Headache as main reason for consultation to a hospital Emergency Department in Spain: a prospective study von Fierro, A., Pérez-Rojí, G., Blanco, A., López, P., Andrés, M., González-Quintanilla, V., Pérez-Pereda, S., Fontanillas, N., Pascual, J.

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Headache as main reason for consultation to a hospital Emergency Department in Spain: a prospective study von Fierro, A, Pérez-Rojí, G, Blanco, A, López, P, Andrés, M, González-Quintanilla, V, Pérez-Pereda, S, Fontanillas, N, Pascual, J

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La cefalea como motivo principal de consulta a un servicio de urgencia hospitalaria en España: un estudio prospectivo von Fierro, A., Pérez-Rojí, G., Blanco, A., López, P., Andrés, M., González-Quintanilla, V., Pérez-Pereda, S., Fontanillas, N., Pascual, J.

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Hemangiomas infantiles de localización vulvar: un reto terapéutico von Parra-Navarro, L., March-Rodriguez, Á., Planella-Fontanillas, N., Pujol, R.M.

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Perception and knowledge of hemorrhoidal disease among healthcare professionals in Spain von Frías Vargas, M, Fontanillas Gamilla, N, Rivera Panizo, I, Fuertes Domínguez, D, Granja Ortega, C, Peiró Morant, J F

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Percepción y conocimiento de la enfermedad hemorroidal en los profesionales sanitarios en España von Frías Vargas, M., Fontanillas Gamilla, N., Rivera Panizo, I., Fuertes Domínguez, D., Granja Ortega, C., Peiró Morant, J.F.

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Colecistitis eosinofílica von Fernández Santiago, Roberto, Fontanillas Garmilla, Noelia, Gutiérrez Fernández, Gonzalo, Fernández Fernández, Fidel, Gómez Fleitas, Manuel

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Spontaneous bacterial peritonitis due to Citrobacter freundii von de Vega, T, Fontanillas, N, Méndez, M A, Casal, S

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Formes de vie von Fontanille, Jacques

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Large-scale GWAS reveals insights into the genetic architecture of same-sex sexual behavior von Ganna, Andrea, Verweij, Karin J H, Nivard, Michel G, Maier, Robert, Wedow, Robbee, Busch, Alexander S, Abdellaoui, Abdel, Guo, Shengru, Sathirapongsasuti, J Fah, Lichtenstein, Paul, Lundström, Sebastian, Långström, Niklas, Auton, Adam, Harris, Kathleen Mullan, Beecham, Gary W, Martin, Eden R, Sanders, Alan R, Perry, John R B, Neale, Benjamin M, Zietsch, Brendan P

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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.

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Multi-trait analysis of genome-wide association summary statistics using MTAG von Turley, Patrick, Walters, Raymond K., Maghzian, Omeed, Okbay, Aysu, Lee, James J., Fontana, Mark Alan, Nguyen-Viet, Tuan Anh, Wedow, Robbee, Zacher, Meghan, Furlotte, Nicholas A., Magnusson, Patrik, Oskarsson, Sven, Johannesson, Magnus, Visscher, Peter M., Laibson, David, Cesarini, David, Neale, Benjamin M., Benjamin, Daniel J.

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Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis von Gallagher, C. S., Mäkinen, N., Harris, H. R., Rahmioglu, N., Uimari, O., Cook, J. P., Shigesi, N., Ferreira, T., Velez-Edwards, D. R., Edwards, T. L., Mortlock, S., Ruhioglu, Z., Day, F., Becker, C. M., Karhunen, V., Martikainen, H., Järvelin, M.-R., Cantor, R. M., Ridker, P. M., Terry, K. L., Buring, J. E., Gordon, S. D., Medland, S. E., Montgomery, G. W., Nyholt, D. R., Hinds, D. A., Tung, J. Y., Perry, J. R. B., Lind, P. A., Painter, J. N., Martin, N. G., Morris, A. P., Chasman, D. I., Missmer, S. A., Zondervan, K. T., Morton, C. C.

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Phenome-wide investigation of health outcomes associated with genetic predisposition to loneliness von Abdellaoui, Abdel, Sanchez-Roige, Sandra, Sealock, Julia, Treur, Jorien L, Dennis, Jessica, Fontanillas, Pierre, Elson, Sarah, Nivard, Michel G, Ip, Hill Fung, van der Zee, Matthijs, Baselmans, Bart M L, Hottenga, Jouke Jan, Willemsen, Gonneke, Mosing, Miriam, Lu, Yi, Pedersen, Nancy L, Denys, Damiaan, Amin, Najaf, M van Duijn, Cornelia, Szilagyi, Ingrid, Tiemeier, Henning, Neumann, Alexander, Verweij, Karin J H, Cacioppo, Stephanie, Cacioppo, John T, Davis, Lea K, Palmer, Abraham A, Boomsma, Dorret I

