Zobrazeno 1 - 10
of 52
pro vyhledávání: '"Magnusson, Sigurdur H"'
Autor:
Jonsdottir, Gudrun A., Einarsson, Gudmundur, Thorleifsson, Gudmar, Magnusson, Sigurdur H., Gunnarsson, Arni F., Frigge, Michael L., Gisladottir, Rosa S., Unnsteinsdottir, Unnur, Gunnarsson, Bjarni, Walters, G. Bragi, Steinthorsdottir, Valgerdur, Helgadottir, Anna, Jonsdottir, Ingileif, Gislason, Thorsteinn, Thorsteinsson, Haraldur S., Sigurdsson, Engilbert, Haraldsson, Magnus, Sigurdsson, Emil L., Bjarnason, Ragnar, Olafsson, Isleifur, Thorgeirsson, Gudmundur, Sulem, Patrick, Holm, Hilma, Thorsteinsdottir, Unnur, Gudbjartsson, Daniel F., Bjornsdottir, Gyda, Thorgeirsson, Thorgeir E., Stefansson, Hreinn, Stefansson, Kari
Publikováno v:
In Intelligence September-October 2021 88
Publikováno v:
In Geothermics September 2021 95
Autor:
Demontis, Ditte, Walters, G. Bragi, Athanasiadis, Georgios, Walters, Raymond, Therrien, Karen, Nielsen, Trine Tollerup, Farajzadeh, Leila, Voloudakis, Georgios, Bendl, Jaroslav, Zeng, Biau, Zhang, Wen, Grove, Jakob, Als, Thomas D., Duan, Jinjie, Satterstrom, F. Kyle, Bybjerg-Grauholm, Jonas, Bækved-Hansen, Marie, Gudmundsson, Olafur O., Magnusson, Sigurdur H., Baldursson, Gisli, Davidsdottir, Katrin, Haraldsdottir, Gyda S., Agerbo, Esben, Hoffman, Gabriel E., Dalsgaard, Søren, Martin, Joanna, Ribasés, Marta, Boomsma, Dorret I., Soler Artigas, Maria, Roth Mota, Nina, Howrigan, Daniel, Medland, Sarah E., Zayats, Tetyana, Rajagopal, Veera M., Havdahl, Alexandra, Doyle, Alysa, Reif, Andreas, Thapar, Anita, Cormand, Bru, Liao, Calwing, Burton, Christie, Bau, Claiton H. D., Rovaris, Diego Luiz, Sonuga-Barke, Edmund, Corfield, Elizabeth, Grevet, Eugenio Horacio, Larsson, Henrik, Gizer, Ian R., Waldman, Irwin, Brikell, Isabell, Haavik, Jan, Crosbie, Jennifer, McGough, James, Kuntsi, Jonna, Glessner, Joseph, Langley, Kate, Lesch, Klaus-Peter, Rohde, Luis Augusto, Hutz, Mara H., Klein, Marieke, Bellgrove, Mark, Tesli, Martin, O’Donovan, Michael C., Andreassen, Ole Andreas, Leung, Patrick W. L., Pan, Pedro M., Joober, Ridha, Schachar, Russel, Loo, Sandra, Witt, Stephanie H., Reichborn-Kjennerud, Ted, Banaschewski, Tobias, Hawi, Ziarih, Daly, Mark J., Mors, Ole, Nordentoft, Merete, Hougaard, David M., Mortensen, Preben Bo, Faraone, Stephen V., Stefansson, Hreinn, Roussos, Panos, Franke, Barbara, Werge, Thomas, Neale, Benjamin M., Stefansson, Kari, Børglum, Anders D.
