Sharing data safely while preserving privacy von Ursin, Giske, Malila, Nea, Chang-Claude, Jenny, Gunter, Marc, Kaaks, Rudolf, Kampman, Ellen, Lambe, Mats, van Leeuwen, Flora, Magnusson, Patrik, Nilbert, Mef C, Romundstad, Pål R, Röösli, Martin, Ryel, Anne Lise, dos-Santos-Silva, Isabel, Stenbeck, Magnus, Storm, Hans H, Swerdlow, Anthony, Vineis, Paolo, Knudsen, Gun Peggy S

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Data must be shared—also with researchers outside of Europe von Ursin, Giske, Stenbeck, Magnus, Chang-Claude, Jenny, Gunter, Marc, Kaaks, Rudolf, Kampman, Ellen, Lambe, Mats, van Leeuwen, Flora, Magnusson, Patrik, Malila, Nea, Nilbert, Mef C, Romundstad, Pål R, Röösli, Martin, Ryel, Anne Lise, dos-Santos-Silva, Isabel, Storm, Hans H, Swerdlow, Anthony, Vineis, Paolo, Knudsen, Gun Peggy S

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Increased skewing of X chromosome inactivation in Rett syndrome patients and their mothers von KNUDSEN, Gun Peggy S, NEILSON, Tracey C. S, PEDERSEN, June, KERR, Alison, SCHWARTZ, Marianne, HULTEN, Maj, BAILEY, Mark E. S, ØRSTAVIK, Karen Helene

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Identification of Genetic Loci Shared Between Attention-Deficit/Hyperactivity Disorder, Intelligence, and Educational Attainment von O’Connell, Kevin S., Shadrin, Alexey, Smeland, Olav B., Bahrami, Shahram, Frei, Oleksandr, Bettella, Francesco, Krull, Florian, Fan, Chun C., Askeland, Ragna B., Knudsen, Gun Peggy S., Halmøy, Anne, Steen, Nils Eiel, Ueland, Torill, Walters, G. Bragi, Davíðsdóttir, Katrín, Haraldsdóttir, Gyða S., Guðmundsson, Ólafur Ó., Stefánsson, Hreinn, Reichborn-Kjennerud, Ted, Haavik, Jan, Dale, Anders M., Stefánsson, Kári, Djurovic, Srdjan, Andreassen, Ole A.

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High Frequency of Skewed X-Chromosome Inactivation in Females with Autoimmune Thyroid Disease: A Possible Explanation for the Female Predisposition to Thyroid Autoimmunity von Brix, Thomas Heiberg, Knudsen, Gun Peggy S., Kristiansen, Marianne, Kyvik, Kirsten Ohm, Ørstavik, Karen Helene, Hegedüs, Laszlo

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Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism von Satterstrom, F. Kyle, Breen, Michael S., Grove, Jakob, Klei, Lambertus, Xu, Xinyi, Norman, Utku, Brand, Harrison, Schwartz, Grace, Barbosa, Mafalda, Bybjerg-Grauholm, Jonas, Carracedo, Angel, Chiocchetti, Andreas G., Chung, Brian H.Y., Coon, Hilary, Cuccaro, Michael L., Dalla Bernardina, Bernardo, Domenici, Enrico, Dong, Shan, Freitag, Christine M., González-Peñas, Javier, Guter, Stephen, He, Xin, Herman, Gail E., Hertz-Picciotto, Irva, Hougaard, David M., Ionita-Laza, Iuliana, Jacob, Suma, Jamison, Jesslyn, Jugessur, Astanand, Kolevzon, Alexander, Kushima, Itaru, Lee, So Lun, Lehtimäki, Terho, Lim, Elaine T., Lipkin, W. Ian, Lopergolo, Diego, Lopes, Fátima, Ludena, Yunin, Maciel, Patricia, Meiri, Gal, Menashe, Idan, Miller, Judith, Montenegro, Eduarda M.S., Muglia, Pierandrea, Nordentoft, Merete, Ozaki, Norio, Palotie, Aarno, Parellada, Mara, Passos-Bueno, Maria Rita, Persico, Antonio M., Pessah, Isaac, Puura, Kaija, Renieri, Alessandra, Riberi, Evelise, Robinson, Elise B., Samocha, Kaitlin E., Sandin, Sven, Santangelo, Susan L., Schellenberg, Gerry, Scherer, Stephen W., Schmitt, Lauren, Silva, Isabela M.W., Singh, Tarjinder, Siper, Paige M., Soares, Gabriela, Susser, Ezra, Szatmari, Peter, Tang, Lara, Tassone, Flora, Teufel, Karoline, Trelles, Maria del Pilar, Werge, Thomas, Werling, Donna M., Wigdor, Emilie M., Yu, Mullin H.C., Zachi, Elaine, Agerbo, Esben, Als, Thomas Damm, Bækvad-Hansen, Marie, Belliveau, Rich, Cerrato, Felecia, Chambert, Kimberly, Churchhouse, Claire, Dumont, Ashley, Hansen, Christine S., Hauberg, Mads Engel, Hollegaard, Mads V., Howrigan, Daniel P., Maller, Julian, Mattheisen, Manuel, Moran, Jennifer, Pallesen, Jonatan, Poulsen, Jesper Buchhave, Ripke, Stephan, Gallagher, Louise, Gill, Michael, Zwick, Michael E., State, Matthew W., Daly, Mark J., Buxbaum, Joseph D.

