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α1-Antitrypsin deficiency · 2: Genetic aspects of α1-antitrypsin deficiency: phenotypes and genetic modifiers of emphysema risk

Thorax, 2004-03, Vol.59 (3), p.259-264

2004

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Associations of IL6 polymorphisms with lung function decline and COPD

Thorax, 2009-08, Vol.64 (8), p.698-704

2009

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Impact of non-linear smoking effects on the identification of gene-by-smoking interactions in COPD genetics studies

Thorax, 2011-10, Vol.66 (10), p.903-909

2011

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Metabolomics in the developmental origins of obesity and its cardiometabolic consequences

Journal of developmental origins of health and disease, 2015-04, Vol.6 (2), p.65-78

2015

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Polymorphic variation in surfactant protein B is associated with COPD exacerbations

The European respiratory journal, 2008-10, Vol.32 (4), p.938-944

2008

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Clinical determinants of exacerbations in severe, early-onset COPD

The European respiratory journal, 2007-12, Vol.30 (6), p.1124-1130

2007

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Women manifest more severe COPD symptoms across the life course

International journal of chronic obstructive pulmonary disease, 2018-01, Vol.13, p.3021-3029

2018

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Development of Predictive Models for Airflow Obstruction in Alpha-1-Antitrypsin Deficiency

American journal of epidemiology, 2009-10, Vol.170 (8), p.1005-1013

2009

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Polymorphisms in the Superoxide Dismutase-3 Gene Are Associated with Emphysema in COPD

Chronic obstructive pulmonary disease, 2010-08, Vol.7 (4), p.262-268

2010

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Familial aggregation of FEF25-75 and FEF25-75/FVC in families with severe, early onset COPD

Thorax, 2004-05, Vol.59 (5), p.396-400

DeMeo, D L

2004

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Unique and shared systemic biomarkers for emphysema in Alpha-1 Antitrypsin deficiency and chronic obstructive pulmonary disease

EBioMedicine, 2022-10, Vol.84, p.104262-104262, Article 104262

2022

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Univariate and multivariate family-based association analysis of the IL-13 ARG130GLN polymorphism in the Childhood Asthma Management program

Genetic epidemiology, 2002-11, Vol.23 (4), p.335-348

2002

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Determinants of airflow obstruction in severe alpha-1-antitrypsin deficiency

Thorax, 2007-09, Vol.62 (9), p.806-813

2007

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Genomic screening and replication using the same data set in family-based association testing

Nature genetics, 2005-07, Vol.37 (7), p.683-691

2005

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COPD: problems in diagnosis and measurement

The European respiratory journal, 2003-06, Vol.21 (Supplement 41), p.4S-12s

2003

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The SERPINE2 Gene Is Associated with Chronic Obstructive Pulmonary Disease

American journal of human genetics, 2006-02, Vol.78 (2), p.253-264

2006

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LUNG TRANSPLANTATION AT THE TURN OF THE CENTURY

Annual review of medicine, 2001-01, Vol.52 (1), p.185-201

2001

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Power and Design Considerations for a General Class of Family-Based Association Tests: Quantitative Traits

American journal of human genetics, 2002-12, Vol.71 (6), p.1330-1341

2002

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Sex and gender: modifiers of health, disease, and medicine

The Lancet (British edition), 2020-08, Vol.396 (10250), p.565-582

2020

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Ambient Air Pollution and Oxygen Saturation

American journal of respiratory and critical care medicine, 2004-08, Vol.170 (4), p.383-387

2004

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Gender differences in COPD: are women more susceptible to smoking effects than men?

Thorax, 2010-06, Vol.65 (6), p.480-485

2010

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Pathogenesis of chronic obstructive pulmonary disease: understanding the contributions of gene–environment interactions across the lifespan

The lancet respiratory medicine, 2022-05, Vol.10 (5), p.512-524

2022

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Heritability of Lung Function in Severe Alpha-1 Antitrypsin Deficiency

Human heredity, 2009-01, Vol.67 (1), p.38-45

2009

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C22 COPD PHENOTYPES: Longitudinal Lung Function And Mortality In Preserved Ratio Impaired Spirometry (prism) In The COPDgene Study

American journal of respiratory and critical care medicine, 2017-01, Vol.195

2017

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α1-Antitrypsin deficiency · 2: Genetic aspects of α1-antitrypsin deficiency: phenotypes and genetic modifiers of emphysema risk

Associations of IL6 polymorphisms with lung function decline and COPD

Impact of non-linear smoking effects on the identification of gene-by-smoking interactions in COPD genetics studies

Metabolomics in the developmental origins of obesity and its cardiometabolic consequences

Polymorphic variation in surfactant protein B is associated with COPD exacerbations

Clinical determinants of exacerbations in severe, early-onset COPD

Women manifest more severe COPD symptoms across the life course

Development of Predictive Models for Airflow Obstruction in Alpha-1-Antitrypsin Deficiency

Polymorphisms in the Superoxide Dismutase-3 Gene Are Associated with Emphysema in COPD

Familial aggregation of FEF25-75 and FEF25-75/FVC in families with severe, early onset COPD

Unique and shared systemic biomarkers for emphysema in Alpha-1 Antitrypsin deficiency and chronic obstructive pulmonary disease

Univariate and multivariate family-based association analysis of the IL-13 ARG130GLN polymorphism in the Childhood Asthma Management program

Determinants of airflow obstruction in severe alpha-1-antitrypsin deficiency

Genomic screening and replication using the same data set in family-based association testing

COPD: problems in diagnosis and measurement

The SERPINE2 Gene Is Associated with Chronic Obstructive Pulmonary Disease

LUNG TRANSPLANTATION AT THE TURN OF THE CENTURY

Power and Design Considerations for a General Class of Family-Based Association Tests: Quantitative Traits

Sex and gender: modifiers of health, disease, and medicine

Ambient Air Pollution and Oxygen Saturation

Gender differences in COPD: are women more susceptible to smoking effects than men?

Pathogenesis of chronic obstructive pulmonary disease: understanding the contributions of gene–environment interactions across the lifespan

Heritability of Lung Function in Severe Alpha-1 Antitrypsin Deficiency

A genome-wide association study of COPD identifies a susceptibility locus on chromosome 19q13

C22 COPD PHENOTYPES: Longitudinal Lung Function And Mortality In Preserved Ratio Impaired Spirometry (prism) In The COPDgene Study

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