Kári Stefánsson (K Stefansson, Kari Stefansson)

ORCID

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 165

Top Venues

Nature genetics

Nature communications

Communications biology

Nature structural & molecular biology

University of Iceland

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

Affiliation History

University of Iceland Sep 01 2013

Iceland

Professor :: Faculty of Medicine

Decode genetics / Amgen Sep 01 1996

Iceland

CEO

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)
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)
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, Lilja Stefansdottir, Gisli Hreinn Halldorsson, Olafur Andri Stefansson, Anna Bjornsdottir, Palmi Jonsson, Vala Palmadottir, Thorgeir E Thorgeirsson, G Bragi Walters, Rosa S Gisladottir, Gyda Bjornsdottir, Gudrun A Jonsdottir, Patrick Sulem, Daníel F Guðbjartsson, Kirk U Knowlton, David A Jones, Aigar Ottas, null null, Ole Birger Vesterager Pedersen, Maria Didriksen, Soren Brunak, Karina Banasik, Thomas Folkmann Hansen, Christian Erikstrup, null null, Jan Haavik, Ole A Andreassen, David Rye, Jannicke Igland, Sisse Rye Ostrowski, Lili A Milani, Lincoln D Nadauld, Hreinn Stefánsson, Kári Stefánsson
GWAS meta-analysis reveals key risk loci in essential tremor pathogenesis. Communications biology 7 (1) (2024)
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)
Katherine A Kentistou, Lena R Kaisinger, Stasa Stankovic, Marc Vaudel, Edson Mendes de Oliveira, Andrea Messina, Robin G Walters, Xiaoxi Liu, Alexander S Busch, Hannes Helgason, Deborah J Thompson, Federico A Santoni, Konstantin M Petricek, Yassine Zouaghi, Isabel Huang-Doran, Daníel F Guðbjartsson, Eirik Bratland, Kuang Lin, Eugene J Gardner, Yajie Zhao, Raina Y Jia, Chikashi C Terao, Marjorie J Riggan, Manjeet K Bolla, Mojgan Yazdanpanah, Nahid Yazdanpanah, Jonathan P Bradfield, Linda Broer, Archie I Campbell, Daniel I Chasman, Diana L Cousminer, Nora Franceschini, Lude H Franke, Giorgia Girotto, Chunyan He, Marjo-Riitta Jarvelin, Peter K Joshi, Yoichiro Kamatani, Robert Karlsson, Jian'an Luan, Kathryn L Lunetta, Reedik Mägi, Massimo Mangino, Sarah E Medland, Christa Meisinger, Raymond Noordam, Teresa Nutile, Maria Pina Concas, Ozren Polašek, Eleonora Porcu, Susan M Ring, Cinzia Felicita Sala, Albert Vernon Smith, Toshiko Tanaka, Peter J van der Most, Veronique Vitart, Carol A Wang, Gonneke Willemsen, Marek Zygmunt, Thomas U Ahearn, Irene L Andrulis, Hoda Anton-Culver, Antonis C Antoniou, Paul L Auer, Catriona L K Barnes, Matthias W Beckmann, Amy Berrington de Gonzalez, Natalia V Bogdanova, Stig Egil Bojesen, Hermann Brenner, Julie E Buring, Federico Canzian, Jenny Chang-Claude, Fergus J Couch, Angela Cox, Laura Crisponi, Kamila Czene, Mary B Daly, Ellen W Demerath, Joe G Dennis, Peter Devilee, Immaculata De Vivo, Thilo Dörk, Alison M Dunning, Miriam V Dwek, Johan G Eriksson, Peter Andreas Fasching, Lindsay Fernández-Rhodes, Liana Ferreli, Olivia Fletcher, Manuela Gago-Dominguez, Montserrat Garcia-Closas, José Angel García-Saenz, Anna González-Neira, Harald Grallert, Pascal Guénel, Christopher