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Áslaug Jónasdóttir

Active 2005–2024

54
Papers
19,619
Citations
48
h-index
53
i10-index

Citations

Citations per year for Áslaug Jónasdóttir1977: 1 citations1982: 1 citations1987: 1 citations2000: 1 citations2005: 18 citations2006: 36 citations2007: 26 citations2008: 103 citations2009: 190 citations2010: 245 citations2011: 229 citations2012: 258 citations2013: 250 citations2014: 262 citations2015: 273 citations2016: 214 citations2017: 246 citations2018: 235 citations2019: 563 citations2020: 1,035 citations2021: 941 citations2022: 471 citations2023: 288 citations2024: 385 citations2025: 190 citations2026: 13 citations1978–1981: no citations, so these years are not shown1983–1986: no citations, so these years are not shown1988–1999: no citations, so these years are not shown2001–2004: no citations, so these years are not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 3,167 citing papers, 24% of this breakdownUnited Kingdom: 1,317 citing papers, 10% of this breakdownGermany: 733 citing papers, 5.6% of this breakdownChina: 619 citing papers, 4.7% of this breakdownNetherlands: 529 citing papers, 4% of this breakdownCanada: 501 citing papers, 3.8% of this breakdownAustralia: 462 citing papers, 3.5% of this breakdownFrance: 434 citing papers, 3.3% of this breakdownItaly: 406 citing papers, 3.1% of this breakdownSweden: 386 citing papers, 2.9% of this breakdownDenmark: 347 citing papers, 2.6% of this breakdownSpain: 297 citing papers, 2.3% of this breakdown
0%24%Other 30.2%

Institutions

Fields

  • Biochemistry, Genetics and Molecular Biology47.9%
  • Medicine38.1%
  • Neuroscience3.9%
  • Immunology and Microbiology2.7%
  • Mathematics2.5%
  • Agricultural and Biological Sciences1.2%
  • Other3.7%

Topics

  • Genetic Associations and Epidemiology5%
  • SARS-CoV-2 and COVID-19 Research4%
  • Genomic variations and chromosomal abnormalities4%
  • Genomics and Rare Diseases3.5%
  • COVID-19 Clinical Research Studies3.4%
  • Genomics and Phylogenetic Studies2.1%
  • Other78%

Coauthors

All papers

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  1. Rate of de novo mutations and the importance of father’s age to disease risk

    Authors: Augustine Kong, Michael L. Frigge, Gísli Másson, Søren Besenbacher, Patrick Sulem, Gísli Magnússon, Sigurjón A. Guðjónsson, Ásgeir Sigurðsson, Áslaug Jónasdóttir, Aðalbjörg Jónasdóttir, Wendy S.W. Wong, Gunnar Sigurðsson, G. Bragi Walters, Stacy Steinberg, Hannes Helgason, Guðmar Þorleifsson, Daníel F. Guðbjartsson, Agnar Helgason, Ólafur Þ. Magnússon, Unnur Þorsteinsdóttir, Kāri Stefánsson - Nature 2012 cited by 2,273

  2. Parental influence on human germline de novo mutations in 1,548 trios from Iceland

    Authors: Hákon Jónsson, Patrick Sulem, Birte Kehr, Snædís Kristmundsdóttir, Florian Zink, Eirikur Hjartarson, Marteinn T. Hardarson, Kristján Eldjárn Hjörleifsson, Hannes P. Eggertsson, Sigurjón A. Guðjónsson, Lucas D. Ward, Gudny A. Arnadottir, Einar A. Helgason, Hannes Helgason, Arnaldur Gylfason, Aðalbjörg Jónasdóttir, Áslaug Jónasdóttir, Þórunn Rafnar, Mike Frigge, Simon Stacey, Ólafur Þ. Magnússon, Unnur Þorsteinsdóttir, Gísli Másson, Augustine Kong, Bjarni V. Halldórsson, Agnar Helgason, Daníel F. Guðbjartsson, Kāri Stefánsson - Nature 2017 cited by 670

