Technical, economic, and environmental feasibility of alternative fuel heavy-duty vehicles in Iceland von Alonso-Villar, Albert, Davíðsdóttir, Brynhildur, Stefánsson, Hlynur, Ásgeirsson, Eyjólfur Ingi, Kristjánsson, Ragnar

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Integrated energy systems’ modeling studies for sub-Saharan Africa: A scoping review von Musonye, Xavier S., Davíðsdóttir, Brynhildur, Kristjánsson, Ragnar, Ásgeirsson, Eyjólfur I., Stefánsson, Hlynur

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Electrification potential for heavy-duty vehicles in harsh climate conditions: A case study based technical feasibility assessment von Alonso-Villar, Albert, Davíðsdóttir, Brynhildur, Stefánsson, Hlynur, Ásgeirsson, Eyjólfur Ingi, Kristjánsson, Ragnar

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Long-read sequencing of 3,622 Icelanders provides insight into the role of structural variants in human diseases and other traits von Beyter, Doruk, Ingimundardottir, Helga, Oddsson, Asmundur, Eggertsson, Hannes P., Bjornsson, Eythor, Jonsson, Hakon, Atlason, Bjarni A., Kristmundsdottir, Snaedis, Mehringer, Svenja, Hardarson, Marteinn T., Gudjonsson, Sigurjon A., Magnusdottir, Droplaug N., Jonasdottir, Aslaug, Jonasdottir, Adalbjorg, Kristjansson, Ragnar P., Sverrisson, Sverrir T., Holley, Guillaume, Palsson, Gunnar, Stefansson, Olafur A., Eyjolfsson, Gudmundur, Olafsson, Isleifur, Sigurdardottir, Olof, Torfason, Bjarni, Masson, Gisli, Helgason, Agnar, Thorsteinsdottir, Unnur, Holm, Hilma, Gudbjartsson, Daniel F., Sulem, Patrick, Magnusson, Olafur T., Halldorsson, Bjarni V., Stefansson, Kari

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Genome-wide association meta-analysis yields 20 loci associated with gallstone disease von Ferkingstad, Egil, Oddsson, Asmundur, Gretarsdottir, Solveig, Benonisdottir, Stefania, Thorleifsson, Gudmar, Deaton, Aimee M., Jonsson, Stefan, Stefansson, Olafur A., Norddahl, Gudmundur L., Zink, Florian, Arnadottir, Gudny A., Gunnarsson, Bjarni, Halldorsson, Gisli H., Helgadottir, Anna, Jensson, Brynjar O., Kristjansson, Ragnar P., Sveinbjornsson, Gardar, Sverrisson, David A., Masson, Gisli, Olafsson, Isleifur, Eyjolfsson, Gudmundur I., Sigurdardottir, Olof, Holm, Hilma, Jonsdottir, Ingileif, Olafsson, Sigurdur, Steingrimsdottir, Thora, Rafnar, Thorunn, Bjornsson, Einar S., Thorsteinsdottir, Unnur, Gudbjartsson, Daniel F., Sulem, Patrick, Stefansson, Kari

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Variants associating with uterine leiomyoma highlight genetic background shared by various cancers and hormone-related traits von Rafnar, Thorunn, Gunnarsson, Bjarni, Stefansson, Olafur A., Sulem, Patrick, Ingason, Andres, Frigge, Michael L., Stefansdottir, Lilja, Sigurdsson, Jon K., Tragante, Vinicius, Steinthorsdottir, Valgerdur, Styrkarsdottir, Unnur, Stacey, Simon N., Gudmundsson, Julius, Arnadottir, Gudny A., Oddsson, Asmundur, Zink, Florian, Halldorsson, Gisli, Sveinbjornsson, Gardar, Kristjansson, Ragnar P., Davidsson, Olafur B., Salvarsdottir, Anna, Thoroddsen, Asgeir, Helgadottir, Elisabet A., Kristjansdottir, Katrin, Ingthorsson, Orri, Gudmundsson, Valur, Geirsson, Reynir T., Arnadottir, Ragnheidur, Gudbjartsson, Daniel F., Masson, Gisli, Asselbergs, Folkert W., Jonasson, Jon G., Olafsson, Karl, Thorsteinsdottir, Unnur, Halldorsson, Bjarni V., Thorleifsson, Gudmar, Stefansson, Kari

