Gardar Sveinbjörnsson (Gardar Sveinbjornsson)

Publication Activity (10 Years)

Years Active: 2021-2024
Publications (10 Years): 42

Top Topics

Gene Expression

Cardiovascular Disease

Genome Wide Association Study

Top Venues

Nature genetics

Nature communications

European heart journal

NPJ Parkinson's disease

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

Publications

David Westergaard, Valgerdur Steinthorsdottir, Lilja Stefansdottir, Palle Duun Rohde, Xiaoping Wu, Frank Geller, Jaakko Tyrmi, Aki S Havulinna, Pol Sole Navais, Christopher Flatley, Sisse Rye Ostrowski, Ole Birger Vesterager Pedersen, Christian Erikstrup, Erik Sørensen, Christina Mikkelsen, Mie Topholm Bruun, Bitten Aagaard Jensen, Thorsten Brodersen, Henrik Ullum, null null, null null, null null, null null, Per M Magnus, Ole Andreas Andreassen, Pal Rasmus Njolstad, Astrid Marie Kolte, Lone Krebs, Mette Nygaard, Thomas Folkmann Hansen, Bjarke Feenstra, Mark Daly, Cecilia M Lindgren, Gudmar Thorleifsson, Olafur Andri Stefansson, Gardar Sveinbjörnsson, Daníel F Guðbjartsson, Unnur Thorsteinsdottir, Karina Banasik, Bo Jacobson, Triin Laisk, Finnpec Hannele Laivuori, Kari Stefansson, Soren Brunak, Henriette Svarre Nielsen
Genome-wide association meta-analysis identifies five loci associated with postpartum hemorrhage. 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 56 (8) (2024)
David Westergaard, Valgerdur Steinthorsdottir, Lilja Stefansdottir, Palle Duun Rohde, Xiaoping Wu, Frank Geller, Jaakko Tyrmi, Aki S Havulinna, Pol Sole Navais, Christopher Flatley, Sisse Rye Ostrowski, Ole Birger Vesterager Pedersen, Christian Erikstrup, Erik Sørensen, Christina Mikkelsen, Mie Topholm Bruun, Bitten Aagaard Jensen, Thorsten Brodersen, Henrik Ullum, null null, null null, null null, null null, Per M Magnus, Ole Andreas Andreassen, Pal Rasmus Njolstad, Astrid Marie Kolte, Lone Krebs, Mette Nygaard, Thomas Folkmann Hansen, Bjarke Feenstra, Mark Daly, Cecilia M Lindgren, Gudmar Thorleifsson, Olafur Andri Stefansson, Gardar Sveinbjörnsson, Daníel F Guðbjartsson, Unnur Thorsteinsdottir, Karina Banasik, Bo Jacobson, Triin Laisk, Finnpec Hannele Laivuori, Kari Stefansson, Soren Brunak, Henriette Svarre Nielsen
Genome-wide association meta-analysis identifies five loci associated with postpartum hemorrhage. Nature genetics 56 (8) (2024)
David Westergaard, Valgerdur Steinthorsdottir, Lilja Stefansdottir, Palle Duun Rohde, Xiaoping Wu, Frank Geller, Jaakko Tyrmi, Aki S Havulinna, Pol Sole Navais, Christopher Flatley, Sisse Rye Ostrowski, Ole Birger Vesterager Pedersen, Christian Erikstrup, Erik Sørensen, Christina Mikkelsen, Mie Topholm Bruun, Bitten Aagaard Jensen, Thorsten Brodersen, Henrik Ullum, null null, null null, null null, null null, Per M Magnus, Ole Andreas Andreassen, Pal Rasmus Njolstad, Astrid Marie Kolte, Lone Krebs, Mette Nygaard, Thomas Folkmann Hansen, Bjarke Feenstra, Mark Daly, Cecilia M Lindgren, Gudmar Thorleifsson, Olafur Andri Stefansson, Gardar Sveinbjörnsson, Daníel F Guðbjartsson, Unnur Thorsteinsdottir, Karina Banasik, Bo Jacobson, Triin Laisk, Finnpec Hannele Laivuori, Kari Stefansson, Soren Brunak, Henriette Svarre Nielsen
Genome-wide association meta-analysis identifies five loci associated with postpartum hemorrhage. Nature genetics 56 (8) (2024)
