Vinicius Tragante

ORCID

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 50

Top Venues

Nature genetics

European heart journal

Communications biology

NPJ Parkinson's disease

deCODE Genetics Inc

University Medical Center Utrecht (PHD)

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

Affiliation History

deCODE Genetics Inc Jul 24 2017

Iceland

Research scientist :: Cardiology

University Medical Center Utrecht Jul 01 2014 - Sep 01 2017

Netherlands

Postdoctoral resesarcher :: Heart & Lungs

Katholieke Universiteit Leuven Departement Computerwetenschappen Apr 06 2009 - Jan 31 2011

Belgium

Research assistant :: Departement Computerwetenschappen

Education History

University Medical Center Utrecht Apr 01 2011 - Jun 24 2014

Netherlands

PHD :: Heart & Lungs

Universidade de São Paulo Mar 01 2007 - Mar 15 2009

Brazil

MSC :: FFCLRP

Universidade de São Paulo Feb 01 2003 - Jan 19 2007

Brazil

BSC :: FFCLRP / FMRP

Publications

Unnur Styrkársdóttir, Vinicius Tragante, Lilja Stefansdottir, Gudmar Thorleifsson, Asmundur Oddsson, Erik Sørensen, Christian Erikstrup, Peter Schwarz, Henrik Løvendahl Jørgensen, Jes Bruun Lauritzen, Soren Brunak, Kirk U Knowlton, Lincoln D Nadauld, Henrik Ullum, Ole Birger Vesterager Pedersen, Sisse Rye Ostrowski, Hilma Hólm, Daniel F Gudbjartsson, Patrick Sulem, Kári Stefánsson
Obesity Variants in the GIPR Gene Are not Associated With Risk of Fracture or Bone Mineral Density. The Journal of clinical endocrinology and metabolism 109 (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)
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)
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)
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)
Karsten Øvretveit, Emma M L Ingeström, Michail Spitieris, Vinicius Tragante, Laurent F Thomas, Ingelin Steinsland, Ben Michael Brumpton, Daníel F Guðbjartsson, Hilma Hólm, Kári Stefánsson, Ulrik Wisløff, Kristian Hveem
Polygenic Interactions With Environmental Exposures in Blood Pressure Regulation: The HUNT Study. Journal of the American Heart Association (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)
Unnur Styrkársdóttir, Vinicius Tragante, Lilja Stefansdottir, Gudmar Thorleifsson, Asmundur Oddsson, Erik Sørensen, Christian Erikstrup, Peter Schwarz, Henrik Løvendahl Jørgensen, Jes Bruun Lauritzen, Soren Brunak, Kirk U Knowlton, Lincoln D Nadauld, Henrik Ullum, Ole Birger Vesterager Pedersen, Sisse Rye Ostrowski, Hilma Hólm, Daniel F Gudbjartsson, Patrick Sulem, Kári Stefánsson
Obesity Variants in the GIPR Gene Are not Associated With Risk of Fracture or Bone Mineral Density. The Journal of clinical endocrinology and metabolism 109 (8) (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)
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)
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)
