Linkage disequilibrium mapping of a breast cancer susceptibility locus near RAI/PPP1R13L/iASPP

Autor: Mains Mette, Hansen Bettina, Koca Cemile, Zhang Xiuqing, Rockenbauer Eszter, Bukowy Zuzanna, Nyegaard Mette, Olsen Anja, Vogel Ulla, Nexø Bjørn A, Hedemand Anne, Kjeldgaard Anette, Laska Magdalena J, Raaschou-Nielsen Ole, Cold Søren, Overvad Kim, Tjønneland Anne, Bolund Lars, Børglum Anders D

Publikováno v: BMC Medical Genetics, Vol 9, Iss 1, p 56 (2008)

Abstract Background Previous results have suggested an association of the region of 19q13.3 with several forms of cancer. In the present study, we investigated 27 public markers within a previously identified 69 kb stretch of chromosome 19q for assoc

Externí odkaz: https://doaj.org/article/76f00bb87ee74f14ae1c93209e5be681

Statistical and functional convergence of common and rare genetic influences on autism at chromosome 16p

Autor: Weiner, Daniel J., Ling, Emi, Erdin, Serkan, Tai, Derek J. C., Yadav, Rachita, Grove, Jakob, Fu, Jack M., Nadig, Ajay, Carey, Caitlin E., Baya, Nikolas, Bybjerg-Grauholm, Jonas, Mortensen, Preben B., Werge, Thomas, Demontis, Ditte, Mors, Ole, Nordentoft, Merete, Als, Thomas D., Baekvad-Hansen, Marie, Rosengren, Anders, Havdahl, Alexandra, Hedemand, Anne, Palotie, Aarno, Chakravarti, Aravinda, Arking, Dan, Sulovari, Arvis, Starnawska, Anna, Thiruvahindrapuram, Bhooma, de Leeuw, Christiaan, Carey, Caitlin, Ladd-Acosta, Christine, van der Merwe, Celia, Devlin, Bernie, Cook, Edwin H., Eichler, Evan, Corfield, Elisabeth, Dieleman, Gwen, Schellenberg, Gerard, Hakonarson, Hakon, Coon, Hilary, Dziobek, Isabel, Vorstman, Jacob, Girault, Jessica, Sutcliffe, James S., Duan, Jinjie, Nurnberger, John, Hallmayer, Joachim, Buxbaum, Joseph, Piven, Joseph, Weiss, Lauren, Davis, Lea, Janecka, Magdalena, Mattheisen, Manuel, State, Matthew W., Gill, Michael, Daly, Mark, Uddin, Mohammed, Andreassen, Ole, Szatmari, Peter, Lee, Phil Hyoun, Anney, Richard, Ripke, Stephan, Satterstrom, Kyle, Santangelo, Susan, Kuo, Susan, van Elst, Ludger Tebartz, Rolland, Thomas, Bougeron, Thomas, Polderman, Tinca, Turner, Tychele, Underwood, Jack, Manikandan, Veera, Pillalamarri, Vamsee, Warrier, Varun, Philipsen, Alexandra, Reif, Andreas, Hinney, Anke, Cormand, Bru, Bau, Claiton H. D., Rovaris, Diego Luiz, Sonuga-Barke, Edmund, Corfield, Elizabeth, Grevet, Eugenio Horacio, Salum, Giovanni, Larsson, Henrik, Buitelaar, Jan, Haavik, Jan, McGough, James, Kuntsi, Jonna, Elia, Josephine, Lesch, Klaus-Peter, Klein, Marieke, Bellgrove, Mark, Tesli, Martin, Leung, Patrick W. L., Pan, Pedro M., Dalsgaard, Soren, Loo, Sandra, Medland, Sarah, Faraone, Stephen V., Reichborn-Kjennerud, Ted, Banaschewski, Tobias, Hawi, Ziarih, Berretta, Sabina, Macosko, Evan Z., Sebat, Jonathan, O’Connor, Luke J., Hougaard, David M., Børglum, Anders D., Talkowski, Michael E., McCarroll, Steven A., Robinson, Elise B.