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Environmental and techno-economic assessment of power system expansion for projected demand levels in Kenya using TIMES modeling framework von Musonye, Xavier S., Davíðsdóttir, Brynhildur, Kristjánsson, Ragnar, Ásgeirsson, Eyjólfur I., Stefánsson, Hlynur

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Common and rare variants associating with serum levels of creatine kinase and lactate dehydrogenase von Kristjansson, Ragnar P., Oddsson, Asmundur, Helgason, Hannes, Sveinbjornsson, Gardar, Arnadottir, Gudny A., Jensson, Brynjar O., Jonasdottir, Aslaug, Jonasdottir, Adalbjorg, Bragi Walters, G., Sulem, Gerald, Oskarsdottir, Arna, Benonisdottir, Stefania, Davidsson, Olafur B., Masson, Gisli, Th Magnusson, Olafur, Holm, Hilma, Sigurdardottir, Olof, Jonsdottir, Ingileif, Eyjolfsson, Gudmundur I., Olafsson, Isleifur, Gudbjartsson, Daniel F., Thorsteinsdottir, Unnur, Sulem, Patrick, Stefansson, Kari

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Epigenetic and genetic components of height regulation von Benonisdottir, Stefania, Oddsson, Asmundur, Helgason, Agnar, Kristjansson, Ragnar P., Sveinbjornsson, Gardar, Oskarsdottir, Arna, Thorleifsson, Gudmar, Davidsson, Olafur B., Arnadottir, Gudny A., Sulem, Gerald, Jensson, Brynjar O., Holm, Hilma, Alexandersson, Kristjan F., Tryggvadottir, Laufey, Walters, G. Bragi, Gudjonsson, Sigurjon A., Ward, Lucas D., Sigurdsson, Jon K., Iordache, Paul D., Frigge, Michael L., Rafnar, Thorunn, Kong, Augustine, Masson, Gisli, Helgason, Hannes, Thorsteinsdottir, Unnur, Gudbjartsson, Daniel F., Sulem, Patrick, Stefansson, Kari

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COPA syndrome in an Icelandic family caused by a recurrent missense mutation in COPA von Jensson, Brynjar O, Hansdottir, Sif, Arnadottir, Gudny A, Sulem, Gerald, Kristjansson, Ragnar P, Oddsson, Asmundur, Benonisdottir, Stefania, Jonsson, Hakon, Helgason, Agnar, Saemundsdottir, Jona, Magnusson, Olafur T, Masson, Gisli, Thorisson, Gudmundur A, Jonasdottir, Adalbjorg, Jonasdottir, Aslaug, Sigurdsson, Asgeir, Jonsdottir, Ingileif, Petursdottir, Vigdis, Kristinsson, Jon R, Gudbjartsson, Daniel F, Thorsteinsdottir, Unnur, Arngrimsson, Reynir, Sulem, Patrick, Gudmundsson, Gunnar, Stefansson, Kari

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Sequence Variants in TAAR5 and Other Loci Affect Human Odor Perception and Naming von Gisladottir, Rosa S., Ivarsdottir, Erna V., Helgason, Agnar, Jonsson, Lina, Hannesdottir, Nanna K., Rutsdottir, Gudrun, Arnadottir, Gudny A., Skuladottir, Astros, Jonsson, Benedikt A., Norddahl, Gudmundur L., Ulfarsson, Magnus O., Helgason, Hannes, Halldorsson, Bjarni V., Nawaz, Muhammad S., Tragante, Vinicius, Sveinbjornsson, Gardar, Thorgeirsson, Thorgeir, Oddsson, Asmundur, Kristjansson, Ragnar P., Bjornsdottir, Gyda, Thorgeirsson, Gudmundur, Jonsdottir, Ingileif, Holm, Hilma, Gudbjartsson, Daniel F., Thorsteinsdottir, Unnur, Stefansson, Hreinn, Sulem, Patrick, Stefansson, Kari

