Treffer 1 - 20 von 22 für Suche 'JANE HENDERSON SHAW', Suchdauer: 1,67s Treffer weiter einschränken
  1. 1
  2. 2
  3. 3
  4. 4
  5. 5
  6. 6
  7. 7
  8. 8
  9. 9
  10. 10
  11. 11

    Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer von Lindstrom, Sara, Dennis, Joe, Maranian, Mel J, Brand, Judith S, Nordestgaard, Børge G, Flyger, Henrik, Rahman, Nazneen, Fletcher, Olivia, Nevanlinna, Heli, Muranen, Taru A, Aaltonen, Kirsimari, Ahsan, Habibul, John, Esther M, Gammon, Marilie D, Ursin, Giske, Schmidt, Daniel F, Gapstur, Susan M, Gaudet, Mia M, Diver, W Ryan, Schumacher, Fredrick, Hoover, Robert N, Lambrechts, Diether, Wildiers, Hans, van Limbergen, Erik, Broeks, Annegien, Cornelissen, Sten, Couch, Fergus J, Olson, Janet E, Hallberg, Emily, Meijers-Heijboer, Hanne, Ito, Hidemi, Iwata, Hiroji, Guénel, Pascal, Sanchez, Marie, Marme, Frederik, Surowy, Harald, Sohn, Christof, Van Den Berg, David, Benitez, Javier, Lu, Wei, Gao, Yu-Tang, Andrulis, Irene L, Knight, Julia A, Mulligan, Anna Marie, Sawyer, Elinor J, Tomlinson, Ian, Kerin, Michael J, Lindblom, Annika, Hollestelle, Antoinette, Collée, J Margriet, Blot, William, Signorello, Lisa B, Cai, Qiuyin, Hou, Ming-Feng, Kristensen, Vessela N, Milne, Roger L, McLean, Catriona, Peeters, Petra, Khaw, Kay-Tee, Palli, Domenico, Mortensen, Lotte Maxild, Dossus, Laure, Meindl, Alfons, Sutter, Christian, Yang, Rongxi, Muir, Kenneth, Siriwanarangsan, Pornthep, Miao, Hui, Chia, Kee Seng, Chan, Ching Wan, Fasching, Peter A, Beckmann, Matthias W, Haeberle, Lothar, Brenner, Hermann, Stegmaier, Christa, Ashworth, Alan, Schoemaker, Minouk J, Brinton, Louise, Zheng, Wei, Grip, Mervi, Brauch, Hiltrud, Radice, Paolo, Manoukian, Siranoush, Bernard, Loris, Dörk, Thilo, Hartikainen, Jaana M, Tollenaar, Robert A E M, Seynaeve, Caroline, Van Asperen, Christi J, Brennan, Paul, McKay, James, Neuhausen, Susan L, Baynes, Caroline, Ahmed, Shahana, Healey, Catherine S, Herrero, Daniel, Simard, Jacques, Chenevix-Trench, Georgia, Hall, Per, Easton, Douglas F

    Veröffentlicht in Nature genetics

    Volltext
    Artikel
  12. 12
  13. 13
  14. 14
  15. 15

    Visual impairment, severe visual impairment, and blindness in children in Britain (BCVIS2): a national observational study von Rahi, Jugnoo S, Adams, Gill, Allen, Louise, Anderson, Christopher, Anwar, Samira, Ash, Isabel, Astagi, Majunath, Balu, Rajesh, Bassi, Zahabiyah, Bates, Adam, Belmour, Linda, Benzimra, James, Blaikie, Andrew, Bolton, Kate, Bos, Ewoud, Bowman, Richard, Bredow, Maria, Butcher, Jeremy, Cane, Clare, Chadwick, Cathryn, Charlton, Ruth, Choi, Jessy, Clifford, Luke, Cox, Rachel, Dattani, Mehul, Dean, Fiona, Devlin, Anita, Dhir, Luna, Doherty, Cora, Dorey, Suzanne, Eaton, Megan, Eckersley, Danielle, Elderkin, Rachel, Ennis, Julia, Escardo-Paton, Julia, Etuwewe, Onajite, Ezekwe, Adjoa, Ferguson, Allison, Galloway, Alexandra, Gibson, Patricia, Goss, Kevin, Graham-Evans, Katherine, Gray, Judith, Guy, Emma, Haddad, Diab, Harris, Sian, Harvey, Phillip, Heath, Dominic, Holden, Roger, Hoole, Janice, Howard, Delyth, Joseph, Annie, Khaw, Peng, Leitch, Jane, Lomas, Tom, MacRae, Mary, Mahmood, Usman, Maling, Sarah, Marr, Jane, Marsh, Catherine, McCartney, Eleanor, McPhee, Derek, Moore, Helen, Nair, Ranjit, Nitsch, Christiane, Palmer, Helen, Papadopoulos, Maria, Parkinson, Shelagh, Parulekar, Manoj, Pennefather, Philippa, Pierrepoint, Marcus, Pollard, Sally, Raina, Jyoti, Ramm, Laura, Rao, Tekki, Reilly, Sheilla, Riordan, Andrew, Roberts, Nerys, Sarvananthan, Nagini, Schmoll, Conrad, Smit, Elisa, Smyth, Katherine, Standring, P, Stanley, Alison, Stanton, Alan, Street, Jessica, Tappin, Alison, Taylor, Kate, Thomas, Megan, Thompson, Dorothy, Thomson, Stephen, Tillett, Angela, Venkatesh, Udupa, Vermaak, Zoe, Walker, David, Walsh, Deidre, Walters, Bronwyn, Ward Platt, Martin, Wong, Chien, Wright, Paul


