Scholars@Duke

• Background
• 

  Education, Training, & Certifications

  • Sleep Medicine Fellowship, Neurology, University of North Carolina at Chapel Hill 2011 - 2012
  • Child Neurology Residency, Pediatrics, Duke University School of Medicine 2008 - 2011
  • Internship and Residency in Pediatrics, Pediatrics, University of North Carolina at Chapel Hill 2006 - 2008
  • M.D., Duke University School of Medicine 2006
• 

  Duke Appointment History

  • Assistant Professor of Pediatrics, Pediatrics, Neurology, Pediatrics 2012 - 2018
• Research
• 

  Selected Grants

  • An integrated and diverse genomic medicine program for undiagnosed diseases awarded by National Institutes of Health 2014 - 2022
  • JAZZ awarded by Jazz Pharmaceuticals 2015 - 2019
  • Ph I Zecuity awarded by Nupathe 2013 - 2016
• Publications & Artistic Works
• 

  Selected Publications

  • Academic Articles

    • Kansagra, S, Ghusayni, R, Kherallah, B, Gunduz, T, McLean, M, Prange, L, Kravitz, RM, and Mikati, MA. "Polysomnography Findings and Sleep Disorders in Children With Alternating Hemiplegia of Childhood." Journal of Clinical Sleep Medicine : Jcsm : Official Publication of the American Academy of Sleep Medicine 15, no. 1 (January 15, 2019): 65-70.  Full Text
    • Khan, TN, Khan, K, Sadeghpour, A, Reynolds, H, Perilla, Y, McDonald, MT, Gallentine, WB, Baig, SM, Task Force for Neonatal Genomics, , Davis, EE, and Katsanis, N. "Mutations in NCAPG2 Cause a Severe Neurodevelopmental Syndrome that Expands the Phenotypic Spectrum of Condensinopathies." American Journal of Human Genetics 104, no. 1 (January 2019): 94-111.  Full Text
    • Marcogliese, PC, Shashi, V, Spillmann, RC, Stong, N, Rosenfeld, JA, Koenig, MK, Martínez-Agosto, JA, Herzog, M, Chen, AH, Dickson, PI, Lin, HJ, Vera, MU, Salamon, N, Graham, JM, Ortiz, D, Infante, E, Steyaert, W, Dermaut, B, Poppe, B, Chung, H-L, Zuo, Z, Lee, P-T, Kanca, O, Xia, F, Yang, Y, Smith, EC, Jasien, J, Kansagra, S, Spiridigliozzi, G, El-Dairi, M, Lark, R, Riley, K, Koeberl, DD, Golden-Grant, K, Program for Undiagnosed Diseases (UD-PrOZA), , Undiagnosed Diseases Network, , Yamamoto, S, Wangler, MF, Mirzaa, G, Hemelsoet, D, Lee, B, Nelson, SF, Goldstein, DB, Bellen, HJ, and Pena, LDM. "IRF2BPL Is Associated with Neurological Phenotypes." American Journal of Human Genetics 103, no. 3 (September 2018): 456-null.  Full Text
    • Marcogliese, PC, Shashi, V, Spillmann, RC, Stong, N, Rosenfeld, JA, Koenig, MK, Martínez-Agosto, JA, Herzog, M, Chen, AH, Dickson, PI, Lin, HJ, Vera, MU, Salamon, N, Graham, JM, Ortiz, D, Infante, E, Steyaert, W, Dermaut, B, Poppe, B, Chung, H-L, Zuo, Z, Lee, P-T, Kanca, O, Xia, F, Yang, Y, Smith, EC, Jasien, J, Kansagra, S, Spiridigliozzi, G, El-Dairi, M, Lark, R, Riley, K, Koeberl, DD, Golden-Grant, K, Program for Undiagnosed Diseases (UD-PrOZA), , Undiagnosed Diseases Network, , Yamamoto, S, Wangler, MF, Mirzaa, G, Hemelsoet, D, Lee, B, Nelson, SF, Goldstein, DB, Bellen, HJ, and Pena, LDM. "IRF2BPL Is Associated with Neurological Phenotypes." American Journal of Human Genetics 103, no. 2 (August 2018): 245-260.  Full Text
