Shifteh Sattar

Title(s)	Clinical Professor, Neurosciences
School	Vc-health Sciences-schools
Address	9500 Gilman Drive # La Jolla CA 92093
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Publications

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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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.

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: 9 Fields:
Gen Genetics
Translation:Humans
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. PMID: 35026043; PMCID: PMC8863643.

View in: PubMed Mentions: 1 Fields:
Gen Genetics
Translation:Humans Cells
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: 6 Fields:
Neu Neurology Ped Pediatrics
Translation:Humans
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: 10 Fields:
Beh Behavioral Sciences Neu Neurology
Translation:Humans Cells PHPublic Health
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: 5 Fields:
Bio Biomedical Engineering Neu Neurology
Translation:Humans
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:
Neu Neurosurgery
Translation:Humans
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: 4 Fields:
Bio Biomedical Engineering Neu Neurology
Translation:Humans
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: 8 Fields:
Bio Biomedical Engineering
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: 4 Fields:
Neu Neurology Ped Pediatrics
Translation:Humans
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:
Neu Neurology Ped Pediatrics
Translation:Humans
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: 59 Fields:
Neu Neurology Ped Pediatrics
Translation:Humans Cells
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: 16 Fields:
Neu Neurology
Translation:Humans