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    Common genetic variants influence human subcortical brain structures von Hibar, Derrek P., Desrivières, Sylvane, Toro, Roberto, Wittfeld, Katharina, Abramovic, Lucija, Bernard, Manon, Chen, Qiang, Giddaluru, Sudheer, Janowitz, Deborah, Lee, Phil H., Ramasamy, Adaikalavan, Risacher, Shannon L., Rose, Emma J., Salami, Alireza, Schmaal, Lianne, Schork, Andrew J., Strike, Lachlan T., Walters, Raymond K., Winkler, Anderson M., Zwiers, Marcel P., Athanasiu, Lavinia, Hakobjan, Marina M. H., Hartberg, Cecilie B., Heister, Angelien J. G. A. M., Hoehn, David, Kasperaviciute, Dalia, Makkinje, Remco R. R., Reese McKay, D., Shen, Li, Walton, Esther, Ames, David, Corvin, Aiden, Curran, Joanne E., Dillman, Allissa, Erk, Susanne, Foroud, Tatiana M., Guelfi, Sebastian, Hegenscheid, Katrin, Hernandez, Dena G., Heslenfeld, Dirk J., Hottenga, Jouke-Jan, Jenkinson, Mark, Kanai, Ryota, Kent, Jack W., McMahon, Katie L., Meisenzahl, Eva, Mohnke, Sebastian, Mühleisen, Thomas W., Nalls, Michael A., Nichols, Thomas E., Potkin, Steven G., Reppermund, Simone, Rujescu, Dan, Schnell, Knut, Thalamuthu, Anbupalam, Turner, Jessica A., van 't Ent, Dennis, Wassink, Thomas H., Westman, Eric, Ashbrook, David G., Lu, Lu, Williams, Robert W., Buckner, Randy L., Calhoun, Vince D., Cavalleri, Gianpiero L., Dale, Anders M., Espeseth, Thomas, Hoffmann, Wolfgang, Le Hellard, Stephanie, Meyer-Lindenberg, Andreas, Müller-Myhsok, Bertram, Nyberg, Lars, Penninx, Brenda W. J. H., van Bokhoven, Hans, van Haren, Neeltje E. M., Völzke, Henry, Weiner, Michael W., White, Tonya, Agartz, Ingrid, Blangero, John, Boomsma, Dorret I., Fernández, Guillén, Fisher, Simon E., Francks, Clyde, Grabe, Hans J., Hashimoto, Ryota, Hulshoff Pol, Hilleke E., Jönsson, Erik G., McIntosh, Andrew M., Singleton, Andrew, Schmidt, Reinhold, Satizabal, Claudia L., Ebling, Maritza, Nyquist, Paul, Vinke, Louis N., Xue, Luting, Mazoyer, Bernard, Martin, Nicholas G., Wright, Margaret J., Schumann, Gunter

    Veröffentlicht in Nature (London)

