28641109Huang AY, Yu D, Davis LK, Sul JH, Tsetsos F, Ramensky V, Zelaya I, Ramos EM, Osiecki L, Chen JA, McGrath LM, Illmann C, Sandor P, Barr CL, Grados M, Singer HS, Nöthen MM, Hebebrand J, King RA, Dion Y, Rouleau G, Budman CL, Depienne C, Worbe Y, Hartmann A, Müller-Vahl KR, Stuhrmann M, Aschauer H, Stamenkovic M, Schloegelhofer M, Konstantinidis A, Lyon GJ, McMahon WM, Barta C, Tarnok Z, Nagy P, Batterson JR, Rizzo R, Cath DC, Wolanczyk T, Berlin C, Malaty IA, Okun MS, Woods DW, Rees E, Pato CN, Pato MT, Knowles JA, Posthuma D, Pauls DL, Cox NJ, Neale BM, Freimer NB, Paschou P, Mathews CA, Scharf JM, Coppola G, Tourette Syndrome Association International Consortium for Genetics (TSAICG), Gilles de la Tourette Syndrome GWAS Replication Initiative (GGRI)NeuronCell Adhesion Molecules, Neuronal; Contactins; DNA Copy Number Variations; Nerve Tissue Proteins; Tourette SyndromeAdolescent; Adult; Calcium-Binding Proteins; Case-Control Studies; Child; Female; Genetic Predisposition to Disease; Genome-Wide Association Study; Genotype; Humans; Male; Neural Cell Adhesion Molecules; Odds Ratio; White People; Young AdultRare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome. Neuron. 2017 Jun 21; 94(6):1101-1111.e7.Neuron2017-06-21T00:00:002017Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome.prns:emailEncryptedemail addressprns:fullNamefull nameprns:hasAuthorListauthor listprns:hasNetworkhas networkprns:hasPublicationVenuepublished inprns:hasSubjectAreaMajorTopicListhas major subject area listprns:hasSubjectAreaMinorTopicListhas minor subject area listprns:informationResourceReferenceinformation resource referenceprns:isPrimaryPositionis primary positionprns:latitudelatitudeprns:longitudelongitudeprns: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:predicateNodepredicate nodeprns:publicationDatepublication dateprns:sortOrdersort orderprns:uniquenessWeightuniqueness weightprns:yearyearAcademic ArticleArticleDocumentbibo:pmidPubMed Identifiervivo:authorRankauthor rank in publicationAuthorshipDepartmentvivo:hasSubjectAreahas subject areavivo:hrJobTitleHR job titleInformation Resourcevivo:informationResourceInAuthorshipauthorsvivo:linkedAuthorlinked authorvivo:linkedInformationResourcelinked information resourcePositionvivo:positionInOrganizationposition in organizationvivo:preferredTitlepreferred titlerdf:predicatepredicaterdf:typetyperdfs:labellabelConceptAgentfoaf:firstNamefirst namefoaf:lastNamelast nameOrganizationPersonD000293Living Beings111389680.400538AdolescentD000328Living Beings1578255770.254432AdultAuthorship 105603450.1563880.1563881authors10.2519has subject areaD002648Living Beings93969130.440034ChildD005879Disorders11250.981132Tourette SyndromeD009419Chemicals & Drugs2005030.780094Nerve Tissue ProteinsD005260Physiology1992444050.191167FemaleD006801Living Beings2262862810.130052HumansD008297Physiology1931408600.201617MaleD015816Chemicals & Drugs19290.98643Cell Adhesion Molecules, NeuronalD016022Procedures53618010.700926Case-Control StudiesD058966Chemicals & Drugs220.998127ContactinsD056915Physiology991710.899103DNA Copy Number VariationsD016017Concepts & Ideas2896770.843104Odds RatioD055106Procedures21716110.566048Genome-Wide Association StudyD002135Chemicals & Drugs851140.937911Calcium-Binding ProteinsD005838Physiology41118500.686726GenotypeD019006Chemicals & Drugs14140.99Neural Cell Adhesion MoleculesD020022Physiology39922670.521961Genetic Predisposition to DiseaseD055815Living Beings97159610.423207Young AdultMedicineUniversity of ChicagoNancy JeanCox2WFmE4EXCuiXhHlsaUXv9Gq0+s+oNancy Jean Cox41.78927490000000-87.601250000000001011Cox, Nancy JeanEmeritus/Emeritatrue1Emeritus/EmeritaEmeritus/Emerita