Unnur Styrkársdóttir (Unnur Styrkarsdottir)

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2014-2024
Publications (10 Years): 23

Top Venues

Nature communications

Nature genetics

Arthritis & rheumatology (Hoboken, N.J.)

Annals of the rheumatic diseases

deCODE genetics

University of Copenhagen (PHD)

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

Affiliation History

deCODE genetics Jan 01 1997

Iceland

Project leader :: Population genomics

Education History

University of Copenhagen

Denmark

PHD :: Genetic institute

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)
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)
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)
Unnur Styrkársdóttir, Lilja Stefansdottir, Gudmar Thorleifsson, Olafur A Stefansson, Saedis Saevarsdottir, Sigrun H Lund, Thorunn Rafnar, Kazuyuki Hoshijima, Kendra Novak, Natividad Oreiro, Ignacio Rego Perez, Channing Hansen, Nikolas Kazmers, Lambertus A Kiemeney, Francisco Javier Blanco, Tyler Barker, Margreet Kloppenburg, Michael J Jurynec, Daniel F Gudbjartsson, Helgi Jonsson, Unnur Thorsteinsdottir, Kari Stefansson
Meta-analysis of erosive hand osteoarthritis identifies four common variants that associate with relatively large effect. Annals of the rheumatic diseases (2023)
Carolina Medina-Gomez, Benjamin H Mullin, Alessandra Chesi, Vid Prijatelj, John P Kemp, Chen Shochat-Carvalho, Katerina Trajanoska, Carol Wang, Raimo Joro, Tavia E Evans, Katharina E Schraut, Ruifang Li-Gao, Tarunveer Singh Ahluwalia, M Carola Zillikens, Kun Zhu, Dennis O Mook-Kanamori, Daniel S Evans, Maria Nethander, Maria J Knol, Gudmar Thorleifsson, Ivana Prokic, Babette S Zemel, Linda Broer, Fiona E McGuigan, Natasja M van Schoor, Sjur Reppe, Mikolaj A Pawlak, Stuart H Ralston, Nathalie van der Velde, Mattias Lorentzon, Kari Stefansson, Hieab H H Adams, Scott G Wilson, Mohammad Arfan Ikram, John P Walsh, Timo A Lakka, Kaare M Gautvik, James F Wilson, Eric S Orwoll, Cornelia M Van Duijn, Klaus Bønnelykke, Andre G Uitterlinden, Unnur Styrkársdóttir, Kristina E Akesson, Timothy D Spector, Jonathan H Tobias, Claes Ohlsson, Janine F Felix, Hans Bisgaard, Struan F A Grant, John Brent Richards, David M Evans, Bram C J van der Eerden, Jeroen van de Peppel, Cheryl L Ackert-Bicknell, David Karasik, Erika Kague, Fernando Rivadeneira
Bone mineral density loci specific to the skull portray potential pleiotropic effects on craniosynostosis. Communications biology 6 (1) (2023)
Cecilie Henkel, Unnur Styrkársdóttir, Gudmar Thorleifsson, Lilja Stefánsdóttir, Gyda Björnsdóttir, Karina Banasik, Søren Brunak, Christian Erikstrup, Khoa Manh Dinh, Thomas Folkmann Hansen, Kaspar René Nielsen, Mie Topholm Bruun, Joseph Dowsett, Thorsten Brodersen, null null, Thorgeir E Thorgeirsson, Kirill Gromov, Mikael Ploug Boesen, Henrik Ullum, Sisse Rye Ostrowski, Ole Birger Pedersen, Kári Stefánsson, Anders Troelsen
Genome-wide association meta-analysis of knee and hip osteoarthritis uncovers genetic differences between patients treated with joint replacement and patients without joint replacement. Annals of the rheumatic diseases (2022)
Unnur Styrkársdóttir, Sigrun H Lund, Gudmar Thorleifsson, Saedis Saevarsdottir, Daniel F Gudbjartsson, Unnur Thorsteinsdottir, Kari Stefansson
