696-P: Increasing CGM Use through Standardized Documentation von DELACEY, SEAN E., SULLIVAN, NAOMI J., FOGEL, NAOMI R.

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Use of Malachite Green-Loop Mediated Isothermal Amplification for Detection of Plasmodium spp. Parasites von Lucchi, Naomi W, Ljolje, Dragan, Silva-Flannery, Luciana, Udhayakumar, Venkatachalam

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Common Disease Is More Complex Than Implied by the Core Gene Omnigenic Model von Wray, Naomi R., Wijmenga, Cisca, Sullivan, Patrick F., Yang, Jian, Visscher, Peter M.

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Genome-wide meta-analysis of depression identifies 102 independent variants and highlights the importance of the prefrontal brain regions von Howard, David M., Adams, Mark J., Clarke, Toni-Kim, Hafferty, Jonathan D., Gibson, Jude, Shirali, Masoud, Coleman, Jonathan R. I., Hagenaars, Saskia P., Ward, Joey, Wigmore, Eleanor M., Alloza, Clara, Shen, Xueyi, Barbu, Miruna C., Xu, Eileen Y., Whalley, Heather C., Marioni, Riccardo E., Porteous, David J., Davies, Gail, Deary, Ian J., Hemani, Gibran, Berger, Klaus, Teismann, Henning, Rawal, Rajesh, Arolt, Volker, Baune, Bernhard T., Dannlowski, Udo, Domschke, Katharina, Tian, Chao, Hinds, David A., Trzaskowski, Maciej, Byrne, Enda M., Ripke, Stephan, Smith, Daniel J., Sullivan, Patrick F., Wray, Naomi R., Breen, Gerome, Lewis, Cathryn M., McIntosh, Andrew M.

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Contrasting genetic architectures of schizophrenia and other complex diseases using fast variance-components analysis von Loh, Po-Ru, Bhatia, Gaurav, Gusev, Alexander, Finucane, Hilary K, Bulik-Sullivan, Brendan K, Pollack, Samuela J, de Candia, Teresa R, Lee, Sang Hong, Wray, Naomi R, Kendler, Kenneth S, O'Donovan, Michael C, Neale, Benjamin M, Patterson, Nick, Price, Alkes L

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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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Estimating the proportion of variation in susceptibility to schizophrenia captured by common SNPs von Lee, S Hong, DeCandia, Teresa R, Ripke, Stephan, Yang, Jian, Sullivan, Patrick F, Goddard, Michael E, Keller, Matthew C, Visscher, Peter M, Wray, Naomi R

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Genome-wide association analysis identifies 13 new risk loci for schizophrenia von Ripke, Stephan, O'Dushlaine, Colm, Chambert, Kimberly, Moran, Jennifer L, Kähler, Anna K, Akterin, Susanne, Bergen, Sarah E, Collins, Ann L, Crowley, James J, Fromer, Menachem, Kim, Yunjung, Lee, Sang Hong, Magnusson, Patrik K E, Sanchez, Nick, Stahl, Eli A, Williams, Stephanie, Wray, Naomi R, Xia, Kai, Bettella, Francesco, Borglum, Anders D, Bulik-Sullivan, Brendan K, Cormican, Paul, Craddock, Nick, de Leeuw, Christiaan, Durmishi, Naser, Gill, Michael, Golimbet, Vera, Hamshere, Marian L, Holmans, Peter, Hougaard, David M, Kendler, Kenneth S, Lin, Kuang, Morris, Derek W, Mors, Ole, Mortensen, Preben B, Neale, Benjamin M, O'Neill, Francis A, Owen, Michael J, Milovancevic, Milica Pejovic, Posthuma, Danielle, Powell, John, Richards, Alexander L, Riley, Brien P, Ruderfer, Douglas, Rujescu, Dan, Sigurdsson, Engilbert, Silagadze, Teimuraz, Smit, August B, Stefansson, Hreinn, Steinberg, Stacy, Suvisaari, Jaana, Tosato, Sarah, Verhage, Matthijs, Walters, James T, Bramon, Elvira, Corvin, Aiden P, O'Donovan, Michael C, Stefansson, Kari, Scolnick, Edward, Purcell, Shaun, McCarroll, Steven A, Sklar, Pamela, Hultman, Christina M, Sullivan, Patrick F

