Genome-wide analysis of insomnia in 1,331,010 individuals identifies new risk loci and functional pathways von Jansen, Philip R., Watanabe, Kyoko, Stringer, Sven, Skene, Nathan, Bryois, Julien, Hammerschlag, Anke R., de Leeuw, Christiaan A., Benjamins, Jeroen S., Muñoz-Manchado, Ana B., Nagel, Mats, Savage, Jeanne E., Tiemeier, Henning, White, Tonya, Tung, Joyce Y., Hinds, David A., Vacic, Vladimir, Wang, Xin, Sullivan, Patrick F., van der Sluis, Sophie, Polderman, Tinca J. C., Smit, August B., Hjerling-Leffler, Jens, Van Someren, Eus J. W., Posthuma, Danielle

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Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria von Day, Felix, Karaderi, Tugce, Jones, Michelle R, Meun, Cindy, He, Chunyan, Drong, Alex, Kraft, Peter, Lin, Nan, Huang, Hongyan, Broer, Linda, Magi, Reedik, Saxena, Richa, Laisk, Triin, Urbanek, Margrit, Hayes, M Geoffrey, Thorleifsson, Gudmar, Fernandez-Tajes, Juan, Mahajan, Anubha, Mullin, Benjamin H, Stuckey, Bronwyn G A, Spector, Timothy D, Wilson, Scott G, Goodarzi, Mark O, Davis, Lea, Obermayer-Pietsch, Barbara, Uitterlinden, André G, Anttila, Verneri, Neale, Benjamin M, Jarvelin, Marjo-Riitta, Fauser, Bart, Kowalska, Irina, Visser, Jenny A, Andersen, Marianne, Ong, Ken, Stener-Victorin, Elisabet, Ehrmann, David, Legro, Richard S, Salumets, Andres, McCarthy, Mark I, Morin-Papunen, Laure, Thorsteinsdottir, Unnur, Stefansson, Kari, Styrkarsdottir, Unnur, Perry, John R B, Dunaif, Andrea, Laven, Joop, Franks, Steve, Lindgren, Cecilia M, Welt, Corrine K

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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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Genome-wide association study of delay discounting in 23,217 adult research participants of European ancestry von Sanchez-Roige, Sandra, Fontanillas, Pierre, Elson, Sarah L., Pandit, Anita, Schmidt, Ellen M., Foerster, Johanna R., Abecasis, Gonçalo R., Gray, Joshua C., de Wit, Harriet, Davis, Lea K., MacKillop, James, Palmer, Abraham A.

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Genetic modifiers of risk and age at onset in GBA associated Parkinson's disease and Lewy body dementia von Blauwendraat, Cornelis, Reed, Xylena, Krohn, Lynne, Heilbron, Karl, Bandres-Ciga, Sara, Tan, Manuela, Gibbs, J. Raphael, Hernandez, Dena G., Kumaran, Ravindran, Langston, Rebekah, Bonet-Ponce, Luis, Alcalay, Roy N., Hassin-Baer, Sharon, Greenbaum, Lior, Iwaki, Hirotaka, Leonard, Hampton L., Grenn, Francis P., Ruskey, Jennifer A., Sabir, Marya, Ahmed, Sarah, Makarious, Mary B., Pihlstrom, Lasse, Toft, Mathias, van Hilten, Jacobus J., Marinus, Johan, Schulte, Claudia, Brockmann, Kathrin, Sharma, Manu, Siitonen, Ari, Majamaa, Kari, Eerola-Rautio, Johanna, Tienari, Pentti J., Pantelyat, Alexander, Hillis, Argye E., Dawson, Ted M., Rosenthal, Liana S., Albert, Marilyn S., Resnick, Susan M., Ferrucci, Luigi, Morris, Christopher M., Pletnikova, Olga, Troncoso, Juan, Grosset, Donald, Lesage, Suzanne, Corvol, Jean-Christophe, Brice, Alexis, Noyce, Alastair J., Masliah, Eliezer, Wood, Nick, Hardy, John, Shulman, Lisa M., Jankovic, Joseph, Shulman, Joshua M., Heutink, Peter, Gasser, Thomas, Cannon, Paul, Scholz, Sonja W., Morris, Huw, Cookson, Mark R., Nalls, Mike A., Gan-Or, Ziv, Singleton, Andrew B.

