Editorial: Complex Immune Mediated Pulmonary Disease: How Genetic Data Can Influence Clinical Practice
Status PubMed-not-MEDLINE Jazyk angličtina Země Švýcarsko Médium electronic-ecollection
Typ dokumentu úvodníky
PubMed
31334234
PubMed Central
PMC6615255
DOI
10.3389/fmed.2019.00150
Knihovny.cz E-zdroje
- Klíčová slova
- bench to bedside, complex lung disease, editorial, genetics, translational medicine,
- Publikační typ
- úvodníky MeSH
Editorial on the Research Topic Complex Immune Mediated Pulmonary Disease: How Genetic Data Can Influence Clinical Practice PubMed
Zobrazit více v PubMed
Baraldo S. Advances in chronic obstructive pulmonary disease genetics: building the picture one piece at a time. Lancet Respir Med. (2019) 7:371–2. 10.1016/S2213-2600(19)30082-7 PubMed DOI
Allen RJ, Guillen-Guio B, Oldham JM, Ma S, Dressen A, Paynton ML, et al. Genome-wide association study of susceptibility to idiopathic pulmonary fibrosis. bioRxiv. (2019). 10.1101/636761 PubMed DOI PMC
Kishore A, Petersen BS, Nutsua M, Müller-Quernheim J, Franke A, Fischer A, et al. Whole-exome sequencing identifies rare genetic variations in German families with pulmonary sarcoidosis. Hum Genet. (2018) 137:705–16. 10.1007/s00439-018-1915-y PubMed DOI
Rivera NV, Ronninger M, Shchetynsky K, Franke A, Nöthen MM, Müller-Quernheim J, et al. High-density genetic mapping identifies new susceptibility variants in sarcoidosis phenotypes and shows genomic-driven phenotypic differences. Am J Respir Crit Care Med. (2016) 193:1008–22. 10.1164/rccm.201507-1372OC PubMed DOI PMC
Vasakova M, Selman M, Morell F, Sterclova M, Molina-Molina M, Raghu G. Hypersensitivity pneumonitis: current concepts of pathogenesis and potential targets for treatment. Am J Respir Crit Care Med. (2019). 10.1164/rccm.201903-0541PP. [Epub ahead of print]. PubMed DOI
Shrine N, Guyatt AL, Erzurumluoglu AM, Jackson VE, Hobbs BD, Melbourne CA, et al. New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries. Nat Genet. (2019) 51:481–93. 10.1038/s41588-018-0321-7 PubMed DOI PMC
Imboden M, Wielscher M, Rezwan FI, Amaral AFS, Schaffner E, Jeong A, et al. Epigenome-wide association study of lung function level and its change. Eur Respir J. (2019). 10.1183/13993003.00457-2019. [Epub ahead of print]. PubMed DOI PMC
James G, Reisberg S, Lepik K, Galwey N, Avillach P, Kolberg L, et al. An exploratory phenome wide association study linking asthma and liver disease genetic variants to electronic health records from the Estonian Biobank. PLoS ONE. (2019) 14:e0215026. 10.1371/journal.pone.0215026 PubMed DOI PMC
Diogo D, Tian C, Franklin CS, Alanne-Kinnunen M, March M, Spencer CCA, et al. Phenome-wide association studies across large population cohorts support drug target validation. Nat Commun. (2018) 9:4285. 10.1038/s41467-018-06540-3 PubMed DOI PMC