    • Pena, LDM, Jiang, Y-H, Schoch, K, Spillmann, RC, Walley, N, Stong, N, Rapisardo Horn, S, Sullivan, JA, McConkie-Rosell, A, Kansagra, S, Smith, EC, El-Dairi, M, Bellet, J, Keels, MA, Jasien, J, Kranz, PG, Noel, R, Nagaraj, SK, Lark, RK, Wechsler, DSG, Del Gaudio, D, Leung, ML, Hendon, LG, Parker, CC, Jones, KL, Undiagnosed Diseases Network Members, , Goldstein, DB, and Shashi, V. "Looking beyond the exome: a phenotype-first approach to molecular diagnostic resolution in rare and undiagnosed diseases." Genetics in Medicine : Official Journal of the American College of Medical Genetics 20, no. 4 (April 2018): 464-469.  Full Text  Open Access Copy
    • Pecoraro, A, Arehart, E, Gallentine, W, Radtke, R, Smith, E, Pizoli, C, Kansagra, S, Abdelnour, E, McLendon, R, and Mikati, MA. "Epilepsy in neurofibromatosis type 1." Epilepsy & Behavior : E&B 73 (August 2017): 137-141.  Full Text
    • Schoch, K, Meng, L, Szelinger, S, Bearden, DR, Stray-Pedersen, A, Busk, OL, Stong, N, Liston, E, Cohn, RD, Scaglia, F, Rosenfeld, JA, Tarpinian, J, Skraban, CM, Deardorff, MA, Friedman, JN, Akdemir, ZC, Walley, N, Mikati, MA, Kranz, PG, Jasien, J, McConkie-Rosell, A, McDonald, M, Wechsler, SB, Freemark, M, Kansagra, S, Freedman, S, Bali, D, Millan, F, Bale, S, Nelson, SF, Lee, H, Dorrani, N, UCLA Clinical Genomics Center, , Undiagnosed Diseases Network, , Goldstein, DB, Xiao, R, Yang, Y, Posey, JE, Martinez-Agosto, JA, Lupski, JR, Wangler, MF, and Shashi, V. "A Recurrent De Novo Variant in NACC1 Causes a Syndrome Characterized by Infantile Epilepsy, Cataracts, and Profound Developmental Delay." American Journal of Human Genetics 100, no. 2 (February 2017): 343-351.  Full Text
    • Kansagra, SM. "Adolescent Chronotype and Self-Regulation: The Power of When." Pediatrics 138, no. 6 (December 2016).  Full Text
    • Gutman, D, Hellriegel, E, Aycardi, E, Bigal, ME, Kunta, J, Chitra, R, Kansagra, S, Kidron, OS, Knebel, H, Linder, S, Ma, Y, Pierce, M, Winner, PK, and Spiegelstein, O. "A Phase I, Open-Label, Single-Dose Safety, Pharmacokinetic, and Tolerability Study of the Sumatriptan Iontophoretic Transdermal System in Adolescent Migraine Patients." Headache 56, no. 8 (September 2016): 1300-1309.  Full Text
    • Kansagra, S, Austin, S, DeArmey, S, Koeberl, D, and Kishnani, PS. "Death from supine asphyxia in late onset pompe disease: Two patients." American journal of medical genetics. Part A 170, no. 7 (July 2016): 1928-1929. (Letter)  Full Text
    • Mastrangelo, M, Scheffer, IE, Bramswig, NC, Nair, LDV, Myers, CT, Dentici, ML, Korenke, GC, Schoch, K, Campeau, PM, White, SM, Shashi, V, Kansagra, S, Van Essen, AJ, and Leuzzi, V. "Epilepsy in KCNH1-related syndromes." Epileptic Disorders : International Epilepsy Journal With Videotape 18, no. 2 (June 2016): 123-136.  Full Text
    • "Longitudinal polysomnographic findings in infantile Pompe disease." American Journal of Medical Genetics, Part A 167, no. 4 (April 1, 2015): 858-861.  Full Text
    • Kansagra, S, Austin, S, DeArmey, S, Kazi, Z, Kravitz, RM, and Kishnani, PS. "Longitudinal polysomnographic findings in infantile Pompe disease." American journal of medical genetics. Part A 167A, no. 4 (April 2015): 858-861.  Full Text
    • "Polysomnographic findings in infantile Pompe disease." American Journal of Medical Genetics, Part A 161, no. 12 (December 1, 2013): 3196-3200.  Full Text
    • Kansagra, S, Austin, S, DeArmey, S, Kishnani, PS, and Kravitz, RM. "Polysomnographic findings in infantile Pompe disease." Am J Med Genet A 161A, no. 12 (December 2013): 3196-3200.  Full Text  Link to Item
