Resultados da pesquisa - Þórunn Rafnar

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  1. 1
    Hypothetical and factual willingness to participate in biobank research

    Hypothetical and factual willingness to participate in biobank research Por Linus Johnsson, Gert Helgesson, Þórunn Rafnar, Ingibjorg Halldorsdottir, K S Chia, Stefan Eriksson, Mats Hansson

    Publicado em 2010
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  2. 2
    Cloning of Amb a I (antigen E), the major allergen family of short ragweed pollen.

    Cloning of Amb a I (antigen E), the major allergen family of short ragweed pollen. Por Þórunn Rafnar, I J Griffith, M C Kuo, Julian F. Bond, Bruce L. Rogers, David G. Klapper

    Publicado em 1991
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  3. 3
    Clinical characteristics of patients with colorectal cancer with double somatic mismatch repair mutations compared with Lynch syndrome

    Clinical characteristics of patients with colorectal cancer with double somatic mismatch repair mutations compared with Lynch syndrome Por Rachel Pearlman, Sigurdís Haraldsdóttir, Albert de la Chapelle, Jón G. Jónasson, Sandya Liyanarachchi, Wendy L. Frankel, Þórunn Rafnar, Kāri Stefánsson, Colin C. Pritchard, Heather Hampel

    Publicado em 2019
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  4. 4
    Prostate Cancer Progression and Survival in BRCA2 Mutation Carriers

    Prostate Cancer Progression and Survival in BRCA2 Mutation Carriers Por Laufey Tryggvadóttír, Linda Vidarsdóttir, Tryggvi Þorgeirsson, Jón G. Jónasson, Elínborg J. Ólafsdóttir, Guðríður H. Ólafsdóttir, Þórunn Rafnar, Steinunn Thorlacius, Eiríkur Jónsson, Jórunn E. Eyfjörd, Hrafn Tulinius

    Publicado em 2007
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  5. 5
    Detection of sharing by descent, long-range phasing and haplotype imputation

    Detection of sharing by descent, long-range phasing and haplotype imputation Por 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

    Publicado em 2008
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  6. 6
    The germline sequence variant rs2736100_C in TERT associates with myeloproliferative neoplasms

    The germline sequence variant rs2736100_C in TERT associates with myeloproliferative neoplasms Por 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

    Publicado em 2014
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  7. 7
    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 Por 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

    Publicado em 2021
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  8. 8
    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 Por 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

    Publicado em 2010
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  9. 9
    Male-pattern baldness susceptibility locus at 20p11

    Male-pattern baldness susceptibility locus at 20p11 Por J. Brent Richards, Xin Yuan, Frank Geller, Dawn Waterworth, Véronique Bataille, Daniel Glass, Kijoung Song, Gérard Waeber, Péter Vollenweider, Katja K.H. Aben, Lambertus A. Kiemeney, G. Bragi Walters, Nicole Soranzo, Unnur Þorsteinsdóttir, Augustine Kong, Þórunn Rafnar, Panos Deloukas, Patrick Sulem, Hreinn Stefánsson, Kāri Stefánsson, Tim D. Spector, Vincent Mooser

    Publicado em 2008
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  10. 10
    Clonal hematopoiesis, with and without candidate driver mutations, is common in the elderly

    Clonal hematopoiesis, with and without candidate driver mutations, is common in the elderly Por Florian Zink, Simon Stacey, Gudmundur L. Norddahl, Michael L. Frigge, Ólafur Þ. Magnússon, Ingileif Jónsdóttir, Thorgeir E. Thorgeirsson, Ásgeir Sigurðsson, Sigurjón A. Guðjónsson, Jūlı́us Guðmundsson, Jón G. Jónasson, Laufey Tryggvadóttír, Þorvaldur Jónsson, Agnar Helgason, Arnaldur Gylfason, Patrick Sulem, Þórunn Rafnar, Unnur Þorsteinsdóttir, Daníel F. Guðbjartsson, Gísli Másson, Augustine Kong, Kāri Stefánsson

    Publicado em 2017
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  11. 11
    Meta-analysis of erosive hand osteoarthritis identifies four common variants that associate with relatively large effect

    Meta-analysis of erosive hand osteoarthritis identifies four common variants that associate with relatively large effect Por Unnur Styrkársdóttir, Lilja Stefánsdóttir, Guðmar Þorleifsson, Ólafur Andri Stefánsson, Saedís Saevarsdóttir, Sigrún H. Lund, Þórunn Rafnar, Kazuyuki Hoshijima, K. Novak, N. Oreiro, Ignacio Rego‐Pérez, Channing Hansen, Nikolas H. Kazmers, Lambertus A. Kiemeney, Francisco J. Blanco, Tyler Barker, M. Kloppenburg, Michael J. Jurynec, Daníel F. Guðbjartsson, Helgi Jónsson, Unnur Þorsteinsdóttir, Kāri Stefánsson

