2023
Congenitally Corrected Transposition of the Great Arteries: Fetal Diagnosis, Associations, and Postnatal Outcome: A Fetal Heart Society Research Collaborative Study
Cohen J, Arya B, Caplan R, Donofrio M, Ferdman D, Harrington J, Ho D, Hogan W, Hornberger L, Jhaveri S, Killen S, Lindblade C, Michelfelder E, Moon‐Grady A, Patel S, Quezada E, Ronai C, Mejia A, Schidlow D, Stiver C, Thakur V, Srivastava S. Congenitally Corrected Transposition of the Great Arteries: Fetal Diagnosis, Associations, and Postnatal Outcome: A Fetal Heart Society Research Collaborative Study. Journal Of The American Heart Association 2023, 12: e029706. PMID: 37259984, PMCID: PMC10381988, DOI: 10.1161/jaha.122.029706.Peer-Reviewed Original ResearchMeSH KeywordsArrhythmias, CardiacAtrioventricular BlockCongenitally Corrected Transposition of the Great ArteriesFemaleFetal DeathFetal HeartFollow-Up StudiesHeart Defects, CongenitalHumansInfantPregnancyPrenatal DiagnosisPulmonary AtresiaRetrospective StudiesTransposition of Great VesselsTricuspid Valve InsufficiencyConceptsDeath/transplantSerial fetal echocardiogramsTricuspid regurgitationAortic obstructionPulmonary atresiaFetal deathGreat arteriesFetal echocardiogramFetal diagnosisAssociated cardiac defectsAssociated cardiac lesionsPulmonary outflow obstructionMedian gestational ageMild tricuspid regurgitationFetal tricuspid regurgitationBiventricular repairExtracardiac anomaliesOutflow obstructionSerial echocardiogramsCardiac lesionsClinical outcomesFetal factorsGestational ageUnivariable analysisAtrioventricular block
2020
De novo damaging variants associated with congenital heart diseases contribute to the connectome
Ji W, Ferdman D, Copel J, Scheinost D, Shabanova V, Brueckner M, Khokha MK, Ment LR. De novo damaging variants associated with congenital heart diseases contribute to the connectome. Scientific Reports 2020, 10: 7046. PMID: 32341405, PMCID: PMC7184603, DOI: 10.1038/s41598-020-63928-2.Peer-Reviewed Original ResearchMeSH KeywordsConnectomeDNA HelicasesDNA-Binding ProteinsExomeFemaleHeart Defects, CongenitalHistone-Lysine N-MethyltransferaseHomeodomain ProteinsHumansMaleMi-2 Nucleosome Remodeling and Deacetylase ComplexMutationMutation, MissenseMyeloid-Lymphoid Leukemia ProteinNerve Tissue ProteinsProtein Tyrosine Phosphatase, Non-Receptor Type 11Receptor, Notch1ConceptsDe novo variantsNDD genesCardiac patterningDe novo damaging variantsDamaging de novo variantsCHD genesDamaging variantsGenesProtein truncatingGenetic originNovo variantsGene mutationsPatterningRecent studiesDendritic developmentVariantsMutationsNeurogenesisSynaptogenesisBonferroni correction
2011
Common Atrium and Pulmonary Vascular Disease
Ferdman DJ, Brady D, Rosenzweig EB. Common Atrium and Pulmonary Vascular Disease. Pediatric Cardiology 2011, 32: 595-598. PMID: 21344289, DOI: 10.1007/s00246-011-9919-6.Peer-Reviewed Original ResearchMeSH KeywordsAdolescentAdultAge FactorsBiopsyCardiac CatheterizationChildChild, PreschoolEchocardiographyFemaleFollow-Up StudiesHeart AtriaHeart Defects, CongenitalHeart Septal Defects, AtrialHeart Septal Defects, VentricularHumansHypertension, PulmonaryInfantMalePulmonary ArteryVascular ResistanceYoung AdultConceptsPulmonary vascular diseaseVascular diseaseCommon atriumEarly pulmonary vascular diseaseSevere pulmonary vascular diseaseLarge atrial septal defectPulmonary hypertension therapyUnderwent surgical repairAtrial septal defectClinical courseSurgical repairCase seriesHypertension therapySeptal defectSurgical correctionPatientsDiseaseAtriumAge 2Early monitoringFirst yearTherapy