Leveraging global multi-ancestry meta-analysis in the study of idiopathic pulmonary fibrosis genetics

The research of rare and devastating orphan diseases, such as idiopathic pulmonary fibrosis (IPF) has been limited by the rarity of the disease itself. The prognosis is poor—the prevalence of IPF is only approximately four times the incidence, limiting the recruitment of patients to trials and studi...

Descripción completa

Detalles Bibliográficos
Autores principales: Partanen, Juulia J., Häppölä, Paavo, Zhou, Wei, Lehisto, Arto A., Ainola, Mari, Sutinen, Eva, Allen, Richard J., Stockwell, Amy D., Leavy, Olivia C., Oldham, Justin M., Guillen-Guio, Beatriz, Cox, Nancy J., Hirbo, Jibril B., Schwartz, David A., Fingerlin, Tasha E., Flores, Carlos, Noth, Imre, Yaspan, Brian L., Jenkins, R. Gisli, Wain, Louise V., Ripatti, Samuli, Pirinen, Matti, Laitinen, Tarja, Kaarteenaho, Riitta, Myllärniemi, Marjukka, Daly, Mark J., Koskela, Jukka T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9903787/
https://www.ncbi.nlm.nih.gov/pubmed/36777997
http://dx.doi.org/10.1016/j.xgen.2022.100181

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9903787/
https://www.ncbi.nlm.nih.gov/pubmed/36777997
http://dx.doi.org/10.1016/j.xgen.2022.100181

Ejemplares similares