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

Functional dissection of inherited non-coding variation influencing multiple myeloma risk

by Ajore, Ram, Niroula, Abhishek, Pertesi, Maroulio, Cafaro, Caterina, Thodberg, Malte, Went, Molly, Bao, Erik L, Duran-Lozano, Laura, Lopez de Lapuente Portilla, Aitzkoa, Olafsdottir, Thorunn, Ugidos-Damboriena, Nerea, Magnusson, Olafur, Samur, Mehmet, Lareau, Caleb A, Halldorsson, Gisli H, Thorleifsson, Gudmar, Norddahl, Gudmundur L, Gunnarsdottir, Kristbjorg, Försti, Asta, Goldschmidt, Hartmut, Hemminki, Kari, van Rhee, Frits, Kimber, Scott, Sperling, Adam S, Kaiser, Martin, Anderson, Kenneth, Jonsdottir, Ingileif, Munshi, Nikhil, Rafnar, Thorunn, Waage, Anders, Weinhold, Niels, Thorsteinsdottir, Unnur, Sankaran, Vijay G, Stefansson, Kari, Houlston, Richard, Nilsson, Björn
Published in Nature communications

The genetic architecture of age-related hearing impairment revealed by genome-wide association analysis

by Ivarsdottir, Erna V, Holm, Hilma, Benonisdottir, Stefania, Olafsdottir, Thorhildur, Sveinbjornsson, Gardar, Thorleifsson, Gudmar, Eggertsson, Hannes P, Halldorsson, Gisli H, Hjorleifsson, Kristjan E, Melsted, Pall, Gylfason, Arnaldur, Arnadottir, Gudny A, Oddsson, Asmundur, Jensson, Brynjar O, Jonasdottir, Aslaug, Jonasdottir, Adalbjorg, Juliusdottir, Thorhildur, Stefansdottir, Lilja, Tragante, Vinicius, Halldorsson, Bjarni V, Petersen, Hannes, Thorgeirsson, Gudmundur, Thorsteinsdottir, Unnur, Sulem, Patrick, Hinriksdottir, Ingibjorg, Jonsdottir, Ingileif, Gudbjartsson, Daniel F, Stefansson, Kari
Published in Communications biology

Author Correction: Functional dissection of inherited non-coding variation influencing multiple myeloma risk

by Ajore, Ram, Niroula, Abhishek, Pertesi, Maroulio, Cafaro, Caterina, Thodberg, Malte, Went, Molly, Bao, Erik L, Duran-Lozano, Laura, Lopez de Lapuente Portilla, Aitzkoa, Olafsdottir, Thorunn, Ugidos-Damboriena, Nerea, Magnusson, Olafur, Samur, Mehmet, Lareau, Caleb A, Halldorsson, Gisli H, Thorleifsson, Gudmar, Norddahl, Gudmundur L, Gunnarsdottir, Kristbjorg, Försti, Asta, Goldschmidt, Hartmut, Hemminki, Kari, van Rhee, Frits, Kimber, Scott, Sperling, Adam S, Kaiser, Martin, Anderson, Kenneth, Jonsdottir, Ingileif, Munshi, Nikhil, Rafnar, Thorunn, Waage, Anders, Weinhold, Niels, Thorsteinsdottir, Unnur, Sankaran, Vijay G, Stefansson, Kari, Houlston, Richard, Nilsson, Björn
Published in Nature communications

