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    De novo variants in the RNU4-2 snRNA cause a frequent neurodevelopmental syndrome von Chen, Yuyang, Kim, Hyung Chul, Ljungdahl, Alicia, Stenton, Sarah L., Lord, Jenny, Lemire, Gabrielle, Martin-Geary, Alexandra C., Ganesh, Vijay S., Ma, Jialan, Ellingford, Jamie M., Delage, Erwan, D’Souza, Elston N., Dong, Shan, Adams, David R., Allan, Kirsten, Bakshi, Madhura, Baldwin, Erin E., Berger, Seth I., Brown, Natasha J., Burrage, Lindsay C., Chapman, Kimberly, Coman, David J., Compton, Alison G., Cunningham, Chloe A., D’Souza, Precilla, Danecek, Petr, Délot, Emmanuèle C., Dias, Kerith-Rae, Elias, Ellen R., Elmslie, Frances, Evans, Care-Anne, Ezell, Kimberly, Fraser, Jamie L., Gallacher, Lyndon, Genetti, Casie A., Grant, Christina L., Haack, Tobias, Higgs, Jenny E., Hinch, Anjali G., Hurles, Matthew E., Kuechler, Alma, Lecoquierre, François, Fevre, Anna Le, Leventer, Richard J., Liebelt, Jan E., Lindsay, Sarah, Lockhart, Paul J., Ma, Alan S., Macnamara, Ellen F., Mendez, Hector R., Metcalfe, Kay, Montgomery, Stephen B., Moosajee, Mariya, Nassogne, Marie-Cécile, Neumann, Serena, O’Donoghue, Michael, O’Leary, Melanie, Palmer, Elizabeth E., Pattani, Nikhil, Pitsava, Georgia, Pysar, Ryan, Rehm, Heidi L., Reuter, Chloe M., Revencu, Nicole, Riess, Angelika, Rodan, Lance, Roscioli, Tony, Rosenfeld, Jill A., Sachdev, Rani, Shaw-Smith, Charles J., Simons, Cas, Sisodiya, Sanjay M., Snell, Penny, St Clair, Laura, Stewart, Helen S., Tan, Natalie B., Temple, Suzanna E. L., Thorburn, David R., Tifft, Cynthia J., VanNoy, Grace E., Vilain, Eric, Viskochil, David H., Wedd, Laura, Wheeler, Matthew T., White, Susan M., Wojcik, Monica, Wolfe, Lynne A., Wolfenson, Zoe, Wright, Caroline F., Xiao, Changrui, Zocche, David, Rubenstein, John L., Markenscoff-Papadimitriou, Eirene, Fica, Sebastian M., Baralle, Diana, Depienne, Christel, MacArthur, Daniel G., Sanders, Stephan J., O’Donnell-Luria, Anne, Whiffin, Nicola

    Veröffentlicht in Nature (London)

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    Genome-wide association study of subtype-specific epithelial ovarian cancer risk alleles using pooled DNA von Earp, Madalene A, Magliocco, Anthony M, Swenerton, Kenneth D, Lu, Yi, Hein, Alexander, Ekici, Arif B, Beckmann, Matthias W, Lambrechts, Diether, Despierre, Evelyn, Vergote, Ignace, Lambrechts, Sandrina, Doherty, Jennifer A, Rossing, Mary Anne, Chang-Claude, Jenny, Friel, Grace, Moysich, Kirsten B, Odunsi, Kunle, Sucheston-Campbell, Lara, Lurie, Galina, Goodman, Marc T, Carney, Michael E, Runnebaum, Ingo B, Dürst, Matthias, Leminen, Arto, Nevanlinna, Heli, Pelttari, Liisa M, Butzow, Ralf, Modugno, Francesmary, Edwards, Robert P, Ness, Roberta B, du Bois, Andreas, Heitz, Florian, Schwaab, Ira, Harter, Philipp, Karlan, Beth Y, Walsh, Christine, Lester, Jenny, Jensen, Allan, Kjær, Susanne K, Høgdall, Claus K, Sellers, Thomas A, Fridley, Brooke L, Cunningham, Julie M, Vierkant, Robert A, Severi, Gianluca, Liang, Dong, Lu, Karen, Levine, Douglas A, Bisogna, Maria, Schildkraut, Joellen M, Iversen, Edwin S, Weber, Rachel Palmieri, Berchuck, Andrew, Cramer, Daniel William, Poole, Elizabeth M, Bandera, Elisa V, Orlow, Irene, Olson, Sara H, Wik, Elisabeth, Bjorge, Line, Halle, Mari K, van Altena, Anne M, Aben, Katja K. H, Kiemeney, Lambertus A, Massuger, Leon F. A. G, Pejovic, Tanja, Bean, Yukie T, Cybulski, Cezary, Gronwald, Jacek, Lubinski, Jan, Wentzensen, Nicolas, Lissowska, Jolanta, Dicks, Ed, Dennis, Joe, Song, Honglin, Tyrer, Jonathan P, Eccles, Diana, Whittemore, Alice S, McGuire, Valerie, Rothstein, Joseph H, Flanagan, James M, Paul, James, Brown, Robert, Phelan, Catherine M, Risch, Harvey A, McLaughlin, John R, Narod, Steven A, Anton-Culver, Hoda, Gentry-Maharaj, Aleksandra, Menon, Usha, Gayther, Simon A, Ramus, Susan J, Wu, Anna H, Pike, Malcolm C, Dansonka-Mieszkowska, Agnieszka, Szafron, Lukasz M, Kupryjanczyk, Jolanta, Cook, Linda S, Le, Nhu D, Brooks-Wilson, Angela


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