| scholarly article | Q13442814 |
| P2093 | author name string | Michael Bamshad | |
| Kathleen C Barnes | |||
| Christoph Lange | |||
| Craig P Hersh | |||
| Edwin K Silverman | |||
| James D Crapo | |||
| Michael H Cho | |||
| Terri H Beaty | |||
| COPDGene Investigators | |||
| Raphael Bueno | |||
| Bartolome R Celli | |||
| Nathaniel Marchetti | |||
| Gerald J Criner | |||
| Victor M Pinto-Plata | |||
| Dandi Qiao | |||
| Jarrett Morrow | |||
| NHLBI Exome Sequencing Project | |||
| Lung GO | |||
| P2860 | cites work | Heterogeneity of barrier function in the lung reflects diversity in endothelial cell junctions | Q43124033 |
| Activated leukocyte cell adhesion molecule is a component of the endothelial junction involved in transendothelial monocyte migration. | Q51808032 | ||
| Genetic epidemiology of severe, early-onset chronic obstructive pulmonary disease. Risk to relatives for airflow obstruction and chronic bronchitis. | Q52241091 | ||
| Exome sequencing identifies mutations in CCDC114 as a cause of primary ciliary dyskinesia | Q24306705 | ||
| Cloning, mapping, and characterization of activated leukocyte-cell adhesion molecule (ALCAM), a CD6 ligand | Q24319426 | ||
| GBF1 bears a novel phosphatidylinositol-phosphate binding module, BP3K, to link PI3Kγ activity with Arf1 activation involved in GPCR-mediated neutrophil chemotaxis and superoxide production | Q24319753 | ||
| Isolation of several human axonemal dynein heavy chain genes: genomic structure of the catalytic site, phylogenetic analysis and chromosomal assignment | Q24322570 | ||
| Exome sequencing identifies the cause of a mendelian disorder | Q24607742 | ||
| Genome-wide association study identifies five loci associated with lung function | Q24629653 | ||
| Meta-analyses of genome-wide association studies identify multiple loci associated with pulmonary function | Q24633262 | ||
| GBF1: A novel Golgi-associated BFA-resistant guanine nucleotide exchange factor that displays specificity for ADP-ribosylation factor 5 | Q24651935 | ||
| STRING 8--a global view on proteins and their functional interactions in 630 organisms | Q24656073 | ||
| Downregulation of FUSE-binding protein and c-myc by tRNA synthetase cofactor p38 is required for lung cell differentiation | Q28181173 | ||
| Whole-exome sequencing reveals TopBP1 as a novel gene in idiopathic pulmonary arterial hypertension | Q28237461 | ||
| Activated leukocyte cell adhesion molecule (ALCAM/CD166/MEMD), a novel actor in invasive growth, controls matrix metalloproteinase activity | Q28275446 | ||
| Exome sequencing identifies WDR35 variants involved in Sensenbrenner syndrome | Q28292428 | ||
| Epidemiology, genetics, and subtyping of preserved ratio impaired spirometry (PRISm) in COPDGene | Q28383674 | ||
| Risk loci for chronic obstructive pulmonary disease: a genome-wide association study and meta-analysis | Q29416987 | ||
| A program for annotating and predicting the effects of single nucleotide polymorphisms, SnpEff: SNPs in the genome of Drosophila melanogaster strain w1118; iso-2; iso-3 | Q29614852 | ||
| Exome sequencing as a tool for Mendelian disease gene discovery | Q29615382 | ||
| A general framework for estimating the relative pathogenicity of human genetic variants | Q29615730 | ||
| Proteomics. Tissue-based map of the human proteome | Q29617248 | ||
| Loss-of-function mutations in APOC3, triglycerides, and coronary disease | Q30408720 | ||
| Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function. | Q30427183 | ||
| Exome sequencing of extreme phenotypes identifies DCTN4 as a modifier of chronic Pseudomonas aeruginosa infection in cystic fibrosis | Q30452653 | ||
| A unified test of linkage analysis and rare-variant association for analysis of pedigree sequence data. | Q30823228 | ||
| Improved scoring of functional groups from gene expression data by decorrelating GO graph structure | Q31036410 | ||
| A genome-wide association study in chronic obstructive pulmonary disease (COPD): identification of two major susceptibility loci. | Q33419815 | ||
| A genome-wide association study of pulmonary function measures in the Framingham Heart Study | Q33419839 | ||
| Whole exome re-sequencing implicates CCDC38 and cilia structure and function in resistance to smoking related airflow obstruction. | Q33553057 | ||
| Transcriptomic analysis of human lung development | Q33555203 | ||
| Variants in FAM13A are associated with chronic obstructive pulmonary disease | Q33687879 | ||