A Haiman, Per Hall, Ute Hamann, Hakon H Hakonarson, Roger J Hart, Martha Hickey, Maartje J Hooning, Reiner Hoppe, John L Hopper, Jouke- Jan Hottenga, Frank B Hu, Hanna Huebner, David J Hunter, null null, Helena Jernström, Esther M John, David Karasik, Elza K Khusnutdinova, Vessela N Kristensen, James V Lacey, Diether Lambrechts, Lenore J Launer, Penelope A Lind, Annika Lindblom, Patrik K E Magnusson, Arto Mannermaa, Mark I McCarthy, Thomas Meitinger, Cristina Menni, Kyriaki Michailidou, Iona Y Millwood, Jonathan Beesley, Grant W Montgomery, Heli Nevanlinna, Ilja Maria Nolte, Dale R Nyholt, Nadia Obi, Katie M O'Brien, Kenneth Offit, Albertine J Oldehinkel, Sisse Rye Ostrowski, Aarno Palotie, Ole Birger Vesterager Pedersen, Annette Peters, Giulia Pianigiani, Dijana Plaseska-Karanfilska, Anneli Pouta, Alfred Pozarickij, Paolo Radice, Gadi Rennert, Frits Richard Rosendaal, Daniela Ruggiero, Emmanouil Saloustros, Dale R Sandler, Sabine Schipf, Carsten Oliver Schmidt, Marjanka K Schmidt, Kerrin S Small, Beatrice Spedicati, Meir Stampfer, Jennifer Stone, Rulla M Tamimi, Lauren R Teras, Emmi Tikkanen, Constance Turman, Celine M Vachon, Qin Wang, Robert Winqvist, Alicja Wolk, Babette S Zemel, Wei Zheng, Ko Willems van Dijk, Behrooz Z Alizadeh, Stefania Bandinelli, Eric Boerwinkle, Dorret I Boomsma, Marina Ciullo, Georgia Chenevix-Trench, Francesco Cucca, Tõnu Esko, Christian Gieger, Struan F A Grant, Vilmundur G Gudnason, Caroline Hayward, Ivana Kolčić, Peter Kraft, Deborah A Lawlor, Nicholas G Martin, Ellen A Nøhr, Nancy L Pedersen, Craig E Pennell, Paul M Ridker, Antonietta Robino, Harold Snieder, Ulla Sovio, Timothy D Spector, Doris Stöckl, Cathie Sudlow, Nicholas John Timpson, Daniela Toniolo, Andre G Uitterlinden, Sheila Ulivi, Henry Völzke, Nicholas J Wareham, Elisabeth Widen, James F Wilson, null null, null null, null null, null null, null null, null null, Paul David Peter Pharoah, Liming Li, Douglas F Easton, Pal Rasmus Njolstad, Patrick Sulem, Joanne M Murabito, Anna Murray, Despoina Manousaki, Anders Juul, Christian Erikstrup, Kári Stefánsson, Momoko Horikoshi, Zhengming Chen, I Sadaf Farooqi, Nelly Pitteloud, Stefan E Johansson, Felix R Day, John R B Perry, Ken K Ong
Understanding the genetic complexity of puberty timing across the allele frequency spectrum. Nature genetics 56 (7) (2024)
Katherine A Kentistou, Lena R Kaisinger, Stasa Stankovic, Marc Vaudel, Edson Mendes de Oliveira, Andrea Messina, Robin G Walters, Xiaoxi Liu, Alexander S Busch, Hannes Helgason, Deborah J Thompson, Federico A Santoni, Konstantin M Petricek, Yassine Zouaghi, Isabel Huang-Doran, Daníel F Guðbjartsson, Eirik Bratland, Kuang Lin, Eugene J Gardner, Yajie Zhao, Raina Y Jia, Chikashi C Terao, Marjorie J Riggan, Manjeet K Bolla, Mojgan Yazdanpanah, Nahid Yazdanpanah, Jonathan P Bradfield, Linda Broer, Archie I Campbell, Daniel I Chasman, Diana L Cousminer, Nora Franceschini, Lude H Franke, Giorgia Girotto, Chunyan He, Marjo-Riitta Jarvelin, Peter K Joshi, Yoichiro Kamatani, Robert Karlsson, Jian'an Luan, Kathryn L Lunetta, Reedik Mägi, Massimo Mangino, Sarah E Medland, Christa