Gisli Hreinn Halldorsson (Gisli Halldorsson, Gisli H Halldorsson)

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 66

Top Topics

Multiple Myeloma

Benign Prostatic Hyperplasia

Chronic Rhinosinusitis

Gene Expression

Top Venues

Nature communications

Nature genetics

Communications biology

European heart journal

This page only lists publications with an associated author ORCID identifier.

Publications

Molly Went, Laura Duran-Lozano, Gisli Hreinn Halldorsson, Andrea Gunnell, Nerea Ugidos-Damboriena, Philip J Law, Ludvig Ekdahl, Amit Sud, Gudmar Thorleifsson, Malte Thodberg, Thorunn Asta Olafsdottir, Antton Lamarca-Arrizabalaga, Caterina Cafaro, Abhishek Niroula, Ram Ajore, Aitzkoa Lopez de Lapuente Portilla, Zain Ali, Maroulio Pertesi, Hartmut Goldschmidt, Lilja Stefansdottir, Sigurdur Y Kristinsson, Simon N Stacey, Thorvardur J Love, Saemundur Rognvaldsson, Roman Hájek, Pavel Vodicka, Ulrika Pettersson-Kymmer, Florentin Späth, Carolina D Schinke, Frits Van Rhee, Patrick Sulem, Egil Ferkingstad, Grimur Hjorleifsson Eldjarn, Ulf-Henrik Mellqvist, Ingileif Jónsdóttir, Gareth J Morgan, Pieter Sonneveld, Anders Waage, Niels Weinhold, Hauke Thomsen, Asta Försti, Markus Hansson, Annette Juul Vangsted, Unnur Thorsteinsdottir, Kari Hemminki, Martin F Kaiser, Thorunn Rafnar, Kári Stefánsson, Richard S Houlston, Björn Nilsson
Deciphering the genetics and mechanisms of predisposition to multiple myeloma. Nature communications 15 (1) (2024)
Astros Th Skuladottir, Lilja Stefansdottir, Gisli Hreinn Halldorsson, Olafur Andri Stefansson, Anna Bjornsdottir, Palmi Jonsson, Vala Palmadottir, Thorgeir E Thorgeirsson, G Bragi Walters, Rosa S Gisladottir, Gyda Bjornsdottir, Gudrun A Jonsdottir, Patrick Sulem, Daníel F Guðbjartsson, Kirk U Knowlton, David A Jones, Aigar Ottas, null null, Ole Birger Vesterager Pedersen, Maria Didriksen, Soren Brunak, Karina Banasik, Thomas Folkmann Hansen, Christian Erikstrup, null null, Jan Haavik, Ole A Andreassen, David Rye, Jannicke Igland, Sisse Rye Ostrowski, Lili A Milani, Lincoln D Nadauld, Hreinn Stefánsson, Kári Stefánsson
GWAS meta-analysis reveals key risk loci in essential tremor pathogenesis. Communications biology 7 (1) (2024)
Olafur Andri Stefansson, Brynja Dogg Sigurpalsdottir, Solvi Rognvaldsson, Gisli Hreinn Halldorsson, Kristinn Juliusson, Gardar Sveinbjörnsson, Bjarni Gunnarsson, Doruk Beyter, Hákon Jónsson, Sigurjon Axel Gudjonsson, Thorunn Asta Olafsdottir, Saedis Saevarsdottir, Magnus Karl Magnusson, Sigrun Helga Lund, Vinicius Tragante, Asmundur Oddsson, Marteinn Thor Hardarson, Hannes Petur Eggertsson, Reynir L Gudmundsson, Sverrir Sverrisson, Michael L Frigge, Florian Zink, Hilma Hólm, Hreinn Stefansson, Thorunn Rafnar, Ingileif Jónsdóttir, Patrick Sulem, Agnar Helgason, Daníel F Guðbjartsson, Bjarni V Halldórsson, Unnur Thorsteinsdottir, Kári Stefánsson
The correlation between CpG methylation and gene expression is driven by sequence variants. Nature genetics 56 (8) (2024)
Thorunn Asta Olafsdottir, Gudmar Thorleifsson, Aitzkoa Lopez de Lapuente Portilla, Stefan Jonsson, Lilja Stefansdottir, Abhishek Niroula, Aslaug Jonasdottir, Hannes Petur Eggertsson, Gisli Hreinn Halldorsson, Gudny E Thorlacius, Asgeir O Arnthorsson, Unnur S Bjornsdottir, Folkert W. Asselbergs, Arthur E H Bentlage, Gudmundur I Eyjolfsson, Steinunn Gudmundsdottir, Kristbjorg Gunnarsdottir, Bjarni V Halldórsson, Hilma Hólm, Bjorn R Ludviksson, Pall Melsted, Gudmundur L Norddahl, Isleifur Olafsson, Saedis Saevarsdottir, Olof Sigurdardottir, Asgeir Sigurdsson, Robin Temming, Pall T Önundarson, Unnur Thorsteinsdottir, Gestur Vidarsson, Patrick Sulem, Daníel F Guðbjartsson, Ingileif Jónsdóttir, Björn Nilsson, Kári Stefánsson
Sequence variants influencing the regulation of serum IgG subclass levels. Nature communications 15 (1) (2024)
Saedis Saevarsdottir, Kristbjörg Bjarnadottir, Thorsteinn Markusson, Jonas Berglund, Thorunn Asta Olafsdottir, Gisli Hreinn Halldorsson, Gudrun Rutsdottir, Kristbjorg Gunnarsdottir, Asgeir Orn Arnthorsson, Sigrun Helga Lund, Lilja Stefansdottir, Julius Gudmundsson, Ari J Johannesson, Arni Sturluson, Asmundur Oddsson, Bjarni V Halldórsson, Björn R Ludviksson, Egil Ferkingstad, Erna V Ivarsdottir, Gardar Sveinbjörnsson, Gerdur Grondal, Gisli Masson, Grimur Hjorleifsson Eldjarn, Gudmundur A Thorisson, Katla Kristjánsdóttir, Kirk U Knowlton, Kristjan Helgi Swerford Moore, Sigurjon A Gudjonsson, Solvi Rognvaldsson, Stacey Knight, Lincoln D Nadauld, Hilma Holm, Olafur T Magnusson, Patrick Sulem, Daníel F Guðbjartsson, Thorunn Rafnar, Gudmar Thorleifsson, Pall Melsted, Gudmundur L Norddahl, Ingileif Jónsdóttir, Kári Stefánsson
Start codon variant in LAG3 is associated with decreased LAG-3 expression and increased risk of autoimmune thyroid disease. Nature communications 15 (1) (2024)
Molly Went, Laura Duran-Lozano, Gisli Hreinn Halldorsson, Andrea Gunnell, Nerea Ugidos-Damboriena, Philip J Law, Ludvig Ekdahl, Amit Sud, Gudmar Thorleifsson, Malte Thodberg, Thorunn Asta Olafsdottir, Antton Lamarca-Arrizabalaga, Caterina Cafaro, Abhishek Niroula, Ram Ajore, Aitzkoa Lopez de Lapuente Portilla, Zain Ali, Maroulio Pertesi, Hartmut Goldschmidt, Lilja Stefansdottir, Sigurdur Y Kristinsson, Simon N Stacey, Thorvardur J Love, Saemundur Rognvaldsson, Roman Hájek, Pavel Vodicka, Ulrika Pettersson-Kymmer, Florentin Späth, Carolina D Schinke, Frits Van Rhee, Patrick Sulem, Egil Ferkingstad, Grimur Hjorleifsson Eldjarn, Ulf-Henrik Mellqvist, Ingileif Jónsdóttir, Gareth J Morgan, Pieter Sonneveld, Anders Waage, Niels Weinhold, Hauke Thomsen, Asta Försti, Markus Hansson, Annette Juul Vangsted, Unnur Thorsteinsdottir, Kari Hemminki, Martin F Kaiser, Thorunn Rafnar, Kári Stefánsson, Richard S Houlston, Björn Nilsson