    Publicado em 2023
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  12. 12
    Sequence variants affecting the genome-wide rate of germline microsatellite mutations

    Sequence variants affecting the genome-wide rate of germline microsatellite mutations Por Snædís Kristmundsdóttir, Hákon Jónsson, Marteinn T. Hardarson, Gunnar Pálsson, Doruk Beyter, Hannes P. Eggertsson, Arnaldur Gylfason, Garðar Sveinbjörnsson, Guillaume Holley, Ólafur Andri Stefánsson, Gísli H. Halldórsson, Sigurgeir Ólafsson, Gudny A. Arnadottir, Pall I. Olason, Ögmundur Eiríksson, Gísli Másson, Unnur Þorsteinsdóttir, Þórunn Rafnar, Patrick Sulem, Agnar Helgason, Daníel F. Guðbjartsson, Bjarni V. Halldórsson, Kāri Stefánsson

    Publicado em 2023
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  13. 13
    Sequence variants in the PTCH1 gene associate with spine bone mineral density and osteoporotic fractures

    Sequence variants in the PTCH1 gene associate with spine bone mineral density and osteoporotic fractures Por Unnur Styrkársdóttir, Guðmar Þorleifsson, Sigurjón A. Guðjónsson, Ásgeir Sigurðsson, Jacqueline R. Center, Seung Hun Lee, Tuan V. Nguyen, Timothy Kwok, Jenny S. W. Lee, Suzanne C. Ho, Jean Woo, Ping-C. Leung, Beom‐Jun Kim, Þórunn Rafnar, Lambertus A. Kiemeney, Þorvaldur Ingvarsson, Jung‐Min Koh, Nelson L.S. Tang, John A. Eisman, Claus Christiansen, Gunnar Sigurðsson, Unnur Þorsteinsdóttir, Kāri Stefánsson

    Publicado em 2016
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  14. 14
    Sequence variants in ARHGAP15, COLQ and FAM155A associate with diverticular disease and diverticulitis

    Sequence variants in ARHGAP15, COLQ and FAM155A associate with diverticular disease and diverticulitis Por Snævar Sigurðsson, Kristjan F. Alexandersson, Patrick Sulem, Bjarke Feenstra, Steinunn Guðmundsdóttir, Gísli H. Halldórsson, Sigurgeir Ólafsson, Ásgeir Sigurðsson, Þórunn Rafnar, Thorgeir E. Thorgeirsson, Erik Sørensen, Andreas Nordholm‐Carstensen, Jakob Burcharth, Jens Rikardt Andersen, Henrik Jørgensen, Emma Possfelt-Møller, Henrik Ullum, Guðmar Þorleifsson, Gísli Másson, Unnur Þorsteinsdóttir, Mads Melbye, Daníel F. Guðbjartsson, Tryggvi Stefánsson, Ingileif Jónsdóttir, Kāri Stefánsson

    Publicado em 2017
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  15. 15
    Association of Folate-Pathway Gene Polymorphisms with the Risk of Prostate Cancer: a Population-Based Nested Case-Control Study, Systematic Review, and Meta-analysis

    Association of Folate-Pathway Gene Polymorphisms with the Risk of Prostate Cancer: a Population-Based Nested Case-Control Study, Systematic Review, and Meta-analysis Por Simon M. Collin, Chris Metcalfe, Luisa Zuccolo, Sarah J. Lewis, Lina Chen, Angela Cox, Michael Davis, J. Athene Lane, Jenny Donovan, George Davey Smith, David E. Neal, Freddie C. Hamdy, Jūlı́us Guðmundsson, Patrick Sulem, Þórunn Rafnar, Kristrún R. Benediktsdóttir, Rosalind A. Eeles, Michelle Guy, Zsofia Kote‐Jarai, Jonathan J. Morrison, Ali Amin Al Olama, Kāri Stefánsson, Douglas F. Easton, Richard M. Martin

    Publicado em 2009
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  16. 16
    Sequence variant at 8q24.21 associates with sciatica caused by lumbar disc herniation

    Sequence variant at 8q24.21 associates with sciatica caused by lumbar disc herniation Por Gyða Björnsdóttir, Stefania Benónísdóttir, Garðar Sveinbjörnsson, Unnur Styrkársdóttir, Guðmar Þorleifsson, G. Bragi Walters, Aron Hjalti Björnsson, Ingvar Hákon Ólafsson, Elfar Úlfarsson, Arnór Víkingsson, Ragnheiður Hansdottir, Karl Orn Karlsson, Þórunn Rafnar, Ingileif Jónsdóttir, Michael L. Frigge, Augustine Kong, Ásmundur Oddsson, Gísli Másson, Ólafur Þ. Magnússon, Tómas Guðbjartsson, Hreinn Stefánsson, Patrick Sulem, Daníel F. Guðbjartsson, Unnur Þorsteinsdóttir, Thorgeir E. Thorgeirsson, Kāri Stefánsson

