Robert King, MD
Emeritus Faculty and Senior Research Scientist in the Child Study CenterDownloadHi-Res Photo
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Appointments
Child Study Center
Primary, Secondary
Contact Info
Child Study Center
PO Box 207900, 230 South Frontage Road
New Haven, CT 06520-7900
United States
About
Titles
Emeritus Faculty and Senior Research Scientist in the Child Study Center
Appointments
Child Study Center
EmeritusPrimaryChild Study Center
Senior Research ScientistSecondary
Other Departments & Organizations
- Child & Adolescent Psychiatry Training Program
- Child Study Center
- Developmental Disabilities Program
- Pituitary Program
- Tic Disorder & Obsessive Compulsive Disorder Program
- Yale Medicine
- Yale Ventures
Education & Training
- Fellow
- Children's Hospital National Medical Center, Washington D.C (1974)
- Fellow
- Boston Children's Hospital Medical Center (1972)
- Resident
- Massachusetts Mental Health Center (1971)
- Resident
- Boston Children's Hospital Medical Center (1969)
- MD
- Harvard University (1968)
Research
Research at a Glance
Yale Co-Authors
Frequent collaborators of Robert King's published research.
Publications Timeline
A big-picture view of Robert King's research output by year.
Lawrence A. Vitulano, PhD, ABPP
Paul Lombroso, MD
James Leckman, MD, PhD
Michael Bloch, MD, MS
Denis Sukhodolsky, PhD
Andrés S Martin, MD, PhD
60Publications
6,372Citations
Publications
2024
Neurodevelopmental Disorders: Stereotypical Movement Disorders and Tic Disorders
Vitulano L, Vitulano M, King R, Yazgan M, Leckman J. Neurodevelopmental Disorders: Stereotypical Movement Disorders and Tic Disorders. 2024, 1685-1707. DOI: 10.1007/978-3-030-51366-5_45.Peer-Reviewed Original ResearchConceptsDevelopmental coordination disorderStereotypic movement disorderTic disordersCoordination disorderMotor skillsBest practice assessmentsNeurodevelopmental disorder groupMotor disordersMovement disordersSelf-bitingHead bangingNeurobiological disorderMotor behaviorHand flappingDisordersPractical assessmentEarly-onsetNonrhythmic movementsChildrenGroup of conditionsJerking movementsMagnetic resonance imaging techniquesSkillsIndividualsThe Challenge of Examining Social Determinants of Health in People Living With Tourette Syndrome
Dy-Hollins M, Carr S, Essa A, Osiecki L, Lackland D, Voeks J, Mejia N, Sharma N, Budman C, Cath D, Grados M, King R, Lyon G, Rouleau G, Sandor P, Singer H, Chibnik L, Mathews C, Scharf J. The Challenge of Examining Social Determinants of Health in People Living With Tourette Syndrome. Pediatric Neurology 2024, 155: 55-61. PMID: 38608551, PMCID: PMC11132913, DOI: 10.1016/j.pediatrneurol.2024.02.008.Peer-Reviewed Original ResearchAltmetricConceptsParental educational attainmentEthnic minority groupsEducational attainmentSocial determinants of healthExamining social determinants of healthNon-Hispanic White individualsDeterminants of healthDiagnosis ageNon-Hispanic whitesMinority groupsHispanic individualsWhite individualsSignificant disparitiesLogistic regressionParental educationNon-whiteComorbid conditionsNon-parametric testsEthnicityGroup differencesSymptom onsetOutcomesParticipantsResearch studiesTourette syndrome
2023
Neurodevelopmental Disorders: Stereotypical Movement Disorders and Tic Disorders
