Introduction: The Invisible (Migrant) Man von Charsley, Katharine, Wray, Helena

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A Thing Apart: Controlling Male Family Migration to the United Kingdom von Wray, Helena

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Kept apart: Routine family separation in the UK family immigration system as times of crises von Charsley, Katharine, Wray, Helena

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An Ideal Husband? Marriages of Convenience, Moral Gate-keeping and Immigration to the UK von Wray, Helena

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Moulding the migrant family von Wray, Helena

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A Family Resemblance? The Regulation of Marriage Migration in Europe von Wray, Helena, Agoston, Agnes, Hutton, Jocelyn

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Introduction to Special Issue: Family Migration in Times of Crisis von Wray, Helena, Charsley, Katharine, Kolbaşı-Muyan, Gizem, Smith, Lothar

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The Aliens Act 1905 and the Immigration Dilemma von Wray, Helena

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A Family Resemblance? The Regulation of Marriage Migration in Europe von Wray, Helena, Agoston, Agnes, Hutton, Jocelyn

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International human rights frameworks in relation to national family reunification policy and administrative practice von Palander, Jaana, Baraka, Usumain, Gustafsson, Hilda, Kvalvaag, Alyssa Marie, Lokot, Michelle, Martuscelli, Patrícia Nabuco, Mesgena, Hadas Yaron, Tuzi, Irene, Wray, Helena

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International human rights frameworks in relation to national family reunification policy and administrative practice von Palander, Jaana, Baraka, Usumain, Gustafsson, Hilda, Kvalvaag, Alyssa Marie, Lokot, Michelle, Martuscelli, Patrícia Nabuco, Mesgena, Hadas Yaron, Tuzi, Irene, Wray, Helena

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International Human Rights Frameworks in Relation to National Family Reunification Policy and Administrative Practice von Palander, Jaana, Baraka, Usumain, Gustafsson, Hilda, Kvalvaag, Alyssa Marie, Lokot, Michelle, Martuscelli, Patrícia N, Yaron Mesgena, Hadas, Tuzi, Irene, Wray, Helena

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Common polygenic variation contributes to risk of schizophrenia and bipolar disorder von Purcell, Shaun M, Wray, Naomi R, Stone, Jennifer L, Visscher, Peter M, O'Donovan, Michael C, Sullivan, Patrick F, Sklar, Pamela

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Analysis of shared heritability in common disorders of the brain von Anttila, Verneri, Bulik-Sullivan, Brendan, Finucane, Hilary K, Walters, Raymond K, Bras, Jose, Duncan, Laramie, Escott-Price, Valentina, Falcone, Guido J, Gormley, Padhraig, Malik, Rainer, Patsopoulos, Nikolaos A, Ripke, Stephan, Wei, Zhi, Yu, Dongmei, Lee, Phil H, Turley, Patrick, Grenier-Boley, Benjamin, Chouraki, Vincent, Kamatani, Yoichiro, Berr, Claudine, Letenneur, Luc, Hannequin, Didier, Amouyel, Philippe, Boland, Anne, Deleuze, Jean-François, Duron, Emmanuelle, Vardarajan, Badri N, Reitz, Christiane, Goate, Alison M, Huentelman, Matthew J, Kamboh, M Ilyas, Larson, Eric B, Rogaeva, Ekaterina, St George-Hyslop, Peter, Hakonarson, Hakon, Kukull, Walter A, Farrer, Lindsay A, Barnes, Lisa L, Beach, Thomas G, Demirci, F Yesim, Head, Elizabeth, Hulette, Christine M, Jicha, Gregory A, Kauwe, John S K, Kaye, Jeffrey A, Leverenz, James B, Levey, Allan I, Lieberman, Andrew P, Pankratz, Vernon S, Poon, Wayne W, Quinn, Joseph F, Saykin, Andrew J, Schneider, Lon S, Smith, Amanda G, Sonnen, Joshua A, Stern, Robert A, Van Deerlin, Vivianna M, Van Eldik, Linda J, Harold, Denise, Russo, Giancarlo, Rubinsztein, David C, Bayer, Anthony, Tsolaki, Magda, Proitsi, Petra, Fox, Nick C, Hampel, Harald, Owen, Michael J, Mead, Simon, Passmore, Peter, Morgan, Kevin, Nöthen, Markus M, Rossor, Martin, Lupton, Michelle K, Hoffmann, Per, Kornhuber, Johannes, Lawlor, Brian, McQuillin, Andrew, Al-Chalabi, Ammar, Bis, Joshua C, Ruiz, Agustin, Boada, Mercè, Seshadri, Sudha, Beiser, Alexa, Rice, Kenneth, van der Lee, Sven J, De Jager, Philip L, Geschwind, Daniel H, Riemenschneider, Matthias, Riedel-Heller, Steffi, Rotter, Jerome I, Ransmayr, Gerhard, Hyman, Bradley T, Cruchaga, Carlos, Alegret, Montserrat, Winsvold, Bendik, Palta, Priit, Farh, Kai-How, Cuenca-Leon, Ester, Furlotte, Nicholas, Kurth, Tobias

