Výsledky vyhledávání - Patrick Sulem

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  1. 1
    Relatedness disequilibrium regression estimates heritability without environmental bias

    Relatedness disequilibrium regression estimates heritability without environmental bias Autor Alexander I. Young, Michael L. Frigge, Daníel F. Guðbjartsson, Guðmar Þorleifsson, Gyða Björnsdóttir, Patrick Sulem, Gísli Másson, Unnur Þorsteinsdóttir, Kāri Stefánsson, Augustine Kong

    Vydáno 2018
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  2. 2
    Cancer as a Complex Phenotype: Pattern of Cancer Distribution within and beyond the Nuclear Family

    Cancer as a Complex Phenotype: Pattern of Cancer Distribution within and beyond the Nuclear Family Autor Laufey T. Ámundadóttir, Sverrir Thorvaldsson, Daníel F. Guðbjartsson, Patrick Sulem, Kristleifur Kristjánsson, Sigurður Árnason, Jeffrey R. Gulcher, Jóhannes Björnsson, Augustine Kong, Unnur Þorsteinsdóttir, Kāri Stefánsson

    Vydáno 2004
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  3. 3
    Multi-nucleotide de novo Mutations in Humans

    Multi-nucleotide de novo Mutations in Humans Autor Søren Besenbacher, Patrick Sulem, Agnar Helgason, Hannes Helgason, Helgi Kristjansson, Áslaug Jónasdóttir, Aðalbjörg Jónasdóttir, Ólafur Þ. Magnússon, Unnur Þorsteinsdóttir, Gísli Másson, Augustine Kong, Daníel F. Guðbjartsson, Kāri Stefánsson

    Vydáno 2016
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  4. 4
    Rare SCARB1 mutations associate with high-density lipoprotein cholesterol but not with coronary artery disease

    Rare SCARB1 mutations associate with high-density lipoprotein cholesterol but not with coronary artery disease Autor Anna Helgadóttir, Patrick Sulem, Guðmundur Þorgeirsson, Sólveig Grétarsdóttir, Guðmar Þorleifsson, Brynjar Ö. Jensson, Gudny A. Arnadottir, Ísleifur Ólafsson, Guðmundur I. Eyjólfsson, Ólöf Sigurðardóttir, Unnur Þorsteinsdóttir, Daníel F. Guðbjartsson, Hilma Hólm, Kāri Stefánsson

    Vydáno 2018
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  5. 5
    The rate of meiotic gene conversion varies by sex and age

    The rate of meiotic gene conversion varies by sex and age Autor Bjarni V. Halldórsson, Marteinn T. Hardarson, Birte Kehr, Unnur Styrkársdóttir, Arnaldur Gylfason, Guðmar Þorleifsson, Florian Zink, Aðalbjörg Jónasdóttir, Áslaug Jónasdóttir, Patrick Sulem, Gísli Másson, Unnur Þorsteinsdóttir, Agnar Helgason, Augustine Kong, Daníel F. Guðbjartsson, Kāri Stefánsson

    Vydáno 2016
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  6. 6
    Selection against variants in the genome associated with educational attainment

    Selection against variants in the genome associated with educational attainment Autor Augustine Kong, Michael L. Frigge, Guðmar Þorleifsson, Hreinn Stefánsson, Alexander I. Young, Florian Zink, Guðrún A. Jónsdóttir, Aysu Okbay, Patrick Sulem, Gísli Másson, Daníel F. Guðbjartsson, Agnar Helgason, Gyða Björnsdóttir, Unnur Þorsteinsdóttir, Kāri Stefánsson

    Vydáno 2017
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  7. 7
    A common biological basis of obesity and nicotine addiction

    A common biological basis of obesity and nicotine addiction Autor Thorgeir E. Thorgeirsson, Daníel F. Guðbjartsson, Patrick Sulem, Søren Besenbacher, Unnur Styrkársdóttir, Guðmar Þorleifsson, G. Bragi Walters, Helena Furberg, Patrick F. Sullivan, Júlio Sérgio Marchini, Mark I. McCarthy, Valgerður Steinthórsdóttir, U. Thorsteinsdottir, Hreinn Stefánsson

    Vydáno 2013
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    Revisão
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  8. 8
    Common and rare variants associated with kidney stones and biochemical traits

    Common and rare variants associated with kidney stones and biochemical traits Autor Ásmundur Oddsson, Patrick Sulem, Hannes Helgason, Viðar Ö. Eðvarðsson, Guðmar Þorleifsson, Garðar Sveinbjörnsson, Eik Haraldsdottir, Guðmundur I. Eyjólfsson, Ólöf Sigurðardóttir, Ísleifur Ólafsson, Gísli Másson, Hilma Hólm, Daníel F. Guðbjartsson, Unnur Þorsteinsdóttir, Ólafur S. Indridason, Runólfur Pálsson, Kāri Stefánsson