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Identification of common genetic risk variants for autism spectrum disorder von Grove, Jakob, Ripke, Stephan, Als, Thomas D., Mattheisen, Manuel, Walters, Raymond K., Won, Hyejung, Pallesen, Jonatan, Agerbo, Esben, Andreassen, Ole A., Anney, Richard, Awashti, Swapnil, Belliveau, Rich, Bettella, Francesco, Buxbaum, Joseph D., Bybjerg-Grauholm, Jonas, Bækvad-Hansen, Marie, Cerrato, Felecia, Chambert, Kimberly, Christensen, Jane H., Churchhouse, Claire, Dellenvall, Karin, Demontis, Ditte, De Rubeis, Silvia, Devlin, Bernie, Djurovic, Srdjan, Dumont, Ashley L., Goldstein, Jacqueline I., Hansen, Christine S., Hauberg, Mads Engel, Hollegaard, Mads V., Hope, Sigrun, Howrigan, Daniel P., Huang, Hailiang, Hultman, Christina M., Klei, Lambertus, Maller, Julian, Martin, Joanna, Martin, Alicia R., Moran, Jennifer L., Nyegaard, Mette, Nærland, Terje, Palmer, Duncan S., Palotie, Aarno, Pedersen, Carsten Bøcker, Pedersen, Marianne Giørtz, dPoterba, Timothy, Poulsen, Jesper Buchhave, Pourcain, Beate St, Qvist, Per, Rehnström, Karola, Reichenberg, Abraham, Reichert, Jennifer, Robinson, Elise B., Roeder, Kathryn, Roussos, Panos, Saemundsen, Evald, Sandin, Sven, Satterstrom, F. Kyle, Davey Smith, George, Stefansson, Hreinn, Steinberg, Stacy, Stevens, Christine R., Sullivan, Patrick F., Turley, Patrick, Walters, G. Bragi, Xu, Xinyi, Stefansson, Kari, Geschwind, Daniel H., Nordentoft, Merete, Hougaard, David M., Werge, Thomas, Mors, Ole, Mortensen, Preben Bo, Neale, Benjamin M., Daly, Mark J., Børglum, Anders D.

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Gastroesophageal reflux GWAS identifies risk loci that also associate with subsequent severe esophageal diseases von An, Jiyuan, Gharahkhani, Puya, Law, Matthew H., Ong, Jue-Sheng, Han, Xikun, Olsen, Catherine M., Neale, Rachel E., Lai, John, Vaughan, Tom L., Gockel, Ines, Thieme, René, Böhmer, Anne C., Jankowski, Janusz, Fitzgerald, Rebecca C., Schumacher, Johannes, Palles, Claire, Whiteman, David C., MacGregor, Stuart

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Genome-wide meta-analysis of depression identifies 102 independent variants and highlights the importance of the prefrontal brain regions von Howard, David M., Adams, Mark J., Clarke, Toni-Kim, Hafferty, Jonathan D., Gibson, Jude, Shirali, Masoud, Coleman, Jonathan R. I., Hagenaars, Saskia P., Ward, Joey, Wigmore, Eleanor M., Alloza, Clara, Shen, Xueyi, Barbu, Miruna C., Xu, Eileen Y., Whalley, Heather C., Marioni, Riccardo E., Porteous, David J., Davies, Gail, Deary, Ian J., Hemani, Gibran, Berger, Klaus, Teismann, Henning, Rawal, Rajesh, Arolt, Volker, Baune, Bernhard T., Dannlowski, Udo, Domschke, Katharina, Tian, Chao, Hinds, David A., Trzaskowski, Maciej, Byrne, Enda M., Ripke, Stephan, Smith, Daniel J., Sullivan, Patrick F., Wray, Naomi R., Breen, Gerome, Lewis, Cathryn M., McIntosh, Andrew M.

