D055028ProceduresE05.393.285.240E05.393.520.500E05.393.661.187580.995653Comparative Genomic Hybridizationcmhprofilesont:personsuffixperson suffixFaculty Rankprns:fullNamefull nameprns: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:meshTreeNumberMeSH tree numberprns: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 IdentifierDepartmentDivisionvivo:hrJobTitleHR job titleInformation Resourcevivo:orcidIdORCID idPositionvivo:positionInOrganizationposition in organizationvivo:preferredTitlepreferred titlevivo:researchAreaOfresearch area ofvivo:subjectAreaForsubject area forrdf:predicatepredicaterdf:typetyperdfs:labellabelConceptAgentfoaf:firstNamefirst namefoaf:lastNamelast nameOrganizationPerson19420922Bittel DC, Yu S, Newkirk H, Kibiryeva N, Holt A, Butler MG, Cooley LDCytogenetic and genome researchBittel DC, Yu S, Newkirk H, Kibiryeva N, Holt A, Butler MG, Cooley LD. Refining the 22q11.2 deletion breakpoints in DiGeorge syndrome by aCGH. Cytogenet Genome Res. 2009; 124(2):113-20.Cytogenet Genome Res2009-05-05T00:00:002009Refining the 22q11.2 deletion breakpoints in DiGeorge syndrome by aCGH.19687311Yu S, Bittel DC, Kibiryeva N, Zwick DL, Cooley LDAmerican journal of clinical pathologyYu S, Bittel DC, Kibiryeva N, Zwick DL, Cooley LD. Validation of the Agilent 244K oligonucleotide array-based comparative genomic hybridization platform for clinical cytogenetic diagnosis. Am J Clin Pathol. 2009 Sep; 132(3):349-60.Am J Clin Pathol2009-09-01T00:00:002009Validation of the Agilent 244K oligonucleotide array-based comparative genomic hybridization platform for clinical cytogenetic diagnosis.20001581Yu S, Kielt M, Stegner AL, Kibiryeva N, Bittel DC, Cooley LDGenetic testing and molecular biomarkersYu S, Kielt M, Stegner AL, Kibiryeva N, Bittel DC, Cooley LD. Quantitative real-time polymerase chain reaction for the verification of genomic imbalances detected by microarray-based comparative genomic hybridization. Genet Test Mol Biomarkers. 2009 Dec; 13(6):751-60.Genet Test Mol Biomarkers2009-12-01T00:00:002009Quantitative real-time polymerase chain reaction for the verification of genomic imbalances detected by microarray-based comparative genomic hybridization.MDSarahSodenSarah E. Soden0.000000000000000.00000000000000111Soden, SarahDivision Director2Associate Professor1Professor0.3755320.02792155research area of0.3792530.09016310subject area for20350984Graf WD, Le Pichon JB, Bittel DC, Abdelmoity AT, Yu SNeurologyGraf WD, Le Pichon JB, Bittel DC, Abdelmoity AT, Yu S. Practice parameter: evaluation of the child with microcephaly (an evidence-based review): report of the quality standards subcommittee of the American Academy of Neurology and the Practice Committee of the Child Neurology Society. Neurology. 2010 Mar 30; 74(13):1080-1; author reply 1081.Neurology2010-03-30T00:00:002010Practice parameter: evaluation of the child with microcephaly (an evidence-based review): report of the quality standards subcommittee of the American Academy of Neurology and the Practice Committee of the Child Neurology Society.MD, FAAP, FAESAhmedAbdelmoityAhmed T. Abdelmoity0.000000000000000.00000000000000147Abdelmoity, AhmedDivision Director, Child NeurologyMD, PhD, FAAPJean-BaptisteLe PichonJean-Baptiste Le Pichon0.000000000000000.00000000000000152Le Pichon, Jean-Baptiste0000-0001-8666-1632Director, Child Neurology Residency ProgramPathology and Laboratory MedicinePediatricsResearchClinicalChildren's Mercy Kansas CityMD, PhD, FCAPMidhatFarooqiMidhat Farooqi0.000000000000000.00000000000000161Farooqi, Midhat0000-0002-5238-1349Director, Molecular Oncology, Center for Pediatric Genomic MedicineMD, FAAP, FACMG, CCDEricRushEric T. Rush0.000000000000000.00000000000000200Rush, Eric0000-0002-8147-7315Medical Director, Office of Faculty Affairs and Development20434696Rush ET, Schaefer GBSeminars in pediatric neurologyRush ET, Schaefer GB. Identification of an X-linked deletion syndrome through comparative genomic hybridization microarray. Semin Pediatr Neurol. 2010 Mar; 17(1):51-3.Semin Pediatr Neurol2010-03-01T00:00:002010Identification of an X-linked deletion syndrome through comparative genomic hybridization microarray.true1Division Director, Child NeurologyDivision Director, Child Neurologytrue1Division DirectorDivision Directortrue1Director, Molecular Oncology, Center for Pediatric Genomic MedicineDirector, Molecular Oncology, Center for Pediatric Genomic Medicinetrue1Director, Child Neurology Residency ProgramDirector, Child Neurology Residency Programtrue1Medical Director, Office of Faculty Affairs and DevelopmentMedical Director, Office of Faculty Affairs and Development