    Vydáno 2015
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  9. 9
    Detection of sharing by descent, long-range phasing and haplotype imputation

    Detection of sharing by descent, long-range phasing and haplotype imputation Autor Augustine Kong, Gísli Másson, Michael L. Frigge, Arnaldur Gylfason, Pasha Zusmanovich, Guðmar Þorleifsson, Pall I. Olason, Andrés Ingason, Stacy Steinberg, Þórunn Rafnar, Patrick Sulem, Magali Mouy, Frosti Jónsson, Unnur Þorsteinsdóttir, Daníel F. Guðbjartsson, Hreinn Stefánsson, Kāri Stefánsson

    Vydáno 2008
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  10. 10
    Sequence variants from whole genome sequencing a large group of Icelanders

    Sequence variants from whole genome sequencing a large group of Icelanders Autor Daníel F. Guðbjartsson, Patrick Sulem, Hannes Helgason, Arnaldur Gylfason, Sigurjón A. Guðjónsson, Florian Zink, Asmundur Oddson, Gísli Magnússon, Bjarni V. Halldórsson, Eirikur Hjartarson, Gunnar Sigurðsson, Augustine Kong, Agnar Helgason, Gísli Másson, Ólafur Þ. Magnússon, Unnur Þorsteinsdóttir, Kāri Stefánsson

    Vydáno 2015
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  11. 11
    Complete human recombination maps

    Complete human recombination maps Autor Gunnar Pálsson, Marteinn T. Hardarson, Hákon Jónsson, Valgerður Steinthórsdóttir, Ólafur Andri Stefánsson, Hannes P. Eggertsson, Sigurjón A. Guðjónsson, Pall I. Olason, Arnaldur Gylfason, Gísli Másson, Unnur Þorsteinsdóttir, Patrick Sulem, Agnar Helgason, Daníel F. Guðbjartsson, Bjarni V. Halldórsson, Kāri Stefánsson

    Vydáno 2025
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  12. 12
    Rare mutations associating with serum creatinine and chronic kidney disease

    Rare mutations associating with serum creatinine and chronic kidney disease Autor Garðar Sveinbjörnsson, Evgenia Mikaelsdottir, Runólfur Pálsson, Ólafur S. Indridason, Hilma Hólm, Áslaug Jónasdóttir, Agnar Helgason, Snævar Sigurðsson, Aðalbjörg Jónasdóttir, Ásgeir Sigurðsson, Guðmundur I. Eyjólfsson, Ólöf Sigurðardóttir, Ólafur Þ. Magnússon, Augustine Kong, Gísli Másson, Patrick Sulem, Ísleifur Ólafsson, Unnur Þorsteinsdóttir, Daníel F. Guðbjartsson, Kāri Stefánsson

    Vydáno 2014
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  13. 13
    The BARD1 Cys557Ser Variant and Breast Cancer Risk in Iceland

    The BARD1 Cys557Ser Variant and Breast Cancer Risk in Iceland Autor Simon Stacey, Patrick Sulem, Oskar T. Johannsson, Agnar Helgason, Jūlı́us Guðmundsson, Jelena P. Kostic, Kristleifur Kristjánsson, Thora Elisabet Jonsdottir, Helgi Sigurðsson, Jón Hrafnkelsson, Jakob Jóhannsson, Þórarinn Sveinsson, Gardar Myrdal, Hlynur Niels Grimsson, Jón Þór Bergþorsson, Laufey T. Ámundadóttir, Jeffrey R. Gulcher, Unnur Þorsteinsdóttir, Augustine Kong, Kāri Stefánsson

    Vydáno 2006
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  14. 14
    The germline sequence variant rs2736100_C in TERT associates with myeloproliferative neoplasms

    The germline sequence variant rs2736100_C in TERT associates with myeloproliferative neoplasms Autor Ásmundur Oddsson, Sigurður Y. Kristinsson, Hannes Helgason, Daníel F. Guðbjartsson, Gísli Másson, Ásgeir Sigurðsson, Áslaug Jónasdóttir, Áslaug Jónasdóttir, Herdis Steingrimsdottir, Brynjar Viðarsson, Sigrún Reykdal, Guðmundur I. Eyjólfsson, Ísleifur Ólafsson, Páll T. Önundarson, Gudmundur Runarsson, Ólöf Sigurðardóttir, Augustine Kong, Þórunn Rafnar, Patrick Sulem, Unnur Þorsteinsdóttir, Kāri Stefánsson

    Vydáno 2014
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  15. 15
    A Missense Variant in PLEC Increases Risk of Atrial Fibrillation

    A Missense Variant in PLEC Increases Risk of Atrial Fibrillation Autor Rósa B. Þórólfsdóttir, Garðar Sveinbjörnsson, Patrick Sulem, Anna Helgadóttir, Sólveig Grétarsdóttir, Stefania Benónísdóttir, Audur Magnusdottir, Olafur B. Davidsson, Sridharan Rajamani, Dan M. Roden, Dawood Darbar, Terje R. Pedersen, Marc S. Sabatine, Ingileif Jónsdóttir, Davíð O. Arnar, Unnur Þorsteinsdóttir, Daníel F. Guðbjartsson, Hilma Hólm, Kāri Stefánsson

