Adjunct Faculty
Adjunct faculty typically have an academic or research appointment at another institution and contribute or collaborate with one or more School of Medicine faculty members or programs.
Adjunct rank detailsKristopher Kahle, MD, PhD
Assistant Professor AdjunctAbout
Research
Publications
2026
188 Single-Cell Profiling of Neurodevelopmental and Neuroinflammatory Dysregulation in Experimental Hydrocephalus
Bonilla M, Dennis E, Michenkova M, Crouthamel J, Lane A, Kahle K, Limbrick D, McAllister J. 188 Single-Cell Profiling of Neurodevelopmental and Neuroinflammatory Dysregulation in Experimental Hydrocephalus. Neurosurgery 2026, 72: 38-38. DOI: 10.1227/neu.0000000000003964_188.Peer-Reviewed Original Research185 Recurrent TRIO De Novo Variants Drive a Novel Neurodevelopmental Syndrome Featuring Human Congenital Hydrocephalus
Dennis E, Mehta N, Allington G, Mekbib K, Davalan W, Phan D, Haider S, Kahle K. 185 Recurrent TRIO De Novo Variants Drive a Novel Neurodevelopmental Syndrome Featuring Human Congenital Hydrocephalus. Neurosurgery 2026, 72: 37-37. DOI: 10.1227/neu.0000000000003964_185.Peer-Reviewed Original ResearchExpanding the scope of pediatric epilepsy surgery: Access, indications, and outcomes in a modern cohort
McLaren J, Muñoz W, Kwon H, Geffrey A, Nanda P, Thibert R, Grossmann L, Stufflebeam S, Jaimes C, Emerton B, Kahle K, Richardson R, Chu C. Expanding the scope of pediatric epilepsy surgery: Access, indications, and outcomes in a modern cohort. Epilepsia Open 2026 PMID: 41915477, DOI: 10.1002/epi4.70257.Peer-Reviewed Original ResearchPediatric epilepsy surgerySeizure reductionGoal of cureEpilepsy surgeryEpilepsy surgery programPediatric epilepsy surgery programResponsive neurostimulationSurgical techniquePrimary outcomeSurgery programsMedian seizure reductionYoung adult patientsOff-label useRNS implantationTreatment proceduresSuper-respondersSurgical candidatesSurgical complicationsSurgical cohortSurgical treatmentAdult patientsAdverse eventsModern cohortTreatment optionsSeizure-freedomDe novo mutations and environmental modifiers: lessons from neural tube defects
Li H, Shen Y, Vong K, Kahle K, Gleeson J. De novo mutations and environmental modifiers: lessons from neural tube defects. Trends In Genetics 2026, 42: 339-349. PMID: 41850968, DOI: 10.1016/j.tig.2026.01.011.Peer-Reviewed Original ResearchSeizure and quality-of-life outcomes following responsive neurostimulation treatment for drug-resistant epilepsy in children and young adults.
Geffrey A, Kwon H, Shi W, Daly N, Philbin A, Sisterson N, Williams Z, Kahle K, Richardson R, Chu C. Seizure and quality-of-life outcomes following responsive neurostimulation treatment for drug-resistant epilepsy in children and young adults. Journal Of Neurosurgery Pediatrics 2026, 37: 309-321. PMID: 41616315, DOI: 10.3171/2025.9.peds25200.Peer-Reviewed Original ResearchDrug-resistant epilepsyMedian Follow-UpFollow-upSeizure reductionQuality-of-life outcomesQuality of lifeClinical characteristicsYounger patientsSeizure responseResponsive neurostimulationResponder rateAuthors' cohortSevere drug-resistant epilepsyYears of follow-upMedian seizure reductionRNS implantationRNS treatmentBilateral thalamicSuper-respondersRetrospective reviewSurgical complicationsPediatric patientsAdverse eventsStimulation-related adverse effectsTreatment optionsDe Novo TRIO Missense Variants Disrupt Ras‐GEF Domains and Cause Congenital Ventriculomegaly and Hydrocephalus
Mehta N, Dennis E, Allington G, Mekbib K, Hale A, Davalan W, Duy P, Zilla E, Fan B, Kasper E, Alper S, Haider S, Kahle K. De Novo TRIO Missense Variants Disrupt Ras‐GEF Domains and Cause Congenital Ventriculomegaly and Hydrocephalus. Human Mutation 2026, 2026: 8870037. PMID: 42051466, PMCID: PMC13115915, DOI: 10.1155/humu/8870037.Peer-Reviewed Original ResearchConceptsRas GEF domainMissense variantsIn silico structural modelingRho GTPase activityClinically relevant genesAutosomal dominant neurodevelopmental disorderGenetic evaluationGenetic architectureGTPase activityRas-GEFMultipotent progenitor populationTranscriptome dataExome sequencingDominant neurodevelopmental disorderRelevant genesCongenital hydrocephalusCongenital ventriculomegalyUnrelated patientsGenesVariantsCerebrospinal fluid diversionSyndromic CHProgenitor populationsStructural brain abnormalitiesNeurodevelopmental disorders