Sara M Willems, Natasha H J Ng, Juan Fernandez, Rebecca S Fine, Eleanor Wheeler, Jennifer Wessel, Hidetoshi Kitajima, Gaelle Marenne, Xueling Sim, Hanieh Yaghootkar, Shuai Wang, Sai Chen, Yuning Chen, Yii-Der Ida Chen, Niels Grarup, Ruifang Li-Gao, Tibor V Varga, Jennifer L Asimit, Shuang Feng, Rona Juliette Strawbridge, Erica L Kleinbrink, Tarunveer S Ahluwalia, Ping An, Emil V Appel, Dan E Arking, Juha Auvinen, Lawrence F Bielak, Nathan A Bihlmeyer, Jette Bork-Jensen, Jennifer A Brody, Archie I Campbell, Audrey Y Chu, Gail Davies, Ayse Demirkan, James S Floyd, Franco Giulianini, Xiuqing Guo, Stefan Gustafsson, Anne U Jackson, Johanna Jakobsdottir, Marjo-Riitta Järvelin, Richard A Jensen, Stavroula Kanoni, Sirkka Keinanen-Kiukaanniemi, Man Li, Yingchang Lu, Jian'an Luan, Alisa K Manning, Jonathan Marten, Karina Meidtner, Dennis O Mook-Kanamori, Taulant Muka, Giorgio Pistis, Bram Prins, Kenneth M Rice, Serena Sanna, Albert Vernon Smith, Jennifer A Smith, Lorraine Southam, Heather M Stringham, Vinicius Tragante, Sander W van der Laan, Helen R Warren, Jie Yao, Andrianos M Yiorkas, Weihua Zhang, Wei Zhao, Mariaelisa Graff, Heather M Highland, Anne E Justice, Eirini Marouli, Carolina Medina-Gomez, Saima Afaq, Wesam A Alhejily, Najaf Amin, Folkert W Asselbergs, Lori L Bonnycastle, Michiel L Bots, Ivan Brandslund, Ji Chen, John Danesh, Renée de Mutsert, Abbas Dehghan, Tapani Ebeling, Paul Elliott, null null, Aliki-Eleni Farmaki, Jessica D Faul, Paul W Franks, Steve Franks, Andreas Fritsche, Anette P Gjesing, Mark O Goodarzi, Vilmundur G Gudnason, Göran Hallmans, Tamara B Harris, Karl-Heinz Herzig, Marie-France Hivert, Torben Jørgensen, Marit E Jørgensen, Pekka Jousilahti, Eero Kajantie, Maria Karaleftheri, Sharon L R Kardia, Leena Kinnunen, Heikki A Koistinen, Pirjo Komulainen, Peter Kovacs, Johanna Kuusisto, Markku Laakso, Leslie A Lange, Lenore J Launer, Aaron Leong, Jaana Lindström, Jocelyn E Manning Fox, Satu Männistö, Nisa M Maruthur, Leena Moilanen, Antonella Mulas, Mike A Nalls, Matthew Neville, James S Pankow, Alison Pattie, Eva R B Petersen, Hannu Puolijoki, Asif Rasheed, Paul Redmond, Frida Renström, Michael Roden, Danish Saleheen, Juha Saltevo, Kai Savonen, Sylvain Sebert, Tea Skaaby, Kerrin S Small, Alena Stančáková, Jakob Stokholm, Konstantin Strauch, E-Shyong Tai, Kent D Taylor, Betina H Thuesen, Anke Tönjes, Emmanouil Tsafantakis, Tiinamaija Tuomi, Jaakko Tuomilehto, null null, Matti Uusitupa, Marja Vääräsmäki, Ilonca Vaartjes, Magdalena Zoledziewska, Goncalo Abecasis, Beverley Balkau, Hans Bisgaard, Alexandra I Blakemore, Matthias Blüher, Heiner Boeing, Eric Boerwinkle, Klaus Bønnelykke, Erwin P Bottinger, Mark J Caulfield, John C Chambers, Daniel I Chasman, Ching-Yu Cheng, Francis S Collins, Josef Coresh, Francesco Cucca, Gert J de Borst, Ian J Deary, George Dedoussis, Panos Deloukas, Hester M den Ruijter, Josée Dupuis, Michele K Evans, Ele Ferrannini, Oscar H Franco, Harald Grallert, Torben Hansen, Andrew T Hattersley, Caroline Hayward, Joel N Hirschhorn, Arfan Ikram, Erik Ingelsson, Fredrik Karpe, Kay-Tee Khaw, Wieland Kiess, Jaspal S Kooner, Antje Körner, Timo Lakka, Claudia Langenberg, Lars Lind, Cecilia M Lindgren, Allan Linneberg, Leonard