Genome-Wide Association Study Points to Novel Locus for Gilles de la Tourette Syndrome

Autor: Barr, Cathy L., Batterson, James R., Berlin, Cheston, Budman, Cathy L., Coppola, Giovanni, Cox, Nancy J., Darrow, Sabrina, Dion, Yves, Freimer, Nelson B., Grados, Marco A., Greenberg, Erica, Hirschtritt, Matthew E., Huang, Alden Y., Illmann, Cornelia, King, Robert A., Kurlan, Roger, Leckman, James F., Lyon, Gholson J., Malaty, Irene A., McMahon, William M., Neale, Benjamin M., Okun, Michael S., Osiecki, Lisa, Robertson, Mary M., Rouleau, Guy A., Sandor, Paul, Singer, Harvey S., Smit, Jan H., Sul, Jae Hoon, Androutsos, Christos, Basha, Entela, Farkas, Luca, Fichna, Jakub, Janik, Piotr, Kapisyzi, Mira, Karagiannidis, Iordanis, Koumoula, Anastasia, Nagy, Peter, Puchala, Joanna, Szejko, Natalia, Szymanska, Urszula, Tsironi, Vaia, Apter, Alan, Ball, Juliane, Bodmer, Benjamin, Bognar, Emese, Buse, Judith, Vela, Marta Correa, Fremer, Carolin, Garcia-Delgar, Blanca, Gulisano, Mariangela, Hagen, Annelieke, Hagstrøm, Julie, Madruga-Garrido, Marcos, Pellico, Alessandra, Ruhrman, Daphna, Schnell, Jaana, Silvestri, Paola Rosaria, Skov, Liselotte, Steinberg, Tamar, Gloor, Friederike Tagwerker, Turner, Victoria L., Weidinger, Elif, Alexander, John, Aranyi, Tamas, Buisman, Wim R., Buitelaar, Jan K., Driessen, Nicole, Drineas, Petros, Fan, Siyan, Forde, Natalie J., Gerasch, Sarah, van den Heuvel, Odile A., Jespersgaard, Cathrine, Kanaan, Ahmad S., Möller, Harald E., Nawaz, Muhammad S., Nespoli, Ester, Pagliaroli, Luca, Poelmans, Geert, Pouwels, Petra J.W., Rizzo, Francesca, Veltman, Dick J., van der Werf, Ysbrand D., Widomska, Joanna, Zilhäo, Nuno R., Brown, Lawrence W., Cheon, Keun-Ah, Coffey, Barbara J., Fernandez, Thomas V., Gilbert, Donald L., Hong, Hyun Ju, Ibanez-Gomez, Laura, Kim, Eun-Joo, Kim, Young Key, Kim, Young-Shin, Koh, Yun-Joo, Kook, Sodahm, Kuperman, Samuel, Leventhal, Bennett L., Maras, Athanasios, Murphy, Tara L., Shin, Eun-Young, Song, Dong-Ho, Song, Jungeun, State, Matthew W., Visscher, Frank, Wang, Sheng, Zinner, Samuel H., Tsetsos, Fotis, Topaloudi, Apostolia, Jain, Pritesh, Yang, Zhiyu, Yu, Dongmei, Kolovos, Petros, Tumer, Zeynep, Rizzo, Renata, Hartmann, Andreas, Depienne, Christel, Worbe, Yulia, Müller-Vahl, Kirsten R., Cath, Danielle C., Boomsma, Dorret I., Wolanczyk, Tomasz, Zekanowski, Cezary, Barta, Csaba, Nemoda, Zsofia, Tarnok, Zsanett, Padmanabhuni, Shanmukha S., Buxbaum, Joseph D., Grice, Dorothy, Glennon, Jeffrey, Stefansson, Hreinn, Hengerer, Bastian, Yannaki, Evangelia, Stamatoyannopoulos, John A., Benaroya-Milshtein, Noa, Cardona, Francesco, Hedderly, Tammy, Heyman, Isobel, Huyser, Chaim, Mir, Pablo, Morer, Astrid, Mueller, Norbert, Munchau, Alexander, Plessen, Kerstin J., Porcelli, Cesare, Roessner, Veit, Walitza, Susanne, Schrag, Anette, Martino, Davide, Tischfield, Jay A., Heiman, Gary A., Willsey, A. Jeremy, Dietrich, Andrea, Davis, Lea K., Crowley, James J., Mathews, Carol A., Scharf, Jeremiah M., Georgitsi, Marianthi, Hoekstra, Pieter J., Paschou, Peristera

Publikováno v: In Biological Psychiatry 15 July 2024 96(2):114-124

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Rare SLC13A1 variants associate with intervertebral disc disorder highlighting role of sulfate in disc pathology