Publikováno v:
Nature Genetics, 55, 2, pp. 198-208
Demontis, D, Walters, G B, Athanasiadis, G, Walters, R, Therrien, K, Nielsen, T T, Farajzadeh, L, Voloudakis, G, Bendl, J, Zeng, B, Zhang, W, Grove, J, Als, T D, Duan, J, Satterstrom, F K, Bybjerg-Grauholm, J, Bækved-Hansen, M, Gudmundsson, O O, Magnusson, S H, Baldursson, G, Davidsdottir, K, Haraldsdottir, G S, Agerbo, E, Hoffman, G E, Dalsgaard, S, Martin, J, Ribasés, M, Boomsma, D I, Soler Artigas, M, Roth Mota, N, Howrigan, D, Medland, S E, Zayats, T, Rajagopal, V M, Nordentoft, M, Mors, O, Hougaard, D M, Mortensen, P B, Daly, M J, Faraone, S V, Stefansson, H, Roussos, P, Franke, B, Werge, T, Neale, B M, Stefansson, K, Børglum, A D & ADHD Working Group of the Psychiatric Genomics Consortium 2023, ' Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains ', Nature Genetics, vol. 55, no. 2, pp. 198-208 . https://doi.org/10.1038/s41588-022-01285-8
Nature Genetics, 55, 198-208
Demontis, D, Walters, G B, Athanasiadis, G, Walters, R, Therrien, K, Nielsen, T T, Farajzadeh, L, Voloudakis, G, Bendl, J, Zeng, B, Zhang, W, Grove, J, Als, T D, Duan, J, Satterstrom, F K, Bybjerg-Grauholm, J, Bækved-Hansen, M, Gudmundsson, O O, Magnusson, S H, Baldursson, G, Davidsdottir, K, Haraldsdottir, G S, Agerbo, E, Hoffman, G E, Dalsgaard, S, Martin, J, Ribasés, M, Boomsma, D I, Soler Artigas, M, Roth Mota, N, Howrigan, D, Medland, S E, Zayats, T, Rajagopal, V M, Havdahl, A, Doyle, A, Reif, A, Thapar, A, Cormand, B, Liao, C, Burton, C, Bau, C H D, Rovaris, D L, Sonuga-Barke, E, Corfield, E, Grevet, E H, Larsson, H, Gizer, I R, Nordentoft, M, Werge, T, ADHD Working Group of the Psychiatric Genomics Consortium & iPSYCH-Broad Consortium 2023, ' Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains ', Nature Genetics, vol. 55, pp. 198–208 . https://doi.org/10.1038/s41588-022-01285-8
Demontis, D, Walters, G B, Athanasiadis, G, Boomsma, D I, Neale, B M, Stefansson, K, Børglum, A D, ADHD Working Group of the Psychiatric Genomics Consortium, iPSYCH-Broad Consortium, Dalsgaard, S & Martin, J 2023, ' Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains ', Nature genetics, vol. 55, no. 2, pp. 198-208 . https://doi.org/10.1038/s41588-022-01285-8
Nature genetics, 55(2), 198-208. Nature Publishing Group
Demontis, D, Walters, G B, Athanasiadis, G, Walters, R, Therrien, K, Nielsen, T T, Farajzadeh, L, Voloudakis, G, Bendl, J, Zeng, B, Zhang, W, Grove, J, Als, T D, Duan, J, Satterstrom, F K, Bybjerg-Grauholm, J, Bækved-Hansen, M, Gudmundsson, O O, Magnusson, S H, Baldursson, G, Davidsdottir, K, Haraldsdottir, G S, Agerbo, E, Hoffman, G E, Dalsgaard, S, Martin, J, Ribasés, M, Boomsma, D I, Soler Artigas, M, Roth Mota, N, Howrigan, D, Medland, S E, Zayats, T, Rajagopal, V M, Nordentoft, M, Mors, O, Hougaard, D M, Mortensen, P B, Daly, M J, Faraone, S V, Stefansson, H, Roussos, P, Franke, B, Werge, T, Neale, B M, Stefansson, K, Børglum, A D & ADHD Working Group of the Psychiatric Genomics Consortium 2023, ' Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains ', Nature Genetics, vol. 55, no. 2, pp. 198-208 . https://doi.org/10.1038/s41588-022-01285-8
Nature Genetics, 55, 198-208
