NINGLIUNING LIU11003LIU, NINGAssistant Professorprns:coAuthorOfcoauthor ofFaculty 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: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:similarTosimilar toprns:sortOrdersort orderprns:uniquenessWeightuniqueness weightprns:yearyearAcademic ArticleArticleDocumentbibo:pmidPubMed IdentifierAddressvivo:address1address line 1vivo:addressCitycityvivo:addressPostalCodepostal codevivo:addressStatestate or provincevivo:authorInAuthorshipselected publicationsvivo:authorRankauthor rank in publicationAuthorshipDepartmentDivisionvivo:hasResearchArearesearch areasvivo:hrJobTitleHR job titleInformation Resourcevivo:linkedAuthorlinked authorvivo:linkedInformationResourcelinked information resourcevivo:mailingAddressmailing addressvivo:personInPositionpositionsPositionvivo:positionInOrganizationposition in organizationvivo:preferredTitlepreferred titlerdf:predicatepredicaterdf:typetyperdfs:labellabelConceptAgentfoaf:firstNamefirst namefoaf:lastNamelast nameOrganizationPersonLeukemiaMD AndersonHAGOP MKANTARJIANHAGOP M KANTARJIAN8501KANTARJIAN, HAGOP MProfessor2450 HOLCOMBEHouston, 77021TX0.8680730.0112031110research areas1.979680.037526836coauthor of12.30732.1258560similar to1114selected publicationsAuthorship 2900931924951112Zhang R, Luo H, Wang S, Chen W, Chen Z, Wang HW, Chen Y, Yang J, Zhang X, Wu W, Zhang SY, Shen S, Dong Q, Zhang Y, Jiang T, Lu D, Zhao S, You Y, Liu N, Wang HNeuro-oncologyMicroRNA-377 inhibited proliferation and invasion of human glioblastoma cells by directly targeting specificity protein 1. Neuro Oncol. 2014 Nov; 16(11):1510-22.Neuro Oncol2014-06-20T00:00:002014MicroRNA-377 inhibited proliferation and invasion of human glioblastoma cells by directly targeting specificity protein 1.74Professor10Assistant Professor14Associate Professor6Adjunct ProfessorAuthorship 6529032127863244Hu B, Wang Q, Wang YA, Hua S, Sauv? CG, Ong D, Lan ZD, Chang Q, Ho YW, Monasterio MM, Lu X, Zhong Y, Zhang J, Deng P, Tan Z, Wang G, Liao WT, Corley LJ, Yan H, Zhang J, You Y, Liu N, Cai L, Finocchiaro G, Phillips JJ, Berger MS, Spring DJ, Hu J, Sulman EP, Fuller GN, Chin L, Verhaak RGW, DePinho RACellEpigenetic Activation of WNT5A Drives Glioblastoma Stem Cell Differentiation and Invasive Growth. Cell. 2016 11 17; 167(5):1281-1295.e18.Cell2016-11-17T00:00:002016Epigenetic Activation of WNT5A Drives Glioblastoma Stem Cell Differentiation and Invasive Growth.Authorship 8799052Authorship 885789128981122Yi S, Liu NN, Hu L, Wang H, Sahni NNature protocolsBase-resolution stratification of cancer mutations using functional variomics. Nat Protoc. 2017 Nov; 12(11):2323-2341.Nat Protoc2017-10-05T00:00:002017Base-resolution stratification of cancer mutations using functional variomics.29726930Liu N, Schoch K, Luo X, Pena LDM, Bhavana VH, Kukolich MK, Stringer S, Powis Z, Radtke K, Mroske C, Deak KL, McDonald MT, McConkie-Rosell A, Markert ML, Kranz PG, Stong N, Need AC, Bick D, Amaral MD, Worthey EA, Levy S, Undiagnosed Diseases Network (UDN), Wangler MF, Bellen HJ, Shashi V, Yamamoto SHuman molecular geneticsFunctional variants in TBX2 are associated with a syndromic cardiovascular and skeletal developmental disorder. Hum Mol Genet. 