Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Kristjan H S, Moore"'
Autor:
Saedis Saevarsdottir, Kristbjörg Bjarnadottir, Thorsteinn Markusson, Jonas Berglund, Thorunn A. Olafsdottir, Gisli H. Halldorsson, Gudrun Rutsdottir, Kristbjorg Gunnarsdottir, Asgeir Orn Arnthorsson, Sigrun H. Lund, Lilja Stefansdottir, Julius Gudmundsson, Ari J. Johannesson, Arni Sturluson, Asmundur Oddsson, Bjarni Halldorsson, Björn R. Ludviksson, Egil Ferkingstad, Erna V. Ivarsdottir, Gardar Sveinbjornsson, Gerdur Grondal, Gisli Masson, Grimur Hjorleifsson Eldjarn, Gudmundur A. Thorisson, Katla Kristjansdottir, Kirk U. Knowlton, Kristjan H. S. Moore, Sigurjon A. Gudjonsson, Solvi Rognvaldsson, Stacey Knight, Lincoln D. Nadauld, Hilma Holm, Olafur T. Magnusson, Patrick Sulem, Daniel F. Gudbjartsson, Thorunn Rafnar, Gudmar Thorleifsson, Pall Melsted, Gudmundur L. Norddahl, Ingileif Jonsdottir, Kari Stefansson
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-12 (2024)
Abstract Autoimmune thyroid disease (AITD) is a common autoimmune disease. In a GWAS meta-analysis of 110,945 cases and 1,084,290 controls, 290 sequence variants at 225 loci are associated with AITD. Of these variants, 115 are previously unreported.
Externí odkaz:
https://doaj.org/article/6749a49ac9b842aa843a6662930b9531
Autor:
Asmundur Oddsson, Patrick Sulem, Gardar Sveinbjornsson, Gudny A. Arnadottir, Valgerdur Steinthorsdottir, Gisli H. Halldorsson, Bjarni A. Atlason, Gudjon R. Oskarsson, Hannes Helgason, Henriette Svarre Nielsen, David Westergaard, Juha M. Karjalainen, Hildigunnur Katrinardottir, Run Fridriksdottir, Brynjar O. Jensson, Vinicius Tragante, Egil Ferkingstad, Hakon Jonsson, Sigurjon A. Gudjonsson, Doruk Beyter, Kristjan H. S. 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 A. Olafsdottir, Geir Selbaek, Mette Nyegaard, Christian Erikstrup, Thorsten Brodersen, Saedis Saevarsdottir, Tomas Olsson, Kaspar Rene Nielsen, Asgeir Haraldsson, Mie Topholm Bruun, Thomas Folkmann Hansen, DBDS Genomic Consortium, Thora Steingrimsdottir, Rikke Louise Jacobsen, Rolv T. Lie, Srdjan Djurovic, Lars Alfredsson, Aitzkoa Lopez de Lapuente Portilla, Soren Brunak, Pall Melsted, Bjarni V. Halldorsson, Jona Saemundsdottir, Olafur Th. Magnusson, Leonid Padyukov, Karina Banasik, Thorunn Rafnar, Johan Askling, Lars Klareskog, Ole Birger Pedersen, Gisli Masson, Alexandra Havdahl, Bjorn Nilsson, Ole A. Andreassen, Mark Daly, Sisse Rye Ostrowski, Ingileif Jonsdottir, Hreinn Stefansson, Hilma Holm, Agnar Helgason, Unnur Thorsteinsdottir, Kari Stefansson, Daniel F. Gudbjartsson
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-15 (2023)
Abstract Genotypes causing pregnancy loss and perinatal mortality are depleted among living individuals and are therefore difficult to find. To explore genetic causes of recessive lethality, we searched for sequence variants with deficit of homozygos
Externí odkaz:
https://doaj.org/article/a4fa595277a74ef2949c5d74d9c4032d
Autor:
Asmundur Oddsson, Patrick Sulem, Gardar Sveinbjornsson, Gudny A. Arnadottir, Valgerdur Steinthorsdottir, Gisli H. Halldorsson, Bjarni A. Atlason, Gudjon R. Oskarsson, Hannes Helgason, Henriette Svarre Nielsen, David Westergaard, Juha M. Karjalainen, Hildigunnur Katrinardottir, Run Fridriksdottir, Brynjar O. Jensson, Vinicius Tragante, Egil Ferkingstad, Hakon Jonsson, Sigurjon A. Gudjonsson, Doruk Beyter, Kristjan H. S. 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 A. Olafsdottir, Geir Selbaek, Mette Nyegaard, Christian Erikstrup, Thorsten Brodersen, Saedis Saevarsdottir, Tomas Olsson, Kaspar Rene Nielsen, Asgeir Haraldsson, Mie Topholm Bruun, Thomas Folkmann Hansen, DBDS Genomic Consortium, Thora Steingrimsdottir, Rikke Louise Jacobsen, Rolv T. Lie, Srdjan Djurovic, Lars Alfredsson, Aitzkoa Lopez de Lapuente Portilla, Soren Brunak, Pall Melsted, Bjarni V. Halldorsson, Jona Saemundsdottir, Olafur Th. Magnusson, Leonid Padyukov, Karina Banasik, Thorunn Rafnar, Johan Askling, Lars Klareskog, Ole Birger Pedersen, Gisli Masson, Alexandra Havdahl, Bjorn Nilsson, Ole A. Andreassen, Mark Daly, Sisse Rye Ostrowski, Ingileif Jonsdottir, Hreinn Stefansson, Hilma Holm, Agnar Helgason, Unnur Thorsteinsdottir, Kari Stefansson, Daniel F. Gudbjartsson
