ALICAGOLDMANALICA GOLDMAN29.70705990000000-95.400460000000003370GOLDMAN, ALICAAssociate Professorprns:coAuthorOfcoauthor ofprns:endDateend dateFaculty Rankprns:fullNamefull nameprns:grantAwardedBygrant awarded byprns:hasAuthorListauthor listprns:hasFacultyRankhas faculty rankprns:hasNetworkhas networkprns:hasPublicationVenuepublished inprns:informationResourceReferenceinformation resource referenceprns:isPrimaryPositionis primary positionprns:latitudelatitudeprns:longitudelongitudeprns:mainImagephotoprns:maxWeightmaximum weightprns:medlineTAjournal title abbreviationprns:meshDescriptorUIMeSH DescriptorUIprns:meshSemanticGroupNameMeSH semantic group nameprns:minWeightminimum weightprns:numberOfAuthorsnumber of authorsprns:numberOfConnectionsnumber of connectionsprns:numberOfPublicationsnumber of publicationsprns:personIdPerson IDprns:personInPrimaryPositionperson in primary positionprns:physicalNeighborOfphysical neighborprns:positionInDepartmentposition in departmentprns:positionInDivisionposition in divisionprns:predicateNodepredicate nodeprns:principalInvestigatorNameprincipal investigator nameprns:publicationDatepublication dateprns:similarTosimilar toprns:sortOrdersort orderprns:startDatestart dateprns:uniquenessWeightuniqueness weightprns:yearyearAcademic ArticleArticleDocumentbibo:pmidPubMed IdentifierAddressvivo:address1address line 1vivo:addressCitycityvivo:addressPostalCodepostal codevivo:addressStatestate or provinceAgreementvivo:authorInAuthorshipselected publicationsvivo:authorRankauthor rank in publicationAuthorshipDepartmentDivisionGrantvivo:hasResearchArearesearch areasvivo:hasResearcherRoleresearch activitiesvivo:hrJobTitleHR job titleInformation Resourcevivo:linkedAuthorlinked authorvivo:linkedInformationResourcelinked information resourcevivo:mailingAddressmailing addressvivo:personInPositionpositionsPositionvivo:positionInOrganizationposition in organizationvivo:preferredTitlepreferred titleResearcher Rolevivo:researcherRoleOfresearcher role ofRolevivo:roleContributesTocontributes tovivo:sponsorAwardIdsponsor award idrdf:predicatepredicaterdf:typetyperdfs:labellabelConceptAgentfoaf:firstNamefirst namefoaf:lastNamelast nameOrganizationPerson25377513Goldman AM, Tuchman REpilepsiaCommentary: Genetic testing in epilepsy: what do patients and families want to know? Epilepsia. 2014 Nov; 55(11):1703-4.Epilepsia2014-11-06T00:00:002014Commentary: Genetic testing in epilepsy: what do patients and families want to know?Authorship 838363Authorship 131266Authorship 1606594Authorship 162692125616485Bergey GK, Morrell MJ, Mizrahi EM, Goldman A, King-Stephens D, Nair D, Srinivasan S, Jobst B, Gross RE, Shields DC, Barkley G, Salanova V, Olejniczak P, Cole A, Cash SS, Noe K, Wharen R, Worrell G, Murro AM, Edwards J, Duchowny M, Spencer D, Smith M, Geller E, Gwinn R, Skidmore C, Eisenschenk S, Berg M, Heck C, Van Ness P, Fountain N, Rutecki P, Massey A, O'Donovan C, Labar D, Duckrow RB, Hirsch LJ, Courtney T, Sun FT, Seale CGNeurologyLong-term treatment with responsive brain stimulation in adults with refractory partial seizures. Neurology. 2015 Feb 24; 84(8):810-7.Neurology2015-01-23T00:00:002015Long-term treatment with responsive brain stimulation in adults with refractory partial seizures.25734955Goldman AMCurrent opinion in neurologyMechanisms of sudden unexplained death in epilepsy. Curr Opin Neurol. 