Deciphering the genetics and mechanisms of predisposition to multiple myeloma. Nature communications 15 (1) (2024)
Asmundur Oddsson, Valgerdur Steinthorsdottir, Gudjon R Oskarsson, Unnur Styrkársdóttir, Kristjan Helgi Swerford Moore, Salvor Isberg, Gisli Hreinn Halldorsson, Gardar Sveinbjörnsson, David Westergaard, Henriette Svarre Nielsen, Run Fridriksdottir, Brynjar Orn Jensson, Gudny Anna Arnadottir, Hákon Jónsson, Arni Sturluson, Audunn S Snaebjarnarson, Ole Andreas Andreassen, G Bragi Walters, Mette Nygaard, Christian Erikstrup, Thora Steingrimsdottir, Rolv Terje Lie, Pall Melsted, Ingileif Jónsdóttir, Bjarni V Halldórsson, Gudmar Thorleifsson, Jona Saemundsdottir, Olafur Th Magnusson, null null, Karina Banasik, Erik Sorensen, Gisli Masson, Ole Birger Vesterager Pedersen, Laufey Tryggvadottir, Jan Haavik, Sisse Rye Ostrowski, Hreinn Stefansson, Hilma Hólm, Thorunn Rafnar, Daníel F Guðbjartsson, Patrick Sulem, Kári Stefánsson
Homozygosity for a stop-gain variant in CCDC201 causes primary ovarian insufficiency. Nature genetics (2024)
Saedis Saevarsdottir, Kristbjörg Bjarnadottir, Thorsteinn Markusson, Jonas Berglund, Thorunn Asta Olafsdottir, Gisli Hreinn Halldorsson, Gudrun Rutsdottir, Kristbjorg Gunnarsdottir, Asgeir Orn Arnthorsson, Sigrun Helga Lund, Lilja Stefansdottir, Julius Gudmundsson, Ari J Johannesson, Arni Sturluson, Asmundur Oddsson, Bjarni V Halldórsson, Björn R Ludviksson, Egil Ferkingstad, Erna V Ivarsdottir, Gardar Sveinbjörnsson, Gerdur Grondal, Gisli Masson, Grimur Hjorleifsson Eldjarn, Gudmundur A Thorisson, Katla Kristjánsdóttir, Kirk U Knowlton, Kristjan Helgi Swerford Moore, Sigurjon A Gudjonsson, Solvi Rognvaldsson, Stacey Knight, Lincoln D Nadauld, Hilma Holm, Olafur T Magnusson, Patrick Sulem, Daníel F Guðbjartsson, Thorunn Rafnar, Gudmar Thorleifsson, Pall Melsted, Gudmundur L Norddahl, Ingileif Jónsdóttir, Kári Stefánsson
Start codon variant in LAG3 is associated with decreased LAG-3 expression and increased risk of autoimmune thyroid disease. Nature communications 15 (1) (2024)
Saedis Saevarsdottir, Kristbjörg Bjarnadottir, Thorsteinn Markusson, Jonas Berglund, Thorunn Asta Olafsdottir, Gisli Hreinn Halldorsson, Gudrun Rutsdottir, Kristbjorg Gunnarsdottir, Asgeir Orn Arnthorsson, Sigrun Helga Lund, Lilja Stefansdottir, Julius Gudmundsson, Ari J Johannesson, Arni Sturluson, Asmundur Oddsson, Bjarni V Halldórsson, Björn R Ludviksson, Egil Ferkingstad, Erna V Ivarsdottir, Gardar Sveinbjörnsson, Gerdur Grondal, Gisli Masson, Grimur Hjorleifsson Eldjarn, Gudmundur A Thorisson, Katla Kristjánsdóttir, Kirk U Knowlton, Kristjan Helgi Swerford Moore, Sigurjon A Gudjonsson, Solvi Rognvaldsson, Stacey Knight, Lincoln D Nadauld, Hilma Holm, Olafur T Magnusson, Patrick Sulem, Daníel F Guðbjartsson, Thorunn Rafnar, Gudmar Thorleifsson, Pall Melsted, Gudmundur L Norddahl, Ingileif Jónsdóttir, Kári Stefánsson
Start codon variant in LAG3 is associated with decreased LAG-3 expression and increased risk of autoimmune thyroid disease. Nature communications 15 (1) (2024)
Olafur Andri Stefansson, Brynja Dogg Sigurpalsdottir, Solvi Rognvaldsson, Gisli Hreinn Halldorsson, Kristinn Juliusson, Gardar Sveinbjörnsson, Bjarni Gunnarsson, Doruk Beyter, Hákon Jónsson, Sigurjon Axel Gudjonsson, Thorunn Asta Olafsdottir, Saedis Saevarsdottir, Magnus Karl Magnusson, Sigrun Helga Lund, Vinicius Tragante, Asmundur Oddsson, Marteinn Thor Hardarson, Hannes Petur Eggertsson, Reynir L Gudmundsson, Sverrir Sverrisson, Michael L Frigge, Florian Zink, Hilma Hólm, Hreinn Stefansson, Thorunn Rafnar, Ingileif Jónsdóttir, Patrick Sulem, Agnar Helgason, Daníel F Guðbjartsson, Bjarni V Halldórsson, Unnur Thorsteinsdottir, Kári Stefánsson
The correlation between CpG methylation and gene expression is driven by sequence variants. Nature genetics 56 (8) (2024)
Astros Th Skuladottir, Lilja Stefansdottir, Gisli Hreinn Halldorsson, Olafur Andri Stefansson, Anna Bjornsdottir, Palmi Jonsson, Vala Palmadottir, Thorgeir E Thorgeirsson, G Bragi Walters, Rosa S Gisladottir, Gyda Bjornsdottir, Gudrun A Jonsdottir, Patrick Sulem, Daníel F Guðbjartsson, Kirk U Knowlton, David A Jones, Aigar Ottas, null null, Ole Birger Vesterager Pedersen, Maria Didriksen, Soren Brunak, Karina Banasik, Thomas Folkmann Hansen, Christian Erikstrup, null null, Jan Haavik, Ole A Andreassen, David Rye, Jannicke Igland, Sisse Rye Ostrowski, Lili A Milani, Lincoln D Nadauld, Hreinn Stefánsson, Kári Stefánsson
GWAS meta-analysis reveals key risk loci in essential tremor pathogenesis. Communications biology 7 (1) (2024)
Olafur Andri Stefansson, Brynja Dogg Sigurpalsdottir, Solvi Rognvaldsson, Gisli Hreinn Halldorsson, Kristinn Juliusson, Gardar Sveinbjörnsson, Bjarni Gunnarsson, Doruk Beyter, Hákon Jónsson, Sigurjon Axel Gudjonsson, Thorunn Asta Olafsdottir, Saedis Saevarsdottir, Magnus Karl Magnusson, Sigrun Helga Lund, Vinicius Tragante, Asmundur Oddsson, Marteinn Thor Hardarson, Hannes Petur Eggertsson, Reynir L Gudmundsson, Sverrir Sverrisson, Michael L Frigge, Florian Zink, Hilma Hólm, Hreinn Stefansson, Thorunn Rafnar, Ingileif Jónsdóttir, Patrick Sulem, Agnar Helgason, Daníel F Guðbjartsson, Bjarni V Halldórsson, Unnur Thorsteinsdottir, Kári Stefánsson
The correlation between CpG methylation and gene expression is driven by sequence variants. Nature genetics 56 (8) (2024)
Olafur Andri Stefansson, Brynja Dogg Sigurpalsdottir, Solvi Rognvaldsson, Gisli Hreinn Halldorsson, Kristinn Juliusson, Gardar Sveinbjörnsson, Bjarni Gunnarsson, Doruk Beyter, Hákon Jónsson, Sigurjon Axel Gudjonsson, Thorunn Asta Olafsdottir, Saedis Saevarsdottir, Magnus Karl Magnusson, Sigrun Helga Lund, Vinicius Tragante, Asmundur Oddsson, Marteinn Thor Hardarson, Hannes Petur Eggertsson, Reynir L Gudmundsson, Sverrir Sverrisson, Michael L Frigge, Florian Zink, Hilma Hólm, Hreinn Stefansson, Thorunn Rafnar, Ingileif Jónsdóttir, Patrick Sulem, Agnar Helgason, Daníel F Guðbjartsson, Bjarni V Halldórsson, Unnur Thorsteinsdottir, Kári Stefánsson
