OR15-2 Risk Variants at the MYO10 Locus are Associated with Metabolic Traits

por Chan, Yee Ming, Styrkarsdottir, Unnur, Welt, Corrine, Zhu, Jia, Battiola, Tess
Publicado 2022

The rate of meiotic gene conversion varies by sex and age

por Halldorsson, Bjarni V., Hardarson, Marteinn T., Kehr, Birte, Styrkarsdottir, Unnur, Gylfason, Arnaldur, Thorleifsson, Gudmar, Zink, Florian, Jonasdottir, Adalbjorg, Jonasdottir, Aslaug, Sulem, Patrick, Masson, Gisli, Thorsteinsdottir, Unnur, Helgason, Agnar, Kong, Augustine, Gudbjartsson, Daniel F., Stefansson, Kari
Publicado 2016

Sequence variation at ANAPC1 accounts for 24% of the variability in corneal endothelial cell density

por Ivarsdottir, Erna V., Benonisdottir, Stefania, Thorleifsson, Gudmar, Sulem, Patrick, Oddsson, Asmundur, Styrkarsdottir, Unnur, Kristmundsdottir, Snaedis, Arnadottir, Gudny A., Thorgeirsson, Gudmundur, Jonsdottir, Ingileif, Zoega, Gunnar M., Thorsteinsdottir, Unnur, Gudbjartsson, Daniel F., Jonasson, Fridbert, Holm, Hilma, Stefansson, Kari
Publicado 2019

Linkage of Osteoporosis to Chromosome 20p12 and Association to BMP2

por Styrkarsdottir, Unnur, Cazier, Jean-Baptiste, Kong, Augustine, Rolfsson, Ottar, Larsen, Helene, Bjarnadottir, Emma, Johannsdottir, Vala D, Sigurdardottir, Margret S, Bagger, Yu, Christiansen, Claus, Reynisdottir, Inga, Grant, Struan F. A, Jonasson, Kristjan, Frigge, Michael L, Gulcher, Jeffrey R, Sigurdsson, Gunnar, Stefansson, Kari
Publicado 2003

Genome-wide association of phenotypes based on clustering patterns of hand osteoarthritis identify WNT9A as novel osteoarthritis gene

por Boer, Cindy Germaine, Yau, Michelle S, Rice, Sarah J, Coutinho de Almeida, Rodrigo, Cheung, Kathleen, Styrkarsdottir, Unnur, Southam, Lorraine, Broer, Linda, Wilkinson, Jeremy Mark, Uitterlinden, André G, Zeggini, Eleftheria, Felson, David, Loughlin, John, Young, Mariel, Capellini, Terence Dante, Meulenbelt, Ingrid, van Meurs, Joyce BJ
Publicado 2021

The CRTAC1 Protein in Plasma Is Associated With Osteoarthritis and Predicts Progression to Joint Replacement: A Large‐Scale Proteomics Scan in Iceland

por Styrkarsdottir, Unnur, Lund, Sigrun H., Saevarsdottir, Saedis, Magnusson, Magnus I., Gunnarsdottir, Kristbjorg, Norddahl, Gudmundur L., Frigge, Michael L., Ivarsdottir, Erna V., Bjornsdottir, Gyda, Holm, Hilma, Thorgeirsson, Gudmundur, Rafnar, Thorunn, Jonsdottir, Ingileif, Ingvarsson, Thorvaldur, Jonsson, Helgi, Sulem, Patrick, Thorsteinsdottir, Unnur, Gudbjartsson, Daniel, Stefansson, Kari
Publicado 2021

Evaluation of shared genetic aetiology between osteoarthritis and bone mineral density identifies SMAD3 as a novel osteoarthritis risk locus

por Hackinger, Sophie, Trajanoska, Katerina, Styrkarsdottir, Unnur, Zengini, Eleni, Steinberg, Julia, Ritchie, Graham R.S., Hatzikotoulas, Konstantinos, Gilly, Arthur, Evangelou, Evangelos, Kemp, John P., Evans, David, Ingvarsson, Thorvaldur, Jonsson, Helgi, Thorsteinsdottir, Unnur, Stefansson, Kari, McCaskie, Andrew W., Brooks, Roger A., Wilkinson, Jeremy M., Rivadeneira, Fernando, Zeggini, Eleftheria
Publicado 2017

