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References from Identification of rare variants in novel candidate genes in pulmonary atresia patients by next generation sequencing. Local targets link to admitted publications; unresolved targets remain external evidence.
Echocardiographic predictors of aortopulmonary collaterals in infants with tetralogy of fallot and pulmonary atresia
10.1016/s0735-1097(02)02960-1 · 2003 · External reference
The functional intraoperative pulmonary blood flow study is a more sensitive predictor than preoperative anatomy for right ventricular pressure and physiologic tolerance of ventricular septal defect closure after complete unifocalization in patients with pulmonary atresia, ventricular septal defect, and major aortopulmonary collaterals
10.1161/circulationaha.108.844084 · 2009 · External reference
10.1016/j.jacc.2011.08.025
10.1016/j.jacc.2011.08.025 · External reference
Advances in molecular genetics for pulmonary atresia
10.1017/s1047951116001487 · 2017 · External reference
10.1016/s0002-9149(96)00212-3
10.1016/s0002-9149(96)00212-3 · External reference
Detecting 22q11.2 deletion in Chinese children with conotruncal heart defects and single nucleotide polymorphisms in the haploid TBX1 locus
10.1186/1471-2350-12-169 · 2011 · External reference
The Congenital Heart Disease Genetic Network Study: rationale, design, and early results
10.1161/circresaha.111.300297 · 2013 · External reference
Early and intermediate outcomes after repair of pulmonary atresia with ventricular septal defect and major aortopulmonary collateral arteries: experience with 85 patients
10.1161/01.cir.101.15.1826 · 2000 · External reference
Long-term outcome following catheter valvotomy for pulmonary atresia with intact ventricular septum
10.1016/j.jacc.2012.01.022 · 2012 · External reference
Fetal pulmonary valvuloplasty for critical pulmonary stenosis or atresia with intact septum
10.1016/s0140-6736(02)11531-5 · 2002 · External reference
Pulmonary atresia with intact ventricular septum: range of morphology in a population-based study
10.1016/s0735-1097(02)01832-6 · 2002 · External reference
10.1038/ng.415
10.1038/ng.415 · External reference
Rare de novo copy number variants in patients with congenital pulmonary atresia
10.1371/journal.pone.0096471 · 2014 · External reference
Alpha-cardiac myosin heavy chain (MYH6) mutations affecting myofibril formation are associated with congenital heart defects
10.1093/hmg/ddq315 · 2010 · External reference
Rare copy number variations in adults with tetralogy of Fallot implicate novel risk gene pathways
10.1371/journal.pgen.1002843 · 2012 · External reference
HEY2 mutations in malformed hearts
10.1002/humu.9390 · 2006 · External reference
10.1016/j.ajhg.2012.08.003
10.1016/j.ajhg.2012.08.003 · External reference
Dihydrofolate reductase deficiency due to a homozygous DHFR mutation causes megaloblastic anemia and cerebral folate deficiency leading to severe neurologic disease
10.1016/j.ajhg.2011.01.007 · 2011 · External reference
Rare copy number variations might not be involved in the molecular pathogenesis of PA-IVS in an unselected Chinese cohort
10.1007/s00246-019-02062-x · 2019 · External reference
10.1093/cvr/cvw195
10.1093/cvr/cvw195 · External reference
10.1097/pat.0b013e32834635a9
10.1097/pat.0b013e32834635a9 · External reference
Prevalence and clinical manifestations of 22q11.2 microdeletion in adults with selected conotruncal anomalies
10.1016/j.jacc.2004.10.056 · 2005 · External reference
10.1093/bioinformatics/btp698
10.1093/bioinformatics/btp698 · External reference
10.1093/bioinformatics/btp352
10.1093/bioinformatics/btp352 · External reference
10.1101/gr.107524.110
10.1101/gr.107524.110 · External reference
10.1093/nar/gkg509
10.1093/nar/gkg509 · External reference
Predicting functional effect of human missense mutations using PolyPhen-2
2013 · External reference
10.1038/nmeth0810-575
10.1038/nmeth0810-575 · External reference
A global reference for human genetic variation
10.1038/nature15393 · 2015 · External reference
10.1093/nar/gkw971
10.1093/nar/gkw971 · External reference
10.1038/gim.2015.30
10.1038/gim.2015.30 · External reference
10.1093/nar/gku1003
10.1093/nar/gku1003 · External reference
Network Analysis Tools: from biological networks to clusters and pathways
10.1038/nprot.2008.100 · 2008 · External reference
10.1101/gr.1239303
10.1101/gr.1239303 · External reference
10.1164/rccm.201306-1086oc
10.1164/rccm.201306-1086oc · External reference
Identification of right heart-enriched genes in a murine model of chronic outflow tract obstruction
10.1016/j.yjmcc.2010.07.014 · 2010 · External reference
Next-generation sequencing identifies novel genes with rare variants in total anomalous pulmonary venous connection
10.1016/j.ebiom.2018.11.008 · 2018 · External reference
10.1038/nprot.2006.236
10.1038/nprot.2006.236 · External reference
10.1038/sj.onc.1205086
10.1038/sj.onc.1205086 · External reference
10.1161/atvbaha.117.310020
10.1161/atvbaha.117.310020 · External reference
Mutations in Hnrnpa1 cause congenital heart defects
2018 · External reference
Rare copy number variants analysis identifies novel candidate genes in heterotaxy syndrome patients with congenital heart defects
10.1186/s13073-018-0549-y · 2018 · External reference
Homozygous frameshift mutations in FAT1 cause a syndrome characterized by colobomatous-microphthalmia, ptosis, nephropathy and syndactyly
10.1038/s41467-019-08547-w · 2019 · External reference
10.1016/j.semcdb.2017.07.016
10.1016/j.semcdb.2017.07.016 · External reference
Defenders and challengers of endothelial barrier function
10.3389/fimmu.2017.01847 · 2017 · External reference
BPAG1 isoform-b: complex distribution pattern in striated and heart muscle and association with plectin and alpha-actinin
10.1016/j.yexcr.2009.11.010 · 2010 · External reference
Expression of fibulin-6 in failing hearts and its role for cardiac fibroblast migration
10.1093/cvr/cvu161 · 2014 · External reference
Therapeutic concentrations of digitoxin inhibit endothelial focal adhesion kinase and angiogenesis induced by different growth factors
10.1111/bph.13944 · 2017 · External reference
10.1073/pnas.1606385113
10.1073/pnas.1606385113 · External reference