  3. Graphtyper enables population-scale genotyping using pangenome graphs

    Authors: Hannes P. Eggertsson, Hákon Jónsson, Snædís Kristmundsdóttir, Eirikur Hjartarson, Birte Kehr, Gísli Másson, Florian Zink, Kristján Eldjárn Hjörleifsson, Áslaug Jónasdóttir, Aðalbjörg Jónasdóttir, Ingileif Jónsdóttir, Daníel F. Guðbjartsson, Páll Melsted, Kāri Stefánsson, Bjarni V. Halldórsson - Nature Genetics 2017 cited by 315

  4. Fine-scale recombination rate differences between sexes, populations and individuals

    Authors: Augustine Kong, Guðmar Þorleifsson, Daníel F. Guðbjartsson, Gísli Másson, Ásgeir Sigurðsson, Áslaug Jónasdóttir, G. Bragi Walters, Aðalbjörg Jónasdóttir, Arnaldur Gylfason, Kári Kristinsson, Sigurjón A. Guðjónsson, Michael L. Frigge, Agnar Helgason, Unnur Þorsteinsdóttir, Kāri Stefánsson - Nature 2010 cited by 664

  5. Variants with large effects on blood lipids and the role of cholesterol and triglycerides in coronary disease

    Authors: Anna Helgadóttir, Sólveig Grétarsdóttir, Guðmar Þorleifsson, Eirikur Hjartarson, Ásgeir Sigurðsson, Audur Magnusdottir, Áslaug Jónasdóttir, Helgi Kristjansson, Patrick Sulem, Ásmundur Oddsson, Garðar Sveinbjörnsson, Valgerður Steinthórsdóttir, Þórunn Rafnar, Gísli Másson, Ingileif Jónsdóttir, Ísleifur Ólafsson, Guðmundur I. Eyjólfsson, Ólöf Sigurðardóttir, Maryam S. Daneshpour, Davood Khalili, Fereidoun Azizi, Dorine W. Swinkels, Lambertus A. Kiemeney, Arshed A. Quyyumi, Allan I. Levey, Riyaz S. Patel, Salim S. Hayek, Ingibjörg Jóna Guðmundsdóttir, Guðmundur Þorgeirsson, Unnur Þorsteinsdóttir, Daníel F. Guðbjartsson, Hilma Hólm, Kāri Stefánsson - Nature Genetics 2016 cited by 265

  6. Lipoprotein(a) Concentration and Risks of Cardiovascular Disease and Diabetes

    Authors: Daníel F. Guðbjartsson, Guðmundur Þorgeirsson, Patrick Sulem, Anna Helgadóttir, Arnaldur Gylfason, Jona Saemundsdottir, Eyþór Björnsson, Gudmundur L. Norddahl, Áslaug Jónasdóttir, Aðalbjörg Jónasdóttir, Hannes P. Eggertsson, Sólveig Grétarsdóttir, Guðmar Þorleifsson, Ólafur S. Indridason, Runólfur Pálsson, Friðbert Jónasson, Ingileif Jónsdóttir, Guðmundur I. Eyjólfsson, Ólöf Sigurðardóttir, Ísleifur Ólafsson, Ragnar Daníelsen, Stefán E. Matthíasson, Snædís Kristmundsdóttir, Bjarni V. Halldórsson, Ástráður B. Hreiðarsson, Einar Már Valdimarsson, Þórarinn Guðnason, Rafn Benediktsson, Valgerður Steinthórsdóttir, Unnur Þorsteinsdóttir, Hilma Hólm, Kāri Stefánsson - Journal of the American College of Cardiology 2019 cited by 221