Meisinger, Raymond Noordam, Teresa Nutile, Maria Pina Concas, Ozren Polašek, Eleonora Porcu, Susan M Ring, Cinzia Felicita Sala, Albert Vernon Smith, Toshiko Tanaka, Peter J van der Most, Veronique Vitart, Carol A Wang, Gonneke Willemsen, Marek Zygmunt, Thomas U Ahearn, Irene L Andrulis, Hoda Anton-Culver, Antonis C Antoniou, Paul L Auer, Catriona L K Barnes, Matthias W Beckmann, Amy Berrington de Gonzalez, Natalia V Bogdanova, Stig Egil Bojesen, Hermann Brenner, Julie E Buring, Federico Canzian, Jenny Chang-Claude, Fergus J Couch, Angela Cox, Laura Crisponi, Kamila Czene, Mary B Daly, Ellen W Demerath, Joe G Dennis, Peter Devilee, Immaculata De Vivo, Thilo Dörk, Alison M Dunning, Miriam V Dwek, Johan G Eriksson, Peter Andreas Fasching, Lindsay Fernández-Rhodes, Liana Ferreli, Olivia Fletcher, Manuela Gago-Dominguez, Montserrat Garcia-Closas, José Angel García-Saenz, Anna González-Neira, Harald Grallert, Pascal Guénel, Christopher A Haiman, Per Hall, Ute Hamann, Hakon H Hakonarson, Roger J Hart, Martha Hickey, Maartje J Hooning, Reiner Hoppe, John L Hopper, Jouke- Jan Hottenga, Frank B Hu, Hanna Huebner, David J Hunter, null null, Helena Jernström, Esther M John, David Karasik, Elza K Khusnutdinova, Vessela N Kristensen, James V Lacey, Diether Lambrechts, Lenore J Launer, Penelope A Lind, Annika Lindblom, Patrik K E Magnusson, Arto Mannermaa, Mark I McCarthy, Thomas Meitinger, Cristina Menni, Kyriaki Michailidou, Iona Y Millwood, Jonathan Beesley, Grant W Montgomery, Heli Nevanlinna, Ilja Maria Nolte, Dale R Nyholt, Nadia Obi, Katie M O'Brien, Kenneth Offit, Albertine J Oldehinkel, Sisse Rye Ostrowski, Aarno Palotie, Ole Birger Vesterager Pedersen, Annette Peters, Giulia Pianigiani, Dijana Plaseska-Karanfilska, Anneli Pouta, Alfred Pozarickij, Paolo Radice, Gadi Rennert, Frits Richard Rosendaal, Daniela Ruggiero, Emmanouil Saloustros, Dale R Sandler, Sabine Schipf, Carsten Oliver Schmidt, Marjanka K Schmidt, Kerrin S Small, Beatrice Spedicati, Meir Stampfer, Jennifer Stone, Rulla M Tamimi, Lauren R Teras, Emmi Tikkanen, Constance Turman, Celine M Vachon, Qin Wang, Robert Winqvist, Alicja Wolk, Babette S Zemel, Wei Zheng, Ko Willems van Dijk, Behrooz Z Alizadeh, Stefania Bandinelli, Eric Boerwinkle, Dorret I Boomsma, Marina Ciullo, Georgia Chenevix-Trench, Francesco Cucca, Tõnu Esko, Christian Gieger, Struan F A Grant, Vilmundur G Gudnason, Caroline Hayward, Ivana Kolčić, Peter Kraft, Deborah A Lawlor, Nicholas G Martin, Ellen A Nøhr, Nancy L Pedersen, Craig E Pennell, Paul M Ridker, Antonietta Robino, Harold Snieder, Ulla Sovio, Timothy D Spector, Doris Stöckl, Cathie Sudlow, Nicholas John Timpson, Daniela Toniolo, Andre G Uitterlinden, Sheila Ulivi, Henry Völzke, Nicholas J Wareham, Elisabeth Widen, James F Wilson, null null, null null, null null, null null, null null, null null, Paul David Peter Pharoah, Liming Li, Douglas F Easton, Pal Rasmus Njolstad, Patrick Sulem, Joanne M Murabito, Anna Murray, Despoina Manousaki, Anders Juul, Christian Erikstrup, Kári Stefánsson, Momoko Horikoshi, Zhengming Chen, I Sadaf Farooqi, Nelly Pitteloud, Stefan E Johansson, Felix R Day, John R B Perry, Ken K Ong