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Genome-wide Association for Major Depression Through Age at Onset Stratification: Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium von Power, Robert A, Tansey, Katherine E, Buttenschøn, Henriette Nørmølle, Cohen-Woods, Sarah, Bigdeli, Tim, Hall, Lynsey S, Kutalik, Zoltán, Lee, S. Hong, Ripke, Stephan, Steinberg, Stacy, Teumer, Alexander, Viktorin, Alexander, Wray, Naomi R, Arolt, Volker, Baune, Bernard T, Boomsma, Dorret I, Børglum, Anders D, Byrne, Enda M, Castelao, Enrique, Craddock, Nick, Craig, Ian W, Dannlowski, Udo, Deary, Ian J, Degenhardt, Franziska, Forstner, Andreas J, Gordon, Scott D, Grabe, Hans J, Grove, Jakob, Hamilton, Steven P, Hayward, Caroline, Heath, Andrew C, Hocking, Lynne J, Homuth, Georg, Hottenga, Jouke J, Kloiber, Stefan, Krogh, Jesper, Landén, Mikael, Lang, Maren, Levinson, Douglas F, Lichtenstein, Paul, Lucae, Susanne, MacIntyre, Donald J, Madden, Pamela, Magnusson, Patrik K.E, Martin, Nicholas G, McIntosh, Andrew M, Middeldorp, Christel M, Milaneschi, Yuri, Montgomery, Grant W, Mors, Ole, Müller-Myhsok, Bertram, Nyholt, Dale R, Oskarsson, Hogni, Owen, Michael J, Padmanabhan, Sandosh, Penninx, Brenda W.J.H, Pergadia, Michele L, Porteous, David J, Potash, James B, Preisig, Martin, Rivera, Margarita, Shi, Jianxin, Shyn, Stanley I, Sigurdsson, Engilbert, Smit, Johannes H, Smith, Blair H, Stefansson, Hreinn, Stefansson, Kari, Strohmaier, Jana, Sullivan, Patrick F, Thomson, Pippa, Thorgeirsson, Thorgeir E, Van der Auwera, Sandra, Weissman, Myrna M, Breen, Gerome, Lewis, Cathryn M

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Oxytocin neurons enable social transmission of maternal behaviour von Carcea, Ioana, Caraballo, Naomi López, Marlin, Bianca J., Ooyama, Rumi, Riceberg, Justin S., Mendoza Navarro, Joyce M., Opendak, Maya, Diaz, Veronica E., Schuster, Luisa, Alvarado Torres, Maria I., Lethin, Harper, Ramos, Daniel, Minder, Jessica, Mendoza, Sebastian L., Bair-Marshall, Chloe J., Samadjopoulos, Grace H., Hidema, Shizu, Falkner, Annegret, Lin, Dayu, Mar, Adam, Wadghiri, Youssef Z., Nishimori, Katsuhiko, Kikusui, Takefumi, Mogi, Kazutaka, Sullivan, Regina M., Froemke, Robert C.

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Polygenic Risk Score, Parental Socioeconomic Status, Family History of Psychiatric Disorders, and the Risk for Schizophrenia: A Danish Population-Based Study and Meta-analysis von Agerbo, Esben, Sullivan, Patrick F, Vilhjálmsson, Bjarni J, Pedersen, Carsten B, Mors, Ole, Børglum, Anders D, Hougaard, David M, Hollegaard, Mads V, Meier, Sandra, Mattheisen, Manuel, Ripke, Stephan, Wray, Naomi R, Mortensen, Preben B