Publikováno v: Nature Genetics, 54(11), 1630-1639. Nature Publishing Group
Nature Genetics
Weiner, D J, Ling, E, Erdin, S, Tai, D J C, Yadav, R, Grove, J, Fu, J M, Nadig, A, Carey, C E, Baya, N, Bybjerg-Grauholm, J, Mortensen, P B, Werge, T, Demontis, D, Mors, O, Nordentoft, M, Als, T D, Baekvad-Hansen, M, Rosengren, A, Havdahl, A, Hedemand, A, Palotie, A, Chakravarti, A, Arking, D, Sulovari, A, Starnawska, A, Thiruvahindrapuram, B, de Leeuw, C, Carey, C, Ladd-Acosta, C, van der Merwe, C, Devlin, B, Cook, E H, Eichler, E, Corfield, E, Dieleman, G, Schellenberg, G, Hakonarson, H, Coon, H, Dziobek, I, Vorstman, J, Girault, J, Sutcliffe, J S, Duan, J, Nurnberger, J, Hallmayer, J, Buxbaum, J, Piven, J, Weiss, L, Davis, L, Janecka, M, Mattheisen, M, State, M W, Gill, M, Daly, M, Uddin, M, Andreassen, O, Szatmari, P, Lee, P H, Anney, R, Ripke, S, Satterstrom, K, Santangelo, S, Kuo, S, van Elst, L T, Rolland, T, Bougeron, T, Polderman, T, Turner, T, Underwood, J, Manikandan, V, Pillalamarri, V, Warrier, V, Philipsen, A, Reif, A, Hinney, A, Cormand, B, Bau, C H D, Rovaris, D L, Sonuga-Barke, E, Corfield, E, Grevet, E H, Salum, G, Larsson, H, Buitelaar, J, Haavik, J, McGough, J, Kuntsi, J, Elia, J, Lesch, K-P, Klein, M, Bellgrove, M, Tesli, M, Leung, P W L, Pan, P M, Dalsgaard, S, Loo, S, Medland, S, iPSYCH Consortium, Faraone, S V, ASD Working Group of the Psychiatric Genomics Consortium, Reichborn-Kjennerud, T, ADHD Working Group of the Psychiatric Genomics Consortium, Banaschewski, T, Hawi, Z, Berretta, S, Macosko, E Z, Sebat, J, O’Connor, L J, Hougaard, D M, Børglum, A D, Talkowski, M E, McCarroll, S A & Robinson, E B 2022, ' Statistical and functional convergence of common and rare genetic influences on autism at chromosome 16p ', Nature Genetics, vol. 54, no. 11, pp. 1630-1639 . https://doi.org/10.1038/s41588-022-01203-y
Weiner, D J, Ling, E, Erdin, S, Tai, D J C, Yadav, R, Grove, J, Fu, J M, Nadig, A, Carey, C, Baya, N, Bybjerg-Grauholm, J, Mortensen, P B, Werge, T, Demontis, D, Mors, O, Nordentoft, M, Als, T D, Baekvad-Hansen, M, Rosengren, A, Havdahl, A, Hedemand, A, Palotie, A, Chakravarti, A, Arking, D, Sulovari, A, Starnawska, A, Thiruvahindrapuram, B, de Leeuw, C, Carey, C, Ladd-Acosta, C, van der Merwe, C, Devlin, B, Cook, E H, Eichler, E, Corfield, E, Dieleman, G, Schellenberg, G, Hakonarson, H, Coon, H, Dziobek, I, Vorstman, J, Girault, J, Sutcliffe, J S, Duan, J, Nurnberger, J, Hallmayer, J, Buxbaum, J, Hinney, A, Larsson, H, Dalsgaard, S, iPSYCH Consortium, ASD Working Group of the Psychiatric Genomics Consortium & ADHD Working Group of the Psychiatric Genomics Consortium 2022, ' Statistical and functional convergence of common and rare genetic influences on autism at chromosome 16p ', Nature Genetics, vol. 54, pp. 1630-1639 . https://doi.org/10.1038/s41588-022-01203-y
Weiner, D J, Ling, E, Erdin, S, Tai, D J C, Yadav, R, Grove, J, Fu, J M, Nadig, A, Carey, C E, Baya, N, Bybjerg-Grauholm, J, iPSYCH Consortium, ASD Working Group of the Psychiatric Genomics Consortium, ADHD Working Group of the Psychiatric Genomics Consortium, Berretta, S, Macosko, E Z, Sebat, J, O'Connor, L J, Hougaard, D M, Børglum, A D, Talkowski, M E, McCarroll, S A & Robinson, E B 2022, ' Statistical and functional convergence of common and rare genetic influences on autism at chromosome 16p ', Nature Genetics, vol. 54, no. 11, pp. 1630-1639 . https://doi.org/10.1038/s41588-022-01203-y
iPSYCH Consortium, ASD Working Group of the Psychiatric Genomics Consortium & ADHD Working Group of the Psychiatric Genomics Consortium 2022, ' Statistical and functional convergence of common and rare genetic influences on autism at chromosome 16p ', Nature genetics, vol. 54, no. 11, pp. 1630-1639 . https://doi.org/10.1038/s41588-022-01203-y
Nature genetics, 54(11), 1630-1639. Nature Publishing Group

in press, weitere Verfasser:innen aus Einrichtungen außerhalb der Universität Duisburg-Essen sind nicht aufgeführt. The canonical paradigm for converting genetic association to mechanism involves iteratively mapping individual associations to the

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4bcf3982bc4fc5cf21c2b7660e0ef09e
https://research.vumc.nl/en/publications/4e6630bb-b283-4456-868d-7258b838f53d

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