David Westergaard, Valgerdur Steinthorsdottir, Lilja Stefansdottir, Palle Duun Rohde, Xiaoping Wu, Frank Geller, Jaakko Tyrmi, Aki S Havulinna, Pol Sole Navais, Christopher Flatley, Sisse Rye Ostrowski, Ole Birger Vesterager Pedersen, Christian Erikstrup, Erik Sørensen, Christina Mikkelsen, Mie Topholm Bruun, Bitten Aagaard Jensen, Thorsten Brodersen, Henrik Ullum, null null, null null, null null, null null, Per M Magnus, Ole Andreas Andreassen, Pal Rasmus Njolstad, Astrid Marie Kolte, Lone Krebs, Mette Nygaard, Thomas Folkmann Hansen, Bjarke Feenstra, Mark Daly, Cecilia M Lindgren, Gudmar Thorleifsson, Olafur Andri Stefansson, Gardar Sveinbjörnsson, Daníel F Guðbjartsson, Unnur Thorsteinsdottir, Karina Banasik, Bo Jacobson, Triin Laisk, Finnpec Hannele Laivuori, Kari Stefansson, Soren Brunak, Henriette Svarre Nielsen
Genome-wide association meta-analysis identifies five loci associated with postpartum hemorrhage. Nature genetics (2024)
Astros Th Skuladottir, Vinicius Tragante, Gardar Sveinbjörnsson, Hannes Helgason, Arni Sturluson, Anna Bjornsdottir, Palmi Jonsson, Vala Palmadottir, Olafur A Sveinsson, Brynjar Orn Jensson, Sigurjon A Gudjonsson, Erna V Ivarsdottir, Rosa S Gisladottir, Arni F Gunnarsson, G Bragi Walters, Gudrun A Jonsdottir, Thorgeir E Thorgeirsson, Gyda Bjornsdottir, Hilma Hólm, Daníel F Guðbjartsson, Patrick Sulem, Hreinn Stefansson, Kári Stefánsson
Loss-of-function variants in ITSN1 confer high risk of Parkinson's disease. NPJ Parkinson's disease 10 (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)
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)
Jonas Ghouse, Gardar Sveinbjörnsson, Marijana Vujkovic, Anne-Sofie Seidelin, Helene Gellert-Kristensen, Gustav Ahlberg, Vinicius Tragante, Søren Albertsen Rand, Joseph Brancale, Silvia Vilarinho, Pia Rengtved Lundegaard, Erik Sørensen, Christian Erikstrup, Mie Topholm Bruun, Bitten Aagaard Jensen, Soren Brunak, Karina Banasik, Henrik Ullum, null null, Niek Verweij, Luca A Lotta, Aris Baras, null null, Tooraj Mirshahi, David J Carey, null null, null null, David E Kaplan, Julie A Lynch, Timothy Morgan, Tae-Hwi Schwantes-An, Daniel R Dochtermann, Saiju Pyarajan, Philip S Tsao, null null, Triin Laisk, Reedik Mägi, Julia Kozlitina, Anne Tybjærg-Hansen, David Jones, Kirk U Knowlton, Lincoln Nadauld, Egil Ferkingstad, Einar S Björnsson, Magnus O Ulfarsson, Árni Sturluson, Patrick Sulem, Ole Birger Vesterager Pedersen, Sisse Rye Ostrowski, Daníel F Guðbjartsson, Kári Stefánsson, Morten Salling Olesen, Kyong-Mi Chang, Hilma Hólm, Henning Bundgaard, Stefan Stender
Integrative common and rare variant analyses provide insights into the genetic architecture of liver cirrhosis. Nature genetics 56 (5) (2024)
Jonas Ghouse, Gardar Sveinbjörnsson, Marijana Vujkovic, Anne-Sofie Seidelin, Helene Gellert-Kristensen, Gustav Ahlberg, Vinicius Tragante, Søren Albertsen Rand, Joseph Brancale, Silvia Vilarinho, Pia Rengtved Lundegaard, Erik Sørensen, Christian Erikstrup, Mie Topholm Bruun, Bitten Aagaard Jensen, Soren Brunak, Karina Banasik, Henrik Ullum, null null, Niek Verweij, Luca A Lotta, Aris Baras, null null, Tooraj Mirshahi, David J Carey, null null, null null, David E Kaplan, Julie A Lynch, Timothy Morgan, Tae-Hwi Schwantes-An, Daniel R Dochtermann, Saiju Pyarajan, Philip S Tsao, null null, Triin Laisk, Reedik Mägi, Julia Kozlitina, Anne Tybjærg-Hansen, David Jones, Kirk U Knowlton, Lincoln Nadauld, Egil Ferkingstad, Einar S Björnsson, Magnus O Ulfarsson, Árni Sturluson, Patrick Sulem, Ole Birger Vesterager Pedersen, Sisse Rye Ostrowski, Daníel F Guðbjartsson, Kári Stefánsson, Morten Salling Olesen, Kyong-Mi Chang, Hilma Hólm, Henning Bundgaard, Stefan Stender