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Sequence variants associating with urinary biomarkers von Benonisdottir, Stefania, Kristjansson, Ragnar P, Oddsson, Asmundur, Steinthorsdottir, Valgerdur, Mikaelsdottir, Evgenia, Kehr, Birte, Jensson, Brynjar O, Arnadottir, Gudny A, Sulem, Gerald, Sveinbjornsson, Gardar, Kristmundsdottir, Snaedis, Ivarsdottir, Erna V, Tragante, Vinicius, Gunnarsson, Bjarni, Runolfsdottir, Hrafnhildur Linnet, Arthur, Joseph G, Deaton, Aimee M, Eyjolfsson, Gudmundur I, Davidsson, Olafur B, Asselbergs, Folkert W, Hreidarsson, Astradur B, Rafnar, Thorunn, Thorleifsson, Gudmar, Edvardsson, Vidar, Sigurdsson, Gunnar, Helgadottir, Anna, Halldorsson, Bjarni V, Masson, Gisli, Holm, Hilma, Onundarson, Pall T, Indridason, Olafur S, Benediktsson, Rafn, Palsson, Runolfur, Gudbjartsson, Daniel F, Olafsson, Isleifur, Thorsteinsdottir, Unnur, Sulem, Patrick, Stefansson, Kari

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Compound heterozygous mutations in UBA5 causing early-onset epileptic encephalopathy in two sisters von Arnadottir, Gudny A, Jensson, Brynjar O, Marelsson, Sigurdur E, Sulem, Gerald, Oddsson, Asmundur, Kristjansson, Ragnar P, Benonisdottir, Stefania, Gudjonsson, Sigurjon A, Masson, Gisli, Thorisson, Gudmundur A, Saemundsdottir, Jona, Magnusson, Olafur Th, Jonasdottir, Adalbjorg, Jonasdottir, Aslaug, Sigurdsson, Asgeir, Gudbjartsson, Daniel F, Thorsteinsdottir, Unnur, Arngrimsson, Reynir, Sulem, Patrick, Stefansson, Kari

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A homozygous loss-of-function mutation leading to CYBC1 deficiency causes chronic granulomatous disease von Arnadottir, Gudny A., Norddahl, Gudmundur L., Gudmundsdottir, Steinunn, Agustsdottir, Arna B., Sigurdsson, Snaevar, Jensson, Brynjar O., Bjarnadottir, Kristbjorg, Theodors, Fannar, Benonisdottir, Stefania, Ivarsdottir, Erna V., Oddsson, Asmundur, Kristjansson, Ragnar P., Sulem, Gerald, Alexandersson, Kristjan F., Juliusdottir, Thorhildur, Gudmundsson, Kjartan R., Saemundsdottir, Jona, Jonasdottir, Adalbjorg, Jonasdottir, Aslaug, Sigurdsson, Asgeir, Manzanillo, Paolo, Gudjonsson, Sigurjon A., Thorisson, Gudmundur A., Magnusson, Olafur Th, Masson, Gisli, Orvar, Kjartan B., Holm, Hilma, Bjornsson, Sigurdur, Arngrimsson, Reynir, Gudbjartsson, Daniel F., Thorsteinsdottir, Unnur, Jonsdottir, Ingileif, Haraldsson, Asgeir, Sulem, Patrick, Stefansson, Kari

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Sequence variant at 4q25 near PITX2 associates with appendicitis von Kristjansson, Ragnar P., Benonisdottir, Stefania, Oddsson, Asmundur, Galesloot, Tessel E., Thorleifsson, Gudmar, Aben, Katja K., Davidsson, Olafur B., Jonsson, Stefan, Arnadottir, Gudny A., Jensson, Brynjar O., Walters, G. Bragi, Sigurdsson, Jon K., Sigurdsson, Snaevar, Holm, Hilma, Arnar, David O., Thorgeirsson, Gudmundur, Alexiusdottir, Kristin, Jonsdottir, Ingileif, Thorsteinsdottir, Unnur, Kiemeney, Lambertus A., Jonsson, Thorvaldur, Gudbjartsson, Daniel F., Rafnar, Thorunn, Sulem, Patrick, Stefansson, Kari

