Search Results

Composition of the founding population of Iceland: Biological distance and morphological variation in early historic Atlantic Europe

by Hallgrímsson, Benedikt, Ó Donnabháin, Barra, Walters, G. Bragi, Cooper, David M.L., Guđbjartsson, Daníel, Stefánsson, Kari
Published in American Journal of Physical Anthropology (2003)

A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke.

by Gudbjartsson, Daniel F, Holm, Hilma, Gretarsdottir, Solveig, Thorleifsson, Gudmar, Walters, G Bragi, Thorgeirsson, Gudmundur, Gulcher, Jeffrey, Mathiesen, Ellisiv B, Njølstad, Inger, Nyrnes, Audhild, Wilsgaard, Tom, Hald, Erin M, Hveem, Kristian, Stoltenberg, Camilla, Kucera, Gayle, Stubblefield, Tanya, Carter, Shannon, Roden, Dan, Ng, Maggie C Y, Baum, Larry, So, Wing Yee, Wong, Ka Sing, Chan, Juliana C N, Gieger, Christian, Wichmann, H-Erich, Gschwendtner, Andreas, Dichgans, Martin, Kuhlenbäumer, Gregor, Berger, Klaus, Ringelstein, E Bernd, Bevan, Steve, Markus, Hugh S, Kostulas, Konstantinos, Hillert, Jan, Sveinbjörnsdóttir, Sigurlaug, Valdimarsson, Einar M, Løchen, Maja-Lisa, Ma, Ronald C W, Darbar, Dawood, Kong, Augustine, Arnar, David O, Thorsteinsdottir, Unnur, Stefansson, Kari
Published in Nature Genetics (2009)

Fourteen sequence variants that associate with multiple sclerosis discovered by meta-analysis informed by genetic correlations

by Sigurgeir Olafsson, Pernilla Stridh, Steffan Daniël Bos, Andres Ingason, Jack Euesden, Patrick Sulem, Gudmar Thorleifsson, Omar Gustafsson, Ari Johannesson, Arni J. Geirsson, Arni V. Thorsson, Bardur Sigurgeirsson, Bjorn Runar Ludviksson, Elias Olafsson, Helga Kristjansdottir, Jon G. Jonasson, Jon Hjaltalin Olafsson, Kjartan B. Orvar, Rafn Benediktsson, Ragnar Bjarnason, Sjofn Kristjansdottir, Thorarinn Gislason, Trausti Valdimarsson, Evgenia Mikaelsdottir, Snaevar Sigurdsson, Stefan Jonsson, Thorunn Rafnar, Dag Aarsland, Srdjan Djurovic, Tormod Fladby, Gun Peggy Knudsen, Elisabeth G. Celius, Kjell-Morten Myhr, Gerdur Grondal, Kristjan Steinsson, Helgi Valdimarsson, Sigurdur Bjornsson, Unnur S. Bjornsdottir, Einar S Bjornsson, Bjorn Nilsson, Ole A. Andreassen, Lars Alfredsson, Jan Hillert, Ingrid Skelton Kockum, Gisli Masson, Unnur Thorsteinsdottir, Daniel F. Gudbjartsson, Hreinn Stefansson, Haukur Hjaltason, Hanne F. Harbo
Published in npj Genomic Medicine (2017)

The effects of sequence variants on cardiac function and disease

by Þórólfsdóttir, Rósa B.
Published 2019

Fourteen sequence variants that associate with multiple sclerosis discovered by meta-analysis informed by genetic correlations

by Ólafsson, Sigurgeir, Stridh, Pernilla, Bos, Steffan Daniël, Ingason, Andrés, Euesden, Jack, sulem, patrick, Thorleifsson, Gudmar, Gústafsson, Ómar, Jóhannesson, Ari, Geirsson, Árni J., Þórsson, Árni V., Sigurgeirsson, Bárður, Ludviksson, Bjorn, Ólafsson, Elías, Kristjansdottir, Helga, Jónasson, Jón G., Ólafsson, Jón Hjaltalín, Örvar, Kjartan B., Benediktsson, Rafn, Bjarnason, Ragnar Grímur, Kristjánsdóttir, Sjöfn, Gislason, Thorarinn, Valdimarsson, Trausti, Mikaelsdóttir, Evgenía, Sigurðsson, Snævar, Jonsson, Stefan, Rafnar, Thorunn, Aarsland, Dag, Djurovic, Srdjan, Fladby, Tormod, Knudsen, Gun Peggy, Celius, Elisabeth G., Myhr, Kjell-Morten, Gröndal, Gerður, Steinsson, Kristján, Valdimarsson, Helgi, Björnsson, Sigurður, Björnsdóttir, Unnur Steina, Björnsson, Einar Stefán, Nilsson, Bjorn, Andreassen, Ole A., Alfredsson, Lars, Hillert, Jan, Kockum, Ingrid Skelton, Másson, Gísli, Thorsteinsdottir, Unnur, Gudbjartsson, Daniel, Stefansson, Hreinn, Hjaltason, Haukur, Harbo, Hanne F.
Published in npj Genomic Medicine (2017)

