CARD15 gene mutations in sarcoidosis Source: Eur Respir J 2003; 22: 748-754 Year: 2003
Positive association of PPARG2 and PPARGC1A gene polymorphisms with sarcoidosis susceptibility Source: Annual Congress 2007 - Novel therapeutic targets and disease markers in pulmonary pathology Year: 2007
Homozygous variant rs2076530 of BTNL2 and familial sarcoidosis: analysis of 5 members of a family Source: Annual Congress 2007 - Novel genetic markers in pathology Year: 2007
Sarcoidosis is associated with a truncating splice site mutation in the BTNL2 gene Source: Eur Respir J 2005; 26: Suppl. 49, 468s Year: 2005
Evaluation of ANXA11 rs1049550 SNP linkage with sarcoidosis susceptibility Source: Annual Congress 2012 - Sarcoidosis Year: 2012
Genetic polymorphism of FOXP3 gene in sarcoidosis patients Source: Eur Respir J 2006; 28: Suppl. 50, 353s Year: 2006
NALP3 and CARD8 genetic polymorphisms and antituberculosis-drugs induced hepatitis Source: Annual Congress 2011 - Tuberculosis: from bench to bedside Year: 2011
CCR5-Δ32 deletion and CCL5 polymorphisms in tuberculosis susceptibility Source: Annual Congress 2010 - Scientific advances in tuberculosis Year: 2010
CARD15/NOD2, CD14, and toll-like receptor 4 gene polymorphisms in Greek patients with sarcoidosis Source: Eur Respir J 2006; 28: Suppl. 50, 520s Year: 2006
Are ADAM33, TNF, LTA, EPHX1 and ADRB2 polymorphisms (SNPs) associated with COPD in a large case-control study when cases and controls are purified? Source: Eur Respir J 2007; 30: Suppl. 51, 131s Year: 2007
Genetic association between COPD and polymorphisms in TNF, ADRB2 and EPHX1 Source: Eur Respir J 2006; 27: 682-688 Year: 2006
No association between COPD and ADAM33, TNF, EPHX1 and ADRB2 polymorphisms (SNPs) in a large case-control study Source: Eur Respir J 2006; 28: Suppl. 50, 584s Year: 2006
Association of IL4 gene polymorphisms with asthma phenotype Source: Annual Congress 2011 - Risk and detection of childhood asthma and allergy Year: 2011
Association of inflammatory bowel disease risk loci with sarcoidosis, and its acute and chronic subphenotypes Source: Eur Respir J 2011; 37: 610-616 Year: 2011
Polymorphism of genes (IL4, IL5) as genetic predisposition to asthma in children Source: International Congress 2018 – Asthma, rhinitis and COPD: cells, mediators, biomarkers and genetics Year: 2018
Potential clinical utility of MUC5B and TOLLIP single nucleotide polymorphisms (SNP) in in the management of patients with IPF. Source: International Congress 2019 – Translational aspects of idiopathic pulmonary fibrosis Year: 2019
Intron-8 polythymidine sequence in Australasian individuals with CF mutations R117H and R117C Source: Eur Respir J 2001; 17: 1195-1200 Year: 2001
M2 allele of alpha1-antitrypsin gene and genetic susceptibility to COPD in Korean men Source: Eur Respir J 2005; 26: Suppl. 49, 442s Year: 2005
Cytokines gene polymorphisms (TNFA, LTA, IL1B, IL1RN and IL10) in children with chronic bronchopulmonary disease and cystic fibrosis Source: Eur Respir J 2004; 24: Suppl. 48, 396s Year: 2004
CTLA4 polymorphisms and COPD Source: Eur Respir J 2010; 35: 457-458 Year: 2010