The management of myelomatosis von Broad, A. F., Godlee, J. N., Emery, E. W., Prankerd, T. A. J.

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URINARY INCONTINENCE FOLLOWING SPINAL INJURY TREATED BY ELECTRONIC IMPLANT von CALDWELL, K P, FLACK, F C, BROAD, A F

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Primary ovarian lymphoma von Cooper, J A, Broad, A F, Salm, R

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SE378897 von BROAD F A

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PRIMARY OVARIAN LYMPHOMA von Cooper, J. A., Broad, A. F., Salm, R.

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URINARY INCONTINENCE FOLLOWING SPINAL INJURY TREATED BY ELECTRONIC IMPLANT von CALDWELL, K

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Autism spectrum disorder and attention deficit hyperactivity disorder have a similar burden of rare protein-truncating variants von Satterstrom, F. Kyle, Walters, Raymond K., Singh, Tarjinder, Wigdor, Emilie M., Lescai, Francesco, Demontis, Ditte, Kosmicki, Jack A., Grove, Jakob, Stevens, Christine, Bybjerg-Grauholm, Jonas, Bækvad-Hansen, Marie, Palmer, Duncan S., Maller, Julian B., Nordentoft, Merete, Mors, Ole, Robinson, Elise B., Hougaard, David M., Werge, Thomas M., Bo Mortensen, Preben, Neale, Benjamin M., Børglum, Anders D., Daly, Mark J.

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A 9-Valent HPV Vaccine against Infection and Intraepithelial Neoplasia in Women von Joura, Elmar A, Giuliano, Anna R, Iversen, Ole-Erik, Bouchard, Celine, Mao, Constance, Mehlsen, Jesper, Moreira, Edson D, Ngan, Yuen, Petersen, Lone Kjeld, Lazcano-Ponce, Eduardo, Pitisuttithum, Punnee, Restrepo, Jaime Alberto, Stuart, Gavin, Woelber, Linn, Yang, Yuh Cheng, Cuzick, Jack, Garland, Suzanne M, Huh, Warner, Kjaer, Susanne K, Bautista, Oliver M, Chan, Ivan S.F, Chen, Joshua, Gesser, Richard, Moeller, Erin, Ritter, Michael, Vuocolo, Scott, Luxembourg, Alain

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Aurora B kinase is recruited to multiple discrete kinetochore and centromere regions in human cells von Broad, Amanda J, DeLuca, Keith F, DeLuca, Jennifer G

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Genetic influences on eight psychiatric disorders based on family data of 4 408 646 full and half-siblings, and genetic data of 333 748 cases and controls von Pettersson, E., Lichtenstein, P., Larsson, H., Song, J., Agrawal, A., Børglum, A. D., Bulik, C. M., Daly, M. J., Davis, L. K., Demontis, D., Edenberg, H. J., Grove, J., Gelernter, J., Neale, B. M., Pardiñas, A. F., Stahl, E., Walters, J. T. R., Walters, R., Sullivan, P. F., Posthuma, D., Polderman, T. J. C.

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Genome-wide association study identifies 16 genomic regions associated with circulating cytokines at birth von Wang, Yunpeng, Nudel, Ron, Benros, Michael E, Skogstrand, Kristin, Fishilevich, Simon, Lancet, Doron, Sun, Jiangming, Hougaard, David M, Andreassen, Ole A, Mortensen, Preben Bo, Buil, Alfonso, Hansen, Thomas F, Thompson, Wesley K, Werge, Thomas

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Genome Sequence, Comparative Analysis, and Population Genetics of the Domestic Horse von Wade, C.M, Giulotto, E, Sigurdsson, S, Zoli, M, Gnerre, S, Imsland, F, Lear, T.L, Adelson, D.L, Bailey, E, Bellone, R.R, Blöcker, H, Distl, O, Edgar, R.C, Garber, M, Leeb, T, Mauceli, E, MacLeod, J.N, Penedo, M.C.T, Raison, J.M, Sharpe, T, Vogel, J, Andersson, L, Antczak, D.F, Biagi, T, Binns, M.M, Chowdhary, B.P, Coleman, S.J, Della Valle, G, Fryc, S, Guérin, G, Hasegawa, T, Hill, E.W, Jurka, J, Kiialainen, A, Lindgren, G, Liu, J, Magnani, E, Mickelson, J.R, Murray, J, Nergadze, S.G, Onofrio, R, Pedroni, S, Piras, M.F, Raudsepp, T, Rocchi, M, Røed, K.H, Ryder, O.A, Searle, S, Skow, L, Swinburne, J.E, Syvänen, A.C, Tozaki, T, Valberg, S.J, Vaudin, M, White, J.R, Zody, M.C, Lander, E.S, Lindblad-Toh, K

