Výsledky vyhledávání - Gudbjartsson, Daniel

“Bias toward the Null” Means Reduced Power Autor Sieberts, Solveig K., Broman, Karl W., Gudbjartsson, Daniel F.

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GWAS of Hematuria Autor Gagliano Taliun, Sarah A., Sulem, Patrick, Sveinbjornsson, Gardar, Gudbjartsson, Daniel F., Stefansson, Kari, Paterson, Andrew D., Barua, Moumita

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A Method for Detecting Long Non-Coding RNAs with Tiled RNA Expression Microarrays Autor Lund, Sigrun Helga, Gudbjartsson, Daniel Fannar, Rafnar, Thorunn, Sigurdsson, Asgeir, Gudjonsson, Sigurjon Axel, Gudmundsson, Julius, Stefansson, Kari, Stefansson, Gunnar

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The mother’s risk of premature death after child loss across two centuries Autor Valdimarsdóttir, Unnur A, Lu, Donghao, Lund, Sigrún H, Fall, Katja, Fang, Fang, Kristjánsson, Þórður, Guðbjartsson, Daníel, Helgason, Agnar, Stefánsson, Kári

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Age and Influenza-Specific Pre-Vaccination Antibodies Strongly Affect Influenza Vaccine Responses in the Icelandic Population whereas Disease and Medication Have Small Effects Autor Olafsdottir, Thorunn A., Alexandersson, Kristjan F., Sveinbjornsson, Gardar, Lapini, Giulia, Palladino, Laura, Montomoli, Emanuele, Del Giudice, Giuseppe, Gudbjartsson, Daniel F., Jonsdottir, Ingileif

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Relatedness disequilibrium regression estimates heritability without environmental bias Autor Young, Alexander I., Frigge, Michael L., Gudbjartsson, Daniel F., Thorleifsson, Gudmar, Bjornsdottir, Gyda, Sulem, Patrick, Masson, Gisli, Thorsteinsdottir, Unnur, Stefansson, Kari, Kong, Augustine

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GraphTyper2 enables population-scale genotyping of structural variation using pangenome graphs Autor Eggertsson, Hannes P., Kristmundsdottir, Snaedis, Beyter, Doruk, Jonsson, Hakon, Skuladottir, Astros, Hardarson, Marteinn T., Gudbjartsson, Daniel F., Stefansson, Kari, Halldorsson, Bjarni V., Melsted, Pall

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Cancer as a Complex Phenotype: Pattern of Cancer Distribution within and beyond the Nuclear Family Autor Amundadottir, Laufey T, Thorvaldsson, Sverrir, Gudbjartsson, Daniel F, Sulem, Patrick, Kristjansson, Kristleifur, Arnason, Sigurdur, Gulcher, Jeffrey R, Bjornsson, Johannes, Kong, Augustine, Thorsteinsdottir, Unnur, Stefansson, Kari

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Multi-nucleotide de novo Mutations in Humans Autor Besenbacher, Søren, Sulem, Patrick, Helgason, Agnar, Helgason, Hannes, Kristjansson, Helgi, Jonasdottir, Aslaug, Jonasdottir, Adalbjorg, Magnusson, Olafur Th., Thorsteinsdottir, Unnur, Masson, Gisli, Kong, Augustine, Gudbjartsson, Daniel F., Stefansson, Kari

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Common Sequence Variants Associated With Coronary Artery Disease Correlate With the Extent of Coronary Atherosclerosis Autor Bjornsson, Eythor, Gudbjartsson, Daniel F., Helgadottir, Anna, Gudnason, Thorarinn, Gudbjartsson, Tomas, Eyjolfsson, Kristjan, Patel, Riyaz S., Ghasemzadeh, Nima, Thorleifsson, Gudmar, Quyyumi, Arshed A., Thorsteinsdottir, Unnur, Thorgeirsson, Gudmundur, Stefansson, Kari

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Genetic Risk of Coronary Artery Disease, Features of Atherosclerosis, and Coronary Plaque Burden Autor Christiansen, Morten Krogh, Nissen, Louise, Winther, Simon, Møller, Peter Loof, Frost, Lars, Johansen, Jane Kirk, Jensen, Henrik Kjærulf, Guðbjartsson, Daníel, Holm, Hilma, Stefánsson, Kári, Bøtker, Hans Erik, Bøttcher, Morten, Nyegaard, Mette

