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
Published in The Lancet (British edition)

Polygenic risk scores for schizophrenia and bipolar disorder predict creativity

by Power, Robert A, Steinberg, Stacy, Bjornsdottir, Gyda, Rietveld, Cornelius A, Abdellaoui, Abdel, Nivard, Michel M, Johannesson, Magnus, Galesloot, Tessel E, Hottenga, Jouke J, Willemsen, Gonneke, Cesarini, David, Benjamin, Daniel J, Magnusson, Patrik K E, Ullén, Fredrik, Tiemeier, Henning, Hofman, Albert, van Rooij, Frank J A, Walters, G Bragi, Sigurdsson, Engilbert, Thorgeirsson, Thorgeir E, Ingason, Andres, Helgason, Agnar, Kong, Augustine, Kiemeney, Lambertus A, Koellinger, Philipp, Boomsma, Dorret I, Gudbjartsson, Daniel, Stefansson, Hreinn, Stefansson, Kari
Published in Nature neuroscience

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.
Published in Biological psychiatry (1969)

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
Published in Nature communications

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
Published in PLoS genetics

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
Published in Nature communications

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.
Published in Communications biology

Cognition in Schizophrenia

by Stefansson, Hreinn, Stefansson, Kari
Published in Biological psychiatry (1969)

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
Published in Communications biology

HLA-DQB1 6672G>C (rs113332494) is associated with clozapine-induced neutropenia and agranulocytosis in individuals of European ancestry

by Konte, Bettina, Walters, James T R, Rujescu, Dan, Legge, Sophie E, Pardiñas, Antonio F, Cohen, Dan, Pirmohamed, Munir, Tiihonen, Jari, Hartmann, Annette M, Bogers, Jan P, van der Weide, Jan, van der Weide, Karen, Putkonen, Anu, Repo-Tiihonen, Eila, Hallikainen, Tero, Silva, Ed, Ingimarsson, Oddur, Sigurdsson, Engilbert, Kennedy, James L, Sullivan, Patrick F, Rietschel, Marcella, Breen, Gerome, Stefansson, Hreinn, Stefansson, Kari, Collier, David A, O'Donovan, Michael C, Giegling, Ina
Published in Translational psychiatry

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
Published in Biological psychiatry (1969)

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
Published in PLoS genetics

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
Published in Molecular psychiatry

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
Published in Communications biology

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
Published in International journal of epidemiology

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
Published in Neuropsychopharmacology (New York, N.Y.)

Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk alleles

by Hautakangas, Heidi, Winsvold, Bendik K S, Ruotsalainen, Sanni, Bjornsdottir, Gyda, Harder, Aster V. E, Kogelman, Lisette J. A, Thomas, Laurent, Noordam, Raymond, Benner, Christian, Gormley, Padhraig, Artto, Ville, Banasik, Karina, Bjornsdottir, Anna, Boomsma, Dorret I, Brumpton, Ben Michael, Burgdorf, Kristoffer Sølvsten, Buring, Julie E, Chalmer, Mona Ameri, de Boer, Irene, Dichgans, Martin, Erikstrup, Christian, Färkkilä, Markus, Gabrielsen, Maiken Elvestad, Ghanbari, Mohsen, Hagen, Knut, Häppölä, Paavo, Hottenga, Jouke-Jan, Hrafnsdottir, Maria G, Hveem, Kristian, Johnsen, Marianne Bakke, Kähönen, Mika, Kristoffersen, Espen Saxhaug, Kurth, Tobias, Lehtimäki, Terho, Lighart, Lannie, Magnusson, Sigurdur H, Malik, Rainer, Pedersen, Ole Birger, Pelzer, Nadine, Penninx, Brenda W. J. H, Ran, Caroline, Ridker, Paul M, Rosendaal, Frits Richard, Sigurdardottir, Gudrun R, Skogholt, Anne Heidi, Sveinsson, Olafur A, Thorgeirsson, Thorgeir E, Ullum, Henrik, Zwart, John Anker Henrik
Published in Nature genetics

