Association between IL-2,IL-4 gene polymorphisms and pulmonary MDRTB Source: International Congress 2017 – Human susceptibility to tuberculosis Year: 2017
Functional assessment of newly identified SFTPA1 and SFTPA2 mutations in patients with idiopathic interstitial pneumonia (IIP) and lung cancer Source: International Congress 2018 – New insights in rare diffuse parenchymal lung diseases (DPLDs) in adults and children Year: 2018
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
Genetic polymorphisms in TNF genes and tuberculosis in cystic fibrosis patients Source: Annual Congress 2011 - Genetics of airway diseases and treatment Year: 2011
Decreased miR-150-5p and miR-23a-3p expressions in patients with active Pulmonary Tuberculosis (TB) disease Source: International Congress 2019 – Tuberculosis: from basic science to patient care Year: 2019
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
Regulator of telomere length 1 (RTEL1 ) mutations are associated with heterogeneous pulmonary and extra-pulmonary phenotypes Source: Eur Respir J, 53 (2) 1800508; 10.1183/13993003.00508-2018 Year: 2019
COPD susceptibility gene on chromosome 4q31 is also associated with lung cancer Source: Annual Congress 2010 - Lung cancer, idiopathic pulmonary fibrosis and sarcoidosis: the genetic approach Year: 2010
Familial interstitial lung disease and ABCA3 gene Gly964Asp mutation Source: Annual Congress 2010 - Pathogenesis of diffuse parenchymal lung disease Year: 2010
Association of VDR, COL1A1 and CALCR genes polymorphisms with susceptibility to steroid osteoporosis in patients with idiopathic pulmonary fibrosis Source: Annual Congress 2010 - Clinical aspects in pulmonary fibrosis Year: 2010
Functional assessment and phenotypic heterogeneity of SFTPA1 and SFTPA2 mutations in interstitial lung diseases and lung cancer Source: Eur Respir J, 56 (6) 2002806; 10.1183/13993003.02806-2020 Year: 2020
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
Prevalence and characteristics of TERT and TERC mutations in suspected genetic pulmonary fibrosis Source: Eur Respir J 2016; 48: 1721-1731 Year: 2016
Cancer gene mutations in congenital pulmonary airway malformation patients Source: ERJ Open Res, 5 (1) 00196-2018; 10.1183/23120541.00196-2018 Year: 2019
Eight novel variants in the SLC34A2 gene in pulmonary alveolar microlithiasis Source: Eur Respir J, 55 (2) 1900806; 10.1183/13993003.00806-2019 Year: 2020
Cytokine gene polymorphisms and mycobacterium tuberculosis : from infection to pulmonary disease Source: Annual Congress 2006 - Immunology of tuberculosis and diagnosis of tuberculosis infection Year: 2006
Polymorphisms A1026G and G369C of CDKN1A/p21 and p53 genes in lung cancer Source: Annual Congress 2011 - Lung cancer: molecular pathology and functional genomics Year: 2011
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
Clinical phenotypes and outcomes of pulmonary veno-occlusive disease in carriers of bi-allelic EIF2AK4 mutations Source: International Congress 2016 – The nature of pulmonary hypertension Year: 2016
Single nucleotide polymorphisms in matrix metalloproteinase genes and lung cancer chemotherapy response and prognosis Source: Eur Respir J 2010; 35: 381-390 Year: 2010