Výsledky vyhledávání - Thorhildur Juliusdottir

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  1. 1
    topr: an R package for viewing and annotating genetic association results

    topr: an R package for viewing and annotating genetic association results Autor Thorhildur Juliusdottir

    Vydáno 2023
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  2. 2
    The genetic architecture of age-related hearing impairment revealed by genome-wide association analysis

    The genetic architecture of age-related hearing impairment revealed by genome-wide association analysis Autor Erna V. Ivarsdottir, Hilma Hólm, Stefania Benónísdóttir, Þórhildur Ólafsdóttir, Garðar Sveinbjörnsson, Guðmar Þorleifsson, Hannes P. Eggertsson, Gísli H. Halldórsson, Kristján Eldjárn Hjörleifsson, Páll Melsted, Arnaldur Gylfason, Gudny A. Arnadottir, Ásmundur Oddsson, Brynjar Ö. Jensson, Áslaug Jónasdóttir, Aðalbjörg Jónasdóttir, Thorhildur Juliusdottir, Lilja Stefánsdóttir, Vinicius Tragante, Bjarni V. Halldórsson, Hannes Petersen, Guðmundur Þorgeirsson, Unnur Þorsteinsdóttir, Patrick Sulem, Ingibjorg Hinriksdottir, Ingileif Jónsdóttir, Daníel F. Guðbjartsson, Kāri Stefánsson

    Vydáno 2021
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  3. 3
    A homozygous loss-of-function mutation leading to CYBC1 deficiency causes chronic granulomatous disease

    A homozygous loss-of-function mutation leading to CYBC1 deficiency causes chronic granulomatous disease Autor Gudny A. Arnadottir, Gudmundur L. Norddahl, Steinunn Guðmundsdóttir, Arna B. Agustsdottir, Snævar Sigurðsson, Brynjar Ö. Jensson, Kristbjörg Bjarnadóttir, Fannar Theódórs, Stefania Benónísdóttir, Erna V. Ivarsdottir, Ásmundur Oddsson, Ragnar P. Kristjansson, Gerald Sulem, Kristjan F. Alexandersson, Thorhildur Juliusdottir, Kjartan R. Guðmundsson, Jona Saemundsdottir, Aðalbjörg Jónasdóttir, Áslaug Jónasdóttir, Ásgeir Sigurðsson, Paolo Manzanillo, Sigurjón A. Guðjónsson, Guðmundur Á. Þórisson, Ólafur Þ. Magnússon, Gísli Másson, Kjartan B. Örvar, Hilma Hólm, Sigurður Björnsson, Reynir Arngrı́msson, Daníel F. Guðbjartsson, Unnur Þorsteinsdóttir, Ingileif Jónsdóttir, Ásgeir Haraldsson, Patrick Sulem, Kāri Stefánsson

    Vydáno 2018
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  4. 4
    Eighty-eight variants highlight the role of T cell regulation and airway remodeling in asthma pathogenesis

    Eighty-eight variants highlight the role of T cell regulation and airway remodeling in asthma pathogenesis Autor Thorunn A. Olafsdottir, Fannar Theódórs, Kristbjörg Bjarnadóttir, Unnur Steina Björnsdóttir, Arna B. Agustsdottir, Ólafur Andri Stefánsson, Erna V. Ivarsdottir, Jon K. Sigurdsson, Stefania Benónísdóttir, Guðmundur I. Eyjólfsson, Davíð Gíslason, Þórarinn Gíslason, Steinunn Guðmundsdóttir, Arnaldur Gylfason, Bjarni V. Halldórsson, Gísli H. Halldórsson, Thorhildur Juliusdottir, Anna M. Kristinsdottir, Dóra Lúðvíksdóttir, Bjórn R. Lúdvíksson, Gísli Másson, Kristján Norland, Páll T. Önundarson, Ísleifur Ólafsson, Ólöf Sigurðardóttir, Lilja Stefánsdóttir, Garðar Sveinbjörnsson, Vinicius Tragante, Daníel F. Guðbjartsson, Guðmar Þorleifsson, Patrick Sulem, Unnur Þorsteinsdóttir, Gudmundur L. Norddahl, Ingileif Jónsdóttir, Kāri Stefánsson

    Vydáno 2020
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  5. 5
    The Genetic Landscape of Renal Complications in Type 1 Diabetes

    The Genetic Landscape of Renal Complications in Type 1 Diabetes Autor Niina Sandholm, Natalie Van Zuydam, Emma Ahlqvist, Thorhildur Juliusdottir, Harshal Deshmukh, Nigel W. Rayner, Barbara Di Camillo, Carol Forsblom, João Fadista, Daniel Ziemek, Rany M. Salem, Linda T. Hiraki, Marcus G. Pezzolesi, David‐Alexandre Trégouët, Emma H. Dahlström, Erkka Valo, Nikolay Oskolkov, Claes Ladenvall, M. Loredana Marcovecchio, Jason D. Cooper, Francesco Sambo, Alberto Malovini, Marco Manfrini, Amy Jayne McKnight, Maria Lajer, Valma Harjutsalo, Daniel Gordin, Maija Parkkonen, Valeriya Lyssenko, Paul McKeigue, Stephen S. Rich, M. Julia Brosnan, Eric B. Fauman, Riccardo Bellazzi, Peter Rossing, Samy Hadjadj, Andrzej S. Królewski, Andrew D. Paterson, Joel N. Hirschhorn, Alexander P. Maxwell, Claudio Cobelli, Helen M. Colhoun, Per‐Henrik Groop, Mark I. McCarthy, Per‐Henrik Groop