Autor: Bjornsdottir, Gyda, Stefánsdóttir, Lilja, Thorleifsson, Gudmar, Sulem, Patrick, Norland, Kristjan, Ferkingstad, Egil, Oddsson, Asmundur, Zink, Florian, Lund, Sigrun H., Nawaz, Muhammad S., Bragi Walters, G., Skuladottir, Astros Th., Gudjonsson, Sigurjon A., Einarsson, Gudmundur, Halldorsson, Gisli H., Bjarnadottir, Valgerdur, Sveinbjornsson, Gardar, Helgadottir, Anna, Styrkársdóttir, Unnur, Gudmundsson, Larus J., Pedersen, Ole B., Hansen, Thomas Folkmann, Werge, Thomas, Banasik, Karina, Troelsen, Anders, Skou, Soren T., Thørner, Lise Wegner, Erikstrup, Christian, Nielsen, Kaspar Rene, Mikkelsen, Susan, Andersen, Steffen, Brunak, Søren, Burgdorf, Kristoffer, Hjalgrim, Henrik, Jemec, Gregor, Jennum, Poul, Johansson, Per Ingemar, Nielsen, Kasper Rene, Nyegaard, Mette, Bruun, Mie Topholm, Pedersen, Ole Birger, Dinh, Khoa Manh, Sørensen, Erik, Ostrowski, Sisse R., Johansson, Pär Ingemar, Gudbjartsson, Daniel F., Stefansson, Hreinn, Þorsteinsdóttir, Unnur, Larsen, Margit Anita Hørup, Didriksen, Maria, Sækmose, Susanne, Zeggini, Eleftheria, Hatzikotoulas, Konstantinos, Southam, Lorraine, Gilly, Arthur, Barysenka, Andrei, van Meurs, Joyce B. J., Boer, Cindy G., Uitterlinden, André G., Jonsson, Helgi, Ingvarsson, Thorvaldur, Esko, Tõnu, Mägi, Reedik, Teder-Laving, Maris, Ikegawa, Shiro, Terao, Chikashi, Takuwa, Hiroshi, Meulenbelt, Ingrid, Coutinho de Almeida, Rodrigo, Kloppenburg, Margreet, Tuerlings, Margo, Slagboom, P. Eline, Nelissen, Rob R. G. H. H., Valdes, Ana M., Mangino, Massimo, Tsezou, Aspasia, Zengini, Eleni, Alexiadis, George, Babis, George C., Cheah, Kathryn S. E., Wu, Tian T., Samartzis, Dino, Cheung, Jason Pui Yin, Sham, Pak Chung, Kraft, Peter, Kang, Jae Hee, Hveem, Kristian, Zwart, John-Anker, Luetge, Almut, Skogholt, Anne Heidi, Johnsen, Marianne B., Thomas, Laurent F., Winsvold, Bendik, Gabrielsen, Maiken E., Lee, Ming Ta Michael, Zhang, Yanfei, Lietman, Steven A., Shivakumar, Manu, Smith, George Davey, Tobias, Jonathan H., Hartley, April, Gaunt, Tom R., Zheng, Jie, Wilkinson, J. Mark, Steinberg, Julia, Morris, Andrew P., Jonsdottir, Ingileif, Bjornsson, Aron, Olafsson, Ingvar H., Ulfarsson, Elfar, Blondal, Josep, Vikingsson, Arnor, Brunak, Soren, Ullum, Henrik, Thorsteinsdottir, Unnur, Thorgeirsson, Thorgeir E., Stefansson, Kari, Consortium, DBDS Genetic, Consortium, GO