The CRTAC1 protein in plasma associates with prevalent osteoarthritis and predicts future risk as well as progression to joint replacements - Results from the UK Biobank resource. Arthritis & rheumatology (Hoboken, N.J.) (2022)
Bjarni V Halldórsson, Hannes Petur Eggertsson, Kristjan H S Moore, Hannes Hauswedell, Ogmundur Eiriksson, Magnus O Ulfarsson, Gunnar Pálsson, Marteinn T Hardarson, Asmundur Oddsson, Brynjar Orn Jensson, Snaedis Kristmundsdottir, Brynja D Sigurpalsdottir, Olafur Andri Stefansson, Doruk Beyter, Guillaume Holley, Vinicius Tragante, Arnaldur Gylfason, Pall I Olason, Florian Zink, Margret Asgeirsdottir, Sverrir T Sverrisson, Brynjar Sigurdsson, Sigurjon A Gudjonsson, Gunnar T Sigurdsson, Gisli Hreinn Halldorsson, Gardar Sveinbjornsson, Kristjan Norland, Unnur Styrkársdóttir, Droplaug N Magnusdottir, Steinunn Snorradottir, Kari Kristinsson, Emilia Sobech, Helgi Jonsson, Arni J Geirsson, Isleifur Olafsson, Palmi Jonsson, Ole Birger Vesterager Pedersen, Christian Erikstrup, Soren Brunak, Sisse Rye Ostrowski, null null, Gudmar Thorleifsson, Frosti Jonsson, Pall Melsted, Ingileif Jónsdóttir, Thorunn Rafnar, Hilma Hólm, Hreinn Stefansson, Jona Saemundsdottir, Daníel F Guðbjartsson, Olafur T Magnusson, Gisli Masson, Unnur Thorsteinsdottir, Agnar Helgason, Hákon Jónsson, Patrick Sulem, Kari Stefansson
The sequences of 150,119 genomes in the UK Biobank. Nature 607 (7920) (2022)
Gyda Bjornsdottir, Lilja Stefansdottir, Gudmar Thorleifsson, Patrick Sulem, Kristjan Norland, Egil Ferkingstad, Asmundur Oddsson, Florian Zink, Sigrun H Lund, Muhammad Sulaman Nawaz, G Bragi Walters, Astros Th Skuladottir, Sigurjon A Gudjonsson, Gudmundur Einarsson, Gisli Hreinn Halldorsson, Valgerdur Bjarnadottir, Gardar Sveinbjornsson, Anna Helgadottir, Unnur Styrkársdóttir, Larus J Gudmundsson, Ole Birger Vesterager Pedersen, Thomas Folkmann Hansen, Thomas M Werge, Karina Banasik, Anders Troelsen, Søren Thorgaard Skou, Lise Wegner Thørner, Christian Erikstrup, Kaspar Rene Nielsen, Susan Mikkelsen, null null, null null, Ingileif Jónsdóttir, Aron Bjornsson, Ingvar H Olafsson, Elfar Ulfarsson, Josep Blondal, Arnor Vikingsson, Soren Brunak, Sisse Rye Ostrowski, Henrik Ullum, Unnur Thorsteinsdottir, Hreinn Stefánsson, Daníel F Guðbjartsson, Thorgeir E Thorgeirsson, Kári Stefánsson
Rare SLC13A1 variants associate with intervertebral disc disorder highlighting role of sulfate in disc pathology. Nature communications 13 (1) (2022)
Gyda Bjornsdottir, Lilja Stefansdottir, Gudmar Thorleifsson, Patrick Sulem, Kristjan Norland, Egil Ferkingstad, Asmundur Oddsson, Florian Zink, Sigrun H Lund, Muhammad Sulaman Nawaz, G Bragi Walters, Astros Th Skuladottir, Sigurjon A Gudjonsson, Gudmundur Einarsson, Gisli Hreinn Halldorsson, Valgerdur Bjarnadottir, Gardar Sveinbjornsson, Anna Helgadottir, Unnur Styrkársdóttir, Larus J Gudmundsson, Ole Birger Vesterager Pedersen, Thomas Folkmann Hansen, Thomas M Werge, Karina Banasik, Anders Troelsen, Søren Thorgaard Skou, Lise Wegner Thørner, Christian Erikstrup, Kaspar Rene Nielsen, Susan Mikkelsen, null null, null null, Ingileif Jónsdóttir, Aron Bjornsson, Ingvar H Olafsson, Elfar Ulfarsson, Josep Blondal, Arnor Vikingsson, Soren Brunak, Sisse Rye Ostrowski, Henrik Ullum, Unnur Thorsteinsdottir, Hreinn Stefánsson, Daníel F Guðbjartsson, Thorgeir E Thorgeirsson, Kári Stefánsson
