Search Results - Taits, M. Yu

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    Identification and molecular characterization of a new ovarian cancer susceptibility locus at 17q21.31 by Shen, Howard C., Velkova, Aneliya, Chen, Zhihua, Lin, Hui-Yi, Ann Chen, Y, Qu, Xiaotao, Ramus, Susan J., Lee, Janet, Lee, Nathan, Larson, Melissa C., Anton-Culver, Hoda, Antoniou, Antonis C., Armasu, Sebastian M., Bacot, François, Baglietto, Laura, Bandera, Elisa V., Bogdanova, Natalia, Brooks-Wilson, Angela, Butzow, Ralf, Cai, Qiuyin, Campbell, Ian, Chang-Claude, Jenny, Chanock, Stephen, Cheng, Jin Q., Cook, Linda S., Couch, Fergus J., Cunningham, Julie M., Dansonka-Mieszkowska, Agnieszka, Doherty, Jennifer A., Easton, Douglas F., Fasching, Peter A., Flanagan, James M., Giles, Graham G., Gonzalez-Bosquet, Jesus, Gore, Martin, Halle, Mari K., Harter, Philipp, Hillemanns, Peter, Hoatlin, Maureen, Høgdall, Claus K., Høgdall, Estrid, Hosono, Satoyo, Jensen, Allan, Jim, Heather, Karlan, Beth Y., Kaye, Stanley B., Kiemeney, Lambertus A., Kikkawa, Fumitaka, Konecny, Gottfried E., Krüger Kjaer, Susanne, Lambrechts, Sandrina, Lancaster, Johnathan M., Leminen, Arto, Levine, Douglas A., Liang, Dong, Kiong Lim, Boon, Lissowska, Jolanta, Lubiński, Jan, McLaughlin, John R., Moysich, Kirsten B., Nakanishi, Toru, Narod, Steven A., Ness, Roberta B., Nickels, Stefan, Noushmehr, Houtan, Odunsi, Kunle, Olson, Sara H., Orlow, Irene, Paul, James, Pelttari, Liisa M., Pike, Malcolm C., Poole, Elizabeth M., Renner, Stefan P., Risch, Harvey A., Rodriguez-Rodriguez, Lorna, Anne Rossing, Mary, Rudolph, Anja, Rzepecka, Iwona K., Salvesen, Helga B., Shu, Xiao-Ou, Shvetsov, Yurii B., Southey, Melissa C., Spiewankiewicz, Beata, Sutphen, Rebecca, van Altena, Anne M., Vincent, Daniel, Vitonis, Allison F., Wentzensen, Nicolas, Wik, Elisabeth, Winterhoff, Boris, Ling Woo, Yin, Yang, Hannah P., Zulkifli, Famida, Schildkraut, Joellen M., Berchuck, Andrew, Goode, Ellen L., Pharoah, Paul D.P., Monteiro, Alvaro N.A., Sellers, Thomas A., Gayther, Simon A.

    Published in Nature communications
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    De Novo Truncating Mutations in WASF1 Cause Intellectual Disability with Seizures by Duarte, Sofia T., Charles, Perinne, Pfundt, Rolph, van Bokhoven, Hans, van Ravenswaaij-Arts, Conny, Morrell, Nicholas W., Thrasher, Adrian, Fletcher, Debra, Veltman, Marijke, Davis, John, Frary, Amy, Martin, Jennifer M., Collins, Janine, Favier, Remi, Hart, Daniel, Heemskerk, Johan W.M., Liesner, Ri, Mangles, Sarah, Roughley, Catherine, Tait, R. Campbell, Thachil, Jecko, Van Geet, Chris, De Vries, Minka, Warner, Timothy Q., Furnell, Abigail, Mapeta, Rutendo, Whitehorn, Deborah, Daugherty, Louise, Deevi, Sri V.V., Hu, Fengyuan, Matser, Vera, Megy, Karyn, Tuna, Salih, von Ziegenweldt, Julie, Haimel, Matthias, Richardson, Sylvia, Rankin, Stuart, Anderson, Julie, Stock, Sophie, Armstrong, Ruth, Bitner-Glindzicz, Maria, Brady, Angie, Clement, Emma, Firth, Helen, Flinter, Frances, French, Courtney, Holder, Muriel, Hurst, Jane, Josifova, Dragana, Krishnakumar, Deepa, Kurian, Manju A., Mehta, Sarju, Moore, Anthony, Rankin, Julia, Reid, Evan, Scott, Richard, Thomas, Ellen, Wassmer, Evangeline, Creaser-Myers, Amanda, Gall, Henning, Ghataorhe, Pavandeep K., Houweling, Arjan C., in’t Veld, Anna Huis, Ross, Rob V. Mackenzie, Rhodes, Christopher J., Soubrier, Florent, Treacy, Carmen M., Vonk Noordegraaf, Anton, Antrobus, Richard, Arumugakani, Gururaj, Bibi, Shahnaz, Devlin, Lisa, Ghurye, Rohit, Grigoriadou, Sofia, Harper, Lorraine, Herwadkar, Archana, Jolles, Stephen, Kumararatne, Dinakantha, Lorenzo, Lorena, Murng, Sai, Nejentsev, Sergey, Quinti, Isabella, Samarghitean, Crina, Savic, Sinisa, Yong, Patrick, Ancliff, Phil, Layton, Mark, Mead, Adam, Roy, Noémi, Chambers, Jenny, Estiu, Cecelia, Simpson, Michael, Emmerson, Ingrid, McCarthy, Mark, Van Zuydam, Natalie, Afzal, Maryam, Colby, Elizabeth, Boycott, Kym M., Majewski, Jacek, Dyment, David

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