Understanding the genetic complexity of puberty timing across the allele frequency spectrum. Nature genetics 56 (7) (2024)
Olafur Andri Stefansson, Brynja Dogg Sigurpalsdottir, Solvi Rognvaldsson, Gisli Hreinn Halldorsson, Kristinn Juliusson, Gardar Sveinbjörnsson, Bjarni Gunnarsson, Doruk Beyter, Hákon Jónsson, Sigurjon Axel Gudjonsson, Thorunn Asta Olafsdottir, Saedis Saevarsdottir, Magnus Karl Magnusson, Sigrun Helga Lund, Vinicius Tragante, Asmundur Oddsson, Marteinn Thor Hardarson, Hannes Petur Eggertsson, Reynir L Gudmundsson, Sverrir Sverrisson, Michael L Frigge, Florian Zink, Hilma Hólm, Hreinn Stefansson, Thorunn Rafnar, Ingileif Jónsdóttir, Patrick Sulem, Agnar Helgason, Daníel F Guðbjartsson, Bjarni V Halldórsson, Unnur Thorsteinsdottir, Kári Stefánsson
The correlation between CpG methylation and gene expression is driven by sequence variants. Nature genetics 56 (8) (2024)
Thorunn Asta Olafsdottir, Gudmar Thorleifsson, Aitzkoa Lopez de Lapuente Portilla, Stefan Jonsson, Lilja Stefansdottir, Abhishek Niroula, Aslaug Jonasdottir, Hannes Petur Eggertsson, Gisli Hreinn Halldorsson, Gudny E Thorlacius, Asgeir O Arnthorsson, Unnur S Bjornsdottir, Folkert W. Asselbergs, Arthur E H Bentlage, Gudmundur I Eyjolfsson, Steinunn Gudmundsdottir, Kristbjorg Gunnarsdottir, Bjarni V Halldórsson, Hilma Hólm, Bjorn R Ludviksson, Pall Melsted, Gudmundur L Norddahl, Isleifur Olafsson, Saedis Saevarsdottir, Olof Sigurdardottir, Asgeir Sigurdsson, Robin Temming, Pall T Önundarson, Unnur Thorsteinsdottir, Gestur Vidarsson, Patrick Sulem, Daníel F Guðbjartsson, Ingileif Jónsdóttir, Björn Nilsson, Kári Stefánsson
Sequence variants influencing the regulation of serum IgG subclass levels. Nature communications 15 (1) (2024)
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)
Katherine A Kentistou, Lena R Kaisinger, Stasa Stankovic, Marc Vaudel, Edson Mendes de Oliveira, Andrea Messina, Robin G Walters, Xiaoxi Liu, Alexander S Busch, Hannes Helgason, Deborah J Thompson, Federico A Santoni, Konstantin M Petricek, Yassine Zouaghi, Isabel Huang-Doran, Daníel F Guðbjartsson, Eirik Bratland, Kuang Lin, Eugene J Gardner, Yajie Zhao, Raina Y Jia, Chikashi C Terao, Marjorie J Riggan, Manjeet K Bolla, Mojgan Yazdanpanah, Nahid Yazdanpanah, Jonathan P Bradfield, Linda Broer, Archie I Campbell, Daniel I Chasman, Diana L Cousminer, Nora Franceschini, Lude H Franke, Giorgia Girotto, Chunyan He, Marjo-Riitta Jarvelin, Peter K Joshi, Yoichiro Kamatani, Robert Karlsson, Jian'an Luan, Kathryn L Lunetta, Reedik Mägi, Massimo Mangino, Sarah E Medland, Christa Meisinger, Raymond Noordam, Teresa Nutile, Maria Pina Concas, Ozren Polašek, Eleonora Porcu, Susan M Ring, Cinzia Felicita Sala, Albert Vernon Smith, Toshiko Tanaka, Peter J van der Most, Veronique Vitart, Carol A Wang, Gonneke Willemsen, Marek Zygmunt, Thomas U Ahearn, Irene L Andrulis, Hoda Anton-Culver, Antonis C Antoniou, Paul L Auer, Catriona L K Barnes, Matthias W Beckmann, Amy Berrington de Gonzalez, Natalia V Bogdanova, Stig Egil Bojesen, Hermann Brenner, Julie E Buring, Federico Canzian, Jenny