Vitulano L, Vitulano M, King R, Yazgan M, Leckman J. Neurodevelopmental Disorders: Stereotypical Movement Disorders and Tic Disorders. 2023, 1-23. DOI: 10.1007/978-3-030-42825-9_45-1.Peer-Reviewed Original ResearchConceptsStereotypic movement disorderTic disordersDevelopmental coordination disorderMovement disordersMotor disordersCoordination disorderMotor skillsNeurodevelopmental disorder groupMagnetic resonance imaging techniquesBest practice assessmentHead bangingHand flappingNeurobiological disorderDisorder groupMotor behaviorDisordersNonrhythmic movementsSuch childrenPractice assessmentUnwanted attentionChildrenImaging techniquesSkillsYearsRecurrent
2022
Mispatterning and interneuron deficit in Tourette Syndrome basal ganglia organoids
Brady M, Mariani J, Koca Y, Szekely A, King R, Bloch M, Landeros-Weisenberger A, Leckman J, Vaccarino F. Mispatterning and interneuron deficit in Tourette Syndrome basal ganglia organoids. Molecular Psychiatry 2022, 27: 5007-5019. PMID: 36447010, PMCID: PMC9949887, DOI: 10.1038/s41380-022-01880-5.Peer-Reviewed Original ResearchCitationsAltmetricMeSH Keywords and ConceptsConceptsTourette syndromeInterneuron deficitsGABAergic interneuronsHealthy controlsNeurodevelopmental underpinningsNeuropathological deficitsBG circuitryNeuropsychiatric disordersDecreased differentiationT patientsInterneuronsAltered expressionPotential mechanismsCilia disruptionSonic hedgehogOrganoidsStem cellsTS individualsPluripotent stem cellsGli transcription factorsDeficitsOrganoid differentiationEarly stagesCholinergicPatientsPhenomenology of Tics and Sensory Urges
Leckman J, Bloch M, Sukhodolsky D, Artukoğlu B, Scahill L, King R. Phenomenology of Tics and Sensory Urges. 2022, 6-25. DOI: 10.1093/med/9780197543214.003.0002.Peer-Reviewed Original ResearchComprehensive Assessment Strategies
King R, Landeros-Weisenberger A. Comprehensive Assessment Strategies. 2022, 335-342. DOI: 10.1093/med/9780197543214.003.0020.Peer-Reviewed Original ResearchConcepts
2017
The PNKD gene is associated with Tourette Disorder or Tic disorder in a multiplex family
Sun N, Nasello C, Deng L, Wang N, Zhang Y, Xu Z, Song Z, Kwan K, King R, Pang Z, Xing J, Heiman G, Tischfield J. The PNKD gene is associated with Tourette Disorder or Tic disorder in a multiplex family. Molecular Psychiatry 2017, 23: 1487-1495. PMID: 28894297, PMCID: PMC5847395, DOI: 10.1038/mp.2017.179.Peer-Reviewed Original ResearchCitationsAltmetricMeSH Keywords and ConceptsConceptsNonsense-mediated mRNA decayNonsense mutationMultiplex familiesPluripotent stem cellsTD phenotypeDeleterious sequence variantsGenetic architectureMRNA decayHouse bioinformatics pipelineDNA sequencesBioinformatics pipelineTD familyWhole-exome sequencingSequence variantsBiochemical assaysMolecular differencesWhole exomeIsoform levelsStem cellsProtein levelsTD etiologyExome sequencingPNKDHeterozygous nonsense mutationGenesGenetic and phenotypic overlap of specific obsessive-compulsive and attention-deficit/hyperactive subtypes with Tourette syndrome
Hirschtritt M, Darrow S, Illmann C, Osiecki L, Grados M, Sandor P, Dion Y, King R, Pauls D, Budman C, Cath D, Greenberg E, Lyon G, Yu D, McGrath L, McMahon W, Lee P, Delucchi K, Scharf J, Mathews C. Genetic and phenotypic overlap of specific obsessive-compulsive and attention-deficit/hyperactive subtypes with Tourette syndrome. Psychological Medicine 2017, 48: 279-293. PMID: 28651666, PMCID: PMC7909616, DOI: 10.1017/s0033291717001672.Peer-Reviewed Original ResearchCitationsAltmetricMeSH Keywords and ConceptsConceptsAttention-deficit/hyperactivity disorderSymmetry/exactnessTourette