Demontis, D, Walters, G B, Athanasiadis, G, Walters, R, Therrien, K, Nielsen, T T, Farajzadeh, L, Voloudakis, G, Bendl, J, Zeng, B, Zhang, W, Grove, J, Als, T D, Duan, J, Satterstrom, F K, Bybjerg-Grauholm, J, Bækved-Hansen, M, Gudmundsson, O O, Magnusson, S H, Baldursson, G, Davidsdottir, K, Haraldsdottir, G S, Agerbo, E, Hoffman, G E, Dalsgaard, S, Martin, J, Ribasés, M, Boomsma, D I, Soler Artigas, M, Roth Mota, N, Howrigan, D, Medland, S E, Zayats, T, Rajagopal, V M, Havdahl, A, Doyle, A, Reif, A, Thapar, A, Cormand, B, Liao, C, Burton, C, Bau, C H D, Rovaris, D L, Sonuga-Barke, E, Corfield, E, Grevet, E H, Larsson, H, Gizer, I R, Nordentoft, M, Werge, T, ADHD Working Group of the Psychiatric Genomics Consortium & iPSYCH-Broad Consortium 2023, ' Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains ', Nature Genetics, vol. 55, pp. 198–208 . https://doi.org/10.1038/s41588-022-01285-8
Demontis, D, Walters, G B, Athanasiadis, G, Boomsma, D I, Neale, B M, Stefansson, K, Børglum, A D, ADHD Working Group of the Psychiatric Genomics Consortium, iPSYCH-Broad Consortium, Dalsgaard, S & Martin, J 2023, ' Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains ', Nature genetics, vol. 55, no. 2, pp. 198-208 . https://doi.org/10.1038/s41588-022-01285-8
Nature genetics, 55(2), 198-208. Nature Publishing Group
Contains fulltext : 290804.pdf (Publisher’s version ) (Closed access) Attention-deficit hyperactivity disorder (ADHD) is a prevalent neurodevelopmental disorder with a major genetic component. Here, we present a genome-wide association study meta-a
Akademický článek
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Autor:
Winsvold, Bendik S., Harder, Aster V. E., Ran, Caroline, Chalmer, Mona A., Dalmasso, Maria Carolina, Ferkingstad, Egil, Tripathi, Kumar Parijat, Bacchelli, Elena, Børte, Sigrid, Fourier, Carmen, Petersen, Anja S., Vijfhuizen, Lisanne S., Magnusson, Sigurdur H., O'Connor, Emer, Bjornsdottir, Gyda, Häppölä, Paavo, Wang, Yen‐Feng, Callesen, Ida, Kelderman, Tim, Gallardo, Victor J
Publikováno v:
Annals of Neurology; Oct2023, Vol. 94 Issue 4, p713-726, 14p
Autor:
Winsvold, Bendik Kristoffer Slagsvold, Harder, Aster V. E., Ran, Caroline, Chalmer, Mona A., Dalmasso, Maria Carolina, Ferkingstad, Egil, Tripathi, Kumar Parijat, Bacchelli, Elena, Børte, Sigrid, Fourier, Carmen, Petersen, Anja S., Vijfhuizen, Lisanne S., Magnusson, Sigurdur H., O'Connor, Emer, Bjornsdottir, Gyda, Häppölä, Paavo, Wang, Yen-Feng, Callesen, Ida, Kelderman, Tim, Gallardo, Victor J, de Boer, Irene, Olofsgård, Felicia Jennysdotter, Heinze, Katja, Lund, Nunu, Thomas, Laurent Francois, Hsu, Chia-Lin, Pirinen, Matti, Hautakangas, Heidi, Ribasés, Marta, Guerzoni, Simona, Sivakumar, Prasanth, Yip, Janice, Heinze, Axel, Küçükali, Fahri, Ostrowski, Sisse R., Pedersen, Ole B., Kristoffersen, Espen Saxhaug, Martinsen, Amy, Artigas, María S., Lagrata, Susie, Cainazzo, Maria Michela, Adebimpe, Joycee, Quinn, Olivia, Göbel, Carl, Cirkel, Anna, Volk, Alexander E., Heilmann-Heimbach, Stefanie, Skogholt, Anne Heidi, Gabrielsen, Maiken Elvestad, Wilbrink, Leopoldine A., Danno, Daisuke, Mehta, Dwij, Guðbjartsson, Daníel F., Rosendaal, Frits Richard, Willems van Dijk, Ko, Fronczek, Rolf, Wagner, Michael, Scherer, Martin, Göbel, Hartmut, Sleegers, Kristel, Sveinsson, Olafur