TitleAssociate Professor
InstitutionBaylor College of Medicine
DepartmentDepartment of Neurology
Address6501 Fannin St
Houston, TX 77030
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    R21NS113015     (GOLDMAN, ALICA M)Jul 1, 2019 - Jun 30, 2021
    Isolating SUDEP Risk conferred by genomic co-variation in candidate SUDEP genes
    Role: Principal Investigator

    U01NS090362     (GOLDMAN, ALICA M)Sep 30, 2014 - Jul 31, 2020
    SUDEP Research Alliance: Systems Medicine Core, Application 3 of 7
    Role: Principal Investigator

    U01NS090406     (GOLDMAN, ALICA M)Sep 30, 2014 - Jul 31, 2020
    SUDEP Research Alliance: Clinical Network Core; Application 2 of 7
    Role: Principal Investigator

    R01NS067013     (GOLDMAN, ALICA M)Feb 1, 2011 - Jul 31, 2015
    Copy Number Variants of Neuro-Cardiac Ion Channel Genes and the Risk of SUDEP
    Role: Principal Investigator

    K08NS047304     (GOLDMAN, ALICA M)Aug 1, 2004 - Jul 31, 2010
    Ion channelopathies co-expressed in heart and brain
    Role: Principal Investigator

    Collapse Bibliographic 
    Collapse selected publications
    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.
    Newest   |   Oldest   |   Most Cited   |   Most Discussed   |   Timeline   |   Field Summary   |   Plain Text
    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. Goldman AM. Oncogenic Pathways Provide Clue to the Etiology of Human Mesial Temporal Lobe Epilepsy. JAMA Neurol. 2023 06 01; 80(6):546-547. PMID: 37126324.
      Citations:    Fields:    Translation:Humans
    2. Goldman AM, Thio KLL. SLC35A2-Related Epilepsy: Global Neuronal Consequences of a Focal Disruption in Glycosylation. Neurology. 2023 01 31; 100(5):225-226. PMID: 36307216.
      Citations:    Fields:    Translation:HumansCells
    3. Goldman AM. Can a Mouse Help Us Unravel the Mysteries of CDKL5-Related Epilepsy? Epilepsy Curr. 2022 Nov-Dec; 22(6):375-377. PMID: 36426191; PMCID: PMC9661619.
    4. Torrealba-Acosta G, Butt H, Edmondson EA, Willaert R, Viswanathan A, Goldman AM. A Neurostimulation-Triggered Trigeminal Neuralgia-like Pain: Risk Factors and Management. Neurol Clin Pract. 2021 Oct; 11(5):e760-e762. PMID: 34840901; PMCID: PMC8610532.
    5. Massey CA, Thompson SJ, Ostrom RW, Drabek J, Sveinsson OA, Haas EA, Mena OJ, Goldman AM, Noebels JL, Tomson T. X-linked serotonin 2C receptor is associated with a non-canonical pathway for sudden unexpected death in epilepsy. Brain Commun. 2021; 3(3):fcab149. PMID: 34396109; PMCID: PMC8361391.
      Citations: 1     
    6. Goldman AM. Peri-ictal Brainstem-Driven Posturing and Its Meaning. Neurology. 2021 01 19; 96(3):89-90. PMID: 33268564.
      Citations:    Fields:    Translation:Humans
    7. Nair DR, Laxer KD, Weber PB, Murro AM, Park YD, Barkley GL, Smith BJ, Gwinn RP, Doherty MJ, Noe KH, Zimmerman RS, Bergey GK, Anderson WS, Heck C, Liu CY, Lee RW, Sadler T, Duckrow RB, Hirsch LJ, Wharen RE, Tatum W, Srinivasan S, McKhann GM, Agostini MA, Alexopoulos AV, Jobst BC, Roberts DW, Salanova V, Witt TC, Cash SS, Cole AJ, Worrell GA, Lundstrom BN, Edwards JC, Halford JJ, Spencer DC, Ernst L, Skidmore CT, Sperling MR, Miller I, Geller EB, Berg MJ, Fessler AJ, Rutecki P, Goldman AM, Mizrahi EM, Gross RE, Shields DC, Schwartz TH, Labar DR, Fountain NB, Elias WJ, Olejniczak PW, Villemarette-Pittman NR, Eisenschenk S, Roper SN, Boggs JG, Courtney TA, Sun FT, Seale CG, Miller KL, Skarpaas TL, Morrell MJ, RNS System LTT Study. Nine-year prospective efficacy and safety of brain-responsive neurostimulation for focal epilepsy. Neurology. 2020 09 01; 95(9):e1244-e1256. PMID: 32690786; PMCID: PMC7538230.
      Citations: 53     Fields:    Translation:Humans
    8. Goldman AM. What does a defect in N-glycosylation mean for neuronal migration and function? Neurol Genet. 2020 Aug; 6(4):e490. PMID: 32754647; PMCID: PMC7357410.
    9. Montier L, Haneef Z, Gavvala J, Yoshor D, North R, Verla T, Van Ness PC, Drabek J, Goldman AM. A somatic mutation in MEN1 gene detected in periventricular nodular heterotopia tissue obtained from depth electrodes. Epilepsia. 2019 10; 60(10):e104-e109. PMID: 31489630; PMCID: PMC6852559.
