Katharine Henderson
Genetic Counselor Diagnostic RadiologyDownloadHi-Res Photo
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Genetic Counselor Diagnostic Radiology
Departments & Organizations
- Advanced Practice Providers (APPs)
- Hereditary Hemorrhagic Telangiectasia (HHT) Program
- Radiology & Biomedical Imaging
Research
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Research at a Glance
Yale Co-Authors
Frequent collaborators of Katharine Henderson's published research.
Publications Timeline
A big-picture view of Katharine Henderson's research output by year.
Jeffrey Pollak, MD
Lawrence Young, MD
Guadalupe Garcia-Tsao, MD, FRCP
Deborah Proctor, MD
Adam Fish
Former YSMRobert I. White Jr, MD
30Publications
1,865Citations
Publications
2024
Criteria for PAVM Reintervention
Fish A, Knight E, Henderson K, Pollak J, Schlachter T. Criteria for PAVM Reintervention. Journal Of Clinical Medicine 2024, 13: 6104. PMID: 39458055, PMCID: PMC11508501, DOI: 10.3390/jcm13206104.Peer-Reviewed Original ResearchCitationsAltmetricConceptsparadoxical embolismretrospective review of patientsreview of patientsmodern embolization techniquesretrospective reviewembolization techniquesreinterventionscreening intervalembolizationlifetime prevalence ratespatientsrecurrencePAVMshemoptysisspontaneous eventsprevalence ratescenters of excellencereperfusioncriteria
2021
Incidence of Spontaneous Pulmonary AVM Rupture in HHT Patients
Fish A, Henderson K, Moushey A, Pollak J, Schlachter T. Incidence of Spontaneous Pulmonary AVM Rupture in HHT Patients. Journal Of Clinical Medicine 2021, 10: 4714. PMID: 34682838, PMCID: PMC8540859, DOI: 10.3390/jcm10204714.Peer-Reviewed Original ResearchCitationsAltmetricConceptsAVM ruptureHHT patientspulmonary hemorrhagepulmonary AVMslife-threatening complicationsinitial presentationtrue incidenceembolization techniquesspontaneous rupturesingle lifetime episodesubsequent embolizationlifetime prevalencelifetime episodespatientsincidencecomplicationshemorrhageAVMrupturehemothoraxembolizationhydrothoraxlesionsprevalencecases
2020
Subaortic Membranes in Patients With Hereditary Hemorrhagic Telangiectasia and Liver Vascular Malformations
Kim AS, Henderson KJ, Pawar S, Kim MJ, Punjani S, Pollak JS, Fahey JT, Garcia‐Tsao G, Sugeng L, Young LH. Subaortic Membranes in Patients With Hereditary Hemorrhagic Telangiectasia and Liver Vascular Malformations. Journal Of The American Heart Association 2020, 9: e016197. PMID: 33054561, PMCID: PMC7763373, DOI: 10.1161/jaha.120.016197.Peer-Reviewed Original ResearchCitationsAltmetricMeSH Keywords and ConceptsMeSH KeywordsActivin Receptors, Type IICardiac Output, HighDiscrete Subaortic StenosisEchocardiographyFemaleHeart Defects, CongenitalHeart FailureHumansLiverMaleMiddle AgedMutationPrognosisRetrospective StudiesSurvival AnalysisTelangiectasia, Hereditary HemorrhagicUnited StatesVascular MalformationsConceptshigh-output cardiac failurehereditary hemorrhagic telangiectasialeft ventricular outflow tractventricular outflow tracthemorrhagic telangiectasiamild obstructionsubaortic membranevascular malformationsoutflow tractactivin receptor-like kinase 1 mutationshereditary hemorrhagic telangiectasia patientsliver vascular malformationsmild aortic insufficiencypulmonary artery pressureright heart catheterizationcohort of patientsretrospective observational analysishigh cardiac outputkinase 1 mutationsartery pressureheart catheterizationpulmonary hypertensionaortic insufficiencyBackground Patientstricuspid regurgitationGenotype–Phenotype Correlations in Children with HHT
Kilian A, Latino GA, White AJ, Clark D, Chakinala MM, Ratjen F, McDonald J, Whitehead K, Gossage JR, Lin D, Henderson K, Pollak J, McWilliams JP, Kim H, Lawton MT, Faughnan ME. Genotype–Phenotype Correlations in Children with HHT. Journal Of Clinical Medicine 2020, 9: 2714. PMID: 32842615, PMCID: PMC7565052, DOI: 10.3390/jcm9092714.Peer-Reviewed Original ResearchCitationsConceptsbrain vascular malformationshereditary hemorrhagic telangiectasiapulmonary arteriovenous malformationsgenotype-phenotype correlationvascular malformationsarteriovenous malformationsHHT patientscentral nervous systemrare autosomal dominant diseasechi-square testautosomal dominant diseasegastrointestinal bleedingpediatric patientsmucocutaneous telangiectasiahemorrhagic telangiectasiagreater prevalencenervous systempatientsphenotypic presentationdominant diseasemalformationsadultschildrentelangiectasiamutations
