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Shifteh Sattar

Title(s)Clinical Professor, Neurosciences
SchoolVc-health Sciences-schools
Address9500 Gilman Drive #
La Jolla CA 92093
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    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Researchers can login to make corrections and additions, or contact us for help. to make corrections and additions.
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    Altmetrics Details 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. Vigabatrin Versus Adrenocorticotropic Hormone After High-Dose Prednisolone Failure for the Treatment of Epileptic Spasms. J Child Neurol. 2025 Aug 03; 8830738251361701. Layton A, Sattar S, Rho JM, Yang JH, Gold J, Zimbric M, Bui J, Sahagian M, Kim-McManus O, Frederick A, Guido-Estrada N, Jindal A, Wiegand S, Dove K, Sweat M, Nespeca M, Montenegro MA. PMID: 40754938.
      View in: PubMed   Mentions:    Fields:    
    2. The development of aperiodic neural activity in the human brain. Nat Hum Behav. 2025 Dec; 9(12):2548-2563. Cross ZR, Gray SM, Dede AJO, Rivera YM, Yin Q, Vahidi P, Rau EMB, Cyr C, Holubecki AM, Asano E, Lin JJ, Kim McManus O, Sattar S, Saez I, Girgis F, King-Stephens D, Weber PB, Laxer KD, Schuele SU, Rosenow JM, Wu JY, Lam SK, Raskin JS, Chang EF, Shaikhouni A, Brunner P, Roland JL, Braga RM, Knight RT, Ofen N, Johnson EL. PMID: 40670699; PMCID: PMC12818177.
      View in: PubMed   Mentions:    Fields:    
    3. Incidental interictal epileptiform discharges in infants with nonepileptic events. Epilepsia. 2025 Sep; 66(9):3571-3577. Montenegro MA, Tsuha M, Sattar S. PMID: 40394879.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    4. Current and Emerging Precision Therapies for Developmental and Epileptic Encephalopathies. Pediatr Neurol. 2025 Jul; 168:67-81. Samanta D, Bhatia S, Hunter SE, Rao CK, Xiong K, Karakas C, Reeders PC, Erdemir G, Sattar S, Axeen E, Sandoval Karamian AG, Fine AL, Keator CG, Nolan D, Schreiber JM. PMID: 40381457.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    5. Reinstatement and transformation of memory traces for recognition. Sci Adv. 2025 Feb 21; 11(8):eadp9336. Rau EMB, Fellner MC, Heinen R, Zhang H, Yin Q, Vahidi P, Kobelt M, Asano E, Kim-McManus O, Sattar S, Lin JJ, Auguste KI, Chang EF, King-Stephens D, Weber PB, Laxer KD, Knight RT, Johnson EL, Ofen N, Axmacher N. PMID: 39970226; PMCID: PMC11838014.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    6. Laser Interstitial Thermal Therapy for the Treatment of Mesial Temporal Lobe Epilepsy in Children. J Child Neurol. 2025 May; 40(5):342-347. Trivedi AM, Montenegro MA, Gonda D, Kim-McManus O, Rismanchi N, Frederick A, Guido-Estrada N, Jindal A, Sattar S. PMID: 39887192.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    7. De novo cerebral pseudoaneurysm formation: a rare delayed complication of stereotactic electroencephalography in children. Childs Nerv Syst. 2024 May; 40(5):1501-1506. Daniel M, Stone LE, Plonsker JH, Sattar S, Ravindra V, Gonda D. PMID: 38240787.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    8. Comprehensive multi-omic profiling of somatic mutations in malformations of cortical development. Nat Genet. 2023 02; 55(2):209-220. Chung C, Yang X, Bae T, Vong KI, Mittal S, Donkels C, Westley Phillips H, Li Z, Marsh APL, Breuss MW, Ball LL, Garcia CAB, George RD, Gu J, Xu M, Barrows C, James KN, Stanley V, Nidhiry AS, Khoury S, Howe G, Riley E, Xu X, Copeland B, Wang Y, Kim SH, Kang HC, Schulze-Bonhage A, Haas CA, Urbach H, Prinz M, Limbrick DD, Gurnett CA, Smyth MD, Sattar S, Nespeca M, Gonda DD, Imai K, Takahashi Y, Chen HH, Tsai JW, Conti V, Guerrini R, Devinsky O, Silva WA, Machado HR, Mathern GW, Abyzov A, Baldassari S, Baulac S, Focal Cortical Dysplasia Neurogenetics Consortium, Brain Somatic Mosaicism Network, Gleeson JG. PMID: 36635388; PMCID: PMC9961399.