A., Pani, Luca, Zoli, Michele, Ramos-Quiroga, Josep A., Dardiotis, Efthimios, Steinberg, Anna, Riedel-Heller, Steffi, Sjöstrand, Christina, Thorgeirsson, Thorgeir E., Stefansson, Hreinn, Southgate, Laura, Trembath, Richard C., Vandrovcova, Jana, Noordam, Raymond, Paemeleire, Koen, Stefansson, Kari, Fann, Cathy Shen-Jang, Waldenlind, Elisabet, Tronvik, Erling Andreas, Jensen, Rigmor H., Chen, Shih-Pin, Houlden, Henry, Terwindt, Gisela M., Kubisch, Christian, Maestrini, Elena, Vikelis, Michail, Pozo-Rosich, Patricia, Belin, Andrea C., Matharu, Manjit, van den Maagdenberg, Arn M.J.M., Hansen, Thomas, Ramirez, Alfredo, Zwart, John Anker Henrik
Publikováno v:
Winsvold, Bendik Kristoffer Slagsvold Harder, Aster V. E. Ran, Caroline Chalmer, Mona A. Dalmasso, Maria Carolina Ferkingstad, Egil Tripathi, Kumar Parijat Bacchelli, Elena Børte, Sigrid Fourier, Carmen Petersen, Anja S. Vijfhuizen, Lisanne S. Magnusson, Sigurdur H. O'Connor, Emer Bjornsdottir, Gyda Häppölä, Paavo Wang, Yen-Feng Callesen, Ida Kelderman, Tim Gallardo, Victor J de Boer, Irene Olofsgård, Felicia Jennysdotter Heinze, Katja Lund, Nunu Thomas, Laurent Francois Hsu, Chia-Lin Pirinen, Matti Hautakangas, Heidi Ribasés, Marta Guerzoni, Simona Sivakumar, Prasanth Yip, Janice Heinze, Axel Küçükali, Fahri Ostrowski, Sisse R. Pedersen, Ole B. Kristoffersen, Espen Saxhaug Martinsen, Amy Artigas, María S. Lagrata, Susie Cainazzo, Maria Michela Adebimpe, Joycee Quinn, Olivia Göbel, Carl Cirkel, Anna Volk, Alexander E. Heilmann-Heimbach, Stefanie Skogholt, Anne Heidi Gabrielsen, Maiken Elvestad Wilbrink, Leopoldine A. Danno, Daisuke Mehta, Dwij Guðbjartsson, Daníel F. Rosendaal, Frits Richard Willems van Dijk, Ko Fronczek, Rolf Wagner, Michael Scherer, Martin Göbel, Hartmut Sleegers, Kristel Sveinsson, Olafur A. Pani, Luca Zoli, Michele Ramos-Quiroga, Josep A. Dardiotis, Efthimios Steinberg, Anna Riedel-Heller, Steffi Sjöstrand, Christina Thorgeirsson, Thorgeir E. Stefansson, Hreinn Southgate, Laura Trembath, Richard C. Vandrovcova, Jana Noordam, Raymond Paemeleire, Koen Stefansson, Kari Fann, Cathy Shen-Jang Waldenlind, Elisabet Tronvik, Erling Andreas Jensen, Rigmor H. Chen, Shih-Pin Houlden, Henry Terwindt, Gisela M. Kubisch, Christian Maestrini, Elena Vikelis, Michail Pozo-Rosich, Patricia Belin, Andrea C. Matharu, Manjit van den Maagdenberg, Arn M.J.M. Hansen, Thomas Ramirez, Alfredo Zwart, John Anker Henrik . Cluster Headache Genomewide Association Study and Meta-Analysis Identifies Eight Loci and Implicates Smoking as Causal Risk Factor. Annals of Neurology. 2023, 94(4), 713-726
Annals of Neurology
Annals of Neurology
Externí odkaz:
http://hdl.handle.net/10852/108212
Autor:
Skuladottir, Astros Th., Bjornsdottir, Gyda, Ferkingstad, Egil, Einarsson, Gudmundur, Stefansdottir, Lilja, Nawaz, Muhammad Sulaman, Oddsson, Asmundur, Olafsdottir, Thorunn A., Saevarsdottir, Saedis, Walters, G. Bragi, Magnusson, Sigurdur H., Bjornsdottir, Anna, Sveinsson, Olafur A., Vikingsson, Arnor, Hansen, Thomas Folkmann, Jacobsen, Rikke Louise, Erikstrup, Christian, Schwinn, Michael, Brunak, Søren, Banasik, Karina, Ostrowski, Sisse Rye, Troelsen, Anders, Henkel, Cecilie, Pedersen, Ole