2015 Apr; 28(2):166-74.Curr Opin Neurol2015-04-01T00:00:002015Mechanisms of sudden unexplained death in epilepsy.MD AndersonEDWARD I-FEICHANGEDWARD I-FEI CHANG9662CHANG, EDWARD I-FEIAssociate ProfessorAuthorship 423653Authorship 5151612Authorship 302627126749013Goldman AM, Behr ER, Semsarian C, Bagnall RD, Sisodiya S, Cooper PNEpilepsiaSudden unexpected death in epilepsy genetics: Molecular diagnostics and prevention. Epilepsia. 2016 Jan; 57 Suppl 1:17-25.Epilepsia2016-01-01T00:00:002016Sudden unexpected death in epilepsy genetics: Molecular diagnostics and prevention.74Professor29Clinical Associate Professor14Associate Professor46Distinguished Emeritus Professor78Professor Emeritus6Adjunct ProfessorEVERTONEDMONDSONEVERTON EDMONDSON0.000000000000000.000000000000004842EDMONDSON, EVERTONProfessor6501 Fannin StHouston, 77030TXAuthorship 327801127330453Goldman 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) EpilEpilepsy currents2014 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.Epilepsy Curr2016-05-01T00:00:0020162014 Epilepsy Benchmarks Area IV: Limit or Prevent Adverse Consequence of Seizures and Their Treatment Across The Lifespan.21785360McGuire 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 SGGenetics in medicine : official journal of the American College of Medical GeneticsTo share or not to share: a randomized trial of consent for data sharing in genome research. Genet Med. 2011 Nov; 13(11):948-55.Genet Med2011-11-01T00:00:002011To share or not to share: a randomized trial of consent for data sharing in genome research.16566870Goldman AM, Potocki L, Walz K, Lynch JK, Glaze DG, Lupski JR, Noebels JLJournal of child neurologyEpilepsy and chromosomal rearrangements in Smith-Magenis Syndrome [del(17)(p11.2p11.2)]. J Child Neurol. 2006 Feb; 21(2):93-8.J Child Neurol2006-02-01T00:00:002006Epilepsy and chromosomal rearrangements in Smith-Magenis Syndrome [del(17)(p11.2p11.2)].17517686Bi W, Yan J, Shi X, Yuva-Paylor LA, Antalffy BA, Goldman A, Yoo JW, Noebels JL, Armstrong DL, Paylor R, Lupski JRHuman molecular geneticsRai1 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.Hum Mol Genet2007-05-21T00:00:002007Rai1 deficiency in mice causes learning impairment and motor dysfunction, whereas Rai1 heterozygous mice display minimal behavioral phenotypes.22796560Klassen TL, von R?den EL, Drabek J, Noebels JL, Goldman AMThe Journal of molecular diagnostics : JMDComparative analytical utility of DNA derived from alternative human specimens for molecular autopsy and diagnostics. J Mol Diagn. 2012 Sep; 14(5):451-7.J Mol Diagn2012-07-13T00:00:002012Comparative analytical utility of DNA derived from alternative human specimens for molecular autopsy and diagnostics.21703448Klassen 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 JCellExome sequencing of ion channel genes reveals complex profiles confounding personal risk assessment in epilepsy. Cell. 2011 Jun 24; 145(7):1036-48.Cell2011-06-24T00:00:002011Exome sequencing of ion channel genes reveals complex profiles confounding personal risk assessment in epilepsy.23408874Chen TT, Klassen TL, Goldman AM, Marini C, Guerrini R, Noebels JLNeurologyNovel brain expression of ClC-1 chloride channels and enrichment of CLCN1 variants in epilepsy. Neurology. 