2018 07 15; 27(14):2454-2465.Hum Mol Genet2018-07-15T00:00:002018Functional variants in TBX2 are associated with a syndromic cardiovascular and skeletal developmental disorder.true1ProfessorProfessortrue1Associate ProfessorAssociate Professortrue1ProfessorProfessorD054067Disorders220.991545Dihydropyrimidine Dehydrogenase DeficiencyD053719Procedures2113670.810926Tandem Mass SpectrometryD050937Chemicals & Drugs690.988441Guanidinoacetate N-MethyltransferaseD003401Chemicals & Drugs44620.961157CreatineD008661Disorders681080.888866Metabolism, Inborn ErrorsDepartment of MedicineDepartment of Molecular & Human GeneticsMedicine-Athero & LipoproteinsMolecular & Human GeneticsBaylor College of MedicineERICBOERWINKLEERIC BOERWINKLE0.000000000000000.000000000000002653BOERWINKLE, ERICAdjunct ProfessorJAMESLUPSKIJAMES LUPSKI29.71073630000000-95.396604500000003140LUPSKI, JAMESProfessorQINSUNQIN SUN0.000000000000000.00000000000000480SUN, QINAssociate ProfessorVERNONSUTTONVERNON SUTTON29.70508570000000-95.401808700000003508SUTTON, VERNONProfessorSARAHELSEASARAH ELSEA0.000000000000000.000000000000004693ELSEA, SARAHProfessortrue1Adjunct ProfessorAdjunct ProfessorAuthorship 989974332439973Alaimo JT, Glinton KE, Liu N, Xiao J, Yang Y, Reid Sutton V, Elsea SHGenetics in medicine : official journal of the American College of Medical GeneticsIntegrated analysis of metabolomic profiling and exome data supplements sequence variant interpretation, classification, and diagnosis. Genet Med. 2020 09; 22(9):1560-1566.Genet Med2020-05-22T00:00:002020Integrated analysis of metabolomic profiling and exome data supplements sequence variant interpretation, classification, and diagnosis.KEVINGLINTONKEVIN GLINTON15928GLINTON, KEVINAssistant Professortrue1Assistant ProfessorAssistant ProfessorAuthorship 999277432909658Pillai NR, Amin H, Gijavanekar C, Liu N, Issaq N, Broniowska KA, Bertuch AA, Sutton VR, Elsea SH, Scaglia FAmerican journal of medical genetics. Part AHematologic presentation and the role of untargeted metabolomics analysis in monitoring treatment for riboflavin transporter deficiency. Am J Med Genet A. 2020 11; 182(11):2781-2787.Am J Med Genet A2020-09-10T00:00:002020Hematologic presentation and the role of untargeted metabolomics analysis in monitoring treatment for riboflavin transporter deficiency.true1Assistant ProfessorAssistant ProfessorAuthorship 1024911134251446Liu N, Xiao J, Gijavanekar C, Pappan KL, Glinton KE, Shayota BJ, Kennedy AD, Sun Q, Sutton VR, Elsea SHJAMA network openComparison of Untargeted Metabolomic Profiling vs Traditional Metabolic Screening to Identify Inborn Errors of Metabolism. JAMA Netw Open. 2021 07 01; 4(7):e2114155.JAMA Netw Open2021-07-01T00:00:002021Comparison of Untargeted Metabolomic Profiling vs Traditional Metabolic Screening to Identify Inborn Errors of Metabolism.Authorship 1031002734605855Marafi D, Fatih JM, Kaiyrzhanov R, Ferla MP, Gijavanekar C, Al-Maraghi A, Liu N, Sites E, Alsaif HS, Al-Owain M, Zakkariah M, El-Anany E, Guliyeva U, Guliyeva S, Gaba C, Haseeb A, Alhashem AM, Danish E, Karageorgou V, Beetz C, Subhi AA, Mullegama SV, Torti E, Sebastin M, Breilyn MS, Duberstein S, Abdel-Hamid MS, Mitani T, Du H, Rosenfeld JA, Jhangiani SN, Coban Akdemir Z, Gibbs RA, Taylor JC, Fakhro KA, Hunter JV, Pehlivan D, Zaki MS, Gleeson JG, Maroofian R, Houlden H, Posey JE, Sutton VR, Alkuraya FS, Elsea SH, Lupski JRBrain : a journal of neurologyBiallelic variants in SLC38A3 encoding a glutamine transporter cause epileptic encephalopathy. Brain. 