D016142DisordersC05.660.207.410C10.500.034.875C16.131.077.410C16.131.260.380C16.131.621.207.410C16.131.666.034.875C16.320.180.3806110.990859Holoprosencephalyplugins:TwitterTwitterFaculty Rankprns:fullNamefull nameprns:hasAuthorListauthor listprns:hasFacultyRankhas faculty rankprns:hasNetworkhas networkprns:hasPublicationVenuepublished inprns:informationResourceReferenceinformation resource referenceprns: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:pluginSearchableDataProfilesRNS Plugin Searchable Dataprns:predicateNodepredicate nodeprns:publicationDatepublication dateprns:sortOrdersort orderprns:uniquenessWeightuniqueness weightprns:yearyearAcademic ArticleArticleDocumentbibo:pmidPubMed IdentifierInformation Resourcevivo:orcidIdORCID idvivo:preferredTitlepreferred titlevivo:researchAreaOfresearch area ofvivo:subjectAreaForsubject area forrdf:predicatepredicaterdf:typetyperdfs:labellabelConceptAgentfoaf:firstNamefirst namefoaf:lastNamelast namePersonRyanAndersonRyan Anderson41.7886000000000087.598699999999993911Anderson, RyanResearch Assistant Professor20104603Klingensmith J, Matsui M, Yang YP, Anderson RMAmerican journal of medical genetics. Part C, Seminars in medical geneticsRoles of bone morphogenetic protein signaling and its antagonism in holoprosencephaly. Am J Med Genet C Semin Med Genet. 2010 Feb 15; 154C(1):43-51.Am J Med Genet C Semin Med Genet2010-02-15T00:00:002010Roles of bone morphogenetic protein signaling and its antagonism in holoprosencephaly.0.5405710.04184256research area of0.5455580.042228511subject area forWilliamDobynsWilliam B. Dobyns0.000000000000000.000000000000002964Dobyns, WilliamPROFESSOR RajatThawaniRajat Thawani41.7886000000000087.598699999999994376Thawani, Rajat0000-0002-5378-9434Assistant Professor26135150Dewan P, Thawani RJournal of paediatrics and child healthCongenital anomaly. J Paediatr Child Health. 2015 Jul; 51(7):739-40.J Paediatr Child Health2015-07-01T00:00:002015Congenital anomaly.AveryTungAvery Tung41.78927490000000-87.601250000000002185Tung, AveryProfessorElizabethGroveElizabeth Grove41.78927490000000-87.60125000000000473Grove, ElizabethProfessorTwitter rajatthawani19346217Lacbawan F, Solomon BD, Roessler E, El-Jaick K, Domené S, Vélez JI, Zhou N, Hadley D, Balog JZ, Long R, Fryer A, Smith W, Omar S, McLean SD, Clarkson K, Lichty A, Clegg NJ, Delgado MR, Levey E, Stashinko E, Potocki L, Vanallen MI, Clayton-Smith J, Donnai D, Bianchi DW, Juliusson PB, Njølstad PR, Brunner HG, Carey JC, Hehr U, Müsebeck J, Wieacker PF, Postra A, Hennekam RC, van den Boogaard MJ, van Haeringen A, Paulussen A, Herbergs J, Schrander-Stumpel CT, Janecke AR, Chitayat D, Hahn J, McDonald-McGinn DM, Zackai EH, Dobyns WB, Muenke MJournal of medical geneticsClinical spectrum of SIX3-associated mutations in holoprosencephaly: correlation between genotype, phenotype and function. J Med Genet. 2009 Jun; 46(6):389-98.J Med Genet2009-04-02T00:00:002009Clinical spectrum of SIX3-associated mutations in holoprosencephaly: correlation between genotype, phenotype and function.25218063Kakar N, Ahmad J, Morris-Rosendahl DJ, Altmüller J, Friedrich K, Barbi G, Nürnberg P, Kubisch C, Dobyns WB, Borck GHuman geneticsSTIL mutation causes autosomal recessive microcephalic lobar holoprosencephaly. Hum Genet. 2015 Jan; 134(1):45-51.Hum Genet2014-09-14T00:00:002014STIL mutation causes autosomal recessive microcephalic lobar holoprosencephaly.19353631Solomon BD, Lacbawan F, Jain M, Domené S, Roessler E, Moore C, Dobyns WB, Muenke MAmerican journal of medical genetics. Part AA novel SIX3 mutation segregates with holoprosencephaly in a large family. Am J Med Genet A. 2009 May; 149A(5):919-25.Am J Med Genet A2009-05-01T00:00:002009A novel SIX3 mutation segregates with holoprosencephaly in a large family.1010