Egil Ferkingstad

ORCID

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 38

Top Venues

Nature communications

Nature genetics

Communications biology

European heart journal

deCODE Genetics Inc

University of Oslo (PHD)

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

Affiliation History

deCODE Genetics Inc Sep 01 2017

Iceland

Research scientist :: Statistics department

University of Iceland Jan 01 2014 - Aug 31 2017

Iceland

Research Scholar (equiv to Research Associate Professor) :: Science institute

University of Zurich Oct 01 2015 - Nov 01 2015

Switzerland

Visting scholar :: Epidemiology, Biostatistics and Prevention Institute

Norwegian University of Science and Technology Jan 01 2015 - Oct 31 2015

Norway

Researcher :: Department of Mathematical Sciences

Norwegian Computing Center Sep 01 2007 - Nov 01 2013

Norway

Research scientist :: Department of Statistical Analysis, Machine Learning and Image Analysis

deCODE Genetics Inc Jan 01 2005 - Jun 30 2005

Iceland

Visiting scholar :: Statistics department

Education History

University of Oslo Jan 01 2004 - Feb 13 2008

Norway

PHD :: Department of Biostatistics

Norwegian University of Science and Technology Aug 01 1998 - Jun 01 2003

Norway

MSC :: Department of Mathematical Sciences

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)
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)
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)
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 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)
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)
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)
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)
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)
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)
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 O Arnar, Jeffrey L Anderson, Kirk U Knowlton, Lincoln D Nadauld, null null, Magnus Haraldsson, Gudmundur Thorgeirsson, Henning Bundgaard, 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 44 (12) (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 55 (3) (2023)
Ragnar P Kristjansson, Gudjon R Oskarsson, Astros Th Skuladottir, Asmundur Oddsson, Solvi Rognvaldsson, Gardar Sveinbjörnsson, Sigrun Helga Lund, Brynjar Orn Jensson, Edda L Styrmisdottir, Gisli Hreinn Halldorsson, Egil Ferkingstad, Grimur Hjorleifsson Eldjarn, Doruk Beyter, Snaedis Kristmundsdottir, Kristinn Juliusson, Run Fridriksdottir, Gudny Anna Arnadottir, Hildigunnur Katrinardottir, Margret H Snorradottir, Vinicius Tragante, Lilja Stefansdottir, Erna V Ivarsdottir, Gyda Bjornsdottir, Bjarni V Halldórsson, Gudmar Thorleifsson, Bjorn R Ludviksson, Pall T Onundarson, Saedis Saevarsdottir, Pall Melsted, Gudmundur L Norddahl, Unnur S Bjornsdottir, Thorunn Asta Olafsdottir, Daníel F Guðbjartsson, Unnur Thorsteinsdottir, Ingileif Jónsdóttir, Patrick Sulem, Kári Stefánsson
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
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
Publisher Correction: Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality. Nature communications 14 (1) (2023)
Muhammad Sulaman Nawaz, Gudmundur Einarsson, Mariana Bustamante, Rosa S Gisladottir, G Bragi Walters, Gudrun A Jonsdottir, Astros Th Skuladottir, Gyda Bjornsdottir, Sigurdur H Magnusson, Bergrun Asbjornsdottir, Unnur Unnsteinsdottir, Engilbert Sigurdsson, Palmi V Jonsson, Vala Kolbrun Palmadottir, Sigurjon A Gudjonsson, Gisli H Halldorsson, Egil Ferkingstad, Ingileif Jónsdóttir, Gudmar Thorleifsson, Hilma Hólm, Unnur Thorsteinsdottir, Patrick Sulem, Daniel F Gudbjartsson, Hreinn Stefánsson, Thorgeir E Thorgeirsson, Magnus O Ulfarsson, Kári Stefánsson
Thirty novel sequence variants impacting human intracranial volume. Brain communications 4 (6) (2022)