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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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Avoiding dynastic, assortative mating, and population stratification biases in Mendelian randomization through within-family analyses von Brumpton, Ben, Sanderson, Eleanor, Heilbron, Karl, Hartwig, Fernando Pires, Harrison, Sean, Vie, Gunnhild Åberge, Cho, Yoonsu, Howe, Laura D., Hughes, Amanda, Boomsma, Dorret I., Havdahl, Alexandra, Hopper, John, Neale, Michael, Nivard, Michel G., Pedersen, Nancy L., Reynolds, Chandra A., Tucker-Drob, Elliot M., Grotzinger, Andrew, Howe, Laurence, Morris, Tim, Li, Shuai, Auton, Adam, Windmeijer, Frank, Chen, Wei-Min, Bjørngaard, Johan Håkon, Hveem, Kristian, Willer, Cristen, Evans, David M., Kaprio, Jaakko, Davey Smith, George, Åsvold, Bjørn Olav, Hemani, Gibran, Davies, Neil M.

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Genomewide Association Studies of LRRK2 Modifiers of Parkinson's Disease von Lai, Dongbing, Alipanahi, Babak, Fontanillas, Pierre, Schwantes‐An, Tae‐Hwi, Aasly, Jan, Alcalay, Roy N., Beecham, Gary W., Berg, Daniela, Bressman, Susan, Brice, Alexis, Brockman, Kathrin, Clark, Lorraine, Cookson, Mark, Das, Sayantan, Van Deerlin, Vivianna, Follett, Jordan, Farrer, Matthew J., Trinh, Joanne, Gasser, Thomas, Goldwurm, Stefano, Gustavsson, Emil, Klein, Christine, Lang, Anthony E., Langston, J. William, Latourelle, Jeanne, Lynch, Timothy, Marder, Karen, Marras, Connie, Martin, Eden R., McLean, Cory Y., Mejia‐Santana, Helen, Molho, Eric, Myers, Richard H., Nuytemans, Karen, Ozelius, Laurie, Payami, Haydeh, Raymond, Deborah, Rogaeva, Ekaterina, Rogers, Michael P., Ross, Owen A., Samii, Ali, Saunders‐Pullman, Rachel, Schüle, Birgitt, Schulte, Claudia, Scott, William K., Tanner, Caroline, Tolosa, Eduardo, Tomkins, James E., Vilas, Dolores, Trojanowski, John Q., Uitti, Ryan, Vance, Jeffery M., Visanji, Naomi P., Wszolek, Zbigniew K., Zabetian, Cyrus P., Mirelman, Anat, Giladi, Nir, Orr Urtreger, Avi, Cannon, Paul, Fiske, Brian, Foroud, Tatiana

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A multi-phenotype analysis reveals 19 susceptibility loci for basal cell carcinoma and 15 for squamous cell carcinoma von Seviiri, Mathias, Law, Matthew H., Ong, Jue-Sheng, Gharahkhani, Puya, Fontanillas, Pierre, Olsen, Catherine M., Whiteman, David C., MacGregor, Stuart

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The Latent Genetic Structure of Impulsivity and Its Relation to Internalizing Psychopathology von Gustavson, Daniel E., Friedman, Naomi P., Fontanillas, Pierre, Elson, Sarah L., Palmer, Abraham A., Sanchez-Roige, Sandra

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Parkinson's disease age at onset genome‐wide association study: Defining heritability, genetic loci, and α‐synuclein mechanisms von Blauwendraat, Cornelis, Heilbron, Karl, Vallerga, Costanza L., Bandres‐Ciga, Sara, von Coelln, Rainer, Pihlstrøm, Lasse, Simón‐Sánchez, Javier, Schulte, Claudia, Sharma, Manu, Krohn, Lynne, Siitonen, Ari, Iwaki, Hirotaka, Leonard, Hampton, Noyce, Alastair J., Tan, Manuela, Gibbs, J. Raphael, Hernandez, Dena G., Scholz, Sonja W., Jankovic, Joseph, Shulman, Lisa M., Lesage, Suzanne, Corvol, Jean‐Christophe, Brice, Alexis, van Hilten, Jacobus J., Marinus, Johan, Eerola‐Rautio, Johanna, Tienari, Pentti, Majamaa, Kari, Toft, Mathias, Grosset, Donald G., Gasser, Thomas, Heutink, Peter, Shulman, Joshua M., Wood, Nicolas, Hardy, John, Morris, Huw R., Hinds, David A., Gratten, Jacob, Visscher, Peter M., Gan‐Or, Ziv, Nalls, Mike A., Singleton, Andrew B.

