Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis by Williams, Nigel M, Dr, Zaharieva, Irina, BSc, Martin, Andrew, BSc, Langley, Kate, PhD, Mantripragada, Kiran, PhD, Fossdal, Ragnheidur, PhD, Stefansson, Hreinn, PhD, Stefansson, Kari, MD, Magnusson, Pall, MD, Gudmundsson, Olafur O, MD, Gustafsson, Omar, PhD, Holmans, Peter, Prof, Owen, Michael J, Prof, O'Donovan, Michael, Prof, Thapar, Anita, Prof

Get full text

Genome-wide Association for Major Depression Through Age at Onset Stratification: Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium by Power, Robert A, Tansey, Katherine E, Buttenschøn, Henriette Nørmølle, Cohen-Woods, Sarah, Bigdeli, Tim, Hall, Lynsey S, Kutalik, Zoltán, Lee, S. Hong, Ripke, Stephan, Steinberg, Stacy, Teumer, Alexander, Viktorin, Alexander, Wray, Naomi R, Arolt, Volker, Baune, Bernard T, Boomsma, Dorret I, Børglum, Anders D, Byrne, Enda M, Castelao, Enrique, Craddock, Nick, Craig, Ian W, Dannlowski, Udo, Deary, Ian J, Degenhardt, Franziska, Forstner, Andreas J, Gordon, Scott D, Grabe, Hans J, Grove, Jakob, Hamilton, Steven P, Hayward, Caroline, Heath, Andrew C, Hocking, Lynne J, Homuth, Georg, Hottenga, Jouke J, Kloiber, Stefan, Krogh, Jesper, Landén, Mikael, Lang, Maren, Levinson, Douglas F, Lichtenstein, Paul, Lucae, Susanne, MacIntyre, Donald J, Madden, Pamela, Magnusson, Patrik K.E, Martin, Nicholas G, McIntosh, Andrew M, Middeldorp, Christel M, Milaneschi, Yuri, Montgomery, Grant W, Mors, Ole, Müller-Myhsok, Bertram, Nyholt, Dale R, Oskarsson, Hogni, Owen, Michael J, Padmanabhan, Sandosh, Penninx, Brenda W.J.H, Pergadia, Michele L, Porteous, David J, Potash, James B, Preisig, Martin, Rivera, Margarita, Shi, Jianxin, Shyn, Stanley I, Sigurdsson, Engilbert, Smit, Johannes H, Smith, Blair H, Stefansson, Hreinn, Stefansson, Kari, Strohmaier, Jana, Sullivan, Patrick F, Thomson, Pippa, Thorgeirsson, Thorgeir E, Van der Auwera, Sandra, Weissman, Myrna M, Breen, Gerome, Lewis, Cathryn M

Get full text

Common variants at VRK2 and TCF4 conferring risk of schizophrenia by Steinberg, Stacy, de Jong, Simone, Andreassen, Ole A., Werge, Thomas, Børglum, Anders D., Mors, Ole, Mortensen, Preben B., Gustafsson, Omar, Costas, Javier, Pietiläinen, Olli P. H., Demontis, Ditte, Papiol, Sergi, Huttenlocher, Johanna, Mattheisen, Manuel, Breuer, René, Vassos, Evangelos, Giegling, Ina, Fraser, Gillian, Walker, Nicholas, Tuulio-Henriksson, Annamari, Suvisaari, Jaana, Lönnqvist, Jouko, Paunio, Tiina, Agartz, Ingrid, Melle, Ingrid, Djurovic, Srdjan, Strengman, Eric, Jürgens, Gesche, Glenthøj, Birte, Terenius, Lars, Hougaard, David M., Ørntoft, Torben, Wiuf, Carsten, Didriksen, Michael, Hollegaard, Mads V., Nordentoft, Merete, van Winkel, Ruud, Kenis, Gunter, Abramova, Lilia, Kaleda, Vasily, Arrojo, Manuel, Sanjuán, Julio, Arango, Celso, Sperling, Swetlana, Rossner, Moritz, Ribolsi, Michele, Magni, Valentina, Siracusano, Alberto, Christiansen, Claus, Kiemeney, Lambertus A., Veldink, Jan, van den Berg, Leonard, Ingason, Andres, Muglia, Pierandrea, Murray, Robin, Nöthen, Markus M., Sigurdsson, Engilbert, Petursson, Hannes, Thorsteinsdottir, Unnur, Kong, Augustine, Rubino, I. Alex, De Hert, Marc, Réthelyi, János M., Bitter, István, Jönsson, Erik G., Golimbet, Vera, Carracedo, Angel, Ehrenreich, Hannelore, Craddock, Nick, Owen, Michael J., O'Donovan, Michael C., Ruggeri, Mirella, Tosato, Sarah, Peltonen, Leena, Ophoff, Roel A., Collier, David A., St Clair, David, Rietschel, Marcella, Cichon, Sven, Stefansson, Hreinn, Rujescu, Dan, Stefansson, Kari