  7. VariantASGR1Associated with a Reduced Risk of Coronary Artery Disease

    Authors: Paul Nioi, Ásgeir Sigurðsson, Guðmar Þorleifsson, Hannes Helgason, Arna B. Agustsdottir, Gudmundur L. Norddahl, Anna Helgadóttir, Audur Magnusdottir, Áslaug Jónasdóttir, Sólveig Grétarsdóttir, Ingileif Jónsdóttir, Valgerður Steinthórsdóttir, Þórunn Rafnar, Dorine W. Swinkels, Tessel E. Galesloot, Niels Grarup, Torben Jørgensen, Henrik Vestergaard, Torben Hansen, Torsten Lauritzen, Allan Linneberg, Nele Friedrich, Nikolaj T. Krarup, Mogens Fenger, Ulrik Abildgaard, Peter Riis Hansen, Anders Galløe, Peter S. Braund, Christopher P. Nelson, Alistair S. Hall, Michael Williams, André M. van Rij, Gregory T. Jones, Riyaz Patel, Allan I. Levey, Salim S. Hayek, Svati H. Shah, Muredach P. Reilly, Guðmundur I. Eyjólfsson, Ólöf Sigurðardóttir, Ísleifur Ólafsson, Lambertus A. Kiemeney, Arshed A. Quyyumi, Daniel J. Rader, William E. Kraus, Nilesh J. Samani, Oluf Pedersen, Guðmundur Þorgeirsson, Gísli Másson, Hilma Hólm, Daníel F. Guðbjartsson, Patrick Sulem, Unnur Þorsteinsdóttir, Kāri Stefánsson - New England Journal of Medicine 2016 cited by 191

  8. A common inversion under selection in Europeans

    Authors: Hreinn Stefánsson, Agnar Helgason, Guðmar Þorleifsson, Valgerður Steinthórsdóttir, Gísli Másson, John Barnard, Adam Baker, Áslaug Jónasdóttir, Andrés Ingason, Vala G Gudnadottir, Natasa Desnica, Andrew A. Hicks, Arnaldur Gylfason, Daníel F. Guðbjartsson, G.M. Jonsdottir, Jesús Sainz, Kari Agnarsson, Birgitta Birgisdottir, Shyamali Ghosh, Aðalheiður Ólafsdóttir, Jean‐Baptiste Cazier, Kristleifur Kristjánsson, Michael L. Frigge, Thorgeir E. Thorgeirsson, Jeffrey R. Gulcher, Augustine Kong, Kāri Stefánsson - Nature Genetics 2005 cited by 872

  9. Common Sequence Variants in the LOXL1 Gene Confer Susceptibility to Exfoliation Glaucoma

    Authors: Guðmar Þorleifsson, Kristinn P. Magnússon, Patrick Sulem, G. Bragi Walters, Daníel F. Guðbjartsson, Hreinn Stefánsson, Thorlakur Jonsson, Aðalbjörg Jónasdóttir, Áslaug Jónasdóttir, Gerður Stefánsdóttir, Gísli Másson, Gudmundur A. Hardarson, Hjörvar Pétursson, Ársæll Már Arnarsson, Mehdi Motallebipour, Ola Wallerman, Claes Wadelius, Jeffrey R. Gulcher, Unnur Þorsteinsdóttir, Augustine Kong, Friðbert Jónasson, Kāri Stefánsson - Science 2007 cited by 681

  10. Rare variants with large effects provide functional insights into the pathology of migraine subtypes, with and without aura