      View in: PubMed   Mentions: 50     Fields:    Translation:Humans
    9. Spatiotemporal dynamics of human high gamma discriminate naturalistic behavioral states. PLoS Comput Biol. 2022 08; 18(8):e1010401. Alasfour A, Gabriel P, Jiang X, Shamie I, Melloni L, Thesen T, Dugan P, Friedman D, Doyle W, Devinsky O, Gonda D, Sattar S, Wang S, Halgren E, Gilja V. PMID: 35939509; PMCID: PMC9387937.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    10. Expanding the phenotypic and molecular spectrum of NFS1-related disorders that cause functional deficiencies in mitochondrial and cytosolic iron-sulfur cluster containing enzymes. Hum Mutat. 2022 03; 43(3):305-315. Yang JH, Friederich MW, Ellsworth KA, Frederick A, Foreman E, Malicki D, Dimmock D, Lenberg J, Prasad C, Yu AC, Anthony Rupar C, Hegele RA, Manickam K, Koboldt DC, Crist E, Choi SS, Farhan SMK, Harvey H, Sattar S, Karp N, Wong T, Haas R, Van Hove JLK, Wigby K, Wigby K. PMID: 35026043; PMCID: PMC8863643.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansCells
    11. Successful Treatment of Pediatric FIRES With Anakinra. Pediatr Neurol. 2021 01; 114:60-61. Yang JH, Nataraj S, Sattar S. PMID: 33227629.
      View in: PubMed   Mentions: 8     Fields:    Translation:Humans
    12. Telehealth in pediatric epilepsy care: A rapid transition during the COVID-19 pandemic. Epilepsy Behav. 2020 10; 111:107282. Sattar S, Kuperman R. PMID: 32759065; PMCID: PMC7386847.
      View in: PubMed   Mentions: 15     Fields:    Translation:HumansCellsPHPublic Health
    13. Neural correlates of unstructured motor behaviors. J Neural Eng. 2019 10 30; 16(6):066026. Gabriel PG, Chen KJ, Alasfour A, Pailla T, Doyle WK, Devinsky O, Friedman D, Dugan P, Melloni L, Thesen T, Gonda D, Sattar S, Wang SG, Gilja V. PMID: 31342926.
      View in: PubMed   Mentions: 6     Fields:    Translation:Humans
    14. Correction: The landscape of epilepsy-related GATOR1 variants. Genet Med. 2019 Aug; 21(8):1896. Baldassari S, Picard F, Verbeek NE, van Kempen M, Brilstra EH, Lesca G, Conti V, Guerrini R, Bisulli F, Licchetta L, Pippucci T, Tinuper P, Hirsch E, de Saint Martin A, Chelly J, Rudolf G, Chipaux M, Ferrand-Sorbets S, Dorfmüller G, Sisodiya S, Balestrini S, Schoeler N, Hernandez-Hernandez L, Krithika S, Oegema R, Hagebeuk E, Gunning B, Deckers C, Berghuis B, Wegner I, Niks EH, Jansen FE, Braun K, de Jong D, Rubboli G, Talvik I, Sander V, Uldall P, Jacquemont ML, Nava C, Leguern E, Julia S, Gambardella A, d'Orsi G, Crichiutti G, Faivre L, Darmency V, Benova B, Krsek P, Biraben A, Lebre AS, Jennesson M, Sattar S, Marchal C, NordliJr DR, Lindstrom K, Striano P, Lomax LB, Kiss C, Bartolomei F, Lepine AF, Schoonjans AS, Stouffs K, Jansen A, Panagiotakaki E, Ricard-Mousnier B, Thevenon J, de Bellescize J, Catenoix H, Dorn T, Zenker M, Müller-Schlüter K, Brandt C, Krey I, Polster T, Wolff M, Balci M, Rostasy K, Achaz G, Zacher P, Becher T, Cloppenborg T, Yuskaitis CJ, Weckhuysen S, Poduri A, Lemke JR, Møller RS, Baulac S. PMID: 30262923; PMCID: PMC7608233.