The correlation between CpG methylation and gene expression is driven by sequence variants. Nature genetics (2024)
Saedis Saevarsdottir, Kristbjörg Bjarnadottir, Thorsteinn Markusson, Jonas Berglund, Thorunn Asta Olafsdottir, Gisli Hreinn Halldorsson, Gudrun Rutsdottir, Kristbjorg Gunnarsdottir, Asgeir Orn Arnthorsson, Sigrun Helga Lund, Lilja Stefansdottir, Julius Gudmundsson, Ari J Johannesson, Arni Sturluson, Asmundur Oddsson, Bjarni V Halldórsson, Björn R Ludviksson, Egil Ferkingstad, Erna V Ivarsdottir, Gardar Sveinbjörnsson, Gerdur Grondal, Gisli Masson, Grimur Hjorleifsson Eldjarn, Gudmundur A Thorisson, Katla Kristjánsdóttir, Kirk U Knowlton, Kristjan Helgi Swerford Moore, Sigurjon A Gudjonsson, Solvi Rognvaldsson, Stacey Knight, Lincoln D Nadauld, Hilma Holm, Olafur T Magnusson, Patrick Sulem, Daníel F Guðbjartsson, Thorunn Rafnar, Gudmar Thorleifsson, Pall Melsted, Gudmundur L Norddahl, Ingileif Jónsdóttir, Kári Stefánsson
Start codon variant in LAG3 is associated with decreased LAG-3 expression and increased risk of autoimmune thyroid disease. Nature communications 15 (1) (2024)
Grimur Hjorleifsson Eldjarn, Egil Ferkingstad, Sigrun Helga Lund, Hannes Helgason, Olafur Th Magnusson, Kristbjorg Gunnarsdottir, Thorunn Asta Olafsdottir, Bjarni V Halldórsson, Pall I Olason, Florian Zink, Sigurjon A Gudjonsson, Gardar Sveinbjörnsson, Magnus I Magnusson, Agnar Helgason, Asmundur Oddsson, Gisli Hreinn Halldorsson, Magnus Karl Magnusson, Saedis Saevarsdottir, Thjodbjorg Eiriksdottir, Gisli Masson, Hreinn Stefansson, Ingileif Jónsdóttir, Hilma Hólm, Thorunn Rafnar, Pall Melsted, Jona Saemundsdottir, Gudmundur L Norddahl, Gudmar Thorleifsson, Magnus O Ulfarsson, Daníel F Guðbjartsson, Unnur Thorsteinsdottir, Patrick Sulem, Kári Stefánsson
Author Correction: Large-scale plasma proteomics comparisons through genetics and disease associations. Nature (2024)
Molly Went, Laura Duran-Lozano, Gisli Hreinn Halldorsson, Andrea Gunnell, Nerea Ugidos-Damboriena, Philip J Law, Ludvig Ekdahl, Amit Sud, Gudmar Thorleifsson, Malte Thodberg, Thorunn Asta Olafsdottir, Antton Lamarca-Arrizabalaga, Caterina Cafaro, Abhishek Niroula, Ram Ajore, Aitzkoa Lopez de Lapuente Portilla, Zain Ali, Maroulio Pertesi, Hartmut Goldschmidt, Lilja Stefansdottir, Sigurdur Y Kristinsson, Simon N Stacey, Thorvardur J Love, Saemundur Rognvaldsson, Roman Hájek, Pavel Vodicka, Ulrika Pettersson-Kymmer, Florentin Späth, Carolina D Schinke, Frits Van Rhee, Patrick Sulem, Egil Ferkingstad, Grimur Hjorleifsson Eldjarn, Ulf-Henrik Mellqvist, Ingileif Jónsdóttir, Gareth J Morgan, Pieter Sonneveld, Anders Waage, Niels Weinhold, Hauke Thomsen, Asta Försti, Markus Hansson, Annette Juul Vangsted, Unnur Thorsteinsdottir, Kari Hemminki, Martin F Kaiser, Thorunn Rafnar, Kári Stefánsson, Richard S Houlston, Björn Nilsson
Deciphering the genetics and mechanisms of predisposition to multiple myeloma. Nature communications 15 (1) (2024)
Jonas Ghouse, Vinicius Tragante, Gustav Ahlberg, Søren A Rand, Jakob B Jespersen, Eva Birgitte Leinøe, Christoffer Rasmus Vissing, Linea C Trudsø, Ingileif Jónsdóttir, Karina Banasik, Soren Brunak, Sisse Rye Ostrowski, Ole B Pedersen, Erik Sørensen, Christian Erikstrup, Mie Topholm Bruun, Kaspar Rene Nielsen, Lars Køber, Alex H Christensen, Kasper Iversen, David Jones, Kirk U Knowlton, Lincoln Nadauld, Gisli Hreinn Halldorsson, Egil Ferkingstad, Isleifur Olafsson, Solveig Gretarsdottir, Pall T Onundarson, Patrick Sulem, Unnur Thorsteinsdottir, Gudmundur Thorgeirsson, Daniel F Gudbjartsson, Kari Stefansson, Hilma Hólm, Morten Salling Olesen, Henning Bundgaard
Genome-wide meta-analysis identifies 93 risk loci and enables risk prediction equivalent to monogenic forms of venous thromboembolism. Nature genetics 55 (3) (2023)
Asmundur Oddsson, Patrick Sulem, Gardar Sveinbjörnsson, Gudny Anna Arnadottir, Valgerdur Steinthorsdottir, Gisli Hreinn Halldorsson, Bjarni A Atlason, Gudjon R Oskarsson, Hannes Helgason, Henriette Svarre Nielsen, David Westergaard, Juha M Karjalainen, Hildigunnur Katrinardottir, Run Fridriksdottir, Brynjar Orn Jensson, Vinicius Tragante, Egil Ferkingstad, Hákon Jónsson, Sigurjon A Gudjonsson, Doruk Beyter, Kristjan Helgi Swerford Moore, Helga B Thordardottir, Snaedis Kristmundsdottir, Olafur A Stefansson, Solbritt Rantapää Dahlqvist, Ida Elken Sonderby, Maria Didriksen, Pernilla Stridh, Jan Haavik, Laufey Tryggvadottir, Oleksandr Frei, G Bragi Walters, Ingrid Kockum, Henrik Hjalgrim, Thorunn Asta Olafsdottir, Geir Selbaek, Mette Nygaard, Christian Erikstrup, Thorsten Brodersen, Saedis Saevarsdottir, Tomas Olsson, Kaspar Rene Nielsen, Asgeir Haraldsson, Mie Topholm Bruun, Thomas Folkmann Hansen, null null, Thora Steingrimsdottir, Rikke Louise Jacobsen, Rolv Terje Lie, Srdjan Djurovic, Lars Alfredsson, Aitzkoa Lopez de Lapuente Portilla, Soren Brunak, Pall Melsted, Bjarni V Halldórsson, Jona Saemundsdottir, Olafur Th Magnusson, Leonid Padyukov, Karina Banasik, Thorunn Rafnar, Johan Askling, Lars Klareskog, Ole Birger Vesterager Pedersen, Gisli Masson, Karoline Alexandra Havdahl, Björn Nilsson, Ole Andreas Andreassen, Mark Daly, Sisse Rye Ostrowski, Ingileif Jónsdóttir, Hreinn Stefansson, Hilma Hólm, Agnar Helgason, Unnur Thorsteinsdottir, Kári Stefánsson, Daníel F Guðbjartsson
Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality. Nature communications 14 (1) (2023)