Chang-Claude, Fergus J Couch, Angela Cox, Laura Crisponi, Kamila Czene, Mary B Daly, Ellen W Demerath, Joe G Dennis, Peter Devilee, Immaculata De Vivo, Thilo Dörk, Alison M Dunning, Miriam V Dwek, Johan G Eriksson, Peter Andreas Fasching, Lindsay Fernández-Rhodes, Liana Ferreli, Olivia Fletcher, Manuela Gago-Dominguez, Montserrat Garcia-Closas, José Angel García-Saenz, Anna González-Neira, Harald Grallert, Pascal Guénel, Christopher A Haiman, Per Hall, Ute Hamann, Hakon H Hakonarson, Roger J Hart, Martha Hickey, Maartje J Hooning, Reiner Hoppe, John L Hopper, Jouke- Jan Hottenga, Frank B Hu, Hanna Huebner, David J Hunter, null null, Helena Jernström, Esther M John, David Karasik, Elza K Khusnutdinova, Vessela N Kristensen, James V Lacey, Diether Lambrechts, Lenore J Launer, Penelope A Lind, Annika Lindblom, Patrik K E Magnusson, Arto Mannermaa, Mark I McCarthy, Thomas Meitinger, Cristina Menni, Kyriaki Michailidou, Iona Y Millwood, Jonathan Beesley, Grant W Montgomery, Heli Nevanlinna, Ilja Maria Nolte, Dale R Nyholt, Nadia Obi, Katie M O'Brien, Kenneth Offit, Albertine J Oldehinkel, Sisse Rye Ostrowski, Aarno Palotie, Ole Birger Vesterager Pedersen, Annette Peters, Giulia Pianigiani, Dijana Plaseska-Karanfilska, Anneli Pouta, Alfred Pozarickij, Paolo Radice, Gadi Rennert, Frits Richard Rosendaal, Daniela Ruggiero, Emmanouil Saloustros, Dale R Sandler, Sabine Schipf, Carsten Oliver Schmidt, Marjanka K Schmidt, Kerrin S Small, Beatrice Spedicati, Meir Stampfer, Jennifer Stone, Rulla M Tamimi, Lauren R Teras, Emmi Tikkanen, Constance Turman, Celine M Vachon, Qin Wang, Robert Winqvist, Alicja Wolk, Babette S Zemel, Wei Zheng, Ko Willems van Dijk, Behrooz Z Alizadeh, Stefania Bandinelli, Eric Boerwinkle, Dorret I Boomsma, Marina Ciullo, Georgia Chenevix-Trench, Francesco Cucca, Tõnu Esko, Christian Gieger, Struan F A Grant, Vilmundur G Gudnason, Caroline Hayward, Ivana Kolčić, Peter Kraft, Deborah A Lawlor, Nicholas G Martin, Ellen A Nøhr, Nancy L Pedersen, Craig E Pennell, Paul M Ridker, Antonietta Robino, Harold Snieder, Ulla Sovio, Timothy D Spector, Doris Stöckl, Cathie Sudlow, Nicholas John Timpson, Daniela Toniolo, Andre G Uitterlinden, Sheila Ulivi, Henry Völzke, Nicholas J Wareham, Elisabeth Widen, James F Wilson, null null, null null, null null, null null, null null, null null, Paul David Peter Pharoah, Liming Li, Douglas F Easton, Pal Rasmus Njolstad, Patrick Sulem, Joanne M Murabito, Anna Murray, Despoina Manousaki, Anders Juul, Christian Erikstrup, Kári Stefánsson, Momoko Horikoshi, Zhengming Chen, I Sadaf Farooqi, Nelly Pitteloud, Stefan E Johansson, Felix R Day, John R B Perry, Ken K Ong
Understanding the genetic complexity of puberty timing across the allele frequency spectrum. Nature genetics 56 (7) (2024)
Anders Breinbjerg, Cecilie Siggaard Jørgensen, G Bragi Walters, Jakob Grove, Thomas Damm Als, Konstantinos Kamperis, Lilja Stéfansdóttir, Janne P Thirstrup, Britt Borg, Clara Albiñana, Bjarni Johann Vilhjalmsson, Viðar Ö Eðvarðsson, Hreinn Stefánsson, Preben Bo Mortensen, Esben Agerbo, Thomas M Werge, Anders Dupont Børglum, Ditte Demontis, Kári Stefánsson, Søren Rittig, Jane Hvarregaard Christensen