Integrative common and rare variant analyses provide insights into the genetic architecture of liver cirrhosis. 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)
Jonas Ghouse, Gardar Sveinbjörnsson, Marijana Vujkovic, Anne-Sofie Seidelin, Helene Gellert-Kristensen, Gustav Ahlberg, Vinicius Tragante, Søren Albertsen Rand, Joseph Brancale, Silvia Vilarinho, Pia Rengtved Lundegaard, Erik Sørensen, Christian Erikstrup, Mie Topholm Bruun, Bitten Aagaard Jensen, Soren Brunak, Karina Banasik, Henrik Ullum, null null, Niek Verweij, Luca A Lotta, Aris Baras, null null, Tooraj Mirshahi, David J Carey, null null, null null, David E Kaplan, Julie A Lynch, Timothy Morgan, Tae-Hwi Schwantes-An, Daniel R Dochtermann, Saiju Pyarajan, Philip S Tsao, null null, Triin Laisk, Reedik Mägi, Julia Kozlitina, Anne Tybjærg-Hansen, David Jones, Kirk U Knowlton, Lincoln Nadauld, Egil Ferkingstad, Einar S Björnsson, Magnus O Ulfarsson, Árni Sturluson, Patrick Sulem, Ole Birger Vesterager Pedersen, Sisse Rye Ostrowski, Daníel F Guðbjartsson, Kári Stefánsson, Morten Salling Olesen, Kyong-Mi Chang, Hilma Hólm, Henning Bundgaard, Stefan Stender
Integrative common and rare variant analyses provide insights into the genetic architecture of liver cirrhosis. Nature genetics 56 (5) (2024)
Astros Th Skuladottir, Vinicius Tragante, Gardar Sveinbjörnsson, Hannes Helgason, Arni Sturluson, Anna Bjornsdottir, Palmi Jonsson, Vala Palmadottir, Olafur A Sveinsson, Brynjar Orn Jensson, Sigurjon A Gudjonsson, Erna V Ivarsdottir, Rosa S Gisladottir, Arni F Gunnarsson, G Bragi Walters, Gudrun A Jonsdottir, Thorgeir E Thorgeirsson, Gyda Bjornsdottir, Hilma Hólm, Daníel F Guðbjartsson, Patrick Sulem, Hreinn Stefansson, Kári Stefánsson
Loss-of-function variants in ITSN1 confer high risk of Parkinson's disease. NPJ Parkinson's disease 10 (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)
Jonas Ghouse, Gardar Sveinbjörnsson, Marijana Vujkovic, Anne-Sofie Seidelin, Helene Gellert-Kristensen, Gustav Ahlberg, Vinicius Tragante, Søren Albertsen Rand, Joseph Brancale, Silvia Vilarinho, Pia Rengtved Lundegaard, Erik Sørensen, Christian Erikstrup, Mie Topholm Bruun, Bitten Aagaard Jensen, Soren Brunak, Karina Banasik, Henrik Ullum, null null, Niek Verweij, Luca A Lotta, Aris Baras, null null, Tooraj Mirshahi, David J Carey, null null, null null, David E Kaplan, Julie A Lynch, Timothy Morgan, Tae-Hwi Schwantes-An, Daniel R Dochtermann, Saiju Pyarajan, Philip S Tsao, null null, Triin Laisk, Reedik Mägi, Julia Kozlitina, Anne Tybjærg-Hansen, David Jones, Kirk U Knowlton, Lincoln Nadauld, Egil Ferkingstad, Einar S Björnsson, Magnus O Ulfarsson, Árni Sturluson, Patrick Sulem, Ole Birger Vesterager Pedersen, Sisse Rye Ostrowski, Daníel F Guðbjartsson, Kári Stefánsson, Morten Salling Olesen, Kyong-Mi Chang, Hilma Hólm, Henning Bundgaard, Stefan Stender
Integrative common and rare variant analyses provide insights into the genetic architecture of liver cirrhosis. Nature genetics 56 (5) (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)