Hildur M Aegisdottir, Rosa B Thorolfsdottir, Gardar Sveinbjörnsson, Olafur Andri Stefansson, Bjarni Gunnarsson, Vinicius Tragante, Gudmar Thorleifsson, Lilja Stefansdottir, Thorgeir E Thorgeirsson, Egil Ferkingstad, Patrick Sulem, Gudmundur Norddahl, Gudrun Rutsdottir, Karina Banasik, Alex Hoerby Christensen, Christina Mikkelsen, Ole Birger Vesterager Pedersen, Soren Brunak, Mie Topholm Bruun, Christian Erikstrup, Rikke Louise Jacobsen, Kaspar René Nielsen, Erik Sørensen, Michael L Frigge, Kristján Eldjárn Hjörleifsson, Erna V Ivarsdottir, Anna Helgadottir, Solveig Gretarsdottir, Valgerdur Steinthorsdottir, Asmundur Oddsson, Hannes Petur Eggertsson, Gisli Hreinn Halldorsson, David A Jones, Jeffrey L Anderson, Kirk U Knowlton, Lincoln D Nadauld, null null, Magnus Haraldsson, Gudmundur Thorgeirsson, Henning Bundgaard, David O Arnar, Unnur Thorsteinsdottir, Daníel F Guðbjartsson, Sisse Rye Ostrowski, Hilma Hólm, Kári Stefánsson
Genetic variants associated with syncope implicate neural and autonomic processes. European heart journal (2023)
Rosa S Gisladottir, Agnar Helgason, Bjarni V Halldórsson, Hannes Helgason, Michal Borsky, Yu-Ren Chien, Jon Gudnason, Sigurjon A Gudjonsson, Scott R Moisik, Dan Dediu, Gudmar Thorleifsson, Vinicius Tragante, Mariana Bustamante, Gudrun A Jonsdottir, Lilja Stefansdottir, Gudrun Rutsdottir, Sigurdur H Magnusson, Marteinn Thor Hardarson, Egil Ferkingstad, Gisli Hreinn Halldorsson, Solvi Rognvaldsson, Astros Th Skuladottir, Erna V Ivarsdottir, Gudmundur Norddahl, Gudmundur Thorgeirsson, Ingileif Jónsdóttir, Magnus O Ulfarsson, Hilma Hólm, Hreinn Stefánsson, Unnur Thorsteinsdottir, Daníel F Guðbjartsson, Patrick Sulem, Kári Stefánsson
Sequence variants affecting voice pitch in humans. Science advances 9 (23) (2023)
Jonas Ghouse, Vinicius Tragante, Gustav Ahlberg, Søren A Rand, Jakob B Jespersen, Eva Birgitte Leinøe, Christoffer Rasmus Vissing, Linea C Trudsø, Ingileif Jónsdóttir, Karina Banasik, Soren Brunak, Sisse Rye Ostrowski, Ole B Pedersen, Erik Sørensen, Christian Erikstrup, Mie Topholm Bruun, Kaspar Rene Nielsen, Lars Køber, Alex H Christensen, Kasper Iversen, David Jones, Kirk U Knowlton, Lincoln Nadauld, Gisli Hreinn Halldorsson, Egil Ferkingstad, Isleifur Olafsson, Solveig Gretarsdottir, Pall T Onundarson, Patrick Sulem, Unnur Thorsteinsdottir, Gudmundur Thorgeirsson, Daniel F Gudbjartsson, Kari Stefansson, Hilma Hólm, Morten Salling Olesen, Henning Bundgaard
Genome-wide meta-analysis identifies 93 risk loci and enables risk prediction equivalent to monogenic forms of venous thromboembolism. Nature genetics (2023)
Snaedis Kristmundsdottir, Hákon Jónsson, Marteinn Thor Hardarson, Gunnar Pálsson, Doruk Beyter, Hannes Petur Eggertsson, Arnaldur Gylfason, Gardar Sveinbjörnsson, Guillaume Holley, Olafur A Stefansson, Gisli Hreinn Halldorsson, Sigurgeir Olafsson, Gudny Anna Arnadottir, Pall I Olason, Ogmundur Eiriksson, Gisli Masson, Unnur Thorsteinsdottir, Thorunn Rafnar, Patrick Sulem, Agnar Helgason, Daníel F Guðbjartsson, Bjarni V Halldórsson, Kári Stefánsson
Sequence variants affecting the genome-wide rate of germline microsatellite mutations. Nature communications 14 (1) (2023)
Gyda Bjornsdottir, Mona Ameri Chalmer, Lilja Stefansdottir, Astros Th Skuladottir, Gudmundur Einarsson, Margret Andresdottir, Doruk Beyter, Egil Ferkingstad, Solveig Gretarsdottir, Bjarni V Halldórsson, Gisli Hreinn Halldorsson, Anna Helgadottir, Hannes Helgason, Grimur Hjorleifsson Eldjarn, Adalbjorg Jonasdottir, Aslaug Jonasdottir, Ingileif Jónsdóttir, Kirk U Knowlton, Lincoln D Nadauld, Sigrun Helga Lund, Olafur Th Magnusson, Pall Melsted, Kristjan Helgi Swerford Moore, Asmundur Oddsson, Pall I Olason, Asgeir Sigurdsson, Olafur Andri Stefansson, Jona Saemundsdottir, Gardar Sveinbjörnsson, Vinicius Tragante, Unnur Unnsteinsdottir, G Bragi Walters, Florian Zink, Linn Rødevand, Ole Andreas Andreassen, Jannicke Igland, Rolv Terje Lie, Jan Haavik, Karina Banasik, Soren Brunak, Maria Didriksen, Mie Topholm Bruun, Christian Erikstrup, Lisette J A Kogelman, Kaspar R Nielsen, Erik Sørensen, Ole Birger Vesterager Pedersen, Henrik Ullum, null null, Gisli Masson, Unnur Thorsteinsdottir, Jes Olesen, Petur Ludvigsson, Olafur Thorarensen, Anna Bjornsdottir, Gudrun R Sigurdardottir, Olafur A Sveinsson, Sisse Rye Ostrowski, Hilma Hólm, Daníel F Guðbjartsson, Gudmar Thorleifsson, Patrick Sulem, Hreinn Stefansson, Thorgeir E Thorgeirsson, Thomas Folkmann Hansen, Kári Stefánsson
Rare variants with large effects provide functional insights into the pathology of migraine subtypes, with and without aura. Nature genetics (2023)
Jonas Ghouse, Vinicius Tragante, Gustav Ahlberg, Søren A Rand, Jakob B Jespersen, Eva Birgitte Leinøe, Christoffer Rasmus Vissing, Linea C Trudsø, Ingileif Jónsdóttir, Karina Banasik, Soren Brunak, Sisse Rye Ostrowski, Ole B Pedersen, Erik Sørensen, Christian Erikstrup, Mie Topholm Bruun, Kaspar Rene Nielsen, Lars Køber, Alex H Christensen, Kasper Iversen, David Jones, Kirk U Knowlton, Lincoln Nadauld, Gisli Hreinn Halldorsson, Egil Ferkingstad, Isleifur Olafsson, Solveig Gretarsdottir, Pall T Onundarson, Patrick Sulem, Unnur Thorsteinsdottir, Gudmundur Thorgeirsson, Daniel F Gudbjartsson, Kari Stefansson, Hilma Hólm, Morten Salling Olesen, Henning Bundgaard
Genome-wide meta-analysis identifies 93 risk loci and enables risk prediction equivalent to monogenic forms of venous thromboembolism. Nature genetics (2023)
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Genetics and epidemiology of mutational barcode-defined clonal hematopoiesis. Nature genetics (2023)
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Sequence variants affecting the genome-wide rate of germline microsatellite mutations. Nature communications 14 (1) (2023)
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Sequence variants affecting the genome-wide rate of germline microsatellite mutations. Nature communications 14 (1) (2023)
