The Impact of Divergence Time on the Nature of Population Structure: An Example from Iceland

por Price, Alkes L., Helgason, Agnar, Palsson, Snaebjorn, Stefansson, Hreinn, St. Clair, David, Andreassen, Ole A., Reich, David, Kong, Augustine, Stefansson, Kari
Publicado 2009

Working memory and reaction time variability mediate the relationship between polygenic risk and ADHD traits in a general population sample

por Moses, Mia, Tiego, Jeggan, Demontis, Ditte, Bragi Walters, G., Stefansson, Hreinn, Stefansson, Kari, Børglum, Anders D., Arnatkeviciute, Aurina, Bellgrove, Mark A.
Publicado 2022

Reciprocal White Matter Changes Associated With Copy Number Variation at 15q11.2 BP1-BP2: A Diffusion Tensor Imaging Study

por Silva, Ana I., Ulfarsson, Magnus O., Stefansson, Hreinn, Gustafsson, Omar, Walters, G. Bragi, Linden, David E.J., Wilkinson, Lawrence S., Drakesmith, Mark, Owen, Michael J., Hall, Jeremy, Stefansson, Kari
Publicado 2019

The cortical thickness phenotype of individuals with DISC1 translocation resembles schizophrenia

por Doyle, Orla M., Bois, Catherine, Thomson, Pippa, Romaniuk, Liana, Whitcher, Brandon, Williams, Steven C.R., Turkheimer, Federico E., Stefansson, Hreinn, McIntosh, Andrew M., Mehta, Mitul A., Lawrie, Stephen M.
Publicado 2015

Analysis of Diffusion Tensor Imaging Data From the UK Biobank Confirms Dosage Effect of 15q11.2 Copy Number Variation on White Matter and Shows Association With Cognition

por Silva, Ana I., Kirov, George, Kendall, Kimberley M., Bracher-Smith, Mathew, Wilkinson, Lawrence S., Hall, Jeremy, Ulfarsson, Magnus O., Walters, G. Bragi, Stefansson, Hreinn, Stefansson, Kari, Linden, David E.J., Caseras, Xavier
Publicado 2021

Polygenic risk scores for schizophrenia and bipolar disorder associate with addiction

por Reginsson, Gunnar W., Ingason, Andres, Euesden, Jack, Bjornsdottir, Gyda, Olafsson, Sigurgeir, Sigurdsson, Engilbert, Oskarsson, Hogni, Tyrfingsson, Thorarinn, Runarsdottir, Valgerdur, Hansdottir, Ingunn, Steinberg, Stacy, Stefansson, Hreinn, Gudbjartsson, Daniel F., Thorgeirsson, Thorgeir E., Stefansson, Kari
Publicado 2017

Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis

por Williams, Nigel M, Zaharieva, Irina, Martin, Andrew, Langley, Kate, Mantripragada, Kiran, Fossdal, Ragnheidur, Stefansson, Hreinn, Stefansson, Kari, Magnusson, Pall, Gudmundsson, Olafur O, Gustafsson, Omar, Holmans, Peter, Owen, Michael J, O'Donovan, Michael, Thapar, Anita
Publicado 2010

Reproductive fitness and genetic risk of psychiatric disorders in the general population

por 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
Publicado 2017

Predicting the probability of death using proteomics

por 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.
Publicado 2021

CFH Y402H Confers Similar Risk of Soft Drusen and Both Forms of Advanced AMD

por Magnusson, Kristinn P, Duan, Shan, Sigurdsson, Haraldur, Petursson, Hjorvar, Yang, Zhenglin, Zhao, Yu, Bernstein, Paul S, Ge, Jian, Jonasson, Fridbert, Stefansson, Einar, Helgadottir, Gudleif, Zabriskie, Norman A, Jonsson, Thorlakur, Björnsson, Asgeir, Thorlacius, Theodora, Jonsson, Palmi V, Thorleifsson, Gudmar, Kong, Augustine, Stefansson, Hreinn, Zhang, Kang, Stefansson, Kari, Gulcher, Jeffrey R
Publicado 2006