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    Sex-Specific Genetic Associations for Barrett’s Esophagus and Esophageal Adenocarcinoma von Dong, Jing, Maj, Carlo, Tsavachidis, Spiridon, Ostrom, Quinn T., Gharahkhani, Puya, Anderson, Lesley A., Wu, Anna H., Ye, Weimin, Bernstein, Leslie, Borisov, Oleg, Schröder, Julia, Chow, Wong-Ho, Gammon, Marilie D., Liu, Geoffrey, Caldas, Carlos, Pharoah, Paul D., Risch, Harvey A., May, Andrea, Gerges, Christian, Anders, Mario, Venerito, Marino, Schmidt, Thomas, Izbicki, Jakob R., Hölscher, Arnulf H., Schumacher, Brigitte, Vashist, Yogesh, Neuhaus, Horst, Rösch, Thomas, Knapp, Michael, Krawitz, Peter, Böhmer, Anne, Iyer, Prasad G., Reid, Brian J., Lagergren, Jesper, Shaheen, Nicholas J., Corley, Douglas A., Gockel, Ines, Fitzgerald, Rebecca C., Dong, Jing, Maj, Carlo, Tsavachidis, Spiridon, Ostrom, Quinn T., Gharahkhani, Puya, Anderson, Lesley A., Wu, Anna H., Ye, Weimin, Bernstein, Leslie, Borisov, Oleg, Schröder, Julia, Chow, Wong-Ho, Gammon, Marilie D., Liu, Geoffrey, Caldas, Carlos, Pharoah, Paul D., Risch, Harvey A., May, Andrea, Gerges, Christian, Anders, Mario, Venerito, Marino, Schmidt, Thomas, Izbicki, Jakob R., Hölscher, Arnulf H., Schumacher, Brigitte, Vashist, Yogesh, Neuhaus, Horst, Rösch, Thomas, Knapp, Michael, Krawitz, Peter, Böhmer, Anne, Iyer, Prasad G., Reid, Brian J., Lagergren, Jesper, Shaheen, Nicholas J., Corley, Douglas A., Gockel, Ines, Fitzgerald, Rebecca C., Cook, Michael B., Whiteman, David C., Vaughan, Thomas L., Schumacher, Johannes, Thrift, Aaron P., Cook, Michael B., Whiteman, David C., Vaughan, Thomas L., Schumacher, Johannes, Thrift, Aaron P.


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    Standardized practices for RNA diagnostics using clinically accessible specimens reclassifies 75% of putative splicing variants von Bommireddipalli, Shobhana, Ades, Lesley, Archibald, Alison D., Berman, Yemima, Bojadzieva, Jasmina, Brown, Natasha J., Bryen, Samantha J., Engel, Amanda, Ewans, Lisa J., Fennell, Andrew, Freckmann, Mary-Louise, Gear, Russell, Goel, Himanshu, Goh, Shuxiang, Harraway, James, Higgins, Megan, Ho, Gladys, Hunter, Matthew F., Joshi, Himanshu, Krzesinski, Emma, Leventer, Richard J., Macaskill, Steven, McCarthy, Hugh J., McLean, Alison, Patel, Chirag, Regan, Matthew, Schindler, Tim, Tantsis, Esther, Tchan, Michel C., van Spaendonck-Zwarts, Karin, White, Susan M., Williams, Mark G., Wright, Dale C., Yap, Patrick, Yeung, Alison, Jones, Kristi J., Cooper, Sandra T., Arts, Peer, Barnett, Christopher, Beshay, Victoria, Blombery, Piers, Boggs, Kirsten, Branford, Susan, Bryen, Samantha J., Canson, Daffodil, Chew, Edward, Chong, Belinda, Chung, Seo-Kyung, Clark, Mike, Compton, Alison, Corbett, Mark, Davis, Mark R., Dudding, Tracy, Ewans, Lisa J., Eyras, Eduardo, Fellowes, Andrew, Field, Michael, Freckmann, Mary-Louise, Gaff, Clara, Galea, Melanie, Hanna, Bernadette, Harraway, James, Hayashi, Rippei, Henderson, Alex, Jackson, Matilda, Jones, Kristi J., Wong, Justin Jong-Leong, Joshi, Himanshu, Krzesinski, Emma, Kumble, Smitha, Laing, Nigel, Lau, Chiyan, Lee, Eric, Lundie, Ben, Mallawaarachchi, Amali, McLean, Alison, Meldrum, Cliff, Mina, Kym, Mowat, David, Oshlack, Alicia, Parsons, Michael, Patel, Chirag, Pinner, Jason R., Quinn, Michael, Ravenscroft, Gina, Regan, Matthew, Ronan, Anne, Sadedin, Simon, Schreiber, Andreas, Scott, Rodney, Simons, Cas, Smyth, Renee, Thompson, Bryony A., Thorburn, David, Trent, Ronald, Tudini, Emma, Wallis, Mathew, Wilson, Meredith J., Winship, Ingrid, Yeung, Alison

    Veröffentlicht in Genetics in medicine

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