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Rates, distribution and implications of postzygotic mosaic mutations in autism spectrum disorder von Lim, Elaine T, Uddin, Mohammed, De Rubeis, Silvia, Chan, Yingleong, Kamumbu, Anne S, Zhang, Xiaochang, D'Gama, Alissa M, Kim, Sonia N, Hill, Robert Sean, Goldberg, Arthur P, Poultney, Christopher, Minshew, Nancy J, Kushima, Itaru, Aleksic, Branko, Ozaki, Norio, Parellada, Mara, Arango, Celso, Penzol, Maria J, Carracedo, Angel, Kolevzon, Alexander, Hultman, Christina M, Weiss, Lauren A, Fromer, Menachem, Chiocchetti, Andreas G, Freitag, Christine M, Church, George M, Scherer, Stephen W, Buxbaum, Joseph D, Walsh, Christopher A

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Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders von Tucker-Drob, Elliot M., Yu, Dongmei, Ge, Tian, Derks, Eske M., Keski-Rahkonen, Anna, Kirov, George, Asherson, Philip, Baldursson, Gísli, Bybjerg-Grauholm, Jonas, Churchhouse, Claire, Crosbie, Jennifer, Demontis, Ditte, Grove, Jakob, Martin, Joanna, McGough, James J., Pedersen, Carsten B., Poulsen, Jesper B., Rothenberger, Aribert, Schachar, Russell, Turley, Patrick, Arking, Dan E., Collins, Ryan L., Coon, Hilary, Delorme, Richard, Hope, Sigrun, Nyegaard, Mette, Pinto, Dalila, Qvist, Per, Talkowski, Michael E., Albani, Diego, Alda, Martin, Bass, Nicholas, Bauer, Michael, Cichon, Sven, Clarke, Toni-Kim, Czerski, Piotr M., Fischer, Sascha B., Frank, Josef, Goes, Fernando S., Holland, Dominic, Jones, Lisa A., Joachim, Oedegaard Ketil, Maaser, Anna, Malt, Ulrik F., McMahon, Francis J., Montgomery, Grant W., Myers, Richard M., Nöthen, Markus M., Perry, Amy, Vieta, Eduard, Aschauer, Harald, Bencko, Vladimir, Burghardt, Roland, Carlberg, Laura, Guo, Yiran, Klump, Kelly L., Le Hellard, Stephanie, Monteleone, Alessio Maria, Seitz, Jochen, Treasure, Janet, Wade, Tracey D., Wichmann, H-Erich, Woodside, D. Blake, Grabe, Hans J., Horn, Carsten, Penninx, Brenda WJH, Schulte, Eva C., Smith, Daniel J., Alexander, Madeline, Begemann, Martin, Campion, Dominique, Ehrenreich, Hannelore, Murphy, Kieran C., Riley, Brien, Sham, Pak C., van Os, Jim, Weiser, Mark, Brown, Lawrence W., Cheon, Keun-Ah, Denys, Damiaan, Gilbert, Donald L., Grados, Marco A., Ibanez-Gomez, Laura, King, Robert A., Leventhal, Bennett L., Okun, Michael S., Piras, Federica, Robertson, Mary, Samuels, Jack F., Spalletta, Gianfranco, Stein, Dan J., Stewart, S Evelyn, Storch, Eric A., Stranger, Barbara, Tübing, Jennifer, Visscher, Frank, Wagner, Michael, Santangelo, Susan L., Thornton, Laura M., Neale, Benjamin M.