Meta-analysis of erosive hand osteoarthritis identifies four common variants that associate with relatively large effect

por Styrkarsdottir, Unnur, Stefansdottir, Lilja, Thorleifsson, Gudmar, Stefansson, Olafur A, Saevarsdottir, Saedis, Lund, Sigrun H, Rafnar, Thorunn, Hoshijima, Kazuyuki, Novak, Kendra, Oreiro, Natividad, Rego-Perez, Ignacio, Hansen, Channing, Kazmers, Nikolas, Kiemeney, Lambertus A, Blanco, Francisco J, Barker, Tyler, Kloppenburg, Margreet, Jurynec, Michael J, Gudbjartsson, Daniel F, Jonsson, Helgi, Thorsteinsdottir, Unnur, Stefansson, Kari
Publicado 2023

The DOT1L rs12982744 polymorphism is associated with osteoarthritis of the hip with genome-wide statistical significance in males

por Evangelou, Evangelos, Valdes, Ana M, Castano-Betancourt, Martha C, Doherty, M, Doherty, Sally, Esko, Tonu, Ingvarsson, Thorvaldur, Ioannidis, John P A, Kloppenburg, Margreet, Metspalu, Andres, Ntzani, Evangelia E, Panoutsopoulou, Kalliope, Slagboom, P Eline, Southam, Lorraine, Spector, Tim D, Styrkarsdottir, Unnur, Stefanson, Kari, Uitterlinden, André G, Wheeler, Margaret, Zeggini, Eleftheria, Meulenbelt, Ingrid, van Meurs, Joyce B
Publicado 2013

Sequence variant at 8q24.21 associates with sciatica caused by lumbar disc herniation

por Bjornsdottir, Gyda, Benonisdottir, Stefania, Sveinbjornsson, Gardar, Styrkarsdottir, Unnur, Thorleifsson, Gudmar, Walters, G. Bragi, Bjornsson, Aron, Olafsson, Ingvar H., Ulfarsson, Elfar, Vikingsson, Arnor, Hansdottir, Ragnheidur, Karlsson, Karl O., Rafnar, Thorunn, Jonsdottir, Ingileif, Frigge, Michael L., Kong, Augustine, Oddsson, Asmundur, Masson, Gisli, Magnusson, Olafur T., Gudbjartsson, Tomas, Stefansson, Hreinn, Sulem, Patrick, Gudbjartsson, Daniel, Thorsteinsdottir, Unnur, Thorgeirsson, Thorgeir E., Stefansson, Kari
Publicado 2017

Genome-wide analyses using UK Biobank data provide insights into the genetic architecture of osteoarthritis

por Zengini, Eleni, Hatzikotoulas, Konstantinos, Tachmazidou, Ioanna, Steinberg, Julia, Hartwig, Fernando P., Southam, Lorraine, Hackinger, Sophie, Boer, Cindy G., Styrkarsdottir, Unnur, Gilly, Arthur, Suveges, Daniel, Killian, Britt, Ingvarsson, Thorvaldur, Jonsson, Helgi, Babis, George C., McCaskie, Andrew, Uitterlinden, Andre G., van Meurs, Joyce B. J., Thorsteinsdottir, Unnur, Stefansson, Kari, Smith, George Davey, Wilkinson, Jeremy M., Zeggini, Eleftheria
Publicado 2018

Large Scale Replication Study of the Association between HLA Class II/BTNL2 Variants and Osteoarthritis of the Knee in European-Descent Populations

por Valdes, Ana M., Styrkarsdottir, Unnur, Doherty, Michael, Morris, David L., Mangino, Massimo, Tamm, Agu, Doherty, Sally A., Kisand, Kalle, Kerna, Irina, Tamm, Ann, Wheeler, Margaret, Maciewicz, Rose A., Zhang, Weiya, Muir, Kenneth R., Dennison, Elaine M., Hart, Deborah J., Metrustry, Sarah, Jonsdottir, Ingileif, Jonsson, Gudbjorn F., Jonsson, Helgi, Ingvarsson, Thorvaldur, Cooper, Cyrus, Vyse, Timothy J., Spector, Tim D., Stefansson, Kari, Arden, Nigel K.
Publicado 2011

