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Kory Keller

Associate Professor of Molecular and Medical Genetics

Oregon Health & Science University

Affiliations

Center Of Child Development And Rehabilitation

Division Of Genetics

Kory Keller is currently serving as a Center Of Child Development And Rehabilitation Associate Professor of Molecular and Medical Genetics at Oregon Health & Science University.

Honors

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Experiences

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Education

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Kory Keller

Oregon Health & Science University

Associate Professor of Molecular and Medical Genetics

You can click a keyword to filter the displayed items

genetics human genetics medical genetics genetic disorders molecular genetics autism neurology immunology hematology neurodevelopmental disorders neuroscience genomics epilepsy medicinal research experimental medicine child neurology intellectual disability mutagenesis genetic basis psychiatric genetics arterial disease rare event estimation microdeletion syndrome schimke immuno-osseous dysplasia hnrnp genes pathogens pathogenesis craniofacial research oral health digestive diseases leukemia clinical transplantation vascular biology attention disorders child psychology biological psychiatry behavioral disorders psychiatric research variant interpretation allelic variant genotype-phenotype association genomic medicine molecular basis developmental anomalies disease gene identification mendelian disorder renal care kidney failure renal function vascular disease angiology vascular adaptation child psychiatry syndromic autism stereotypic movement disorder developmental disorders genotype-phenotype study clinical spectrum neonatal hypotonia molecular delineation missense mutations seizure activity genotype-phenotype analysis pitt-hopkins syndrome shows autism spectrum disorder reciprocal deletion xy sex reversal genetic disturbances spinal features

Notable Scholarly Works

Notable Federal Grants

Collaborators

Additional File 1 of Rare Deleterious Mutations of Hnrnp Genes Result in Shared Neurodevelopmental Disorders. Open MIND (2021)

Madelyn A. GillentineTianyun WangKendra HoekzemaJill RosenfeldPengfei LiuHui GuoChang N. KimBert B. A. De VriesLisenka E. L. M. VissersMagnus NordenskjoldMalin KvarnungAnna LindstrandAnn NordgrenJozef GeczMaria IasconeAnna CeredaAgnese ScatignoSilvia MaitzGinevra ZanniEnrico BertiniChristiane ZweierSarah SchuhmannAntje WiesenerMicah PepperHeena PanjwaniErin TortiFarida AbidIrina AnselmSiddharth SrivastavaPaldeep AtwalCarlos A. BacinoGifty BhatKatherine CobianLynne M. BirdJennifer FriedmanMeredith S. WrightBert CallewaertFlorence PetitSophie MathieuAlexandra AfenjarCelenie K. ChristensenKerry M. WhiteOrly ElpelegItai BergerEdward J. EspineliChristina FagerbergCharlotte Brasch-AndersenLars Kjærsgaard HansenTimothy FeymaSusan HughesIsabelle ThiffaultBonnie SullivanShuang YanKory KellerBoris KerenCyril MignotFrank KooyMarije MeuwissenAlice BasingerMary KukolichMeredith PhilipsLucia OrtegaMargaret Drummond-BorgMathilde LauridsenKristina SorensenAnna LehmanElena Lopez-RangelPaul LevyDavor LesselTimothy LotzeSuneeta Madan-KhetarpalJessica SebastianJodie VentoDivya VatsL. Manace BenmanShane MckeeGhayda M. MirzaaCandace MussJohn PappasHilde PeetersCorrado RomanoMaurizio EliaOrnella GalesiMarleen E. H. SimonKoen L. I. Van GassenKara SimpsonRobert StrattonSabeen SyedJulien ThevenonIrene Valenzuela PalafollAntonio VitobelloMarie BournezLaurence FaivreKun XiaRachel K. EarlTomasz NowakowskiRaphael A. BernierEvan E. Eichler

human geneticshnrnp genesgeneticsrare deleterious mutations

Rare Deleterious Mutations of Hnrnp Genes Result in Shared Neurodevelopmental Disorders. Genome Medicine (2021)