Common and Rare Sequence Variants Influencing Tumor Biomarkers in Blood

by Olafsson, Sigurgeir, Alexandersson, Kristjan F, Gizurarson, Johann G K, Hauksdottir, Katrin, Gunnarsson, Orvar, Olafsson, Karl, Gudmundsson, Julius, Stacey, Simon N, Sveinbjornsson, Gardar, Saemundsdottir, Jona, Bjornsson, Einar S, Olafsson, Sigurdur, Bjornsson, Sigurdur, Orvar, Kjartan B, Vikingsson, Arnor, Geirsson, Arni J, Arinbjarnarson, Sturla, Bjornsdottir, Gyda, Thorgeirsson, Thorgeir E, Sigurdsson, Snaevar, Halldorsson, Gisli H, Magnusson, Olafur T, Masson, Gisli, Holm, Hilma, Jonsdottir, Ingileif, Sigurdardottir, Olof, Eyjolfsson, Gudmundur I, Olafsson, Isleifur, Sulem, Patrick, Thorsteinsdottir, Unnur, Jonsson, Thorvaldur, Rafnar, Thorunn, Gudbjartsson, Daniel F, Stefansson, Kari
Published in Cancer epidemiology, biomarkers & prevention

Author Correction: Rare SLC13A1 variants associate with intervertebral disc disorder highlighting role of sulfate in disc pathology

by Bjornsdottir, Gyda, Stefansdottir, Lilja, Thorleifsson, Gudmar, Sulem, Patrick, Norland, Kristjan, Ferkingstad, Egil, Oddsson, Asmundur, Zink, Florian, Lund, Sigrun H, Nawaz, Muhammad S, Bragi Walters, G, Skuladottir, Astros Th, Gudjonsson, Sigurjon A, Einarsson, Gudmundur, Halldorsson, Gisli H, Bjarnadottir, Valgerdur, Sveinbjornsson, Gardar, Helgadottir, Anna, Styrkarsdottir, Unnur, Gudmundsson, Larus J, Pedersen, Ole B, Hansen, Thomas Folkmann, Werge, Thomas, Banasik, Karina, Troelsen, Anders, Skou, Soren T, Thørner, Lise Wegner, Erikstrup, Christian, Nielsen, Kaspar Rene, Mikkelsen, Susan, Jonsdottir, Ingileif, Bjornsson, Aron, Olafsson, Ingvar H, Ulfarsson, Elfar, Blondal, Josep, Vikingsson, Arnor, Brunak, Soren, Ostrowski, Sisse R, Ullum, Henrik, Thorsteinsdottir, Unnur, Stefansson, Hreinn, Gudbjartsson, Daniel F, Thorgeirsson, Thorgeir E, Stefansson, Kari
Published in Nature communications

Genetic insight into sick sinus syndrome

by Thorolfsdottir, Rosa B, Sveinbjornsson, Gardar, Aegisdottir, Hildur M, Benonisdottir, Stefania, Stefansdottir, Lilja, Ivarsdottir, Erna V, Halldorsson, Gisli H, Sigurdsson, Jon K, Torp-Pedersen, Christian, Weeke, Peter E, Brunak, Søren, Westergaard, David, Pedersen, Ole B, Sorensen, Erik, Nielsen, Kaspar R, Burgdorf, Kristoffer S, Banasik, Karina, Brumpton, Ben, Zhou, Wei, Oddsson, Asmundur, Tragante, Vinicius, Hjorleifsson, Kristjan E, Davidsson, Olafur B, Rajamani, Sridharan, Jonsson, Stefan, Torfason, Bjarni, Valgardsson, Atli S, Thorgeirsson, Gudmundur, Frigge, Michael L, Thorleifsson, Gudmar, Norddahl, Gudmundur L, Helgadottir, Anna, Gretarsdottir, Solveig, Sulem, Patrick, Jonsdottir, Ingileif, Willer, Cristen J, Hveem, Kristian, Bundgaard, Henning, Ullum, Henrik, Arnar, David O, Thorsteinsdottir, Unnur, Gudbjartsson, Daniel F, Holm, Hilma, Stefansson, Kari
Published in European heart journal

