D005808Genes & Molecular SequencesPhenomenaG05.360.340.024.340.415G05.420.325780.99519Genes, RecessiveFaculty 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 ResourcePositionvivo:positionInOrganizationposition in organizationvivo:preferredTitlepreferred titlevivo:researchAreaOfresearch area ofvivo:subjectAreaForsubject area forrdf:predicatepredicaterdf:typetyperdfs:labellabelConceptAgentfoaf:firstNamefirst namefoaf:lastNamelast nameOrganizationPerson30255572Bhatt N, Loew JM, Gallagher P, Mittal NPediatric blood & cancerSevere nondominant hereditary spherocytosis in an infant with coinheritance of three rare alpha-spectrin gene defects. Pediatr Blood Cancer. 2019 01; 66(1):e27480.Pediatr Blood Cancer2018-09-25T00:00:002018Severe nondominant hereditary spherocytosis in an infant with coinheritance of three rare alpha-spectrin gene defects.26366463Ghani M, Reitz C, Cheng R, Vardarajan BN, Jun G, Sato C, Naj A, Rajbhandary R, Wang LS, Valladares O, Lin CF, Larson EB, Graff-Radford NR, Evans D, De Jager PL, Crane PK, Buxbaum JD, Murrell JR, Raj T, Ertekin-Taner N, Logue M, Baldwin CT, Green RC, Barnes LL, Cantwell LB, Fallin MD, Go RC, Griffith PA, Obisesan TO, Manly JJ, Lunetta KL, Kamboh MI, Lopez OL, Bennett DA, Hendrie H, Hall KS, Goate AM, Byrd GS, Kukull WA, Foroud TM, Haines JL, Farrer LA, Pericak-Vance MA, Lee JH, Schellenberg GD, St George-Hyslop P, Mayeux R, Rogaeva EJAMA neurologyAssociation of Long Runs of Homozygosity With Alzheimer Disease Among African American Individuals. JAMA Neurol. 2015 Nov; 72(11):1313-23.JAMA Neurol2015-11-01T00:00:002015Association of Long Runs of Homozygosity With Alzheimer Disease Among African American Individuals.PathologyPediatricsPsychiatryJeromeLoewJerome Loew349407Loew, JeromeAssociate Professor6Assistant Professor5Associate Professor4Professor0.6806220.007929147research area of0.6839120.01539546subject area for15342989Blackman SC, Lurain NS, Witte DP, Filipovich AH, Groen P, Schleiss MRJournal of pediatric hematology/oncologyEmergence and compartmentalization of fatal multi-drug-resistant cytomegalovirus infection in a patient with autosomal-recessive severe combined immune deficiency. J Pediatr Hematol Oncol. 2004 Sep; 26(9):601-5.J Pediatr Hematol Oncol2004-09-01T00:00:002004Emergence and compartmentalization of fatal multi-drug-resistant cytomegalovirus infection in a patient with autosomal-recessive severe combined immune deficiency.Neurological SciencesRush University, Rush Medical CollegeDavidBennettDavid A. Bennett41.87328300000000-87.66936330000000349004Bennett, DavidProfessorLisaBarnesLisa L. Barnes41.87328300000000-87.66936330000000349014Barnes, LisaProfessortrue1Assistant ProfessorAssistant Professortrue1Associate ProfessorAssociate ProfessorJudithBadnerJudith Badner349859Badner, JudithAssociate ProfessorNupurMittalNupur Mittal349863Mittal, NupurAssistant Professor3666434Chakravarti A, Badner JA, Li CCGenetic epidemiologyTests of linkage and heterogeneity in Mendelian diseases using identity by descent scores. Genet Epidemiol. 1987; 4(4):255-66.Genet Epidemiol1987-01-01T00:00:001987Tests of linkage and heterogeneity in Mendelian diseases using identity by descent scores.true1Associate ProfessorAssociate Professor8074150Nevin NC, Silvestri J, Kernohan DC, Hutchinson WMAmerican journal of medical geneticsOral-facial-digital syndrome with retinal abnormalities: OFDS type IX. A further case report. Am J Med Genet. 1994 Jul 01; 51(3):228-31.Am J Med Genet1994-07-01T00:00:001994Oral-facial-digital syndrome with retinal abnormalities: OFDS type IX. A further case report.true1ProfessorProfessortrue1ProfessorProfessor