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-1 (2023)
Externí odkaz:
https://doaj.org/article/5f67c08c01ba468598a7f011b98dd4d8
Autor:
David W Clark, Yukinori Okada, Kristjan H S Moore, Dan Mason, Nicola Pirastu, Ilaria Gandin, Hannele Mattsson, Catriona L K Barnes, Kuang Lin, Jing Hua Zhao, Patrick Deelen, Rebecca Rohde, Claudia Schurmann, Xiuqing Guo, Franco Giulianini, Weihua Zhang, Carolina Medina-Gomez, Robert Karlsson, Yanchun Bao, Traci M Bartz, Clemens Baumbach, Ginevra Biino, Matthew J Bixley, Marco Brumat, Jin-Fang Chai, Tanguy Corre, Diana L Cousminer, Annelot M Dekker, David A Eccles, Kristel R van Eijk, Christian Fuchsberger, He Gao, Marine Germain, Scott D Gordon, Hugoline G de Haan, Sarah E Harris, Edith Hofer, Alicia Huerta-Chagoya, Catherine Igartua, Iris E Jansen, Yucheng Jia, Tim Kacprowski, Torgny Karlsson, Marcus E Kleber, Shengchao Alfred Li, Ruifang Li-Gao, Anubha Mahajan, Koichi Matsuda, Karina Meidtner, Weihua Meng, May E Montasser, Peter J van der Most, Matthias Munz, Teresa Nutile, Teemu Palviainen, Gauri Prasad, Rashmi B Prasad, Tallapragada Divya Sri Priyanka, Federica Rizzi, Erika Salvi, Bishwa R Sapkota, Daniel Shriner, Line Skotte, Melissa C Smart, Albert Vernon Smith, Ashley van der Spek, Cassandra N Spracklen, Rona J Strawbridge, Salman M Tajuddin, Stella Trompet, Constance Turman, Niek Verweij, Clara Viberti, Lihua Wang, Helen R Warren, Robyn E Wootton, Lisa R Yanek, Jie Yao, Noha A Yousri, Wei Zhao, Adebowale A Adeyemo, Saima Afaq, Carlos Alberto Aguilar-Salinas, Masato Akiyama, Matthew L Albert, Matthew A Allison, Maris Alver, Tin Aung, Fereidoun Azizi, Amy R Bentley, Heiner Boeing, Eric Boerwinkle, Judith B Borja, Gert J de Borst, Erwin P Bottinger, Linda Broer, Harry Campbell, Stephen Chanock, Miao-Li Chee, Guanjie Chen, Yii-Der I Chen, Zhengming Chen, Yen-Feng Chiu, Massimiliano Cocca, Francis S Collins, Maria Pina Concas, Janie Corley, Giovanni Cugliari, Rob M van Dam, Anna Damulina, Maryam S Daneshpour, Felix R Day, Graciela E Delgado, Klodian Dhana, Alexander S F Doney, Marcus Dörr, Ayo P Doumatey, Nduna Dzimiri, S Sunna Ebenesersdóttir, Joshua Elliott, Paul Elliott, Ralf Ewert, Janine F Felix, Krista Fischer, Barry I Freedman, Giorgia Girotto, Anuj Goel, Martin Gögele, Mark O Goodarzi, Mariaelisa Graff, Einat Granot-Hershkovitz, Francine Grodstein, Simonetta Guarrera, Daniel F Gudbjartsson, Kamran Guity, Bjarni Gunnarsson, Yu Guo, Saskia P Hagenaars, Christopher A Haiman, Avner Halevy, Tamara B Harris, Mehdi Hedayati, David A van Heel, Makoto Hirata, Imo Höfer, Chao Agnes Hsiung, Jinyan Huang, Yi-Jen Hung, M Arfan Ikram, Anuradha Jagadeesan, Pekka Jousilahti, Yoichiro Kamatani, Masahiro Kanai, Nicola D Kerrison, Thorsten Kessler, Kay-Tee Khaw, Chiea Chuen Khor, Dominique P V de Kleijn, Woon-Puay Koh, Ivana Kolcic, Peter Kraft, Bernhard K Krämer, Zoltán Kutalik, Johanna Kuusisto, Claudia Langenberg, Lenore J Launer, Deborah A Lawlor, I-Te Lee, Wen-Jane Lee, Markus M Lerch, Liming Li, Jianjun Liu, Marie Loh, Stephanie J London, Stephanie Loomis, Yingchang Lu, Jian’an Luan, Reedik Mägi, Ani W Manichaikul, Paolo Manunta, Gísli Másson, Nana Matoba, Xue W Mei, Christa Meisinger, Thomas Meitinger, Massimo Mezzavilla, Lili Milani, Iona Y Millwood, Yukihide Momozawa, Amy Moore, Pierre-Emmanuel Morange, Hortensia Moreno-Macías, Trevor A Mori, Alanna C Morrison, Taulant Muka, Yoshinori Murakami, Alison D Murray, Renée de Mutsert, Josyf C Mychaleckyj, Mike A Nalls, Matthias Nauck, Matt J Neville, Ilja M Nolte, Ken K Ong, Lorena Orozco, Sandosh Padmanabhan, Gunnar Pálsson, James S Pankow, Cristian Pattaro, Alison Pattie, Ozren Polasek, Neil Poulter, Peter P Pramstaller, Lluis Quintana-Murci, Katri Räikkönen, Sarju Ralhan, Dabeeru C Rao, Wouter van Rheenen, Stephen S Rich, Paul M Ridker, Cornelius A Rietveld, Antonietta Robino, Frank J A van Rooij, Daniela Ruggiero, Yasaman Saba, Charumathi Sabanayagam, Maria Sabater-Lleal, Cinzia Felicita Sala, Veikko Salomaa, Kevin Sandow, Helena Schmidt, Laura J Scott, William R Scott, Bahareh Sedaghati-Khayat, Bengt Sennblad, Jessica van Setten, Peter J Sever, Wayne H-H Sheu, Yuan Shi, Smeeta Shrestha, Sharvari Rahul Shukla, Jon K Sigurdsson, Timo