Lipovich, Ching-Ti Liu, Jun Liu, Yongmei Liu, Ruth J F Loos, Patrick E MacDonald, Karen L Mohlke, Andrew D Morris, Patricia B Munroe, Alison D Murray, Sandosh Padmanabhan, Colin N A Palmer, Gerard Pasterkamp, Oluf Pedersen, Patricia A Peyser, Ozren Polasek, David J Porteous, Michael A Province, Bruce M Psaty, Rainer Rauramaa, Paul M Ridker, Olov Rolandsson, Patrik Rorsman, Frits R Rosendaal, Igor Rudan, Veikko V Salomaa, Matthias B Schulze, Robert Sladek, Blair Hamilton Smith, Timothy D Spector, John M Starr, Michael Stumvoll, Cornelia M Van Duijn, Mark Walker, Nicholas J Wareham, David R Weir, James G Wilson, Tien Yin Wong, Eleftheria Zeggini, Alan B Zonderman, Jerome I Rotter, Andrew P Morris, Michael Boehnke, Jose C Florez, Mark I McCarthy, James B Meigs, Anubha Mahajan, Robert A Scott, Anna L Gloyn, Inês A Barroso
Large-scale exome array summary statistics resources for glycemic traits to aid effector gene prioritization. Wellcome open research 8 (2023)
Hilma Hólm, Erna V Ivarsdottir, Thorhildur Olafsdottir, Rosa B Thorolfsdottir, Elias Eythorsson, Kristjan Norland, Rosa S Gisladottir, Gudrun Jonsdottir, Unnur Unnsteinsdottir, Kristin E Sveinsdottir, Benedikt A Jonsson, Margret Andresdottir, David O Arnar, Asgeir O Arnthorsson, Kolbrún Birgisdottir, Kristbjorg Bjarnadottir, Solveig Bjarnadottir, Gyda Bjornsdottir, Gudmundur Einarsson, Berglind Eiriksdottir, Elisabet Eir Gardarsdottir, Thorarinn Gislason, Magnus Gottfredsson, Steinunn Gudmundsdottir, Julius Gudmundsson, Kristbjorg Gunnarsdottir, Anna Helgadottir, Dadi Helgason, Ingibjorg Hinriksdottir, Ragnar F Ingvarsson, Sigga S Jonasdottir, Ingileif Jónsdóttir, Tekla H Karlsdottir, Anna M Kristinsdottir, Sigurdur Yngvi Kristinsson, Steinunn Kristjansdottir, Thorvardur J Love, Dora Ludviksdottir, Gisli Masson, Gudmundur Norddahl, Thorunn Asta Olafsdottir, Isleifur Olafsson, Thorunn Rafnar, Hrafnhildur L Runolfsdottir, Jona Saemundsdottir, Svanur Sigurbjornsson, Kristin Sigurdardottir, Engilbert Sigurdsson, Martin I Sigurdsson, Emil L Sigurdsson, Valgerdur Steinthorsdottir, Gardar Sveinbjornsson, Emil A Thorarensen, Bjarni Thorbjornsson, Brynja Thorsteinsdottir, Vinicius Tragante, Magnus O Ulfarsson, Hreinn Stefansson, Thorsteinn Gislason, Mar Kristjansson, Runolfur Palsson, Patrick Sulem, Unnur Thorsteinsdottir, Gudmundur Thorgeirsson, Daníel F Guðbjartsson, Kári Stefánsson
Physical and cognitive impact following SARS-CoV-2 infection in a large population-based case-control study. Communications medicine 3 (1) (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)
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)
Simon N Stacey, Florian Zink, Gisli Hreinn Halldorsson, Lilja Stefansdottir, Sigurjon A Gudjonsson, Gudmundur Einarsson, Grimur Hjorleifsson Eldjarn, Thjodbjorg Eiriksdottir, Anna Helgadottir, Gyda Bjornsdottir, Thorgeir E Thorgeirsson, Thorunn Asta Olafsdottir, Ingileif Jónsdóttir, Solveig Gretarsdottir, Vinicius Tragante, Magnus Karl Magnusson, Hákon Jónsson, Julius Gudmundsson, Sigurgeir Olafsson, Hilma Hólm, Daníel F Guðbjartsson, Patrick Sulem, Agnar Helgason, Unnur Thorsteinsdottir, Laufey Tryggvadottir, Thorunn Rafnar, Pall Melsted, Magnus Ö Ulfarsson, Brynjar Vidarsson, Gudmar Thorleifsson, Kári Stefánsson