Sequence variants in the PTCH1 gene associate with spine bone mineral density and osteoporotic fractures

por Styrkarsdottir, Unnur, Thorleifsson, Gudmar, Gudjonsson, Sigurjon A., Sigurdsson, Asgeir, Center, Jacqueline R., Lee, Seung Hun, Nguyen, Tuan V., Kwok, Timothy C.Y., Lee, Jenny S.W., Ho, Suzanne C., Woo, Jean, Leung, Ping-C., Kim, Beom-Jun, Rafnar, Thorunn, Kiemeney, Lambertus A., Ingvarsson, Thorvaldur, Koh, Jung-Min, Tang, Nelson L.S., Eisman, John A., Christiansen, Claus, Sigurdsson, Gunnar, Thorsteinsdottir, Unnur, Stefansson, Kari
Publicado 2016

MEPE loss-of-function variant associates with decreased bone mineral density and increased fracture risk

por Surakka, Ida, Fritsche, Lars G., Zhou, Wei, Backman, Joshua, Kosmicki, Jack A., Lu, Haocheng, Brumpton, Ben, Nielsen, Jonas B., Gabrielsen, Maiken E., Skogholt, Anne Heidi, Wolford, Brooke, Graham, Sarah E., Chen, Y. Eugene, Lee, Seunggeun, Kang, Hyun Min, Langhammer, Arnulf, Forsmo, Siri, Åsvold, Bjørn O., Styrkarsdottir, Unnur, Holm, Hilma, Gudbjartsson, Daniel, Stefansson, Kari, Baras, Aris, Abecasis, Goncalo R., Hveem, Kristian, Willer, Cristen J.
Publicado 2020

European Bone Mineral Density Loci Are Also Associated with BMD in East-Asian Populations

por Styrkarsdottir, Unnur, Halldorsson, Bjarni V., Gudbjartsson, Daniel F., Tang, Nelson L. S., Koh, Jung-Min, Xiao, Su-mei, Kwok, Timothy C. Y., Kim, Ghi Su, Chan, Juliana C. N., Cherny, Stacey, Lee, Seung Hun, Kwok, Anthony, Ho, Suzanne, Gretarsdottir, Solveig, Pop Kostic, Jelena, Palsson, Stefan Th., Sigurdsson, Gunnar, Sham, Pak C., Kim, Beom-Jun, Kung, Annie W. C., Kim, Shin-Yoon, Woo, Jean, Leung, Ping-C., Kong, Augustine, Thorsteinsdottir, Unnur, Stefansson, Kari
Publicado 2010

Causal mechanisms and balancing selection inferred from genetic associations with polycystic ovary syndrome

por Day, Felix R., Hinds, David A., Tung, Joyce Y., Stolk, Lisette, Styrkarsdottir, Unnur, Saxena, Richa, Bjonnes, Andrew, Broer, Linda, Dunger, David B., Halldorsson, Bjarni V., Lawlor, Debbie A., Laval, Guillaume, Mathieson, Iain, McCardle, Wendy L., Louwers, Yvonne, Meun, Cindy, Ring, Susan, Scott, Robert A., Sulem, Patrick, Uitterlinden, André G., Wareham, Nicholas J., Thorsteinsdottir, Unnur, Welt, Corrine, Stefansson, Kari, Laven, Joop S. E., Ong, Ken K., Perry, John R. B.
Publicado 2015

