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Recommendations for a Standardized Pulmonary Function Report. An Official American Thoracic Society Technical Statement

American journal of respiratory and critical care medicine, 2017-12, Vol.196 (11), p.1463-1472

2017

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Polygenic architecture of rare coding variation across 394,783 exomes

Nature (London), 2023-02, Vol.614 (7948), p.492-499

2023

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Measurement of FEF25-75% and FEF75% does not contribute to clinical decision making

The European respiratory journal, 2014-04, Vol.43 (4), p.1051-1058

2014

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Paternal-age-related de novo mutations and risk for five disorders

Nature communications, 2019-07, Vol.10 (1), p.3043-9, Article 3043

2019

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Assessment of clinical response to ivacaftor with lung clearance index in cystic fibrosis patients with a G551D- CFTR mutation and preserved spirometry: a randomised controlled trial

The lancet respiratory medicine, 2013-10, Vol.1 (8), p.630-638

2013

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Hypersensitivity Pneumonitis and Acute Respiratory Distress Syndrome From E-Cigarette Use

Pediatrics (Evanston), 2018-06, Vol.141 (6), p.e20163927

2018

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Experiences and Perspectives of Individuals with Cystic Fibrosis and Their Families Related to Food Insecurity

Nutrients, 2022-06, Vol.14 (13), p.2573

2022

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Geospatial Analysis of Food Deserts and Their Impact on Health Outcomes in Children with Cystic Fibrosis

Nutrients, 2021-11, Vol.13 (11), p.3996

2021

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Human Airway Epithelial Cells Sense Pseudomonas aeruginosa Infection via Recognition of Flagellin by Toll-Like Receptor 5

Infection and Immunity, 2005-11, Vol.73 (11), p.7151-7160

2005

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Genetic influences on externalizing psychopathology overlap with cognitive functioning and show developmental variation

European psychiatry, 2021-03, Vol.64 (1), p.e29-e29, Article e29

2021

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The female protective effect against autism spectrum disorder

Cell genomics, 2022-06, Vol.2 (6), p.100134, Article 100134

2022

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Provider Attitudes and Practices toward Sexual and Reproductive Health Care for Young Women with Cystic Fibrosis

Journal of pediatric & adolescent gynecology, 2017-10, Vol.30 (5), p.546-552

2017

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Combining SNP-to-gene linking strategies to identify disease genes and assess disease omnigenicity

Nature genetics, 2022-06, Vol.54 (6), p.827-836

2022

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Spirometry Interpretation After Implementation of Race-Neutral Reference Equations in Children

JAMA pediatrics, 2024-07, Vol.178 (7), p.699

2024

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β-Defensin 1 Contributes to Pulmonary Innate Immunity in Mice

Infection and Immunity, 2002-06, Vol.70 (6), p.3068-3072

2002

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First trimester ondansetron exposure and risk of structural birth defects

Reproductive toxicology (Elmsford, N.Y.), 2019-01, Vol.83, p.14-20

2019

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Advances in Pediatric Lung Function Testing Techniques

Clinics in chest medicine, 2024-09, Vol.45 (3), p.543-553

2024

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Obesity and Airway Dysanapsis in Children with and without Asthma

American journal of respiratory and critical care medicine, 2017-02, Vol.195 (3), p.314-323

2017

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Use of the Mechanical In-Exsufflator in Pediatric Patients With Neuromuscular Disease and Impaired Cough

Chest, 2004-04, Vol.125 (4), p.1406-1412

2004

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Impact of Respiratory Developmental Stage on Sensitivity to Late Effects of Radiation in Pediatric Cancer Survivors

Advances in radiation oncology, 2020-05, Vol.5 (3), p.426-433

2020

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Race and Ethnicity in Pulmonary Function Test Interpretation: An Official American Thoracic Society Statement

American journal of respiratory and critical care medicine, 2023-04, Vol.207 (8), p.978-995

2023

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Overweight and obesity in patients with cystic fibrosis: A center-based analysis

Pediatric pulmonology, 2015-01, Vol.50 (1), p.35-41

2015

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Historic Use of Race-Based Spirometry Values Lowered Transplant Priority for Black Patients

Chest, 2024-02, Vol.165 (2), p.381-388

2024

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Nasal epithelial cell culture fluorescence recovery after photobleaching predicts cystic fibrosis therapeutic response

ERJ open research, 2022-10, Vol.8 (4), p.382

2022

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Recommendations for a Standardized Pulmonary Function Report. An Official American Thoracic Society Technical Statement

Polygenic architecture of rare coding variation across 394,783 exomes

Measurement of FEF25-75% and FEF75% does not contribute to clinical decision making

Paternal-age-related de novo mutations and risk for five disorders

Assessment of clinical response to ivacaftor with lung clearance index in cystic fibrosis patients with a G551D- CFTR mutation and preserved spirometry: a randomised controlled trial

Hypersensitivity Pneumonitis and Acute Respiratory Distress Syndrome From E-Cigarette Use

Experiences and Perspectives of Individuals with Cystic Fibrosis and Their Families Related to Food Insecurity

Geospatial Analysis of Food Deserts and Their Impact on Health Outcomes in Children with Cystic Fibrosis

Human Airway Epithelial Cells Sense Pseudomonas aeruginosa Infection via Recognition of Flagellin by Toll-Like Receptor 5

Genetic influences on externalizing psychopathology overlap with cognitive functioning and show developmental variation

The female protective effect against autism spectrum disorder

Provider Attitudes and Practices toward Sexual and Reproductive Health Care for Young Women with Cystic Fibrosis

Combining SNP-to-gene linking strategies to identify disease genes and assess disease omnigenicity

Spirometry Interpretation After Implementation of Race-Neutral Reference Equations in Children

β-Defensin 1 Contributes to Pulmonary Innate Immunity in Mice

Recommendations for surveillance of pulmonary dysfunction among childhood, adolescent, and young adult cancer survivors: a report from the International Late Effects of Childhood Cancer Guideline Harmonization Group

First trimester ondansetron exposure and risk of structural birth defects

Advances in Pediatric Lung Function Testing Techniques

Obesity and Airway Dysanapsis in Children with and without Asthma

Use of the Mechanical In-Exsufflator in Pediatric Patients With Neuromuscular Disease and Impaired Cough

Impact of Respiratory Developmental Stage on Sensitivity to Late Effects of Radiation in Pediatric Cancer Survivors

Race and Ethnicity in Pulmonary Function Test Interpretation: An Official American Thoracic Society Statement

Overweight and obesity in patients with cystic fibrosis: A center-based analysis

Historic Use of Race-Based Spirometry Values Lowered Transplant Priority for Black Patients

Nasal epithelial cell culture fluorescence recovery after photobleaching predicts cystic fibrosis therapeutic response

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