2013 Mar 19; 80(12):1078-85.Neurology2013-02-13T00:00:002013Novel brain expression of ClC-1 chloride channels and enrichment of CLCN1 variants in epilepsy.true1ProfessorProfessortrue1ProfessorProfessortrue1Associate ProfessorAssociate ProfessorD003645Disorders46590.946872Death, SuddenD004828Disorders421110.909362Epilepsies, PartialD004833Disorders411010.893471Epilepsy, Temporal LobeD004827Disorders2568730.550536EpilepsyAuthorship 936989630552298Marafi D, Suter B, Schultz R, Glaze D, Pavlik VN, Goldman AMNeurologySpectrum and time course of epilepsy and the associated cognitive decline in MECP2 duplication syndrome. Neurology. 2019 01 08; 92(2):e108-e114.Neurology2018-12-14T00:00:002018Spectrum and time course of epilepsy and the associated cognitive decline in MECP2 duplication syndrome.2020-07-31NIHGOLDMAN, ALICA M2014-09-30SUDEP Research Alliance: Systems Medicine Core, Application 3 of 7U01NS0903622015-07-31NIHGOLDMAN, ALICA M2011-02-01Copy Number Variants of Neuro-Cardiac Ion Channel Genes and the Risk of SUDEPR01NS0670132010-07-31NIHGOLDMAN, ALICA M2004-08-01Ion channelopathies co-expressed in heart and brainK08NS0473042020-07-31NIHGOLDMAN, ALICA M2014-09-30SUDEP Research Alliance: Clinical Network Core; Application 2 of 7U01NS090406Principal InvestigatorPrincipal InvestigatorPrincipal InvestigatorPrincipal InvestigatorD004829Disorders48710.920165Epilepsy, GeneralizedPlastic SurgeryDepartment of MedicineDepartment of NeurologyDepartment of PediatricsDepartment of Molecular & Human GeneticsDepartment of NeurosurgeryMedicine-CardiologyMolecular & Human GeneticsNeurologyNeurosurgeryPediatrics-NeurologyBaylor College of MedicineVITORPACHECOVITOR PACHECO29.70705990000000-95.400460000000001343PACHECO, VITORClinical Associate ProfessorDANIELGLAZEDANIEL GLAZE29.70508570000000-95.401808700000002349GLAZE, DANIELDistinguished Emeritus ProfessorASHWINVISWANATHANASHWIN VISWANATHAN0.000000000000000.0000000000000090VISWANATHAN, ASHWINProfessorJAMESLUPSKIJAMES LUPSKI29.71073630000000-95.396604500000003140LUPSKI, JAMESProfessor2.06560.00410192124research areas0.628480.025806729coauthor of36.89993.4355760similar to1122selected publicationsZULFIHANEEFZULFI HANEEF0.000000000000000.000000000000003975HANEEF, ZULFIAssociate ProfessorLEOSIMPSONLEO SIMPSON29.70705990000000-95.40046000000000895SIMPSON, LEOAssociate ProfessorRICHARDHRACHOVYRICHARD HRACHOVY29.70705990000000-95.400460000000002391HRACHOVY, RICHARDDistinguished Emeritus Professor30850373Assia Batzir N, Bhagwat PK, Eble TN, Liu P, Eng CM, Elsea SH, Robak LA, Scaglia F, Goldman AM, Dhar SU, Wangler MFCold Spring Harbor molecular case studiesDe 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).Cold Spring Harb Mol Case Stud2019-06-03T00:00:002019De novo missense variant in the GTPase effector domain (GED) of DNM1L leads to static encephalopathy and seizures.JEFFREYNOEBELSJEFFREY NOEBELS0.000000000000000.000000000000003151NOEBELS, JEFFREYProfessorAuthorship 94819492021-06-30NIHGOLDMAN, ALICA M2019-07-01Isolating SUDEP Risk conferred by genomic co-variation in candidate SUDEP genesR21NS113015Principal InvestigatorAuthorship 955008931489630Montier L, Haneef Z, Gavvala J, Yoshor D, North R, Verla T, Van Ness PC, Drabek J, Goldman AMEpilepsiaA somatic mutation in MEN1 gene detected in periventricular nodular heterotopia tissue obtained from depth electrodes. Epilepsia. 