Get full text

Predicting the probability of death using proteomics by Eiriksdottir, Thjodbjorg, Ardal, Steinthor, Jonsson, Benedikt A., Lund, Sigrun H., Ivarsdottir, Erna V., Norland, Kristjan, Ferkingstad, Egil, Stefansson, Hreinn, Jonsdottir, Ingileif, Holm, Hilma, Rafnar, Thorunn, Saemundsdottir, Jona, Norddahl, Gudmundur L., Thorgeirsson, Gudmundur, Gudbjartsson, Daniel F., Sulem, Patrick, Thorsteinsdottir, Unnur, Stefansson, Kari, Ulfarsson, Magnus O.

Get full text

Sequence variant at 8q24.21 associates with sciatica caused by lumbar disc herniation by Bjornsdottir, Gyda, Benonisdottir, Stefania, Sveinbjornsson, Gardar, Styrkarsdottir, Unnur, Thorleifsson, Gudmar, Walters, G. Bragi, Bjornsson, Aron, Olafsson, Ingvar H., Ulfarsson, Elfar, Vikingsson, Arnor, Hansdottir, Ragnheidur, Karlsson, Karl O., Rafnar, Thorunn, Jonsdottir, Ingileif, Frigge, Michael L., Kong, Augustine, Oddsson, Asmundur, Masson, Gisli, Magnusson, Olafur T., Gudbjartsson, Tomas, Stefansson, Hreinn, Sulem, Patrick, Gudbjartsson, Daniel, Thorsteinsdottir, Unnur, Thorgeirsson, Thorgeir E., Stefansson, Kari

Get full text

Large genome-wide association study identifies three novel risk variants for restless legs syndrome by Didriksen, Maria, Nawaz, Muhammad Sulaman, Dowsett, Joseph, Bell, Steven, Erikstrup, Christian, Pedersen, Ole B., Sørensen, Erik, Jennum, Poul J., Burgdorf, Kristoffer S., Burchell, Brendan, Butterworth, Adam S., Soranzo, Nicole, Rye, David B., Trotti, Lynn Marie, Saini, Prabhjyot, Stefansdottir, Lilja, Magnusson, Sigurdur H., Thorleifsson, Gudmar, Sigmundsson, Thordur, Sigurdsson, Albert P., Van Den Hurk, Katja, Quee, Franke, Tanck, Michael W. T., Ouwehand, Willem H., Roberts, David J., Earley, Eric J., Busch, Michael P., Mast, Alan E., Page, Grier P., Danesh, John, Di Angelantonio, Emanuele, Stefansson, Hreinn, Ullum, Henrik, Stefansson, Kari

Get full text

Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases by Li, Rui, Brockschmidt, Felix F, Kiefer, Amy K, Stefansson, Hreinn, Nyholt, Dale R, Song, Kijoung, Vermeulen, Sita H, Kanoni, Stavroula, Glass, Daniel, Medland, Sarah E, Dimitriou, Maria, Waterworth, Dawn, Tung, Joyce Y, Geller, Frank, Heilmann, Stefanie, Hillmer, Axel M, Bataille, Veronique, Eigelshoven, Sibylle, Hanneken, Sandra, Moebus, Susanne, Herold, Christine, den Heijer, Martin, Montgomery, Grant W, Deloukas, Panos, Eriksson, Nicholas, Heath, Andrew C, Becker, Tim, Sulem, Patrick, Mangino, Massimo, Vollenweider, Peter, Spector, Tim D, Dedoussis, George, Martin, Nicholas G, Kiemeney, Lambertus A, Mooser, Vincent, Stefansson, Kari, Hinds, David A, Nöthen, Markus M, Richards, J Brent

