Computation of the head-related transfer function via the fast multipole accelerated boundary element method and its spherical harmonic representation von GUMEROV, Nail A, O'DONOVAN, Adam E, DURAISWAMI, Ramani, ZOTKIN, Dmitry N

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Coupled Groups of g-Modes in a Sun with a Mixed Core von Wolff, Charles L, O’Donovan, Adam E

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Automatic matched filter recovery via the audio camera von O'Donovan, Adam E, Duraiswami, Ramani, Zotkin, Dmitry N

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Chain architecture: An efficient hardware solution for a large microphone array system von Zotkin, Dmitry N., Adelman, Ross, O'Donovan, Adam E., Duraiswami, Ramani

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Chain architecture: An efficient hardware solution for a large microphone array system von Zotkin, Dmitry N., Adelman, Ross, O'Donovan, Adam E., Duraiswami, Ramani

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Spectro-temporal analysis, visualization and identification of listening-space measurements von O'Donovan, Adam E., Zotkin, Dmitry N., Duraiswami, Ramani

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Exome sequencing in bipolar disorder identifies AKAP11 as a risk gene shared with schizophrenia von Palmer, Duncan S., Howrigan, Daniel P., Chapman, Sinéad B., Adolfsson, Rolf, Bass, Nick, Blackwood, Douglas, Boks, Marco P. M., Chen, Chia-Yen, Churchhouse, Claire, Corvin, Aiden P., Craddock, Nicholas, Curtis, David, Di Florio, Arianna, Dickerson, Faith, Freimer, Nelson B., Goes, Fernando S., Jia, Xiaoming, Jones, Ian, Jones, Lisa, Jonsson, Lina, Kahn, Rene S., Landén, Mikael, Locke, Adam E., McIntosh, Andrew M., McQuillin, Andrew, Morris, Derek W., O’Donovan, Michael C., Ophoff, Roel A., Owen, Michael J., Pedersen, Nancy L., Posthuma, Danielle, Reif, Andreas, Risch, Neil, Schaefer, Catherine, Scott, Laura, Singh, Tarjinder, Smoller, Jordan W., Solomonson, Matthew, Clair, David St, Stahl, Eli A., Vreeker, Annabel, Walters, James T. R., Wang, Weiqing, Watts, Nicholas A., Yolken, Robert, Zandi, Peter P., Neale, Benjamin M.

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Corticostriatal dysfunction and social interaction deficits in mice lacking the cystine/glutamate antiporter von Bentea, Eduard, Villers, Agnès, Moore, Cynthia, Funk, Adam J., O’Donovan, Sinead M., Verbruggen, Lise, Lara, Olaya, Janssen, Pauline, De Pauw, Laura, Declerck, Noemi B., DePasquale, Erica A. K., Churchill, Madeline J., Sato, Hideyo, Hermans, Emmanuel, Arckens, Lutgarde, Meshul, Charles K., Ris, Laurence, McCullumsmith, Robert E., Massie, Ann

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Assessing the effects of antipsychotic medications on schizophrenia functional analysis: a postmortem proteome study von Alnafisah, Rawan S, Reigle, James, Eladawi, Mahmoud Ali, O'Donovan, Sinead M, Funk, Adam J, Meller, Jaroslaw, Mccullumsmith, Robert E, Shukla, Rammohan

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Measurement of lactate levels in postmortem brain, iPSCs, and animal models of schizophrenia von Sullivan, Courtney R., Mielnik, Catharine A., Funk, Adam, O’Donovan, Sinead M., Bentea, Eduard, Pletnikov, Mikhail, Ramsey, Amy J., Wen, Zhexing, Rowland, Laura M., McCullumsmith, Robert E.

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Transcriptional programs regulating neuronal differentiation are disrupted in DLG2 knockout human embryonic stem cells and enriched for schizophrenia and related disorders risk var... von Sanders, Bret, D’Andrea, Daniel, Collins, Mark O., Rees, Elliott, Steward, Tom G. J., Zhu, Ying, Chapman, Gareth, Legge, Sophie E., Pardiñas, Antonio F., Harwood, Adrian J., Gray, William P., O’Donovan, Michael C., Owen, Michael J., Errington, Adam C., Blake, Derek J., Whitcomb, Daniel J., Pocklington, Andrew J., Shin, Eunju

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Connectivity Analyses of Bioenergetic Changes in Schizophrenia: Identification of Novel Treatments von Sullivan, Courtney R., Mielnik, Catharine A., O’Donovan, Sinead M., Funk, Adam J., Bentea, Eduard, DePasquale, Erica A., Alganem, Khaled, Wen, Zhexing, Haroutunian, Vahram, Katsel, Pavel, Ramsey, Amy J., Meller, Jarek, McCullumsmith, Robert E.