Genome-wide association analysis of insomnia complaints identifies risk genes and genetic overlap with psychiatric and metabolic traits

por Hammerschlag, Anke R, Stringer, Sven, de Leeuw, Christiaan A, Sniekers, Suzanne, Taskesen, Erdogan, Watanabe, Kyoko, Blanken, Tessa F, Dekker, Kim, te Lindert, Bart HW, Wassing, Rick, Jonsdottir, Ingileif, Thorleifsson, Gudmar, Stefansson, Hreinn, Gislason, Thorarinn, Berger, Klaus, Schormair, Barbara, Wellmann, Juergen, Winkelmann, Juliane, Stefansson, Kari, Oexle, Konrad, Van Someren, Eus JW, Posthuma, Danielle
Publicado 2017

Sequence variant at 8q24.21 associates with sciatica caused by lumbar disc herniation

por 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
Publicado 2017

A polygenic resilience score moderates the genetic risk for schizophrenia

por Hess, Jonathan L., Tylee, Daniel S., Mattheisen, Manuel, Børglum, Anders D., Als, Thomas D., Grove, Jakob, Werge, Thomas, Mortensen, Preben Bo, Mors, Ole, Nordentoft, Merete, Hougaard, David M., Byberg-Grauholm, Jonas, Bækvad-Hansen, Marie, Greenwood, Tiffany A., Tsuang, Ming T., Curtis, David, Steinberg, Stacy, Sigurdsson, Engilbert, Stefánsson, Hreinn, Stefánsson, Kári, Edenberg, Howard J., Holmans, Peter, Faraone, Stephen V., Glatt, Stephen J.
Publicado 2019

DanMAC5: a browser of aggregated sequence variants from 8,671 whole genome sequenced Danish individuals

por Banasik, Karina, Møller, Peter L., Techlo, Tanya R., Holm, Peter C., Walters, G. Bragi, Ingason, Andrés, Rosengren, Anders, Rohde, Palle D., Kogelman, Lisette J. A., Westergaard, David, Siggaard, Troels, Chmura, Piotr J., Chalmer, Mona A., Magnússon, Ólafur Þ., Þórisson, Guðmundur Á., Stefánsson, Hreinn, Guðbjartsson, Daníel F., Stefánsson, Kári, Olesen, Jes, Winther, Simon, Bøttcher, Morten, Brunak, Søren, Werge, Thomas, Nyegaard, Mette, Hansen, Thomas F.
Publicado 2023

Testing for pharmacogenomic predictors of ppRNFL thinning in individuals exposed to vigabatrin

por Boothman, Isabelle, Clayton, Lisa M., McCormack, Mark, Driscoll, Alexandra McKibben, Stevelink, Remi, Moloney, Patrick, Krause, Roland, Kunz, Wolfram S., Diehl, Sarah, O’Brien, Terence J., Sills, Graeme J., de Haan, Gerrit-Jan, Zara, Federico, Koeleman, Bobby P., Depondt, Chantal, Marson, Anthony G., Stefansson, Hreinn, Stefansson, Kari, Craig, John, Johnson, Michael R., Striano, Pasquale, Lerche, Holger, Furney, Simon J., Delanty, Norman, Sisodiya, Sanjay M., Cavalleri, Gianpiero L.
Publicado 2023

MAP1B mutations cause intellectual disability and extensive white matter deficit

por Walters, G. Bragi, Gustafsson, Omar, Sveinbjornsson, Gardar, Eiriksdottir, Valgerdur K., Agustsdottir, Arna B., Jonsdottir, Gudrun A., Steinberg, Stacy, Gunnarsson, Arni F., Magnusson, Magnus I., Unnsteinsdottir, Unnur, Lee, Amy L., Jonasdottir, Adalbjorg, Sigurdsson, Asgeir, Jonasdottir, Aslaug, Skuladottir, Astros, Jonsson, Lina, Nawaz, Muhammad S., Sulem, Patrick, Frigge, Mike, Ingason, Andres, Love, Askell, Norddhal, Gudmundur L., Zervas, Mark, Gudbjartsson, Daniel F., Ulfarsson, Magnus O., Saemundsen, Evald, Stefansson, Hreinn, Stefansson, Kari
Publicado 2018

