Exome sequencing identifies gene variants and networks associated with extreme respiratory outcomes following preterm birth

Ancestry and Genetic Associations with Bronchopulmonary Dysplasia in Preterm Infants

(2018) Dara G Torgerson et al.   AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY

Csk/Src/EGFR signaling regulates migration of myofibroblasts and alveolarization

(2016) Jianhui Li et al.   AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY

Antiinflammatory Effects of Budesonide in Human Fetal Lung

(2016) Anne Marie Barrette et al.   AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY

The genetic predisposition to bronchopulmonary dysplasia

(2016) Kun-Hsing Yu et al.   CURRENT OPINION IN PEDIATRICS

Pulmonary hypertension associated with acute or chronic lung diseases in the preterm and term neonate and infant. The European Paediatric Pulmonary Vascular Disease Network, endorsed by ISHLT and DGPK

(2016) Anne Hilgendorff et al.   HEART

Targeted Sequencing and Meta-Analysis of Preterm Birth

(2016) Alper Uzun et al.   PLoS One

Exome Sequencing of Neonatal Blood Spots and the Identification of Genes Implicated in Bronchopulmonary Dysplasia

(2015) Jingjing Li et al.   AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE

Prematurity and respiratory outcomes program (PROP): study protocol of a prospective multicenter study of respiratory outcomes of preterm infants in the United States

(2015) Gloria S Pryhuber et al.   BMC Pediatrics

Exome sequencing and pathway analysis for identification of genetic variability relevant for bronchopulmonary dysplasia (BPD) in preterm newborns: A pilot study

(2015) Paola Carrera et al.   CLINICA CHIMICA ACTA

Exome-based case–control association study using extreme phenotype design reveals novel candidates with protective effect in diabetic retinopathy

(2015) Corina Shtir et al.   HUMAN GENETICS

Trends in Care Practices, Morbidity, and Mortality of Extremely Preterm Neonates, 1993-2012

(2015) Barbara J. Stoll et al.   JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION

Integrated Genomic Analyses in Bronchopulmonary Dysplasia

(2015) Namasivayam Ambalavanan et al.   JOURNAL OF PEDIATRICS

Genetic predisposition to bronchopulmonary dysplasia

(2015) Charitharth Vivek Lal et al.   SEMINARS IN PERINATOLOGY

Exome Sequencing of Phenotypic Extremes Identifies CAV2 and TMC6 as Interacting Modifiers of Chronic Pseudomonas aeruginosa Infection in Cystic Fibrosis

(2015) Mary J. Emond et al.   PLoS Genetics

An Update on the Impact of Postnatal Systemic Corticosteroids on Mortality and Cerebral Palsy in Preterm Infants: Effect Modification by Risk of Bronchopulmonary Dysplasia

(2014) Lex W. Doyle et al.   JOURNAL OF PEDIATRICS

FFBSKAT: Fast Family-Based Sequence Kernel Association Test

(2014) Gulnara R. Svishcheva et al.   PLoS One

Sequence Kernel Association Tests for the Combined Effect of Rare and Common Variants

(2013) Iuliana Ionita-Laza et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Multiple Genetic Variant Association Testing by Collapsing and Kernel Methods With Pedigree or Population Structured Data

(2013) Daniel J. Schaid et al.   GENETIC EPIDEMIOLOGY

A Genome-Wide Association Study (GWAS) for Bronchopulmonary Dysplasia

(2013) H. Wang et al.   PEDIATRICS

Gene Expression Profiling in Preterm Infants: New Aspects of Bronchopulmonary Dysplasia Development

(2013) Jacek J. Pietrzyk et al.   PLoS One

Genome-Wide Transcriptional Profiling Reveals Connective Tissue Mast Cell Accumulation in Bronchopulmonary Dysplasia

(2012) Soumyaroop Bhattacharya et al.   AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE

Genome-wide efficient mixed-model analysis for association studies

(2012) Xiang Zhou et al.   NATURE GENETICS

Risk of bronchopulmonary dysplasia by second-trimester maternal serum levels of α-fetoprotein, human chorionic gonadotropin, and unconjugated estriol

(2012) Laura L. Jelliffe-Pawlowski et al.   PEDIATRIC RESEARCH

Mortality and Neonatal Morbidity Among Infants 501 to 1500 Grams From 2000 to 2009

(2012) J. D. Horbar et al.   PEDIATRICS

Rare-Variant Association Testing for Sequencing Data with the Sequence Kernel Association Test

(2011) Michael C. Wu et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Identification ofSPOCK2As a Susceptibility Gene for Bronchopulmonary Dysplasia

(2011) Alice Hadchouel et al.   AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE

Risk Factors for Pulmonary Artery Hypertension in Preterm Infants with Moderate or Severe Bronchopulmonary Dysplasia

(2011) Do-Hyun Kim et al.   Neonatology

Robust relationship inference in genome-wide association studies

(2010) Ani Manichaikul et al.   BIOINFORMATICS

ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data

(2010) K. Wang et al.   NUCLEIC ACIDS RESEARCH

Identifying a High Fraction of the Human Genome to be under Selective Constraint Using GERP++

(2010) Eugene V. Davydov et al.   PLoS Computational Biology

Postnatal Estradiol Up-regulates Lung Nitric Oxide Synthases and Improves Lung Function in Bronchopulmonary Dysplasia

(2009) Donald C. McCurnin et al.   AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE

Transcriptomic Analysis of Human Lung Development

(2009) Alvin T. Kho et al.   AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE

Gastrin-Releasing Peptide, Immune Responses, and Lung Disease

(2009) Simone Degan et al.   Annals of the New York Academy of Sciences

Heritability of Bronchopulmonary Dysplasia, Defined According to the Consensus Statement of the National Institutes of Health

(2008) P. M. Lavoie et al.   PEDIATRICS