Birger, Andersen, Steffen, Burgdorf, Kristoffer, Didriksen, Maria, Dinh, Khoa Manh, Hjalgrim, Henrik, Jemec, Gregor, Jennum, Poul, Johansson, Pär Ingemar, Larsen, Margit Anita Hørup, Mikkelsen, Susan, Nielsen, Kasper Rene, Nyegaard, Mette, Stefánsson, Hreinn, Sækmose, Susanne, Sørensen, Erik, Thorsteinsdottir, Unnur, Bruun, Mie Topholm, Ullum, Henrik, Werge, Thomas, Jonsdottir, Ingileif, Gudbjartsson, Daniel F., Sulem, Patrick, Thorgeirsson, Thorgeir E., Stefansson, Hreinn, Stefansson, Kari
Publikováno v:
Skuladottir, A T, Bjornsdottir, G, Ferkingstad, E, Einarsson, G, Stefansdottir, L, Nawaz, M S, Oddsson, A, Olafsdottir, T A, Saevarsdottir, S, Walters, G B, Magnusson, S H, Bjornsdottir, A, Sveinsson, O A, Vikingsson, A, Hansen, T F, Jacobsen, R L, Erikstrup, C, Schwinn, M, Brunak, S, Banasik, K, Ostrowski, S R, Troelsen, A, Henkel, C, Pedersen, O B, DBDS Genetic Consortium, Jonsdottir, I, Gudbjartsson, D F, Sulem, P, Thorgeirsson, T E, Stefansson, H & Stefansson, K 2022, ' A genome-wide meta-analysis identifies 50 genetic loci associated with carpal tunnel syndrome ', Nature Communications, vol. 13, 1598 . https://doi.org/10.1038/s41467-022-29133-7
Skuladottir, A T, Bjornsdottir, G, Ferkingstad, E, Einarsson, G, Stefansdottir, L, Nawaz, M S, Oddsson, A, Olafsdottir, T A, Saevarsdottir, S, Walters, G B, Magnusson, S H, Bjornsdottir, A, Sveinsson, O A, Vikingsson, A, Hansen, T F, Jacobsen, R L, Erikstrup, C, Schwinn, M, Brunak, S, Banasik, K, Ostrowski, S R, Troelsen, A, Henkel, C, Pedersen, O B, Jonsdottir, I, Gudbjartsson, D F, Sulem, P, Thorgeirsson, T E, Stefansson, H, Stefansson, K, DBDS Genetic Consortium, Nyegaard, M & Nielsen, K R 2022, ' A genome-wide meta-analysis identifies 50 genetic loci associated with carpal tunnel syndrome ', Nature Communications, vol. 13, no. 1, 1598 . https://doi.org/10.1038/s41467-022-29133-7
Skuladottir, A T, Bjornsdottir, G, Ferkingstad, E, Einarsson, G, Stefansdottir, L, Nawaz, M S, Oddsson, A, Olafsdottir, T A, Saevarsdottir, S, Walters, G B, Magnusson, S H, Bjornsdottir, A, Sveinsson, O A, Vikingsson, A, Hansen, T F, Jacobsen, R L, Erikstrup, C, Schwinn, M, Brunak, S, Banasik, K, Ostrowski, S R, Troelsen, A, Henkel, C, Pedersen, O B, Jonsdottir, I, Gudbjartsson, D F, Sulem, P, Thorgeirsson, T E, Stefansson, H, Stefansson, K & DBDS Genetic Consortium 2022, ' A genome-wide meta-analysis identifies 50 genetic loci associated with carpal tunnel syndrome ', Nature Communications, vol. 13, no. 1, 1598 . https://doi.org/10.1038/s41467-022-29133-7
Nature Communications
Skuladottir, A T, Bjornsdottir, G, Ferkingstad, E, Einarsson, G, Stefansdottir, L, Nawaz, M S, Oddsson, A, Olafsdottir, T A, Saevarsdottir, S, Walters, G B, Magnusson, S H, Bjornsdottir, A, Sveinsson, O A, Vikingsson, A, Hansen, T F, Jacobsen, R L, Erikstrup, C, Schwinn, M, Brunak, S, Banasik, K, Ostrowski, S R, Troelsen, A, Henkel, C, Pedersen, O B, Jonsdottir, I, Gudbjartsson, D F, Sulem, P, Thorgeirsson, T E, Stefansson, H, Stefansson, K, DBDS Genetic Consortium & Bruun, M T 2022, ' A genome-wide meta-analysis identifies 50 genetic loci associated with carpal tunnel syndrome ', Nature Communications, vol. 13, no. 1, 1598 . https://doi.org/10.1038/s41467-022-29133-7