Sequence variants affecting voice pitch in humans

by Gisladottir, Rosa S, Helgason, Agnar, Halldorsson, Bjarni V, Helgason, Hannes, Borsky, Michal, Chien, Yu-Ren, Gudnason, Jon, Gudjonsson, Sigurjon A, Moisik, Scott, Dediu, Dan, Thorleifsson, Gudmar, Tragante, Vinicius, Bustamante, Mariana, Jonsdottir, Gudrun A, Stefansdottir, Lilja, Rutsdottir, Gudrun, Magnusson, Sigurdur H, Hardarson, Marteinn, Ferkingstad, Egil, Halldorsson, Gisli H, Rognvaldsson, Solvi, Skuladottir, Astros, Ivarsdottir, Erna V, Norddahl, Gudmundur, Thorgeirsson, Gudmundur, Jonsdottir, Ingileif, Ulfarsson, Magnus O, Holm, Hilma, Stefansson, Hreinn, Thorsteinsdottir, Unnur, Gudbjartsson, Daniel F, Sulem, Patrick, Stefansson, Kari
Published in Science advances

Publisher Correction: GWAS of bone size yields twelve loci that also affect height, BMD, osteoarthritis or fractures

by Styrkarsdottir, Unnur, Stefansson, Olafur A, Gunnarsdottir, Kristbjorg, Thorleifsson, Gudmar, Lund, Sigrun H, Stefansdottir, Lilja, Juliusson, Kristinn, Agustsdottir, Arna B, Zink, Florian, Halldorsson, Gisli H, Ivarsdottir, Erna V, Benonisdottir, Stefania, Jonsson, Hakon, Gylfason, Arnaldur, Norland, Kristjan, Trajanoska, Katerina, Boer, Cindy G, Southam, Lorraine, Leung, Jason C S, Tang, Nelson L S, Kwok, Timothy C Y, Lee, Jenny S W, Ho, Suzanne C, Byrjalsen, Inger, Center, Jacqueline R, Lee, Seung Hun, Koh, Jung-Min, Lohmander, L Stefan, Ho-Pham, Lan T, Nguyen, Tuan V, Eisman, John A, Woo, Jean, Leung, Ping-C, Loughlin, John, Zeggini, Eleftheria, Christiansen, Claus, Rivadeneira, Fernando, van Meurs, Joyce, Uitterlinden, Andre G, Mogensen, Brynjolfur, Jonsson, Helgi, Ingvarsson, Thorvaldur, Sigurdsson, Gunnar, Benediktsson, Rafn, Sulem, Patrick, Jonsdottir, Ingileif, Masson, Gisli, Holm, Hilma, Norddahl, Gudmundur L, Thorsteinsdottir, Unnur, Gudbjartsson, Daniel F, Stefansson, Kari
Published in Nature communications

HLA alleles, disease severity, and age associate with T-cell responses following infection with SARS-CoV-2

by Olafsdottir, Thorunn A, Bjarnadottir, Kristbjorg, Norddahl, Gudmundur L, Halldorsson, Gisli H, Melsted, Pall, Gunnarsdottir, Kristbjorg, Ivarsdottir, Erna, Olafsdottir, Thorhildur, Arnthorsson, Asgeir O, Theodors, Fannar, Eythorsson, Elias, Helgason, Dadi, Eggertsson, Hannes P, Masson, Gisli, Bjarnadottir, Sólveig, Saevarsdottir, Saedis, Runolfsdottir, Hrafnhildur L, Olafsson, Isleifur, Saemundsdottir, Jona, Sigurdsson, Martin I, Ingvarsson, Ragnar F, Palsson, Runolfur, Thorgeirsson, Gudmundur, Halldorsson, Bjarni V, Holm, Hilma, Kristjansson, Mar, Sulem, Patrick, Thorsteinsdottir, Unnur, Jonsdottir, Ingileif, Gudbjartsson, Daniel F, Stefansson, Kari
Published in Communications biology

Coding variants in RPL3L and MYZAP 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