A genome‐wide association study of sodium levels and drug metabolism in an epilepsy cohort treated with carbamazepine and oxcarbazepine

por Berghuis, Bianca, Stapleton, Caragh, Sonsma, Anja C. M., Hulst, Janic, de Haan, Gerrit‐Jan, Lindhout, Dick, Demurtas, Rita, Krause, Roland, Depondt, Chantal, Kunz, Wolfram S., Zara, Federico, Striano, Pasquale, Craig, John, Auce, Pauls, Marson, Anthony G., Stefansson, Hreinn, O'Brien, Terence J., Johnson, Michael R., Sills, Graeme J., Wolking, Stefan, Lerche, Holger, Sisodiya, Sanjay M., Sander, Josemir W., Cavalleri, Gianpiero L., Koeleman, Bobby P. C., McCormack, Mark
Publicado 2019

Attention-deficit hyperactivity disorder shares copy number variant risk with schizophrenia and autism spectrum disorder

por Gudmundsson, Olafur O., Walters, G. Bragi, Ingason, Andres, Johansson, Stefan, Zayats, Tetyana, Athanasiu, Lavinia, Sonderby, Ida Elken, Gustafsson, Omar, Nawaz, Muhammad S., Jonsson, Gudbjorn F., Jonsson, Lina, Knappskog, Per-Morten, Ingvarsdottir, Ester, Davidsdottir, Katrin, Djurovic, Srdjan, Knudsen, Gun Peggy Strømstad, Askeland, Ragna Bugge, Haraldsdottir, Gyda S., Baldursson, Gisli, Magnusson, Pall, Sigurdsson, Engilbert, Gudbjartsson, Daniel F., Stefansson, Hreinn, Andreassen, Ole A., Haavik, Jan, Reichborn-Kjennerud, Ted, Stefansson, Kari
Publicado 2019

A pharmacogenomic assessment of psychiatric adverse drug reactions to levetiracetam

por Campbell, Ciarán, McCormack, Mark, Patel, Sonn, Stapleton, Caragh, Bobbili, Dheeraj, Krause, Roland, Depondt, Chantal, Sills, Graeme J., Koeleman, Bobby P., Striano, Pasquale, Zara, Federico, Sander, Josemir W., Lerche, Holger, Kunz, Wolfram S., Stefansson, Kari, Stefansson, Hreinn, Doherty, Colin P., Heinzen, Erin L., Scheffer, Ingrid E., Goldstein, David B., O'Brien, Terence, Cotter, David, Berkovic, Samuel F., Sisodiya, Sanjay M., Delanty, Norman, Cavalleri, Gianpiero L.
Publicado 2022

Thirty novel sequence variants impacting human intracranial volume

por Nawaz, Muhammad Sulaman, Einarsson, Gudmundur, Bustamante, Mariana, Gisladottir, Rosa S, Walters, G Bragi, Jonsdottir, Gudrun A, Skuladottir, Astros Th, Bjornsdottir, Gyda, Magnusson, Sigurdur H, Asbjornsdottir, Bergrun, Unnsteinsdottir, Unnur, Sigurdsson, Engilbert, Jonsson, Palmi V, Palmadottir, Vala Kolbrun, Gudjonsson, Sigurjon A, Halldorsson, Gisli H, Ferkingstad, Egil, Jonsdottir, Ingileif, Thorleifsson, Gudmar, Holm, Hilma, Thorsteinsdottir, Unnur, Sulem, Patrick, Gudbjartsson, Daniel F, Stefansson, Hreinn, Thorgeirsson, Thorgeir E, Ulfarsson, Magnus O, Stefansson, Kari
Publicado 2022