Gudny Anna Arnadottir (Gudny A Arnadottir)

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 33

Top Topics

Genome Wide Association

Intellectual Disability

Top Venues

Nature communications

Nature structural & molecular biology

Communications biology

Nature genetics

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

Publications

Valgerdur Steinthorsdottir, Bjarni V Halldórsson, Hákon Jónsson, Gunnar Pálsson, Asmundur Oddsson, David Westergaard, Gudny Anna Arnadottir, Lilja Stefansdottir, Karina Banasik, M Sean Esplin, Thomas Folkmann Hansen, Soren Brunak, Mette Nygaard, Sisse Rye Ostrowski, Ole Birger Vesterager Pedersen, Christian Erikstrup, null null, Gudmar Thorleifsson, Lincoln D Nadauld, Ásgeir Haraldsson, Thora Steingrimsdottir, Laufey Tryggvadottir, Ingileif Jónsdóttir, Daníel F Guðbjartsson, Eva R Hoffman, Patrick Sulem, Hilma Hólm, Henriette Svarre Nielsen, Kári Stefánsson
Variant in the synaptonemal complex protein SYCE2 associates with pregnancy loss through effect on recombination. Nature structural & molecular biology (2024)
Valgerdur Steinthorsdottir, Bjarni V Halldórsson, Hákon Jónsson, Gunnar Pálsson, Asmundur Oddsson, David Westergaard, Gudny Anna Arnadottir, Lilja Stefansdottir, Karina Banasik, M Sean Esplin, Thomas Folkmann Hansen, Soren Brunak, Mette Nygaard, Sisse Rye Ostrowski, Ole Birger Vesterager Pedersen, Christian Erikstrup, null null, Gudmar Thorleifsson, Lincoln D Nadauld, Ásgeir Haraldsson, Thora Steingrimsdottir, Laufey Tryggvadottir, Ingileif Jónsdóttir, Daníel F Guðbjartsson, Eva R Hoffman, Patrick Sulem, Hilma Hólm, Henriette Svarre Nielsen, Kári Stefánsson
Variant in the synaptonemal complex protein SYCE2 associates with pregnancy loss through effect on recombination. Nature structural & molecular biology 31 (4) (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)
Valgerdur Steinthorsdottir, Bjarni V Halldórsson, Hákon Jónsson, Gunnar Pálsson, Asmundur Oddsson, David Westergaard, Gudny Anna Arnadottir, Lilja Stefansdottir, Karina Banasik, M Sean Esplin, Thomas Folkmann Hansen, Soren Brunak, Mette Nygaard, Sisse Rye Ostrowski, Ole Birger Vesterager Pedersen, Christian Erikstrup, null null, Gudmar Thorleifsson, Lincoln D Nadauld, Ásgeir Haraldsson, Thora Steingrimsdottir, Laufey Tryggvadottir, Ingileif Jónsdóttir, Daníel F Guðbjartsson, Eva R Hoffman, Patrick Sulem, Hilma Hólm, Henriette Svarre Nielsen, Kári Stefánsson
Variant in the synaptonemal complex protein SYCE2 associates with pregnancy loss through effect on recombination. Nature structural & molecular biology 31 (4) (2024)
Valgerdur Steinthorsdottir, Bjarni V Halldórsson, Hákon Jónsson, Gunnar Pálsson, Asmundur Oddsson, David Westergaard, Gudny Anna Arnadottir, Lilja Stefansdottir, Karina Banasik, M Sean Esplin, Thomas Folkmann Hansen, Soren Brunak, Mette Nygaard, Sisse Rye Ostrowski, Ole Birger Vesterager Pedersen, Christian Erikstrup, null null, Gudmar Thorleifsson, Lincoln D Nadauld, Ásgeir Haraldsson, Thora Steingrimsdottir, Laufey Tryggvadottir, Ingileif Jónsdóttir, Daníel F Guðbjartsson, Eva R Hoffman, Patrick Sulem, Hilma Hólm, Henriette Svarre Nielsen, Kári Stefánsson
Variant in the synaptonemal complex protein SYCE2 associates with pregnancy loss through effect on recombination. Nature structural & molecular biology (2024)
Valgerdur Steinthorsdottir, Bjarni V Halldórsson, Hákon Jónsson, Gunnar Pálsson, Asmundur Oddsson, David Westergaard, Gudny Anna Arnadottir, Lilja Stefansdottir, Karina Banasik, M Sean Esplin, Thomas Folkmann Hansen, Soren Brunak, Mette Nygaard, Sisse Rye Ostrowski, Ole Birger Vesterager Pedersen, Christian Erikstrup, null null, Gudmar Thorleifsson, Lincoln D Nadauld, Ásgeir Haraldsson, Thora Steingrimsdottir, Laufey Tryggvadottir, Ingileif Jónsdóttir, Daníel F Guðbjartsson, Eva R Hoffman, Patrick Sulem, Hilma Hólm, Henriette Svarre Nielsen, Kári Stefánsson