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Adenosine Kinase Expression in the Frontal Cortex in Schizophrenia von Moody, Cassidy L, Funk, Adam J, Devine, Emily, Devore Homan, Ryan C, Boison, Detlev, McCullumsmith, Robert E, O’Donovan, Sinead M

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Remote sensing of the decant pond of tailings dams: Insights from a South African case study von O'Donovan, C, Adam, E, Torres-Cruz, L.A

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Genome-wide Association Study Identifies Genetic Variation in Neurocan as a Susceptibility Factor for Bipolar Disorder von Cichon, Sven, Mühleisen, Thomas W., Degenhardt, Franziska A., Mattheisen, Manuel, Miró, Xavier, Strohmaier, Jana, Steffens, Michael, Meesters, Christian, Herms, Stefan, Weingarten, Moritz, Priebe, Lutz, Haenisch, Britta, Alexander, Michael, Vollmer, Jennifer, Breuer, René, Schmäl, Christine, Tessmann, Peter, Moebus, Susanne, Wichmann, H.-Erich, Schreiber, Stefan, Müller-Myhsok, Bertram, Lucae, Susanne, Jamain, Stéphane, Leboyer, Marion, Bellivier, Frank, Etain, Bruno, Henry, Chantal, Kahn, Jean-Pierre, Heath, Simon, Hamshere, Marian, O'Donovan, Michael C., Owen, Michael J., Craddock, Nick, Schwarz, Markus, Vedder, Helmut, Kammerer-Ciernioch, Jutta, Reif, Andreas, Sasse, Johanna, Bauer, Michael, Hautzinger, Martin, Wright, Adam, Mitchell, Philip B., Schofield, Peter R., Montgomery, Grant W., Medland, Sarah E., Gordon, Scott D., Martin, Nicholas G., Gustafsson, Omar, Andreassen, Ole, Djurovic, Srdjan, Sigurdsson, Engilbert, Steinberg, Stacy, Stefansson, Hreinn, Stefansson, Kari, Kapur-Pojskic, Lejla, Oruc, Liliana, Rivas, Fabio, Mayoral, Fermín, Chuchalin, Alexander, Babadjanova, Gulja, Tiganov, Alexander S., Pantelejeva, Galina, Abramova, Lilia I., Grigoroiu-Serbanescu, Maria, Diaconu, Carmen C., Czerski, Piotr M., Hauser, Joanna, Zimmer, Andreas, Lathrop, Mark, Schulze, Thomas G., Wienker, Thomas F., Schumacher, Johannes, Maier, Wolfgang, Propping, Peter, Rietschel, Marcella, Nöthen, Markus M.

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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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Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder von Jia, Xiaoming, Goes, Fernando S., Locke, Adam E., Palmer, Duncan, Wang, Weiqing, Cohen-Woods, Sarah, Genovese, Giulio, Jackson, Anne U., Jiang, Chen, Kvale, Mark, Mullins, Niamh, Nguyen, Hoang, Pirooznia, Mehdi, Rivera, Margarita, Ruderfer, Douglas M., Shen, Ling, Thai, Khanh, Zawistowski, Matthew, Zhuang, Yongwen, Abecasis, Gonçalo, Akil, Huda, Bergen, Sarah, Burmeister, Margit, Chapman, Sinéad, DelaBastide, Melissa, Juréus, Anders, Kang, Hyun Min, Kwok, Pui-Yan, Li, Jun Z., Levy, Shawn E., Monson, Eric T., Moran, Jennifer, Sobell, Janet, Watson, Stanley, Willour, Virginia, Zöllner, Sebastian, Adolfsson, Rolf, Blackwood, Douglas, Boehnke, Michael, Breen, Gerome, Corvin, Aiden, Craddock, Nick, DiFlorio, Arianna, Hultman, Christina M., Landen, Mikael, Lewis, Cathryn, McCarroll, Steven A., Richard McCombie, W., McGuffin, Peter, McIntosh, Andrew, McQuillin, Andrew, Morris, Derek, Myers, Richard M., O’Donovan, Michael, Ophoff, Roel, Boks, Marco, Kahn, Rene, Ouwehand, Willem, Owen, Michael, Pato, Carlos, Pato, Michele, Posthuma, Danielle, Potash, James B., Reif, Andreas, Sklar, Pamela, Smoller, Jordan, Sullivan, Patrick F., Vincent, John, Walters, James, Neale, Benjamin, Purcell, Shaun, Risch, Neil, Schaefer, Catherine, Stahl, Eli A., Zandi, Peter P., Scott, Laura J.

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Widespread genomic influences on phenotype in Dravet syndrome, a ‘monogenic’ condition von Martins Custodio, Helena, Clayton, Lisa M, Bellampalli, Ravishankara, Pagni, Susanna, Silvennoinen, Katri, Caswell, Richard, Brunklaus, Andreas, Guerrini, Renzo, Koeleman, Bobby P C, Lemke, Johannes R, Møller, Rikke S, Scheffer, Ingrid E, Weckhuysen, Sarah, Zara, Federico, Zuberi, Sameer, Kuchenbaecker, Karoline, Balestrini, Simona, Mills, James D, Sisodiya, Sanjay M

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Signatures of TOP1 transcription-associated mutagenesis in cancer and germline von Reijns, Martin A. M., Parry, David A., Williams, Thomas C., Nadeu, Ferran, Hindshaw, Rebecca L., Rios Szwed, Diana O., Nicholson, Michael D., Carroll, Paula, Boyle, Shelagh, Royo, Romina, Cornish, Alex J., Xiang, Hang, Ridout, Kate, Schuh, Anna, Aden, Konrad, Palles, Claire, Campo, Elias, Stankovic, Tatjana, Taylor, Martin S., Jackson, Andrew P.

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Spectrum of mutational signatures in T-cell lymphoma reveals a key role for UV radiation in cutaneous T-cell lymphoma von Jones, Christine L., Degasperi, Andrea, Grandi, Vieri, Amarante, Tauanne D., Mitchell, Tracey J., Nik-Zainal, Serena, Whittaker, Sean J.

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