Author Correction: Rare SLC13A1 variants associate with intervertebral disc disorder highlighting role of sulfate in disc pathology. Nature communications 13 (1) (2022)
Unnur Styrkársdóttir, Sigrun H Lund, Saedis Saevarsdottir, Magnus I Magnusson, Kristbjorg Gunnarsdottir, Gudmundur L Norddahl, Michael L Frigge, Erna V Ivarsdottir, Gyda Bjornsdottir, Hilma Holm, Gudmundur Thorgeirsson, Thorunn Rafnar, Ingileif Jonsdottir, Thorvaldur Ingvarsson, Helgi Jonsson, Patrick Sulem, Unnur Thorsteinsdottir, Daniel Gudbjartsson, Kári Stefánsson
The CRTAC1 Protein in Plasma Is Associated With Osteoarthritis and Predicts Progression to Joint Replacement: A Large-Scale Proteomics Scan in Iceland. Arthritis & rheumatology (Hoboken, N.J.) 73 (11) (2021)
Ida Surakka, Lars G Fritsche, Wei Zhou, Joshua Backman, Jack A Kosmicki, Haocheng Lu, Ben Brumpton, Jonas Bille Nielsen, Maiken E Gabrielsen, Anne Heidi Skogholt, Brooke N Wolford, Sarah E Graham, Y Eugene Chen, Seunggeun Lee, Hyun Min Kang, Arnulf Langhammer, Siri Forsmo, Bjørn Olav Åsvold, Unnur Styrkársdóttir, Hilma Hólm, Daníel F Guðbjartsson, Kari Stefansson, Aris Baras, null null, Goncalo R Abecasis, Kristian Hveem, Cristen J Willer
MEPE loss-of-function variant associates with decreased bone mineral density and increased fracture risk. Nature communications 11 (1) (2020)
Unnur Styrkársdóttir, Olafur A Stefansson, Kristbjorg Gunnarsdottir, Gudmar Thorleifsson, Sigrun H Lund, Lilja Stefansdottir, Kristinn Juliusson, Arna B Agustsdottir, Florian Zink, Gisli Hreinn Halldorsson, Erna V Ivarsdottir, Stefania Benonisdottir, Hákon Jónsson, Arnaldur Gylfason, Kristjan Norland, Katerina Trajanoska, Cindy Germaine Boer, Lorraine Southam, Jason C S Leung, Nelson Leung-Sang Tang, Timothy C Y Kwok, Jenny S W Lee, Suzanne C Ho, Inger Byrjalsen, Jacqueline R Center, Seung Hun Lee, Jung-Min Koh, L Stefan Lohmander, Lan T Ho-Pham, Tuan V Nguyen, John A Eisman, Jean Woo, Ping-C Leung, John Loughlin, Eleftheria Zeggini, Claus Christiansen, Fernando Rivadeneira, Joyce van Meurs, Andre G Uitterlinden, Brynjolfur Mogensen, Helgi Jonsson, Thorvaldur Ingvarsson, Gunnar Sigurdsson, Rafn Benediktsson, Patrick Sulem, Ingileif Jonsdottir, Gisli Masson, Hilma Holm, Gudmundur L Norddahl, Unnur Thorsteinsdottir, Daníel F Guðbjartsson, Kári Stefánsson
Publisher Correction: GWAS of bone size yields twelve loci that also affect height, BMD, osteoarthritis or fractures. Nature communications 10 (1) (2019)
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)
Unnur Styrkársdóttir, Olafur A Stefansson, Kristbjorg Gunnarsdottir, Gudmar Thorleifsson, Sigrun H Lund, Lilja Stefansdottir, Kristinn Juliusson, Arna B Agustsdottir, Florian Zink, Gisli Hreinn Halldorsson, Erna V Ivarsdottir, Stefania Benonisdottir, Hákon Jónsson, Arnaldur Gylfason, Kristjan Norland, Katerina Trajanoska, Cindy Germaine Boer, Lorraine Southam, Jason C S Leung, Nelson Leung-Sang Tang, Timothy C Y Kwok, Jenny S W Lee, Suzanne C Ho, Inger Byrjalsen, Jacqueline R Center, Seung Hun Lee, Jung-Min Koh, L Stefan Lohmander, Lan T Ho-Pham, Tuan V Nguyen, John A Eisman, Jean Woo, Ping-C Leung, John Loughlin, Eleftheria Zeggini, Claus Christiansen, Fernando Rivadeneira, Joyce van Meurs, Andre G Uitterlinden, Brynjolfur Mogensen, Helgi Jonsson, Thorvaldur Ingvarsson, Gunnar Sigurdsson, Rafn Benediktsson, Patrick Sulem, Ingileif Jonsdottir, Gisli Masson, Hilma Holm, Gudmundur L Norddahl, Unnur Thorsteinsdottir, Daníel F Guðbjartsson, Kári Stefánsson
