D059472Genes & Molecular SequencesG05.360.340.01115410.98483Exomecmhprofilesont:personsuffixperson suffixprns:fullNamefull nameprns:hasAuthorListauthor listprns: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 ResourcePositionvivo:positionInOrganizationposition in organizationvivo:preferredTitlepreferred titlevivo:researchAreaOfresearch area ofvivo:subjectAreaForsubject area forrdf:predicatepredicaterdf:typetyperdfs:labellabelConceptAgentfoaf:firstNamefirst namefoaf:lastNamelast nameOrganizationPerson25372662Shortt K, Chaudhary S, Grigoryev D, Heruth DP, Venkitachalam L, Zhang LQ, Ye SQPloS oneShortt K, Chaudhary S, Grigoryev D, Heruth DP, Venkitachalam L, Zhang LQ, Ye SQ. Identification of novel single nucleotide polymorphisms associated with acute respiratory distress syndrome by exome-seq. PLoS One. 2014; 9(11):e111953.PLoS One2014-11-05T00:00:002014Identification of novel single nucleotide polymorphisms associated with acute respiratory distress syndrome by exome-seq.MDSarahSodenSarah E. Soden0.000000000000000.00000000000000111Soden, SarahDivision DirectorMD, PhDTomiPastinenTomi Pastinen0.000000000000000.00000000000000113Pastinen, TomiDirector, Center for Pediatric Genomic Medicine 25473036Soden SE, Saunders CJ, Willig LK, Farrow EG, Smith LD, Petrikin JE, LePichon JB, Miller NA, Thiffault I, Dinwiddie DL, Twist G, Noll A, Heese BA, Zellmer L, Atherton AM, Abdelmoity AT, Safina N, Nyp SS, Zuccarelli B, Larson IA, Modrcin A, Herd S, Creed M, Ye Z, Yuan X, Brodsky RA, Kingsmore SFScience translational medicineSoden SE, Saunders CJ, Willig LK, Farrow EG, Smith LD, Petrikin JE, LePichon JB, Miller NA, Thiffault I, Dinwiddie DL, Twist G, Noll A, Heese BA, Zellmer L, Atherton AM, Abdelmoity AT, Safina N, Nyp SS, Zuccarelli B, Larson IA, Modrcin A, Herd S, Creed M, Ye Z, Yuan X, Brodsky RA, Kingsmore SF. Effectiveness of exome and genome sequencing guided by acuity of illness for diagnosis of neurodevelopmental disorders. Sci Transl Med. 2014 Dec 03; 6(265):265ra168.Sci Transl Med2014-12-03T00:00:002014Effectiveness of exome and genome sequencing guided by acuity of illness for diagnosis of neurodevelopmental disorders.26616883Siuko M, Valori M, Kivel? T, Set?l? K, Morin A, Kwan T, Pastinen T, Tienari PJournal of neuroimmunologySiuko M, Valori M, Kivel? T, Set?l? K, Morin A, Kwan T, Pastinen T, Tienari P. Exome and regulatory element sequencing of neuromyelitis optica patients. J Neuroimmunol. 2015 Dec 15; 289:139-42.J Neuroimmunol2015-11-03T00:00:002015Exome and regulatory element sequencing of neuromyelitis optica patients.27125219Magne F, Ge B, Larriv?e-Vanier S, Van Vliet G, Samuels ME, Pastinen T, Delado?y JThyroid : official journal of the American Thyroid AssociationMagne F, Ge B, Larriv?e-Vanier S, Van Vliet G, Samuels ME, Pastinen T, Delado?y J. Demonstration of Autosomal Monoallelic Expression in Thyroid Tissue Assessed by Whole-Exome and Bulk RNA Sequencing. Thyroid. 2016 06; 26(6):852-9.Thyroid2016-05-18T00:00:002016Demonstration of Autosomal Monoallelic Expression in Thyroid Tissue Assessed by Whole-Exome and Bulk RNA Sequencing.PhD, CGCEmilyFarrowEmily G. Farrow0.000000000000000.00000000000000124Farrow, EmilyDirector of Lab Operations0.7982450.034080915research area of0.5802650.11775832subject area for26684335Smith LD, Willig LK, Kingsmore SFCold Spring Harbor perspectives in medicineSmith LD, Willig LK, Kingsmore SF. Whole-Exome Sequencing and Whole-Genome Sequencing in Critically Ill Neonates Suspected to Have Single-Gene Disorders. Cold Spring Harb Perspect Med. 2015 Dec 18; 6(2):a023168.Cold Spring Harb Perspect Med2015-12-18T00:00:002015Whole-Exome Sequencing and Whole-Genome Sequencing in Critically Ill Neonates Suspected to Have Single-Gene Disorders.MD, FAAP, FAESAhmedAbdelmoityAhmed T. Abdelmoity0.000000000000000.00000000000000147Abdelmoity, AhmedDivision Director, Child NeurologyMDLaurelWilligLaurel K. Willig0.000000000000000.00000000000000154Willig, LaurelMedical Director, Center for Pediatric Genomic Medicine PediatricsResearchClinicalChildren's Mercy Kansas Citytrue1Division Director, Child NeurologyDivision Director, Child Neurologytrue1Medical Director, Center for Pediatric Genomic Medicine Medical Director, Center for Pediatric Genomic Medicine true1Division DirectorDivision Directortrue1Director, Center for Pediatric Genomic Medicine Director, Center for Pediatric Genomic Medicine true1Director of Lab OperationsDirector of Lab Operations