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The LifeCycle Project-EU Child Cohort Network: a federated analysis infrastructure and harmonized data of more than 250,000 children and parents von Jaddoe, Vincent W. V., Felix, Janine F., Andersen, Anne-Marie Nybo, Charles, Marie-Aline, Chatzi, Leda, Corpeleijn, Eva, Donner, Nina, Elhakeem, Ahmed, Eriksson, Johan G., Foong, Rachel, Grote, Veit, Haakma, Sido, Hanson, Mark, Harris, Jennifer R., Heude, Barbara, Huang, Rae-Chi, Inskip, Hazel, Järvelin, Marjo-Riitta, Koletzko, Berthold, Lawlor, Deborah A., Lindeboom, Maarten, McEachan, Rosemary R. C., Mikkola, Tuija M., Nader, Johanna L. T., de Moira, Angela Pinot, Pizzi, Costanza, Richiardi, Lorenzo, Sebert, Sylvain, Schwalber, Ameli, Sunyer, Jordi, Swertz, Morris A., Vafeiadi, Marina, Vrijheid, Martine, Wright, John, Duijts, Liesbeth

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Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa von Hübel, Christopher, Bryois, Julien, Hinney, Anke, Leppä, Virpi M., Mattheisen, Manuel, Medland, Sarah E., Giusti-Rodríguez, Paola, Alfredsson, Lars, Berrettini, Wade H., Boni, Claudette, Burghardt, Roland, Cichon, Sven, Cone, Roger D., Courtet, Philippe, Crowley, James J., Davis, Oliver S. P., de Zwaan, Martina, Dikeos, Dimitris, Dina, Christian, Duncan, Laramie E., Egberts, Karin, Estivill, Xavier, Favaro, Angela, Fernández-Aranda, Fernando, Fichter, Manfred M., Forstner, Andreas J., Forzan, Monica, Franklin, Christopher S., Giegling, Ina, Guillaume, Sébastien, Hakonarson, Hakon, Hatzikotoulas, Konstantinos, Hauser, Joanna, Helder, Sietske G., Herpertz-Dahlmann, Beate, Herzog, Wolfgang, Huckins, Laura M., Hudson, James I., Inoko, Hidetoshi, Janout, Vladimir, Julià, Antonio, Kalsi, Gursharan, Kaminská, Deborah, Karhunen, Leila, Keski-Rahkonen, Anna, Kim, Youl-Ri, Knudsen, Gun Peggy S., La Via, Maria C., Levitan, Robert D., Lin, Bochao Danae, Luykx, Jurjen, Marsal, Sara, Marshall, Christian R., McDevitt, Sara, McGuffin, Peter, Metspalu, Andres, Monteleone, Alessio Maria, Monteleone, Palmiero, Munn-Chernoff, Melissa A., Navratilova, Marie, O’Toole, Julie K., Palotie, Aarno, Raevuori, Anu, Ramoz, Nicolas, Reichborn-Kjennerud, Ted, Ritschel, Franziska, Roberts, Marion, Rotondo, Alessandro, Rujescu, Dan, Rybakowski, Filip, Santonastaso, Paolo, Scherer, Stephen W., Schmidt, Ulrike, Schosser, Alexandra, Slagboom, P. Eline, Sorbi, Sandro, Szatkiewicz, Jin P., Tenconi, Elena, Tortorella, Alfonso, Treasure, Janet, Tziouvas, Konstantinos, van Elburg, Annemarie A., van Furth, Eric F., Zipfel, Stephan, Bergen, Andrew W., Boden, Joseph M., Johnson, Craig, Kaye, Walter H., Mitchell, James E., Olsen, Catherine M., Woodside, D. Blake, Stuber, Garret D., Gordon, Scott, Henders, Anjali K., Juréus, Anders, Petersen, Liselotte, Wade, Tracey D., Landén, Mikael, Sullivan, Patrick F., Breen, Gerome

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Prenatal Phthalates, Maternal Thyroid Function, and Risk of Attention-Deficit Hyperactivity Disorder in the Norwegian Mother and Child Cohort von Engel, Stephanie M, Villanger, Gro D, Nethery, Rachel C, Thomsen, Cathrine, Sakhi, Amrit K, Drover, Samantha S M, Hoppin, Jane A, Zeiner, Pal, Knudsen, Gun Peggy, Reichborn-Kjennerud, Ted, Herring, Amy H, Aase, Heidi

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No Link Between X Chromosome Inactivation Pattern and Simple Goiter in Females: Evidence from a Twin Study von Brix, Thomas Heiberg, Hansen, Pia Skov, Knudsen, Gun Peggy S., Kringen, Marianne K., Kyvik, Kirsten Ohm, Ørstavik, Karen Helene, Hegedüs, Laszlo