Tonis Sikka, Jai Rup Singh, Blair H Smith, Alena Stančáková, Alice Stanton, John M Starr, Lilja Stefansdottir, Leon Straker, Patrick Sulem, Gardar Sveinbjornsson, Morris A Swertz, Adele M Taylor, Kent D Taylor, Natalie Terzikhan, Yih-Chung Tham, Gudmar Thorleifsson, Unnur Thorsteinsdottir, Annika Tillander, Russell P Tracy, Teresa Tusié-Luna, Ioanna Tzoulaki, Simona Vaccargiu, Jagadish Vangipurapu, Jan H Veldink, Veronique Vitart, Uwe Völker, Eero Vuoksimaa, Salma M Wakil, Melanie Waldenberger, Gurpreet S Wander, Ya Xing Wang, Nicholas J Wareham, Sarah Wild, Chittaranjan S Yajnik, Jian-Min Yuan, Lingyao Zeng, Liang Zhang, Jie Zhou, Najaf Amin, Folkert W Asselbergs, Stephan J L Bakker, Diane M Becker, Benjamin Lehne, David A Bennett, Leonard H van den Berg, Sonja I Berndt, Dwaipayan Bharadwaj, Lawrence F Bielak, Murielle Bochud, Mike Boehnke, Claude Bouchard, Jonathan P Bradfield, Jennifer A Brody, Archie Campbell, Shai Carmi, Mark J Caulfield, David Cesarini, John C Chambers, Giriraj Ratan Chandak, Ching-Yu Cheng, Marina Ciullo, Marilyn Cornelis, Daniele Cusi, George Davey Smith, Ian J Deary, Rajkumar Dorajoo, Cornelia M van Duijn, David Ellinghaus, Jeanette Erdmann, Johan G Eriksson, Evangelos Evangelou, Michele K Evans, Jessica D Faul, Bjarke Feenstra, Mary Feitosa, Sylvain Foisy, Andre Franke, Yechiel Friedlander, Paolo Gasparini, Christian Gieger, Clicerio Gonzalez, Philippe Goyette, Struan F A Grant, Lyn R Griffiths, Leif Groop, Vilmundur Gudnason, Ulf Gyllensten, Hakon Hakonarson, Anders Hamsten, Pim van der Harst, Chew-Kiat Heng, Andrew A Hicks, Hagit Hochner, Heikki Huikuri, Steven C Hunt, Vincent W V Jaddoe, Philip L De Jager, Magnus Johannesson, Åsa Johansson, Jost B Jonas, J Wouter Jukema, Juhani Junttila, Jaakko Kaprio, Sharon L. R. Kardia, Fredrik Karpe, Meena Kumari, Markku Laakso, Sander W van der Laan, Jari Lahti, Matthias Laudes, Rodney A Lea, Wolfgang Lieb, Thomas Lumley, Nicholas G Martin, Winfried März, Giuseppe Matullo, Mark I McCarthy, Sarah E Medland, Tony R Merriman, Andres Metspalu, Brian F Meyer, Karen L Mohlke, Grant W Montgomery, Dennis Mook-Kanamori, Patricia B Munroe, Kari E North, Dale R Nyholt, Jeffery R O’connell, Carole Ober, Albertine J Oldehinkel, Walter Palmas, Colin Palmer, Gerard G Pasterkamp, Etienne Patin, Craig E Pennell, Louis Perusse, Patricia A Peyser, Mario Pirastu, Tinca J. C. Polderman, David J Porteous, Danielle Posthuma, Bruce M Psaty, John D Rioux, Fernando Rivadeneira, Charles Rotimi, Jerome I Rotter, Igor Rudan, Hester M Den Ruijter, Dharambir K Sanghera, Naveed Sattar, Reinhold Schmidt, Matthias B Schulze, Heribert Schunkert, Robert A Scott, Alan R Shuldiner, Xueling Sim, Neil Small, Jennifer A Smith, Nona Sotoodehnia, E-Shyong Tai, Alexander Teumer, Nicholas J Timpson, Daniela Toniolo, David-Alexandre Tregouet, Tiinamaija Tuomi, Peter Vollenweider, Carol A Wang, David R Weir, John B Whitfield, Cisca Wijmenga, Tien-Yin Wong, John Wright, Jingyun Yang, Lei Yu, Babette S Zemel, Alan B Zonderman, Markus Perola, Patrik K. E. Magnusson, André G Uitterlinden, Jaspal S Kooner, Daniel I Chasman, Ruth J. F. Loos, Nora Franceschini, Lude Franke, Chris S Haley, Caroline Hayward, Robin G Walters, John R. B. Perry, Tōnu Esko, Agnar Helgason, Kari Stefansson, Peter K Joshi, Michiaki Kubo, James F Wilson
Publikováno v:
Nature Communications, Vol 10, Iss 1, Pp 1-17 (2019)
Inbreeding depression has been observed in many different species, but in humans a systematic analysis has been difficult so far. Here, analysing more than 1.3 million individuals, the authors show that a genomic inbreeding coefficient (FROH) is asso
Externí odkaz:
https://doaj.org/article/701d2fda0b6343e98f5974339f0a8eb7
Autor:
Joscha Gretzinger, Duncan Sayer, Pierre Justeau, Eveline Altena, Maria Pala, Katharina Dulias, Ceiridwen J. Edwards, Susanne Jodoin, Laura Lacher, Susanna Sabin, Åshild J. Vågene, Wolfgang Haak, S. Sunna Ebenesersdóttir, Kristjan H. S. Moore, Rita Radzeviciute, Kara Schmidt, Selina Brace, Martina Abenhus Bager, Nick Patterson, Luka Papac, Nasreen Broomandkhoshbacht, Kimberly Callan, Éadaoin Harney, Lora Iliev, Ann Marie Lawson, Megan Michel, Kristin Stewardson, Fatma Zalzala, Nadin Rohland, Stefanie Kappelhoff-Beckmann, Frank Both, Daniel Winger, Daniel Neumann, Lars Saalow, Stefan Krabath, Sophie Beckett, Melanie Van Twest, Neil Faulkner, Chris Read, Tabatha Barton, Joanna Caruth, John Hines, Ben Krause-Kyora, Ursula Warnke, Verena J. Schuenemann, Ian Barnes, Hanna Dahlström, Jane Jark Clausen, Andrew Richardson, Elizabeth Popescu, Natasha Dodwell, Stuart Ladd, Tom Phillips, Richard Mortimer, Faye Sayer, Diana Swales, Allison Stewart, Dominic Powlesland, Robert Kenyon, Lilian Ladle, Christina Peek, Silke Grefen-Peters, Paola Ponce, Robin Daniels, Cecily Spall, Jennifer Woolcock, Andy M. Jones, Amy V. Roberts, Robert Symmons, Anooshka C. Rawden, Alan Cooper, Kirsten I. Bos, Tom Booth, Hannes Schroeder, Mark G. Thomas, Agnar Helgason, Martin B. Richards, David Reich, Johannes Krause, Stephan Schiffels
Publikováno v:
Nature
Gretzinger, J, Sayer, D, Justeau, P, Altena, E, Pala, M, Dulias, K, Edwards, C J, Jodoin, S, Lacher, L, Sabin, S, Vågene, Å J, Haak, W, Ebenesersdóttir, S S, Moore, K H S, Radzeviciute, R, Schmidt, K, Brace, S, Bager, M A, Patterson, N, Papac, L, Broomandkhoshbacht, N, Callan, K, Harney, É, Iliev, L, Lawson, A M, Michel, M, Stewardson, K, Zalzala, F, Rohland, N, Kappelhoff-Beckmann, S, Both, F, Winger, D, Neumann, D, Saalow, L, Krabath, S, Beckett, S, Van Twest, M, Faulkner, N, Read, C, Barton, T, Caruth, J, Hines, J, Krause-Kyora, B, Warnke, U, Schuenemann, V J, Barnes, I, Dahlström, H, Clausen, J J, Richardson, A, Popescu, E, Dodwell, N, Ladd, S, Phillips, T, Mortimer, R, Sayer, F, Swales, D, Stewart, A, Powlesland, D, Kenyon, R, Ladle, L, Peek, C, Grefen-Peters, S, Ponce, P, Daniels, R, Spall, C, Woolcock, J, Jones, A M, Roberts, A V, Symmons, R, Rawden, A C, Cooper, A, Bos, K I, Booth, T, Schroeder, H, Thomas, M G, Helgason, A, Richards, M B, Reich, D, Krause, J & Schiffels, S 2022, ' The Anglo-Saxon migration and the formation of the early English gene pool ', Nature, vol. 610, pp. 112-119 . https://doi.org/10.1038/s41586-022-05247-2
Nature, 610(7930), 112-+. NATURE PORTFOLIO
Gretzinger, J, Sayer, D, Justeau, P, Altena, E, Pala, M, Dulias, K, Edwards, C J, Jodoin, S, Lacher, L, Sabin, S, Vågene, Å J, Haak, W, Ebenesersdóttir, S S, Moore, K H S, Radzeviciute, R, Schmidt, K, Brace, S, Bager, M A, Patterson, N, Papac, L, Broomandkhoshbacht, N, Callan, K, Harney, É, Iliev, L, Lawson, A M, Michel, M, Stewardson, K, Zalzala, F, Rohland, N, Kappelhoff-Beckmann, S, Both, F, Winger, D, Neumann, D, Saalow, L, Krabath, S, Beckett, S, Van Twest, M, Faulkner, N, Read, C, Barton, T, Caruth, J, Hines, J, Krause-Kyora, B, Warnke, U, Schuenemann, V J, Barnes, I, Dahlström, H, Clausen, J J, Richardson, A, Popescu, E, Dodwell, N, Ladd, S, Phillips, T, Mortimer, R, Sayer, F, Swales, D, Stewart, A, Powlesland, D, Kenyon, R, Ladle, L, Peek, C, Grefen-Peters, S, Ponce, P, Daniels, R, Spall, C, Woolcock, J, Jones, A M, Roberts, A V, Symmons, R, Rawden, A C, Cooper, A, Bos, K I, Booth, T, Schroeder, H, Thomas, M G, Helgason, A, Richards, M B, Reich, D, Krause, J & Schiffels, S 2022, ' The Anglo-Saxon migration and the formation of the early English gene pool ', Nature, vol. 610, pp. 112-119 . https://doi.org/10.1038/s41586-022-05247-2
Nature, 610(7930), 112-+. NATURE PORTFOLIO
The history of the British Isles and Ireland is characterized by multiple periods of major cultural change, including the influential transformation after the end of Roman rule, which precipitated shifts in language, settlement patterns and material
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b5be5e57f72b6a17148e0cefd0aa7636
https://eprints.bournemouth.ac.uk/37579/1/s41586-022-05247-2.pdf
https://eprints.bournemouth.ac.uk/37579/1/s41586-022-05247-2.pdf
Autor:
Thorgeir E. Thorgeirsson, Sigurdur H. Magnusson, Helene M. Paarup, Astros Skuladottir, Erik Elgaard Sørensen, Olafur A. Sveinsson, Gardar Sveinbjornsson, Brynja D. Sigurpalsdottir, Hreinn Stefansson, Christian Erikstrup, Muhammad Sulaman Nawaz, Gyda Bjornsdottir, Maria Gudlaug Hrafnsdottir, Gudrun R. Sigurdardottir, Pall I. Olason, G. Bragi Walters, Mie Topholm Bruun, Ingileif Jonsdottir, Thomas Hansen, Gudmar Thorleifsson, Bjarni V. Halldorsson, Kristoffer Sølvsten Burgdorf, Anna Bjornsdottir, Ole Birger Pedersen, Karina Banasik, Asmundur Oddsson, Henrik Ullum, Mads Klokker, Kari Stefansson, Kaspar René Nielsen, Arnor Vikingsson, Hannes P. Eggertsson, Kristjan H. S. Moore
