Genetic analyses identify widespread sex-differential participation bias

Autor: Pirastu N., Cordioli M., Nandakumar P., Mignogna G., Abdellaoui A., Hollis B., Kanai M., Rajagopal V. M., Parolo P. D. B., Baya N., Carey C. E., Karjalainen J., Als T. D., Van der Zee M. D., Day F. R., Ong K. K., Agee M., Aslibekyan S., Bell R. K., Bryc K., Clark S. K., Elson S. L., Fletez-Brant K., Fontanillas P., Furlotte N. A., Gandhi P. M., Heilbron K., Hicks B., Huber K. E., Jewett E. M., Jiang Y., Kleinman A., Lin K. -H., Litterman N. K., Luff M. K., McIntyre M. H., McManus K. F., Mountain J. L., Mozaffari S. V., Noblin E. S., Northover C. A. M., O'Connell J., Petrakovitz A. A., Pitts S. J., Poznik G. D., Sathirapongsasuti J. F., Shelton J. F., Shringarpure S., Tian C., Tung J. Y., Tunney R. J., Vacic V., Wang X., Zare A., Mortensen P. B., Mors O., Werge T., Nordentoft M., Hougaard D. M., Bybjerg-Grauholm J., Baekvad-Hansen M., Morisaki T., de Geus E., Bellocco R., Okada Y., Borglum A. D., Joshi P., Auton A., Hinds D., Neale B. M., Walters R. K., Nivard M. G., Perry J. R. B., Ganna A.

Publikováno v: Nature Genetics, 53(5), 663-671. Nature Publishing Group
Nature genetics, 53(5), 663-671. Nature Publishing Group
Pirastu, N, Cordioli, M, Nandakumar, P, Mignogna, G, Abdellaoui, A, Hollis, B, Kanai, M, Rajagopal, V M, Parolo, P D B, Baya, N, Carey, C E, Karjalainen, J, Als, T D, Zee, M D V D, Day, F R, Ong, K K, Morisaki, T, Geus, E D, Bellocco, R, Okada, Y, Børglum, A D, Joshi, P, Auton, A, Hinds, D, Neale, B M, Walters, R K, Nivard, M G, Perry, J R B & Ganna, A 2021, ' Genetic analyses identify widespread sex-differential participation bias ', Nature Genetics, vol. 53, 53, pp. 663 . https://doi.org/10.1038/s41588-021-00846-7
Pirastu, N, Cordioli, M, Nandakumar, P, Mignogna, G, Abdellaoui, A, Hollis, B, Kanai, M, Rajagopal, V M, Parolo, P D B, Baya, N, Carey, C E, Karjalainen, J, Als, T D, Van der Zee, M D, Day, F R, Ong, K K, Morisaki, T, de Geus, E, Bellocco, R, Okada, Y, Børglum, A D, Joshi, P, Auton, A, Hinds, D, Neale, B M, Walters, R K, Nivard, M G, Perry, J R B, Ganna, A, FinnGen Study, 23andMe Research Team & iPSYCH Consortium 2021, ' Genetic analyses identify widespread sex-differential participation bias ', Nature Genetics, vol. 53, no. 5, pp. 663-671 . https://doi.org/10.1038/s41588-021-00846-7
Nat Genet
Pirastu, N, Cordioli, M, Nandakumar, P, Mignogna, G, Abdellaoui, A, Hollis, B, Kanai, M, Rajagopal, V M, Parolo, P D B, Baya, N, Carey, C E, Karjalainen, J, Als, T D, Van Der Zee, M D, Day, F R, Ong, K K, Morisaki, T, De Geus, E, Bellocco, R, Okada, Y, Børglum, A D, Joshi, P, Auton, A, Hinds, D, Neale, B M, Walters, R K, Nivard, M G, Perry, J R B & Ganna, A 2021, ' Genetic analyses identify widespread sex-differential participation bias ', Nature Genetics, vol. 53, no. 5, pp. 663-671 . https://doi.org/10.1038/s41588-021-00846-7

