Correction: Whole exome sequencing reveals HSPA1L as a genetic risk factor for spontaneous preterm birth.

Autor: Johanna M Huusko, Minna K Karjalainen, Britney E Graham, Ge Zhang, Emily G Farrow, Neil A Miller, Bo Jacobsson, Haley R Eidem, Jeffrey C Murray, Bruce Bedell, Patrick Breheny, Noah W Brown, Frans L Bødker, Nadia K Litterman, Pan-Pan Jiang, Laura Russell, David A Hinds, Youna Hu, andMe Research Team, Antonis Rokas, Kari Teramo, Kaare Christensen, Scott M Williams, Mika Rämet, Stephen F Kingsmore, Kelli K Ryckman, Mikko Hallman, Louis J Muglia

Publikováno v: PLoS Genetics, Vol 14, Iss 9, p e1007673 (2018)

[This corrects the article DOI: 10.1371/journal.pgen.1007394.].

Externí odkaz: https://doaj.org/article/68534e5341a74437bcb568d25963de72

The Danish Twin Registry:Linking surveys, national registers, and biological information

Autor: Lars Hvidberg, Niels V. Holm, Paul Bingley, Morten Nielsen, Qihua Tan, Kaare Christensen, Lene Christiansen, Frans L Bødker, Matt McGue, Kirsten Ohm Kyvik, Axel Skytthe, Jacob v. B. Hjelmborg, James W. Vaupel, Inge Petersen

Publikováno v: Skytthe, A, Christiansen, L, Kyvik, K O, Bødker, F L, Hvidberg, L, Petersen, I, Nielsen, M M F, Bingley, P, Hjelmborg, J, Tan, Q, Holm, N V, Vaupel, J W, McGue, M & Christensen, K 2013, ' The Danish Twin Registry : Linking surveys, national registers, and biological information ', Twin Research and Human Genetics, vol. 16, no. 1, pp. 104-111 . https://doi.org/10.1017/thg.2012.77

Over the last 60 years, the resources and the research in the Danish Twin Registry (DTR) have periodically been summarized. Here, we give a short overview of the DTR and a more comprehensive description of new developments in the twenty-first century

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::360bb07011aca3e8aa9fd6ec84b61ab6
https://portal.findresearcher.sdu.dk/da/publications/9b1c39a9-4f5a-4058-92c1-209c8227905f

Integrative genetic, genomic and transcriptomic analysis of heat shock protein and nuclear hormone receptor gene associations with spontaneous preterm birth.

Autor: Huusko, Johanna M.^1,2,3, Tiensuu, Heli^1,2, Haapalainen, Antti M.^1,2, Pasanen, Anu^1,2, Tissarinen, Pinja^1,2, Karjalainen, Minna K.^1,2, Zhang, Ge³, Christensen, Kaare⁴, Ryckman, Kelli K.⁵, Jacobsson, Bo^6,7, Murray, Jeffrey C.⁸, Kingsmore, Stephen F.⁹, Hallman, Mikko^1,2, Muglia, Louis J.^3,10, Rämet, Mika^1,2,11 mika.ramet@oulu.fi

Publikováno v: Scientific Reports. 8/24/2021, Vol. 11 Issue 1, p1-13. 13p.

Correction: Whole exome sequencing reveals HSPA1L as a genetic risk factor for spontaneous preterm birth.

Autor: Huusko, Johanna M., Karjalainen, Minna K., Graham, Britney E., Zhang, Ge, Farrow, Emily G., Miller, Neil A., Jacobsson, Bo, Eidem, Haley R., Murray, Jeffrey C., Bedell, Bruce, Breheny, Patrick, Brown, Noah W., Bødker, Frans L., Litterman, Nadia K., Jiang, Pan-Pan, Russell, Laura, Hinds, David A., Hu, Youna, Rokas, Antonis, Teramo, Kari

Publikováno v: PLoS Genetics. 9/13/2018, Vol. 14 Issue 9, p1-1. 1p.