Astros Th Skuladottir, Gyda Bjornsdottir, Egil Ferkingstad, Gudmundur Einarsson, Lilja Stefansdottir, Muhammad Sulaman Nawaz, Asmundur Oddsson, Thorunn Asta Olafsdottir, Saedis Saevarsdottir, G Bragi Walters, Sigurður H Magnusson, Anna Bjornsdottir, Olafur A Sveinsson, Arnor Vikingsson, Thomas Folkmann Hansen, Rikke Louise Jacobsen, Christian Erikstrup, Michael Schwinn, Soren Brunak, Karina Banasik, Sisse Rye Ostrowski, Anders Troelsen, Cecilie Henkel, Ole Birger Vesterager Pedersen, null null, Ingileif Jónsdóttir, Daníel F Guðbjartsson, Patrick Sulem, Thorgeir E Thorgeirsson, Hreinn Stefansson, Kári Stefánsson
A genome-wide meta-analysis identifies 50 genetic loci associated with carpal tunnel syndrome. Nature communications 13 (1) (2022)
Gyda Bjornsdottir, Lilja Stefansdottir, Gudmar Thorleifsson, Patrick Sulem, Kristjan Norland, Egil Ferkingstad, Asmundur Oddsson, Florian Zink, Sigrun H Lund, Muhammad Sulaman Nawaz, G Bragi Walters, Astros Th Skuladottir, Sigurjon A Gudjonsson, Gudmundur Einarsson, Gisli Hreinn Halldorsson, Valgerdur Bjarnadottir, Gardar Sveinbjornsson, Anna Helgadottir, Unnur Styrkársdóttir, Larus J Gudmundsson, Ole Birger Vesterager Pedersen, Thomas Folkmann Hansen, Thomas M Werge, Karina Banasik, Anders Troelsen, Søren Thorgaard Skou, Lise Wegner Thørner, Christian Erikstrup, Kaspar Rene Nielsen, Susan Mikkelsen, null null, null null, Ingileif Jónsdóttir, Aron Bjornsson, Ingvar H Olafsson, Elfar Ulfarsson, Josep Blondal, Arnor Vikingsson, Soren Brunak, Sisse Rye Ostrowski, Henrik Ullum, Unnur Thorsteinsdottir, Hreinn Stefánsson, Daníel F Guðbjartsson, Thorgeir E Thorgeirsson, Kári Stefánsson
Rare SLC13A1 variants associate with intervertebral disc disorder highlighting role of sulfate in disc pathology. Nature communications 13 (1) (2022)
Gyda Bjornsdottir, Lilja Stefansdottir, Gudmar Thorleifsson, Patrick Sulem, Kristjan Norland, Egil Ferkingstad, Asmundur Oddsson, Florian Zink, Sigrun H Lund, Muhammad Sulaman Nawaz, G Bragi Walters, Astros Th Skuladottir, Sigurjon A Gudjonsson, Gudmundur Einarsson, Gisli Hreinn Halldorsson, Valgerdur Bjarnadottir, Gardar Sveinbjornsson, Anna Helgadottir, Unnur Styrkársdóttir, Larus J Gudmundsson, Ole Birger Vesterager Pedersen, Thomas Folkmann Hansen, Thomas M Werge, Karina Banasik, Anders Troelsen, Søren Thorgaard Skou, Lise Wegner Thørner, Christian Erikstrup, Kaspar Rene Nielsen, Susan Mikkelsen, null null, null null, Ingileif Jónsdóttir, Aron Bjornsson, Ingvar H Olafsson, Elfar Ulfarsson, Josep Blondal, Arnor Vikingsson, Soren Brunak, Sisse Rye Ostrowski, Henrik Ullum, Unnur Thorsteinsdottir, Hreinn Stefánsson, Daníel F Guðbjartsson, Thorgeir E Thorgeirsson, Kári Stefánsson
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)
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)
Thjodbjorg Eiriksdottir, Steinthor Ardal, Benedikt A Jonsson, Sigrun Helga Lund, Erna V Ivarsdottir, Kristjan Norland, Egil Ferkingstad, Hreinn Stefansson, Ingileif Jónsdóttir, Hilma Hólm, Thorunn Rafnar, Jona Saemundsdottir, Gudmundur L Norddahl, Gudmundur Thorgeirsson, Daníel F Guðbjartsson, Patrick Sulem, Unnur Thorsteinsdottir, Kári Stefánsson, Magnus O Ulfarsson
Predicting the probability of death using proteomics. Communications biology 4 (1) (2021)
Joseph Dowsett, Egil Ferkingstad, Line Jee Hartmann Rasmussen, Lise Wegner Thørner, Magnus Karl Magnusson, Karen Sugden, Gudmar Thorleifsson, Michael L Frigge, Kristoffer Sølvsten Burgdorf, Sisse Rye Ostrowski, Erik Sørensen, Christian Erikstrup, Ole Birger Vesterager Pedersen, Thomas Folkmann Hansen, Karina Banasik, Soren Brunak, null null, Vinicius Tragante, Sigrun Helga Lund, Lilja Stefansdottir, Bjarni Gunnarson, Richie Poulton, Louise Arseneault, Avshalom Caspi, Terrie E Moffitt, Daníel F Guðbjartsson, Jesper Eugen-Olsen, Hreinn Stefánsson, Kári Stefánsson, Henrik Ullum
Eleven genomic loci affect plasma levels of chronic inflammation marker soluble urokinase-type plasminogen activator receptor. Communications biology 4 (1) (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)
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)

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Egil Ferkingstad