Identifying a Deletion Affecting Total Lung Capacity Among Subjects in the COPDGene Study Cohort

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Identifying a Deletion Affecting Total Lung Capacity Among Subjects in the COPDGene Study Cohort is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1002/GEPI.21943
P932PMC publication ID4679532
P698PubMed publication ID26643968

P2093author name stringJames Crapo
David A Lynch
Douglas Curran-Everett
Edwin K Silverman
Michael H Cho
Terri H Beaty
Ingo Ruczinski
Robert B Scharpf
Jacqueline B Hetmanski
Margaret M Parker
Ferdouse Begum
Shengchao Li
P2860cites workThe SERPINE2 gene is associated with chronic obstructive pulmonary disease in two large populations.Q53572756
Genomic copy number determines functional expression of {beta}-defensin 2 in airway epithelial cells and associates with chronic obstructive pulmonary disease.Q54433238
Genome-wide association study of copy number variations associated with pulmonary function measures in Korea Associated Resource (KARE) cohortsQ57226791
DNAH5 is associated with total lung capacity in chronic obstructive pulmonary diseaseQ57757087
Evaluation of COPD Longitudinally to Identify Predictive Surrogate End-points (ECLIPSE)Q57955885
Accurate airway wall estimation using phase congruencyQ62490747
The phenotypic spectrum of duplication 5q35.2-q35.3 encompassing NSD1: is it really a reversed Sotos syndrome?Q87196000
Towards a proteome-scale map of the human protein–protein interaction networkQ21735930
Standardisation of the measurement of lung volumesQ28269989
Interpretative strategies for lung function testsQ28279970
Epidemiology, genetics, and subtyping of preserved ratio impaired spirometry (PRISm) in COPDGeneQ28383674
The Genotype-Tissue Expression (GTEx) projectQ28657968
Risk loci for chronic obstructive pulmonary disease: a genome-wide association study and meta-analysisQ29416987
STRING v9.1: protein-protein interaction networks, with increased coverage and integrationQ29614691
LocusZoom: regional visualization of genome-wide association scan resultsQ29614868
PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping dataQ29614933
The Atherosclerosis Risk in Communities (ARIC) Study: design and objectives. The ARIC investigatorsQ29614947
Global strategy for the diagnosis, management, and prevention of chronic obstructive pulmonary disease: GOLD executive summaryQ29614970
Clinical and radiographic predictors of GOLD-unclassified smokers in the COPDGene studyQ30504247
A genome-wide study of de novo deletions identifies a candidate locus for non-syndromic isolated cleft lip/palate riskQ31151570
Dynamic lung hyperinflation and its clinical implication in COPDQ33441638
Genetic syndromes associated with overgrowth in childhoodQ33635229
Variants in FAM13A are associated with chronic obstructive pulmonary diseaseQ33687879
Copy number polymorphisms near SLC2A9 are associated with serum uric acid concentrationsQ33986398
Genetic epidemiology of COPD (COPDGene) study designQ34074731
Fast computation and applications of genome mappabilityQ34140534
The short and long term effects of exercise training in non-cystic fibrosis bronchiectasis--a randomised controlled trialQ34216188
Admixture mapping identifies a quantitative trait locus associated with FEV1/FVC in the COPDGene StudyQ34308364
Fast detection of de novo copy number variants from SNP arrays for case-parent triosQ34509681
High-resolution genomic profiling of chromosomal aberrations using Infinium whole-genome genotypingQ35012994
Malan syndrome: Sotos-like overgrowth with de novo NFIX sequence variants and deletions in six new patients and a review of the literatureQ35477955
A genome-wide association study of COPD identifies a susceptibility locus on chromosome 19q13.Q35816887
Interobserver variability in the determination of upper lobe-predominant emphysemaQ36734384
Paired inspiratory-expiratory chest CT scans to assess for small airways disease in COPD.Q36769613
Adjustment of genomic waves in signal intensities from whole-genome SNP genotyping platformsQ36959677
Copy number variation of the beta-defensin genes in europeans: no supporting evidence for association with lung function, chronic obstructive pulmonary disease or asthmaQ37431463
Deaths: Leading Causes for 2011.Q40682159
Pulmonary hyperinflation a clinical overviewQ41289358
PLEIAD/SIMC1/C5orf25, a novel autolysis regulator for a skeletal-muscle-specific calpain, CAPN3, scaffolds a CAPN3 substrate, CTBP1.Q41562535
A GC-wave correction algorithm that improves the analytical performance of aCGH.Q44844596
Quantitative computed tomography: emphysema and airway wall thickness by sex, age and smoking.Q51647885
P433issue1
P304page(s)81-88
P577publication date2015-12-07
P1433published inGenetic EpidemiologyQ5532864
P1476titleIdentifying a Deletion Affecting Total Lung Capacity Among Subjects in the COPDGene Study Cohort
P478volume40

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cites work (P2860)
Q61804807Gene fingerprint model for literature based detection of the associations among complex diseases: a case study of COPD
Q36155424Hemizygous Deletion on Chromosome 3p26.1 Is Associated with Heavy Smoking among African American Subjects in the COPDGene Study

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