    Authors: Gyða Björnsdóttir, Mona Ameri Chalmer, Lilja Stefánsdóttir, Ástrós Skúladóttir, Guðmundur Einarsson, Margrét B. Andrésdóttir, Doruk Beyter, Egil Ferkingstad, Sólveig Grétarsdóttir, Bjarni V. Halldórsson, Gísli H. Halldórsson, Anna Helgadóttir, Hannes Helgason, Grímur Hjörleifsson Eldjárn, Aðalbjörg Jónasdóttir, Áslaug Jónasdóttir, Ingileif Jónsdóttir, Kirk U. Knowlton, Lincoln Nadauld, Sigrún H. Lund, Ólafur Þ. Magnússon, Páll Melsted, Kristjan H. S. Moore, Ásmundur Oddsson, Pall I. Olason, Ásgeir Sigurðsson, Ólafur Andri Stefánsson, Jona Saemundsdottir, Garðar Sveinbjörnsson, Vinicius Tragante, Unnur Unnsteinsdóttir, G. Bragi Walters, Florian Zink, Linn Rødevand, Ole A. Andreassen, Jannicke Igland, Rolv T. Lie, Jan Haavik, Karina Banasik, Søren Brunak, Maria Didriksen, Mie Topholm Bruun, Christian Erikstrup, Lisette J. A. Kogelman, Kaspar René Nielsen, Erik Sørensen, Ole Birger Pedersen, Henrik Ullum, Jakob Thaning Bay, Jens Kjærgaard Boldsen, Thorsten Brodersen, Kristoffer Sølvsten Burgdorf, Khoa Manh Dinh, Joseph Dowsett, Bjarke Feenstra, Frank Geller, Lotte Hindhede, Henrik Hjalgrim, Rikke Louise Jacobsen, Gregor B. E. Jemec, Katrine Kaspersen, Bertram D. Kjerulf, Margit Anita Hørup Larsen, Ioannis Louloudis, Agnete Troen Lundgaard, Susan Mikkelsen, Christina Mikkelsen, Janna Nissen, Mette Nyegaard, Alexander Pil Henriksen, Palle Duun Rohde, Klaus Rostgaard, Michael Swinn, Lise Wegner Thørner, Mie Topholm Bruun, Thomas Werge, David Westergaard, Gísli Másson, Unnur Þorsteinsdóttir, Jes Olesen, Pétur Lúðvígsson, Ólafur Thorarensen, Anna Bjornsdottir, Gudrun R. Sigurdardottir, Ólafur Sveinsson, Sisse Rye Ostrowski, Hilma Hólm, Daníel F. Guðbjartsson, Guðmar Þorleifsson, Patrick Sulem, Hreinn Stefánsson, Thorgeir E. Thorgeirsson, Thomas Folkmann Hansen, Kāri Stefánsson - Nature Genetics 2023 cited by 55

  11. Genetics of gene expression and its effect on disease

    Authors: Valur Emilsson, Guðmar Þorleifsson, Bin Zhang, Amy Leonardson, Florian Zink, Jun Zhu, Sonia Carlson, Agnar Helgason, G. Bragi Walters, Steinunn Gunnarsdottir, Magali Mouy, Valgerður Steinthórsdóttir, Gudrun H. Eiriksdottir, Gyða Björnsdóttir, Inga Reynisdóttir, Daníel F. Guðbjartsson, Anna Helgadóttir, Áslaug Jónasdóttir, Aðalbjörg Jónasdóttir, Unnur Styrkársdóttir, Sólveig Grétarsdóttir, Kristinn P. Magnússon, Hreinn Stefánsson, Ragnheiður Fossdal, Kristleifur Kristjánsson, Hjörtur Gíslason, Tryggvi Stefánsson, Björn Geir Leifsson, Unnur Þorsteinsdóttir, John R. Lamb, Jeffrey R. Gulcher, Marc L. Reitman, Augustine Kong, Eric E. Schadt, Kāri Stefánsson - Nature 2008 cited by 1,347

  12. Whole genome characterization of sequence diversity of 15,220 Icelanders

    Authors: Hákon Jónsson, Patrick Sulem, Birte Kehr, Snædís Kristmundsdóttir, Florian Zink, Eirikur Hjartarson, Marteinn T. Hardarson, Kristján Eldjárn Hjörleifsson, Hannes P. Eggertsson, Sigurjón A. Guðjónsson, Lucas D. Ward, Gudny A. Arnadottir, Einar A. Helgason, Hannes Helgason, Arnaldur Gylfason, Aðalbjörg Jónasdóttir, Áslaug Jónasdóttir, Þórunn Rafnar, Søren Besenbacher, Michael L. Frigge, Simon Stacey, Ólafur Þ. Magnússon, Unnur Þorsteinsdóttir, Gísli Másson, Augustine Kong, Bjarni V. Halldórsson, Agnar Helgason, Daníel F. Guðbjartsson, Kāri Stefánsson - Scientific Data 2017 cited by 124

  13. The rate of meiotic gene conversion varies by sex and age

    Authors: 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 - Nature Genetics 2016 cited by 112