Madelyn A. GillentineTianyun WangKendra HoekzemaJill RosenfeldPengfei LiuHui GuoChang N. KimBert B. A. De VriesLisenka E. L. M. VissersMagnus NordenskjoldMalin KvarnungAnna LindstrandAnn NordgrenJozef GeczMaria IasconeAnna CeredaAgnese ScatignoSilvia MaitzGinevra ZanniEnrico BertiniChristiane ZweierSarah SchuhmannAntje WiesenerMicah PepperHeena PanjwaniErin TortiFarida AbidIrina AnselmSiddharth SrivastavaPaldeep AtwalCarlos A. BacinoGifty BhatKatherine CobianLynne M. BirdJennifer FriedmanMeredith S. WrightBert CallewaertFlorence PetitSophie MathieuAlexandra AfenjarCelenie K. ChristensenKerry M. WhiteOrly ElpelegItai BergerEdward J. EspineliChristina FagerbergCharlotte Brasch-AndersenLars Kjærsgaard HansenTimothy FeymaSusan HughesIsabelle ThiffaultBonnie SullivanShuang YanKory KellerBoris KerenCyril MignotFrank KooyMarije MeuwissenAlice BasingerMary KukolichMeredith PhilipsLucia OrtegaMargaret Drummond-BorgMathilde LauridsenKristina SorensenAnna LehmanElena Lopez-RangelPaul LevyDavor LesselTimothy LotzeSuneeta Madan-KhetarpalJessica SebastianJodie VentoDivya VatsL. Manace BenmanShane MckeeGhayda M. MirzaaCandace MussJohn PappasHilde PeetersCorrado RomanoMaurizio EliaOrnella GalesiMarleen E. H. SimonKoen L. I. van GassenKara SimpsonRobert StrattonSabeen SyedJulien ThevenonIrene Valenzuela PalafollAntonio VitobelloMarie BournezLaurence FaivreKun XiaJohn AcampadoAndrea J. AceAlpha AmatyaIrina AstrovskayaAsif BasharElizabeth Brooks

geneticsgenomic medicinehnrnp genesgenomicsmolecular basisneurodevelopmental disordersgenetic disorders

Autism and Attention‐Deficit/Hyperactivity Disorders and Symptoms in Children With Neurofibromatosis Type 1. Developmental Medicine & Child Neurology (2020)

Hadley MorottiSarah MastelKory KellerRebecca A BarnardTrevor HallBrian J O'RoakEric Fombonne

cognitive impairmentautismchild psychiatrycognitive developmentmental healthneurodevelopmental disorderschild neurologyneurologyattention disorderschild psychologychild development

Autism Questionnaire Scores Do Not Only Rise Because of Autism. Developmental Medicine & Child Neurology (2020)

Eric FombonneHadley MorottiSarah MastelKory KellerRebecca A BarnardTrevor HallBrian J O’Roak

psychologyautism questionnaire scoresautismchild neurology

Clinical Spectrum of Individuals With Pathogenic N F1 Missense Variants Affecting P.Met1149, P.Arg1276, and P.Lys1423: Genotype–Phenotype Study in Neurofibromatosis Type 1. Human Mutation (2019)

Magdalena KoczkowskaTom CallensYunjia ChenAlicia GomesAlesha D. HicksAngela SharpEric JohnsKim Armfield UhasLinlea ArmstrongKatherine Armstrong BosankoDusica Babovic‐VuksanovicLaura BakerDonald G. BaselMario BengalaJames T. BennettChelsea ChambersLola K. ClarksonMaurizio ClementiFanny M. CortésMitch CunninghamM. Daniela D'AgostinoMartin B. DelatyckiMaria C. DigilioLaura DosaSilvia EspositoStephanie FoxMary‐Louise FreckmannChristine FauthTeresa GiuglianoSandra GiustiniAllison GoetschYael GoldbergRobert S. GreenwoodCristin GriffisKaren W. GrippPunita GuptaEric HaanRachel K. HachenTamara L. HaygarthConcepción Hernández‐ChicoKatelyn HodgeRobert J. HopkinLouanne HudginsSandra JanssensKory KellerGeraldine Kelly‐MancusoAaina KochharBruce R. KorfAndrea M. LewisJan LiebeltAngie LichtyRobert H. ListernickMichael J. LyonsIsabelle MaystadtMayra Martinez OjedaCarey McDougallLesley K. McGregorDaniela MelisNancy MendelsohnMalgorzata J.M. NowaczykJune OrtenbergKarin PanzerJohn G. PappasMary Ella PierpontGiulio PilusoValentina PinnaEniko K. PivnickDinel A. PondCynthia M. PowellCaleb RogersNoa Ruhrman ShaharS. Lane RutledgeVeronica SalettiSarah A. SandaraduraClaudia SantoroUlrich A. SchatzAllison SchreiberDaryl A. ScottElizabeth A. SellarsRuth ShefferElizabeth SiqvelandJohn M. SlopisRosemarie SmithAlberto SpaliceDavid W. StocktonHaley StreffAmy TheosGail E. TomlinsonGrace TranPamela L. TrapaneEva TrevissonNicole J. UllrichJenneke Van den EndeSamantha A. Schrier VerganoStephanie E. WallaceMichael F. WanglerDavid D. WeaverKaleb H. YohayElaine ZackaiJonathan Zonana

variant interpretationgeneticshuman geneticspathogenesisgenotype-phenotype associationclinical spectrumpathogensneurologyallelic variantgenotype-phenotype studygenetic variationpathology

