Genetic studies of lung disease in Cystic Fibrosis are hampered by the lack of a severity measure that accounts for chronic disease progression and mortality attrition. Further, combining analyses across studies requires common phenotypes that are robust to study design and patient ascertainment
AbstractCystic fibrosis (CF) is a life-shortening genetic disease characterized by variability in ag...
Since the 1989 discovery that mutations in the cystic fibrosis transmembrane conductance regulator (...
AbstractBackgroundAlthough there are more than 1000 mutations in the cystic fibrosis transmembrane c...
Genetic studies of lung disease in Cystic Fibrosis are hampered by the lack of a severity measure th...
Genetic studies of lung disease in Cystic Fibrosis are faced with the challenge of identifying a sev...
Rationale: The study of genetic modifiers in cystic fibrosis (CF) lung disease requires rigorous phe...
The identification of small molecules that target specific CFTR variants has ushered in a new era of...
BACKGROUND: Lung disease is the major source of morbidity and mortality in cystic fibrosis (CF), wit...
BACKGROUND: Polymorphisms in genes other than the cystic fibrosis transmembrane conductance regulato...
Our understanding of cystic fibrosis (CF) has grown exponentially since the discovery of the cystic ...
Technological advances in genetics have made feasible and affordable large studies to identify genet...
In many respects, genetic studies in cystic fibrosis (CF) serve as a paradigm for a human Mendelian ...
Cystic fibrosis (CF) is a single gene Mendelian disorder characterized by pulmonary disease and panc...
Rationale: Variability in pulmonary disease severity is found in patients with cystic fibrosis (CF) ...
Cystic Fibrosis (CF) is the most common monogenic disease among people of Western European descent a...
AbstractCystic fibrosis (CF) is a life-shortening genetic disease characterized by variability in ag...
Since the 1989 discovery that mutations in the cystic fibrosis transmembrane conductance regulator (...
AbstractBackgroundAlthough there are more than 1000 mutations in the cystic fibrosis transmembrane c...
Genetic studies of lung disease in Cystic Fibrosis are hampered by the lack of a severity measure th...
Genetic studies of lung disease in Cystic Fibrosis are faced with the challenge of identifying a sev...
Rationale: The study of genetic modifiers in cystic fibrosis (CF) lung disease requires rigorous phe...
The identification of small molecules that target specific CFTR variants has ushered in a new era of...
BACKGROUND: Lung disease is the major source of morbidity and mortality in cystic fibrosis (CF), wit...
BACKGROUND: Polymorphisms in genes other than the cystic fibrosis transmembrane conductance regulato...
Our understanding of cystic fibrosis (CF) has grown exponentially since the discovery of the cystic ...
Technological advances in genetics have made feasible and affordable large studies to identify genet...
In many respects, genetic studies in cystic fibrosis (CF) serve as a paradigm for a human Mendelian ...
Cystic fibrosis (CF) is a single gene Mendelian disorder characterized by pulmonary disease and panc...
Rationale: Variability in pulmonary disease severity is found in patients with cystic fibrosis (CF) ...
Cystic Fibrosis (CF) is the most common monogenic disease among people of Western European descent a...
AbstractCystic fibrosis (CF) is a life-shortening genetic disease characterized by variability in ag...
Since the 1989 discovery that mutations in the cystic fibrosis transmembrane conductance regulator (...
AbstractBackgroundAlthough there are more than 1000 mutations in the cystic fibrosis transmembrane c...