    Publicado em 2017
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  17. 17
    A common variant at 8q24.21 is associated with renal cell cancer

    A common variant at 8q24.21 is associated with renal cell cancer Por Jūlı́us Guðmundsson, Patrick Sulem, Daníel F. Guðbjartsson, Gísli Másson, Vigdís Pétursdóttir, Sverrir Harðarson, Sigurjón A. Guðjónsson, Hrefna Johannsdottir, Hafdís T. Helgadóttir, Simon Stacey, Ólafur Þ. Magnússon, Hannes Helgason, Angeles Panadero, Loes F. van der Zanden, Katja K.H. Aben, Sita H. Vermeulen, Egbert Oosterwijk, Augustine Kong, José Mayordomo, Ásgerður Sverrisdóttir, Eiríkur Jónsson, Tómas Guðbjartsson, Guðmundur Einarsson, Lambertus A. Kiemeney, Unnur Þorsteinsdóttir, Þórunn Rafnar, Kāri Stefánsson

    Publicado em 2013
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  18. 18
    Comprehensive population-wide analysis of Lynch syndrome in Iceland reveals founder mutations in MSH6 and PMS2

    Comprehensive population-wide analysis of Lynch syndrome in Iceland reveals founder mutations in MSH6 and PMS2 Por Sigurdís Haraldsdóttir, Þórunn Rafnar, Wendy L. Frankel, Sylvia Einarsdottir, Ásgeir Sigurðsson, Heather Hampel, Pétur Snæbjörnsson, Gísli Másson, Daniel Weng, Reynir Arngrı́msson, Birte Kehr, Ahmet Yılmaz, Stefán Haraldsson, Patrick Sulem, Tryggvi Stefánsson, Peter G. Shields, Fridbjörn Sigurdsson, Tanios Bekaii‐Saab, Páll Helgi Möller, Margrét Steinarsdóttir, Kristín Alexíusdóttir, Megan P. Hitchins, Colin C. Pritchard, Albert de la Chapelle, Jón G. Jónasson, Richard M. Goldberg, Kāri Stefánsson

    Publicado em 2017
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  19. 19
    Genome-wide associations for benign prostatic hyperplasia reveal a genetic correlation with serum levels of PSA

    Genome-wide associations for benign prostatic hyperplasia reveal a genetic correlation with serum levels of PSA Por Jūlı́us Guðmundsson, Jon K. Sigurdsson, Lilja Stefánsdóttir, Bjarni A. Agnarsson, Helgi J. Ísaksson, Ólafur Andri Stefánsson, Sigurjón A. Guðjónsson, Daníel F. Guðbjartsson, Gísli Másson, Michael L. Frigge, Simon Stacey, Patrick Sulem, Gísli H. Halldórsson, Vinicius Tragante, Hilma Hólm, Guðmundur I. Eyjólfsson, Ólöf Sigurðardóttir, Ísleifur Ólafsson, Þorvaldur Jónsson, Eiríkur Jónsson, Rósa B. Barkardóttir, Rafn Hilmarsson, Folkert W. Asselbergs, Guðmundur Geirsson, Unnur Þorsteinsdóttir, Þórunn Rafnar, Guðmar Þorleifsson, Kāri Stefánsson

    Publicado em 2018
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  20. 20
    A rare variant in MYH6 is associated with high risk of sick sinus syndrome

    A rare variant in MYH6 is associated with high risk of sick sinus syndrome Por Hilma Hólm, Daníel F. Guðbjartsson, Patrick Sulem, Gísli Másson, Hafdís T. Helgadóttir, Carlo Zanon, Ólafur Þ. Magnússon, Agnar Helgason, Jona Saemundsdottir, Arnaldur Gylfason, Hrafnhildur Stefansdottir, Sólveig Grétarsdóttir, Stefán E. Matthíasson, Gu∂mundur Thorgeirsson, Áslaug Jónasdóttir, Ásgeir Sigurðsson, Hreinn Stefánsson, Thomas Werge, Þórunn Rafnar, Lambertus A. Kiemeney, Babar Parvez, Raafia Muhammad, Dan M. Roden, Dawood Darbar, Guðmar Þorleifsson, G. Bragi Walters, Augustine Kong, Unnur Þorsteinsdóttir, Davíð O. Arnar, Kāri Stefánsson

    Publicado em 2011
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