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References from Rare-variant collapsing analyses identified risk genes for neonatal acute respiratory distress syndrome. Local targets link to admitted publications; unresolved targets remain external evidence.
Epidemiology of Neonatal Acute Respiratory Distress Syndrome: Prospective, Multicenter, International Cohort Study
10.1097/pcc.0000000000002961 · 2022 · External reference
The Montreux definition of neonatal ARDS: biological and clinical background behind the description of a new entity
10.1016/s2213-2600(17)30214-x · 2017 · External reference
Surfactant therapies for pediatric and neonatal ARDS: ESPNIC expert consensus opinion for future research steps
10.1186/s13054-021-03489-6 · 2021 · External reference
Respiratory syncytial virus seropositivity at birth is associated with adverse neonatal respiratory outcomes
10.1002/ppul.25001 · 2020 · External reference
Risk Factors and Clinical Characteristics of Neonatal Acute Respiratory Distress Syndrome Caused by Early Onset Sepsis
10.3389/fped.2022.847827 · 2022 · External reference
The surfactant system protects both fetus and newborn
10.1159/000349994 · 2013 · External reference
Surfactant proteins gene variants in premature newborn infants with severe respiratory distress syndrome
10.1038/s41372-017-0018-2 · 2018 · External reference
ABCA3 gene mutations shape the clinical profiles of severe unexplained respiratory distress syndrome in late preterm and term infants
10.21037/tp-20-283 · 2021 · External reference
In Lysinuric Protein Intolerance system y+L activity is defective in monocytes and in GM-CSF-differentiated macrophages
10.1186/1750-1172-5-32 · 2010 · External reference
10.1006/dbio.2001.0322
10.1006/dbio.2001.0322 · External reference
10.1042/cs20080068
10.1042/cs20080068 · External reference
Association of polymorphisms in the human surfactant protein-D (SFTPD) gene and postnatal pulmonary adaptation in the preterm infant
10.1111/j.1651-2227.2008.01014.x · 2009 · External reference
Genetic Polymorphisms of LPCAT1, CHPT1 and PCYT1B and Risk of Neonatal Respiratory Distress Syndrome among a Chinese Han Population
10.1016/j.pedneo.2019.12.012 · 2020 · External reference
Endothelial NOS gene Glu298Asp polymorphism in preterm neonates with respiratory distress syndrome
10.1002/ppul.22759 · 2013 · External reference
Integrated genomic analyses in bronchopulmonary dysplasia
10.1016/j.jpeds.2014.09.052 · 2015 · External reference
Association of SCNN1A Single Nucleotide Polymorphisms with neonatal respiratory distress syndrome
10.1038/srep17317 · 2015 · External reference
Genetic Polymorphisms of SP-A, SP-B, and SP-D and Risk of Respiratory Distress Syndrome in Preterm Neonates
10.12659/msm.898553 · 2016 · External reference
A study based on whole-genome sequencing yields a rare variant at 8q24 associated with prostate cancer
10.1038/ng.2437 · 2012 · External reference
10.1038/nrg3118
10.1038/nrg3118 · External reference
Proband-only medical exome sequencing as a cost-effective first-tier genetic diagnostic test for patients without prior molecular tests and clinical diagnosis in a developing country: the China experience
10.1038/gim.2017.195 · 2018 · External reference
10.1146/annurev-pathol-012513-104644
10.1146/annurev-pathol-012513-104644 · External reference
10.1172/jci130143
10.1172/jci130143 · External reference
Establishing the entity of neonatal acute respiratory distress syndrome
10.21037/jtd.2017.10.64 · 2017 · External reference
10.1056/nejmra1608077
10.1056/nejmra1608077 · External reference
Transcriptomic analysis of human lung development
10.1164/rccm.200907-1063oc · 2010 · External reference
Nitric oxide decreases surfactant protein gene expression in primary cultures of type II pneumocytes
10.1152/ajplung.00210.2004 · 2005 · External reference
10.1016/j.molcel.2020.10.042
10.1016/j.molcel.2020.10.042 · External reference
Functional characterization of four ATP-binding cassette transporter A3 gene (ABCA3) variants
10.1002/humu.24014 · 2020 · External reference
Toxic effects of perinatal maternal exposure to nonylphenol on lung inflammation in male offspring rats
10.1016/j.scitotenv.2020.139238 · 2020 · External reference
Heterozygous endothelin receptor B (EDNRB) mutations in isolated Hirschsprung disease
10.1093/hmg/5.3.355 · 1996 · External reference
10.1056/nejmoa032178
10.1056/nejmoa032178 · External reference
Exome sequencing and pathway analysis for identification of genetic variability relevant for bronchopulmonary dysplasia (BPD) in preterm newborns: A pilot study
10.1016/j.cca.2015.01.001 · 2015 · External reference
10.1164/rccm.201501-0168oc
10.1164/rccm.201501-0168oc · External reference
Exome sequencing identifies gene variants and networks associated with extreme respiratory outcomes following preterm birth
10.1186/s12863-018-0679-7 · 2018 · External reference
Whole exome sequencing identifies a novel variant in ABCA3 in an individual with fatal congenital surfactant protein deficiency
10.24953/turkjped.2021.04.019 · 2021 · External reference
10.1038/nrg2918
10.1038/nrg2918 · External reference
Lists2Networks: integrated analysis of gene/protein lists
10.1186/1471-2105-11-87 · 2010 · External reference