GWAS of bone size yields twelve loci that also affect height, BMD, osteoarthritis or fractures. Nature communications 10 (1) (2019)
Thorunn Rafnar, Bjarni Gunnarsson, Olafur A Stefansson, Patrick Sulem, Andres Ingason, Michael L Frigge, Lilja Stefansdottir, Jon K Sigurdsson, Vinicius Tragante, Valgerdur Steinthorsdottir, Unnur Styrkársdóttir, Simon N Stacey, Julius Gudmundsson, Gudny Anna Arnadottir, Asmundur Oddsson, Florian Zink, Gisli Hreinn Halldorsson, Gardar Sveinbjornsson, Ragnar P Kristjansson, Olafur B Davidsson, Anna Salvarsdottir, Asgeir Thoroddsen, Elisabet A Helgadottir, Katrin Kristjansdottir, Orri Ingthorsson, Valur Gudmundsson, Reynir T Geirsson, Ragnheidur Arnadottir, Daníel F Guðbjartsson, Gisli Masson, Folkert W Asselbergs, Jon G Jonasson, Karl Olafsson, Unnur Thorsteinsdottir, Bjarni V Halldórsson, Gudmar Thorleifsson, Kari Stefansson
Variants associating with uterine leiomyoma highlight genetic background shared by various cancers and hormone-related traits. Nature communications 9 (1) (2018)
Eleni Zengini, Konstantinos Hatzikotoulas, Ioanna Tachmazidou, Julia Steinberg, Fernando Pires Hartwig, Lorraine Southam, Sophie Hackinger, Cindy Germaine Boer, Unnur Styrkársdóttir, Arthur Gilly, Daniel Suveges, Britt Killian, Thorvaldur Ingvarsson, Helgi Jonsson, George C Babis, Andrew McCaskie, Andre G Uitterlinden, Joyce B J van Meurs, Unnur Thorsteinsdottir, Kari Stefansson, George Davey Smith, Jeremy Mark Wilkinson, Eleftheria Zeggini
Genome-wide analyses using UK Biobank data provide insights into the genetic architecture of osteoarthritis. Nature genetics 50 (4) (2018)
Unnur Styrkársdóttir, Sigrun Helga Lund, Gudmar Thorleifsson, Florian Zink, Olafur A Stefansson, Jon K Sigurdsson, Kristinn Juliusson, Kristbjörg Bjarnadottir, Sara Sigurbjornsdottir, Stefan Jonsson, Kristjan Norland, Lilja Stefansdottir, Asgeir Sigurdsson, Gardar Sveinbjornsson, Asmundur Oddsson, Gyda Bjornsdottir, Reynir L Gudmundsson, Gisli Hreinn Halldorsson, Thorunn Rafnar, Ingileif Jónsdóttir, Eirikur Steingrimsson, Gudmundur L Norddahl, Gisli Masson, Patrick Sulem, Helgi Jonsson, Thorvaldur Ingvarsson, Daníel F Guðbjartsson, Unnur Thorsteinsdottir, Kári Stefánsson
Meta-analysis of Icelandic and UK data sets identifies missense variants in SMO, IL11, COL11A1 and 13 more new loci associated with osteoarthritis. Nature genetics 50 (12) (2018)
Felix R Day, Tugce Karaderi, Michelle R Jones, Cindy Meun, Chunyan He, Alex Drong, Peter Kraft, Nan Lin, Hongyan Huang, Linda Broer, Reedik Magi, Richa Saxena, Triin Laisk, Margrit Urbanek, M Geoffrey Hayes, Gudmar Thorleifsson, Juan Fernandez-Tajes, Anubha Mahajan, Benjamin H Mullin, Bronwyn G A Stuckey, Timothy D Spector, Scott G Wilson, Mark O Goodarzi, Lea Davis, Barbara Obermayer-Pietsch, André G Uitterlinden, Verneri Anttila, Benjamin M Neale, Marjo-Riitta Jarvelin, Bart Fauser, Irina Kowalska, Jenny A Visser, Marianne Andersen, Ken K Ong, Elisabet Stener-Victorin, David Ehrmann, Richard S Legro, Andres Salumets, Mark I McCarthy, Laure Morin-Papunen, Unnur Thorsteinsdottir, Kari Stefansson, null null, Unnur Styrkársdóttir, John R B Perry, Andrea Dunaif, Joop Laven, Steve Franks, Cecilia M Lindgren, Corrine K Welt
Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria. PLoS genetics 14 (12) (2018)
Gyda Bjornsdottir, Stefania Benonisdottir, Gardar Sveinbjornsson, Unnur Styrkársdóttir, Gudmar Thorleifsson, G Bragi Walters, Aron Bjornsson, Ingvar H Olafsson, Elfar Ulfarsson, Arnor Vikingsson, Ragnheidur Hansdottir, Karl O Karlsson, Thorunn Rafnar, Ingileif Jonsdottir, Michael L Frigge, Augustine Kong, Asmundur Oddsson, Gisli Masson, Olafur T Magnusson, Tomas Gudbjartsson, Hreinn Stefansson, Patrick Sulem, Daníel F Guðbjartsson, Unnur Thorsteinsdottir, Thorgeir E Thorgeirsson, Kari Stefansson
Sequence variant at 8q24.21 associates with sciatica caused by lumbar disc herniation. Nature communications 8 (2017)
Unnur Styrkársdóttir, Hannes Helgason, Asgeir Sigurdsson, Gudmundur L Norddahl, Arna B Agustsdottir, Louise N Reynard, Amanda Villalvilla, Gisli H Halldorsson, Aslaug Jonasdottir, Audur Magnusdottir, Asmundur Oddsson, Gerald Sulem, Florian Zink, Gardar Sveinbjornsson, Agnar Helgason, Hrefna S Johannsdottir, Anna Helgadottir, Hreinn Stefansson, Solveig Gretarsdottir, Thorunn Rafnar, Ina S Almdahl, Anne Brækhus, Tormod Fladby, Geir Selbæk, Farhad Hosseinpanah, Fereidoun Azizi, Jung Min Koh, Nelson Leung-Sang Tang, Maryam S Daneshpour, Jose I Mayordomo, Corrine Welt, Peter S Braund, Nilesh J Samani, Lambertus A Kiemeney, L Stefan Lohmander, Claus Christiansen, Ole Andreas Andreassen, null null, Olafur Magnusson, Gisli Masson, Augustine Kong, Ingileif Jónsdóttir, Daníel F Guðbjartsson, Patrick Sulem, Helgi Jonsson, John Loughlin, Thorvaldur Ingvarsson, Unnur Thorsteinsdottir, Kari Stefansson
Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritis. Nature genetics 49 (5) (2017)
Felix R Day, David A Hinds, Joyce Y Tung, Lisette Stolk, Unnur Styrkársdóttir, Richa Saxena, Andrew Bjonnes, Linda Broer, Professor David Dunger, Bjarni V Halldorsson, Debbie A Lawlor, Guillaume Laval, Iain Mathieson, Wendy L McCardle, Yvonne Louwers, Cindy Meun, Susan Ring, Robert A Scott, Patrick Sulem, André G Uitterlinden, Nicholas J Wareham, Unnur Thorsteinsdottir, Corrine Welt, Kari Stefansson, Joop S E Laven, Ken K Ong, John R B Perry
Causal mechanisms and balancing selection inferred from genetic associations with polycystic ovary syndrome. Nature communications 6 (2015)
Unnur Styrkársdóttir, Gudmar Thorleifsson, Hafdis T Helgadottir, Nils Bomer, Sarah Metrustry, S Bierma-Zeinstra, Annelieke M Strijbosch, Evangelos Evangelou, Deborah Hart, Marian Beekman, Aslaug Jonasdottir, Asgeir Sigurdsson, Finnur F Eiriksson, Margret Thorsteinsdottir, Michael L Frigge, Augustine Kong, Sigurjon A Gudjonsson, Olafur T Magnusson, Gisli Masson, null null, null null, Albert Hofman, Nigel K Arden, Thorvaldur Ingvarsson, Stefan Lohmander, Margreet Kloppenburg, Fernando Rivadeneira, Rob G H H Nelissen, Tim Spector, Andre Uitterlinden, P Eline Slagboom, Unnur Thorsteinsdottir, Ingileif Jonsdottir, Ana M Valdes, Ingrid Meulenbelt, Joyce van Meurs, Helgi Jonsson, Kari Stefansson
Severe osteoarthritis of the hand associates with common variants within the ALDH1A2 gene and with rare variants at 1p31. Nature genetics 46 (5) (2014)

Unnur Styrkársdóttir.css-eqlu8i{font-size:small;padding-left:4px;} (Unnur Styrkarsdottir)

Publication Activity (10 Years)

Top Topics

Top Venues

Unnur Styrkársdóttir (Unnur Styrkarsdottir)