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Sequence variant affects GCSAML splicing, mast cell specific proteins, and risk of urticaria. Communications biology 6 (1) (2023)
Jonas Ghouse, Vinicius Tragante, Gustav Ahlberg, Søren A Rand, Jakob B Jespersen, Eva Birgitte Leinøe, Christoffer Rasmus Vissing, Linea C Trudsø, Ingileif Jónsdóttir, Karina Banasik, Soren Brunak, Sisse Rye Ostrowski, Ole B Pedersen, Erik Sørensen, Christian Erikstrup, Mie Topholm Bruun, Kaspar Rene Nielsen, Lars Køber, Alex H Christensen, Kasper Iversen, David Jones, Kirk U Knowlton, Lincoln Nadauld, Gisli Hreinn Halldorsson, Egil Ferkingstad, Isleifur Olafsson, Solveig Gretarsdottir, Pall T Onundarson, Patrick Sulem, Unnur Thorsteinsdottir, Gudmundur Thorgeirsson, Daniel F Gudbjartsson, Kari Stefansson, Hilma Hólm, Morten Salling Olesen, Henning Bundgaard
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Rosa B Thorolfsdottir, Gardar Sveinbjörnsson, Hildur M Aegisdottir, Stefania Benonisdottir, Lilja Stefansdottir, Erna V Ivarsdottir, Gisli Hreinn Halldorsson, Jon K Sigurdsson, Christian Torp-Pedersen, Peter E Weeke, Søren Brunak, David Westergaard, Ole Birger Vesterager Pedersen, Erik Sorensen, Kaspar René Nielsen, Kristoffer Sølvsten Burgdorf, Karina Banasik, Ben Michael Brumpton, Wei Zhou, Asmundur Oddsson, Vinicius Tragante, Kristján Eldjárn Hjörleifsson, Olafur B Davidsson, Sridharan Rajamani, Stefan Jonsson, Bjarni Torfason, Atli S Valgardsson, Gudmundur Thorgeirsson, Michael L Frigge, Gudmar Thorleifsson, Gudmundur L Norddahl, Anna Helgadottir, Solveig Gretarsdottir, Patrick Sulem, Ingileif Jónsdóttir, Cristen J Willer, Kristian Hveem, Henning Bundgaard, Henrik Ullum, David O Arnar, Unnur Thorsteinsdottir, Daníel F Guðbjartsson, Hilma Hólm, Kári Stefánsson, null null
Genetic insight into sick sinus syndrome. European heart journal 42 (20) (2022)
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The sequences of 150,119 genomes in the UK Biobank. Nature 607 (7920) (2022)
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Functional dissection of inherited non-coding variation influencing multiple myeloma risk. Nature communications 13 (1) (2022)
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Rare SLC13A1 variants associate with intervertebral disc disorder highlighting role of sulfate in disc pathology. Nature communications 13 (1) (2022)
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Author Correction: Functional dissection of inherited non-coding variation influencing multiple myeloma risk. Nature communications 13 (1) (2022)
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HLA alleles, disease severity, and age associate with T-cell responses following infection with SARS-CoV-2. Communications biology 5 (1) (2022)
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Author Correction: Rare SLC13A1 variants associate with intervertebral disc disorder highlighting role of sulfate in disc pathology. Nature communications 13 (1) (2022)
Gudjon R Oskarsson, Magnus Karl Magnusson, Asmundur Oddsson, Brynjar Orn Jensson, Run Fridriksdottir, Gudny Anna Arnadottir, Hildigunnur Katrinardottir, Solvi Rognvaldsson, Gisli Hreinn Halldorsson, Gardar Sveinbjornsson, Erna V Ivarsdottir, Lilja Stefansdottir, Egil Ferkingstad, Kristjan Norland, Vinicius Tragante, Jona Saemundsdottir, Aslaug Jonasdottir, Adalbjorg Jonasdottir, Svanhvit Sigurjonsdottir, Karen O Petursdottir, Olafur B Davidsson, Thorunn Rafnar, Hilma Hólm, Isleifur Olafsson, Pall T Onundarson, Brynjar Vidarsson, Olof Sigurdardottir, Gisli Masson, Daníel F Guðbjartsson, Ingileif Jónsdóttir, Gudmundur L Norddahl, Unnur Thorsteinsdottir, Patrick Sulem, Kári Stefánsson
Genetic architecture of band neutrophil fraction in Iceland. Communications biology 5 (1) (2022)
Ram Ajore, Abhishek Niroula, Maroulio Pertesi, Caterina Cafaro, Malte Thodberg, Molly Went, Erik L Bao, Laura Duran-Lozano, Aitzkoa Lopez de Lapuente Portilla, Thorunn Asta Olafsdottir, Nerea Ugidos-Damboriena, Olafur Magnusson, Mehmet Kemal Samur, Caleb A Lareau, Gisli Hreinn Halldorsson, Gudmar Thorleifsson, Gudmundur L Norddahl, Kristbjorg Gunnarsdottir, Asta Försti, Hartmut Goldschmidt, Kari Hemminki, Frits van Rhee, Scott Kimber, Adam S Sperling, Martin F Kaiser, Kenneth C Anderson, Ingileif Jónsdóttir, Nikhil C Munshi, Thorunn Rafnar, Anders Waage, Niels Weinhold, Unnur Thorsteinsdottir, Vijay G Sankaran, Kári Stefánsson, Richard S Houlston, Björn Nilsson
Author Correction: Functional dissection of inherited non-coding variation influencing multiple myeloma risk. Nature communications 13 (1) (2022)
Gudmundur L Norddahl, Pall Melsted, Kristbjorg Gunnarsdottir, Gisli Hreinn Halldorsson, Thorunn Asta Olafsdottir, Arnaldur Gylfason, Mar Kristjansson, Olafur T Magnusson, Patrick Sulem, Daníel F Guðbjartsson, Unnur Thorsteinsdottir, Ingileif Jónsdóttir, Kári Stefánsson
Effect of booster vaccination against Delta and Omicron SARS-CoV-2 variants in Iceland. Nature communications 13 (1) (2022)
Steven Bell, Andreas S Rigas, Magnus Karl Magnusson, Egil Ferkingstad, Elias Allara, Gyda Bjornsdottir, Anna Ramond, Erik Sørensen, Gisli Hreinn Halldorsson, Dirk S Paul, Kristoffer S Burgdorf, Hannes Petur Eggertsson, Joanna M M Howson, Lise W Thørner, Snaedis Kristmundsdottir, William J Astle, Christian Erikstrup, Jon K Sigurdsson, Dragana Vuckovic, Khoa M Dinh, Vinicius Tragante, Praveen Surendran, Ole Birger Vesterager Pedersen, Brynjar Vidarsson, Tao Jiang, Helene Martina Paarup, Pall T Onundarson, Parsa Akbari, Kaspar R Nielsen, Sigrun Helga Lund, Kristinn Juliusson, Magnus I Magnusson, Michael L Frigge, Asmundur Oddsson, Isleifur Olafsson, Stephen Kaptoge, Henrik Hjalgrim, Gudmundur Runarsson, Angela M Wood, Ingileif Jónsdóttir, Thomas Folkmann Hansen, Olof Sigurdardottir, Hreinn Stefánsson, David Rye, null null, James E Peters, David Westergaard, Hilma Hólm, Nicole Soranzo, Karina Banasik, Gudmar Thorleifsson, Willem Hendrik Ouwehand, Unnur Thorsteinsdottir, David J Roberts, Patrick Sulem, Adam S Butterworth, Daníel F Guðbjartsson, John Danesh, Soren Brunak, Emanuele Di Angelantonio, Henrik Ullum, Kári Stefánsson