Identification of Genetic Loci Shared Between Attention-Deficit/Hyperactivity Disorder, Intelligence, and Educational Attainment

by 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.
Published in Biological psychiatry (1969)

Genome-wide association study identifies 48 common genetic variants associated with handedness

by Cuellar-Partida, Gabriel, Eriksson, Nicholas, Albrecht, Eva, Aliev, Fazil, Barroso, Inês, Beckmann, Jacques S, Boks, Marco P, Boomsma, Dorret I, Campbell, Harry, Chasman, Daniel I, Cherkas, Lynn F, Davies, Gail, de Geus, Eco J C, Deary, Ian J, Deloukas, Panos, Dick, Danielle M, Duffy, David L, Eriksson, Johan G, Esko, Tõnu, Feenstra, Bjarke, Geller, Frank, Gieger, Christian, Giegling, Ina, Gordon, Scott D, Han, Jiali, Hansen, Thomas F, Hartmann, Annette M, Hayward, Caroline, Heikkilä, Kauko, Hicks, Andrew A, Hirschhorn, Joel N, Hottenga, Jouke-Jan, Huffman, Jennifer E, Hwang, Liang-Dar, Ikram, M Arfan, Kaprio, Jaakko, Kemp, John P, Khaw, Kay-Tee, Konte, Bettina, Kutalik, Zoltan, Lahti, Jari, Li, Xin, Luciano, Michelle, Magnusson, Sigurdur H, Mangino, Massimo, Martin, Nicholas G, McArdle, Wendy L, McCarthy, Mark I, Medina-Gomez, Carolina, Melville, Scott A, Metspalu, Andres, Milani, Lili, Nelis, Mari, Nyholt, Dale R, O'Connell, Kevin S, Ophoff, Roel A, Palmer, Cameron, Palotie, Aarno, Peltonen, Leena, Penninx, Brenda W J H, Polasek, Ozren, Pramstaller, Peter P, Prokopenko, Inga, Raikkonen, Katri, Ripatti, Samuli, Rivadeneira, Fernando, Rudan, Igor, Rujescu, Dan, Smit, Johannes H, Smoller, Jordan W, Soranzo, Nicole, Spector, Tim D, Pourcain, Beate St, Starr, John M, Stefánsson, Hreinn, Steinberg, Stacy, Teder-Laving, Maris, Thorleifsson, Gudmar, Stefánsson, Kári, Timpson, Nicholas J, Uitterlinden, André G, Vollenweider, Peter, Vuoksimaa, Eero, Waeber, Gérard, Wareham, Nicholas J, Warrington, Nicole, Waterworth, Dawn, Wichmann, H-Erich, Widen, Elisabeth, Willemsen, Gonneke, Wright, Margaret J, Xu, Mousheng, Zhao, Jing Hua, Kraft, Peter, Hinds, David A, Lindgren, Cecilia M, Mägi, Reedik, Neale, Benjamin M, Evans, David M, Medland, Sarah E
Published in Nature human behaviour

A mutation in APP protects against Alzheimer's disease and age-related cognitive decline

by JONSSON, Thorlakur, ATWAL, Jasvinder K, HOYTE, Kwame, GUSTAFSON, Amy, LIU, Yichin, YANMEI LU, BHANGALE, Tushar, GRAHAM, Robert R, HUTTENLOCHER, Johanna, BJORNSDOTTIR, Gyda, ANDREASSEN, Ole A, JÖNSSON, Erik G, STEINBERG, Stacy, PALOTIE, Aarno, BEHRENS, Timothy W, MAGNUSSON, Olafur T, KONG, Augustine, THORSTEINSDOTTIR, Unnur, WATTS, Ryan J, STEFANSSON, Kari, SNAEDAL, Jon, JONSSON, Palmi V, BJORNSSON, Sigurbjorn, STEFANSSON, Hreinn, SULEM, Patrick, GUDBJARTSSON, Daniel, MALONEY, Janice
Published in Nature (London)