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Rare SCARB1 mutations associate with high-density lipoprotein cholesterol but not with coronary artery disease Autor Helgadottir, Anna, Sulem, Patrick, Thorgeirsson, Gudmundur, Gretarsdottir, Solveig, Thorleifsson, Gudmar, Jensson, Brynjar Ö, Arnadottir, Gudny A, Olafsson, Isleifur, Eyjolfsson, Gudmundur I, Sigurdardottir, Olof, Thorsteinsdottir, Unnur, Gudbjartsson, Daniel F, Holm, Hilma, Stefansson, Kari

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Polygenic risk scores for schizophrenia and bipolar disorder associate with addiction Autor 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

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A Susceptibility Gene for Psoriatic Arthritis Maps to Chromosome 16q: Evidence for Imprinting Autor Karason, Ari, Gudjonsson, Johann E., Upmanyu, Ruchi, Antonsdottir, Arna A., Hauksson, Valdimar B., Runasdottir, E. Hjaltey, Jonsson, Hjortur H., Gudbjartsson, Daniel F., Frigge, Michael L., Kong, Augustine, Stefansson, Kari, Valdimarsson, Helgi, Gulcher, Jeffrey R.

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The rate of meiotic gene conversion varies by sex and age Autor Halldorsson, Bjarni V., Hardarson, Marteinn T., Kehr, Birte, Styrkarsdottir, Unnur, Gylfason, Arnaldur, Thorleifsson, Gudmar, Zink, Florian, Jonasdottir, Adalbjorg, Jonasdottir, Aslaug, Sulem, Patrick, Masson, Gisli, Thorsteinsdottir, Unnur, Helgason, Agnar, Kong, Augustine, Gudbjartsson, Daniel F., Stefansson, Kari

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Selection against variants in the genome associated with educational attainment Autor Kong, Augustine, Frigge, Michael L., Thorleifsson, Gudmar, Stefansson, Hreinn, Young, Alexander I., Zink, Florian, Jonsdottir, Gudrun A., Okbay, Aysu, Sulem, Patrick, Masson, Gisli, Gudbjartsson, Daniel F., Helgason, Agnar, Bjornsdottir, Gyda, Thorsteinsdottir, Unnur, Stefansson, Kari

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Allele frequency of variants reported to cause adenine phosphoribosyltransferase deficiency Autor Runolfsdottir, Hrafnhildur L., Sayer, John A., Indridason, Olafur S., Edvardsson, Vidar O., Jensson, Brynjar O., Arnadottir, Gudny A., Gudjonsson, Sigurjon A., Fridriksdottir, Run, Katrinardottir, Hildigunnur, Gudbjartsson, Daniel, Thorsteinsdottir, Unnur, Sulem, Patrick, Stefansson, Kari, Palsson, Runolfur

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Common variants upstream of KDR encoding VEGFR2 and in TTC39B associate with endometriosis Autor Steinthorsdottir, Valgerdur, Thorleifsson, Gudmar, Aradottir, Kristrun, Feenstra, Bjarke, Sigurdsson, Asgeir, Stefansdottir, Lilja, Kristinsdottir, Anna M., Zink, Florian, Halldorsson, Gisli H., Munk Nielsen, Nete, Geller, Frank, Melbye, Mads, Gudbjartsson, Daniel F., Geirsson, Reynir T., Thorsteinsdottir, Unnur, Stefansson, Kari

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Sequence variation at ANAPC1 accounts for 24% of the variability in corneal endothelial cell density Autor Ivarsdottir, Erna V., Benonisdottir, Stefania, Thorleifsson, Gudmar, Sulem, Patrick, Oddsson, Asmundur, Styrkarsdottir, Unnur, Kristmundsdottir, Snaedis, Arnadottir, Gudny A., Thorgeirsson, Gudmundur, Jonsdottir, Ingileif, Zoega, Gunnar M., Thorsteinsdottir, Unnur, Gudbjartsson, Daniel F., Jonasson, Fridbert, Holm, Hilma, Stefansson, Kari

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Detection of sharing by descent, long-range phasing and haplotype imputation Autor Kong, Augustine, Masson, Gisli, Frigge, Michael L., Gylfason, Arnaldur, Zusmanovich, Pasha, Thorleifsson, Gudmar, Olason, Pall I., Ingason, Andres, Steinberg, Stacy, Rafnar, Thorunn, Sulem, Patrick, Mouy, Magali, Jonsson, Frosti, Thorsteinsdottir, Unnur, Gudbjartsson, Daniel F., Stefansson, Hreinn, Stefansson, Kari

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