Exploring the Genetic Risk of Childhood Daytime Urinary Incontinence: A Genome-Wide Association Study. The Journal of urology (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)
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Understanding the genetic complexity of puberty timing across the allele frequency spectrum. Nature genetics 56 (7) (2024)
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Genome-wide analyses identify 21 infertility loci and over 400 reproductive hormone loci across the allele frequency spectrum. medRxiv : the preprint server for health sciences (2024)
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Start codon variant in LAG3 is associated with decreased LAG-3 expression and increased risk of autoimmune thyroid disease. Nature communications 15 (1) (2024)
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Start codon variant in LAG3 is associated with decreased LAG-3 expression and increased risk of autoimmune thyroid disease. Nature communications 15 (1) (2024)
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Variant in the synaptonemal complex protein SYCE2 associates with pregnancy loss through effect on recombination. Nature structural & molecular biology 31 (4) (2024)
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Understanding the genetic complexity of puberty timing across the allele frequency spectrum. Nature genetics 56 (7) (2024)
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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)
Markus Scholz, Katrin Horn, Janne Pott, Matthias Wuttke, Andreas Kühnapfel, M Kamal Nasr, Holger Kirsten, Yong Li, Anselm Hoppmann, Mathias Gorski, Sahar Ghasemi, Man Li, Adrienne Tin, Jin-Fang Chai, Massimiliano Cocca, Judy Wang, Teresa Nutile, Masato Akiyama, Bjørn Olav Åsvold, Nisha Bansal, Mary L Biggs, Thibaud Boutin, Hermann Brenner, Ben Michael Brumpton, Ralph Burkhardt, Jianwen Cai, Archie I Campbell, Harry Campbell, John Chalmers, Daniel I Chasman, Miao Ling Chee, Miao Li Chee, Xu Chen, Ching-Yu Cheng, Renata Cifkova, Martha Daviglus, Graciela Delgado, Katalin Dittrich, Todd L Edwards, Karlhans Endlich, J Michael Gaziano, Ayush Giri, Franco Giulianini, Scott D Gordon, Daniel F Gudbjartsson, Stein Hallan, Pavel Hamet, Catharina A Hartman, Caroline Hayward, Iris M Heid, Jacklyn N Hellwege, Bernd Holleczek, Hilma Hólm, Nina Hutri-Kähönen, Kristian Hveem, Berend Isermann, Jost Bruno Jonas, Peter K Joshi, Yoichiro Kamatani, Masahiro Kanai, Mika Kastarinen, Chiea Chuen Khor, Wieland Kiess, Marcus Edi Kleber, Antje Körner, Peter Kovacs, Alena Krajcoviechova, Holly J Kramer, Bernhard K Krämer, Mikko Kuokkanen, Mika Kähönen, Leslie A Lange, James P Lash, Terho Lehtimäki, Hengtong Li, Bridget M Lin, Jian-Jun Liu, Markus Loeffler, Leo-Pekka Lyytikainen, Patrik K E Magnusson, Nicholas G Martin, Koichi Matsuda, Yuri Milaneschi, Pashupati P Mishra, Nina Mononen, Grant W Montgomery, Dennis O Mook-Kanamori, Josyf C Mychaleckyi, Winfried März, Matthias Nauck, Kjell Nikus, Ilja Maria Nolte, Raymond Noordam, Yukinori