| Publication |
PUBMEDID |
| Potential role of modifier genes influencing transforming growth factor-beta1 levels in the development of vascular defects in endoglin heterozygous mice with hereditary hemorrhagic telangiectasia. |
11395379 |
| Reduced endothelial secretion and plasma levels of transforming growth factor-beta1 in patients with hereditary hemorrhagic telangiectasia type 1. |
15907823 |
| Splice-site mutations in the TRIC gene underlie autosomal recessive nonsyndromic hearing impairment in Pakistani families. |
18084694 |
| Mapping of a new autosomal recessive non-syndromic hearing impairment locus (DFNB45) to chromosome 1q43-q44. |
18325041 |
| Novel autosomal recessive non-syndromic hearing impairment locus (DFNB71) maps to chromosome 8p22-21.3. |
19229252 |
| Recurrent chromosome 16p13.1 duplications are a risk factor for aortic dissections. |
21698135 |
| Genome-wide association study identifies a susceptibility locus for thoracic aortic aneurysms and aortic dissections spanning FBN1 at 15q21.1. |
21909107 |
| The chicken frizzle feather is due to an α-keratin (KRT75) mutation that causes a defective rachis. |
22829773 |
| Genetic association of cyclic AMP signaling genes with bipolar disorder. |
23032945 |
| Beyond GWAS in COPD: probing the landscape between gene-set associations, genome-wide associations and protein-protein interaction networks. |
25171373 |
| Quantitative computed tomography measures of pectoralis muscle area and disease severity in chronic obstructive pulmonary disease. A cross-sectional study. |
24558953 |
| Risk loci for chronic obstructive pulmonary disease: a genome-wide association study and meta-analysis. |
24621683 |
| A comparative analysis of family-based and population-based association tests using whole genome sequence data. |
25519381 |
| The clinical and genetic features of COPD-asthma overlap syndrome. |
24876173 |
| Genome-wide association identifies regulatory Loci associated with distinct local histogram emphysema patterns. |
25006744 |
| DNAH5 is associated with total lung capacity in chronic obstructive pulmonary disease. |
25134640 |
| Genetic susceptibility for chronic bronchitis in chronic obstructive pulmonary disease. |
25241909 |
| Phenotypic and genetic heterogeneity among subjects with mild airflow obstruction in COPDGene. |
25154699 |
| Chest CT measures of muscle and adipose tissue in COPD: gender-based differences in content and in relationships with blood biomarkers. |
25088837 |
| Common genetic variants associated with resting oxygenation in chronic obstructive pulmonary disease. |
24825563 |
| IREB2 and GALC are associated with pulmonary artery enlargement in chronic obstructive pulmonary disease. |
25101718 |
| Reduced Bone Density and Vertebral Fractures in Smokers. Men and COPD Patients at Increased Risk. |
25719895 |
| Continuous fat-free mass decline in COPD: fact or fiction? |
26381518 |
| A genome-wide association study identifies risk loci for spirometric measures among smokers of European and African ancestry. |
26634245 |
| Sarcopenic Obesity, Functional Outcomes, and Systemic Inflammation in Patients With Chronic Obstructive Pulmonary Disease. |
27161848 |
| A genome-wide analysis of the response to inhaled β2-agonists in chronic obstructive pulmonary disease. |
26503814 |
| Clinical, physiologic, and radiographic factors contributing to development of hypoxemia in moderate to severe COPD: a cohort study. |
27903260 |
| Susceptibility to Childhood Pneumonia: A Genome-Wide Analysis. |
27508494 |
| Obesity Is Associated With Increased Morbidity in Moderate to Severe COPD. |
27568229 |
| Body mass index change in gastrointestinal cancer and chronic obstructive pulmonary disease is associated with Dedicator of Cytokinesis 1. |
28044437 |
| Sex-Based Genetic Association Study Identifies CELSR1 as a Possible Chronic Obstructive Pulmonary Disease Risk Locus among Women. |
27854507 |