Genetic architecture of band neutrophil fraction in Iceland

by Oskarsson, Gudjon R, Magnusson, Magnus K, Oddsson, Asmundur, Jensson, Brynjar O, Fridriksdottir, Run, Arnadottir, Gudny A, Katrinardottir, Hildigunnur, Rognvaldsson, Solvi, Halldorsson, Gisli H, Sveinbjornsson, Gardar, Ivarsdottir, Erna V, Stefansdottir, Lilja, Ferkingstad, Egil, Norland, Kristjan, Tragante, Vinicius, Saemundsdottir, Jona, Jonasdottir, Aslaug, Jonasdottir, Adalbjorg, Sigurjonsdottir, Svanhvit, Petursdottir, Karen O, Davidsson, Olafur B, Rafnar, Thorunn, Holm, Hilma, Olafsson, Isleifur, Onundarson, Pall T, Vidarsson, Brynjar, Sigurdardottir, Olof, Masson, Gisli, Gudbjartsson, Daniel F, Jonsdottir, Ingileif, Norddahl, Gudmundur L, Thorsteinsdottir, Unnur, Sulem, Patrick, Stefansson, Kari
Published in Communications biology

Thirty novel sequence variants impacting human intracranial volume

by 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
Published in Brain communications

The sequences of 150,119 genomes in the UK Biobank

by Halldorsson, Bjarni V, Eggertsson, Hannes P, Moore, Kristjan H S, Hauswedell, Hannes, Eiriksson, Ogmundur, Ulfarsson, Magnus O, Palsson, Gunnar, Hardarson, Marteinn T, Oddsson, Asmundur, Jensson, Brynjar O, Kristmundsdottir, Snaedis, Sigurpalsdottir, Brynja D, Stefansson, Olafur A, Beyter, Doruk, Holley, Guillaume, Tragante, Vinicius, Gylfason, Arnaldur, Olason, Pall I, Zink, Florian, Asgeirsdottir, Margret, Sverrisson, Sverrir T, Sigurdsson, Brynjar, Gudjonsson, Sigurjon A, Sigurdsson, Gunnar T, Halldorsson, Gisli H, Sveinbjornsson, Gardar, Norland, Kristjan, Styrkarsdottir, Unnur, Magnusdottir, Droplaug N, Snorradottir, Steinunn, Kristinsson, Kari, Sobech, Emilia, Jonsson, Helgi, Geirsson, Arni J, Olafsson, Isleifur, Jonsson, Palmi, Pedersen, Ole Birger, Erikstrup, Christian, Brunak, Søren, Ostrowski, Sisse Rye, Thorleifsson, Gudmar, Jonsson, Frosti, Melsted, Pall, Jonsdottir, Ingileif, Rafnar, Thorunn, Holm, Hilma, Stefansson, Hreinn, Saemundsdottir, Jona, Gudbjartsson, Daniel F, Magnusson, Olafur T, Masson, Gisli, Thorsteinsdottir, Unnur, Helgason, Agnar, Jonsson, Hakon, Sulem, Patrick, Stefansson, Kari
Published in Nature (London)

FLT3 stop mutation increases FLT3 ligand level and risk of autoimmune thyroid disease

by Saevarsdottir, Saedis, Olafsdottir, Thorunn A, Ivarsdottir, Erna V, Halldorsson, Gisli H, Gunnarsdottir, Kristbjorg, Sigurdsson, Asgeir, Johannesson, Ari, Sigurdsson, Jon K, Juliusdottir, Thorhildur, Lund, Sigrun H, Arnthorsson, Asgeir O, Styrmisdottir, Edda L, Gudmundsson, Julius, Grondal, Gerdur M, Steinsson, Kristjan, Alfredsson, Lars, Askling, Johan, Benediktsson, Rafn, Bjarnason, Ragnar, Geirsson, Arni J, Gudbjornsson, Bjorn, Gudjonsson, Hallgrimur, Hjaltason, Haukur, Hreidarsson, Astradur B, Klareskog, Lars, Kockum, Ingrid, Kristjansdottir, Helga, Love, Thorvardur J, Ludviksson, Bjorn R, Olsson, Tomas, Onundarson, Pall T, Orvar, Kjartan B, Padyukov, Leonid, Sigurgeirsson, Bardur, Tragante, Vinicius, Bjarnadottir, Kristbjorg, Rafnar, Thorunn, Masson, Gisli, Sulem, Patrick, Gudbjartsson, Daniel F, Melsted, Pall, Thorleifsson, Gudmar, Norddahl, Gudmundur L, Thorsteinsdottir, Unnur, Jonsdottir, Ingileif, Stefansson, Kari
Published in Nature (London)