  14. Actionable Genotypes and Their Association with Life Span in Iceland

    Authors: Brynjar Ö. Jensson, Gudny A. Arnadottir, Hildigunnur Katrínardóttir, Rún Friðriksdóttir, Hannes Helgason, Ásmundur Oddsson, Garðar Sveinbjörnsson, Hannes P. Eggertsson, Gísli H. Halldórsson, Bjarni A. Atlason, Hákon Jónsson, Gudjon R. Oskarsson, Árni Sturluson, Sigurjón A. Guðjónsson, Guðmundur Á. Þórisson, Florian Zink, Kristjan H. S. Moore, Gunnar Pálsson, Ásgeir Sigurðsson, Aðalbjörg Jónasdóttir, Áslaug Jónasdóttir, Magnus K. Magnusson, Anna Helgadóttir, Valgerður Steinthórsdóttir, Jūlı́us Guðmundsson, Simon Stacey, Rafn Hilmarsson, Ísleifur Ólafsson, Oskar T. Johannsson, Davíð O. Arnar, Jona Saemundsdottir, Ólafur Þ. Magnússon, Gísli Másson, Bjarni V. Halldórsson, Agnar Helgason, Hreinn Stefánsson, Ingileif Jónsdóttir, Hilma Hólm, Þórunn Rafnar, Unnur Þorsteinsdóttir, Daníel F. Guðbjartsson, Kāri Stefánsson, Patrick Sulem - New England Journal of Medicine 2023 cited by 56

  15. Differences between germline genomes of monozygotic twins

    Authors: Hákon Jónsson, Erna Magnúsdóttir, Hannes P. Eggertsson, Ólafur Andri Stefánsson, Gudny A. Arnadottir, Ögmundur Eiríksson, Florian Zink, Einar A. Helgason, Ingileif Jónsdóttir, Arnaldur Gylfason, Aðalbjörg Jónasdóttir, Áslaug Jónasdóttir, Doruk Beyter, Þóra Steingrímsdóttir, Gudmundur L. Norddahl, Ólafur Þ. Magnússon, Gísli Másson, Bjarni V. Halldórsson, Unnur Þorsteinsdóttir, Agnar Helgason, Patrick Sulem, Daníel F. Guðbjartsson, Kāri Stefánsson - Nature Genetics 2021 cited by 183

  16. Multiple transmissions of de novo mutations in families

    Authors: Hákon Jónsson, Patrick Sulem, Gudny A. Arnadottir, Gunnar Pálsson, Hannes P. Eggertsson, Snædís Kristmundsdóttir, Florian Zink, Birte Kehr, Kristján Eldjárn Hjörleifsson, Brynjar Ö. Jensson, Ingileif Jónsdóttir, Sigurdur Einar Marelsson, Sigurjón A. Guðjónsson, Arnaldur Gylfason, Aðalbjörg Jónasdóttir, Áslaug Jónasdóttir, Simon Stacey, Ólafur Þ. Magnússon, Unnur Þorsteinsdóttir, Gísli Másson, Augustine Kong, Bjarni V. Halldórsson, Agnar Helgason, Daníel F. Guðbjartsson, Kāri Stefánsson - Nature Genetics 2018 cited by 128

  17. Mutations in BRIP1 confer high risk of ovarian cancer

    Authors: Þórunn Rafnar, Daníel F. Guðbjartsson, Patrick Sulem, Áslaug Jónasdóttir, Ásgeir Sigurðsson, Aðalbjörg Jónasdóttir, Søren Besenbacher, Pär Lundin, Simon Stacey, Jūlı́us Guðmundsson, Ólafur Þ. Magnússon, Louise le Roux, Gudbjorg Orlygsdottir, Hafdís T. Helgadóttir, Hrefna Johannsdottir, Arnaldur Gylfason, Laufey Tryggvadóttír, Jón G. Jónasson, Ana De Juan, Eugenia Ortega, José Manuel Ramón-Cajal, María Dolores García-Prats, C. Sanchez Mayordomo, Angeles Panadero, Fernando Rivera, Katja K.H. Aben, Anne M. van Altena, Leon F.A.G. Massuger, Mervi Aavikko, Paula Kujala, Synnöve Staff, Lauri A. Aaltonen, Kristrún Ólafsdóttir, Jóhannes Björnsson, Augustine Kong, Anna Salvarsdottir, Hafsteinn Saemundsson, Karl Olafsson, Kristrún R. Benediktsdóttir, Jeffrey R. Gulcher, Gísli Másson, Lambertus A. Kiemeney, José Mayordomo, Unnur Þorsteinsdóttir, Kāri Stefánsson - Nature Genetics 2011 cited by 427