Publikováno v: Nature Communications, 13(1):634. Nature Publishing Group
Nature Communications, Vol 13, Iss 1, Pp 1-13 (2022)
Bjornsdottir, G, Stefansdottir, L, Thorleifsson, G, Sulem, P, Norland, K, Ferkingstad, E, Oddsson, A, Zink, F, Lund, S H, Nawaz, M S, Bragi Walters, G, Skuladottir, A T, Gudjonsson, S A, Einarsson, G, Halldorsson, G H, Bjarnadottir, V, Sveinbjornsson, G, Helgadottir, A, Styrkarsdottir, U, Gudmundsson, L J, Pedersen, O B, Hansen, T F, Werge, T, Banasik, K, Troelsen, A, Skou, S T, Thørner, L W, Erikstrup, C, Nielsen, K R, Mikkelsen, S, Jonsdottir, I, Bjornsson, A, Olafsson, I H, Ulfarsson, E, Blondal, J, Vikingsson, A, Brunak, S, Ostrowski, S R, Ullum, H, Thorsteinsdottir, U, Stefansson, H, Gudbjartsson, D F, Thorgeirsson, T E, Stefansson, K, DBDS Genetic Consortium & GO Consortium 2022, ' Rare SLC13A1 variants associate with intervertebral disc disorder highlighting role of sulfate in disc pathology ', Nature Communications, vol. 13, 634 . https://doi.org/10.1038/s41467-022-28167-1
Bjornsdottir, G, Stefánsdóttir, L, Thorleifsson, G, Sulem, P, Norland, K, Ferkingstad, E, Oddsson, A, Zink, F, Lund, S H, Nawaz, M S, Bragi Walters, G, Skuladottir, A T, Gudjonsson, S A, Einarsson, G, Halldorsson, G H, Bjarnadottir, V, Sveinbjornsson, G, Helgadottir, A, Styrkársdóttir, U, Gudmundsson, L J, Pedersen, O B, Hansen, T F, Werge, T, Banasik, K, Troelsen, A, Skou, S T, Thørner, L W, Erikstrup, C, Nielsen, K R, Mikkelsen, S, Andersen, S, Brunak, S, Burgdorf, K, Hjalgrim, H, Jemec, G, Jennum, P, Johansson, P I, Nielsen, K R, Nyegaard, M, Bruun, M T, Pedersen, O B, Dinh, K M, Sørensen, E, Ostrowski, S R, Johansson, P I, Gudbjartsson, D F, Stefansson, H, Þorsteinsdóttir, U, Larsen, M A H, Didriksen, M, Sækmose, S, Zeggini, E, Hatzikotoulas, K, Southam, L, Gilly, A, Barysenka, A, van Meurs, J B J, Boer, C G, Uitterlinden, A G, Styrkársdóttir, U, Stefánsdóttir, L, Jonsson, H, Ingvarsson, T, Esko, T, Mägi, R, Teder-Laving, M, Ikegawa, S, Terao, C, Takuwa, H, Meulenbelt, I, Coutinho de Almeida, R, Kloppenburg, M, Tuerlings, M, Slagboom, P E, Nelissen, R R G H H, Valdes, A M, Mangino, M, Tsezou, A, Zengini, E, Alexiadis, G, Babis, G C, Cheah, K S E, Wu, T T, Samartzis, D, Cheung, J P Y, Sham, P C, Kraft, P, Kang, J H, Hveem, K, Zwart, J-A, Luetge, A, Skogholt, A H, Johnsen, M B, Thomas, L F, Winsvold, B, Gabrielsen, M E, Lee, M T M, Zhang, Y, Lietman, S A, Shivakumar, M, Smith, G D, Tobias, J H, Hartley, A, Gaunt, T R, Zheng, J, Wilkinson, J M, Steinberg, J, Morris, A P, Jonsdottir, I, Bjornsson, A, Olafsson, I H, Ulfarsson, E, Blondal, J, Vikingsson, A, Brunak, S, Ostrowski, S R, Ullum, H, Thorsteinsdottir, U, Stefansson, H, Gudbjartsson, D F, Thorgeirsson, T E, Stefansson, K, Consortium, DBDS G & Consortium, GO 2022, ' Rare SLC13A1 variants associate with intervertebral disc disorder highlighting role of sulfate in disc pathology ', Nature Communications, vol. 13, no. 1, 634 . https://doi.org/10.1038/s41467-022-28167-1
Bjornsdottir, G, Stefansdottir, L, Thorleifsson, G, Sulem, P, Norland, K, Ferkingstad, E, Oddsson, A, Zink, F, Lund, S H, Nawaz, M S, Bragi Walters, G, Skuladottir, A T, Gudjonsson, S A, Einarsson, G, Halldorsson, G H, Bjarnadottir, V, Sveinbjornsson, G, Helgadottir, A, Styrkarsdottir, U, Gudmundsson, L J, Pedersen, O B, Hansen, T F, Werge, T, Banasik, K, Troelsen, A, Skou, S T, Thørner, L W, Erikstrup, C, Nielsen, K R, Mikkelsen, S, DBDS Genetic Consortium, Jonsdottir, I, Bjornsson, A, Olafsson, I H, Ulfarsson, E, Blondal, J, Vikingsson, A, Brunak, S, Ostrowski, S R, Ullum, H, Thorsteinsdottir, U, Stefansson, H, Gudbjartsson, D F, Thorgeirsson, T E, Stefansson, K & Nyegaard, M 2022, ' Rare SLC13A1 variants associate with intervertebral disc disorder highlighting role of sulfate in disc pathology ', Nature Communications, vol. 13, no. 1, 634 . https://doi.org/10.1038/s41467-022-28167-1
Bjornsdottir, G, Stefánsdóttir, L, Thorleifsson, G, Sulem, P, Norland, K, Ferkingstad, E, Oddsson, A, Zink, F, Lund, S H, Nawaz, M S, Bragi Walters, G, Skuladottir, A T, Gudjonsson, S A, Einarsson, G, Halldorsson, G H, Bjarnadottir, V, Sveinbjornsson, G, Helgadottir, A, Styrkársdóttir, U, Gudmundsson, L J, Pedersen, O B, Hansen, T F, Werge, T, Banasik, K, Troelsen, A, Skou, S T, Thørner, L W, Erikstrup, C, Nielsen, K R, Mikkelsen, S, DBDS Genetic Consortium, GO Consortium, Jonsdottir, I, Bjornsson, A, Olafsson, I H, Ulfarsson, E, Blondal, J, Vikingsson, A, Brunak, S, Ostrowski, S R, Ullum, H, Thorsteinsdottir, U, Stefansson, H, Gudbjartsson, D F, Thorgeirsson, T E & Nyegaard, M 2022, ' Rare SLC13A1 variants associate with intervertebral disc disorder highlighting role of sulfate in disc pathology ', Nature Communications, vol. 13, 634 . https://doi.org/10.1038/s41467-022-28167-1