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Associations Between Attention-Deficit/Hyperactivity Disorder and Various Eating Disorders: A Swedish Nationwide Population Study Using Multiple Genetically Informative Approaches von Yao, Shuyang, Kuja-Halkola, Ralf, Lu, Yi, Birgegård, Andreas, Yilmaz, Zeynep, Coleman, Joni, Courtet, Philippe, Crawford, Steven, Crow, Scott, Crowley, James, Danner, Unna, Dikeos, Dimitris, Docampo, Elisa, Ehrlich, Stefan, Estivill, Xavier, Favaro, Angela, Fichter, Manfred, Foretova, Lenka, Forzan, Monica, Franklin, Christopher, Gaspar, Héléna, Gonidakis, Fragiskos, Gorwood, Philip, Guo, Yiran, Hakonarson, Hakon, Hatzikotoulas, Konstantinos, Hebebrand, Johannes, Hendriks, Judith, Hilliard, Christopher, Hinney, Anke, Huckins, Laura, Hudson, James, Huemer, Julia, Imgart, Hartmut, Inoko, Hidetoshi, Johnson, Craig, Jordan, Jenny, Juréus, Anders, Kalsi, Gursharan, Karhunen, Leila, Karwautz, Andreas, Kas, Martien, Kennedy, James, Keski-Rahkonen, Anna, Koubek, Doris, Levitan, Robert, Lichtenstein, Paul, Mannik, Katrin, Martin, Nicholas, Merl, Elisabeth, Metspalu, Andres, Meulenbelt, Ingrid, Mitchell, James, Monteleone, Palmiero, Munn-Chernoff, Melissa, Nilsson, Ida, Norring, Claes, Ntalla, Ioanna, Parker, Richard, Rabionet, Raquel, Raevuori, Anu, Rajewski, Andrzej, Reichborn-Kjennerud, Ted, Ritschel, Franziska, Scherag, André, Schmidt, Ulrike, Seitz, Jochen, Slachtova, Lenka, Slopien, Agnieszka, Strober, Michael, Sullivan, Patrick, Szatkiewicz, Jin, Tenconi, Elena, Thornton, Laura, Treasure, Janet, Wagner, Gudrun, Walton, Esther, Woodside, D. Blake, Zeggini, Eleftheria, Zerwas, Stephanie, Andreassen, Ole, Aschauer, Harald, Barrett, Jeffrey, Bencko, Vladimir, Espeseth, Thomas, Floyd, James, Gallinger, Steven, Gambaro, Giovanni, Giegling, Ina, Herms, Stefan, Julià, Antonio, Klareskog, Lars, Le Hellard, Stephanie, Navratilova, Marie, Ophoff, Roel, Pinto, Dalila, Rujescu, Dan, Sladek, Robert, Wichmann, H-Erich, Magnusson, Patrik K.

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Dissecting the Shared Genetic Architecture of Suicide Attempt, Psychiatric Disorders, and Known Risk Factors von Mullins, Niamh, Campos, Adrian I., Shabalin, Andrey, Hafferty, Jonathan D., Okazaki, Satoshi, Bohus, Martin, Johnson, Craig, Li, Dong, Magistretti, Pierre J., Van der Auwera, Sandra, Byrne, Enda M., Casas, Miguel, Jonsson, Lina, O’Donovan, Michael C., Pato, Carlos, Ramos-Quiroga, Josep Antoni, Sánchez-Mora, Cristina, Smeland, Olav B., Shannon Weickert, Cynthia, Hauser, Elizabeth R., Andlauer, Till F.M., Colodro-Conde, Lucía, Craddock, Nick, Derks, Eske M., Escott-Price, Valentina, Gordon, Scott D., Wu, Yang, Xi, Hualin S., Esko, Tõnu, Kohane, Isaac S., McGrath, Patrick, McGuffin, Peter, Middeldorp, Christel M., Milaneschi, Yuri, Nauck, Matthias, Nyholt, Dale R., Nöthen, Markus M., Pedersen, Nancy L., Pedersen, Carsten Bøcker, Steinberg, Stacy, Potash, James B., Schaefer, Catherine, Smoller, Jordan W., Völzke, Henry, Drange, Ole Kristian, Ikeda, Masashi, Panagiotaropoulou, Georgia, Sloofman, Laura G., Casas, Miquel, Ferrier, I. Nicol, Guzman-Parra, José, Kogevinas, Manolis, Lee, Phil H., Magnusson, Sigurdur H., Mühleisen, Thomas W., Sirignano, Lea, Adolfsson, Rolf, Alda, Martin, Catts, Stanley, Corvin, Aiden, Craddock, Nicholas, Fullerton, Janice M., Iwata, Nakao, Mayoral, Fermin, Mowry, Bryan, McQuillin, Andrew, Bulik, Cynthia M., Courtet, Philippe, Dina, Christian, Fichter, Manfred M., Föcker, Manuel, Hinney, Anke, Hübel, Christopher, Purves, Kirstin L., Rujescu, Dan, Scherer, Stephen W., Slagboom, P. Eline, Steen, Vidar W., Karhunen, Leila, Kennedy, Martin A., Tsitsika, Artemis, Yao, Shuyang, Schwarze, Cornelia E., Bohus, Martin, Crivelli, Silvia, Muralidhar, Sumitra, Huang, Grant, Moser, Jennifer, Brewer, Jessica V., Connor, Todd, Humphries, Donald E., Hauser, Elizabeth, Whittle, Jeffrey, Hammer, Kimberly, Godschalk, Michael, Sriram, Peruvemba, Liangpunsakul, Suthat, Wallbom, Agnes, Esko, Tõnu, Martin, Nicholas G.