    Volltext
    Artikel
  16. 16
  17. 17
  18. 18

    Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt Signaling von Snijders Blok, Lot, Madsen, Erik, Juusola, Jane, Gilissen, Christian, Baralle, Diana, Reijnders, Margot R F, Venselaar, Hanka, Helsmoortel, Céline, Cho, Megan T, Hoischen, Alexander, Vissers, Lisenka E L M, Koemans, Tom S, Wissink-Lindhout, Willemijn, Eichler, Evan E, Romano, Corrado, Van Esch, Hilde, Stumpel, Connie, Vreeburg, Maaike, Smeets, Eric, Oberndorff, Karin, Van Bon, Bregje W M, Shaw, Marie, Gecz, Jozef, Haan, Eric, Bienek, Melanie, Jensen, Corinna, Loeys, Bart L, Van Dijck, Anke, Innes, A. Micheil, Racher, Hilary, Vermeer, Sascha, Di Donato, Nataliya, Rump, Andreas, Tatton-Brown, Katrina, Parker, Michael J, Henderson, Alex, Lynch, Sally A, Fryer, Alan, Ross, Alison, Vasudevan, Pradeep, Kini, Usha, Newbury-Ecob, Ruth, Chandler, Kate, Male, Alison, Dijkstra, Sybe, Schieving, Jolanda, Giltay, Jacques, Van gassen, Koen L I, Schuurs-Hoeijmakers, Janneke, Tan, Perciliz L, Pediaditakis, Igor, Haas, Stefan A, Retterer, Kyle, Reed, Patrick, Monaghan, Kristin G, Haverfield, Eden, Natowicz, Marvin, Myers, Angela, Kruer, Michael C, Stein, Quinn, Strauss, Kevin A, Brigatti, Karlla W, Keating, Katherine, Burton, Barbara K, Kim, Katherine H, Charrow, Joel, Norman, Jennifer, Foster-Barber, Audrey, Kline, Antonie D, Kimball, Amy, Zackai, Elaine, Harr, Margaret, Fox, Joyce, McLaughlin, Julie, Lindstrom, Kristin, Haude, Katrina M, Van Roozendaal, Kees, Brunner, Han, Chung, Wendy K, Kooy, R. Frank, Pfundt, Rolph, Kalscheuer, Vera, Mehta, Sarju G, Katsanis, Nicholas, Kleefstra, Tjitske


    Volltext
    Artikel
  19. 19

    Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt Signaling von Snijders Blok, Lot, Madsen, Erik, Juusola, Jane, Gilissen, Christian, Baralle, Diana, Reijnders, Margot R.F, Venselaar, Hanka, Helsmoorte, Céline, Cho, Megan T, Hoischen, Alexander, Vissers, Lisenka E.L.M, Koemans, Tom S, Wissink-Lindhout, Willemijn, Eichler, Evan E, Romano, Corrado, Van Esch, Hilde, Stumpel, Connie, Vreeburg, Maaike, Smeets, Eric, Obemdorff, Karin, van Bon, Bregje W.M, Shaw, Marie, Gecz, Jozef, Haan, Eric, Bienek, Melanie, Jensen, Corinna, Loeys, Bart L, Van Dijck, Anke, Innes, A. Micheil, Racher, Hilary, Vermeer, Sascha, Di Donato, Nataliya, Rump, Andreas, Tatton-Brown, Katrina, Parker, Michael J, Henderson, Alex, Lynch, Sally A, Fryer, Alan, Ross, Alison, Vasudevan, Pradeep, Kini, Usha, Newbury-Ecob, Ruth, Chandler, Kate, Male, Alison, the DDD Study, Dijkstra, Sybe, Schieving, Jolanda, Giltay, Jacques, van Gassen, Koen L.I, Schuurs-Hoeijmakers, Janneke, Tan, Perciliz L, Pediaditakis, Igor, Haas, Stefan A, Retterer, Kyle, Reed, Patrick, Monaghan, Kristin G, Haverfield, Eden, Natowicz, Marvin, Myers, Angela, Kruer, Michael C, Stein, Quinn, Strauss, Kevin A, Brigatti, Karlla W, Keating, Katherine, Burton, Barbara K, Kim, Katherine H, Charrow, Joel, Norman, Jennifer, Foster-Barber, Audrey, Kline, Antonie D, Kimball, Amy, Zackai, Elaine, Harr, Margaret, Fox, Joyce, McLaughlin, Julie, Lindstrom, Kristin, Haude, Katrina M, van Roozendaal, Kees, Brunner, Han, Chung, Wendy K, Kooy, R. Frank, Pfundt, Rolph, Kalscheuer, Vera, Mehta, Sarju G, Katsanis, Nicholas, Kleefstra, Tjitske


    Volltext
    Artikel
  20. 20