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Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism von Satterstrom, F. Kyle, Breen, Michael S., Grove, Jakob, Klei, Lambertus, Xu, Xinyi, Norman, Utku, Brand, Harrison, Schwartz, Grace, Barbosa, Mafalda, Bybjerg-Grauholm, Jonas, Carracedo, Angel, Chiocchetti, Andreas G., Chung, Brian H.Y., Coon, Hilary, Cuccaro, Michael L., Dalla Bernardina, Bernardo, Domenici, Enrico, Dong, Shan, Freitag, Christine M., González-Peñas, Javier, Guter, Stephen, He, Xin, Herman, Gail E., Hertz-Picciotto, Irva, Hougaard, David M., Ionita-Laza, Iuliana, Jacob, Suma, Jamison, Jesslyn, Jugessur, Astanand, Kolevzon, Alexander, Kushima, Itaru, Lee, So Lun, Lehtimäki, Terho, Lim, Elaine T., Lipkin, W. Ian, Lopergolo, Diego, Lopes, Fátima, Ludena, Yunin, Maciel, Patricia, Meiri, Gal, Menashe, Idan, Miller, Judith, Montenegro, Eduarda M.S., Muglia, Pierandrea, Nordentoft, Merete, Ozaki, Norio, Palotie, Aarno, Parellada, Mara, Passos-Bueno, Maria Rita, Persico, Antonio M., Pessah, Isaac, Puura, Kaija, Renieri, Alessandra, Riberi, Evelise, Robinson, Elise B., Samocha, Kaitlin E., Sandin, Sven, Santangelo, Susan L., Schellenberg, Gerry, Scherer, Stephen W., Schmitt, Lauren, Silva, Isabela M.W., Singh, Tarjinder, Siper, Paige M., Soares, Gabriela, Susser, Ezra, Szatmari, Peter, Tang, Lara, Tassone, Flora, Teufel, Karoline, Trelles, Maria del Pilar, Werge, Thomas, Werling, Donna M., Wigdor, Emilie M., Yu, Mullin H.C., Zachi, Elaine, Agerbo, Esben, Als, Thomas Damm, Bækvad-Hansen, Marie, Belliveau, Rich, Cerrato, Felecia, Chambert, Kimberly, Churchhouse, Claire, Dumont, Ashley, Hansen, Christine S., Hauberg, Mads Engel, Hollegaard, Mads V., Howrigan, Daniel P., Maller, Julian, Mattheisen, Manuel, Moran, Jennifer, Pallesen, Jonatan, Poulsen, Jesper Buchhave, Ripke, Stephan, Gallagher, Louise, Gill, Michael, Zwick, Michael E., State, Matthew W., Daly, Mark J., Buxbaum, Joseph D.

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Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population von Robinson, Elise B, St Pourcain, Beate, Anttila, Verneri, Kosmicki, Jack A, Bulik-Sullivan, Brendan, Grove, Jakob, Maller, Julian, Samocha, Kaitlin E, Sanders, Stephan J, Ripke, Stephan, Martin, Joanna, Hollegaard, Mads V, Werge, Thomas, Hougaard, David M, Neale, Benjamin M, Evans, David M, Skuse, David, Mortensen, Preben Bo, Børglum, Anders D, Ronald, Angelica, Smith, George Davey, Daly, Mark J

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Shared molecular neuropathology across major psychiatric disorders parallels polygenic overlap von Gandal, Michael J, Haney, Jillian R, Parikshak, Neelroop N, Leppa, Virpi, Ramaswami, Gokul, Hartl, Chris, Schork, Andrew J, Appadurai, Vivek, Buil, Alfonso, Werge, Thomas M, Liu, Chunyu, White, Kevin P, Horvath, Steve, Geschwind, Daniel H

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SYT1-associated neurodevelopmental disorder: a case series von Baker, Kate, Gordon, Sarah L, Melland, Holly, Bumbak, Fabian, Scott, Daniel J, Jiang, Tess J, Owen, David, Turner, Bradley J, Boyd, Stewart G, Rossi, Mari, Al-Raqad, Mohammed, Elpeleg, Orly, Peck, Dawn, Mancini, Grazia M S, Wilke, Martina, Zollino, Marcella, Marangi, Giuseppe, Weigand, Heike, Borggraefe, Ingo, Haack, Tobias, Stark, Zornitza, Sadedin, Simon, Tan, Tiong Yang, Jiang, Yunyun, Gibbs, Richard A, Ellingwood, Sara, Amaral, Michelle, Kelley, Whitley, Kurian, Manju A, Cousin, Michael A, Raymond, F Lucy