      Citations: 3     Fields:    Translation:Humans
    10. Assia Batzir N, Bhagwat PK, Eble TN, Liu P, Eng CM, Elsea SH, Robak LA, Scaglia F, Goldman AM, Dhar SU, Wangler MF. De novo missense variant in the GTPase effector domain (GED) of DNM1L leads to static encephalopathy and seizures. Cold Spring Harb Mol Case Stud. 2019 06; 5(3). PMID: 30850373; PMCID: PMC6549558.
      Citations: 11     Fields:    Translation:HumansCells
    11. Marafi D, Suter B, Schultz R, Glaze D, Pavlik VN, Goldman AM. Spectrum and time course of epilepsy and the associated cognitive decline in MECP2 duplication syndrome. Neurology. 2019 01 08; 92(2):e108-e114. PMID: 30552298; PMCID: PMC6340341.
      Citations: 10     Fields:    Translation:Humans
    12. Goldman AM, LaFrance WC, Benke T, Asato M, Drane D, Pack A, Syed T, Doss R, Lhatoo S, Fureman B, Dingledine R, American Epilepsy Society (AES)/National Institute of Neurological Disorders and Stroke (NINDS) Epil. 2014 Epilepsy Benchmarks Area IV: Limit or Prevent Adverse Consequence of Seizures and Their Treatment Across The Lifespan. Epilepsy Curr. 2016 May-Jun; 16(3):198-205. PMID: 27330453; PMCID: PMC4913859.
      Citations: 6     
    13. Goldman AM, Behr ER, Semsarian C, Bagnall RD, Sisodiya S, Cooper PN. Sudden unexpected death in epilepsy genetics: Molecular diagnostics and prevention. Epilepsia. 2016 Jan; 57 Suppl 1:17-25. PMID: 26749013; PMCID: PMC5034873.
    14. Goldman AM. Mechanisms of sudden unexplained death in epilepsy. Curr Opin Neurol. 2015 Apr; 28(2):166-74. PMID: 25734955; PMCID: PMC5034868.
    15. Goldman AM, Tuchman R. Commentary: Genetic testing in epilepsy: what do patients and families want to know? Epilepsia. 2014 Nov; 55(11):1703-4. PMID: 25377513.
    16. Chen TT, Klassen TL, Goldman AM, Marini C, Guerrini R, Noebels JL. Novel brain expression of ClC-1 chloride channels and enrichment of CLCN1 variants in epilepsy. Neurology. 2013 Mar 19; 80(12):1078-85. PMID: 23408874; PMCID: PMC3662306.
      Citations: 24     Fields:    Translation:HumansAnimals
    17. Klassen TL, Drabek J, Noebels JL, Goldman AM, von R?den EL. Comparative analytical utility of DNA derived from alternative human specimens for molecular autopsy and diagnostics. J Mol Diagn. 2012 Sep; 14(5):451-7. PMID: 22796560; PMCID: PMC5803546.
      Citations: 4     Fields:    Translation:Humans
    18. McGuire AL, Oliver JM, Slashinski MJ, Graves JL, Wang T, Kelly PA, Fisher W, Lau CC, Goss J, Okcu M, Treadwell-Deering D, Goldman AM, Noebels JL, Hilsenbeck SG. To share or not to share: a randomized trial of consent for data sharing in genome research. Genet Med. 2011 Nov; 13(11):948-55. PMID: 21785360; PMCID: PMC3203320.
      Citations: 48     Fields:    Translation:Humans
    19. Klassen T, Davis C, Goldman A, Burgess D, Chen T, Wheeler D, McPherson J, Bourquin T, Lewis L, Villasana D, Morgan M, Muzny D, Gibbs R, Noebels J. Exome sequencing of ion channel genes reveals complex profiles confounding personal risk assessment in epilepsy. Cell. 2011 Jun 24; 145(7):1036-48. PMID: 21703448; PMCID: PMC3131217.
      Citations: 161     Fields:    Translation:HumansCells
    20. Bi W, Yan J, Shi X, Yuva-Paylor LA, Antalffy BA, Goldman A, Yoo JW, Noebels JL, Armstrong DL, Paylor R, Lupski JR. Rai1 deficiency in mice causes learning impairment and motor dysfunction, whereas Rai1 heterozygous mice display minimal behavioral phenotypes. Hum Mol Genet. 2007 Aug 01; 16(15):1802-13. PMID: 17517686.
      Citations: 38     Fields:    Translation:Animals
    21. Goldman AM, Potocki L, Walz K, Lynch JK, Glaze DG, Lupski JR, Noebels JL. Epilepsy and chromosomal rearrangements in Smith-Magenis Syndrome [del(17)(p11.2p11.2)]. J Child Neurol. 2006 Feb; 21(2):93-8. PMID: 16566870.
      Citations: 13     Fields:    Translation:HumansCells
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