2025
Transient Receptor Potential channels (TRP) in GtoPdb v.2025.4
Blair N, McKemy D, Nilius B, Oancea E, Owsianik G, Riccio A, Sah R, Stotz S, Tian J, Tong D, Vriens J, Wu L, Xu H, Yang F, Yang W, Yue L, Liu Q, Liu B, Caceres A, Carvacho I, Chaudhuri D, Clapham D, De Clercq K, Delling M, Doerner J, Fan L, Grimm C, Ha K, Hu M, Jabba S, Jordt S, Julius D, Kahle K, Zhu M. Transient Receptor Potential channels (TRP) in GtoPdb v.2025.4. IUPHAR/BPS Guide To Pharmacology CITE 2025, 2025 DOI: 10.2218/gtopdb/f78/2025.4.Peer-Reviewed Original ResearchTRPC channelsTransient receptor potential channelsDetection of noxious heatCongenital stationary night blindnessCalcium-activated cationStore-operated channelsPlacental trophoblast cellsNMDA receptorsAdenosine diphosphate riboseSlow afterdepolarizationNoxious heatC-terminal kinase regionSplice variantsIntracellular ATP levelsCation channelsChannel activityNeurodegenerative disorder mucolipidosis type IVTRPA1 activationDepletion of intracellular calcium storesMucolipidosis type IVTRP channelsAssociated with conduction defectsDevelopment of heat hyperalgesiaDevelopment of thermal hyperalgesiaDynamic intracellular vesicular structuresEffect of GLP‐1 receptor agonists on idiopathic intracranial hypertension: A systematic review
de Oliveira H, Ruelas M, Fonseca P, Diaz C, de Paula G, da Costa P, Parker T, Kahle K. Effect of GLP‐1 receptor agonists on idiopathic intracranial hypertension: A systematic review. Headache The Journal Of Head And Face Pain 2025, 66: 286-297. PMID: 41246926, DOI: 10.1111/head.70005.Peer-Reviewed Original ResearchIdiopathic intracranial hypertensionGLP-1 RAsInternational Prospective RegisterCochrane Central RegisterGLP-1Receptor agonistsGLP-1RAIntracranial hypertensionWorld Health Organization-International Clinical Trials Registry PlatformHeadache burdenEffects of GLP-1 receptor agonistsClinical effectsEffects of glucagon-like peptide-1 receptor agonistsGlucagon-like peptide-1 receptor agonistsPeptide-1 receptor agonistsGLP-1 receptor agonistsInternational Prospective Register of Systematic ReviewsSystematic reviewProspective Register of Systematic ReviewsMild gastrointestinal symptomsCochrane Central Register of Controlled TrialsCentral Register of Controlled TrialsGLP-1RA treatmentRegister of Controlled TrialsElevated intracranial pressureConcurrent Chiari malformation type I and hydrocephalus: Integrating mechanistic and pathophysiological insights toward a unified management paradigm
Davalan W, Mehta N, Jackson E, Rocque B, Duy P, Muñoz W, Kundishora A, Mekbib K, Limbrick D, Kahle K. Concurrent Chiari malformation type I and hydrocephalus: Integrating mechanistic and pathophysiological insights toward a unified management paradigm. Experimental Neurology 2025, 396: 115535. PMID: 41173227, DOI: 10.1016/j.expneurol.2025.115535.Peer-Reviewed Original ResearchConceptsChiari malformation type IPosterior fossa decompressionCM-ICerebrospinal fluidPosterior fossa hypoplasiaCSF diversionCraniospinal pressure dissociationPremature suture fusionVenous outflow restrictionType ITonsillar descentCerebrospinal fluid dynamicsHindbrain herniationSurgical outcomesSyndromic craniosynostosesSecondary hydrocephalusSyndrome casesClinical managementDevelopmental anomaliesDiagnostic accuracyPathophysiological mechanismsAnatomical classificationTreatment selectionHydrocephalusPathophysiological insightsSomatic TEK Mutation Identified in a Patient with Calvarial Venous Malformations
Fan B, Dennis E, Mehta N, Davalan W, Fortes C, Swamy A, Muñoz W, Jaimes C, Hale A, Kahle K. Somatic TEK Mutation Identified in a Patient with Calvarial Venous Malformations. Genes 2025, 16: 1123. PMID: 41153341, PMCID: PMC12564052, DOI: 10.3390/genes16101123.Peer-Reviewed Original ResearchConceptsVenous malformationsScRNA-seqScRNA-seq data analysisSingle-cell RNA sequencingSporadic venous malformationsExome sequencingRNA sequencingPathway enrichmentGermline DNAMolecular consequencesTEK mutationsBlood DNANeurosurgical resectionMutationsPediatric casesVascular anomaliesGenetic testingMolecular implicationsSporadic casesEndothelial cellsDNATherapeutic targetSequenceMalformationsPopulation database