A PRPH splice-donor variant associates with reduced sural nerve amplitude and risk of peripheral neuropathy

por Bjornsdottir, Gyda, Ivarsdottir, Erna V., Bjarnadottir, Kristbjorg, Benonisdottir, Stefania, Gylfadottir, Sandra Sif, Arnadottir, Gudny A., Benediktsson, Rafn, Halldorsson, Gisli Hreinn, Helgadottir, Anna, Jonasdottir, Adalbjorg, Jonasdottir, Aslaug, Jonsdottir, Ingileif, Kristinsdottir, Anna Margret, Magnusson, Olafur Th., Masson, Gisli, Melsted, Pall, Rafnar, Thorunn, Sigurdsson, Asgeir, Sigurdsson, Gunnar, Skuladottir, Astros, Steinthorsdottir, Valgerdur, Styrkarsdottir, Unnur, Thorgeirsson, Gudmundur, Thorleifsson, Gudmar, Vikingsson, Arnor, Gudbjartsson, Daniel F., Holm, Hilma, Stefansson, Hreinn, Thorsteinsdottir, Unnur, Norddahl, Gudmundur L., Sulem, Patrick, Thorgeirsson, Thorgeir E., Stefansson, Kari
Publicado 2019

Genome-wide association identifies seven loci for pelvic organ prolapse in Iceland and the UK Biobank

por Olafsdottir, Thorhildur, Thorleifsson, Gudmar, Sulem, Patrick, Stefansson, Olafur A., Medek, Helga, Olafsson, Karl, Ingthorsson, Orri, Gudmundsson, Valur, Jonsdottir, Ingileif, Halldorsson, Gisli H., Kristjansson, Ragnar P., Frigge, Michael L., Stefansdottir, Lilja, Sigurdsson, Jon K., Oddsson, Asmundur, Sigurdsson, Asgeir, Eggertsson, Hannes P., Melsted, Pall, Halldorsson, Bjarni V., Lund, Sigrun H., Styrkarsdottir, Unnur, Steinthorsdottir, Valgerdur, Gudmundsson, Julius, Holm, Hilma, Tragante, Vinicius, Asselbergs, Folkert W., Thorsteinsdottir, Unnur, Gudbjartsson, Daniel F., Jonsdottir, Kristin, Rafnar, Thorunn, Stefansson, Kari
Publicado 2020

An atlas of genetic determinants of forearm fracture

por Nethander, Maria, Movérare-Skrtic, Sofia, Kämpe, Anders, Coward, Eivind, Reimann, Ene, Grahnemo, Louise, Borbély, Éva, Helyes, Zsuzsanna, Funck-Brentano, Thomas, Cohen-Solal, Martine, Tuukkanen, Juha, Koskela, Antti, Wu, Jianyao, Li, Lei, Lu, Tianyuan, Gabrielsen, Maiken E., Mägi, Reedik, Hoff, Mari, Lerner, Ulf H., Henning, Petra, Ullum, Henrik, Erikstrup, Christian, Brunak, Søren, Langhammer, Arnulf, Tuomi, Tiinamaija, Oddsson, Asmundur, Stefansson, Kari, Pettersson-Kymmer, Ulrika, Ostrowski, Sisse Rye, Pedersen, Ole Birger Vesterager, Styrkarsdottir, Unnur, Mäkitie, Outi, Hveem, Kristian, Richards, J. Brent, Ohlsson, Claes
Publicado 2023

Genome-Wide Meta-Analysis for Serum Calcium Identifies Significantly Associated SNPs near the Calcium-Sensing Receptor (CASR) Gene

por Kapur, Karen, Johnson, Toby, Beckmann, Noam D., Sehmi, Joban, Tanaka, Toshiko, Kutalik, Zoltán, Styrkarsdottir, Unnur, Zhang, Weihua, Marek, Diana, Gudbjartsson, Daniel F., Milaneschi, Yuri, Holm, Hilma, DiIorio, Angelo, Waterworth, Dawn, Li, Yun, Singleton, Andrew B., Bjornsdottir, Unnur S., Sigurdsson, Gunnar, Hernandez, Dena G., DeSilva, Ranil, Elliott, Paul, Eyjolfsson, Gudmundur I., Guralnik, Jack M., Scott, James, Thorsteinsdottir, Unnur, Bandinelli, Stefania, Chambers, John, Stefansson, Kari, Waeber, Gérard, Ferrucci, Luigi, Kooner, Jaspal S., Mooser, Vincent, Vollenweider, Peter, Beckmann, Jacques S., Bochud, Murielle, Bergmann, Sven
Publicado 2010