Genetic association results are often interpreted with the assumption that study participation does not affect downstream analyses. Understanding the genetic basis of participation bias is challenging since it requires the genotypes of unseen individ

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::a71745af8272663af6b52258d6ed8794
https://doi.org/10.1038/s41588-021-00846-7

Genome-wide association study of REM sleep behavior disorder identifies polygenic risk and brain expression effects

Autor: Krohn, L., Heilbron, K., Blauwendraat, C., Reynolds, R. H., Yu, E., Senkevich, K., Rudakou, U., Estiar, M. A., Gustavsson, E. K., Brolin, K., Ruskey, J. A., Freeman, K., Asayesh, F., Chia, R., Arnulf, I., M. T. M., Hu, Montplaisir, J. Y., Gagnon, J. -F., Desautels, A., Dauvilliers, Y., Gigli, G. L., Valente, M., Janes, F., Bernardini, A., Hogl, B., Stefani, A., Ibrahim, A., Sonka, K., Kemlink, D., Oertel, W., Janzen, A., Plazzi, G., Biscarini, F., Antelmi, E., Figorilli, M., Puligheddu, M., Mollenhauer, B., Trenkwalder, C., Sixel-Doring, F., Cochen De Cock, V., Monaca, C. C., Heidbreder, A., Ferini-Strambi, L., Dijkstra, F., Viaene, M., Abril, B., Boeve, B. F., Aslibekyan, S., Auton, A., Babalola, E., Bell, R. K., Bielenberg, J., Bryc, K., Bullis, E., Coker, D., Partida, G. C., Dhamija, D., Das, S., Elson, S. L., Filshtein, T., Fletez-Brant, K., Fontanillas, P., Freyman, W., Gandhi, P. M., Hicks, B., Hinds, D. A., Jewett, E. M., Jiang, Y., Kukar, K., Lin, K. -H., Lowe, M., Mccreight, J. C., Mcintyre, M. H., Micheletti, S. J., Moreno, M. E., Mountain, J. L., Nandakumar, P., Noblin, E. S., O'Connell, J., Petrakovitz, A. A., Poznik, G. D., Schumacher, M., Shastri, A. J., Shelton, J. F., Shi, J., Shringarpure, S., Tran, V., Tung, J. Y., Wang, X., Wang, W., Weldon, C. H., Wilton, P., Hernandez, A., Wong, C., Tchakoute, C. T., Scholz, S. W., Ryten, M., Bandres-Ciga, S., Noyce, A., Cannon, P., Pihlstrom, L., Nalls, M. A., Singleton, A. B., Rouleau, G. A., Postuma, R. B., Gan-Or, Z.

Publikováno v: Nature communications

Rapid-eye movement (REM) sleep behavior disorder (RBD), enactment of dreams during REM sleep, is an early clinical symptom of alpha-synucleinopathies and defines a more severe subtype. The genetic background of RBD and its underlying mechanisms are n

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9fcdc569abde0b0f8b22a0fa00ba2e69
https://hdl.handle.net/10067/1961640151162165141

Gastroesophageal reflux GWAS identifies risk loci that also associate with subsequent severe esophageal diseases

Autor: An, Jiyuan, Gharahkhani, Puya, Law, Matthew H., Ong, Jue-Sheng, Han, Xikun, Olsen, Catherine M., Neale, Rachel E., Lai, John, Vaughan, Tom L., Gockel, Ines, Thieme, René, Böhmer, Anne C., Jankowski, Janusz, Fitzgerald, Rebecca C., Schumacher, Johannes, Palles, Claire, Whiteman, David C., MacGregor, Stuart, Gammon, Marilie D., Corley, Douglas A., Shaheen, Nicholas J., Bird, Nigel C., Hardie, Laura J., Murray, Liam J., Reid, Brian J., Chow, Wong-Ho, Risch, Harvey A., Ye, Weimin, Liu, Geoffrey, Romero, Yvonne, Bernstein, Leslie, Wu, Anna H., Agee, M., Alipanahi, B., Auton, A., Bell, R. K., Bryc, K., Elson, S. L., Fontanillas, P., Furlotte, N. A., Hinds, D. A., Huber, K. E., Kleinman, A., Litterman, N. K., McIntyre, M. H., Mountain, J. L., Noblin, E. S., Northover, C. A. M., Pitts, S. J., Sathirapongsasuti, J. Fah, Sazonova, O. V., Shelton, J. F., Shringarpure, S., Tian, C., Tung, J. Y., Vacic, V., Wilson, C. H.