    Vydáno 2016
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  6. 6
    Genetic effects on the timing of parturition and links to fetal birth weight

    Genetic effects on the timing of parturition and links to fetal birth weight Autor Pol Solé-Navais, Christopher Flatley, Valgerður Steinthórsdóttir, Marc Vaudel, Julius Juodakis, Jing Chen, Triin Laisk, Abigail L. LaBella, David Westergaard, Jonas Bacelis, Ben Brumpton, Line Skotte, Maria Carolina Borges, Øyvind Helgeland, Anubha Mahajan, Matthias Wielscher, Frederick T. J. Lin, Catherine Briggs, Carol A. Wang, Gunn-Helen Moen, Robin N. Beaumont, Jonathan P. Bradfield, Abin Abraham, Guðmar Þorleifsson, Maiken E. Gabrielsen, Sisse Rye Ostrowski, Dominika Modzelewska, Ellen A. Nøhr, Elina Hyppönen, Amit Srivastava, Octavious Talbot, Catherine Allard, Scott M. Williams, Ramkumar Menon, Beverley M. Shields, Garðar Sveinbjörnsson, Huan Xu, Mads Melbye, William L. Lowe, Luigi Bouchard, Emily Oken, Ole Birger Pedersen, Daníel F. Guðbjartsson, Christian Erikstrup, Erik Sørensen, Rolv T. Lie, Kari Teramo, Mikko Hallman, Thorhildur Juliusdottir, Hakon Hakonarson, Henrik Ullum, Andrew T. Hattersley, Line Sletner, Mario Merialdi, Sheryl L. Rifas‐Shiman, Thora Steingrimsdottir, Denise Scholtens, Christine Power, Jane West, Mette Nyegaard, John A Capra, Anne Heidi Skogholt, Per Magnus, Ole A. Andreassen, Unnur Thorsteinsdottir, Struan F.A. Grant, Elisabeth Qvigstad, Craig E. Pennell, Marie‐France Hivert, M. Geoffrey Hayes, Marjo‐Riitta Järvelin, Mark I McCarthy, Debbie A. Lawlor, Henriette Svarre Nielsen, Reedik Mägi, Antonis Rokas, Kristian Hveem, Kāri Stefánsson, Bjarke Feenstra, Pål R. Njølstad, Louis J Muglia, Rachel M. Freathy, Stefan Johansson, Ge Zhang, Bo Jacobsson

    Vydáno 2023
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  7. 7
    Genetic predisposition to hypertension is associated with preeclampsia in European and Central Asian women

    Genetic predisposition to hypertension is associated with preeclampsia in European and Central Asian women Autor Valgerður Steinthórsdóttir, Ralph McGinnis, Nicholas Williams, Lilja Stefánsdóttir, Guðmar Þorleifsson, Scott Shooter, João Fadista, Jon K. Sigurdsson, Kirsi Auro, Galina Berezina, Maria Carolina Borges, Suzannah Bumpstead, Jonas Bybjerg‐Grauholm, Irina Colgiu, Vivien A. Dolby, Frank Dudbridge, Stephanie M. Engel, Christopher Franklin, Michael L. Frigge, Yr Frisbæk, Reynir Tómas Geirsson, Frank Geller, Sólveig Grétarsdóttir, Daníel F. Guðbjartsson, Quaker E. Harmon, David M. Hougaard, Tatyana Hegay, Anna Helgadóttir, Sigrun Hjartardottir, Tiina Jääskeläinen, Hrefna Johannsdottir, Ingileif Jónsdóttir, Thorhildur Juliusdottir, Noor Kalsheker, A. K. Kasimov, John P. Kemp, Katja Kivinen, Kari Klungsøyr, Wai Lee, Mads Melbye, Zosia Miedzybrodska, Ashley Moffett, Dilbar Najmutdinova, F Nishanova, Thorunn A. Olafsdottir, Markus Perola, Fiona Broughton Pipkin, Lucilla Poston, Gordon Prescott, Saedís Saevarsdóttir, Damilya Salimbayeva, Paula J. Scaife, Line Skotte, Eleonora Staines-Urias, Ólafur Andri Stefánsson, Karina Meden Sørensen, Liv Cecilie Vestrheim Thomsen, Vinicius Tragante, Lill Trogstad, Nigel Simpson, Hannele Laivuori, Seppo Heinonen, Eero Kajantie, Juha Kere, Katja Kivinen, Anneli Pouta, Linda Morgan, Fiona Broughton Pipkin, Noor Kalsheker, James J. Walker, Sheila Macphail, Mark D. Kilby, Marwan Habiba, Catherine Williamson, Kevin M. O’Shaughnessy, Shaughn O’Brien, Alan C. Cameron, Christopher W.G. Redman, Martin Farrall, Mark J. Caulfield, Anna F. Dominiczak, Tamara Aripova, Juan P. Casas, Anna F. Dominiczak, James J. Walker, Unnur Þorsteinsdóttir, Ann‐Charlotte Iversen, Bjarke Feenstra, Debbie A. Lawlor, Heather A. Boyd, Per Magnus, Hannele Laivuori, Nodira Zakhidova, Gulnara Svyatova, Kāri Stefánsson, Linda Morgan

    Vydáno 2020
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