Editorial: Complex Immune Mediated Pulmonary Disease: How Genetic Data Can Influence Clinical Practice

. 2019 ; 6 () : 150. [epub] 20190702

Status PubMed-not-MEDLINE Jazyk angličtina Země Švýcarsko Médium electronic-ecollection

Typ dokumentu úvodníky

Perzistentní odkaz   https://www.medvik.cz/link/pmid31334234
Komentář

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

Najít záznam

Citační ukazatele

Nahrávání dat ...

Možnosti archivace

Nahrávání dat ...