Publisher Correction: Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality

by Oddsson, Asmundur, Sulem, Patrick, Sveinbjornsson, Gardar, Arnadottir, Gudny A, Steinthorsdottir, Valgerdur, Halldorsson, Gisli H, Atlason, Bjarni A, Oskarsson, Gudjon R, Helgason, Hannes, Nielsen, Henriette Svarre, Westergaard, David, Karjalainen, Juha M, Katrinardottir, Hildigunnur, Fridriksdottir, Run, Jensson, Brynjar O, Tragante, Vinicius, Ferkingstad, Egil, Jonsson, Hakon, Gudjonsson, Sigurjon A, Beyter, Doruk, Moore, Kristjan H S, Thordardottir, Helga B, Kristmundsdottir, Snaedis, Stefansson, Olafur A, Rantapää-Dahlqvist, Solbritt, Sonderby, Ida Elken, Didriksen, Maria, Stridh, Pernilla, Haavik, Jan, Tryggvadottir, Laufey, Frei, Oleksandr, Walters, G Bragi, Kockum, Ingrid, Hjalgrim, Henrik, Olafsdottir, Thorunn A, Selbaek, Geir, Nyegaard, Mette, Erikstrup, Christian, Brodersen, Thorsten, Saevarsdottir, Saedis, Olsson, Tomas, Nielsen, Kaspar Rene, Haraldsson, Asgeir, Bruun, Mie Topholm, Hansen, Thomas Folkmann, Steingrimsdottir, Thora, Jacobsen, Rikke Louise, Lie, Rolv T, Djurovic, Srdjan, Alfredsson, Lars, Lopez de Lapuente Portilla, Aitzkoa, Brunak, Soren, Melsted, Pall, Halldorsson, Bjarni V, Saemundsdottir, Jona, Magnusson, Olafur Th, Padyukov, Leonid, Banasik, Karina, Rafnar, Thorunn, Askling, Johan, Klareskog, Lars, Pedersen, Ole Birger, Masson, Gisli, Havdahl, Alexandra, Nilsson, Bjorn, Andreassen, Ole A, Daly, Mark, Ostrowski, Sisse Rye, Jonsdottir, Ingileif, Stefansson, Hreinn, Holm, Hilma, Helgason, Agnar, Thorsteinsdottir, Unnur, Stefansson, Kari, Gudbjartsson, Daniel F
Published in Nature communications

Rare variants with large effects provide functional insights into the pathology of migraine subtypes, with and without aura