The Association of Neurofibromatosis and Autism Symptomatology is Confounded by Behavioral Problems. medRxiv (2019)

autism symptomatologypsychiatryneuropathologyautismbiological psychiatryabnormal child psychologypsychiatric researchneurosciencedevelopmental disorderspsychopathologybehavioral disordersneuropsychologyneurodevelopmental disordersbehavioral problemssyndromic autismpsychologydevelopmental psychopathologystereotypic movement disorder

De Novo Apparent Loss-Of-Function Mutations in Prr12 in Three Patients With Intellectual Disability and Iris Abnormalities. Human Genetics (2018)

Magalie S. LeducMarianne McguireSuneeta Madan-KhetarpalDamara OrtizSusan HayflickKory KellerChristine M. EngYaping YangWeimin Bi

geneticsintellectual disabilitymolecular geneticsiris abnormalitiesmedical geneticshuman geneticsapparent loss-of-function mutations

Two De Novo Novel Mutations in One Shank3 Allele in a Patient With Autism and Moderate Intellectual Disability. American Journal of Medical Genetics Part A (2018)

Wenmiao ZhuJianli LiStella ChenJinglan ZhangFrancesco VetriniAlicia BraxtonChristine M. EngYaping YangFan XiaKory L. KellerLeila Okinaka‐HuChung LeeJ. Lloyd HolderWeimin Bi

geneticsintellectual disabilitynovel mutationsautismpsychiatric geneticsmoderate intellectual disabilitygenetic basismedical geneticsgenetic disordershuman genetics

Puf60 Variants Cause a Syndrome of Id, Short Stature, Microcephaly, Coloboma, Craniofacial, Cardiac, Renal and Spinal Features. European Journal of Human Genetics (2017)

geneticsmedicinepuf60 variantsspinal featuresdisease gene identificationanatomical pathologydevelopmental anomaliescraniofacial researchshort staturemedical geneticsgenetic disordershuman geneticsmendelian disorder

Increased Wnt and Notch Signaling: A Clue to the Renal Disease in Schimke Immuno-Osseous Dysplasia?. Orphanet Journal of Rare Diseases (2016)

Marie MorimotoClara MyungKimberly BeirnesKunho ChoiYumi AsakuraArend BokenkampDominique BonneauMilena BrugnaraJoel CharrowEstelle ColinAmira DavisGeorges DeschenesMattia GentileMario GiordanoAndrew K. GormleyRajeshree GovenderMark JosephKory KellerEvelyne LerutElena LevtchenkoLaura MassellaChristy MayfieldBehzad NajafianDavid ParhamJurgen SprangerPeter StenzelUluc YisZhongxin YuJonathan ZonanaGlenda HendsonCornelius F. Boerkoel

rare event estimationpediatricsleukemiarenal functionchronic kidney diseasestrokenotch signalingrenal diseaserenal caregeneticsdigestive diseasesclinical transplantationkidney failureclinical epidemiologyarterial diseaseimmunologynephrologymedicinal researchhematologyexperimental medicine

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Kory Keller

Associate Professor of Molecular and Medical Genetics

Oregon Health & Science University

Affiliations

Center Of Child Development And Rehabilitation

Division Of Genetics

Kory Keller is currently serving as a Center Of Child Development And Rehabilitation Associate Professor of Molecular and Medical Genetics at Oregon Health & Science University.

Honors

Create free account to unlock more features

Experiences

Create free account to unlock more features

Education

Create free account to unlock more features

Kory Keller

Oregon Health & Science University

Associate Professor of Molecular and Medical Genetics

You can click a keyword to filter the displayed items

Notable Scholarly Works

Notable Federal Grants

Collaborators

Additional File 1 of Rare Deleterious Mutations of Hnrnp Genes Result in Shared Neurodevelopmental Disorders. Open MIND (2021)

human geneticshnrnp genesgeneticsrare deleterious mutations

Rare Deleterious Mutations of Hnrnp Genes Result in Shared Neurodevelopmental Disorders. Genome Medicine (2021)