Get full text

Reproductive fitness and genetic risk of psychiatric disorders in the general population by Mullins, Niamh, Ingason, Andrés, Porter, Heather, Euesden, Jack, Gillett, Alexandra, Ólafsson, Sigurgeir, Gudbjartsson, Daniel F., Lewis, Cathryn M., Sigurdsson, Engilbert, Saemundsen, Evald, Gudmundsson, Ólafur Ó, Frigge, Michael L., Kong, Augustine, Helgason, Agnar, Walters, G. Bragi, Gustafsson, Omar, Stefansson, Hreinn, Stefansson, Kari

Get full text

Maternally Derived Microduplications at 15q11-q13: Implication of Imprinted Genes in Psychotic Illness by Ingason, Andrés, Kirov, George, Giegling, Ina, Hansen, Thomas, Isles, Anthony R., Jakobsen, Klaus D., Kristinsson, Kari T., le Roux, Louise, Gustafsson, Omar, Craddock, Nick, Möller, Hans-Jürgen, McQuillin, Andrew, Muglia, Pierandrea, Cichon, Sven, Rietschel, Marcella, Ophoff, Roel A., Djurovic, Srdjan, Andreassen, Ole A., Pietiläinen, Olli P.H., Peltonen, Leena, Dempster, Emma, Collier, David A., St. Clair, David, Rasmussen, Henrik B., Glenthøj, Birte Y., Kiemeney, Lambertus A., Franke, Barbara, Tosato, Sarah, Bonetto, Chiara, Saemundsen, Evald, Hreidarsson, Stefán J., Nöthen, Markus M., Gurling, Hugh, O'Donovan, Michael C., Owen, Michael J., Sigurdsson, Engilbert, Petursson, Hannes, Stefansson, Hreinn, Rujescu, Dan, Stefansson, Kari, Werge, Thomas

Get full text

Cognition in Schizophrenia by Stefansson, Hreinn, Stefansson, Kari

Get full text

Genome-Wide Analysis Shows Increased Frequency of Copy Number Variation Deletions in Dutch Schizophrenia Patients by Buizer-Voskamp, Jacobine E, Muntjewerff, Jan-Willem, Strengman, Eric, Sabatti, Chiara, Stefansson, Hreinn, Vorstman, Jacob A.S, Ophoff, Roel A

Get full text

The impact of divergence time on the nature of population structure: an example from Iceland by Price, Alkes L, Helgason, Agnar, Palsson, Snaebjorn, Stefansson, Hreinn, St Clair, David, Andreassen, Ole A, Reich, David, Kong, Augustine, Stefansson, Kari

Get full text

The association between candidate migraine susceptibility loci and severe migraine phenotype in a clinical sample by Esserlind, Ann-Louise, Christensen, Anne Francke, Steinberg, Stacy, Grarup, Niels, Pedersen, Oluf, Hansen, Torben, Werge, Thomas, Hansen, Thomas Folkmann, Husemoen, Lise Lotte N, Linneberg, Allan, Budtz-Jorgensen, Esben, Westergaard, Maria Lurenda, Stefansson, Hreinn, Olesen, Jes

Request full text

A genome-wide meta-analysis yields 46 new loci associating with biomarkers of iron homeostasis by Bell, Steven, Rigas, Andreas S., Magnusson, Magnus K., Ferkingstad, Egil, Allara, Elias, Bjornsdottir, Gyda, Ramond, Anna, Sørensen, Erik, Halldorsson, Gisli H., Paul, Dirk S., Burgdorf, Kristoffer S., Eggertsson, Hannes P., Howson, Joanna M. M., Thørner, Lise W., Kristmundsdottir, Snaedis, Astle, William J., Erikstrup, Christian, Sigurdsson, Jon K., Vuckovic, Dragana, Dinh, Khoa M., Tragante, Vinicius, Surendran, Praveen, Pedersen, Ole B., Vidarsson, Brynjar, Jiang, Tao, Paarup, Helene M., Onundarson, Pall T., Akbari, Parsa, Nielsen, Kaspar R., Lund, Sigrun H., Juliusson, Kristinn, Magnusson, Magnus I., Frigge, Michael L., Oddsson, Asmundur, Olafsson, Isleifur, Kaptoge, Stephen, Hjalgrim, Henrik, Runarsson, Gudmundur, Wood, Angela M., Jonsdottir, Ingileif, Hansen, Thomas F., Sigurdardottir, Olof, Stefansson, Hreinn, Rye, David, Peters, James E., Westergaard, David, Holm, Hilma, Soranzo, Nicole, Banasik, Karina, Thorleifsson, Gudmar, Ouwehand, Willem H., Thorsteinsdottir, Unnur, Roberts, David J., Sulem, Patrick, Butterworth, Adam S., Gudbjartsson, Daniel F., Danesh, John, Brunak, Søren, Di Angelantonio, Emanuele, Ullum, Henrik, Stefansson, Kari