by Bjornsdottir, Gyda, Chalmer, Mona A, Stefansdottir, Lilja, Skuladottir, Astros Th, Einarsson, Gudmundur, Andresdottir, Margret, Beyter, Doruk, Ferkingstad, Egil, Gretarsdottir, Solveig, Halldorsson, Bjarni V, Halldorsson, Gisli H, Helgadottir, Anna, Helgason, Hannes, Hjorleifsson Eldjarn, Grimur, Jonasdottir, Adalbjorg, Jonasdottir, Aslaug, Jonsdottir, Ingileif, Knowlton, Kirk U, Nadauld, Lincoln D, Lund, Sigrun H, Magnusson, Olafur Th, Melsted, Pall, Moore, Kristjan H. S, Oddsson, Asmundur, Olason, Pall I, Sigurdsson, Asgeir, Stefansson, Olafur A, Saemundsdottir, Jona, Sveinbjornsson, Gardar, Tragante, Vinicius, Unnsteinsdottir, Unnur, Walters, G. Bragi, Zink, Florian, Rødevand, Linn, Andreassen, Ole, Igland, Jannicke, Lie, Rolv T, Haavik, Jan, Banasik, Karina, Brunak, Søren, Didriksen, Maria, T. Bruun, Mie, Erikstrup, Christian, Kogelman, Lisette J. A, Nielsen, Kaspar R, Sørensen, Erik, Pedersen, Ole B, Ullum, Henrik, Bay, Jakob, Boldsen, Jens K, Brodersen, Thorsten, Burgdorf, Kristoffer, Dinh, Khoa M, Dowsett, Joseph, Feenstra, Bjarke, Geller, Frank, Hindhede, Lotte, Hjalgrim, Henrik, Jacobsen, Rikke L, Jemec, Gregor, Kaspersen, Katrine, Kjerulf, Bertram D, Larsen, Margit A. H, Louloudis, Ioannis, Lundgaard, Agnete, Mikkelsen, Susan, Mikkelsen, Christina, Nissen, Ioanna, Nyegaard, Mette, Henriksen, Alexander P, Rohde, Palle D, Rostgaard, Klaus, Swinn, Michael, Thørner, Lise W, Bruun, Mie T, Werge, Thomas, Westergaard, David, Masson, Gisli, Thorsteinsdottir, Unnur, Olesen, Jes, Ludvigsson, Petur, Thorarensen, Olafur, Bjornsdottir, Anna, Sigurdardottir, Gudrun R, Sveinsson, Olafur A, Ostrowski, Sisse R, Holm, Hilma, Gudbjartsson, Daniel F, Thorleifsson, Gudmar, Sulem, Patrick, Stefansson, Hreinn, Thorgeirsson, Thorgeir E, Hansen, Thomas F, Stefansson, Kari
Published in Nature genetics

Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality

by Oddsson, Asmundur, Sulem, Patrick, Sveinbjornsson, Gardar, Arnadottir, Gudny A, Steinthorsdottir, Valgerdur, Halldorsson, Gisli H, Atlason, Bjarni A, Oskarsson, Gudjon R, Helgason, Hannes, Nielsen, Henriette Svarre, Westergaard, David, Karjalainen, Juha M, Katrinardottir, Hildigunnur, Fridriksdottir, Run, Jensson, Brynjar O, Tragante, Vinicius, Ferkingstad, Egil, Jonsson, Hakon, Gudjonsson, Sigurjon A, Beyter, Doruk, Moore, Kristjan H S, Thordardottir, Helga B, Kristmundsdottir, Snaedis, Stefansson, Olafur A, Rantapää-Dahlqvist, Solbritt, Sonderby, Ida Elken, Didriksen, Maria, Stridh, Pernilla, Haavik, Jan, Tryggvadottir, Laufey, Frei, Oleksandr, Walters, G Bragi, Kockum, Ingrid, Hjalgrim, Henrik, Olafsdottir, Thorunn A, Selbaek, Geir, Nyegaard, Mette, Erikstrup, Christian, Brodersen, Thorsten, Saevarsdottir, Saedis, Olsson, Tomas, Nielsen, Kaspar Rene, Haraldsson, Asgeir, Bruun, Mie Topholm, Hansen, Thomas Folkmann, Steingrimsdottir, Thora, Jacobsen, Rikke Louise, Lie, Rolv T, Djurovic, Srdjan, Alfredsson, Lars, Lopez de Lapuente Portilla, Aitzkoa, Brunak, Soren, Melsted, Pall, Halldorsson, Bjarni V, Saemundsdottir, Jona, Magnusson, Olafur Th, Padyukov, Leonid, Banasik, Karina, Rafnar, Thorunn, Askling, Johan, Klareskog, Lars, Pedersen, Ole Birger, Masson, Gisli, Havdahl, Alexandra, Nilsson, Bjorn, Andreassen, Ole A, Daly, Mark, Ostrowski, Sisse Rye, Jonsdottir, Ingileif, Stefansson, Hreinn, Holm, Hilma, Helgason, Agnar, Thorsteinsdottir, Unnur, Stefansson, Kari, Gudbjartsson, Daniel F
Published in Nature communications