A genome-wide meta-analysis yields 46 new loci associating with biomarkers of iron homeostasis. Communications biology 4 (1) (2021)
Egil Ferkingstad, Patrick Sulem, Bjarni A Atlason, Gardar Sveinbjornsson, Magnus I Magnusson, Edda L Styrmisdottir, Kristbjorg Gunnarsdottir, Agnar Helgason, Asmundur Oddsson, Bjarni V Halldórsson, Brynjar O Jensson, Florian Zink, Gisli Hreinn Halldorsson, Gisli Masson, Gudny Anna Arnadottir, Hildigunnur Katrinardottir, Kristinn Juliusson, Magnus Karl Magnusson, Olafur Th Magnusson, Run Fridriksdottir, Saedis Saevarsdottir, Sigurjon A Gudjonsson, Simon N Stacey, Solvi Rognvaldsson, Thjodbjorg Eiriksdottir, Thorunn A Olafsdottir, Valgerdur Steinthorsdottir, Vinicius Tragante, Magnus O Ulfarsson, Hreinn Stefánsson, Ingileif Jónsdóttir, Hilma Hólm, Thorunn Rafnar, Pall Melsted, Jona Saemundsdottir, Gudmundur L Norddahl, Sigrun Helga Lund, Daníel F Guðbjartsson, Unnur Thorsteinsdottir, Kári Stefánsson
Large-scale integration of the plasma proteome with genetics and disease. Nature genetics 53 (12) (2021)
Rosa B Thorolfsdottir, Gardar Sveinbjörnsson, Hildur M Aegisdottir, Stefania Benonisdottir, Lilja Stefansdottir, Erna V Ivarsdottir, Gisli Hreinn Halldorsson, Jon K Sigurdsson, Christian Torp-Pedersen, Peter E Weeke, Søren Brunak, David Westergaard, Ole Birger Vesterager Pedersen, Erik Sorensen, Kaspar René Nielsen, Kristoffer Sølvsten Burgdorf, Karina Banasik, Ben Michael Brumpton, Wei Zhou, Asmundur Oddsson, Vinicius Tragante, Kristján Eldjárn Hjörleifsson, Olafur B Davidsson, Sridharan Rajamani, Stefan Jonsson, Bjarni Torfason, Atli S Valgardsson, Gudmundur Thorgeirsson, Michael L Frigge, Gudmar Thorleifsson, Gudmundur L Norddahl, Anna Helgadottir, Solveig Gretarsdottir, Patrick Sulem, Ingileif Jónsdóttir, Cristen J Willer, Kristian Hveem, Henning Bundgaard, Henrik Ullum, David O Arnar, Unnur Thorsteinsdottir, Daníel F Guðbjartsson, Hilma Hólm, Kári Stefánsson, null null
Genetic insight into sick sinus syndrome. European heart journal 42 (20) (2021)
Laura Duran-Lozano, Gudmar Thorleifsson, Aitzkoa Lopez de Lapuente Portilla, Abhishek Niroula, Molly Went, Malte Thodberg, Maroulio Pertesi, Ram Ajore, Caterina Cafaro, Pall I Olason, Lilja Stefansdottir, G Bragi Walters, Gisli Hreinn Halldorsson, Ingemar Turesson, Martin F Kaiser, Niels Weinhold, Niels Abildgaard, Niels Frost Andersen, Ulf-Henrik Mellqvist, Anders Waage, Annette Juul Vangsted, Unnur Thorsteinsdottir, Markus Hansson, Richard S Houlston, Thorunn Rafnar, Kari Stefansson, Björn Nilsson
Author Correction: Germline variants at SOHLH2 influence multiple myeloma risk. Blood cancer journal 11 (11) (2021)
Erna V Ivarsdottir, Hilma Hólm, Stefania Benonisdottir, Thorhildur Olafsdottir, Gardar Sveinbjornsson, Gudmar Thorleifsson, Hannes Petur Eggertsson, Gisli Hreinn Halldorsson, Kristján Eldjárn Hjörleifsson, Pall Melsted, Arnaldur Gylfason, Gudny Anna Arnadottir, Asmundur Oddsson, Brynjar O Jensson, Aslaug Jonasdottir, Adalbjorg Jonasdottir, Thorhildur Juliusdottir, Lilja Stefansdottir, Vinicius Tragante, Bjarni V Halldórsson, Hannes Petersen, Gudmundur Thorgeirsson, Unnur Thorsteinsdottir, Patrick Sulem, Ingibjorg Hinriksdottir, Ingileif Jónsdóttir, Daníel F Guðbjartsson, Kari Stefansson
The genetic architecture of age-related hearing impairment revealed by genome-wide association analysis. Communications biology 4 (1) (2021)
Evgenia Mikaelsdottir, Gudmar Thorleifsson, Lilja Stefansdottir, Gisli Hreinn Halldorsson, Jon K Sigurdsson, Sigrun Helga Lund, Vinicius Tragante, Pall Melsted, Solvi Rognvaldsson, Kristjan Norland, Anna Helgadottir, Magnus Karl Magnusson, Gunnar B Ragnarsson, Sigurdur Y Kristinsson, Sigrun Reykdal, Brynjar Vidarsson, Ingibjorg Jona Gudmundsdottir, Isleifur Olafsson, Pall T Onundarson, Olof Sigurdardottir, Emil L Sigurdsson, Gerdur Grondal, Arni J Geirsson, Gudmundur Geirsson, Julius Gudmundsson, Hilma Hólm, Saedis Saevarsdottir, Ingileif Jónsdóttir, Gudmundur Thorgeirsson, Daníel F Guðbjartsson, Unnur Thorsteinsdottir, Thorunn Rafnar, Kári Stefánsson
Genetic variants associated with platelet count are predictive of human disease and physiological markers. Communications biology 4 (1) (2021)
Laura Duran-Lozano, Gudmar Thorleifsson, Aitzkoa Lopez de Lapuente Portilla, Abhishek Niroula, Molly Went, Malte Thodberg, Maroulio Pertesi, Ram Ajore, Caterina Cafaro, Pall I Olason, Lilja Stefansdottir, G Bragi Walters, Gisli Hreinn Halldorsson, Ingemar Turesson, Martin F Kaiser, Niels Weinhold, Niels Abildgaard, Niels Frost Andersen, Ulf-Henrik Mellqvist, Anders Waage, Annette Juul Vangsted, Unnur Thorsteinsdottir, Markus Hansson, Richard S Houlston, Thorunn Rafnar, Kari Stefansson, Björn Nilsson
Germline variants at SOHLH2 influence multiple myeloma risk. Blood cancer journal 11 (4) (2021)
Gudjon R Oskarsson, Asmundur Oddsson, Magnus K Magnusson, Ragnar P Kristjansson, Gisli Hreinn Halldorsson, Egil Ferkingstad, Florian Zink, Anna Helgadottir, Erna V Ivarsdottir, Gudny Anna Arnadottir, Brynjar O Jensson, Hildigunnur Katrinardottir, Gardar Sveinbjornsson, Anna M Kristinsdottir, Amy L Lee, Jona Saemundsdottir, Lilja Stefansdottir, Jon K Sigurdsson, Olafur B Davidsson, Stefania Benonisdottir, Aslaug Jonasdottir, Adalbjorg Jonasdottir, Stefan Jonsson, Reynir L Gudmundsson, Folkert W. Asselbergs, Vinicius Tragante, Bjarni Gunnarsson, Gisli Masson, Gudmar Thorleifsson, Thorunn Rafnar, Hilma Holm, Isleifur Olafsson, Pall T Onundarson, Daníel F Guðbjartsson, Gudmundur L Norddahl, Unnur Thorsteinsdottir, Patrick Sulem, Kári Stefánsson