2022 04 29; 145(3):909-924.Brain2022-04-29T00:00:002022Biallelic variants in SLC38A3 encoding a glutamine transporter cause epileptic encephalopathy.Authorship 1031524434648945Huo KG, Notsuda H, Fang Z, Liu NF, Gebregiworgis T, Li Q, Pham NA, Li M, Liu N, Shepherd FA, Marshall CB, Ikura M, Moghal N, Tsao MSJournal of thoracic oncology : official publication of the International Association for the Study of Lung CancerLung Cancer Driven by BRAFG469V Mutation Is Targetable by EGFR Kinase Inhibitors. J Thorac Oncol. 2022 02; 17(2):277-288.J Thorac Oncol2021-10-12T00:00:002021Lung Cancer Driven by BRAFG469V Mutation Is Targetable by EGFR Kinase Inhibitors.Authorship 1038417935294868Marcogliese PC, Deal SL, Andrews J, Harnish JM, Bhavana VH, Graves HK, Jangam S, Luo X, Liu N, Bei D, Chao YH, Hull B, Lee PT, Pan H, Bhadane P, Huang MC, Longley CM, Chao HT, Chung HL, Haelterman NA, Kanca O, Manivannan SN, Rossetti LZ, German RJ, Gerard A, Schwaibold EMC, Fehr S, Guerrini R, Vetro A, England E, Murali CN, Barakat TS, van Dooren MF, Wilke M, van Slegtenhorst M, Lesca G, Sabatier I, Chatron N, Brownstein CA, Madden JA, Agrawal PB, Keren B, Courtin T, Perrin L, Brugger M, Roser T, Leiz S, Mau-Them FT, Delanne J, Sukarova-Angelovska E, Trajkova S, Rosenhahn E, Strehlow V, Platzer K, Keller R, Pavinato L, Brusco A, Rosenfeld JA, Marom R, Wangler MF, Yamamoto SCell reportsDrosophila functional screening of de novo variants in autism uncovers damaging variants and facilitates discovery of rare neurodevelopmental diseases. Cell Rep. 2022 03 15; 38(11):110517.Cell Rep2022-03-15T00:00:002022Drosophila functional screening of de novo variants in autism uncovers damaging variants and facilitates discovery of rare neurodevelopmental diseases.Authorship 1050552835822097Tallis E, Karsenty CL, Grimes AB, Karam LB, Elsea SH, Sutton VR, Rawls-Castillo BL, Liu N, Soler-Alfonso CJIMD reportsUntargeted metabolomic profiling in a patient with glycogen storage disease Ib receiving empagliflozin treatment. JIMD Rep. 2022 Jul; 63(4):309-315.JIMD Rep2022-05-22T00:00:002022Untargeted metabolomic profiling in a patient with glycogen storage disease Ib receiving empagliflozin treatment.true1ProfessorProfessorAuthorship 10589921Authorship 1056224136127584Liu N, Sun QMethods in molecular biology (Clifton, N.J.)Laboratory Diagnosis of Cerebral Creatine Deficiency Syndromes by Determining Creatine and Guanidinoacetate in Plasma and Urine. Methods Mol Biol. 2022; 2546:129-140.Methods Mol Biol2022-01-01T00:00:002022Laboratory Diagnosis of Cerebral Creatine Deficiency Syndromes by Determining Creatine and Guanidinoacetate in Plasma and Urine.36127610Liu N, Sun QMethods in molecular biology (Clifton, N.J.)Quantitation of Pyrimidine in Urine by Ultra-Performance Liquid Chromatography-Tandem Mass Spectrometry. Methods Mol Biol. 2022; 2546:431-437.Methods Mol Biol2022-01-01T00:00:002022Quantitation of Pyrimidine in Urine by Ultra-Performance Liquid Chromatography-Tandem Mass Spectrometry.CHARULGIJAVANEKARCHARUL GIJAVANEKAR18911GIJAVANEKAR, CHARULAssistant Professortrue1Assistant ProfessorAssistant Professor37717413Glinton KE, Minard CG, Liu N, Sun Q, Elsea SH, Burrage LC, Nagamani SCSMolecular genetics and metabolismMonitoring the treatment of urea cycle disorders using phenylbutyrate metabolite analyses: Still many lessons to learn. Mol Genet Metab. 2023 11; 140(3):107699.Mol Genet Metab2023-09-11T00:00:002023Monitoring the treatment of urea cycle disorders using phenylbutyrate metabolite analyses: Still many lessons to learn.Authorship 10801233true1ProfessorProfessor