Dr. Christina Gurnett, MD

• Epilepsy & Seizure Disorders

• Pediatric Neurology

*Healthgrades does not verify qualifications for medical specialties. Please verify your provider's specialty and qualifications directly with your provider and applicable medical board.

• Washington University

  Fellowship Hospital, 2003

• Washington University

  Residency Hospital, 2001

• University Ia

  Residency Hospital, 2000

• University Of Iowa Carver College Of Medicine

  Medical School, 1998

• Sex- and mutation-specific p53 gain-of-function activity in gliomagenesis, 2021-12-15

• SARS-CoV-2 Screening Testing in Schools for Children with Intellectual and Developmental Disabilities, 2021-07-20

• SARS-CoV-2 screening testing in schools for children with intellectual and developmental disabilities, 2021-09-01

• Massively parallel single nucleotide mutagenesis using reversibly-terminated inosine, 2016-10-03

• Exome Sequencing Identifies a RareHSPG2Variant Associated with Familial Idiopathic Scoliosis, 2014-12-12

• The cartilage matrisome in adolescent idiopathic scoliosis, 2020-03-09

• Missense variants in the chromatin remodelerCHD1are associated with neurodevelopmental disability, 2017-09-02

• Obex position is associated with syringomyelia and use of posterior fossa decompression among patients with Chiari I malformation, 2020-04-10

• Axial distribution of myosin binding protein-C is unaffected by mutations in human cardiac and skeletal muscle, 2012-03-14

• ATRAIDregulates the action of nitrogen-containing bisphosphonates on bone, 2020-05-20

• Diagnostic yield of exome sequencing in congenital vertical talus, 2022-04-27

• Distal chromosome 16p11.2 duplications containingSH2B1in patients with scoliosis, 2019-02-25

• Mutations in the novel protein PRRT2 cause paroxysmal kinesigenic dyskinesia with infantile convulsions, 2011-12-15

• Summary of the first inaugural joint meeting of the International Consortium for scoliosis genetics and the International Consortium for vertebral anomalies and scoliosis, March 16-18, 2017, Dallas, Texas, 2017-11-21

• Evaluation of GPR50, hMel-1B, and ROR-Alpha Melatonin-Related Receptors and the Etiology of Adolescent Idiopathic Scoliosis, 2010-07-19

• Rare andde novoDuplications ContainingSHOXin Clubfoot, 2020-06-09

• Genome-Wide Copy Number Variation in Epilepsy: Novel Susceptibility Loci in Idiopathic Generalized and Focal Epilepsies, 2010-05-20

• Models of Distal Arthrogryposis and Lethal Congenital Contracture Syndrome, 2021-06-20

• Identification of Medically Actionable Secondary Findings in the 1000 Genomes, 2015-09-02

• Prevalence and impact of underlying diagnosis and comorbidities on Chiari 1 malformation, 2020-01-21

• A Decade in Review after Idiopathic Scoliosis Was First Called a Complex Trait-A Tribute to the Late Dr. Yves Cotrel for His Support in Studies of Etiology of Scoliosis, 2021-07-01

• Genetic Linkage Localizes an Adolescent Idiopathic Scoliosis and Pectus Excavatum Gene to the 18q Chromosome, 2009-01-15

• A missense variant inSLC39A8is associated with severe idiopathic scoliosis, 2018-10-09

• Deletions of 5' HOXC genes are associated with lower extremity malformations including clubfoot and vertical talus, 2016-01-04

• MYH 3-associated distal arthrogryposis zebrafish model is normalized with para-aminoblebbistatin, 2020-10-05

• GermlineDICER1Mutations in Familial Pleuropulmonary Blastoma, 2009-06-25

• Supporting COVID-19 School Safety for Children with Disabilities and Medical Complexity, 2022-02-01

• Mutations inKinesin family member 6reveal specific role in ependymal cell ciliogenesis and human neurological development, 2018-11-26

• Kinesin Family Member 6 (kif6) Is Necessary for Spine Development in Zebrafish, 2014-10-20

• Human iPSC-Derived Neuronal Cells FromCTBP1-Mutated Patients Reveal Altered Expression of Neurodevelopmental Gene Networks, 2020-10-27

• Novel SCN3A Variants Associated with Focal Epilepsy in Children, 2013-10-21

• Common polymorphisms in human lysyl oxidase genes are not associated with the adolescent idiopathic scoliosis phenotype, 2011-07-08

• Diverse monogenic subforms of human spermatogenic failure, 2022-12-26

• ComprehensiveIn VivoInterrogation Reveals Phenotypic Impact of Human Enhancer Variants, 2020-03-12

• Genetic counseling as preventive intervention: toward individual specification of transgenerational autism risk, 2021-09-16