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-8 (2021)
Scientific Reports
Skuladottir, A T, Bjornsdottir, G, Thorleifsson, G, Walters, G B, Nawaz, M S, Moore, K H S, Olason, P I, Thorgeirsson, T E, Sigurpalsdottir, B, Sveinbjornsson, G, Eggertsson, H P, Magnusson, S H, Oddsson, A, Bjornsdottir, A, Vikingsson, A, Sveinsson, O A, Hrafnsdottir, M G, Sigurdardottir, G R, Halldorsson, B V, Hansen, T F, Paarup, H, Erikstrup, C, Nielsen, K, Klokker, M, Bruun, M T, Sorensen, E, Banasik, K, Burgdorf, K S, Pedersen, O B, Ullum, H, Jonsdottir, I, Stefansson, H & Stefansson, K 2021, ' A meta-analysis uncovers the first sequence variant conferring risk of Bell’s palsy ', Scientific Reports, vol. 11, no. 1, 4188 . https://doi.org/10.1038/s41598-021-82736-w
Skuladottir, A T, Bjornsdottir, G, Thorleifsson, G, Walters, G B, Nawaz, M S, Moore, K H S, Olason, P I, Thorgeirsson, T E, Sigurpalsdottir, B, Sveinbjornsson, G, Eggertsson, H P, Magnusson, S H, Oddsson, A, Bjornsdottir, A, Vikingsson, A, Sveinsson, O A, Hrafnsdottir, M G, Sigurdardottir, G R, Halldorsson, B V, Hansen, T F, Paarup, H, Erikstrup, C, Nielsen, K, Klokker, M, Bruun, M T, Sorensen, E, Banasik, K, Burgdorf, K S, Pedersen, O B, Ullum, H, Jonsdottir, I, Stefansson, H & Stefansson, K 2021, ' A meta-analysis uncovers the first sequence variant conferring risk of Bell’s palsy ', Scientific Reports, vol. 11, 4188 . https://doi.org/10.1038/s41598-021-82736-w
Skuladottir, A T, Bjornsdottir, G, Thorleifsson, G, Walters, G B, Nawaz, M S, Moore, K H S, Olason, P I, Thorgeirsson, T E, Sigurpalsdottir, B, Sveinbjornsson, G, Eggertsson, H P, Magnusson, S H, Oddsson, A, Bjornsdottir, A, Vikingsson, A, Sveinsson, O A, Hrafnsdottir, M G, Sigurdardottir, G R, Halldorsson, B V, Hansen, T F, Paarup, H, Erikstrup, C, Nielsen, K, Klokker, M, Bruun, M T, Sørensen, E, Banasik, K, Burgdorf, K S, Pedersen, O B, Ullum, H, Jonsdottir, I, Stefansson, H & Stefansson, K 2021, ' A meta-analysis uncovers the first sequence variant conferring risk of Bell’s palsy ', Scientific Reports, vol. 11, no. 1, 4188 . https://doi.org/10.1038/s41598-021-82736-w
Scientific Reports
Skuladottir, A T, Bjornsdottir, G, Thorleifsson, G, Walters, G B, Nawaz, M S, Moore, K H S, Olason, P I, Thorgeirsson, T E, Sigurpalsdottir, B, Sveinbjornsson, G, Eggertsson, H P, Magnusson, S H, Oddsson, A, Bjornsdottir, A, Vikingsson, A, Sveinsson, O A, Hrafnsdottir, M G, Sigurdardottir, G R, Halldorsson, B V, Hansen, T F, Paarup, H, Erikstrup, C, Nielsen, K, Klokker, M, Bruun, M T, Sorensen, E, Banasik, K, Burgdorf, K S, Pedersen, O B, Ullum, H, Jonsdottir, I, Stefansson, H & Stefansson, K 2021, ' A meta-analysis uncovers the first sequence variant conferring risk of Bell’s palsy ', Scientific Reports, vol. 11, no. 1, 4188 . https://doi.org/10.1038/s41598-021-82736-w
Skuladottir, A T, Bjornsdottir, G, Thorleifsson, G, Walters, G B, Nawaz, M S, Moore, K H S, Olason, P I, Thorgeirsson, T E, Sigurpalsdottir, B, Sveinbjornsson, G, Eggertsson, H P, Magnusson, S H, Oddsson, A, Bjornsdottir, A, Vikingsson, A, Sveinsson, O A, Hrafnsdottir, M G, Sigurdardottir, G R, Halldorsson, B V, Hansen, T F, Paarup, H, Erikstrup, C, Nielsen, K, Klokker, M, Bruun, M T, Sorensen, E, Banasik, K, Burgdorf, K S, Pedersen, O B, Ullum, H, Jonsdottir, I, Stefansson, H & Stefansson, K 2021, ' A meta-analysis uncovers the first sequence variant conferring risk of Bell’s palsy ', Scientific Reports, vol. 11, 4188 . https://doi.org/10.1038/s41598-021-82736-w
Skuladottir, A T, Bjornsdottir, G, Thorleifsson, G, Walters, G B, Nawaz, M S, Moore, K H S, Olason, P I, Thorgeirsson, T E, Sigurpalsdottir, B, Sveinbjornsson, G, Eggertsson, H P, Magnusson, S H, Oddsson, A, Bjornsdottir, A, Vikingsson, A, Sveinsson, O A, Hrafnsdottir, M G, Sigurdardottir, G R, Halldorsson, B V, Hansen, T F, Paarup, H, Erikstrup, C, Nielsen, K, Klokker, M, Bruun, M T, Sørensen, E, Banasik, K, Burgdorf, K S, Pedersen, O B, Ullum, H, Jonsdottir, I, Stefansson, H & Stefansson, K 2021, ' A meta-analysis uncovers the first sequence variant conferring risk of Bell’s palsy ', Scientific Reports, vol. 11, no. 1, 4188 . https://doi.org/10.1038/s41598-021-82736-w
