22442429Alcalay RN, Caccappolo E, Mejia-Santana H, Tang M-, Rosado L, Orbe Reilly M, Ruiz D, Ross B, Verbitsky M, Kisselev S, Louis E, Comella C, Colcher A, Jennings D, Nance M, Bressman S, Scott WK, Tanner C, Mickel S, Andrews H, Waters C, Fahn S, Cote L, Frucht S, Ford B, Rezak M, Novak K, Friedman JH, Pfeiffer R, Marsh L, Hiner B, Siderowf A, Payami H, Molho E, Factor S, Ottman R, Clark LN, Marder KNeurologyCognitive Dysfunction; DNA Mutational Analysis; Genetic Carrier Screening; Glucosylceramidase; Neuropsychological Tests; Parkinson DiseaseAdult; Basal Ganglia Diseases; beta-Glucosidase; Dementia; Depressive Disorder; Female; Genetic Testing; Genotype; Humans; Leucine-Rich Repeat Serine-Threonine Protein Kinase-2; Male; Memory Disorders; Mental Status Schedule; Middle Aged; Olfaction Disorders; Phenotype; Protein Serine-Threonine Kinases; Ubiquitin-Protein LigasesCognitive performance of GBA mutation carriers with early-onset PD: the CORE-PD study. Neurology. 2012 May 01; 78(18):1434-40.Neurology2012-03-21T00:00:002012Cognitive performance of GBA mutation carriers with early-onset PD: the CORE-PD study.Faculty Rankprns:fullNamefull nameprns:hasAuthorListauthor listprns:hasFacultyRankhas faculty rankprns:hasNetworkhas networkprns:hasPublicationVenuepublished inprns:hasSubjectAreaMajorTopicListhas major subject area listprns:hasSubjectAreaMinorTopicListhas minor subject area listprns:informationResourceReferenceinformation resource referenceprns:isPrimaryPositionis primary positionprns: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:positionInDepartmentposition in departmentprns:positionInDivisionposition in divisionprns:predicateNodepredicate nodeprns:publicationDatepublication dateprns:sortOrdersort orderprns:uniquenessWeightuniqueness weightprns:yearyearAcademic ArticleArticleDocumentbibo:pmidPubMed Identifiervivo:authorRankauthor rank in publicationAuthorshipDepartmentDivisionvivo:hasSubjectAreahas subject areavivo:hrJobTitleHR job titleInformation Resourcevivo:informationResourceInAuthorshipauthorsvivo:linkedAuthorlinked authorvivo:linkedInformationResourcelinked information resourcePositionvivo:positionInOrganizationposition in organizationvivo:preferredTitlepreferred titlerdf:predicatepredicaterdf:typetyperdfs:labellabelConceptAgentfoaf:firstNamefirst namefoaf:lastNamelast nameOrganizationPersonD003866Disorders611870.89492Depressive DisorderD006580Procedures4120.994442Genetic Carrier ScreeningD005838Physiology924050.891534GenotypeD003704Disorders585210.667901DementiaD000857Disorders16530.938588Olfaction DisordersD008609Concepts & IdeasProcedures391130.967278Mental Status ScheduleCynthiaComellaCynthia Comella349619Comella, CynthiaProfessor4ProfessorD008875Concepts & IdeasLiving Beings48398170.373681Middle AgedD009483Concepts & IdeasProcedures9912510.714918Neuropsychological TestsD010641Physiology1263530.897565PhenotypeD010300Disorders6311640.510774Parkinson DiseaseD001480Disorders7110.995165Basal Ganglia DiseasesD000328Living Beings51685930.393483AdultAuthorship 1949412D008297Physiology564156270.299065Male0.1086740.1086741authors10.2523has subject areaD005260Physiology579162020.293532FemaleD004252Procedures30560.985126DNA Mutational AnalysisNeurological SciencesRush University, Rush Medical CollegeD006801Living Beings643293340.211949HumansD008569Disorders441740.877255Memory DisordersD044767Chemicals & Drugs20350.980018Ubiquitin-Protein LigasesD0000711584100.996683Leucine-Rich Repeat Serine-Threonine Protein Kinase-2true1ProfessorProfessorD060825Disorders729380.516432Cognitive DysfunctionD001617Chemicals & Drugs110.999864beta-GlucosidaseD005962Chemicals & Drugs12260.980269GlucosylceramidaseD005820Procedures33640.96832Genetic Testing