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ALICA M GOLDMAN

TitleAssociate Professor
InstitutionBaylor College of Medicine
DepartmentDepartment of Neurology
DivisionNeurology
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    K08NS047304     (GOLDMAN, ALICA M)Aug 1, 2004 - Jul 31, 2010
    NIH/NINDS
    Ion channelopathies co-expressed in heart and brain
    Role: Principal Investigator

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

    U01NS090362     (GOLDMAN, ALICA M)Sep 30, 2014 - Jul 31, 2019
    NIH/NINDS
    SUDEP Research Alliance: Systems Medicine Core, Application 3 of 7
    Role: Principal Investigator

    U01NS090406     (GOLDMAN, ALICA M)Sep 30, 2014 - Jul 31, 2019
    NIH/NINDS
    SUDEP Research Alliance: Clinical Network Core; Application 2 of 7
    Role: Principal Investigator

    R21NS113015     (GOLDMAN, ALICA M)Jul 1, 2019 - Jun 30, 2021
    NIH/NINDS
    Isolating SUDEP Risk conferred by genomic co-variation in candidate SUDEP genes
    Role: Principal Investigator

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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. 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 Jun; 5(3). PMID: 30850373.
      View in: PubMed
    2. Mueller SG, Bateman LM, Nei M, Goldman AM, Laxer KD. Brainstem atrophy in focal epilepsy destabilizes brainstem-brain interactions: Preliminary findings. Neuroimage Clin. 2019 Jun 03; 23:101888. PMID: 31203171.
      View in: PubMed
    3. 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 Jan 08; 92(2):e108-e114. PMID: 30552298.
      View in: PubMed
    4. Frasier CR, Zhang H, Offord J, Dang LT, Auerbach DS, Shi H, Chen C, Goldman AM, Eckhardt LL, Bezzerides VJ, Parent JM, Isom LL. Channelopathy as a SUDEP Biomarker in Dravet Syndrome Patient-Derived Cardiac Myocytes. Stem Cell Reports. 2018 09 11; 11(3):626-634. PMID: 30146492.
      View in: PubMed
    5. Mueller SG, Nei M, Bateman LM, Knowlton R, Laxer KD, Friedman D, Devinsky O, Goldman AM. Brainstem network disruption: A pathway to sudden unexplained death in epilepsy? Hum Brain Mapp. 2018 12; 39(12):4820-4830. PMID: 30096213.
      View in: PubMed
    6. Jobst BC, Kapur R, Barkley GL, Bazil CW, Berg MJ, Bergey GK, Boggs JG, Cash SS, Cole AJ, Duchowny MS, Duckrow RB, Edwards JC, Eisenschenk S, Fessler AJ, Fountain NB, Geller EB, Goldman AM, Goodman RR, Gross RE, Gwinn RP, Heck C, Herekar AA, Hirsch LJ, King-Stephens D, Labar DR, Marsh WR, Meador KJ, Miller I, Mizrahi EM, Murro AM, Nair DR, Noe KH, Olejniczak PW, Park YD, Rutecki P, Salanova V, Sheth RD, Skidmore C, Smith MC, Spencer DC, Srinivasan S, Tatum W, Van Ness P, Vossler DG, Wharen RE, Worrell GA, Yoshor D, Zimmerman RS, Skarpaas TL, Morrell MJ. Brain-responsive neurostimulation in patients with medically intractable seizures arising from eloquent and other neocortical areas. Epilepsia. 2017 06; 58(6):1005-1014. PMID: 28387951.
      View in: PubMed
    7. Goldman AM, LaFrance WC, Benke T, Asato M, Drane D, Pack A, Syed T, Doss R, Lhatoo S, Fureman B, Dingledine R. 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.
      View in: PubMed
    8. 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.
      View in: PubMed
    9. Goldman AM. Mechanisms of sudden unexplained death in epilepsy. Curr Opin Neurol. 2015 Apr; 28(2):166-74. PMID: 25734955.
      View in: PubMed
    10. 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.
      View in: PubMed
    11. Hirose S, Scheffer IE, Marini C, De Jonghe P, Andermann E, Goldman AM, Kauffman M, Tan NC, Lowenstein DH, Sisodiya SM, Ottman R, Berkovic SF. SCN1A testing for epilepsy: application in clinical practice. Epilepsia. 2013 May; 54(5):946-52. PMID: 23586701.
      View in: PubMed
    12. 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.
      View in: PubMed
    13. Klassen TL, von RĂ¼den EL, Drabek J, Noebels JL, Goldman AM. 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.
      View in: PubMed
    14. 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.
      View in: PubMed
    15. 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.
      View in: PubMed
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