Multiomics analysis of rheumatoid arthritis yields sequence variants that have large effects on risk of the seropositive subset

by Saevarsdottir, Saedis, Stefansdottir, Lilja, Sulem, Patrick, Thorleifsson, Gudmar, Ferkingstad, Egil, Rutsdottir, Gudrun, Glintborg, Bente, Westerlind, Helga, Grondal, Gerdur, Loft, Isabella C, Sorensen, Signe Bek, Lie, Benedicte Alexandra, Brink, Mikael, Arlestig, Lisbeth, Arnthorsson, Asgeir Orn, Baecklund, Eva, Banasik, Karina, Bank, Steffen, Bjorkman, Lena I, Ellingsen, Torkell, Erikstrup, Christian, Frei, Oleksandr, Gjertsson, Inger, Gudbjartsson, Daniel F, Gudjonsson, Sigurjon A, Halldorsson, Gisli H, Hendricks, Oliver, Hillert, Jan, Hogdall, Estrid, Jacobsen, Søren, Jensen, Dorte Vendelbo, Jonsson, Helgi Freyr, Kastbom, Alf, Kockum, Ingrid, Kristensen, Salome, Kristjansdottir, Helga, Larsen, Margit H, Linauskas, Asta, Hauge, Ellen-Margrethe, Loft, Anne G, Ludviksson, Bjorn R, Lund, Sigrun H, Markusson, Thorsteinn, Masson, Gisli, Melsted, Pall, Moore, Kristjan H S, Munk, Heidi, Nielsen, Kaspar R, Norddahl, Gudmundur L, Oddsson, Asmundur, Olafsdottir, Thorunn A, Olason, Pall I, Olsson, Tomas, Ostrowski, Sisse Rye, Hørslev-Petersen, Kim, Rognvaldsson, Solvi, Sanner, Helga, Silberberg, Gilad N, Stefansson, Hreinn, Sørensen, Erik, Sørensen, Inge J, Turesson, Carl, Bergman, Thomas, Alfredsson, Lars, Kvien, Tore Kristian, Brunak, Søren, Steinsson, Kristján, Andersen, Vibeke, Andreassen, Ole, Rantapää-Dahlqvist, Solbritt, Hetland, Merete Lund, Klareskog, Lars, Askling, Johan, Padyukov, Leonid, Pedersen, Ole Bv, Thorsteinsdottir, Unnur, Jonsdottir, Ingileif, Stefansson, Kari
Published in Annals of the rheumatic diseases

Sequence variant affects GCSAML splicing, mast cell specific proteins, and risk of urticaria

by Kristjansson, Ragnar P, Oskarsson, Gudjon R, Skuladottir, Astros, Oddsson, Asmundur, Rognvaldsson, Solvi, Sveinbjornsson, Gardar, Lund, Sigrun H, Jensson, Brynjar O, Styrmisdottir, Edda L, Halldorsson, Gisli H, Ferkingstad, Egil, Eldjarn, Grimur Hjorleifsson, Beyter, Doruk, Kristmundsdottir, Snædis, Juliusson, Kristinn, Fridriksdottir, Run, Arnadottir, Gudny A, Katrinardottir, Hildigunnur, Snorradottir, Margret H, Tragante, Vinicius, Stefansdottir, Lilja, Ivarsdottir, Erna V, Bjornsdottir, Gyda, Halldorsson, Bjarni V, Thorleifsson, Gudmar, Ludviksson, Bjorn R, Onundarson, Pall T, Saevarsdottir, Saedis, Melsted, Pall, Norddahl, Gudmundur L, Bjornsdottir, Unnur S, Olafsdottir, Thorunn, Gudbjartsson, Daniel F, Thorsteinsdottir, Unnur, Jonsdottir, Ingileif, Sulem, Patrick, Stefansson, Kari
Published in Communications biology