Coding variants in and increase risk of atrial fibrillation.

by Thorolfsdottir, Rosa B, Sveinbjornsson, Gardar, Sulem, Patrick, Nielsen, Jonas B, Jonsson, Stefan, Halldorsson, Gisli H, Melsted, Pall, Ivarsdottir, Erna V, Davidsson, Olafur B, Kristjansson, Ragnar P, Thorleifsson, Gudmar, Helgadottir, Anna, Gretarsdottir, Solveig, Norddahl, Gudmundur, Rajamani, Sridharan, Torfason, Bjarni, Valgardsson, Atli S, Sverrisson, Jon T, Tragante, Vinicius, Holmen, Oddgeir L, Asselbergs, Folkert W, Roden, Dan M, Darbar, Dawood, Pedersen, Terje R, Sabatine, Marc S, Willer, Cristen J, Løchen, Maja-Lisa, Halldorsson, Bjarni V, Jonsdottir, Ingileif, Hveem, Kristian, Arnar, David O, Thorsteinsdottir, Unnur, Gudbjartsson, Daniel F, Holm, Hilma, Stefansson, Kari
Published in Communications Biology (2019)

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
Published in Scientific Reports (2019)

A genome-wide cross-phenotype meta-analysis of the association of blood pressure with migraine

by Guo, Y. (Yanjun), Rist, P. M. (Pamela M.), Daghlas, I. (Iyas), Giulianini, F. (Franco), Kurth, T. (Tobias), Chasman, D. I. (Daniel, I)
Published 2020

Hair cortisol in twins:heritability and genetic overlap with psychological variables and stress-system genes

by Rietschel, L. (Liz), Streit, F. (Fabian), Zhu, G. (Gu), McAlone, K. (Kerrie), Frank, J. (Josef), Couvy-Duchesne, B. (Baptiste), Witt, S. H. (Stephanie H.), Binz, T. M. (Tina M.), McGrath, J. (John), Hickie, I. B. (Ian B.), Hansel, N. K. (Narelle K.), Wright, M. J. (Margaret J.), Gillespie, N. A. (Nathan A.), Forstner, A. J. (Andreas J.), Schulze, T. G. (Thomas G.), Wüst, S. (Stefan), Nöthen, M. M. (Markus M.), Baumgartner, M. R. (Markus R.), Walker, B. R. (Brian R.), Crawford, A. A. (Andrew A.), Colodro-Conde, L. (Lucía), Medland, S. E. (Sarah E.), Martin, N. G. (Nicholas G.), Rietschel, M. (Marcella)
Published 2017

Gene expression imputation across multiple brain regions provides insights into schizophrenia risk

by Huckins, L. M. (Laura M.), Dobbyn, A. (Amanda), Ruderfer, D. M. (Douglas M.), Hoffman, G. (Gabriel), Wang, W. (Weiqing), Pardiñas, A. (Antonio), Rajagopal, V. M. (Veera M.), Als, T. D. (Thomas D.), Nguyen, H. (Hoang), Girdhar, K. (Kiran), Boocock, J. (James), Roussos, P. (Panos), Fromer, M. (Menachem), Kramer, R. (Robin), Domencini, E. (Enrico), Gamazon, E. (Eric), Purcell, S. (Shaun), C. C. (CommonMind Consortium), T. S. (The Schizophrenia Working Group of the Psychiatric Genomics Consortium), i. S. (iPSYCH-GEMS Schizophrenia Working Group), Demontis, D. (Ditte), Børglum, A. D. (Anders D.), Walters, J. T. (James T. R.), O'Donovan, M. C. (Michael C.), Sullivan, P. (Patrick), Owen, M. J. (Michael J.), Devlin, B. (Bernie), Sieberts, S. K. (Solveig K.), Cox, N. J. (Nancy J.), Im, H. K. (Hae Kyung), Sklar, P. (Pamela), Stahl, E. A. (Eli A.)
Published 2019

Age at first birth in women is genetically associated with increased risk of schizophrenia

by Ni, G. (Guiyan), Gratten, J. (Jacob), Wray, N. R. (Naomi R.), Lee, S. H. (Sang Hong), S. W. (Schizophrenia Working Group of the Psychiatric Genomics Consortium)
Published 2018