Variant in the synaptonemal complex protein SYCE2 associates with pregnancy loss through effect on recombination. Nature structural & molecular biology 31 (4) (2024)
Valgerdur Steinthorsdottir, Bjarni V Halldórsson, Hákon Jónsson, Gunnar Pálsson, Asmundur Oddsson, David Westergaard, Gudny Anna Arnadottir, Lilja Stefansdottir, Karina Banasik, M Sean Esplin, Thomas Folkmann Hansen, Soren Brunak, Mette Nygaard, Sisse Rye Ostrowski, Ole Birger Vesterager Pedersen, Christian Erikstrup, null null, Gudmar Thorleifsson, Lincoln D Nadauld, Ásgeir Haraldsson, Thora Steingrimsdottir, Laufey Tryggvadottir, Ingileif Jónsdóttir, Daníel F Guðbjartsson, Eva R Hoffman, Patrick Sulem, Hilma Hólm, Henriette Svarre Nielsen, Kári Stefánsson
Variant in the synaptonemal complex protein SYCE2 associates with pregnancy loss through effect on recombination. Nature structural & molecular biology 31 (4) (2024)
Valgerdur Steinthorsdottir, Bjarni V Halldórsson, Hákon Jónsson, Gunnar Pálsson, Asmundur Oddsson, David Westergaard, Gudny Anna Arnadottir, Lilja Stefansdottir, Karina Banasik, M Sean Esplin, Thomas Folkmann Hansen, Soren Brunak, Mette Nygaard, Sisse Rye Ostrowski, Ole Birger Vesterager Pedersen, Christian Erikstrup, null null, Gudmar Thorleifsson, Lincoln D Nadauld, Ásgeir Haraldsson, Thora Steingrimsdottir, Laufey Tryggvadottir, Ingileif Jónsdóttir, Daníel F Guðbjartsson, Eva R Hoffman, Patrick Sulem, Hilma Hólm, Henriette Svarre Nielsen, Kári Stefánsson
Variant in the synaptonemal complex protein SYCE2 associates with pregnancy loss through effect on recombination. Nature structural & molecular biology 31 (4) (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)
Gardar Sveinbjörnsson, Bara D Benediktsdottir, Gunnlaugur Sigfusson, Kristjan Norland, Olafur B Davidsson, Rosa B Thorolfsdottir, Vinicius Tragante, Gudny Anna Arnadottir, Brynjar O Jensson, Hildigunnur Katrinardottir, Run Fridriksdottir, Hallbera Gudmundsdottir, Hildur M Aegisdottir, Brynjar Fridriksson, Gudmundur Thorgeirsson, Vidar Magnusson, Asmundur Oddsson, Patrick Sulem, Daniel F Gudbjartsson, Hilma Hólm, David O Arnar, Kari Stefansson
Screening for Rare Coding Variants That Associate With the QTc Interval in Iceland. Journal of the American Heart Association (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)
Elin Ola Klemenzdottir, Gudny Anna Arnadottir, Brynjar Orn Jensson, Adalbjorg Jonasdottir, Hildigunnur Katrinardottir, Run Fridriksdottir, Aslaug Jonasdottir, Asgeir Sigurdsson, Sigurjon Axel Gudjonsson, Jon Johannes Jonsson, Vigdis Stefansdottir, Ragnar Danielsen, Astridur Palsdottir, Hakon Jonsson, Agnar Helgason, Olafur Thor Magnusson, Unnur Thorsteinsdottir, Hans Tomas Bjornsson, Kári Stefánsson, Patrick Sulem
A population-based survey of FBN1 variants in Iceland reveals underdiagnosis of Marfan syndrome. European journal of human genetics : EJHG (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)
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)
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)
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)
Gudny Anna Arnadottir, Asmundur Oddsson, Brynjar O Jensson, Svanborg Gisladottir, Mariella T Simon, Asgeir O Arnthorsson, Hildigunnur Katrinardottir, Run Fridriksdottir, Erna V Ivarsdottir, Adalbjorg Jonasdottir, Aslaug Jonasdottir, Rebekah Barrick, Jona Saemundsdottir, Louise le Roux, Gudjon R Oskarsson, Jurate Asmundsson, Thora Steffensen, Kjartan R Gudmundsson, Petur Ludvigsson, Jon J Jonsson, Gisli Masson, Ingileif Jónsdóttir, Hilma Hólm, Jon G Jonasson, Olafur Th Magnusson, Olafur Thorarensen, Jose Abdenur, Gudmundur L Norddahl, Daníel F Guðbjartsson, Hans T Bjornsson, Unnur Thorsteinsdottir, Patrick Sulem, Kári Stefánsson
