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    The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions von Rahmioglu, Nilufer, Mortlock, Sally, Ghiasi, Marzieh, Møller, Peter L., Stefansdottir, Lilja, Galarneau, Geneviève, Turman, Constance, Danning, Rebecca, Law, Matthew H., Sapkota, Yadav, Christofidou, Paraskevi, Skarp, Sini, Krassowski, Michal, Lepamets, Maarja, Marciniak, Błażej, Sobalska-Kwapis, Marta, Topbas-Selcuki, Nura F., Vitonis, Allison, Westergaard, David, Arnadottir, Ragnheidur, Burgdorf, Kristoffer S., Campbell, Archie, Cheuk, Cecilia S. K., DiVasta, Amy, Dorien, O., Donoghue, Jacqueline F., Fontanillas, Pierre, Geirsson, Reynir T., Girling, Jane E., Harkki, Paivi, Harris, Holly R., Heikinheimo, Oskari, Hostettler, Isabel C., Houlden, Henry, Houshdaran, Sahar, Jarvelin, Marjo-Riitta, Kamatani, Yoichiro, Kennedy, Stephen H., Kettunen, Johannes, Kubo, Michiaki, Kulig, Bartosz, Laivuori, Hannele, Laufer, Marc R., Lindgren, Cecilia M., MacGregor, Stuart, Mangino, Massimo, Martin, Nicholas G., Matalliotakis, Michail, Murray, Alison D., Ndungu, Anne, Nezhat, Camran, Opoku-Anane, Jessica, Padmanabhan, Sandosh, Peters, Maire, Polak, Grzegorz, Porteous, David J., Rexrode, Kathyrn M., Romanowicz, Hanna, Saare, Merli, Saavalainen, Liisu, Schork, Andrew J., Sen, Sushmita, Shafrir, Amy L., Siewierska-Górska, Anna, Smith, Blair H., Szaflik, Tomasz, Takahashi, Atsushi, Terry, Kathryn L., Tomassetti, Carla, Vanhie, Arne, Vincent, Katy, Vo, Kim C., Werring, David J., Zervou, Maria I., Adachi, Sosuke, Buring, Julie E., Ridker, Paul M., D’Hooghe, Thomas, Hapangama, Dharani K., Hayward, Caroline, Low, Siew-Kee, Martikainen, Hannu, Chasman, Daniel I., Saunders, Philippa T., Sirota, Marina, Spector, Tim, Strapagiel, Dominik, Tung, Joyce Y., Whiteman, David C., Velez-Edwards, Digna R., Uimari, Outi, Kraft, Peter, Salumets, Andres, Nyholt, Dale R., Stefansson, Kari, Becker, Christian M., Nyegaard, Mette, Missmer, Stacey A., Montgomery, Grant W., Morris, Andrew P.

    Veröffentlicht in Nature genetics

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    Association of the PHACTR1/EDN1 Genetic Locus With Spontaneous Coronary Artery Dissection von Adlam, David, Al-Hussaini, Abtehale, Bouajila, Sara, d’Escamard, Valentina, Huang, Siying, Margaritis, Marios, Nelson, Christopher P., Welch, Catherine A., Jeunemaitre, Xavier, Barnay, Pierre, Rioufol, Gilles, Range, Grégoire, Harbaoui, Brahim, Cayla, Guillaume, Champin, Stanislas, Saint-Etienne, Christophe, Marliere, Stéphanie, Karrillon, Gaëtan, Gerbay, Antoine, Houpe, David, Wong, Claire Mei Yi, Giannoulatou, Eleni, Sweeting, Michael, McGrath-Cadell, Lucy, Dunwoodie, Sally L., Harvey, Richard, Holloway, Cameron, Nikpay, Majid, Goel, Anuj, Won, Hong-Hee, Willenborg, Christina, Kanoni, Stavroula, Kyriakou, Theodosios, Nelson, Christopher P., Webb, Thomas R., Alver, Maris, Auro, Kirsi, Bjonnes, Andrew, Chasman, Daniel I., Franceschini, Nora, Gieger, Christian, Hwang, Shih-Jen, Kleber, Marcus E., Morrison, Alanna, Rose, Lynda M., Scholz, Markus, Smith, Albert V., Uitterlinden, Andre, Beutner, Frank, Gauguier, Dominique, Goodall, Alison H., Gottesman, Omri, Han, Bok-Ghee, Kessler, Thorsten, König, Inke R., Lannfelt, Lars, Lind, Lars, Lindgren, Cecilia M., Mallick, Nadeem H., Meitinger, Thomas, Morris, Andrew P., Nieminen, Markku S., Pedersen, Nancy L., Rasheed, Asif, Sinisalo, Juha, Trompet, Stella, Wang, Laiyuan, Boerwinkle, Eric, Demuth, Ilja, Epstein, Stephen E., Esko, Tõnu, Franco, Oscar H., Franzosi, Maria Grazia, Granger, Christopher B., Harris, Tamara B., Hofman, Albert, Ingelsson, Erik, Iribarren, Carlos, Jukema, J Wouter, Karhunen, Pekka J., Kim, Bong-Jo, Kooner, Jaspal S., Kullo, Iftikhar J., Palmer, Colin N., Perola, Markus, Ridker, Paul M., Ripatti, Samuli, Salomaa, Veikko, Seedorf, Udo, Stewart, Alexandre F., Stott, David J., Thiery, Joachim, Zalloua, Pierre A., Reilly, Muredach P., Clarke, Robert, Watkins, Hugh, Samani, Nilesh J., Farrall, Martin, Hayes, Sharonne N., Samani, Nilesh J.


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