      View in: PubMed   Mentions: 3     Fields:    
    15. Correction to: The landscape of epilepsy-related GATOR1 variants. Genet Med. 2019 Jul; 21(7):1671. Baldassari S, Picard F, Verbeek NE, van Kempen M, Brilstra EH, Lesca G, Conti V, Guerrini R, Bisulli F, Licchetta L, Pippucci T, Tinuper P, Hirsch E, Martin AS, Chelly J, Rudolf G, Chipaux M, Ferrand-Sorbets S, Dorfmüller G, Sisodiya S, Balestrini S, Schoeler N, Hernandez-Hernandez L, Krithika S, Oegema R, Hagebeuk E, Gunning B, Deckers C, Berghuis B, Wegner I, Niks E, Jansen F, Braun K, Jong D, Rubboli G, Talvik I, Sander V, Uldall P, Jacquemont ML, Nava C, Leguern E, Julia S, Gambardella A, d'Orsi G, Crichiutti G, Faivre L, Darmency V, Benova B, Krsek P, Biraben A, Lebre AS, Jennesson M, Sattar S, Marchal C, NordliJr DR, Lindstrom K, Striano P, Lomax LB, Kiss C, Bartolomei F, Lepine AF, Schoonjans AS, Stouffs K, Jansen A, Panagiotakaki E, Ricard-Mousnier B, Thevenon J, Bellescize J, Catenoix H, Dorn T, Zenker M, Müller-Schlüter K, Brandt C, Krey I, Polster T, Wolff M, Balci M, Rostasy K, Achaz G, Zacher P, Becher T, Cloppenborg T, Yuskaitis CJ, Weckhuysen S, Poduri A, Lemke JR, Møller RS, Baulac S. PMID: 30158694; PMCID: PMC7608347.
      View in: PubMed   Mentions:    Fields:    
    16. Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and Epilepsy. Am J Hum Genet. 2019 06 06; 104(6):1210-1222. O'Donnell-Luria AH, Pais LS, Faundes V, Wood JC, Sveden A, Luria V, Abou Jamra R, Accogli A, Amburgey K, Anderlid BM, Azzarello-Burri S, Basinger AA, Bianchini C, Bird LM, Buchert R, Carre W, Ceulemans S, Charles P, Cox H, Culliton L, Currò A, Deciphering Developmental Disorders (DDD) Study, Demurger F, Dowling JJ, Duban-Bedu B, Dubourg C, Eiset SE, Escobar LF, Ferrarini A, Haack TB, Hashim M, Heide S, Helbig KL, Helbig I, Heredia R, Héron D, Isidor B, Jonasson AR, Joset P, Keren B, Kok F, Kroes HY, Lavillaureix A, Lu X, Maas SM, Maegawa GHB, Marcelis CLM, Mark PR, Masruha MR, McLaughlin HM, McWalter K, Melchinger EU, Mercimek-Andrews S, Nava C, Pendziwiat M, Person R, Ramelli GP, Ramos LLP, Rauch A, Reavey C, Renieri A, Rieß A, Sanchez-Valle A, Sattar S, Saunders C, Schwarz N, Smol T, Srour M, Steindl K, Syrbe S, Taylor JC, Telegrafi A, Thiffault I, Trauner DA, van der Linden H, van Koningsbruggen S, Villard L, Vogel I, Vogt J, Weber YG, Wentzensen IM, Widjaja E, Zak J, Baxter S, Banka S, Rodan LH. PMID: 31079897; PMCID: PMC6556837.
      View in: PubMed   Mentions: 44     Fields:    Translation:Humans
    17. Laser Ablation of a Nonlesional Cingulate Gyrus Epileptogenic Zone Using Robotic-Assisted Stereotactic EEG Localization: A Case Report. Stereotact Funct Neurosurg. 2019; 97(1):10-17. Upadhyayula PS, Rennert RC, Hoshide R, Sattar S, Gonda DD. PMID: 30943498.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    18. Coarse behavioral context decoding. J Neural Eng. 2019 02; 16(1):016021. Alasfour A, Gabriel P, Jiang X, Shamie I, Melloni L, Thesen T, Dugan P, Friedman D, Doyle W, Devinsky O, Gonda D, Sattar S, Wang S, Halgren E, Gilja V. PMID: 30523860.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
    19. Patient-Specific Pose Estimation in Clinical Environments. IEEE J Transl Eng Health Med. 2018; 6:2101111. Chen K, Gabriel P, Alasfour A, Gong C, Doyle WK, Devinsky O, Friedman D, Dugan P, Melloni L, Thesen T, Gonda D, Sattar S, Wang S, Gilja V. PMID: 30483453; PMCID: PMC6255526.