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Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression von Ripke, Stephan, Trzaskowski, Maciej, Byrne, Enda M., Adams, Mark J., Andlauer, Till M. F., Bacanu, Silviu-Alin, Beekman, Aartjan F. T., Bigdeli, Tim B., Binder, Elisabeth B., Blackwood, Douglas R. H., Bybjerg-Grauholm, Jonas, Castelao, Enrique, Couvy-Duchesne, Baptiste, Craddock, Nick, Deary, Ian J., Finucane, Hilary K., Forstner, Andreas J., Frank, Josef, Gill, Michael, Goes, Fernando S., Grove, Jakob, Hall, Lynsey S., Hannon, Eilis, Hansen, Thomas F., Hickie, Ian B., Hoffmann, Per, Horn, Carsten, Hougaard, David M., Hyde, Craig L., Jorgenson, Eric, Knowles, James A., Kraft, Julia, Krogh, Jesper, Kutalik, Zoltán, Lane, Jacqueline M., Li, Yihan, Li, Yun, Liu, Xiaoxiao, Lu, Leina, MacIntyre, Donald J., MacKinnon, Dean F., Maier, Robert M., Marchini, Jonathan, Mbarek, Hamdi, McGrath, Patrick, Mehta, Divya, Montgomery, Grant W., Nauck, Matthias, Nivard, Michel G., Pedersen, Carsten Bøcker, Posthuma, Danielle, Purcell, Shaun M., Quiroz, Jorge A., Saeed Mirza, Saira, Schoevers, Robert, Schulte, Eva C., Shi, Jianxin, Shyn, Stanley I., Smit, Johannes H., Smith, Daniel J., Stockmeier, Craig A., Teumer, Alexander, Thompson, Wesley, Thomson, Pippa A., Thorgeirsson, Thorgeir E., Tian, Chao, Treutlein, Jens, van Hemert, Albert M., Viktorin, Alexander, Visscher, Peter M., Wang, Yunpeng, Weinsheimer, Shantel Marie, Wellmann, Jürgen, Witt, Stephanie H., Wu, Yang, Xi, Hualin S., Yang, Jian, Zhang, Futao, Baune, Bernhard T., Berger, Klaus, de Geus, E. C. J., Domschke, Katharina, Esko, Tõnu, Hinds, David A., Li, Qingqin S., McIntosh, Andrew M., Metspalu, Andres, Mors, Ole, Müller-Myhsok, Bertram, O’Donovan, Michael C., Paciga, Sara A., Pedersen, Nancy L., Perlis, Roy H., Potash, James B., Schaefer, Catherine, Schulze, Thomas G., Uher, Rudolf, Völzke, Henry, Winslow, Ashley R., Børglum, Anders D.

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A Genetic Investigation of Sex Bias in the Prevalence of Attention-Deficit/Hyperactivity Disorder von Walters, Raymond K., Lee, S. Hong, Brikell, Isabell, Ghirardi, Laura, Larsson, Henrik, Lichtenstein, Paul, Bell, Robert K., Bryc, Katarzyna, Fontanillas, Pierre, Hromatka, Bethann S., Huber, Karen E., Litterman, Nadia K., McIntyre, Matthew H., Mountain, Joanna L., Pitts, Steven J., Vacic, Vladimir, Anney, Richard J.L., Vasquez, Alejandro Arias, Arranz, Maria Jesús, Banaschewski, Tobias, Banaschewski, Tobias J., Mortensen, Preben Bo, Børglum, Anders, Charach, Alice, Crosbie, Jennifer, Dalsgaard, Soeren, Demontis, Ditte, Dempfle, Astrid, Elia, Josephine, Faraone, Stephen V., Franke, Barbara, Freitag, Christine, Gelernter, Joel, Grevet, Eugenio, Haavik, Jan, Hakonarson, Hakon, Hawi, Ziarih, Hinney, Anke, Holmans, Peter, Ickowitz, Abel, Kent, Lindsey, Kittel-Schneider, Sarah, Langley, Kate, Lesch, Klaus-Peter, Loo, Sandra K., Martin, Joanna, Medland, Sarah E., Mulas, Fernando, Mulligan, Aisling, O’Donovan, Michael C., Oades, Robert D., Palmason, Haukur, Rhode, Luis, Roeyers, Herbert, Romanos, Marcel, Romanos, Jasmin, Rothenberger, Aribert, Schäfer, Helmut, Scherag, André, Schimmelmann, Benno G., Sergeant, Joseph, Smalley, Susan L., Sonuga-Barke, Edmund J.S., Steinhausen, Hans-Christoph, Sullivan, Patrick F., Todorov, Alexandre, Waldman, Irwin, Wang, Yufeng, Warnke, Andreas, Williams, Nigel, Witt, Stephanie H., Yang, Li, Agerbo, Esben, Belliveau, Rich, Børglum, Anders D., Chambert, Kimberly, Dalsgaard, Søren, Dumont, Ashley, Goldstein, Jacqueline, Grove, Jakob, Howrigan, Daniel P., Huang, Hailiang, Martin, Alicia R., Mattheisen, Manuel, Moran, Jennifer, Mors, Ole, Pallesen, Jonatan, Poterba, Timothy, Poulsen, Jesper Buchhave, Robinson, Elise B., Satterstrom, F. Kyle, Stevens, Christine, Turley, Patrick, Pedersen, Marianne Giørtz, Mors, Ole, Nordentoft, Merete, Hougaard, David M., Bybjerg-Grauholm, Jonas, Franke, Barbara, Neale, Benjamin M.