Genetics and epidemiology of mutational barcode-defined clonal hematopoiesis. Nature genetics (2023)
Karsten Øvretveit, Emma M L Ingeström, Michail Spitieris, Vinicius Tragante, Kaitlin H Wade, Laurent Thomas, Brooke N Wolford, Ulrik Wisløff, Daniel F Gudbjartsson, Hilma Hólm, Kári Stefánsson, Ben M Brumpton, Kristian Hveem
Polygenic risk scores associate with blood pressure traits across the lifespan. European journal of preventive cardiology (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)
Unnur Styrkarsdottir, Vinicius Tragante, Lilja Stefansdottir, Gudmar Thorleifsson, Asmundur Oddsson, Erik Sørensen, Christian Erikstrup, Peter Schwarz, Henrik Løvendahl Jørgensen, Jes Bruun Lauritzen, Soren Brunak, Kirk U Knowlton, Lincoln D Nadauld, Henrik Ullum, Ole Birger Vesterager Pedersen, Sisse Rye Ostrowski, Hilma Hólm, Daniel F Gudbjartsson, Patrick Sulem, Kari Stefansson
Obesity variants in the GIPR gene do not associate with risk of fracture or bone mineral density. The Journal of clinical endocrinology and metabolism (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)
Jonas Ghouse, Vinicius Tragante, Ayesha Muhammad, Gustav Ahlberg, Morten W Skov, Dan M Roden, Ingileif Jónsdóttir, Laura Andreasen, Pia Rengtved Lundegaard, Linea C Trudsø, Karina Banasik, Søren Brunak, Sisse Rye Ostrowski, null null, Christian Torp-Pedersen, Ole V Pedersen, Erik Sørensen, Lars Valeur Køber, Kasper Iversen, Unnur Thorsteinsdottir, Gudmundur Thorgeirsson, Henrik Ullum, Daniel F Gudbjartsson, Jonathan D Mosley, Hilma Hólm, Kári Stefánsson, Henning Bundgaard, Morten Salling Olesen
Polygenic risk score for ACE-inhibitor-associated cough based on the discovery of new genetic loci. European heart journal 43 (45) (2022)
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)
Anna Helgadottir, Gudmar Thorleifsson, Audunn Snaebjarnarson, Lilja Stefansdottir, Gardar Sveinbjörnsson, Vinicius Tragante, Eyþór Björnsson, Valgerdur Steinthorsdottir, Solveig Gretarsdottir, Hannes Helgason, Jona Saemundsdottir, Isleifur Olafsson, Jens Jakob Thune, Anna Axelsson Raja, Jonas Ghouse, Morten Salling Olesen, Alex Christensen, Rikke Louise Jacobsen, Joseph Dowsett, Mie Topholm Bruun, Kaspar Nielsen, Kirk U Knowlton, Lincoln Nadauld, Rafn Benediktsson, Christian Erikstrup, Ole B Pedersen, Karina Banasik, Søren Brunak, null null, Henning Bundgaard, Sisse R Ostrowski, Patrick Sulem, David O Arnar, Gudmundur Thorgeirsson, Unnur Thorsteinsdottir, Daniel F Gudbjartsson, Kari Stefansson, Hilma Hólm
Cholesterol not particle concentration mediates the atherogenic risk conferred by apolipoprotein B particles - A Mendelian randomization analysis. European journal of preventive cardiology (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)
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)