Get full text

Identification of genetic overlap and novel risk loci for attention-deficit/hyperactivity disorder and bipolar disorder by O’Connell, Kevin S., Shadrin, Alexey, Bahrami, Shahram, Smeland, Olav B., Bettella, Francesco, Frei, Oleksandr, Krull, Florian, Askeland, Ragna B., Walters, G. Bragi, Davíðsdóttir, Katrín, Haraldsdóttir, Gyða S., Guðmundsson, Ólafur Ó., Stefánsson, Hreinn, Fan, Chun C., Steen, Nils Eiel, Reichborn-Kjennerud, Ted, Dale, Anders M., Stefánsson, Kári, Djurovic, Srdjan, Andreassen, Ole A.

Get full text

Data Resource Profile: The Copenhagen Hospital Biobank (CHB) by Sørensen, Erik, Christiansen, Lene, Wilkowski, Bartlomiej, Larsen, Margit H, Burgdorf, Kristoffer S, Thørner, Lise W, Nissen, Janna, Pedersen, Ole B, Banasik, Karina, Brunak, Søren, Bundgaard, Henning, Stefánsson, Hreinn, Stefánsson, Kari, Melbye, Mads, Ullum, Henrik

Get full text

The influence of genetic constitution on migraine drug responses by Christensen, Anne Francke, Esserlind, Ann-Louise, Werge, Thomas, Stefánsson, Hreinn, Stefánsson, Kári, Olesen, Jes

Request full text

Predicting ADHD in alcohol dependence using polygenic risk scores for ADHD by Patel, Kejal H. S., Walters, G. Bragi, Stefánsson, Hreinn, Stefánsson, Kári, Degenhardt, Franziska, Nothen, Markus, Van Der Veen, Tracey, Demontis, Ditte, Borglum, Anders, Kristiansen, Mark, Bass, Nicholas J., McQuillin, Andrew

Get full text

GBA and APOE ε4 associate with sporadic dementia with Lewy bodies in European genome wide association study by Rongve, Arvid, Witoelar, Aree, Ruiz, Agustín, Athanasiu, Lavinia, Abdelnour, Carla, Clarimon, Jordi, Heilmann-Heimbach, Stefanie, Hernández, Isabel, Moreno-Grau, Sonia, de Rojas, Itziar, Morenas-Rodríguez, Estrella, Fladby, Tormod, Sando, Sigrid B., Bråthen, Geir, Blanc, Frédéric, Bousiges, Olivier, Lemstra, Afina W., van Steenoven, Inger, Londos, Elisabet, Almdahl, Ina S., Pålhaugen, Lene, Eriksen, Jon A., Djurovic, Srdjan, Stordal, Eystein, Saltvedt, Ingvild, Ulstein, Ingun D., Bettella, Francesco, Desikan, Rahul S., Idland, Ane-Victoria, Toft, Mathias, Pihlstrøm, Lasse, Snaedal, Jon, Tárraga, Lluís, Boada, Mercè, Lleó, Alberto, Stefánsson, Hreinn, Stefánsson, Kári, Ramírez, Alfredo, Aarsland, Dag, Andreassen, Ole A.

Get full text

Polygenic liability for antipsychotic dosage and polypharmacy - a real-world registry and biobank study by Koch, Elise, Kämpe, Anders, Alver, Maris, Sigurðarson, Sindri, Einarsson, Guðmundur, Partanen, Juulia, Smith, Robert L, Jaholkowski, Piotr, Taipale, Heidi, Lähteenvuo, Markku, Steen, Nils Eiel, Smeland, Olav B, Djurovic, Srdjan, Molden, Espen, Sigurdsson, Engilbert, Stefánsson, Hreinn, Stefánsson, Kári, Palotie, Aarno, Milani, Lili, O'Connell, Kevin S, Andreassen, Ole A

Get full text