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Common polygenic variation contributes to risk of schizophrenia and bipolar disorder von Purcell, Shaun M, Wray, Naomi R, Stone, Jennifer L, Visscher, Peter M, O'Donovan, Michael C, Sullivan, Patrick F, Sklar, Pamela

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Genome-wide association study identifies 30 loci associated with bipolar disorder von Forstner, Andreas J., Wang, Yunpeng, Steinberg, Stacy, Trzaskowski, Maciej, Byrne, Enda M., Abbott, Liam, Akil, Huda, Anjorin, Adebayo, Antilla, Verneri, Barchas, Jack D., Belliveau, Richard, Pedersen, Carsten Bøcker, Bøen, Erlend, Budde, Monika, Bunney, William, Churchhouse, Claire, Clarke, Toni-Kim, Craig, David W., Cruceanu, Cristiana, Czerski, Piotr M., de Jong, Simone, Dumont, Ashley, Fischer, Sascha B., Frisén, Louise, Garnham, Julie, Giambartolomei, Claudia, Pedersen, Marianne Giørtz, Goldstein, Jaqueline, Gordon, Scott D., Green, Melissa J., Grove, Jakob, Heilbronner, Urs, Herms, Stefan, Huckins, Laura, Johnson, Jessica S., Juréus, Anders, Kandaswamy, Radhika, Knowles, James A., Lavebratt, Catharina, Lawrence, Jacob, Lee, Phil H., Levy, Shawn E., Li, Jun Z., Lucae, Susanne, Maaser, Anna, Maier, Wolfgang, McCarroll, Steve, McKay, James D., Meng, Fan, Montgomery, Grant W., Mühleisen, Thomas W., Nguyen, Hoang, Nievergelt, Caroline M., O’Donovan, Claire, Loohuis, Loes M. Olde, Ori, Anil P. S., Ösby, Urban, Perlis, Roy H., Pfennig, Andrea, Potash, James B., Reif, Andreas, Reinbold, Céline S., Rivera, Margarita, Roussos, Panos, Ryu, Euijung, Sánchez-Mora, Cristina, Slaney, Claire, Steffens, Michael, Strauss, John S., Zhang, Peng, Adolfsson, Rolf, Agartz, Ingrid, Alda, Martin, Baune, Bernhard T., Berrettini, Wade H., Biernacka, Joanna M., Blackwood, Douglas H. R., Børglum, Anders D., Corvin, Aiden, Hauser, Joanna, Kahn, René S., Lewis, Cathryn M., Li, Qingqin S., Melle, Ingrid, Morken, Gunnar, O’Donovan, Michael C., Paciga, Sara A., Pato, Carlos, Ramos-Quiroga, Josep Antoni, Ribasés, Marta, Rouleau, Guy A., Schulze, Thomas G., Sullivan, Patrick F., Vaaler, Arne E., Vincent, John B., Nurnberger, John I., Wray, Naomi R., Cichon, Sven, Scott, Laura J., Andreassen, Ole A.