syndromeLatent class analysisSymptom patternsADHD symptomsHigher psychiatric comorbidity ratesPsychiatric comorbidity ratesExploratory factor analysisHyperactive subtypeComorbidity ratesTS patientsClinical relevanceSpecific subtypesSum scoreUnique phenotypicHyperactivity disorderSymptomsPhenotypic overlapThree-class solutionTraditional diagnostic boundariesAggressive urgesSyndromeSubtypesDiagnostic boundaries896 Genetic and Phenotypic Overlap of Specific Obsessive-Compulsive Subtypes with Tourette Syndrome
Hirschtritt M, Darrow S, Illmann C, Osiecki L, Grados M, Sandor P, Dion Y, King R, Pauls D, Budman C, Cath D, Greenberg E, Lyon G, Yu D, McGrath L, McMahon W, Lee P, Delucchi K, Scharf J, Mathews C. 896 Genetic and Phenotypic Overlap of Specific Obsessive-Compulsive Subtypes with Tourette Syndrome. Biological Psychiatry 2017, 81: s361-s362. DOI: 10.1016/j.biopsych.2017.02.621.Peer-Reviewed Original Research
2015
Neurodevelopmental Disorders: Motor Disorders
Vitulano L, Vitulano M, King R, Leckman J. Neurodevelopmental Disorders: Motor Disorders. 2015, 779-790. DOI: 10.1002/9781118753378.ch47.Peer-Reviewed Original ResearchCitations
Academic Achievements & Community Involvement
activity Neuropsychiatric Disorders
ResearchDetails01/01/2008 - PresentIsraelAbstract/SynopsisProfessor King collaborates with the Schneider Children's Hospital of Israel and Geha Psychiatric Hospital, both affiliated with University of Tel Aviv School of Medicine, on studies of neuropsychiatric disorders of childhood -- Tourette's syndrome, obsessive compulsive disorder; epidemiology and prevention of adolescent suicide.
activity Psychoanalysis of Children
ResearchDetails01/01/2008 - PresentUnited KingdomAbstract/SynopsisProfessor King collaborates with the Anna Freud Centre (Hampstead, London) on the study of intensive psychodynamic and psychoanalytic treatment of children.
Clinical Care
Overview
Clinical Specialties
Psychiatry; Pediatric Developmental and Behavioral Medicine; Child and Adolescent Psychiatry
Fact Sheets
Attention Deficit Hyperactivity Disorder (ADHD)
Learn More on Yale MedicineObsessive-Compulsive Disorder in Children
Learn More on Yale MedicineDevelopmental Delay
Learn More on Yale MedicineLearning Disorders
Learn More on Yale Medicine
Board Certifications
Child & Adolescent Psychiatry
- Certification Organization
- AB of Psychiatry & Neurology
- Original Certification Date
- 1981
Psychiatry
- Certification Organization
- AB of Psychiatry & Neurology
- Original Certification Date
- 1974
Yale Medicine News
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News
- July 05, 2022
Yale Child Study Center Honors Retirees & Award Recipients
- June 19, 2020
Yale Medicine Inaugurates Distinguished Clinical Career Award
- June 14, 2019
Over 200 Yale Medicine Physicians Make 2019 ‘Best Doctors’ List
- January 03, 2018
Tourette disorder study judged among top 5 articles in 2017 by journal Neuron
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Contacts
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Mailing Address
Child Study Center
PO Box 207900, 230 South Frontage Road
New Haven, CT 06520-7900
United States
Locations
Neison Irving Harris Building
Academic Office
230 South Frontage Road
New Haven, CT 06519
Patient Care Locations
Are You a Patient? View this doctor's clinical profile on the Yale Medicine website for information about the services we offer and making an appointment.