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A rare splice donor mutation in the haptoglobin gene associates with blood lipid levels and coronary artery disease von Bjornsson, Eythor, Helgason, Hannes, Halldorsson, Gisli, Helgadottir, Anna, Gylfason, Arnaldur, Kehr, Birte, Jonasdottir, Adalbjorg, Jonasdottir, Aslaug, Sigurdsson, Asgeir, Oddsson, Asmundur, Thorleifsson, Gudmar, Magnusson, Olafur Th, Gretarsdottir, Solveig, Zink, Florian, Kristjansson, Ragnar P, Asgeirsdottir, Margret, Swinkels, Dorine W, Kiemeney, Lambertus A, Eyjolfsson, Gudmundur I, Sigurdardottir, Olof, Masson, Gisli, Olafsson, Isleifur, Thorgeirsson, Gudmundur, Holm, Hilma, Thorsteinsdottir, Unnur, Gudbjartsson, Daniel F, Sulem, Patrick, Stefansson, Kari

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Genome-wide association study reveals a locus in ADARB2 for complete freedom from headache in Danish Blood Donors von Olofsson, Isa Amalie, Kristjansson, Ragnar P., Callesen, Ida, Davidsson, Olafur, Winsvold, Bendik, Hjalgrim, Henrik, Ostrowski, Sisse R., Erikstrup, Christian, Bruun, Mie Topholm, Pedersen, Ole Birger, Burgdorf, Kristoffer S., Banasik, Karina, Sørensen, Erik, Mikkelsen, Christina, Didriksen, Maria, Dinh, Khoa Manh, Mikkelsen, Susan, Brunak, Søren, Ullum, Henrik, Chalmer, Mona Ameri, Olesen, Jes, Kogelman, Lisette J. A., Hansen, Thomas Folkmann

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Predicted loss and gain of function mutations in ACO1 are associated with erythropoiesis von Oskarsson, Gudjon R., Oddsson, Asmundur, Magnusson, Magnus K., Kristjansson, Ragnar P., Halldorsson, Gisli H., Ferkingstad, Egil, Zink, Florian, Helgadottir, Anna, Ivarsdottir, Erna V., Arnadottir, Gudny A., Jensson, Brynjar O., Katrinardottir, Hildigunnur, Sveinbjornsson, Gardar, Kristinsdottir, Anna M., Lee, Amy L., Saemundsdottir, Jona, Stefansdottir, Lilja, Sigurdsson, Jon K., Davidsson, Olafur B., Benonisdottir, Stefania, Jonasdottir, Aslaug, Jonasdottir, Adalbjorg, Jonsson, Stefan, Gudmundsson, Reynir L., Asselbergs, Folkert W., Tragante, Vinicius, Gunnarsson, Bjarni, Masson, Gisli, Thorleifsson, Gudmar, Rafnar, Thorunn, Holm, Hilma, Olafsson, Isleifur, Onundarson, Pall T., Gudbjartsson, Daniel F., Norddahl, Gudmundur L., Thorsteinsdottir, Unnur, Sulem, Patrick, Stefansson, Kari

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Coding variants in RPL3L and MYZAP increase risk of atrial fibrillation von 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

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Genome-wide association identifies seven loci for pelvic organ prolapse in Iceland and the UK Biobank von Olafsdottir, Thorhildur, Thorleifsson, Gudmar, Sulem, Patrick, Stefansson, Olafur A., Medek, Helga, Olafsson, Karl, Ingthorsson, Orri, Gudmundsson, Valur, Jonsdottir, Ingileif, Halldorsson, Gisli H., Kristjansson, Ragnar P., Frigge, Michael L., Stefansdottir, Lilja, Sigurdsson, Jon K., Oddsson, Asmundur, Sigurdsson, Asgeir, Eggertsson, Hannes P., Melsted, Pall, Halldorsson, Bjarni V., Lund, Sigrun H., Styrkarsdottir, Unnur, Steinthorsdottir, Valgerdur, Gudmundsson, Julius, Holm, Hilma, Tragante, Vinicius, Asselbergs, Folkert W., Thorsteinsdottir, Unnur, Gudbjartsson, Daniel F., Jonsdottir, Kristin, Rafnar, Thorunn, Stefansson, Kari

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