2018
Tissue‐specific mosaicism in hereditary hemorrhagic telangiectasia: Implications for genetic testing in families
McDonald J, Wooderchak‐Donahue W, Henderson K, Paul E, Morris A, Bayrak‐Toydemir P. Tissue‐specific mosaicism in hereditary hemorrhagic telangiectasia: Implications for genetic testing in families. American Journal Of Medical Genetics Part A 2018, 176: 1618-1621. PMID: 29736967, DOI: 10.1002/ajmg.a.38695.Peer-Reviewed Original ResearchCitationsMeSH Keywords and ConceptsConceptspathogenic variantsdetection of mosaicismdisease-causing mutationsgenetic testing algorithmtissue-specific mosaicismhemorrhagic telangiectasiaexome sequencingSanger sequencingdeletion/duplication analysisfamilial probandsgenetic testingprobandsblood sampleshereditary hemorrhagic telangiectasiamosaicismgeneshemorrhagic telangiectasia patientsmutationsvariantsmolecular findingssequencebulb samplesHHT patientsperipheral bloodfamilyApplicability of the Curaçao Criteria for the Diagnosis of Hereditary Hemorrhagic Telangiectasia in the Pediatric Population
Pahl KS, Choudhury A, Wusik K, Hammill A, White A, Henderson K, Pollak J, Kasthuri RS. Applicability of the Curaçao Criteria for the Diagnosis of Hereditary Hemorrhagic Telangiectasia in the Pediatric Population. The Journal Of Pediatrics 2018, 197: 207-213. PMID: 29655863, DOI: 10.1016/j.jpeds.2018.01.079.Peer-Reviewed Original ResearchCitationsAltmetricMeSH Keywords and ConceptsTHREE TYPES OF INTRAHEPATIC SHUNTS PRESENTING IN A SINGLE PATIENT WITH HEREDITARY HEMORRHAGIC TELANGIECTASIA
Brandt E, Haghighat L, Garcia-Tsao G, Henderson K, Pollak J, Proctor D, Young L. THREE TYPES OF INTRAHEPATIC SHUNTS PRESENTING IN A SINGLE PATIENT WITH HEREDITARY HEMORRHAGIC TELANGIECTASIA. Journal Of The American College Of Cardiology 2018, 71: a2393. DOI: 10.1016/s0735-1097(18)32934-6.Peer-Reviewed Case Reports and Technical NotesCitations
2017
Pulmonary Hypertension Prevalence and Prognosis in a Cohort of Patients with Hereditary Hemorrhagic Telangiectasia Undergoing Embolization of Pulmonary Arteriovenous Malformations
Chizinga M, Rudkovskaia AA, Henderson K, Pollak J, Garcia-Tsao G, Young LH, Fares WH. Pulmonary Hypertension Prevalence and Prognosis in a Cohort of Patients with Hereditary Hemorrhagic Telangiectasia Undergoing Embolization of Pulmonary Arteriovenous Malformations. American Journal Of Respiratory And Critical Care Medicine 2017, 196: 1353-1356. PMID: 28375020, DOI: 10.1164/rccm.201702-0267le.Peer-Reviewed Original ResearchCitationsAltmetricMeSH Keywords and ConceptsClinical Significance of Pulmonary Arteriovenous Malformation Reperfusion
Kaufman C, Henderson K, Pollak J. Clinical Significance of Pulmonary Arteriovenous Malformation Reperfusion. Journal Of Clinical Interventional Radiology ISVIR 2017, 01: 156-160. DOI: 10.1055/s-0037-1604096.Peer-Reviewed Original ResearchCitationsConceptssymptomatic patientsclinical significancepulmonary arteriovenous malformation (PAVM) embolizationtime of diagnosispulmonary arteriovenous malformationstime of embolizationtime of presentationarteriovenous malformation embolizationHHT Centerinitial embolizationmedical comorbiditiesretrospective reviewclinical historysevere manifestationsPAVM embolizationarteriovenous malformationsinitial procedureembolization procedurestreatment periodembolizationpatientsmild manifestationsreperfusionsymptomsPAVMsPrevalence of Pulmonary Hypertension in a Large Cohort of Hereditary Hemorrhagic Telangiectasia Patients
Chizinga M, Rudkovskaia A, Henderson K, Pollak J, Garcia-Tsao G, Young L, Fares W. Prevalence of Pulmonary Hypertension in a Large Cohort of Hereditary Hemorrhagic Telangiectasia Patients. American Journal Of Respiratory And Critical Care Medicine 2017, 195: a7035-a7035. DOI: 10.1164/ajrccm-conference.2017.195.1_meetingabstracts.a7035.Peer-Reviewed Original Research
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