Bell’s palsy is the most common cause of unilateral facial paralysis and is defined as an idiopathic and acute inability to control movements of the facial muscles on the affected side. While the pathogenesis remains unknown, previous studies have
Autor:
Saedis, Saevarsdottir, Lilja, Stefansdottir, Patrick, Sulem, Gudmar, Thorleifsson, Egil, Ferkingstad, Gudrun, Rutsdottir, Bente, Glintborg, Helga, Westerlind, Gerdur, Grondal, Isabella C, Loft, Signe Bek, Sorensen, Benedicte A, Lie, Mikael, Brink, Lisbeth, Ärlestig, Asgeir Orn, Arnthorsson, Eva, Baecklund, Karina, Banasik, Steffen, Bank, Lena I, Bjorkman, Torkell, Ellingsen, Christian, Erikstrup, Oleksandr, Frei, Inger, Gjertsson, Daniel F, Gudbjartsson, Sigurjon A, Gudjonsson, Gisli H, Halldorsson, Oliver, Hendricks, Jan, Hillert, Estrid, Hogdall, Søren, Jacobsen, Dorte Vendelbo, Jensen, Helgi, Jonsson, Alf, Kastbom, Ingrid, Kockum, Salome, Kristensen, Helga, Kristjansdottir, Margit H, Larsen, Asta, Linauskas, Ellen-Margrethe, Hauge, Anne G, Loft, Bjorn R, Ludviksson, Sigrun H, Lund, Thorsteinn, Markusson, Gisli, Masson, Pall, Melsted, Kristjan H S, Moore, Heidi, Munk, Kaspar R, Nielsen, Gudmundur L, Norddahl, Asmundur, Oddsson, Thorunn A, Olafsdottir, Pall I, Olason, Tomas, Olsson, Sisse Rye, Ostrowski, Kim, Hørslev-Petersen, Solvi, Rognvaldsson, Helga, Sanner, Gilad N, Silberberg, Hreinn, Stefansson, Erik, Sørensen, Inge J, Sørensen, Carl, Turesson, Thomas, Bergman, Lars, Alfredsson, Tore K, Kvien, Søren, Brunak, Kristján, Steinsson, Vibeke, Andersen, Ole A, Andreassen, Solbritt, Rantapää-Dahlqvist, Merete Lund, Hetland, Lars, Klareskog, Johan, Askling, Leonid, Padyukov, Ole Bv, Pedersen, Unnur, Thorsteinsdottir, Ingileif, Jonsdottir, Kari, Stefansson
Publikováno v:
Saevarsdottir, S, Stefansdottir, L, Sulem, P, Thorleifsson, G, Ferkingstad, E, Rutsdottir, G, Glintborg, B, Westerlind, H, Grondal, G, Loft, I C, Sorensen, S B, Lie, B A, Brink, M, Ärlestig, L, Arnthorsson, A O, Baecklund, E, Banasik, K, Bank, S, Bjorkman, L I, Ellingsen, T, Erikstrup, C, Frei, O, Gjertsson, I, Gudbjartsson, D F, Gudjonsson, S A, Halldorsson, G H, Hendricks, O, Hillert, J, Hogdall, E, Jacobsen, S, Jensen, D V, Jonsson, H, Kastbom, A, Kockum, I, Kristensen, S, Kristjansdottir, H, Larsen, M H, Linauskas, A, Hauge, E-M, Loft, A G, Ludviksson, B R, Lund, S H, Ostrowski, S R, Sørensen, E, Sørensen, I J, Brunak, S, Andersen, V, Hetland, M L, Askling, J, Pedersen, O B & Members of the DBDS Genomic Consortium 2022, ' Multiomics analysis of rheumatoid arthritis yields sequence variants that have large effects on risk of the seropositive subset ', Annals of the Rheumatic Diseases, vol. 81, no. 8, pp. 1085-1095 . https://doi.org/10.1136/annrheumdis-2021-221754
Saevarsdottir, S, Stefansdottir, L, Sulem, P, Thorleifsson, G, Ferkingstad, E, Rutsdottir, G, Glintborg, B, Westerlind, H, Grondal, G, Loft, I C, Sorensen, S B, Lie, B A, Brink, M, Arlestig, L, Arnthorsson, A O, Baecklund, E, Banasik, K, Bank, S, Bjorkman, L I, Ellingsen, T, Erikstrup, C, Frei, O, Gjertsson, I, Gudbjartsson, D F, Gudjonsson, S A, Halldorsson, G H, Hendricks, O, Hillert, J, Hogdall, E, Jacobsen, S, Jensen, D V, Jonsson, H, Kastbom, A, Kockum, I, Kristensen, S, Kristjansdottir, H, Larsen, M H, Linauskas, A, Hauge, E M, Loft, A G, Ludviksson, B R, Lund, S H, Markusson, T, Masson, G, Melsted, P, Moore, K H S, Munk, H, Nielsen, K R, Norddahl, G L, Oddsson, A, DBDS Genomic Consortium, The Danish RA Genetics Working Group & The Swedish Rheumatology Quality Register Biobank Study Group (SRQb) 2022, ' Multiomics analysis of rheumatoid arthritis yields sequence variants that have large effects on risk of the seropositive subset ', Annals of the Rheumatic Diseases, vol. 81, no. 8, pp. 1085-1095 . https://doi.org/10.1136/annrheumdis-2021-221754
Annals of the Rheumatic Diseases