Back pain is a common and debilitating disorder with largely unknown underlying biology. Here we report a genome-wide association study of back pain using diagnoses assigned in clinical practice; dorsalgia (119,100 cases, 909,847 controls) and interv

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a437f3a611a9b487e04c29f022013bff
https://pure.eur.nl/en/publications/1ed1ee69-849e-44a6-99a5-da9d852b2852

Author Correction: Rare SLC13A1 variants associate with intervertebral disc disorder highlighting role of sulfate in disc pathology

Autor: Bjornsdottir, Gyda, Stefansdottir, Lilja, Thorleifsson, Gudmar, Sulem, Patrick, Norland, Kristjan, Ferkingstad, Egil, Oddsson, Asmundur, Zink, Florian, Lund, Sigrun H, Nawaz, Muhammad S, Bragi Walters, G, Skuladottir, Astros Th, Gudjonsson, Sigurjon A, Einarsson, Gudmundur, Halldorsson, Gisli H, Bjarnadottir, Valgerdur, Sveinbjornsson, Gardar, Helgadottir, Anna, Styrkarsdottir, Unnur, Gudmundsson, Larus J, Pedersen, Ole B, Hansen, Thomas Folkmann, Werge, Thomas, Banasik, Karina, Troelsen, Anders, Skou, Soren T, Thørner, Lise Wegner, Erikstrup, Christian, Nielsen, Kaspar Rene, Mikkelsen, Susan, Jonsdottir, Ingileif, Bjornsson, Aron, Olafsson, Ingvar H, Ulfarsson, Elfar, Blondal, Josep, Vikingsson, Arnor, Brunak, Soren, Ostrowski, Sisse R, Ullum, Henrik, Thorsteinsdottir, Unnur, Stefansson, Hreinn, Gudbjartsson, Daniel F, Thorgeirsson, Thorgeir E, Stefansson, Kari

Publikováno v: Bjornsdottir, G, Stefansdottir, L, Thorleifsson, G, Sulem, P, Norland, K, Ferkingstad, E, Oddsson, A, Zink, F, Lund, S H, Nawaz, M S, Bragi Walters, G, Skuladottir, A T, Gudjonsson, S A, Einarsson, G, Halldorsson, G H, Bjarnadottir, V, Sveinbjornsson, G, Helgadottir, A, Styrkarsdottir, U, Gudmundsson, L J, Pedersen, O B, Hansen, T F, Werge, T, Banasik, K, Troelsen, A, Skou, S T, Thørner, L W, Erikstrup, C, Nielsen, K R, Mikkelsen, S, DBDS Genetic Consortium, Jonsdottir, I, Bjornsson, A, Olafsson, I H, Ulfarsson, E, Blondal, J, Vikingsson, A, Brunak, S, Ostrowski, S R, Ullum, H, Thorsteinsdottir, U, Stefansson, H, Gudbjartsson, D F, Thorgeirsson, T E & Stefansson, K 2022, ' Author Correction: Rare SLC13A1 variants associate with intervertebral disc disorder highlighting role of sulfate in disc pathology ', Nature Communications, vol. 13, no. 1, 2419 . https://doi.org/10.1038/s41467-022-30129-6

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4517c1a8447dab991bbd0fc4db6a8e47
https://findresearcher.sdu.dk:8443/ws/files/202268138/s41467_022_30129_6.pdf

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