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Genome‐wide association study of alcohol use disorder identification test (AUDIT) scores in 20 328 research participants of European ancestry von Sanchez‐Roige, Sandra, Fontanillas, Pierre, Elson, Sarah L., Gray, Joshua C., Wit, Harriet, Davis, Lea K., MacKillop, James, Palmer, Abraham A.

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Genome-wide association study identifies nine novel loci for 2D:4D finger ratio, a putative retrospective biomarker of testosterone exposure in utero von Warrington, Nicole M, Shevroja, Enisa, Hemani, Gibran, Hysi, Pirro G, Jiang, Yunxuan, Auton, Adam, Boer, Cindy G, Mangino, Massimo, Wang, Carol A, Kemp, John P, McMahon, George, Medina-Gomez, Carolina, Hickey, Martha, Trajanoska, Katerina, Wolke, Dieter, Ikram, M Arfan, Montgomery, Grant W, Felix, Janine F, Wright, Margaret J, Mackey, David A, Jaddoe, Vincent W, Martin, Nicholas G, Tung, Joyce Y, Davey Smith, George, Pennell, Craig E, Spector, Tim D, van Meurs, Joyce, Rivadeneira, Fernando, Medland, Sarah E, Evans, David M

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Transcriptome-wide association study identifies new susceptibility genes and pathways for depression von Li, Xiaoyan, Su, Xi, Liu, Jiewei, Li, Huijuan, Li, Ming, Li, Wenqiang, Luo, Xiong-Jian

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Author Correction: 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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The association of clinical phenotypes to known AD/FTD genetic risk loci and their inter-relationship von Li, Qingqin S., Tian, Chao, Hinds, David, Seabrook, Guy R.

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Genome-wide association and HLA fine-mapping studies identify risk loci and genetic pathways underlying allergic rhinitis von Waage, Johannes, Standl, Marie, Curtin, John A., Jessen, Leon E., Thorsen, Jonathan, Tian, Chao, Schoettler, Nathan, Flores, Carlos, Abdellaoui, Abdel, Ahluwalia, Tarunveer S., Alves, Alexessander C., Amaral, Andre F. S., Antó, Josep M., Arnold, Andreas, Barreto-Luis, Amalia, Baurecht, Hansjörg, van Beijsterveldt, Catharina E. M., Bleecker, Eugene R., Bonàs-Guarch, Sílvia, Boomsma, Dorret I., Brix, Susanne, Bunyavanich, Supinda, Burchard, Esteban G., Chen, Zhanghua, Curjuric, Ivan, Custovic, Adnan, den Dekker, Herman T., Dharmage, Shyamali C., Dmitrieva, Julia, Duijts, Liesbeth, Ege, Markus J., Gauderman, W. James, Georges, Michel, Gieger, Christian, Gilliland, Frank, Granell, Raquel, Gui, Hongsheng, Hansen, Torben, Heinrich, Joachim, Henderson, John, Hernandez-Pacheco, Natalia, Holt, Patrick, Imboden, Medea, Jaddoe, Vincent W. V., Jarvelin, Marjo-Riitta, Jarvis, Deborah L., Jensen, Kamilla K., Jónsdóttir, Ingileif, Kabesch, Michael, Kaprio, Jaakko, Kumar, Ashish, Lee, Young-Ae, Levin, Albert M., Li, Xingnan, Lorenzo-Diaz, Fabian, Melén, Erik, Mercader, Josep M., Meyers, Deborah A., Myers, Rachel, Nicolae, Dan L., Nohr, Ellen A., Palviainen, Teemu, Paternoster, Lavinia, Pennell, Craig E., Pershagen, Göran, Pino-Yanes, Maria, Probst-Hensch, Nicole M., Rüschendorf, Franz, Simpson, Angela, Stefansson, Kari, Sunyer, Jordi, Sveinbjornsson, Gardar, Thiering, Elisabeth, Thompson, Philip J., Torrent, Maties, Torrents, David, Tung, Joyce Y., Wang, Carol A., Weidinger, Stephan, Weiss, Scott, Willemsen, Gonneke, Williams, L. Keoki, Ober, Carole, Hinds, David A., Ferreira, Manuel A., Bisgaard, Hans, Strachan, David P., Bønnelykke, Klaus

