W., Slagboom, P. Eline, Steen, Vidar W., Karhunen, Leila, Kennedy, Martin A., Tsitsika, Artemis, Yao, Shuyang, Schwarze, Cornelia E., Bohus, Martin, Crivelli, Silvia, Muralidhar, Sumitra, Huang, Grant, Moser, Jennifer, Brewer, Jessica V., Connor, Todd, Humphries, Donald E., Hauser, Elizabeth, Whittle, Jeffrey, Hammer, Kimberly, Godschalk, Michael, Sriram, Peruvemba, Liangpunsakul, Suthat, Wallbom, Agnes, Esko, Tõnu, Martin, Nicholas G.

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Genome-Wide Association Study of Male Sexual Orientation by Sanders, Alan R., Beecham, Gary W., Guo, Shengru, Dawood, Khytam, Rieger, Gerulf, Badner, Judith A., Gershon, Elliot S., Krishnappa, Ritesha S., Kolundzija, Alana B., Duan, Jubao, Gejman, Pablo V., Bailey, J. Michael, Martin, Eden R.

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No Significant Association of 14 Candidate Genes With Schizophrenia in a Large European Ancestry Sample: Implications for Psychiatric Genetics by Sanders, Alan R., Duan, Jubao, Levinson, Douglas F., Shi, Jianxin, He, Deli, Hou, Cuiping, Burrell, Gregory J., Rice, John P., Nertney, Deborah A., Olincy, Ann, Rozic, Pablo, Vinogradov, Sophia, Buccola, Nancy G., Mowry, Bryan J., Freedman, Robert, Amin, Farooq, Black, Donald W., Silverman, Jeremy M., Byerley, William F., Crowe, Raymond R., Cloninger, C. Robert, Martinez, Maria, Gejman, Pablo V.

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Racial-ethnic disparities in management and outcomes among children with type 1 diabetes by Willi, Steven M, Miller, Kellee M, DiMeglio, Linda A, Klingensmith, Georgeanna J, Simmons, Jill H, Tamborlane, William V, Nadeau, Kristen J, Kittelsrud, Julie M, Huckfeldt, Peter, Beck, Roy W, Lipman, Terri H

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The T1D Exchange Clinic Registry by Beck, Roy W, Tamborlane, William V, Bergenstal, Richard M, Miller, Kellee M, DuBose, Stephanie N, Hall, Callyn A, for the T1D Exchange Clinic Network

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Evaluation of Percutaneous Intradiscal Amniotic Suspension Allograft in a Rabbit Model of Intervertebral Disc Degeneration by Luo, Tianyi David, Vines, Jeremy B., Zabarsky, Zachary K., Mowry, Katie C., Marquez-Lara, Alejandro, Jinnah, Alexander H., Ma, Xue, Berwick, Benjamin W., Willey, Jeffrey S., Smith, Thomas L., Li, Zhongyu, O’Gara, Tadhg J.

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Severe Hypoglycemia and Diabetic Ketoacidosis in Adults With Type 1 Diabetes: Results From the T1D Exchange Clinic Registry by Weinstock, Ruth S, Xing, Dongyuan, Maahs, David M, Michels, Aaron, Rickels, Michael R, Peters, Anne L, Bergenstal, Richard M, Harris, Breanne, DuBose, Stephanie N, Miller, Kellee M, Beck, Roy W, for the T1D Exchange Clinic Network

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