Madelyn A. GillentineTianyun WangKendra HoekzemaJill RosenfeldPengfei LiuHui GuoChang N. KimBert B. A. De VriesLisenka E. L. M. VissersMagnus NordenskjoldMalin KvarnungAnna LindstrandAnn NordgrenJozef GeczMaria IasconeAnna CeredaAgnese ScatignoSilvia MaitzGinevra ZanniEnrico BertiniChristiane ZweierSarah SchuhmannAntje WiesenerMicah PepperHeena PanjwaniErin TortiFarida AbidIrina AnselmSiddharth SrivastavaPaldeep AtwalCarlos A. BacinoGifty BhatKatherine CobianLynne M. BirdJennifer FriedmanMeredith S. WrightBert CallewaertFlorence PetitSophie MathieuAlexandra AfenjarCelenie K. ChristensenKerry M. WhiteOrly ElpelegItai BergerEdward J. EspineliChristina FagerbergCharlotte Brasch-AndersenLars Kjærsgaard HansenTimothy FeymaSusan HughesIsabelle ThiffaultBonnie SullivanShuang YanKory KellerBoris KerenCyril MignotFrank KooyMarije MeuwissenAlice BasingerMary KukolichMeredith PhilipsLucia OrtegaMargaret Drummond-BorgMathilde LauridsenKristina SorensenAnna LehmanElena Lopez-RangelPaul LevyDavor LesselTimothy LotzeSuneeta Madan-KhetarpalJessica SebastianJodie VentoDivya VatsL. Manace BenmanShane MckeeGhayda M. MirzaaCandace MussJohn PappasHilde PeetersCorrado RomanoMaurizio EliaOrnella GalesiMarleen E. H. SimonKoen L. I. van GassenKara SimpsonRobert StrattonSabeen SyedJulien ThevenonIrene Valenzuela PalafollAntonio VitobelloMarie BournezLaurence FaivreKun XiaJohn AcampadoAndrea J. AceAlpha AmatyaIrina AstrovskayaAsif BasharElizabeth Brooks

geneticsgenomic medicinehnrnp genesgenomicsmolecular basisneurodevelopmental disordersgenetic disorders

Autism and Attention‐Deficit/Hyperactivity Disorders and Symptoms in Children With Neurofibromatosis Type 1. Developmental Medicine & Child Neurology (2020)

Hadley MorottiSarah MastelKory KellerRebecca A BarnardTrevor HallBrian J O'RoakEric Fombonne

cognitive impairmentautismchild psychiatrycognitive developmentmental healthneurodevelopmental disorderschild neurologyneurologyattention disorderschild psychologychild development

Autism Questionnaire Scores Do Not Only Rise Because of Autism. Developmental Medicine & Child Neurology (2020)

Eric FombonneHadley MorottiSarah MastelKory KellerRebecca A BarnardTrevor HallBrian J O’Roak

psychologyautism questionnaire scoresautismchild neurology

Clinical Spectrum of Individuals With Pathogenic N F1 Missense Variants Affecting P.Met1149, P.Arg1276, and P.Lys1423: Genotype–Phenotype Study in Neurofibromatosis Type 1. Human Mutation (2019)

variant interpretationgeneticshuman geneticspathogenesisgenotype-phenotype associationclinical spectrumpathogensneurologyallelic variantgenotype-phenotype studygenetic variationpathology

The Association of Neurofibromatosis and Autism Symptomatology is Confounded by Behavioral Problems. medRxiv (2019)

De Novo Apparent Loss-Of-Function Mutations in Prr12 in Three Patients With Intellectual Disability and Iris Abnormalities. Human Genetics (2018)

Magalie S. LeducMarianne McguireSuneeta Madan-KhetarpalDamara OrtizSusan HayflickKory KellerChristine M. EngYaping YangWeimin Bi

geneticsintellectual disabilitymolecular geneticsiris abnormalitiesmedical geneticshuman geneticsapparent loss-of-function mutations

Two De Novo Novel Mutations in One Shank3 Allele in a Patient With Autism and Moderate Intellectual Disability. American Journal of Medical Genetics Part A (2018)

Wenmiao ZhuJianli LiStella ChenJinglan ZhangFrancesco VetriniAlicia BraxtonChristine M. EngYaping YangFan XiaKory L. KellerLeila Okinaka‐HuChung LeeJ. Lloyd HolderWeimin Bi

geneticsintellectual disabilitynovel mutationsautismpsychiatric geneticsmoderate intellectual disabilitygenetic basismedical geneticsgenetic disordershuman genetics

Puf60 Variants Cause a Syndrome of Id, Short Stature, Microcephaly, Coloboma, Craniofacial, Cardiac, Renal and Spinal Features. European Journal of Human Genetics (2017)

Increased Wnt and Notch Signaling: A Clue to the Renal Disease in Schimke Immuno-Osseous Dysplasia?. Orphanet Journal of Rare Diseases (2016)

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