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Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes von Ruderfer, Douglas M., Boocock, James, Stahl, Eli A., Charney, Alexander W., Ori, Anil P.S., Alliey-Rodriguez, Ney, Anjorin, Adebayo, Badner, Judith A., Band, Gavin, Bruggeman, Richard, Buccola, Nancy G., Bumpstead, Suzannah J., Casas, Juan P., Chan, Raymond C.K., Chen, Ronald Y.L., Collier, David A., Cormican, Paul, Craddock, Nicholas, Crowley, James J., Curtis, David, Dannlowski, Udo, Davidson, Michael, Demontis, Ditte, Dronov, Serge, Elvsashagen, Torbjorn, Etain, Bruno, Fan, Chun Chieh, Forty, Liz, Fraser, Christine, Garnham, Julie, Gill, Michael, Gillman, Matthew, Gratten, Jacob, Gwilliam, Rhian, Hammer, Christian, Hansen, Thomas, Henskens, Frans A., Jamain, Stephane, Jankowski, Janusz, Joa, Inge, Julia, Antonio, Kandaswamy, Radhika, Kavanagh, David, Keller, Matthew C., Khrunin, Andrey, Lee, Phil H., Legge, Sophie E., Lencz, Todd, Levinson, Douglas F., Levy, Shawn E., Li, Tao, Lin, Kuang, Macek, Milan, McCarley, Robert W., McGuffin, Peter, McInnis, Melvin G., Meijer, Carin J., Melegh, Bela, Mesholam-Gately, Raquelle I., Myin-Germeys, Inez, Nicodemus, Kristin K., Nimgaonkar, Vishwajit, Nordin, Annelie, Nöthen, Markus M., Van Os, Jim, Owen, Michael J., Palmer, Colin N.A., Palotie, Aarno, Papadimitriou, George N., Pato, Michele T., Perlis, Roy H., Petryshen, Tracey L., Plomin, Robert, Potash, James B., Powell, John, Ramos-Quiroga, Josep Antoni, Rautanen, Anna, Reichenberg, Abraham, Ribases, Marta, Rice, John P., Richards, Alexander L., Ricketts, Michelle, Sanchez-Mora, Cristina, Sanders, Alan R., Schall, Ulrich, Serretti, Alessandro, Sham, Pak C., Straub, Richard E., Strauss, John S., Szatkiewicz, Jin P., Thompson, Robert C., Thorgeirsson, Thorgeir E., Treutlein, Jens, Vedder, Helmut, Wang, Qiang, Wu, Jing Qin, Sullivan, Patrick F., Wray, Naomi R., Sklar, Pamela, Kendler, Kenneth S.

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Conditional GWAS analysis to identify disorder-specific SNPs for psychiatric disorders von Byrne, Enda M., Zhu, Zhihong, Qi, Ting, Skene, Nathan G., Bryois, Julien, Pardinas, Antonio F., Stahl, Eli, Smoller, Jordan W., Rietschel, Marcella, Owen, Michael J., Walters, James T. R., O’Donovan, Michael C., McGrath, John G., Hjerling-Leffler, Jens, Sullivan, Patrick F., Goddard, Michael E., Visscher, Peter M., Yang, Jian, Wray, Naomi R.

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Evidence of causal effect of major depression on alcohol dependence: findings from the psychiatric genomics consortium von Polimanti, Renato, Peterson, Roseann E., Ong, Jue-Sheng, MacGregor, Stuart, Edwards, Alexis C., Clarke, Toni-Kim, Frank, Josef, Gerring, Zachary, Gillespie, Nathan A., Lind, Penelope A., Maes, Hermine H., Martin, Nicholas G., Mbarek, Hamdi, Medland, Sarah E., Streit, Fabian, Agrawal, Arpana, Edenberg, Howard J., Kendler, Kenneth S., Lewis, Cathryn M., Sullivan, Patrick F., Wray, Naomi R., Gelernter, Joel, Derks, Eske M.

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Still Searching for a Suitable Molecular Test to Detect Hidden Plasmodium Infection: A Proposal for Blood Donor Screening in Brazil von Lima, Giselle Fernandes Maciel de Castro, Lucchi, Naomi W, Silva-Flannery, Luciana, Macedo-de-Oliveira, Alexandre, Hristov, Angelica D, Inoue, Juliana, Costa-Nascimento, Maria de Jesus, Udhayakumar, Venkatachalam, Di Santi, Silvia M

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Relation of Brachial and Digital Measures of Vascular Function in the Community: The Framingham Heart Study von Hamburg, Naomi M, Palmisano, Joseph, Larson, Martin G, Sullivan, Lisa M, Lehman, Birgitta T, Vasan, Ramachandran S, Levy, Daniel, Mitchell, Gary F, Vita, Joseph A, Benjamin, Emelia J

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