Thorhildur Juliusdottir, Valgerdur Steinthorsdottir, Lilja Stefansdottir, Gardar Sveinbjornsson, Erna V Ivarsdottir, Rosa B Thorolfsdottir, Jon K Sigurdsson, Vinicius Tragante, Kristjan E Hjorleifsson, Anna Helgadottir, Michael L Frigge, Gudmundur Thorgeirsson, Rafn Benediktsson, Emil L Sigurdsson, David O Arnar, Thora Steingrimsdottir, Ingileif Jónsdóttir, Hilma Hólm, Daníel F Guðbjartsson, Gudmar Thorleifsson, Unnur Thorsteinsdottir, Kári Stefánsson
Distinction between the effects of parental and fetal genomes on fetal growth. Nature genetics 53 (8) (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)
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)
Stefan J Schunk, Marcus Edi Kleber, Winfried März, Shichao Pang, Stephen Zewinger, Sarah Triem, Philipp Ege, Matthias Christian Reichert, Marcin Krawczyk, Susanne N Weber, Isabella Jaumann, David Schmit, Tamim Sarakpi, Stefan Wagenpfeil, Rafael Kramann, Eric Boerwinkle, Christie M Ballantyne, Megan L Grove, Vinicius Tragante, Anna P Pilbrow, Arthur Mark Richards, Vicky A Cameron, Robert N Doughty, Marie-Pierre Dubé, Jean Claude Tardif, Yassamin Feroz-Zada, Maxine Sun, Chang Liu, Yi-An Ko, Arshed A Quyyumi, Jaana A Hartiala, Wai Hong Wilson Tang, Stanley L Hazen, Hooman Allayee, Caitrin W McDonough, Yan Gong, Rhonda M Cooper-DeHoff, Julie A Johnson, Markus Scholz, Andrej Teren, Ralph Burkhardt, Andreas Martinsson, J Gustav Smith, Lars Wallentin, Stefan K James, Niclas Eriksson, Harvey D White, Claes Held, Dawn M Waterworth, Stella Trompet, Johan Wouter Jukema, Ian Ford, David J Stott, Naveed Sattar, Sharon Cresci, John A Spertus, Hannah Campbell, Sascha Tierling, Jörn Walter, Emmanuel Ampofo, Barbara A Niemeyer, Peter Lipp, Heribert Schunkert, Michael Böhm, Wolfgang Koenig, Danilo Fliser, Ulrich Laufs, Thimoteus Speer, null null, null null
Genetically determined NLRP3 inflammasome activation associates with systemic inflammation and cardiovascular mortality. European heart journal 42 (18) (2021)
Hilma Hólm, Patrick Sulem, Vinicius Tragante, Unnur Thorsteinsdottir, Daníel F Guðbjartsson, Kári Stefánsson
Comment on "Evaluating the cardiovascular safety of sclerostin inhibition using evidence from meta-analysis of clinical trials and human genetics". Science translational medicine 13 (622) (2021)
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)
Elisabetta Manduchi, Daiane Hemerich, Jessica van Setten, Vinicius Tragante, Magdalena Harakalova, Jiayi Pei, Scott M Williams, Pim van der Harst, Folkert W. Asselbergs, Jason H Moore
A comparison of two workflows for regulome and transcriptome-based prioritization of genetic variants associated with myocardial mass. Genetic epidemiology 43 (6) (2019)
Vinicius Tragante, Johannes M I H Gho, Janine F Felix, Ramachandran S Vasan, Nicholas L Smith, Benjamin F Voight, null null, Colin Palmer, Pim van der Harst, Jason H Moore, Folkert W Asselbergs
Gene Set Enrichment Analyses: lessons learned from the heart failure phenotype. BioData mining 10 (2017)

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