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Genome-Wide Association Study Meta-Analysis of the Alcohol Use Disorders Identification Test (AUDIT) in Two Population-Based Cohorts von Sanchez-Roige, Sandra, Palmer, Abraham A, Fontanillas, Pierre, Elson, Sarah L, Adams, Mark J, Howard, David M, Edenberg, Howard J, Davies, Gail, Crist, Richard C, Deary, Ian J, McIntosh, Andrew M, Clarke, Toni-Kim

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Genome-wide analysis of 944 133 individuals provides insights into the etiology of haemorrhoidal disease von Zheng, Tenghao, Ellinghaus, David, Juzenas, Simonas, Cossais, François, Burmeister, Greta, Mayr, Gabriele, Jørgensen, Isabella Friis, Teder-Laving, Maris, Skogholt, Anne Heidi, Chen, Sisi, Strege, Peter R, Ito, Go, Banasik, Karina, Becker, Thomas, Bokelmann, Frank, Brunak, Søren, Buch, Stephan, Clausnitzer, Hartmut, Datz, Christian, Degenhardt, Frauke, Doniec, Marek, Erikstrup, Christian, Esko, Tõnu, Forster, Michael, Frey, Norbert, Fritsche, Lars G, Gabrielsen, Maiken Elvestad, Gräßle, Tobias, Gsur, Andrea, Gross, Justus, Hampe, Jochen, Hendricks, Alexander, Hinz, Sebastian, Hveem, Kristian, Jongen, Johannes, Junker, Ralf, Karlsen, Tom Hemming, Hemmrich-Stanisak, Georg, Kruis, Wolfgang, Kupcinskas, Juozas, Laubert, Tilman, Rosenstiel, Philip C, Röcken, Christoph, Laudes, Matthias, Leendertz, Fabian H, Lieb, Wolfgang, Limperger, Verena, Margetis, Nikolaos, Mätz-Rensing, Kerstin, Németh, Christopher Georg, Ness-Jensen, Eivind, Nowak-Göttl, Ulrike, Pandit, Anita, Pedersen, Ole Birger, Peleikis, Hans Günter, Peuker, Kenneth, Rodriguez, Cristina Leal, Rühlemann, Malte Christoph, Schniewind, Bodo, Schulzky, Martin, Skieceviciene, Jurgita, Tepel, Jürgen, Thomas, Laurent, Uellendahl-Werth, Florian, Ullum, Henrik, Vogel, Ilka, Volzke, Henry, von Fersen, Lorenzo, von Schönfels, Witigo, Vanderwerff, Brett, Wilking, Julia, Wittig, Michael, Zeissig, Sebastian, Zobel, Myrko, Zawistowski, Matthew, Vacic, Vladimir, Sazonova, Olga, Noblin, Elizabeth S, Farrugia, Gianrico, Beyder, Arthur, Wedel, Thilo, Kahlke, Volker, Schafmayer, Clemens, D'Amato, Mauro, Franke, Andre

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Whole exome sequencing reveals HSPA1L as a genetic risk factor for spontaneous preterm birth von Huusko, Johanna M, Karjalainen, Minna K, Graham, Britney E, Zhang, Ge, Farrow, Emily G, Miller, Neil A, Jacobsson, Bo, Eidem, Haley R, Murray, Jeffrey C, Bedell, Bruce, Breheny, Patrick, Brown, Noah W, Bødker, Frans L, Litterman, Nadia K, Jiang, Pan-Pan, Russell, Laura, Hinds, David A, Hu, Youna, Rokas, Antonis, Teramo, Kari, Christensen, Kaare, Williams, Scott M, Rämet, Mika, Kingsmore, Stephen F, Ryckman, Kelli K, Hallman, Mikko, Muglia, Louis J

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