Skuladottir, A T, Bjornsdottir, G, Ferkingstad, E, Einarsson, G, Stefansdottir, L, Nawaz, M S, Oddsson, A, Olafsdottir, T A, Saevarsdottir, S, Walters, G B, Magnusson, S H, Bjornsdottir, A, Sveinsson, O A, Vikingsson, A, Hansen, T F, Jacobsen, R L, Erikstrup, C, Schwinn, M, Brunak, S, Banasik, K, Ostrowski, S R, Troelsen, A, Henkel, C, Pedersen, O B, Jonsdottir, I, Gudbjartsson, D F, Sulem, P, Thorgeirsson, T E, Stefansson, H, Stefansson, K, DBDS Genetic Consortium, Nyegaard, M & Nielsen, K R 2022, ' A genome-wide meta-analysis identifies 50 genetic loci associated with carpal tunnel syndrome ', Nature Communications, vol. 13, no. 1, 1598 . https://doi.org/10.1038/s41467-022-29133-7
Skuladottir, A T, Bjornsdottir, G, Ferkingstad, E, Einarsson, G, Stefansdottir, L, Nawaz, M S, Oddsson, A, Olafsdottir, T A, Saevarsdottir, S, Walters, G B, Magnusson, S H, Bjornsdottir, A, Sveinsson, O A, Vikingsson, A, Hansen, T F, Jacobsen, R L, Erikstrup, C, Schwinn, M, Brunak, S, Banasik, K, Ostrowski, S R, Troelsen, A, Henkel, C, Pedersen, O B, Jonsdottir, I, Gudbjartsson, D F, Sulem, P, Thorgeirsson, T E, Stefansson, H, Stefansson, K & DBDS Genetic Consortium 2022, ' A genome-wide meta-analysis identifies 50 genetic loci associated with carpal tunnel syndrome ', Nature Communications, vol. 13, no. 1, 1598 . https://doi.org/10.1038/s41467-022-29133-7
Nature Communications
Skuladottir, A T, Bjornsdottir, G, Ferkingstad, E, Einarsson, G, Stefansdottir, L, Nawaz, M S, Oddsson, A, Olafsdottir, T A, Saevarsdottir, S, Walters, G B, Magnusson, S H, Bjornsdottir, A, Sveinsson, O A, Vikingsson, A, Hansen, T F, Jacobsen, R L, Erikstrup, C, Schwinn, M, Brunak, S, Banasik, K, Ostrowski, S R, Troelsen, A, Henkel, C, Pedersen, O B, Jonsdottir, I, Gudbjartsson, D F, Sulem, P, Thorgeirsson, T E, Stefansson, H, Stefansson, K, DBDS Genetic Consortium & Bruun, M T 2022, ' A genome-wide meta-analysis identifies 50 genetic loci associated with carpal tunnel syndrome ', Nature Communications, vol. 13, no. 1, 1598 . https://doi.org/10.1038/s41467-022-29133-7
Carpal tunnel syndrome (CTS) is the most common entrapment neuropathy and has a largely unknown underlying biology. In a genome-wide association study of CTS (48,843 cases and 1,190,837 controls), we found 53 sequence variants at 50 loci associated w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f0e1fb461e6039948999410e47252af3
https://pure.au.dk/portal/da/publications/a-genomewide-metaanalysis-identifies-50-genetic-loci-associated-with-carpal-tunnel-syndrome(b0b10990-726d-4553-8a3e-3a36045f9933).html
https://pure.au.dk/portal/da/publications/a-genomewide-metaanalysis-identifies-50-genetic-loci-associated-with-carpal-tunnel-syndrome(b0b10990-726d-4553-8a3e-3a36045f9933).html
Autor:
Hautakangas, Heidi, Winsvold, Bendik K S, Ruotsalainen, Sanni, Bjornsdottir, Gyda, Harder, Aster V. E., Kogelman, Lisette J. A., Thomas, Laurent, Noordam, Raymond, Benner, Christian, Gormley, Padhraig, Artto, Ville, Banasik, Karina, Bjornsdottir, Anna, Boomsma, Dorret I., Brumpton, Ben Michael, Burgdorf, Kristoffer Sølvsten, Buring, Julie E., Chalmer, Mona Ameri, de Boer, Irene, Dichgans, Martin, Erikstrup, Christian, Färkkilä, Markus, Gabrielsen, Maiken Elvestad, Ghanbari, Mohsen, Hagen, Knut, Häppölä, Paavo, Hottenga, Jouke-Jan, Hrafnsdottir, Maria G., Hveem, Kristian, Johnsen, Marianne Bakke, Kähönen, Mika, Kristoffersen, Espen Saxhaug, Kurth, Tobias, Lehtimäki, Terho, Lighart, Lannie, Magnusson, Sigurdur H., Malik, Rainer, Pedersen, Ole Birger, Pelzer, Nadine, Penninx, Brenda W. J. H., Ran, Caroline, Ridker, Paul M., Rosendaal, Frits Richard, Sigurdardottir, Gudrun R., Skogholt, Anne Heidi, Sveinsson, Olafur A., Thorgeirsson, Thorgeir E., Ullum, Henrik, Zwart, John Anker Henrik
Externí odkaz:
https://hdl.handle.net/11250/3042137
Akademický článek
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Autor:
Cuellar-Partida, Gabriel, Tung, Joyce Y, Eriksson, Nicholas, Albrecht, Eva, Aliev, Fazil, Andreassen, Ole A, Barroso, Inês, Beckmann, Jacques S, Boks, Marco P, Boomsma, Dorret I, Boyd, Heather A, Breteler, Monique MB, Campbell, Harry, Chasman, Daniel I, Cherkas, Lynn F, Davies, Gail, de Geus, Eco JC, Deary, Ian J, Deloukas, Panos, Dick, Danielle M, Duffy, David L, Eriksson, Johan G, Esko, Tõnu, Feenstra, Bjarke, Geller, Frank, Gieger, Christian, Giegling, Ina, Gordon, Scott D, Han, Jiali, Hansen, Thomas F, Hartmann, Annette M, Hayward, Caroline, Heikkilä, Kauko, Hicks, Andrew A, Hirschhorn, Joel N, Hottenga, Jouke-Jan, Huffman, Jennifer E, Hwang, Liang-Dar, Ikram, M Arfan, Kaprio, Jaakko, Kemp, John P, Khaw, Kay-Tee, Klopp, Norman, Konte, Bettina, Kutalik, Zoltan, Lahti, Jari, Li, Xin, Loos, Ruth JF, Luciano, Michelle, Magnusson, Sigurdur H, Mangino, Massimo, Marques-Vidal, Pedro, Martin, Nicholas G, McArdle, Wendy L, McCarthy, Mark I, Medina-Gomez, Carolina, Melbye, Mads, Melville, Scott A, Metspalu, Andres, Milani, Lili, Mooser, Vincent, Nelis, Mari, Nyholt, Dale R, O'Connell, Kevin S, Ophoff, Roel A, Palmer, Cameron, Palotie, Aarno, Palviainen, Teemu, Pare, Guillaume, Paternoster, Lavinia, Peltonen, Leena, Penninx, Brenda WJH, Polasek, Ozren, Pramstaller, Peter P, Prokopenko, Inga, Raikkonen, Katri, Ripatti, Samuli, Rivadeneira, Fernando, Rudan, Igor, Rujescu, Dan, Smit, Johannes H, Smith, George Davey, Smoller, Jordan W, Soranzo, Nicole, Spector, Tim D, Pourcain, Beate St, Starr, John M, Stefánsson, Hreinn, Steinberg, Stacy, Teder-Laving, Maris, Thorleifsson, Gudmar, Stefánsson, Kári, Timpson, Nicholas J, Uitterlinden, André G, van Duijn, Cornelia M, van Rooij, Frank JA, Vink, Jaqueline M, Vollenweider, Peter, Vuoksimaa, Eero, Waeber, Gérard, Wareham, Nicholas J, Warrington, Nicole, Waterworth, Dawn, Werge, Thomas, Wichmann, H-Erich, Widen, Elisabeth, Willemsen, Gonneke, Wright, Alan F, Wright, Margaret J, Xu, Mousheng, Zhao, Jing Hua, Kraft, Peter, Hinds, David A, Lindgren, Cecilia M, Mägi, Reedik, Neale, Benjamin M, Evans, David M, Medland, Sarah E
Handedness has been extensively studied because of its relationship with language and the over-representation of left-handers in some neurodevelopmental disorders. Using data from the UK Biobank, 23andMe and the International Handedness Consortium, w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______109::cf50cf38c09bc2f14910c61c9d7b9b7f
https://www.repository.cam.ac.uk/handle/1810/309425
https://www.repository.cam.ac.uk/handle/1810/309425