Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Kitaba, Negusse Tadesse"'
Autor:
Kitaba, Negusse Tadesse1 (AUTHOR), Knudsen, Gerd Toril Mørkve2,3 (AUTHOR), Johannessen, Ane4 (AUTHOR), Rezwan, Faisal I.5 (AUTHOR), Malinovschi, Andrei6 (AUTHOR), Oudin, Anna7 (AUTHOR), Benediktsdottir, Bryndis8,9 (AUTHOR), Martino, David10 (AUTHOR), González, Francisco Javier Callejas11 (AUTHOR), Gómez, Leopoldo Palacios12 (AUTHOR), Holm, Mathias13 (AUTHOR), Jõgi, Nils Oskar2,3 (AUTHOR), Dharmage, Shyamali C.14 (AUTHOR), Skulstad, Svein Magne3 (AUTHOR), Watkins, Sarah H.15 (AUTHOR), Suderman, Matthew15 (AUTHOR), Gómez-Real, Francisco2,16 (AUTHOR), Schlünssen, Vivi17,18 (AUTHOR), Svanes, Cecilie3,4 (AUTHOR), Holloway, John W.1,19 (AUTHOR) J.W.Holloway@soton.ac.uk
Publikováno v:
Clinical Epigenetics. 8/31/2023, Vol. 15 Issue 1, p1-16. 16p.
Akademický článek
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Autor:
Granell, Raquel, Curtin, John, Haider, Sadia, Kitaba, Negusse Tadesse, Mathie, Sara A, Custovic, Adnan
Publikováno v:
Granell, R, Curtin, J, Haider, S, Kitaba, N T, Mathie, S A & Custovic, A 2023, ' A meta-analysis of genome-wide association studies of childhood wheezing phenotypes identifies ANXA1 as a susceptibility locus for persistent wheezing ', eLife, vol. 12, e84315 . https://doi.org/10.7554/eLife.84315
Background:Many genes associated with asthma explain only a fraction of its heritability. Most genome-wide association studies (GWASs) used a broad definition of 'doctor-diagnosed asthma', thereby diluting genetic signals by not considering asthma he
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2642::3aa60af171455aecb63767679864a9dd
https://research-information.bris.ac.uk/en/publications/c3cc6a9f-baf6-42ea-9e92-b8388f9d1b62
https://research-information.bris.ac.uk/en/publications/c3cc6a9f-baf6-42ea-9e92-b8388f9d1b62