Predicted loss and gain of function mutations in ACO1 are associated with erythropoiesis. Communications biology 3 (1) (2020)
Thorhildur Olafsdottir, Gudmar Thorleifsson, Patrick Sulem, Olafur A Stefansson, Helga Medek, Karl Olafsson, Orri Ingthorsson, Valur Gudmundsson, Ingileif Jónsdóttir, Gisli Hreinn Halldorsson, Ragnar P Kristjansson, Michael L Frigge, Lilja Stefansdottir, Jon K Sigurdsson, Asmundur Oddsson, Asgeir Sigurdsson, Hannes P Eggertsson, Pall Melsted, Bjarni V Halldórsson, Sigrun Helga Lund, Unnur Styrkarsdottir, Valgerdur Steinthorsdottir, Julius Gudmundsson, Hilma Holm, Vinicius Tragante, Folkert W. Asselbergs, Unnur Thorsteinsdottir, Daníel F Guðbjartsson, Kristin Jonsdottir, Thorunn Rafnar, Kári Stefánsson
Genome-wide association identifies seven loci for pelvic organ prolapse in Iceland and the UK Biobank. Communications biology 3 (1) (2020)
Thorunn A Olafsdottir, Fannar Theodors, Kristbjorg Bjarnadottir, Unnur Steina Bjornsdottir, Arna B Agustsdottir, Olafur A Stefansson, Erna V Ivarsdottir, Jon K Sigurdsson, Stefania Benonisdottir, Gudmundur I Eyjolfsson, David Gislason, Thorarinn Gislason, Steinunn Guðmundsdóttir, Arnaldur Gylfason, Bjarni V Halldórsson, Gisli Hreinn Halldorsson, Thorhildur Juliusdottir, Anna M Kristinsdottir, Dora Ludviksdottir, Bjorn R Ludviksson, Gisli Masson, Kristjan Norland, Pall T Onundarson, Isleifur Olafsson, Olof Sigurdardottir, Lilja Stefansdottir, Gardar Sveinbjornsson, Vinicius Tragante, Daníel F Guðbjartsson, Gudmar Thorleifsson, Patrick Sulem, Unnur Thorsteinsdottir, Gudmundur L Norddahl, Ingileif Jónsdóttir, Kári Stefánsson
Eighty-eight variants highlight the role of T cell regulation and airway remodeling in asthma pathogenesis. Nature communications 11 (1) (2020)
Bjarni V Halldórsson, Gunnar Pálsson, Olafur A Stefansson, Hákon Jónsson, Marteinn Thor Hardarson, Hannes Petur Eggertsson, Bjarni Gunnarsson, Asmundur Oddsson, Gisli Hreinn Halldorsson, Florian Zink, Sigurjon A Gudjonsson, Michael L Frigge, Gudmar Thorleifsson, Asgeir Sigurdsson, Simon N Stacey, Patrick Sulem, Gisli Masson, Agnar Helgason, Daníel F Guðbjartsson, Unnur Thorsteinsdottir, Kári Stefánsson
Characterizing mutagenic effects of recombination through a sequence-level genetic map. Science (New York, N.Y.) 363 (6425) (2019)
Unnur Styrkársdóttir, Olafur A Stefansson, Kristbjorg Gunnarsdottir, Gudmar Thorleifsson, Sigrun H Lund, Lilja Stefansdottir, Kristinn Juliusson, Arna B Agustsdottir, Florian Zink, Gisli Hreinn Halldorsson, Erna V Ivarsdottir, Stefania Benonisdottir, Hákon Jónsson, Arnaldur Gylfason, Kristjan Norland, Katerina Trajanoska, Cindy Germaine Boer, Lorraine Southam, Jason C S Leung, Nelson Leung-Sang Tang, Timothy C Y Kwok, Jenny S W Lee, Suzanne C Ho, Inger Byrjalsen, Jacqueline R Center, Seung Hun Lee, Jung-Min Koh, L Stefan Lohmander, Lan T Ho-Pham, Tuan V Nguyen, John A Eisman, Jean Woo, Ping-C Leung, John Loughlin, Eleftheria Zeggini, Claus Christiansen, Fernando Rivadeneira, Joyce van Meurs, Andre G Uitterlinden, Brynjolfur Mogensen, Helgi Jonsson, Thorvaldur Ingvarsson, Gunnar Sigurdsson, Rafn Benediktsson, Patrick Sulem, Ingileif Jonsdottir, Gisli Masson, Hilma Holm, Gudmundur L Norddahl, Unnur Thorsteinsdottir, Daníel F Guðbjartsson, Kári Stefánsson
Publisher Correction: GWAS of bone size yields twelve loci that also affect height, BMD, osteoarthritis or fractures. Nature communications 10 (1) (2019)
Gyda Bjornsdottir, Erna V Ivarsdottir, Kristbjorg Bjarnadottir, Stefania Benonisdottir, Sandra Sif Gylfadottir, Gudny Anna Arnadottir, Rafn Benediktsson, Gisli Hreinn Halldorsson, Anna Helgadottir, Adalbjorg Jonasdottir, Aslaug Jonasdottir, Ingileif Jonsdottir, Anna Margret Kristinsdottir, Olafur Th Magnusson, Gisli Masson, Pall Melsted, Thorunn Rafnar, Asgeir Sigurdsson, Gunnar Sigurdsson, Astros Skuladottir, Valgerdur Steinthorsdottir, Unnur Styrkársdóttir, Gudmundur Thorgeirsson, Gudmar Thorleifsson, Arnor Vikingsson, Daníel F Guðbjartsson, Hilma Holm, Hreinn Stefánsson, Unnur Thorsteinsdottir, Gudmundur L Norddahl, Patrick Sulem, Thorgeir E Thorgeirsson, Kari Stefansson
A PRPH splice-donor variant associates with reduced sural nerve amplitude and risk of peripheral neuropathy. Nature communications 10 (1) (2019)
Ragnar P Kristjansson, Stefania Benonisdottir, Olafur B Davidsson, Asmundur Oddsson, Vinicius Tragante, Jon K Sigurdsson, Lilja Stefansdottir, Stefan Jonsson, Brynjar O Jensson, Joseph G Arthur, Gudny Anna Arnadottir, Gerald Sulem, Bjarni V Halldórsson, Bjarni Gunnarsson, Gisli Hreinn Halldorsson, Olafur A Stefansson, Gudjon R Oskarsson, Aimee M Deaton, Isleifur Olafsson, Gudmundur I Eyjolfsson, Olof Sigurdardottir, Pall T Onundarson, David Gislason, Thorarinn Gislason, Bjorn R Ludviksson, Dora Ludviksdottir, Thorunn A Olafsdottir, Thorunn Rafnar, Gisli Masson, Florian Zink, Gyda Bjornsdottir, Olafur Th Magnusson, Unnur S Bjornsdottir, Gudmar Thorleifsson, Gudmundur L Norddahl, Daníel F Guðbjartsson, Unnur Thorsteinsdottir, Ingileif Jónsdóttir, Patrick Sulem, Kári Stefánsson
A loss-of-function variant in ALOX15 protects against nasal polyps and chronic rhinosinusitis. Nature genetics 51 (2) (2019)
