ROHINI COORG

TitleAssociate Professor
InstitutionBaylor College of Medicine
DepartmentDepartment of Pediatrics
Address6701 FANNIN
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    Other Positions
    TitleAssociate Professor
    InstitutionBaylor College of Medicine
    DepartmentDepartment of Neurology
    DivisionNeurology


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    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
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    PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
    1. Berecki G, Tao E, Howell KB, Coorg RK, Andersen E, Kahlig K, Wolff M, Corry B, Petrou S. Nav1.2 channel mutations preventing fast inactivation lead to SCN2A encephalopathy. Brain. 2024 Jun 28. PMID: 38939966.
      Citations: 1     Fields:    
    2. Melendez-Zaidi AE, Pence KL, Coorg R. Early Subclinical Status Epilepticus May Contribute to Developmental Delays in Infants With Tuberous Sclerosis Complex. Pediatr Neurol. 2024 Aug; 157:39-41. PMID: 38865948.
      Citations:    Fields:    Translation:Humans
    3. Hentrich L, Parnes M, Lotze TE, Coorg R, de Koning TJ, Nguyen KM, Yip CK, Jungbluth H, Koy A, Dafsari HS. Novel Genetic and Phenotypic Expansion in GOSR2-Related Progressive Myoclonus Epilepsy. Genes (Basel). 2023 09 25; 14(10). PMID: 37895210; PMCID: PMC10606070.
      Citations: 2     Fields:    Translation:Humans
    4. Karakas C, Houck K, Handoko M, Trandafir C, Coorg R, Haneef Z, Riviello JJ, Weiner HL, Curry D, Ali I. Responsive Neurostimulation for the Treatment of Children With Drug-Resistant Epilepsy in Tuberous Sclerosis Complex. Pediatr Neurol. 2023 Aug; 145:97-101. PMID: 37302216.
      Citations: 1     Fields:    Translation:Humans
    5. Ravindra VM, Ruggieri L, Gadgil N, Addison AP, Patino I, Gonda DD, Chu J, Whitehead L, Anderson A, Diaz-Medina G, Houck K, Katyayan A, Masters L, Nath A, Quach M, Riviello JJ, Seto E, Sully KE, Agurs L, Sen S, Handoko M, Coorg R, Ali I, Ikeda D, Weiner H, Curry DJ. An Initial Experience of Completion Hemispherotomy via Magnetic Resonance-Guided Laser Interstitial Therapy. Stereotact Funct Neurosurg. 2023; 101(3):179-187. PMID: 37062282.
      Citations:    Fields:    Translation:Humans
    6. M?ller P, Takacs DS, Hedrich UBS, Coorg R, Masters L, Glinton KE, Dai H, Cokley JA, Riviello JJ, Lerche H, Cooper EC. KCNA1 gain-of-function epileptic encephalopathy treated with 4-aminopyridine. Ann Clin Transl Neurol. 2023 04; 10(4):656-663. PMID: 36793218; PMCID: PMC10109319.
      Citations: 4     Fields:    Translation:Humans
    7. Ravindra VM, Karas PJ, Lazaro TT, Coorg R, Awad AW, Patino I, McClernon EE, Clarke D, Cairampoma Whitehead L, Anderson A, Diaz-Medina G, Houck K, Katyayan A, Masters L, Nath A, Quach M, Riviello J, Seto ES, Sully K, Agurs L, Sen S, Handoko M, LoPresti M, Ali I, Curry DJ, Weiner HL. Epilepsy Surgery in Young Children With Tuberous Sclerosis Complex: A Novel Hybrid Multimodal Surgical Approach. Neurosurgery. 2023 02 01; 92(2):398-406. PMID: 36637274.
      Citations:    Fields:    Translation:Humans
    8. Khan AQ, Marini C, Myers KA, Coorg RK, Gill D. Koolen-de Vries syndrome associated with continuous spike-wave in sleep Epileptic Disord. 2022 10 01; 24(5):928-933. PMID: 35811432.
      Citations:    Fields:    Translation:HumansCells
    9. Ahring PK, Liao VWY, Gardella E, Johannesen KM, Krey I, Selmer KK, Stadheim BF, Davis H, Peinhardt C, Coorg RK, Syrbe S, Bertsche A, Santiago-Sim T, Diemer T, Fenger CD, Platzer K, Eichler EE, Lemke JR, Chebib M, Koko M, Lerche H, M?ller RS. Gain-of-function variants in GABRD reveal a novel pathway for neurodevelopmental disorders and epilepsy. Brain. 2022 05 24; 145(4):1299-1309. PMID: 34633442; PMCID: PMC9630717.
      Citations: 4     Fields:    Translation:Humans
    10. Seto ES, Coorg R. Epilepsy Surgery: Monitoring and Novel Surgical Techniques. Neurol Clin. 2021 08; 39(3):723-742. PMID: 34215384.
      Citations:    Fields:    Translation:Humans
    11. Jimenez-Gomez A, Niu S, Andujar-Perez F, McQuade EA, Balasa A, Huss D, Coorg R, Quach M, Vinson S, Risen S, Holder JL. Phenotypic characterization of individuals with SYNGAP1 pathogenic variants reveals a potential correlation between posterior dominant rhythm and developmental progression. J Neurodev Disord. 2019 08 08; 11(1):18. PMID: 31395010; PMCID: PMC6688356.
      Citations: 9     Fields:    Translation:Humans
    12. Coorg R, Weisenberg JL. Successful Treatment of Electrographic Status Epilepticus of Sleep With Felbamate in a Patient With SLC9A6 Mutation. Pediatr Neurol. 2015 Dec; 53(6):527-31. PMID: 26421989.
      Citations: 6     Fields:    Translation:Humans
    13. COORG R, Thio LL. 5-Minute Pediatric Consult (Cabana MD, ed). Seizures-Febrile. 2015.
    14. Shinawi M, Coorg R, Shimony JS, Grange DK, Al-Kateb H. Intragenic CAMTA1 deletions are associated with a spectrum of neurobehavioral phenotypes. Clin Genet. 2015 May; 87(5):478-82. PMID: 24738973.
      Citations: 9     Fields:    Translation:Humans
    15. Weisenberg JL, Wong M, Coorg R. Clinical neurogenetics: recent advances in the genetics of epilepsy. Neurol Clin. 2013 Nov; 31(4):891-913. PMID: 24176415.
      Citations: 2     Fields:    Translation:Humans
    16. Coorg R, Lotze TE. Child Neurology: a case of PMM2-CDG (CDG 1a) presenting with unusual eye movements. Neurology. 2012 Oct 09; 79(15):e131-3. PMID: 23045520.
      Citations: 2     Fields:    Translation:Humans
    17. Coorg R, Tournay A. Filicide-suicide involving children with disabilities. J Child Neurol. 2013 Jun; 28(6):745-51. PMID: 22826515.
      Citations: 3     Fields:    Translation:Humans
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