e-learning
resources
Paris 2018
Wednesday, 19.09.2018
New developments in paediatric asthma
Login
Search all ERS
e-learning
resources
Disease Areas
Airways Diseases
Interstitial Lung Diseases
Respiratory Critical Care
Respiratory Infections
Paediatric Respiratory Diseases
Pulmonary Vascular Diseases
Sleep and Breathing Disorders
Thoracic Oncology
Events
International Congress
Courses
Webinars
Conferences
Research Seminars
Journal Clubs
Publications
Breathe
Monograph
ERJ
ERJ Open Research
ERR
European Lung White Book
Handbook Series
Guidelines
All ERS guidelines
e-learning
CME Online
Case reports
Short Videos
SpirXpert
Procedure Videos
CME tests
Reference Database of Respiratory Sounds
Radiology Image Challenge
Brief tobacco interventions
EU Projects
VALUE-Dx
ERN-LUNG
ECRAID
UNITE4TB
Disease Areas
Events
Publications
Guidelines
e-learning
EU Projects
Login
Search
Whole-genome sequencing of Costa Rican children with asthma identifies CRISPLD2 as a candidate gene for lung function
B. Chawes (Copenhagen, Denmark), J. Hecker (Bonn, Germany), C. Lange (Boston, United States of America), S. Weiss (Boston, United States of America), J. Lasky-Su (Boston, United States of America)
Source:
International Congress 2018 – New developments in paediatric asthma
Session:
New developments in paediatric asthma
Session type:
Poster Discussion
Number:
5432
Disease area:
Airway diseases, Paediatric lung diseases
Rating:
You must
login
to grade this presentation.
Share or cite this content
Citations should be made in the following way:
B. Chawes (Copenhagen, Denmark), J. Hecker (Bonn, Germany), C. Lange (Boston, United States of America), S. Weiss (Boston, United States of America), J. Lasky-Su (Boston, United States of America). Whole-genome sequencing of Costa Rican children with asthma identifies CRISPLD2 as a candidate gene for lung function. 5432
You must
login
to share this Presentation/Article on Twitter, Facebook, LinkedIn or by email.
Member's Comments
No comment yet.
You must
Login
to comment this presentation.
Related content which might interest you:
Late Breaking Abstract - Implications of treatable traits and treatment choices on exacerbation risk in moderate-severe asthma
Observational cohort study of pulmonary exacerbations in alpha-1 antitrypsin deficiency
Management of Severe Asthma in Pediatric Patients by an Interdisciplinary Team in a Public Hospital Setting.
Related content which might interest you:
Genome-wide association study identifies new COPD risk locus, PDE4D, in Korean population
Source: Annual Congress 2013 –Genetics and genomics of lung disease
Year: 2013
Targeted sequencing of 130 asthma candidate genes and association testing of rare variants with age of onset in Norwegian asthma patients.
Source: Virtual Congress 2021 – Epidemiology and burden of tuberculosis and other lung diseases
Year: 2021
Biochip analysis of xenobiotic-metabolizing gene polymorphisms in children with bronchial asthma
Source: Annual Congress 2009 - New results in molecular pathology and functional genomics of non-neoplastic lung diseases
Year: 2009
A large-scale genome-wide association analysis of lung function in the Chinese population identifies novel loci and highlights shared genetic aetiology with obesity
Source: Eur Respir J, 58 (4) 2100199; 10.1183/13993003.00199-2021
Year: 2021
Gene polymorphisms, gene expression and inflammatory markers in preschool children with and without wheeze
Source: Annual Congress 2012 - Gene-environment treatment and asthma
Year: 2012
Common genes underlying asthma and COPD? Genome-wide analysis on the Dutch hypothesis
Source: Eur Respir J 2014; 44: 860-872
Year: 2014
Human exome analysis of candidate genetic variants for susceptibility to high-altitude pulmonary edema in Japanese
Source: Virtual Congress 2020 – Asthma and COPD: How genetic and environment influences its developement?
Year: 2020
Re-sequencing of
PLAUR
in severe asthma patients identifies novel variation
Source: International Congress 2014 – Genetics and environmental factors underlying asthma and COPD
Year: 2014
Influence of two novel mutations in surfactant protein-c on lung function and disease: resequencing of 760 individuals followed by genotyping of 48,000 individuals from the general population
Source: Annual Congress 2009 - Risk factors for COPD
Year: 2009
A meta-analysis of genome-wide association studies of asthma in Puerto Ricans
Source: Eur Respir J, 49 (5) 1601505; 10.1183/13993003.01505-2016
Year: 2017
A pooling based genome-wide analysis identifies new potential candidate genes for atopy in the echrs study
Source: Annual Congress 2009 - Asthma genetics: from genome wide to single nucleotide polymorphisms
Year: 2009
Investigation for candidate genes of glucocorticoid resistance by genome-wide gene expression profiling in animal model of asthma
Source: Annual Congress 2011 - New mechanisms in airway disease
Year: 2011
Gene–gene interaction among polymorphisms of
Eotaxin
gene family in Korean asthmatics
Source: Eur Respir J 2005; 26: Suppl. 49, 263s
Year: 2005
Genetics and epigenetics of childhood asthma
Source: Eur Respir Mon 2012; 56: 97-114
Year: 2012
SNPs identified by GWAS affect asthma risk through DNA methylation and expression of
cis
-genes in airway epithelium
Source: Eur Respir J, 55 (4) 1902079; 10.1183/13993003.02079-2019
Year: 2020
Array-based diagnostic gene expression score for atopy and asthma
Source: Eur Respir J 2001; 18: Suppl. 33, 529s
Year: 2001
Gene polymorphisms in bronchial asthma
Source: Annual Congress 2007 - PG9 - Molecular pathology and genetics in lung diseases
Year: 2007
Whole exome sequencing (WES) of a Chinese Han family with familial pulmonary sarcoidosis
Source: Virtual Congress 2020 – Genetics and biomarkers for diagnosis and prognosis of granulomatous lung diseases
Year: 2020
We use cookies on our website to give you the most relevant experience by remembering your preferences and repeat visits. By clicking "Accept", you consent to the use of the cookies.
Accept