Population-level deficit of homozygosity unveils CPSF3 as an intellectual disability syndrome gene. 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)
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)
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)
Run Fridriksdottir, Arnar J Jonsson, Brynjar O Jensson, Kristinn Ö Sverrisson, Gudny Anna Arnadottir, Sigurbjorg J Skarphedinsdottir, Hildigunnur Katrinardottir, Steinunn Snaebjornsdottir, Hakon Jonsson, Ogmundur Eiriksson, Gudjon R Oskarsson, Asmundur Oddsson, Adalbjorg Jonasdottir, Aslaug Jonasdottir, Gisli H Sigurdsson, Einar P Indridason, Stefan B Sigurdsson, Gyda Bjornsdottir, Jona Saemundsdottir, Olafur T Magnusson, Hans T Bjornsson, Unnur Thorsteinsdottir, Theodor S Sigurdsson, Patrick Sulem, Martin I Sigurdsson, Kári Stefánsson
Sequence variants in malignant hyperthermia genes in Iceland: classification and actionable findings in a population database. European journal of human genetics : EJHG 29 (12) (2021)
Hákon Jónsson, Erna Magnusdottir, Hannes Petur Eggertsson, Olafur A Stefansson, Gudny Anna Arnadottir, Ogmundur Eiriksson, Florian Zink, Einar A Helgason, Ingileif Jónsdóttir, Arnaldur Gylfason, Adalbjorg Jonasdottir, Aslaug Jonasdottir, Doruk Beyter, Thora Steingrimsdottir, Gudmundur L Norddahl, Olafur Th Magnusson, Gisli Masson, Bjarni V Halldórsson, Unnur Thorsteinsdottir, Agnar Helgason, Patrick Sulem, Daníel F Guðbjartsson, Kári Stefánsson
Differences between germline genomes of monozygotic twins. Nature genetics 53 (1) (2021)
Hrafnhildur L Runolfsdottir, John Andrew Sayer, Olafur S Indridason, Viðar Ö Eðvarðsson, Brynjar O Jensson, Gudny Anna Arnadottir, Sigurjon A Gudjonsson, Run Fridriksdottir, Hildigunnur Katrinardottir, Daniel Gudbjartsson, Unnur Thorsteinsdottir, Patrick Sulem, Kari Stefansson, Runolfur Palsson
Allele frequency of variants reported to cause adenine phosphoribosyltransferase deficiency. European journal of human genetics : EJHG 29 (7) (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)
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)
Erna V Ivarsdottir, Stefania Benonisdottir, Gudmar Thorleifsson, Patrick Sulem, Asmundur Oddsson, Unnur Styrkársdóttir, Snaedis Kristmundsdottir, Gudny Anna Arnadottir, Gudmundur Thorgeirsson, Ingileif Jonsdottir, Gunnar M Zoega, Unnur Thorsteinsdottir, Daníel F Guðbjartsson, Fridbert Jonasson, Hilma Holm, Kári Stefánsson
Sequence variation at ANAPC1 accounts for 24% of the variability in corneal endothelial cell density. 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)
Gudny Anna Arnadottir, Gudmundur L Norddahl, Steinunn Gudmundsdottir, Arna B Agustsdottir, Snaevar Sigurdsson, Brynjar O Jensson, Kristbjorg Bjarnadottir, Fannar Theodors, Stefania Benonisdottir, Erna V Ivarsdottir, Asmundur Oddsson, Ragnar P Kristjansson, Gerald Sulem, Kristjan F Alexandersson, Thorhildur Juliusdottir, Kjartan R Gudmundsson, Jona Saemundsdottir, Adalbjorg Jonasdottir, Aslaug Jonasdottir, Asgeir Sigurdsson, Paolo Manzanillo, Sigurjon A Gudjonsson, Gudmundur A Thorisson, Olafur Th Magnusson, Gisli Masson, Kjartan B Orvar, Hilma Holm, Sigurdur Bjornsson, Reynir Arngrimsson, Daníel F Guðbjartsson, Unnur Thorsteinsdottir, Ingileif Jonsdottir, Asgeir Haraldsson, Patrick Sulem, Kari Stefansson
A homozygous loss-of-function mutation leading to CYBC1 deficiency causes chronic granulomatous disease. Nature communications 9 (1) (2018)
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Genome-wide association meta-analysis yields 20 loci associated with gallstone disease. Nature communications 9 (1) (2018)