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Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder von Demontis, Ditte, Walters, Raymond K., Martin, Joanna, Mattheisen, Manuel, Als, Thomas D., Agerbo, Esben, Baldursson, Gísli, Belliveau, Rich, Bybjerg-Grauholm, Jonas, Bækvad-Hansen, Marie, Cerrato, Felecia, Chambert, Kimberly, Churchhouse, Claire, Dumont, Ashley, Eriksson, Nicholas, Gandal, Michael, Goldstein, Jacqueline I., Grasby, Katrina L., Grove, Jakob, Gudmundsson, Olafur O., Hansen, Christine S., Hauberg, Mads Engel, Hollegaard, Mads V., Howrigan, Daniel P., Huang, Hailiang, Maller, Julian B., Martin, Alicia R., Martin, Nicholas G., Moran, Jennifer, Pallesen, Jonatan, Palmer, Duncan S., Pedersen, Carsten Bøcker, Pedersen, Marianne Giørtz, Poterba, Timothy, Poulsen, Jesper Buchhave, Ripke, Stephan, Robinson, Elise B., Satterstrom, F. Kyle, Stefansson, Hreinn, Stevens, Christine, Turley, Patrick, Walters, G. Bragi, Won, Hyejung, Wright, Margaret J., Andreassen, Ole A., Asherson, Philip, Burton, Christie L., Boomsma, Dorret I., Cormand, Bru, Dalsgaard, Søren, Franke, Barbara, Gelernter, Joel, Geschwind, Daniel, Hakonarson, Hakon, Haavik, Jan, Kranzler, Henry R., Kuntsi, Jonna, Langley, Kate, Lesch, Klaus-Peter, Middeldorp, Christel, Reif, Andreas, Rohde, Luis Augusto, Roussos, Panos, Schachar, Russell, Sklar, Pamela, Sonuga-Barke, Edmund J. S., Sullivan, Patrick F., Thapar, Anita, Tung, Joyce Y., Waldman, Irwin D., Medland, Sarah E., Stefansson, Kari, Nordentoft, Merete, Hougaard, David M., Werge, Thomas, Mors, Ole, Mortensen, Preben Bo, Daly, Mark J., Faraone, Stephen V., Børglum, Anders D., Neale, Benjamin M.

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Genetic Consequences of the Transatlantic Slave Trade in the Americas von Micheletti, Steven J., Bryc, Kasia, Ancona Esselmann, Samantha G., Freyman, William A., Moreno, Meghan E., Poznik, G. David, Shastri, Anjali J., Agee, M., Aslibekyan, S., Auton, A., Bell, R., Clark, S., Das, S., Elson, S., Fletez-Brant, K., Fontanillas, P., Gandhi, P., Heilbron, K., Hicks, B., Hinds, D., Huber, K., Jewett, E., Jiang, Y., Kleinman, A., Lin, K., Litterman, N., McCreight, J., McIntyre, M., McManus, K., Mozaffari, S., Nandakumar, P., Noblin, L., Northover, C., O’Connell, J., Petrakovitz, A., Pitts, S., Shelton, J., Shringarpure, S., Tian, C., Tung, J., Tunney, R., Vacic, V., Wang, X., Zare, A., Beleza, Sandra, Mountain, Joanna L.

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Genetic insights into biological mechanisms governing human ovarian ageing von Hussain, Jazib, Abe, Hironori, Fontanillas, Pierre, Bakker, Olivier B., Sulem, Patrick, Terao, Chikashi, Horikoshi, Momoko, Shukla, Vallari, Borup, Rehannah, Olsen, Kristina W., Ferrer-Roda, Mònica, Timmers, Paul R. H. J., Ahearn, Thomas U., Naderi, Elnaz, Barbieri, Caterina M., Beaumont, Robin N., Becher, Heiko, Beckmann, Matthias W., Bochud, Murielle, Boomsma, Dorret I., Bowker, Nicholas, Campbell, Harry, Catamo, Eulalia, Chanock, Stephen J., Ciullo, Marina, Corre, Tanguy, Couch, Fergus J., Cox, Angela, Cross, Simon S., Cucca, Francesco, Czene, Kamila, Smith, George Davey, Faul, Jessica D., Ferrucci, Luigi, Franceschini, Nora, Gago-Dominguez, Manuela, Mezzavilla, Massimo, Grallert, Harald, Hayward, Caroline, Høffding, Miya K., Hu, Frank, Joaquim, Micaella D. R., John, Esther M., Joshi, Peter K., Kardia, Sharon L. R., Kartsonaki, Christiana, Kooperberg, Charles, Kurian, Allison W., Kutalik, Zoltan, LaChance, Genevieve, Langenberg, Claudia, Laven, Joop S. E., Lawlor, Deborah A., Le Marchand, Loic, Li, Jingmei, Lindblom, Annika, Mangino, Massimo, Mannermaa, Arto, Marten, Jonathan, McKnight, Barbara, Medland, Sarah E., Menni, Cristina, Milani, Lili, Mulas, Antonella, Mulligan, Anna M., Newman, Anne, Noordam, Raymond, Nutile, Teresa, Nyholt, Dale R., Pedersen, Nancy L., Porcu, Eleonora, Psaty, Bruce M., Rennert, Gad, Rennert, Hedy S., Ruggiero, Daniela, Sawyer, Elinor J., Schoemaker, Minouk J., Schraut, Katharina E., Smith, Albert V., Smith, Blair H., Sorice, Rossella, Spinelli, John J., van Meurs, Joyce B. J., Troester, Melissa A., Truong, Thérèse, Vachon, Celine M., Vitart, Veronique, Vollenweider, Peter, Wang, Qin, Weinberg, Clarice R., Franke, Lude, Burgess, Stephen, Pers, Tune H., Lopez-Contreras, Andres J., Visser, Jenny A., Namekawa, Satoshi H., Murabito, Joanne M., Ong, Ken K., Murray, Anna, Perry, John R. B.

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