  18. Large recurrent microdeletions associated with schizophrenia

    Authors: GROUP, Hreinn Stefánsson, Dan Rujescu, Sven Cichon, Olli Pietiläinen, Andrés Ingason, Stacy Steinberg, Ragnheiður Fossdal, Engilbert Sigurðsson, Thordur Sigmundsson, Jacobine E. Buizer‐Voskamp, Thomas Folkmann Hansen, Klaus D. Jakobsen, Pierandrea Muglia, Clyde Francks, Paul M. Matthews, Arnaldur Gylfason, Bjarni V. Halldórsson, Daníel F. Guðbjartsson, Thorgeir E. Thorgeirsson, Ásgeir Sigurðsson, Aðalbjörg Jónasdóttir, Áslaug Jónasdóttir, Ásgeir Björnsson, Sigurborg Mattiasdottir, Thórarinn Blöndal, Magnús Haraldsson, Brynja B. Magnúsdóttir, Ina Giegling, Hans‐Jürgen Möller, Annette M. Hartmann, Kevin V. Shianna, Dongliang Ge, Anna C. Need, Caroline Crombie, Gillian Fraser, Nicholas Walker, Jouko Lönnqvist, Jaana Suvisaari, Annamarie Tuulio-Henriksson, Tiina Paunio, Timi Toulopoulou, Elvira Bramon, Marta Di Forti, Robin Murray, Mirella Ruggeri, Evangelos Vassos, Sarah Tosato, Muriel Walshe, Tao Li, Catalina Vasilescu, Thomas W. Mühleisen, August G. Wang, Henrik Ullum, Srdjan Djurovic, Ingrid Melle, Jes Olesen, Lambertus A. Kiemeney, Barbara Franke, Chiara Sabatti, Nelson B. Freimer, Jeffrey R. Gulcher, Unnur Þorsteinsdóttir, Augustine Kong, Ole A. Andreassen, Roel A. Ophoff, Alexander Georgi, Marcella Rietschel, Thomas Werge, Hannes Pétursson, David B. Goldstein, Markus M. Nöthen, Leena Peltonen, David Collier, David St Clair, Kāri Stefánsson - Nature 2008 cited by 1,782

  19. Long read sequencing of 3,622 Icelanders provides insight into the role of structural variants in human diseases and other traits

    Authors: Doruk Beyter, Helga Ingimundardóttir, Ásmundur Oddsson, Hannes P. Eggertsson, Eyþór Björnsson, Hákon Jónsson, Bjarni A. Atlason, Snædís Kristmundsdóttir, Svenja Mehringer, Marteinn T. Hardarson, Sigurjón A. Guðjónsson, Droplaug N. Magnúsdóttir, Áslaug Jónasdóttir, Aðalbjörg Jónasdóttir, Ragnar P. Kristjansson, Sverrir T. Sverrisson, Guillaume Holley, Gunnar Pálsson, Ólafur Andri Stefánsson, Guðmundur I. Eyjólfsson, Ísleifur Ólafsson, Ólöf Sigurðardóttir, Bjarni Torfason, Gísli Másson, Agnar Helgason, Unnur Þorsteinsdóttir, Hilma Hólm, Daníel F. Guðbjartsson, Patrick Sulem, Ólafur Þ. Magnússon, Bjarni V. Halldórsson, Kāri Stefánsson - Nature Genetics 2019 cited by 287

