CARD15/NOD2 3020insC (1007fs) mutation is not a genetic marker for cytokine network in sarcoidosis Source: Eur Respir J 2006; 28: Suppl. 50, 520s Year: 2006
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
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
HLA-DRB1* alleles and symptoms associated with Heerfordt's syndrome in sarcoidosis Source: Eur Respir J 2011; 38: 1151-1157 Year: 2011
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
Genome-wide association analysis reveals 12q13.3–q14.1 as new risk locus for sarcoidosis Source: Eur Respir J 2013; 41: 888-900 Year: 2013
A BTNL2 gene variant confers to sarcoidosis susceptibility by an increased risk towards the chronic form of the disease Source: Eur Respir J 2006; 28: Suppl. 50, 148s Year: 2006
Intersitial lung disease in chlidren with mutation in the SFTPC and SFPTB gene: A two case report Source: International Congress 2017 – Pulmonary infection and inflammation Year: 2017
Pulmonary fibrosis in non-mutation carriers of families with short telomere syndrome gene mutations. Source: Virtual Congress 2021 – Genetics and translational aspects of idiopathic pulmonary fibrosis Year: 2021
CARD15/NOD2 polymorphisms are associated with severe pulmonary sarcoidosis Source: Eur Respir J 2010; 35: 324-330 Year: 2010
Mutations in SFTPC, SFTPA2 and TERT explain 60% of familial pulmonary fibrosis and correlate to specific disease phenotypes Source: Annual Congress 2011 - Genetic and molecular background in pulmonary fibrosis Year: 2011
Familial interstitial lung disease and ABCA3 gene Gly964Asp mutation Source: Annual Congress 2010 - Pathogenesis of diffuse parenchymal lung disease Year: 2010
Is the BTNL2 genotype associated with specific HLA-DRB1 and DRB3/4/5 alleles in Danish sarcoidosis patients? Source: International Congress 2015 – Sarcoidosis: pathogenesis Year: 2015
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
Association of single nucleotide polymorphisms in 4 genes (VDR, COL1A1, CALCR and BGLAP) with susceptibility to steroid osteoporosis in patients with idiopathic pulmonary fibrosis (IPF) Source: Annual Congress 2011 - Genetic and molecular background in pulmonary fibrosis Year: 2011
Sarcoidosis is associated with a truncating splice site mutation in the BTNL2 gene Source: Eur Respir J 2005; 26: Suppl. 49, 468s Year: 2005
Disease modifier genes in cystic fibrosis Source: ISSN=ISSN 1025-448x, ISBN=ISBN 1-904097-46-6, page=50 Year: 2006
Toll-like receptor (TLR) 2 promotor polymorphism is associated with the disease course in sarcoidosis patients Source: Annual Congress 2006 - Lung vascular and parenchymal remodeling Year: 2006
Polymorphic variants of genes ADRB2, NR3C1, MDR1 in patients with chronic obstructive pulmonary disease and obesity Source: International Congress 2015 – Genetics and environmental factors in phenotypes of asthma and COPD Year: 2015
Polymorphisms of the aph-1 homolog A, gamma-secretase subunit (APH1A) gene in Japanese patients with aspirin-exacerbated respiratory disease (AERD). Source: International Congress 2017 – Asthma genetics and genomics in patients and populations Year: 2017