      View in: PubMed   Mentions: 16     Fields:    
    20. The landscape of epilepsy-related GATOR1 variants. Genet Med. 2019 02; 21(2):398-408. Baldassari S, Picard F, Verbeek NE, van Kempen M, Brilstra EH, Lesca G, Conti V, Guerrini R, Bisulli F, Licchetta L, Pippucci T, Tinuper P, Hirsch E, de Saint Martin A, Chelly J, Rudolf G, Chipaux M, Ferrand-Sorbets S, Dorfmüller G, Sisodiya S, Balestrini S, Schoeler N, Hernandez-Hernandez L, Krithika S, Oegema R, Hagebeuk E, Gunning B, Deckers C, Berghuis B, Wegner I, Niks E, Jansen FE, Braun K, de Jong D, Rubboli G, Talvik I, Sander V, Uldall P, Jacquemont ML, Nava C, Leguern E, Julia S, Gambardella A, d'Orsi G, Crichiutti G, Faivre L, Darmency V, Benova B, Krsek P, Biraben A, Lebre AS, Jennesson M, Sattar S, Marchal C, Nordli DR, Lindstrom K, Striano P, Lomax LB, Kiss C, Bartolomei F, Lepine AF, Schoonjans AS, Stouffs K, Jansen A, Panagiotakaki E, Ricard-Mousnier B, Thevenon J, de Bellescize J, Catenoix H, Dorn T, Zenker M, Müller-Schlüter K, Brandt C, Krey I, Polster T, Wolff M, Balci M, Rostasy K, Achaz G, Zacher P, Becher T, Cloppenborg T, Yuskaitis CJ, Weckhuysen S, Poduri A, Lemke JR, Møller RS, Baulac S. PMID: 30093711; PMCID: PMC6292495.
      View in: PubMed   Mentions: 110     Fields:    Translation:HumansCells
    21. Neurological Outcomes After Presumed Childhood Encephalitis. Pediatr Neurol. 2015 Sep; 53(3):200-6. Rismanchi N, Gold JJ, Sattar S, Glaser C, Sheriff H, Proudfoot J, Mower A, Nespeca M, Crawford JR, Wang SG. PMID: 26220354.
      View in: PubMed   Mentions: 6     Fields:    Translation:Humans
    22. Epilepsy After Resolution of Presumed Childhood Encephalitis. Pediatr Neurol. 2015 Jul; 53(1):65-72. Rismanchi N, Gold JJ, Sattar S, Glaser CA, Sheriff H, Proudfoot J, Mower A, Crawford JR, Nespeca M, Wang SG. PMID: 26092415.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    23. Co-occurrence of distinct ciliopathy diseases in single families suggests genetic modifiers. Am J Med Genet A. 2011 Dec; 155A(12):3042-9. Zaki MS, Sattar S, Massoudi RA, Gleeson JG. PMID: 22002901; PMCID: PMC3415794.
      View in: PubMed   Mentions: 24     Fields:    Translation:Humans
    24. New recessive syndrome of microcephaly, cerebellar hypoplasia, and congenital heart conduction defect. Am J Med Genet A. 2011 Dec; 155A(12):3035-41. Zaki MS, Salam GM, Saleem SN, Dobyns WB, Issa MY, Sattar S, Gleeson JG. PMID: 22002884; PMCID: PMC3415795.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    25. The ciliopathies in neuronal development: a clinical approach to investigation of Joubert syndrome and Joubert syndrome-related disorders. Dev Med Child Neurol. 2011 Sep; 53(9):793-798. Sattar S, Gleeson JG. PMID: 21679365; PMCID: PMC3984879.
      View in: PubMed   Mentions: 72     Fields:    Translation:HumansCells
    26. Distinguishing 3 classes of corpus callosal abnormalities in consanguineous families. Neurology. 2011 Jan 25; 76(4):373-82. Hanna RM, Marsh SE, Swistun D, Al-Gazali L, Zaki MS, Abdel-Salam GM, Al-Tawari A, Bastaki L, Kayserili H, Rajab A, Boglárka B, Dietrich RB, Dobyns WB, Truwit CL, Sattar S, Chuang NA, Sherr EH, Gleeson JG. PMID: 21263138; PMCID: PMC3034417.
      View in: PubMed   Mentions: 19     Fields:    Translation:Humans
    27. Expanding the clinical spectrum of SPG11 gene mutations in recessive hereditary spastic paraplegia with thin corpus callosum. Eur J Med Genet. 2011 Jan-Feb; 54(1):82-5. Abdel Aleem A, Abu-Shahba N, Swistun D, Silhavy J, Bielas SL, Sattar S, Gleeson JG, Zaki MS. PMID: 20971220; PMCID: PMC3073376.
      View in: PubMed   Mentions: 4     Fields:    Translation:HumansCells
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