  20. Spread of SARS-CoV-2 in the Icelandic Population

    Authors: Daníel F. Guðbjartsson, Agnar Helgason, Hákon Jónsson, Ólafur Þ. Magnússon, Páll Melsted, Gudmundur L. Norddahl, Jona Saemundsdottir, Ásgeir Sigurðsson, Patrick Sulem, Arna B. Agustsdottir, Berglind Eiríksdottir, Rún Friðriksdóttir, Elisabet E Gardarsdottir, G. Georgsson, Olafia S. Gretarsdottir, Kjartan R. Guðmundsson, Thora R Gunnarsdottir, Arnaldur Gylfason, Hilma Hólm, Brynjar Ö. Jensson, Áslaug Jónasdóttir, Frosti Jónsson, Kamilla S. Josefsdottir, Þórður Kristjánsson, Droplaug N. Magnúsdóttir, Louise le Roux, Guðrún Sigmundsdóttir, Garðar Sveinbjörnsson, Kristin E. Sveinsdottir, Maney Sveinsdottir, Emil Aron Thorarensen, Bjarni Thorbjornsson, Arthur D. Love, Gísli Másson, Ingileif Jónsdóttir, Alma D. Möller, Þórólfur Guðnason, Karl G. Kristinsson, Unnur Þorsteinsdóttir, Kāri Stefánsson - New England Journal of Medicine 2020 cited by 1,413

  21. Humoral Immune Response to SARS-CoV-2 in Iceland

    Authors: Daníel F. Guðbjartsson, Gudmundur L. Norddahl, Páll Melsted, Kristbjörg Gunnarsdóttir, Hilma Hólm, Elías Eyþórsson, Asgeir Ö. Arnthórsson, Daði Helgason, Kristbjörg Bjarnadóttir, Ragnar Freyr Ingvarsson, Brynja Thorsteinsdottir, Steinunn Kristjánsdóttir, Kolbrún Birgisdottir, Anna M. Kristinsdottir, Martin I. Sigurðsson, Gudny A. Arnadottir, Erna V. Ivarsdottir, Margrét B. Andrésdóttir, Frosti Jónsson, Arna B. Agustsdottir, Jonas Berglund, Berglind Eiríksdottir, Rún Friðriksdóttir, Elisabet E Gardarsdottir, Magnús Gottfreðsson, Olafia S. Gretarsdottir, Steinunn Guðmundsdóttir, Kjartan R. Guðmundsson, Thora R Gunnarsdottir, Arnaldur Gylfason, Agnar Helgason, Brynjar Ö. Jensson, Áslaug Jónasdóttir, Hákon Jónsson, Þórður Kristjánsson, Karl G. Kristinsson, Droplaug N. Magnúsdóttir, Ólafur Þ. Magnússon, Lovisa Bjork Olafsdóttir, Sölvi Rögnvaldsson, Louise le Roux, Guðrún Sigmundsdóttir, Ásgeir Sigurðsson, Garðar Sveinbjörnsson, Kristin E. Sveinsdottir, Maney Sveinsdottir, Emil Aron Thorarensen, Bjarni Thorbjornsson, Maríanna Þórðardóttir, Jona Saemundsdottir, Sigurður Kristjánsson, Kamilla S. Josefsdottir, Gísli Másson, G. Georgsson, Már Kristjánsson, Alma D. Möller, Runólfur Pálsson, Þórólfur Guðnason, Unnur Þorsteinsdóttir, Ingileif Jónsdóttir, Patrick Sulem, Kāri Stefánsson - New England Journal of Medicine 2020 cited by 1,040

  22. HLA class II sequence variants influence tuberculosis risk in populations of European ancestry

    Authors: Garðar Sveinbjörnsson, Daníel F. Guðbjartsson, Bjarni V. Halldórsson, Karl G. Kristinsson, Magnús Gottfreðsson, Jeffrey C. Barrett, Lárus J. Gudmundsson, Kai Blöndal, Arnaldur Gylfason, Sigurjón A. Guðjónsson, Hafdís T. Helgadóttir, Aðalbjörg Jónasdóttir, Áslaug Jónasdóttir, Ari Kárason, Ljiljana Bulat Kardum, Jelena Knežević, Helgi Kristjansson, Már Kristjánsson, Arthur Löve, Yang Luo, Ólafur Þ. Magnússon, Patrick Sulem, Augustine Kong, Gísli Másson, Unnur Þorsteinsdóttir, Zlatko Dembić, Sergey Nejentsev, Þorsteinn Blöndal, Ingileif Jónsdóttir, Kāri Stefánsson - Nature Genetics 2016 cited by 156

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

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