Guidance for elective single-embryo transfer should be applied to frozen embryo transfer cycles von Freeman, Melanie R., Hinds, M. Shaun, Howard, Kay G., Howard, Julie M., Hill, George A.

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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 second generation human haplotype map of over 3.1 million SNPs von Frazer, Kelly A, Ballinger, Dennis G, Cox, David R, Hinds, David A, Stuve, Laura L, Gibbs, Richard A, Belmont, John W, Boudreau, Andrew, Hardenbol, Paul, Leal, Suzanne M, Pasternak, Shiran, Wheeler, David A, Willis, Thomas D, Yu, Fuli, Yang, Huanming, Zeng, Changqing, Gao, Yang, Hu, Haoran, Hu, Weitao, Li, Chaohua, Lin, Wei, Liu, Siqi, Pan, Hao, Tang, Xiaoli, Wang, Jian, Wang, Wei, Yu, Jun, Zhang, Bo, Zhang, Qingrun, Zhao, Hongbin, Zhao, Hui, Zhou, Jun, Gabriel, Stacey B, Barry, Rachel, Blumenstiel, Brendan, Camargo, Amy, Defelice, Matthew, Faggart, Maura, Goyette, Mary, Gupta, Supriya, Moore, Jamie, Nguyen, Huy, Onofrio, Robert C, Parkin, Melissa, Roy, Jessica, Stahl, Erich, Winchester, Ellen, Ziaugra, Liuda, Altshuler, David, Shen, Yan, Yao, Zhijian, Huang, Wei, Chu, Xun, He, Yungang, Jin, Li, Liu, Yangfan, Shen, Yayun, Sun, Weiwei, Wang, Haifeng, Wang, Yi, Wang, Ying, Xiong, Xiaoyan, Xu, Liang, Waye, Mary M Y, Tsui, Stephen K W, Xue, Hong, Wong, J Tze-Fei, Galver, Luana M, Fan, Jian-Bing, Gunderson, Kevin, Murray, Sarah S, Oliphant, Arnold R, Chee, Mark S, Montpetit, Alexandre, Chagnon, Fanny, Ferretti, Vincent, Leboeuf, Martin, Olivier, Jean-François, Phillips, Michael S, Roumy, Stéphanie, Sallée, Clémentine, Verner, Andrei, Hudson, Thomas J, Kwok, Pui-Yan, Cai, Dongmei, Koboldt, Daniel C, Miller, Raymond D, Pawlikowska, Ludmila, Taillon-Miller, Patricia, Xiao, Ming, Tsui, Lap-Chee, Mak, William, Song, You Qiang, Tam, Paul K H, Nakamura, Yusuke, Kawaguchi, Takahisa, Kitamoto, Takuya, Morizono, Takashi, Nagashima, Atsushi, Ohnishi, Yozo

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Genome-wide detection and characterization of positive selection in human populations von Sabeti, Pardis C., Varilly, Patrick, Fry, Ben, Lohmueller, Jason, Hostetter, Elizabeth, Cotsapas, Chris, Xie, Xiaohui, Byrne, Elizabeth H., McCarroll, Steven A., Gaudet, Rachelle, Schaffner, Stephen F., Lander, Eric S.

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Stratified analyses refine association between TLR7 rare variants and severe COVID-19 von Millar, Johnny, Pereira, Alexandre C., Aravindan, Latha, Das, Sukamal, Fourman, Max Head, Golightly, Ailsa, Law, Dawn, Law, Sarah, Murphy, Sheena, Ward, Mairi, Arbane, Gill, Xavier, Kugan, Banach, Dorota, Hutton, Paula, Barclay, Lucy, Peasgood, Emily, Ezeobu, Obiageri, Da Gloria, Edna Fernandes, Kent, Alissa, Bamford, Peter, Dykes, Joseph, Hijazi, Muhammad, Thomas, Jacqueline, Fine, Christopher, Ali, Syamlan, Gibson, Sian, McNeela, Fiona, Krishnamurthy, Vinodh, Trotman, Sallyanne, Cabrelli, Louise, Butler, Aaron, Gardner, Amy, Davis, Caroline, Durie, Alison, Morgan, Aled, Purewal, Manjit, Walton, Olivia, Ward, Luke, Thomson, Nicola, Savill, Heather, Bhatia, Nikhil, Webster, Andrea, Anderson, Felicity, Harvey, Alice, Poulaka, Maria, Baxter, Nicola, Akeroyd, Louise, Hudig, Lisa, Jones, Cathy, Pritchard, Kelly, Butcher, Deborah, Rowland-Jones, Sarah, Pinnell, Jez, Hibbert, Meg, Branney, Debbie, Ma, Louise, Parmar, Chetan, Jose, Sanal, Mahenthran, Mervin, Creagh-Brown, Ben, Mayangao, Irving, Marriott, Cheryl, Hierons, Sarah, Howie, Lucy, Ramos, Lidia, Menzies, Daniel, Davies, Llinos, Coton, Zoe, Vedage, Dave, Morrison, Alan, Symon, Lesley, Kannan, Thogulava, Barron, Anthony, Mitra, Atideb, Pollard, Rachel, Stead, Rachael, Skinner, Denise, Crickmore, Vikki, Deery, Joanne, Turki, Salah, Tutton, Rebecca, Waldron, Joanne, Rekha, Patel, King, Bernadette, Tyl, David, Johnson, Laura, Little, Jeff, McParland, Chantal, George, Linsha, Lewis, Tracy, Saunderson, Paula, Thornton, Lorraine, Allibone, Suzanne, Fagan, Andrew, Thomas, Helen, Jackson, Peter, Carter, Sasha, Hall, Kathryn, Hardy, John, Rawlik, Konrad

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Showcasing E-Book Platform Features von Shaun R. Bennett, Xiaoyan Song, Danica M. Lewis

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