Saevarsdottir, S, Stefansdottir, L, Sulem, P, Thorleifsson, G, Ferkingstad, E, Rutsdottir, G, Glintborg, B, Westerlind, H, Grondal, G, Loft, I C, Sorensen, S B, Lie, B A, Brink, M, Ärlestig, L, Arnthorsson, A O, Baecklund, E, Banasik, K, Bank, S, Bjorkman, L I, Ellingsen, T, Erikstrup, C, Frei, O, Gjertsson, I, Gudbjartsson, D F, Gudjonsson, S A, Halldorsson, G H, Hendricks, O, Hillert, J, Hogdall, E, Jacobsen, S, Jensen, D V, Jonsson, H, Kastbom, A, Kockum, I, Kristensen, S, Kristjansdottir, H, Larsen, M H, Linauskas, A, Hauge, E-M, Loft, A G, Ludviksson, B R, Lund, S H, Markusson, T, Masson, G, Melsted, P, Moore, K H S, Munk, H, Nielsen, K R, Norddahl, G L, Oddsson, A, Olafsdottir, T A, Olason, P I, Olsson, T, Ostrowski, S R, Hørslev-Petersen, K, Rognvaldsson, S, Sanner, H, Silberberg, G N, Stefansson, H, Sørensen, E, Sørensen, I J, Turesson, C, Bergman, T, Alfredsson, L, Kvien, T K, Brunak, S, Steinsson, K, Andersen, V, Andreassen, O A, Rantapää-Dahlqvist, S, Hetland, M L, Klareskog, L, Askling, J, Padyukov, L, Pedersen, O B, Thorsteinsdottir, U, Jonsdottir, I, Stefansson, K, Members of the DBDS Genomic Consortium & Nyegaard, M 2022, ' Multiomics analysis of rheumatoid arthritis yields sequence variants that have large effects on risk of the seropositive subset ', Annals of the Rheumatic Diseases, vol. 81, no. 8, 221754, pp. 1085-1095 . https://doi.org/10.1136/annrheumdis-2021-221754
Saevarsdottir, S, Stefansdottir, L, Sulem, P, Thorleifsson, G, Ferkingstad, E, Rutsdottir, G, Glintborg, B, Westerlind, H, Grondal, G, Loft, I C, Sorensen, S B, Lie, B A, Brink, M, Arlestig, L, Arnthorsson, A O, Baecklund, E, Banasik, K, Bank, S, Bjorkman, L I, Ellingsen, T, Erikstrup, C, Frei, O, Gjertsson, I, Gudbjartsson, D F, Gudjonsson, S A, Halldorsson, G H, Hendricks, O, Hillert, J, Hogdall, E, Jacobsen, S, Jensen, D V, Jonsson, H, Kastbom, A, Kockum, I, Kristensen, S, Kristjansdottir, H, Larsen, M H, Linauskas, A, Hauge, E M, Loft, A G, Ludviksson, B R, Lund, S H, Markusson, T, Masson, G, Melsted, P, Moore, K H S, Munk, H, Nielsen, K R, Norddahl, G L, Oddsson, A, DBDS Genomic Consortium, The Danish RA Genetics Working Group & The Swedish Rheumatology Quality Register Biobank Study Group (SRQb) 2022, ' Multiomics analysis of rheumatoid arthritis yields sequence variants that have large effects on risk of the seropositive subset ', Annals of the Rheumatic Diseases, vol. 81, no. 8, pp. 1085-1095 . https://doi.org/10.1136/annrheumdis-2021-221754
Annals of the Rheumatic Diseases
Saevarsdottir, S, Stefansdottir, L, Sulem, P, Thorleifsson, G, Ferkingstad, E, Rutsdottir, G, Glintborg, B, Westerlind, H, Grondal, G, Loft, I C, Sorensen, S B, Lie, B A, Brink, M, Ärlestig, L, Arnthorsson, A O, Baecklund, E, Banasik, K, Bank, S, Bjorkman, L I, Ellingsen, T, Erikstrup, C, Frei, O, Gjertsson, I, Gudbjartsson, D F, Gudjonsson, S A, Halldorsson, G H, Hendricks, O, Hillert, J, Hogdall, E, Jacobsen, S, Jensen, D V, Jonsson, H, Kastbom, A, Kockum, I, Kristensen, S, Kristjansdottir, H, Larsen, M H, Linauskas, A, Hauge, E-M, Loft, A G, Ludviksson, B R, Lund, S H, Markusson, T, Masson, G, Melsted, P, Moore, K H S, Munk, H, Nielsen, K R, Norddahl, G L, Oddsson, A, Olafsdottir, T A, Olason, P I, Olsson, T, Ostrowski, S R, Hørslev-Petersen, K, Rognvaldsson, S, Sanner, H, Silberberg, G N, Stefansson, H, Sørensen, E, Sørensen, I J, Turesson, C, Bergman, T, Alfredsson, L, Kvien, T K, Brunak, S, Steinsson, K, Andersen, V, Andreassen, O A, Rantapää-Dahlqvist, S, Hetland, M L, Klareskog, L, Askling, J, Padyukov, L, Pedersen, O B, Thorsteinsdottir, U, Jonsdottir, I, Stefansson, K, Members of the DBDS Genomic Consortium & Nyegaard, M 2022, ' Multiomics analysis of rheumatoid arthritis yields sequence variants that have large effects on risk of the seropositive subset ', Annals of the Rheumatic Diseases, vol. 81, no. 8, 221754, pp. 1085-1095 . https://doi.org/10.1136/annrheumdis-2021-221754
Objectives To find causal genes for rheumatoid arthritis (RA) and its seropositive (RF and/or ACPA positive) and seronegative subsets. Methods We performed a genome-wide association study (GWAS) of 31 313 RA cases (68% seropositive) and similar to 1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bfa559b7172b3407158d15a52860ec6e
https://curis.ku.dk/portal/da/publications/multiomics-analysis-of-rheumatoid-arthritis-yields-sequence-variants-that-have-large-effects-on-risk-of-the-seropositive-subset(ac8972ce-4933-4e08-88e5-2da877e76a2b).html
