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Sarah R. Risen

TitleAssistant Professor
InstitutionBaylor College of Medicine
DepartmentDepartment of Pediatrics
DivisionPediatrics-Neurology
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    Other Positions
    TitleAssistant 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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    1. Orman G, Kralik SF, Meoded A, Desai N, Risen S, Huisman TAGM. MRI Findings in Pediatric Abusive Head Trauma: A Review. J Neuroimaging. 2019 Nov 06. PMID: 31696594.
      View in: PubMed
    2. 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 Aug 08; 11(1):18. PMID: 31395010.
      View in: PubMed
    3. Handoko M, Hong W, Espineli E, Saxena K, Muscal E, Risen S. Autoimmune Glial Fibrillary Acidic Protein Astrocytopathy Following Herpes Simplex Virus Encephalitis in a Pediatric Patient. Pediatr Neurol. 2019 Sep; 98:85-86. PMID: 31248671.
      View in: PubMed
    4. Lyons-Warren AM, Risen SR, Clark G. Infant Botulism With Asymmetric Cranial Nerve Palsies. Pediatr Neurol. 2019 03; 92:71-72. PMID: 30639248.
      View in: PubMed
    5. Lapin WB, Lyons-Warren AM, Risen SR, Rathore N, Slone JS, Elghetany MT, Marcus M. A 14-Year-Old Boy With Fevers, Cytopenias, and Neurocognitive Decline. Pediatrics. 2018 09; 142(3). PMID: 30072574.
      View in: PubMed
    6. Palmer EE, Kumar R, Gordon CT, Shaw M, Hubert L, Carroll R, Rio M, Murray L, Leffler M, Dudding-Byth T, Oufadem M, Lalani SR, Lewis AM, Xia F, Tam A, Webster R, Brammah S, Filippini F, Pollard J, Spies J, Minoche AE, Cowley MJ, Risen S, Powell-Hamilton NN, Tusi JE, Immken L, Nagakura H, Bole-Feysot C, Nitschké P, Garrigue A, de Saint Basile G, Kivuva E, Scott RH, Rendon A, Munnich A, Newman W, Kerr B, Besmond C, Rosenfeld JA, Amiel J, Field M, Gecz J. A Recurrent De Novo Nonsense Variant in ZSWIM6 Results in Severe Intellectual Disability without Frontonasal or Limb Malformations. Am J Hum Genet. 2017 Dec 07; 101(6):995-1005. PMID: 29198722.
      View in: PubMed
    7. Stephens JA, Salorio CF, Barber AD, Risen SR, Mostofsky SH, Suskauer SJ. Preliminary findings of altered functional connectivity of the default mode network linked to functional outcomes one year after pediatric traumatic brain injury. Dev Neurorehabil. 2018 Oct; 21(7):423-430. PMID: 28692408.
      View in: PubMed
    8. Shukla NM, Risen S. A 15-Year-Old Boy With Refractory Status Epilepticus. Semin Pediatr Neurol. 2018 07; 26:101-103. PMID: 29961495.
      View in: PubMed
    9. Risen SR, Reesman J, Yenokyan G, Slomine BS, Suskauer SJ. The Course of Concussion Recovery in Children 6-12 Years of Age: Experience From an Interdisciplinary Rehabilitation Clinic. PM R. 2017 Sep; 9(9):874-883. PMID: 28082178.
      View in: PubMed
    10. Risen SR, Barber AD, Mostofsky SH, Suskauer SJ. Altered functional connectivity in children with mild to moderate TBI relates to motor control. J Pediatr Rehabil Med. 2015; 8(4):309-19. PMID: 26684071.
      View in: PubMed
    11. Risen SR, Suskauer SJ, Dematt EJ, Slomine BS, Salorio CF. Functional outcomes in children with abusive head trauma receiving inpatient rehabilitation compared with children with nonabusive head trauma. J Pediatr. 2014 Mar; 164(3):613-9.e1-2. PMID: 24321537.
      View in: PubMed
    12. Poretti A, Mall V, Smitka M, Grunt S, Risen S, Toelle SP, Benson JE, Yoshida S, Jung NH, Tinschert S, Neuhann TM, Rauch A, Steinlin M, Meoded A, Huisman TA, Boltshauser E. Macrocerebellum: significance and pathogenic considerations. Cerebellum. 2012 Dec; 11(4):1026-36. PMID: 22528964.
      View in: PubMed
    13. Anderson BH, Kasher PR, Mayer J, Szynkiewicz M, Jenkinson EM, Bhaskar SS, Urquhart JE, Daly SB, Dickerson JE, O'Sullivan J, Leibundgut EO, Muter J, Abdel-Salem GM, Babul-Hirji R, Baxter P, Berger A, Bonafé L, Brunstom-Hernandez JE, Buckard JA, Chitayat D, Chong WK, Cordelli DM, Ferreira P, Fluss J, Forrest EH, Franzoni E, Garone C, Hammans SR, Houge G, Hughes I, Jacquemont S, Jeannet PY, Jefferson RJ, Kumar R, Kutschke G, Lundberg S, Lourenço CM, Mehta R, Naidu S, Nischal KK, Nunes L, Ounap K, Philippart M, Prabhakar P, Risen SR, Schiffmann R, Soh C, Stephenson JB, Stewart H, Stone J, Tolmie JL, van der Knaap MS, Vieira JP, Vilain CN, Wakeling EL, Wermenbol V, Whitney A, Lovell SC, Meyer S, Livingston JH, Baerlocher GM, Black GC, Rice GI, Crow YJ. Mutations in CTC1, encoding conserved telomere maintenance component 1, cause Coats plus. Nat Genet. 2012 Jan 22; 44(3):338-42. PMID: 22267198.
      View in: PubMed
    14. Osorio MJ, Risen S, Alper G. An unusual presentation of juvenile Alexander disease. J Child Neurol. 2012 Apr; 27(4):507-10. PMID: 21940697.
      View in: PubMed
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