Unnur Styrkársdóttir, Olafur A Stefansson, Kristbjorg Gunnarsdottir, Gudmar Thorleifsson, Sigrun H Lund, Lilja Stefansdottir, Kristinn Juliusson, Arna B Agustsdottir, Florian Zink, Gisli Hreinn Halldorsson, Erna V Ivarsdottir, Stefania Benonisdottir, Hákon Jónsson, Arnaldur Gylfason, Kristjan Norland, Katerina Trajanoska, Cindy Germaine Boer, Lorraine Southam, Jason C S Leung, Nelson Leung-Sang Tang, Timothy C Y Kwok, Jenny S W Lee, Suzanne C Ho, Inger Byrjalsen, Jacqueline R Center, Seung Hun Lee, Jung-Min Koh, L Stefan Lohmander, Lan T Ho-Pham, Tuan V Nguyen, John A Eisman, Jean Woo, Ping-C Leung, John Loughlin, Eleftheria Zeggini, Claus Christiansen, Fernando Rivadeneira, Joyce van Meurs, Andre G Uitterlinden, Brynjolfur Mogensen, Helgi Jonsson, Thorvaldur Ingvarsson, Gunnar Sigurdsson, Rafn Benediktsson, Patrick Sulem, Ingileif Jonsdottir, Gisli Masson, Hilma Holm, Gudmundur L Norddahl, Unnur Thorsteinsdottir, Daníel F Guðbjartsson, Kári Stefánsson
GWAS of bone size yields twelve loci that also affect height, BMD, osteoarthritis or fractures. Nature communications 10 (1) (2019)
Thorunn Rafnar, Bjarni Gunnarsson, Olafur A Stefansson, Patrick Sulem, Andres Ingason, Michael L Frigge, Lilja Stefansdottir, Jon K Sigurdsson, Vinicius Tragante, Valgerdur Steinthorsdottir, Unnur Styrkársdóttir, Simon N Stacey, Julius Gudmundsson, Gudny Anna Arnadottir, Asmundur Oddsson, Florian Zink, Gisli Hreinn Halldorsson, Gardar Sveinbjornsson, Ragnar P Kristjansson, Olafur B Davidsson, Anna Salvarsdottir, Asgeir Thoroddsen, Elisabet A Helgadottir, Katrin Kristjansdottir, Orri Ingthorsson, Valur Gudmundsson, Reynir T Geirsson, Ragnheidur Arnadottir, Daníel F Guðbjartsson, Gisli Masson, Folkert W Asselbergs, Jon G Jonasson, Karl Olafsson, Unnur Thorsteinsdottir, Bjarni V Halldórsson, Gudmar Thorleifsson, Kari Stefansson
Variants associating with uterine leiomyoma highlight genetic background shared by various cancers and hormone-related traits. Nature communications 9 (1) (2018)
Gudjon R Oskarsson, Ragnar P Kristjansson, Amy L Lee, Gardar Sveinbjornsson, Magnus K Magnusson, Erna V Ivarsdottir, Stefania Benonisdottir, Asmundur Oddsson, Olafur B Davidsson, Jona Saemundsdottir, Gisli Hreinn Halldorsson, Joseph Arthur, Gudny Anna Arnadottir, Gisli Masson, Brynjar O Jensson, Hilma Holm, Isleifur Olafsson, Pall T Onundarson, Daníel F Guðbjartsson, Gudmundur L Norddahl, Unnur Thorsteinsdottir, Patrick Sulem, Kari Stefansson
A truncating mutation in EPOR leads to hypo-responsiveness to erythropoietin with normal haemoglobin. Communications biology 1 (2018)
Florian Zink, Droplaug N Magnusdottir, Olafur T Magnusson, Nicolas J Walker, Tiffany J Morris, Asgeir Sigurdsson, Gisli Hreinn Halldorsson, Sigurjon A Gudjonsson, Pall Melsted, Helga Ingimundardottir, Snædis Kristmundsdottir, Kristjan F Alexandersson, Anna Helgadottir, Julius Gudmundsson, Thorunn Rafnar, Ingileif Jónsdóttir, Hilma Holm, Gudmundur Ingi Eyjolfsson, Olof Sigurdardottir, Isleifur Olafsson, Gisli Masson, Daníel F Guðbjartsson, Unnur Thorsteinsdottir, Bjarni V Halldórsson, Simon N Stacey, Kari Stefansson
Insights into imprinting from parent-of-origin phased methylomes and transcriptomes. Nature genetics 50 (11) (2018)
Julius Gudmundsson, Jon K Sigurdsson, Lilja Stefansdottir, Bjarni A Agnarsson, Helgi J Isaksson, Olafur A Stefansson, Sigurjon A Gudjonsson, Daníel F Guðbjartsson, Gisli Masson, Michael L Frigge, Simon N Stacey, Patrick Sulem, Gisli Hreinn Halldorsson, Vinicius Tragante, Hilma Holm, Gudmundur I Eyjolfsson, Olof Sigurdardottir, Isleifur Olafsson, Thorvaldur Jonsson, Eirikur Jonsson, Rosa B Barkardottir, Rafn Hilmarsson, Folkert W. Asselbergs, Gudmundur Geirsson, Unnur Thorsteinsdottir, Thorunn Rafnar, Gudmar Thorleifsson, Kári Stefánsson
Genome-wide associations for benign prostatic hyperplasia reveal a genetic correlation with serum levels of PSA. Nature communications 9 (1) (2018)
Unnur Styrkársdóttir, Sigrun Helga Lund, Gudmar Thorleifsson, Florian Zink, Olafur A Stefansson, Jon K Sigurdsson, Kristinn Juliusson, Kristbjörg Bjarnadottir, Sara Sigurbjornsdottir, Stefan Jonsson, Kristjan Norland, Lilja Stefansdottir, Asgeir Sigurdsson, Gardar Sveinbjornsson, Asmundur Oddsson, Gyda Bjornsdottir, Reynir L Gudmundsson, Gisli Hreinn Halldorsson, Thorunn Rafnar, Ingileif Jónsdóttir, Eirikur Steingrimsson, Gudmundur L Norddahl, Gisli Masson, Patrick Sulem, Helgi Jonsson, Thorvaldur Ingvarsson, Daníel F Guðbjartsson, Unnur Thorsteinsdottir, Kári Stefánsson
Meta-analysis of Icelandic and UK data sets identifies missense variants in SMO, IL11, COL11A1 and 13 more new loci associated with osteoarthritis. Nature genetics 50 (12) (2018)
Egil Ferkingstad, Asmundur Oddsson, Solveig Gretarsdottir, Stefania Benonisdottir, Gudmar Thorleifsson, Aimee M Deaton, Stefan Jonsson, Olafur A Stefansson, Gudmundur L Norddahl, Florian Zink, Gudny Anna Arnadottir, Bjarni Gunnarsson, Gisli Hreinn Halldorsson, Anna Helgadottir, Brynjar O Jensson, Ragnar P Kristjansson, Gardar Sveinbjornsson, David A Sverrisson, Gisli Masson, Isleifur Olafsson, Gudmundur I Eyjolfsson, Olof Sigurdardottir, Hilma Holm, Ingileif Jonsdottir, Sigurdur Olafsson, Thora Steingrimsdottir, Thorunn Rafnar, Einar S Bjornsson, Unnur Thorsteinsdottir, Daníel F Guðbjartsson, Patrick Sulem, Kári Stefánsson
Genome-wide association meta-analysis yields 20 loci associated with gallstone disease. Nature communications 9 (1) (2018)
Rosa B Thorolfsdottir, Gardar Sveinbjornsson, Patrick Sulem, Jonas Bille Nielsen, Stefan Jonsson, Gisli Hreinn Halldorsson, Pall Melsted, Erna V Ivarsdottir, Olafur B Davidsson, Ragnar P Kristjansson, Gudmar Thorleifsson, Anna Helgadottir, Solveig Gretarsdottir, Gudmundur Norddahl, Sridharan Rajamani, Bjarni Torfason, Atli S Valgardsson, Jon T Sverrisson, Vinicius Tragante, Oddgeir L Holmen, Folkert W Asselbergs, Dan M Roden, Dawood Darbar, Terje R Pedersen, Marc S Sabatine, Cristen J Willer, Maja-Lisa Løchen, Bjarni V Halldórsson, Ingileif Jonsdottir, Kristian Hveem, David O Arnar, Unnur Thorsteinsdottir, Daniel F Gudbjartsson, Hilma Holm, Kari Stefansson
Coding variants in RPL3L and MYZAP increase risk of atrial fibrillation. Communications biology 1 (2018)