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The association of second trimester biomarkers in amniotic fluid and fetal outcome von Sterpu, Irene, Anfelter, Peter, Wray, Susan, Kaihola, Helena, Åkerud, Helena, Wiberg-Itzel, Eva

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Genome-wide copy number variation association study in anorexia nervosa von Walker, Alicia, Karlsson, Robert, Szatkiewicz, Jin P, Thornton, Laura M, Yilmaz, Zeynep, Leppä, Virpi M, Savva, Androula, Lin, Tian, Sidorenko, Julia, McRae, Allan, Kirov, George, Davies, Helena L, Fundín, Bengt T, Chawner, Samuel J R A, Song, Jie, Borg, Stina, Wen, Jia, Watson, Hunna J, Munn-Chernoff, Melissa A, Baker, Jessica H, Gordon, Scott, Berrettini, Wade H, Brandt, Harry, Crawford, Steven, Halmi, Katherine A, Kaplan, Allan S, Kaye, Walter H, Mitchell, James, Strober, Michael, Woodside, D Blake, Pedersen, Nancy L, Parker, Richard, Jordan, Jennifer, Kennedy, Martin A, Birgegård, Andreas, Landén, Mikael, Martin, Nicholas G, Sullivan, Patrick F, Bulik, Cynthia M, Wray, Naomi R

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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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Genetic comorbidity between major depression and cardio‐metabolic traits, stratified by age at onset of major depression von Hagenaars, Saskia P., Coleman, Jonathan R. I., Choi, Shing Wan, Gaspar, Héléna, Adams, Mark J., Howard, David M., Hodgson, Karen, Traylor, Matthew, Air, Tracy M., Andlauer, Till F. M., Arolt, Volker, Baune, Bernhard T., Binder, Elisabeth B., Blackwood, Douglas H. R., Boomsma, Dorret I., Campbell, Archie, Cearns, Micah, Czamara, Darina, Dannlowski, Udo, Domschke, Katharina, Geus, Eco J. C., Hamilton, Steven P., Hayward, Caroline, Hickie, Ian B., Hottenga, Jouke Jan, Ising, Marcus, Jones, Ian, Jones, Lisa, Kutalik, Zoltan, Lucae, Susanne, Martin, Nicholas G., Milaneschi, Yuri, Mueller‐Myhsok, Bertram, Owen, Michael J., Padmanabhan, Sandosh, Penninx, Brenda W. J. H., Pistis, Giorgio, Porteous, David J., Preisig, Martin, Ripke, Stephan, Shyn, Stanley I., Sullivan, Patrick F., Whitfield, John B., Wray, Naomi R., McIntosh, Andrew M., Deary, Ian J., Breen, Gerome, Lewis, Cathryn M.

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Molecular pathways involved in neuronal cell adhesion and membrane scaffolding contribute to schizophrenia and bipolar disorder susceptibility von O'Dushlaine, C, Kenny, E, Heron, E, Donohoe, G, Gill, M, Morris, D, Corvin, A

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Genome-wide gene-environment analyses of major depressive disorder and reported lifetime traumatic experiences in UK Biobank von Coleman, Jonathan R. I., Peyrot, Wouter J., Purves, Kirstin L., Davis, Katrina A. S., Rayner, Christopher, Choi, Shing Wan, Hübel, Christopher, Gaspar, Héléna A., Kan, Carol, Van der Auwera, Sandra, Adams, Mark James, Lyall, Donald M., Choi, Karmel W., Dunn, Erin C., Vassos, Evangelos, Danese, Andrea, Maughan, Barbara, Grabe, Hans J., Lewis, Cathryn M., O’Reilly, Paul F., McIntosh, Andrew M., Smith, Daniel J., Wray, Naomi R., Hotopf, Matthew, Eley, Thalia C., Breen, Gerome

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