2019 10; 60(10):e104-e109.Epilepsia2019-09-06T00:00:002019A somatic mutation in MEN1 gene detected in periventricular nodular heterotopia tissue obtained from depth electrodes.true1Distinguished Emeritus ProfessorDistinguished Emeritus Professor32690786Nair 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 StudyNeurologyNine-year prospective efficacy and safety of brain-responsive neurostimulation for focal epilepsy. Neurology. 2020 09 01; 95(9):e1244-e1256.Neurology2020-07-20T00:00:002020Nine-year prospective efficacy and safety of brain-responsive neurostimulation for focal epilepsy.true1ProfessorProfessortrue1ProfessorProfessorAuthorship 10092361Authorship 100924645Authorship 1009380132754647Goldman AMNeurology. GeneticsWhat does a defect in N-glycosylation mean for neuronal migration and function? Neurol Genet. 2020 Aug; 6(4):e490.Neurol Genet2020-07-07T00:00:002020What does a defect in N-glycosylation mean for neuronal migration and function?33268564Goldman AMNeurologyPeri-ictal Brainstem-Driven Posturing and Its Meaning. Neurology. 2021 01 19; 96(3):89-90.Neurology2020-12-02T00:00:002020Peri-ictal Brainstem-Driven Posturing and Its Meaning.true1Associate ProfessorAssociate ProfessorCHSA Pedi-NeurologyAuthorship 1027835834396109Massey CA, Thompson SJ, Ostrom RW, Drabek J, Sveinsson OA, Tomson T, Haas EA, Mena OJ, Goldman AM, Noebels JLBrain communicationsX-linked serotonin 2C receptor is associated with a non-canonical pathway for sudden unexpected death in epilepsy. Brain Commun. 2021; 3(3):fcab149.Brain Commun2021-07-09T00:00:002021X-linked serotonin 2C receptor is associated with a non-canonical pathway for sudden unexpected death in epilepsy.Authorship 1034574634840901Torrealba-Acosta G, Butt H, Edmondson EA, Willaert R, Viswanathan A, Goldman AMNeurology. Clinical practiceA Neurostimulation-Triggered Trigeminal Neuralgia-like Pain: Risk Factors and Management. Neurol Clin Pract. 2021 Oct; 11(5):e760-e762.Neurol Clin Pract2021-10-01T00:00:002021A Neurostimulation-Triggered Trigeminal Neuralgia-like Pain: Risk Factors and Management.true1Associate ProfessorAssociate ProfessorAuthorship 10619671Authorship 1055213136426191Goldman AMEpilepsy currentsCan a Mouse Help Us Unravel the Mysteries of CDKL5-Related Epilepsy? Epilepsy Curr. 2022 Nov-Dec; 22(6):375-377.Epilepsy Curr2022-09-22T00:00:002022Can a Mouse Help Us Unravel the Mysteries of CDKL5-Related Epilepsy?36307216Goldman AM, Thio KLLNeurologySLC35A2-Related Epilepsy: Global Neuronal Consequences of a Focal Disruption in Glycosylation. Neurology. 2023 01 31; 100(5):225-226.Neurology2022-10-28T00:00:002022SLC35A2-Related Epilepsy: Global Neuronal Consequences of a Focal Disruption in Glycosylation.Authorship 1068307137126324Goldman AMJAMA neurologyOncogenic Pathways Provide Clue to the Etiology of Human Mesial Temporal Lobe Epilepsy. JAMA Neurol. 2023 06 01; 80(6):546-547.JAMA Neurol2023-06-01T00:00:002023Oncogenic Pathways Provide Clue to the Etiology of Human Mesial Temporal Lobe Epilepsy.true1Clinical Associate ProfessorClinical Associate Professortrue1Distinguished Emeritus ProfessorDistinguished Emeritus Professortrue1Adjunct ProfessorAdjunct ProfessorAuthorship 210581true1Professor EmeritusProfessor Emeritustrue1Associate ProfessorAssociate ProfessorAuthorship 252974YU-TZENGYU-TZE NG7903NG, YU-TZEAdjunct ProfessorPAULVAN NESSPAUL VAN NESS8179VAN NESS, PAULProfessor EmeritusAuthorship 1551811