31327508Kanca O, Andrews JC, Lee PT, Patel C, Braddock SR, Slavotinek AM, Cohen JS, Gubbels CS, Aldinger KA, Williams J, Indaram M, Fatemi A, Yu TW, Agrawal PB, Vezina G, Simons C, Crawford J, Lau CC, Undiagnosed Diseases Network, Chung WK, Markello TC, Dobyns WB, Adams DR, Gahl WA, Wangler MF, Yamamoto S, Bellen HJ, Malicdan MCVAmerican journal of human geneticsBody Dysmorphic Disorders; Cerebellum; Coloboma; Developmental Disabilities; Epilepsy; Intellectual Disability; Mutation; Nervous System Malformations; WD40 RepeatsAdult; Amino Acid Sequence; Animals; Child; Drosophila melanogaster; Female; Humans; Infant; Infant, Newborn; Male; Microfilament Proteins; Phenotype; Sequence Homology; Young AdultDe Novo Variants in WDR37 Are Associated with Epilepsy, Colobomas, Dysmorphism, Developmental Delay, Intellectual Disability, and Cerebellar Hypoplasia. Am J Hum Genet. 2019 08 01; 105(2):413-424.Am J Hum Genet2019-07-18T00:00:002019De Novo Variants in WDR37 Are Associated with Epilepsy, Colobomas, Dysmorphism, Developmental Delay, Intellectual Disability, and Cerebellar Hypoplasia.prns: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 nameOrganizationPersonD000595Genes & Molecular Sequences43920620.7368Amino Acid SequenceD000328Living Beings1578255770.254432AdultD000818Living Beings1457265180.249624AnimalsD002648Living Beings93969130.440034ChildD002531Anatomy842470.851307CerebellumD002658Disorders631940.865811Developmental DisabilitiesD003103Disorders4120.992567ColobomaD004827Disorders803950.728702EpilepsyD004331Living Beings1115960.694543Drosophila melanogasterD007231Living Beings50923690.641593Infant, NewbornD007223Living Beings60430360.61304InfantD008840Chemicals & Drugs792060.874789Microfilament ProteinsD008607Disorders651850.890678Intellectual DisabilityD009154Physiology70239520.442648MutationAuthorship 131790220.1805490.1805491authors10.2523has subject areaD005260Physiology1992444050.191167FemaleD006801Living Beings2262862810.130052HumansWilliamDobynsWilliam B. Dobyns0.000000000000000.000000000000002964Dobyns, WilliamPROFESSOR D008297Physiology1931408600.201617MaleD009421Disorders8460.963395Nervous System MalformationsD017385Concepts & IdeasGenes & Molecular Sequences27280.993483Sequence HomologyD057215Disorders3120.982287Body Dysmorphic DisordersD000071678110.999098WD40 RepeatsD010641Physiology64723750.615854PhenotypeD055815Living Beings97159610.423207Young AdultHuman GeneticsUniversity of Chicagotrue1PROFESSOR PROFESSOR