Okada, Isleifur Olafsson, Albertine J Oldehinkel, Brenda W J H Penninx, Markus Perola, Nicola Pirastu, Ozren Polasek, David J Porteous, Tanja Poulain, Bruce M Psaty, Ton J Rabelink, Laura M Raffield, Olli T Raitakari, Humaira Rasheed, Dermot F Reilly, Kenneth M Rice, Anne Richmond, Paul M Ridker, Jerome I Rotter, Igor Rudan, Charumathi Sabanayagam, Veikko V Salomaa, Neil Schneiderman, Ben Schöttker, Mario Sims, Harold Snieder, Klaus J Stark, Kári Stefánsson, Hannah R Stocker, Michael Stumvoll, Patrick Sulem, Gardar Sveinbjornsson, Per O Svensson, E-Shyong Tai, Kent D Taylor, Bamidele O Tayo, Andrej Teren, Yih-Chung Tham, Joachim Thiery, Chris H L Thio, Laurent F Thomas, Johanne Tremblay, Anke Tönjes, Peter J van der Most, Veronique Vitart, Linus Völker, Ya-Xing Wang, Chaolong Wang, Wen Bin Wei, John B Whitfield, Sarah D Wild, James F Wilson, Thomas W Winkler, Tien-Yin Wong, Mark Woodward, Xueling S Sim, Audrey Y Chu, Mary F Feitosa, Unnur Thorsteinsdottir, Adriana M Hung, Alexander Teumer, Nora Franceschini, Afshin Parsa, Anna Kottgen, Pascal Schlosser, Cristian Pattaro
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The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions. Nature genetics 55 (3) (2023)
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The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions. Nature genetics 55 (3) (2023)
Ditte Demontis, G Bragi Walters, Georgios Athanasiadis, Raymond K Walters, Karen Therrien, Trine Tollerup Nielsen, Leila Farajzadeh, Georgios Voloudakis, Jaroslav Bendl, Biau Zeng, Wen Zhang, Jakob Grove, Thomas Damm Als, Jinjie Duan, F Kyle Satterstrom, Jonas Byberg-Grauholm, Marie Bækved-Hansen, Ólafur Ó Guðmundsson, Sigurður H Magnusson, Gisli Baldursson, Katrin Davidsdottir, Gyda S Haraldsdottir, Esben Agerbo, Gabriel E Hoffman, Søren Dalsgaard, Joanna Martin, Marta Ribases, Dorret I Boomsma, Artigas María Soler, Nina Roth Mota, Daniel P Howrigan, Sarah E Medland, Tetyana Zayats, Veera Manikandan Rajagopal, null null, null null, Merete Nordentoft, Ole Mors, David Michael Hougaard, Preben Bo Mortensen, Mark J Daly, Stephen V Faraone, Hreinn Stefansson, Panagiotis Roussos, Barbara Franke, Thomas M Werge, Benjamin M Neale, Kári Stefánsson, Anders Dupont Børglum
Author Correction: Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains. Nature genetics (2023)
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Author Correction: Genetic effects on the timing of parturition and links to fetal birth weight. Nature genetics (2023)
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Physical and cognitive impact following SARS-CoV-2 infection in a large population-based case-control study. Communications medicine 3 (1) (2023)
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Author Correction: Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains. Nature genetics (2023)
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Sequence variants affecting voice pitch in humans. Science advances 9 (23) (2023)
Elise A Lucotte, Valdís Björt Guðmundsdóttir, Jacob M Jensen, Laurits Skov, Moisès Coll Macià, Kristian Almstrup, Mikkel Heide Schierup, Agnar Helgason, Kári Stefánsson
