D020325DisordersC10.228.140.546.399.750.250440.996261Migraine with Auraprns:fullNamefull nameprns:hasAuthorListauthor listprns:hasNetworkhas networkprns:hasPublicationVenuepublished inprns:informationResourceReferenceinformation resource referenceprns:isPrimaryPositionis primary positionprns:latitudelatitudeprns:longitudelongitudeprns:maxWeightmaximum weightprns:medlineTAjournal title abbreviationprns:meshDescriptorUIMeSH DescriptorUIprns:meshSemanticGroupNameMeSH semantic group nameprns:meshTreeNumberMeSH tree numberprns:minWeightminimum weightprns:numberOfAuthorsnumber of authorsprns:numberOfConnectionsnumber of connectionsprns:numberOfPublicationsnumber of publicationsprns:personIdPerson IDprns:personInPrimaryPositionperson in primary positionprns:positionInDepartmentposition in departmentprns:predicateNodepredicate nodeprns:publicationDatepublication dateprns:sortOrdersort orderprns:uniquenessWeightuniqueness weightprns:yearyearAcademic ArticleArticleDocumentbibo:pmidPubMed IdentifierDepartmentvivo:hrJobTitleHR job titleInformation ResourcePositionvivo:positionInOrganizationposition in organizationvivo:preferredTitlepreferred titlevivo:researchAreaOfresearch area ofvivo:subjectAreaForsubject area forrdf:predicatepredicaterdf:typetyperdfs:labellabelConceptAgentfoaf:firstNamefirst namefoaf:lastNamelast nameOrganizationPerson15174025Swoboda KJ, Kanavakis E, Xaidara A, Johnson JE, Leppert MF, Schlesinger-Massart MB, Ptacek LJ, Silver K, Youroukos SAnnals of neurologyAlternating hemiplegia of childhood or familial hemiplegic migraine? A novel ATP1A2 mutation. Ann Neurol. 2004 Jun; 55(6):884-7.Ann Neurol2004-06-01T00:00:002004Alternating hemiplegia of childhood or familial hemiplegic migraine? A novel ATP1A2 mutation.30690204Monteiro FP, Curry CJ, Hevner R, Elliott S, Fisher JH, Turocy J, Dobyns WB, Costa LA, Freitas E, Kitajima JP, Kok FEuropean journal of medical geneticsBiallelic loss of function variants in ATP1A2 cause hydrops fetalis, microcephaly, arthrogryposis and extensive cortical malformations. Eur J Med Genet. 2020 Jan; 63(1):103624.Eur J Med Genet2019-01-25T00:00:002019Biallelic loss of function variants in ATP1A2 cause hydrops fetalis, microcephaly, arthrogryposis and extensive cortical malformations.ElishevaColemanElisheva Coleman41.7886000000000087.598699999999993910Coleman, ElishevaAssistant ProfessorWilliamDobynsWilliam B. Dobyns0.000000000000000.000000000000002964Dobyns, WilliamPROFESSOR 14620879Kunkler PE, Kraig RPHippocampusHippocampal spreading depression bilaterally activates the caudal trigeminal nucleus in rodents. Hippocampus. 2003; 13(7):835-44.Hippocampus2003-01-01T00:00:002003Hippocampal spreading depression bilaterally activates the caudal trigeminal nucleus in rodents.21945891Coleman ER, Grosberg BM, Robbins MSCephalalgia : an international journal of headacheOlfactory hallucinations in primary headache disorders: case series and literature review. Cephalalgia. 2011 Oct; 31(14):1477-89.Cephalalgia2011-09-23T00:00:002011Olfactory hallucinations in primary headache disorders: case series and literature review.0.2418920.1046324research area of0.9711980.1050255subject area forHuman GeneticsNeurologyUniversity of ChicagoRichardKraigRichard Kraig41.78927490000000-87.601250000000002091Kraig, RichardProfessorPallMelstedPall Melsted41.78927490000000-87.60125000000000339Melsted, Pall37884687Bjornsdottir G, Chalmer MA, Stefansdottir L, Skuladottir AT, Einarsson G, Andresdottir M, Beyter D, Ferkingstad E, Gretarsdottir S, Halldorsson BV, Halldorsson GH, Helgadottir A, Helgason H, Hjorleifsson Eldjarn G, Jonasdottir A, Jonasdottir A, Jonsdottir I, Knowlton KU, Nadauld LD, Lund SH, Magnusson OT, Melsted P, Moore KHS, Oddsson A, Olason PI, Sigurdsson A, Stefansson OA, Saemundsdottir J, Sveinbjornsson G, Tragante V, Unnsteinsdottir U, Walters GB, Zink F, Rødevand L, Andreassen OA, Igland J, Lie RT, Haavik J, Banasik K, Brunak S, Didriksen M, T Bruun M, Erikstrup C, Kogelman LJA, Nielsen KR, Sørensen E, Pedersen OB, Ullum H, DBDS Genetic Consortium, Masson G, Thorsteinsdottir U, Olesen J, Ludvigsson P, Thorarensen O, Bjornsdottir A, Sigurdardottir GR, Sveinsson OA, Ostrowski SR, Holm H, Gudbjartsson DF, Thorleifsson G, Sulem P, Stefansson H, Thorgeirsson TE, Hansen TF, Stefansson KNature geneticsRare variants with large effects provide functional insights into the pathology of migraine subtypes, with and without aura. Nat Genet. 2023 Nov; 55(11):1843-1853.Nat Genet2023-10-26T00:00:002023Rare variants with large effects provide functional insights into the pathology of migraine subtypes, with and without aura.true1true1PROFESSOR PROFESSOR true1ProfessorProfessortrue1Assistant ProfessorAssistant Professor