Astros Th Skuladottir, Vinicius Tragante, Gardar Sveinbjörnsson, Hannes Helgason, Arni Sturluson, Anna Bjornsdottir, Palmi Jonsson, Vala Palmadottir, Olafur A Sveinsson, Brynjar Orn Jensson, Sigurjon A Gudjonsson, Erna V Ivarsdottir, Rosa S Gisladottir, Arni F Gunnarsson, G Bragi Walters, Gudrun A Jonsdottir, Thorgeir E Thorgeirsson, Gyda Bjornsdottir, Hilma Hólm, Daníel F Guðbjartsson, Patrick Sulem, Hreinn Stefansson, Kári Stefánsson
Loss-of-function variants in ITSN1 confer high risk of Parkinson's disease. NPJ Parkinson's disease 10 (1) (2024)
Jonas Ghouse, Gardar Sveinbjörnsson, Marijana Vujkovic, Anne-Sofie Seidelin, Helene Gellert-Kristensen, Gustav Ahlberg, Vinicius Tragante, Søren Albertsen Rand, Joseph Brancale, Silvia Vilarinho, Pia Rengtved Lundegaard, Erik Sørensen, Christian Erikstrup, Mie Topholm Bruun, Bitten Aagaard Jensen, Soren Brunak, Karina Banasik, Henrik Ullum, null null, Niek Verweij, Luca A Lotta, Aris Baras, null null, Tooraj Mirshahi, David J Carey, null null, null null, David E Kaplan, Julie A Lynch, Timothy Morgan, Tae-Hwi Schwantes-An, Daniel R Dochtermann, Saiju Pyarajan, Philip S Tsao, null null, Triin Laisk, Reedik Mägi, Julia Kozlitina, Anne Tybjærg-Hansen, David Jones, Kirk U Knowlton, Lincoln Nadauld, Egil Ferkingstad, Einar S Björnsson, Magnus O Ulfarsson, Árni Sturluson, Patrick Sulem, Ole Birger Vesterager Pedersen, Sisse Rye Ostrowski, Daníel F Guðbjartsson, Kári Stefánsson, Morten Salling Olesen, Kyong-Mi Chang, Hilma Hólm, Henning Bundgaard, Stefan Stender
Integrative common and rare variant analyses provide insights into the genetic architecture of liver cirrhosis. Nature genetics 56 (5) (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)
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)
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Screening for Rare Coding Variants That Associate With the QTc Interval in Iceland. Journal of the American Heart Association (2023)
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Author Correction: Genetic effects on the timing of parturition and links to fetal birth weight. 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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Rare variants with large effects provide functional insights into the pathology of migraine subtypes, with and without aura. Nature genetics (2023)
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
Large-scale plasma proteomics comparisons through genetics and disease associations. Nature (2023)
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Sequence variant affects GCSAML splicing, mast cell specific proteins, and risk of urticaria. Communications biology 6 (1) (2023)
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Genetic insights into resting heart rate and its role in cardiovascular disease. Nature communications 14 (1) (2023)
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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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Multiomics study of nonalcoholic fatty liver disease. Nature genetics 54 (11) (2022)
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GWAS of Hematuria. Clinical journal of the American Society of Nephrology : CJASN (2022)
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Cholesterol not particle concentration mediates the atherogenic risk conferred by apolipoprotein B particles - A Mendelian randomization analysis. European journal of preventive cardiology (2022)
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