Characterizing the evolution and phenotypic impact of ampliconic Y chromosome regions. Nature communications 14 (1) (2023)
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Genetic effects on the timing of parturition and links to fetal birth weight. Nature genetics (2023)
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Rare variants with large effects provide functional insights into the pathology of migraine subtypes, with and without aura. Nature genetics (2023)
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Genome-wide association meta-analysis identifies risk loci for abdominal aortic aneurysm and highlights PCSK9 as a therapeutic target. Nature genetics (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)
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The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions. Nature genetics 55 (3) (2023)
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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)
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)
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)
Krishna G Aragam, Tao Jiang, Anuj Goel, Stavroula Kanoni, Brooke N Wolford, Deepak S Atri, Elle M Weeks, Minxian Wang, George Hindy, Wei Zhou, Christopher Grace, Carolina Roselli, Nicholas A Marston, Frederick K Kamanu, Ida Surakka, Loreto Muñoz Venegas, Paul Sherliker, Satoshi Koyama, Kazuyoshi Ishigaki, Bjørn Olav Åsvold, Michael R Brown, Ben Michael Brumpton, Paul S de Vries, Olga Giannakopoulou, Panagiota Giardoglou, Daníel F Guðbjartsson, Ulrich Güldener, Syed M Ijlal Haider, Anna Helgadottir, Maysson Ibrahim, Adnan Kastrati, Thorsten Kessler, Theodosios Kyriakou, Tomasz Konopka, Ling Li, Lijiang Ma, Thomas Meitinger, Sören Mucha, Matthias Munz, Federico Murgia, Jonas B Nielsen, Markus M Nöthen, Shichao Pang, Tobias Reinberger, Gavin Schnitzler, Damian Smedley, Gudmar Thorleifsson, Moritz von Scheidt, Jacob C Ulirsch, null null, null null, David O Arnar, Noël P Burtt, Maria C Costanzo, Jason Flannick, Shefali S Verma, Dong-Keun Jang, Yoichiro Kamatani, Amit V Khera, Issei Komuro, Iftikhar J Kullo, Luca A Lotta, Christopher P Nelson, Robert Roberts, Gudmundur Thorgeirsson, Unnur Thorsteinsdottir, Thomas R Webb, Aris Baras, Johan L M Bjorkegren, Eric Boerwinkle, George Dedoussis, Hilma Hólm, Kristian Hveem, Olle Melander, Alanna C Morrison, Marju Orho-Melander, Loukianos S Rallidis, Arno Ruusalepp, Marc S Sabatine, Kári Stefánsson, Pierre Zalloua, Patrick T Ellinor, Martin Farrall, John Danesh, Christian T Ruff, Hilary K Finucane, Jemma C Hopewell, Robert J Clarke, Rajat M Gupta, Jeanette Erdmann, Nilesh J Samani, Heribert Schunkert, Hugh C Watkins, Cristen J Willer, Panos Deloukas, Sekar Kathiresan, Adam S Butterworth, null null
Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants. Nature genetics 54 (12) (2022)

Kári Stefánsson.css-eqlu8i{font-size:small;padding-left:4px;} (K Stefansson, Kari Stefansson)

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Kári Stefánsson (K Stefansson, Kari Stefansson)