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Rare coding variation provides insight into the genetic architecture and phenotypic context of autism von Fu, Jack M., Satterstrom, F. Kyle, Peng, Minshi, Brand, Harrison, Collins, Ryan L., Dong, Shan, Wamsley, Brie, Klei, Lambertus, Wang, Lily, Hao, Stephanie P., Stevens, Christine R., Cusick, Caroline, Babadi, Mehrtash, Banks, Eric, Collins, Brett, Dodge, Sheila, Gabriel, Stacey B., Gauthier, Laura, Lee, Samuel K., Liang, Lindsay, Ljungdahl, Alicia, Mahjani, Behrang, Sloofman, Laura, Smirnov, Andrey N., Barbosa, Mafalda, Betancur, Catalina, Brusco, Alfredo, Chung, Brian H. Y., Cook, Edwin H., Cuccaro, Michael L., Domenici, Enrico, Ferrero, Giovanni Battista, Gargus, J. Jay, Herman, Gail E., Hertz-Picciotto, Irva, Maciel, Patricia, Manoach, Dara S., Passos-Bueno, Maria Rita, Persico, Antonio M., Renieri, Alessandra, Sutcliffe, James S., Tassone, Flora, Trabetti, Elisabetta, Campos, Gabriele, Cardaropoli, Simona, Carli, Diana, Chan, Marcus C. Y., Fallerini, Chiara, Giorgio, Elisa, Girardi, Ana Cristina, Hansen-Kiss, Emily, Lee, So Lun, Lintas, Carla, Ludena, Yunin, Nguyen, Rachel, Pavinato, Lisa, Pericak-Vance, Margaret, Pessah, Isaac N., Schmidt, Rebecca J., Smith, Moyra, Costa, Claudia I. S., Trajkova, Slavica, Wang, Jaqueline Y. T., Yu, Mullin H. C., Cutler, David J., De Rubeis, Silvia, Buxbaum, Joseph D., Daly, Mark J., Devlin, Bernie, Roeder, Kathryn, Sanders, Stephan J., Talkowski, Michael E.

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Meta-analysis identifies five novel loci associated with endometriosis highlighting key genes involved in hormone metabolism von Sapkota, Yadav, Steinthorsdottir, Valgerdur, Morris, Andrew P., Fassbender, Amelie, Rahmioglu, Nilufer, De Vivo, Immaculata, Buring, Julie E., Zhang, Futao, Edwards, Todd L., Jones, Sarah, O, Dorien, Peterse, Daniëlle, Rexrode, Kathryn M., Ridker, Paul M., Schork, Andrew J., MacGregor, Stuart, Martin, Nicholas G., Becker, Christian M., Adachi, Sosuke, Yoshihara, Kosuke, Enomoto, Takayuki, Takahashi, Atsushi, Kamatani, Yoichiro, Matsuda, Koichi, Kubo, Michiaki, Thorleifsson, Gudmar, Geirsson, Reynir T., Thorsteinsdottir, Unnur, Wallace, Leanne M., Yang, Jian, Velez Edwards, Digna R., Nyegaard, Mette, Low, Siew-Kee, Zondervan, Krina T., Missmer, Stacey A., D'Hooghe, Thomas, Montgomery, Grant W., Chasman, Daniel I., Stefansson, Kari, Tung, Joyce Y., Nyholt, Dale R.

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Genome-Wide Association Studies of a Broad Spectrum of Antisocial Behavior von Tielbeek, Jorim J, Johansson, Ada, Polderman, Tinca J. C, Rautiainen, Marja-Riitta, Jansen, Philip, Taylor, Michelle, Tong, Xiaoran, Lu, Qing, Burt, Alexandra S, Tiemeier, Henning, Viding, Essi, Plomin, Robert, Martin, Nicholas G, Heath, Andrew C, Madden, Pamela A. F, Montgomery, Grant, Beaver, Kevin M, Waldman, Irwin, Gelernter, Joel, Kranzler, Henry R, Farrer, Lindsay A, Perry, John R. B, Munafò, Marcus, LoParo, Devon, Paunio, Tiina, Tiihonen, Jari, Mous, Sabine E, Pappa, Irene, de Leeuw, Christiaan, Watanabe, Kyoko, Hammerschlag, Anke R, Salvatore, Jessica E, Aliev, Fazil, Bigdeli, Tim B, Dick, Danielle, Faraone, Stephen V, Popma, Arne, Medland, Sarah E, Posthuma, Danielle

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Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders von Weiner, Daniel J, Wigdor, Emilie M, Ripke, Stephan, Walters, Raymond K, Kosmicki, Jack A, Grove, Jakob, Samocha, Kaitlin E, Goldstein, Jacqueline I, Okbay, Aysu, Bybjerg-Grauholm, Jonas, Werge, Thomas, Hougaard, David M, Taylor, Jacob, Skuse, David, Devlin, Bernie, Anney, Richard, Sanders, Stephan J, Bishop, Somer, Mortensen, Preben Bo, Børglum, Anders D, Smith, George Davey, Daly, Mark J, Robinson, Elise B

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