    Vydáno 2017
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  16. 16
    A rare missense mutation in <i>MYH6</i> associates with non-syndromic coarctation of the aorta

    A rare missense mutation in <i>MYH6</i> associates with non-syndromic coarctation of the aorta Autor Þorsteinn Björnsson, Rósa B. Þórólfsdóttir, Garðar Sveinbjörnsson, Patrick Sulem, Gudmundur L. Norddahl, Anna Helgadóttir, Sólveig Grétarsdóttir, Audur Magnusdottir, Ragnar Daníelsen, Engilbert Sigurðsson, Berglind Aðalsteinsdóttir, Sverrir I. Gunnarsson, Ingileif Jónsdóttir, Davíð O. Arnar, Hróðmar Helgason, Tómas Guðbjartsson, Daníel F. Guðbjartsson, Unnur Þorsteinsdóttir, Hilma Hólm, Kāri Stefánsson

    Vydáno 2018
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  17. 17
    The CRTAC1 Protein in Plasma Is Associated With Osteoarthritis and Predicts Progression to Joint Replacement: A Large‐Scale Proteomics Scan in Iceland

    The CRTAC1 Protein in Plasma Is Associated With Osteoarthritis and Predicts Progression to Joint Replacement: A Large‐Scale Proteomics Scan in Iceland Autor Unnur Styrkársdóttir, Sigrún H. Lund, Saedís Saevarsdóttir, Magnus I. Magnusson, Kristbjörg Gunnarsdóttir, Gudmundur L. Norddahl, Michael L. Frigge, Erna V. Ivarsdottir, Gyða Björnsdóttir, Hilma Hólm, Guðmundur Þorgeirsson, Þórunn Rafnar, Ingileif Jónsdóttir, Þorvaldur Ingvarsson, Helgi Jónsson, Patrick Sulem, Unnur Þorsteinsdóttir, Daníel F. Guðbjartsson, Kāri Stefánsson

    Vydáno 2021
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  18. 18
    Biallelic variants in <i>GTF3C3</i> encoding a subunit of the TFIIIC2 complex are associated with neurodevelopmental phenotypes in humans and zebrafish

    Biallelic variants in <i>GTF3C3</i> encoding a subunit of the TFIIIC2 complex are associated with neurodevelopmental phenotypes in humans and zebrafish Autor Mohamed S. Abdel‐Hamid, Adeline Paimboeuf, Maha S. Zaki, Fernanda Barbosa Figueiredo, Sherif F. Abdel‐Ghafar, Sabrina Maher, Rún Friðriksdóttir, Patrick Sulem, Hákon Björn Högnason, Sigrún Hallgrímsdóttir, Catarina Falleiros Nogueira Rojas, Fernando Kok, Mohnish Suri, César Augusto Pinheiro Ferreira Alves, Henry Houlden, Reza Maroofian, Shunmoogum A. Patten

    Vydáno 2025
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  19. 19
    Association of Variants at UMOD with Chronic Kidney Disease and Kidney Stones—Role of Age and Comorbid Diseases

    Association of Variants at UMOD with Chronic Kidney Disease and Kidney Stones—Role of Age and Comorbid Diseases Autor Daníel F. Guðbjartsson, Hilma Hólm, Ólafur S. Indridason, Guðmar Þorleifsson, Viðar Ö. Eðvarðsson, Patrick Sulem, Femmie de Vegt, Frank d’Ancona, Martin den Heijer, Leifur Franzson, Þórunn Rafnar, Kristleifur Kristjánsson, Unnur Steina Björnsdóttir, Guðmundur I. Eyjólfsson, Lambertus A. Kiemeney, Augustine Kong, Runólfur Pálsson, Unnur Þorsteinsdóttir, Kāri Stefánsson

    Vydáno 2010
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  20. 20
    Compound heterozygous mutations in UBA5 causing early-onset epileptic encephalopathy in two sisters

    Compound heterozygous mutations in UBA5 causing early-onset epileptic encephalopathy in two sisters Autor Gudny A. Arnadottir, Brynjar Ö. Jensson, S Marelsson, Gerald Sulem, Ásmundur Oddsson, Ragnar P. Kristjansson, Stefania Benónísdóttir, Sigurjón A. Guðjónsson, Gísli Másson, Guðmundur Á. Þórisson, Jona Saemundsdottir, Ólafur Þ. Magnússon, Aðalbjörg Jónasdóttir, Áslaug Jónasdóttir, Ásgeir Sigurðsson, Daníel F. Guðbjartsson, Unnur Þorsteinsdóttir, Reynir Arngrı́msson, Patrick Sulem, Kāri Stefánsson

    Vydáno 2017
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