| Loss-of-function mutations in SLC30A8 protect against type 2 diabetes | Q33734046 | ||
| Genetic epidemiology of COPD (COPDGene) study design | Q34074731 | ||
| Finding disease variants in Mendelian disorders by using sequence data: methods and applications | Q34089812 | ||
| Loss-of-function mutations in APOC3 and risk of ischemic vascular disease | Q34425444 | ||
| Chronic obstructive pulmonary disease surveillance--United States, 1971-2000. | Q34527761 | ||
| Improving the assessment of the outcome of nonsynonymous SNVs with a consensus deleteriousness score, Condel. | Q34768428 | ||
| A general framework for detecting disease associations with rare variants in sequencing studies | Q35204927 | ||
| A genome-wide association study of COPD identifies a susceptibility locus on chromosome 19q13. | Q35816887 | ||
| Novel insights into the genetics of smoking behaviour, lung function, and chronic obstructive pulmonary disease (UK BiLEVE): a genetic association study in UK Biobank | Q36123192 | ||
| Aminoacyl tRNA synthetases and their connections to disease | Q36837363 | ||
| A novel channelopathy in pulmonary arterial hypertension | Q37219463 | ||
| Heritability of chronic obstructive pulmonary disease and related phenotypes in smokers | Q37304387 | ||
| Defining the disease liability of variants in the cystic fibrosis transmembrane conductance regulator gene | Q37418902 | ||
| Cigarette smoke induces systemic defects in cystic fibrosis transmembrane conductance regulator function | Q37572359 | ||
| Impact of heterozygote CFTR mutations in COPD patients with chronic bronchitis | Q37586134 | ||
| New anti-inflammatory targets for chronic obstructive pulmonary disease. | Q38131512 | ||
| P433 | issue | 12 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | chronic obstructive pulmonary disease | Q199804 |
| P304 | page(s) | 1353-1363 | |
| P577 | publication date | 2016-01-06 | |
| P1433 | published in | American Journal of Respiratory and Critical Care Medicine | Q4744267 |
| P1476 | title | Exome Sequencing Analysis in Severe, Early-Onset Chronic Obstructive Pulmonary Disease | |
| P478 | volume | 193 |
| Q54959257 | A Genome-Wide Linkage Study for Chronic Obstructive Pulmonary Disease in a Dutch Genetic Isolate Identifies Novel Rare Candidate Variants. |
| Q39373353 | Boosting Gene Mapping Power and Efficiency with Efficient Exact Variance Component Tests of Single Nucleotide Polymorphism Sets. |
| Q54225498 | COPD: time to improve its taxonomy? |
| Q38757264 | Extreme Trait Whole-Genome Sequencing Identifies PTPRO as a Novel Candidate Gene in Emphysema with Severe Airflow Obstruction. |
| Q38964529 | Gene-based segregation method for identifying rare variants in family-based sequencing studies |
| Q30252379 | Genome-wide association study of subclinical interstitial lung disease in MESA. |
| Q62602871 | High-Throughput Sequencing in Respiratory, Critical Care, and Sleep Medicine Research. An Official American Thoracic Society Workshop Report |
| Q37342111 | Increasing Generality and Power of Rare-Variant Tests by Utilizing Extended Pedigrees |
| Q93265639 | Initiating drug therapy in early stage chronic obstructive pulmonary disease: does it impact the course and outcome? |
| Q47120721 | Natural history of COPD: gaps and opportunities |
| Q90281013 | Proper conditional analysis in the presence of missing data: Application to large scale meta-analysis of tobacco use phenotypes |
| Q52728819 | RNAseq analysis of bronchial epithelial cells to identify COPD-associated genes and SNPs. |
| Q42689380 | The Advent of High-Throughput Sequencing Studies of Chronic Obstructive Pulmonary Disease |
| Q48343913 | Update in Chronic Obstructive Pulmonary Disease 2016. |
| Q38642884 | Using omics approaches to understand pulmonary diseases |
| Q47801457 | What do polymorphisms tell us about the mechanisms of COPD? |
| Q56355677 | Whole Genome Sequencing in Severe Chronic Obstructive Pulmonary Disease |
| Q90636929 | Whole exome sequencing analysis in severe chronic obstructive pulmonary disease |
| Q47833625 | Whole-Genome Sequencing in Common Respiratory Diseases. Ready, Set, Go! |
| Q87895169 | Whole-Transcriptome Sequencing: a Powerful Tool for Vascular Tissue Engineering and Endothelial Mechanobiology |
| Q91639265 | metaFARVAT: An Efficient Tool for Meta-Analysis of Family-Based, Case-Control, and Population-Based Rare Variant Association Studies |
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