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Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index von Hinney, A, Kesselmeier, M, Jall, S, Volckmar, A-L, Föcker, M, Antel, J, Heid, I M, Winkler, T W, Grant, S F A, Guo, Y, Bergen, A W, Kaye, W, Berrettini, W, Hakonarson, H, Herpertz-Dahlmann, B, de Zwaan, M, Herzog, W, Ehrlich, S, Zipfel, S, Egberts, K M, Adan, R, Brandys, M, van Elburg, A, Boraska Perica, V, Franklin, C S, Tschöp, M H, Zeggini, E, Bulik, C M, Collier, D, Scherag, A, Müller, T D, Hebebrand, J

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Maternal fever during pregnancy and offspring attention deficit hyperactivity disorder von Gustavson, Kristin, Ask, Helga, Ystrom, Eivind, Stoltenberg, Camilla, Lipkin, W. Ian, Surén, Pål, Håberg, Siri E., Magnus, Per, Knudsen, Gun Peggy, Eilertsen, Espen, Bresnahan, Michaeline, Aase, Heidi, Mjaaland, Siri, Susser, Ezra S., Hornig, Mady, Reichborn-Kjennerud, Ted

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Midlife vascular risk factors and their association with dementia deaths: Results from a Norwegian prospective study followed up for 35 years von Strand, Bjørn Heine, Langballe, Ellen Melbye, Hjellvik, Vidar, Handal, Marte, Næss, Øyvind, Knudsen, Gunn Peggy, Refsum, Helga, Tambs, Kristian, Nafstad, Per, Schirmer, Henrik, Bergem, Astrid Liv Mina, Selmer, Randi, Engedal, Knut, Magnus, Per, Bjertness, Espen

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Severe hypohidrotic ectodermal dysplasia in a girl caused by a de novo 9;X insertion that includes XIST and disrupts the EDA gene von Ørstavik, Karen Helene, Knudsen, Gun Peggy S., Nordgarden, Hilde, Ormerod, Eli, Strømme, Petter, Lazarou, Lazarous P., Rosser, Lyndon G., Prescott, Trine, Houge, Gunnar

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Continuity of Genetic Risk for Aggressive Behavior Across the Life-Course von van der Laan, Camiel M., Morosoli-García, José J., van de Weijer, Steve G. A., Colodro-Conde, Lucía, Lupton, Michelle K., Mitchell, Brittany L., McAloney, Kerrie, Parker, Richard, Burns, Jane M., Hickie, Ian B., Pool, René, Hottenga, Jouke-Jan, Martin, Nicholas G., Medland, Sarah E., Nivard, Michel G., Boomsma, Dorret I.

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A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling von Li, Dong, Chang, Xiao, Connolly, John J., Tian, Lifeng, Liu, Yichuan, Bhoj, Elizabeth J., Robinson, Nora, Abrams, Debra, Li, Yun R., Bradfield, Jonathan P., Kim, Cecilia E., Li, Jin, Wang, Fengxiang, Snyder, James, Lemma, Maria, Hou, Cuiping, Wei, Zhi, Guo, Yiran, Qiu, Haijun, Mentch, Frank D., Thomas, Kelly A., Chiavacci, Rosetta M., Cone, Roger, Li, Bingshan, Sleiman, Patrick A., Hakonarson, Hakon

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