https://curis.ku.dk/portal/da/publications/multiomics-analysis-of-rheumatoid-arthritis-yields-sequence-variants-that-have-large-effects-on-risk-of-the-seropositive-subset(ac8972ce-4933-4e08-88e5-2da877e76a2b).html
Autor:
Jona Saemundsdottir, Arnaldur Gylfason, Hreinn Stefansson, Steinunn Snorradottir, Gudmar Thorleifsson, Brynjar O. Jensson, Sverrir T. Sverrisson, Gisli Masson, Brynjar Sigurdsson, Olafur Th Magnusson, Agnar Helgason, Unnur Styrkarsdottir, Olafur A. Stefansson, Sigurjon A. Gudjonsson, Hannes Hauswedell, Pall I. Olason, Margret Asgeirsdottir, Páll Melsted, Droplaug N Magnusdottir, Marteinn T. Hardarson, Asmundur Oddsson, Gisli H. Halldorsson, Kristjan Norland, Hannes P. Eggertsson, Thorunn Rafnar, Kari Stefansson, Hilma Holm, Unnur Thorsteinsdottir, Emilia Sobech, Doruk Beyter, Ogmundur Eiriksson, Kristjan H. S. Moore, Brynja D. Sigurpalsdottir, Gunnar Th. Sigurdsson, Ingileif Jonsdottir, Guillaume Holley, Snaedis Kristmundsdottir, Kari Kristinsson, Bjarni V. Halldorsson, Gunnar K. Pálsson, Magnus O. Ulfarsson, Frosti Jonsson, Daniel F. Gudbjartsson, Vinicius Tragante, Patrick Sulem, Florian Zink, Gardar Sveinbjornsson, Hakon Jonsson
We describe the analysis of whole genome sequences (WGS) of 150,119 individuals from the UK biobank (UKB). This constitutes a set of high quality variants, including 585,040,410 SNPs, representing 7.0% of all possible human SNPs, and 58,707,036 indel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3ec97dcc172cfe882dfcfb8c2d1ae42a
https://doi.org/10.1101/2021.11.16.468246
https://doi.org/10.1101/2021.11.16.468246
Autor:
Bjarni V, Halldorsson, Hannes P, Eggertsson, Kristjan H S, Moore, Hannes, Hauswedell, Ogmundur, Eiriksson, Magnus O, Ulfarsson, Gunnar, Palsson, Marteinn T, Hardarson, Asmundur, Oddsson, Brynjar O, Jensson, Snaedis, Kristmundsdottir, Brynja D, Sigurpalsdottir, Olafur A, 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 H, Halldorsson, Gardar, Sveinbjornsson, Kristjan, Norland, Unnur, Styrkarsdottir, Droplaug N, Magnusdottir, Steinunn, Snorradottir, Kari, Kristinsson, Emilia, Sobech, Helgi, Jonsson, Arni J, Geirsson, Isleifur, Olafsson, Palmi, Jonsson, Ole Birger, Pedersen, Christian, Erikstrup, Søren, Brunak, Sisse Rye, Ostrowski, Gudmar, Thorleifsson, Frosti, Jonsson, Pall, Melsted, Ingileif, Jonsdottir, Thorunn, Rafnar, Hilma, Holm, Hreinn, Stefansson, Jona, Saemundsdottir, Daniel F, Gudbjartsson, Olafur T, Magnusson, Gisli, Masson, Unnur, Thorsteinsdottir, Agnar, Helgason, Hakon, Jonsson, Patrick, Sulem, Thomas, Werge
Publikováno v:
Nature. 607(7920)
Detailed knowledge of how diversity in the sequence of the human genome affects phenotypic diversity depends on a comprehensive and reliable characterization of both sequences and phenotypic variation. Over the past decade, insights into this relatio
Autor:
Joscha Gretzinger, Duncan Sayer, Pierre Justeau, Eveline Altena, Maria Pala, Katharina Dulias, Ceiridwen J. Edwards, Susanne Jodoin, Laura Lacher, Susanna Sabin, Åshild J. Vågene, Wolfgang Haak, S. Sunna Ebenesersdóttir, Kristjan H. S. Moore, Rita Radzeviciute, Kara Schmidt, Selina Brace, Martina Abenhus Bager, Nick Patterson, Luka Papac, Nasreen Broomandkhoshbacht, Kimberly Callan, Éadaoin Harney, Lora Iliev, Ann Marie Lawson, Megan Michel, Kristin Stewardson, Fatma Zalzala, Nadin Rohland, Stefanie Kappelhoff-Beckmann, Frank Both, Daniel Winger, Daniel Neumann, Lars Saalow, Stefan Krabath, Sophie Beckett, Melanie Van Twest, Neil Faulkner, Chris Read, Tabatha Barton, Joanna Caruth, John Hines, Ben Krause-Kyora, Ursula Warnke, Verena J. Schuenemann, Ian Barnes, Hanna Dahlström, Jane Jark Clausen, Andrew Richardson, Elizabeth Popescu, Natasha Dodwell, Stuart Ladd, Tom Phillips, Richard Mortimer, Faye Sayer, Diana Swales, Allison Stewart, Dominic Powlesland, Robert Kenyon, Lilian Ladle, Christina Peek, Silke Grefen-Peters, Paola Ponce, Robin Daniels, Cecily Spall, Jennifer Woolcock, Andy M. Jones, Amy V. Roberts, Robert Symmons, Anooshka C. Rawden, Alan Cooper, Kirsten I. Bos, Tom Booth, Hannes Schroeder, Mark G. Thomas, Agnar Helgason, Martin B. Richards, David Reich, Johannes Krause, Stephan Schiffels
Publikováno v:
Nature. 611:E3-E3