    • Kansagra, S, and Vaughn, B. "Pediatric sleep apnea Five things you might not know." Neurology: Clinical Practice 3, no. 4 (August 1, 2013): 321-325.  Full Text
    • Kansagra, S, Mikati, MA, and Vigevano, F. "Alternating hemiplegia of childhood." Handbook of Clinical Neurology 112 (January 2013): 821-826. (Review)  Full Text
    • Kansagra, S, Walter, R, and Vaughn, B. "Nocturnal temazepam in the treatment of narcolepsy." Journal of Clinical Sleep Medicine 9, no. 5 (2013): 499-500.  Full Text
    • Nguyen, L, Kansagra, S, Shaw, A, and McLean, H. "Index of suspicion case 3: Ptosis and diplopia after a respiratory infection in a 7-year-old girl (Pediatrics in Review (2012) 33, 2 (89-94))." Pediatrics in Review 33, no. 10 (October 1, 2012): 468-null.  Full Text
    • Ananthanarayanan, S, Gereige, R, Al-Owain, M, Nguyen, L, Kansagra, S, Shaw, A, and McLean, H. "Index of suspicion. Case 1: Lymphadenopathy, prolonged hematuria, proteinuria, and weight loss in a teenage boy. Case 2: Red, Swollen, painful eye in a 12-year-old boy with methylmalonic acidemia. Case 3: Ptosis and diplopia after a respiratory infection in a 7-year-old girl." Pediatrics in review / American Academy of Pediatrics 33, no. 2 (2012): 89-94.  Full Text
    • Kansagra, S, D'Cruz, O, Noah, TL, and Vaughn, BV. "Sleep-disordered breathing in Beckwith-Wiedemann syndrome: Three patients." American Journal of Medical Genetics, Part A 158 A, no. 11 (2012): 2956-2958.  Full Text
    • Nguyen, L, Kansagra, S, Shaw, A, and McLean, H. "Case 3: Ptosis and diplopia after a respiratory infection in a 7-year-old girl." Pediatrics in Review 33, no. 2 (2012): 90+92-90+94.  Full Text
    • Kansagra, SM, and Gallentine, WB. "Cytokine storm of acute necrotizing encephalopathy." Pediatr Neurol 45, no. 6 (December 2011): 400-402.  Full Text  Link to Item
    • Veerapandiyan, A, Gallentine, WB, Winchester, SA, Baker, J, Kansagra, SM, and Mikati, MA. "Oculogyric crises secondary to lamotrigine overdosage." Epilepsia 52, no. 3 (March 2011): e4-e6.  Full Text
    • Veerapandiyan, A, Winchester, SA, Gallentine, WB, Smith, EC, Kansagra, S, Hyland, K, and Mikati, MA. "Electroencephalographic and seizure manifestations of pyridoxal 5'-phosphate-dependent epilepsy." Epilepsy Behav 20, no. 3 (March 2011): 494-501. (Review)  Full Text  Link to Item
    • Kansagra, S, Ataya, N, Lewis, D, Gallentine, W, and Mikati, MA. "The effect of vagus nerve stimulation therapy on body mass index in children." Epilepsy & Behavior : E&B 19, no. 1 (September 2010): 50-51.  Full Text
    • Mikati, MA, Ataya, NF, El-Ferezli, JC, Baghdadi, TS, Turkmani, AH, Comair, YG, Kansagra, S, and Najjar, MW. "Quality of life after vagal nerve stimulator insertion." Epileptic Disord 11, no. 1 (March 2009): 67-74.  Full Text  Link to Item

  • Book Sections

    • Kansagra, S, and Vaughn, BV. "REM behavior disorder in adults." In Parasomnias: Clinical Characteristics and Treatment, 221-235. January 1, 2013.  Full Text
• Teaching & Mentoring
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  Recent Courses

  • PEDS 226C: Pediatric Neurology 2019
  • PEDS 436C: Pediatric Neurology 2019

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