Funder: The Swedish Esophageal Cancer Study was funded by grants (R01 CA57947-03) from the National Cancer Institute he California Tobacco Related Research Program (3RT-0122; and; 10RT-0251) Marit Peterson Fund for Melanoma Research. CIDR is supporte

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::63e787bf315ca4c794c643db06019563
https://www.repository.cam.ac.uk/handle/1810/310289

Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error

Autor: TEDJA, M. S., WOJCIECHOWSKI, R., HYSI, P. G., ERIKSSON, N., FURLOTTE, N. A., VERHOEVEN, V. J. M., IGLESIAS, A. I., MEESTER-SMOOR, M. A., TOMPSON, S. W., Fan, Q., KHAWAJA, A. P., CHENG, C. Y., HOHN, R., YAMASHIRO, K., WENOCUR, A., GRAZAL, C., Haller, T., Metspalu, A., WEDENOJA, J., JONAS, J. B., WANG, Y. X., Xie, J., Mitchell, P., FOSTER, P. J., KLEIN, B. E. K., Klein, R., PATERSON, A. D., HOSSEINI, S. M., SHAH, R. L., Williams, C., TEO, Y. Y., THAM, Y. C., Gupta, P., Zhao, W., Shi, Y., SAW, W. Y., TAI, E. S., SIM, X. L., HUFFMAN, J. E., POLASEK, O., Hayward, C., BENCIC, G., RUDAN, I., WILSON, J. F., Joshi, P. K., TSUJIKAWA, A., Matsuda, F., WHISENHUNT, K. N., Zeller, T., VAN DER SPEK, P. J., HAAK, R., Meijers-Heijboer, H., VAN LEEUWEN, E. M., IYENGAR, S. K., LASS, J. H., Hofman, A., Rivadeneira, F., UITTERLINDEN, A. G., VINGERLING, J. R., LEHTIMAKI, T., RAITAKARI, O. T., BIINO, G., CONCAS, M. P., SCHWANTES-AN, T. H., IGO, R. P., Jr., CUELLAR-PARTIDA, G., Martin, N. G., CRAIG, J. E., GHARAHKHANI, P., Williams, K. M., NAG, A., RAHI, J. S., CUMBERLAND, P. M., Delcourt, Cécile, Bellenguez, C., RIED, J. S., BERGEN, A. A., Meitinger, T., Gieger, C., WONG, T. Y., HEWITT, A. W., MACKEY, D. A., SIMPSON, C. L., Pfeiffer, N., PARSSINEN, O., BAIRD, P. N., Vitart, V., Amin, N., VAN DUIJN, C. M., BAILEY-WILSON, J. E., YOUNG, T. L., SAW, S. M., STAMBOLIAN, D., MACGREGOR, S., GUGGENHEIM, J. A., TUNG, J. Y., HAMMOND, C. J., KLAVER, C. C. W.

Publikováno v: Nature Genetics
Nature Genetics, Nature Publishing Group, 2018, 50 (6), pp.834-848. ⟨10.1038/s41588-018-0127-7⟩

Refractive errors, including myopia, are the most frequent eye disorders worldwide and an increasingly common cause of blindness. This genome-wide association meta-analysis in 160,420 participants and replication in 95,505 participants increased the

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::5b2086cfb69a2e2d507998cfe6580144
https://hal.archives-ouvertes.fr/hal-03193823

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