Edwin K Silverman researcher
Silverman, Edwin K.
VIAF ID: 29051819 (Personal)
Permalink: http://viaf.org/viaf/29051819
Preferred Forms
- 100 0 _ ‡a Edwin K Silverman ‡c researcher
- 100 1 _ ‡a Silverman, Edwin K
- 100 1 _ ‡a Silverman, Edwin K
- 100 1 _ ‡a Silverman, Edwin K.
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- 100 1 _ ‡a Silverman, Edwin K.
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4xx's: Alternate Name Forms (3)
Works
Title | Sources |
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Assessing the reproducibility of asthma candidate gene associations, using genome-wide data | |
Association between hemochromatosis genotype and lead exposure among elderly men: the normative aging study | |
Association between occupational exposure and lung function, respiratory symptoms, and high-resolution computed tomography imaging in COPDGene | |
Association Between Telomere Length and Risk of Cancer and Non-Neoplastic Diseases: A Mendelian Randomization Study | |
Association Between Titin Loss-of-Function Variants and Early-Onset Atrial Fibrillation | |
The association of a SNP upstream of INSIG2 with body mass index is reproduced in several but not all cohorts | |
Asthma-susceptibility variants identified using probands in case-control and family-based analyses | |
The chronic bronchitic phenotype of COPD: an analysis of the COPDGene Study | |
Clinical and radiographic predictors of GOLD-unclassified smokers in the COPDGene study | |
Clinical and Radiologic Disease in Smokers With Normal Spirometry | |
Cluster analysis in severe emphysema subjects using phenotype and genotype data: an exploratory investigation | |
Cluster analysis in the COPDGene study identifies subtypes of smokers with distinct patterns of airway disease and emphysema | |
A combined pulmonary-radiology workshop for visual evaluation of COPD: study design, chest CT findings and concordance with quantitative evaluation | |
Common Genetic Polymorphisms Influence Blood Biomarker Measurements in COPD. | |
Comorbidities of COPD have a major impact on clinical outcomes, particularly in African Americans | |
Connecting COPD GWAS Genes: FAM13A Controls TGFβ2 Secretion by Modulating AP-3 Transport | |
The COPD genetic association compendium: a comprehensive online database of COPD genetic associations | |
Corticosteroid pharmacogenetics: association of sequence variants in CRHR1 with improved lung function in asthmatics treated with inhaled corticosteroids | |
CT-based Visual Classification of Emphysema: Association with Mortality in the COPDGene Study | |
CT measurements of central pulmonary vasculature as predictors of severe exacerbation in COPD. | |
Family-based tests for associating haplotypes with general phenotype data: application to asthma genetics | |
Folliculin mutations are not associated with severe COPD. | |
Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstruction | |
Genome-wide association study identifies BICD1 as a susceptibility gene for emphysema | |
A genome-wide association study of pulmonary function measures in the Framingham Heart Study | |
Genome-wide association study of smoking behaviours in patients with COPD | |
Genome-wide site-specific differential methylation in the blood of individuals with Klinefelter syndrome | |
Genome-wide study of percent emphysema on computed tomography in the general population. The Multi-Ethnic Study of Atherosclerosis Lung/SNP Health Association Resource Study | |
Genomic screening and replication using the same data set in family-based association testing | |
GOLD 2011 disease severity classification in COPDGene: a prospective cohort study | |
A high-resolution HLA reference panel capturing global population diversity enables multi-ancestry fine-mapping in HIV host response | |
Histone deacetylase 6-mediated selective autophagy regulates COPD-associated cilia dysfunction | |
Identifying Smoking-Related Disease on Lung Cancer Screening CT Scans: Increasing the Value | |
Improved prediction of smoking status via isoform-aware RNA-seq deep learning models | |
Inherited causes of clonal haematopoiesis in 97,691 whole genomes | |
Integration of mouse and human genome-wide association data identifies KCNIP4 as an asthma gene | |
Intrathoracic tracheal volume and collapsibility on inspiratory and end-expiratory ct scans correlations with lung volume and pulmonary function in 85 smokers | |
Longitudinal Phenotypes and Mortality in Preserved Ratio Impaired Spirometry in the COPDGene Study | |
Lung Mass in Smokers | |
Microarray data-based prioritization of chronic obstructive pulmonary disease susceptibility genes. | |
Molecular networks in Network Medicine: Development and applications | |
Mortality and Exacerbations by Global Initiative for Chronic Obstructive Lung Disease Groups ABCD: 2011 Versus 2017 in the COPDGene® Cohort | |
Network medicine : complex systems in human disease and therapeutics | |
On the analysis of genome-wide association studies in family-based designs: a universal, robust analysis approach and an application to four genome-wide association studies | |
Overlap of Genetic Risk between Interstitial Lung Abnormalities and Idiopathic Pulmonary Fibrosis | |
Paired inspiratory-expiratory chest CT scans to assess for small airways disease in COPD. | |
Parsing the effects of individual SNPs in candidate genes with family data. | |
Personalized respiratory medicine: exploring the horizon, addressing the issues. Summary of a BRN-AJRCCM workshop held in Barcelona on June 12, 2014 | |
Prediction of acute respiratory disease in current and former smokers with and without COPD | |
Pulmonary arterial enlargement and acute exacerbations of COPD | |
Pulmonary hypertension and computed tomography measurement of small pulmonary vessels in severe emphysema | |
Racial differences in CT phenotypes in COPD. | |
Reported environmental exposures are inversely associated with obtaining a genetic diagnosis in the Undiagnosed Diseases Network | |
Respiratory genetics | |
Sequencing Analysis at 8p23 Identifies Multiple Rare Variants in DLC1 Associated with Sleep-Related Oxyhemoglobin Saturation Level | |
Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program | |
Single nucleotide polymorphisms in innate immunity genes: abundant variation and potential role in complex human disease | |
Subtypes of COPD Have Unique Distributions and Differential Risk of Mortality | |
T-bet polymorphisms are associated with asthma and airway hyperresponsiveness | |
TOLL-like receptor 10 genetic variation is associated with asthma in two independent samples | |
Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations | |
Utilizing the Jaccard index to reveal population stratification in sequencing data: a simulation study and an application to the 1000 Genomes Project | |
Variants in FAM13A are associated with chronic obstructive pulmonary disease | |
Whole genome sequence analysis of pulmonary function and COPD in 19,996 multi-ethnic participants |