List of works - Scott M Blackman

A novel lung disease phenotype adjusted for mortality attrition for cystic fibrosis genetic modifier studies.

scientific article

A susceptibility gene for type 2 diabetes confers substantial risk for diabetes complicating cystic fibrosis

scientific article

Cat and dog exposure and respiratory morbidities in cystic fibrosis.

scientific article

Deep resequencing of CFTR in 762 F508del homozygotes reveals clusters of non-coding variants associated with cystic fibrosis disease traits.

scientific article

Diabetes-related mortality in adults with cystic fibrosis. Role of genotype and sex

scientific article

Flexibility of the cytoplasmic domain of the anion exchange protein, band 3, in human erythrocytes

scientific article

Genetic modifiers of cystic fibrosis-related diabetes

scientific article published on 13 May 2013

Genome-wide association and linkage identify modifier loci of lung disease severity in cystic fibrosis at 11p13 and 20q13.2.

scientific article

Genome-wide association meta-analysis identifies five modifier loci of lung disease severity in cystic fibrosis

scientific article

Heritability of respiratory infection with Pseudomonas aeruginosa in cystic fibrosis

scientific article published on 23 February 2012

Hyperglycemia in Young Children with Cystic Fibrosis.

scientific article

Insulin pump use in young children in the T1D Exchange clinic registry is associated with lower hemoglobin A1c levels than injection therapy

scientific article

Interactions between secondhand smoke and genes that affect cystic fibrosis lung disease

scientific article

Modifier gene study of meconium ileus in cystic fibrosis: statistical considerations and gene mapping results

scientific article

Most youth with type 1 diabetes in the T1D Exchange Clinic Registry do not meet American Diabetes Association or International Society for Pediatric and Adolescent Diabetes clinical guidelines

scientific article

Multiple apical plasma membrane constituents are associated with susceptibility to meconium ileus in individuals with cystic fibrosis

scientific article

Mutations that permit residual CFTR function delay acquisition of multiple respiratory pathogens in CF patients.

scientific article

Oligomeric state of human erythrocyte band 3 measured by fluorescence resonance energy homotransfer.

scientific article

Quantitative imaging of green fluorescent protein in cultured cells: comparison of microscopic techniques, use in fusion proteins and detection limits.

scientific article published on November 1995

Self-reported exercise and longitudinal outcomes in cystic fibrosis: a retrospective cohort study

scientific article

Severe hypoglycemia and diabetic ketoacidosis in adults with type 1 diabetes: results from the T1D Exchange clinic registry

scientific article

The T1D Exchange clinic registry

scientific article

The orientation of eosin-5-maleimide on human erythrocyte band 3 measured by fluorescence polarization microscopy

scientific article

Understanding the population structure of North American patients with cystic fibrosis

scientific article

Use of a modeling framework to evaluate the effect of a modifier gene (MBL2) on variation in cystic fibrosis.

scientific article

Variation in MSRA modifies risk of neonatal intestinal obstruction in cystic fibrosis.

scientific article

List of works by Scott M Blackman

A novel lung disease phenotype adjusted for mortality attrition for cystic fibrosis genetic modifier studies.

A susceptibility gene for type 2 diabetes confers substantial risk for diabetes complicating cystic fibrosis

Cat and dog exposure and respiratory morbidities in cystic fibrosis.

Deep resequencing of CFTR in 762 F508del homozygotes reveals clusters of non-coding variants associated with cystic fibrosis disease traits.

Diabetes-related mortality in adults with cystic fibrosis. Role of genotype and sex

Flexibility of the cytoplasmic domain of the anion exchange protein, band 3, in human erythrocytes

Genetic modifiers of cystic fibrosis-related diabetes

Genome-wide association and linkage identify modifier loci of lung disease severity in cystic fibrosis at 11p13 and 20q13.2.

Genome-wide association meta-analysis identifies five modifier loci of lung disease severity in cystic fibrosis

Heritability of respiratory infection with Pseudomonas aeruginosa in cystic fibrosis

Hyperglycemia in Young Children with Cystic Fibrosis.

Insulin pump use in young children in the T1D Exchange clinic registry is associated with lower hemoglobin A1c levels than injection therapy

Interactions between secondhand smoke and genes that affect cystic fibrosis lung disease

Modifier gene study of meconium ileus in cystic fibrosis: statistical considerations and gene mapping results

Most youth with type 1 diabetes in the T1D Exchange Clinic Registry do not meet American Diabetes Association or International Society for Pediatric and Adolescent Diabetes clinical guidelines

Multiple apical plasma membrane constituents are associated with susceptibility to meconium ileus in individuals with cystic fibrosis

Mutations that permit residual CFTR function delay acquisition of multiple respiratory pathogens in CF patients.

Oligomeric state of human erythrocyte band 3 measured by fluorescence resonance energy homotransfer.

Quantitative imaging of green fluorescent protein in cultured cells: comparison of microscopic techniques, use in fusion proteins and detection limits.

Self-reported exercise and longitudinal outcomes in cystic fibrosis: a retrospective cohort study

Severe hypoglycemia and diabetic ketoacidosis in adults with type 1 diabetes: results from the T1D Exchange clinic registry

The T1D Exchange clinic registry

The orientation of eosin-5-maleimide on human erythrocyte band 3 measured by fluorescence polarization microscopy

Understanding the population structure of North American patients with cystic fibrosis

Use of a modeling framework to evaluate the effect of a modifier gene (MBL2) on variation in cystic fibrosis.

Variation in MSRA modifies risk of neonatal intestinal obstruction in cystic fibrosis.