Faculty

Institution

Unit

Venue

Karen Weck

Professor

University of North Carolina at Chapel Hill

Affiliations

School of Medicine

Pathology and Laboratory Medicine

Karen Weck is currently serving as a Pathology And Laboratory Medicine Professor at University of North Carolina At Chapel Hill.

Honors

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Experiences

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Karen Weck

University of North Carolina at Chapel Hill

Professor

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genetics genomics medicine pharmacology molecular diagnostics medical genetics human genetics oncology clinical research molecular biology bioinformatics cancer research genome sequencing hematology genome biology laboratory medicine molecular genetics respiratory medicine next-generation sequencing cancer biology pharmacotherapy cancer genomics molecular pathology cancer care medicinal research dna sequencing genomic medicine pharmacogenomics percutaneous coronary intervention cardiovascular interventions cancer genetics neonatology clinical implementation cytogenetics clinical microbiology molecular cancer obstetrics and gynaecology histopathology clinical pharmacology genome analysis genetic disorders clinical outcomes primary ciliary dyskinesia exome sequencing angiology cancer treatment precision medicine allelic variant clinical evidence viral diagnostics colorectal cancer germline variants molecular genetic testing cancer imaging thoracic oncology pharmacological research mammalian biology population genomics clinical mycology clinical toxicology digital archives medical microbiology electronic health records computational genomics pharmacokinetics abnormal development multicenter study allele selection genomic sequencing warfarin sensitivity antiplatelet therapy laboratory performance laboratory standards american pathologists genetic variants african-american individuals pathology personalized medicine

Notable Scholarly Works

Notable Federal Grants

Collaborators

CORRECTION: Foss Et Al. the Rise of Population Genomic Screening: Characteristics of Current Programs and the Need for Evidence Regarding Optimal Implementation. J. Pers. Med. 2022, 12, 692. Carolina Digital Repository (University of North Carolina at Chapel Hill) (2024)

Foss, Kimberly S.O’Daniel, Julianne M.Berg, Jonathan S.Powell, Sabrina N.Cadigan, Rosemary JeanKuczynski, Kristine J.Milko, Laura V.Saylor, Katherine W.Roberts, MeganWeck, KarenHenderson, Gail E.

public healthmedicineoptimal implementationpersonalized medicinepopulation genomic screeningcurrent programshealth sciences

Dpyd Genotyping Recommendations. Journal of Molecular Diagnostics (2024)

Victoria M. PrattLarisa H. CavallariMakenzie L. FulmerAndrea GaedigkHouda HachadYuan JiLisa V. KalmanReynold C. LyAnn M. MoyerStuart A. ScottAmy J. TurnerRon H.N. van SchaikMichelle Whirl-CarrilloKaren E. Weck

genomicsgenome biologyimaging genomicsgene expressionfunctional genomicsnext-generation sequencinggenomic medicinebiomarker discoverysystems biologygeneticsclinical proteomicscomputational genomicsnucleic acidsmolecular diagnosticsmolecular biologymolecular informaticshuman geneticsbioinformatics

Editorial Board. Brachytherapy (2024)

A SyedMichael ZelefskyBethany AndersonGastrointestinal StrnadSteven FrankMatthew HarkenriderMitchell KamravaEye HeadPhillip DevlinChirag ShahGilad CohenMark RivardInvited FeaturesScott GlaserUsa TheranosticsNeil TaunkJaroslaw HepelJean Michael Hannoun-LeviFrance GastrointestinalPeter HassAlexandra StewartAmandeep TaggarMira KeyesGerard MortonPeter OrioChad TangEmma FieldsEric LeungWilliam SmallNeck SkinAngeles RovirosaLuca TagliaferriNikhil JoshiMartin TomAntonio DamatoChristopher DeufelDaniel ScanderbegDavid Aramburu NúñezIvan BuzurovicMauricio CambeiroMark CorkumJean-Marc CossetBrett CoxJuanita CrookJoao LuisDa SilvaBrian DavisLaura DoylePatricia EifelShirin EngerGabriel FonsecaRazvan GalalaeJose GuinotChristina GutiérrezLara HathoutEric HorwitzPeter HoskinJun ItamiChristian KirisitsManon KisselMarisa KollmeierRajat KudchadkerUsama MahmoodPatrick MclaughlinKevin MartellCanada Victor Munoz-GarzonBradley PietersCsaba PolgarAron PopovtzerLouis PottersBradley PrestidgeMarcus RandallSusan RichardsonMack RoachSimona ShaitelmanFrank-Andre SiebertNelson StoneEric VigneaultAkila ViswanathanTe VuongJunjie WangChina WernickeCatheryn YasharAtsunori YoruzuDavid Newcombe

Wdr44 Loss‐of‐Function Promoter Deletion in a Male Newborn With a Ciliopathy Phenotype. American Journal of Medical Genetics Part A (2024)

Tam P. SneddonKelly L. GilmoreMai XiongKaren E. WeckBradford C. PowellNeeta L. Vora

ciliopathy phenotypegeneticsmedical geneticshuman geneticsgenetic disorders

P735: Structural Variant Analysis Unveils Loss-Of-Function Promoter Deletion in Candidate Gene Wdr44. Genetics in Medicine Open (2024)

Tam SneddonMai XiongKelly GilmoreKaren WeckBradford PowellNeeta Vora

genomicsmedicinegeneticsmolecular geneticsepigeneticsmedical geneticshuman genetics

Abrogation of Map4K4 Protein Function Causes Congenital Anomalies in Humans and Zebrafish. Science Advances (2023)

Victoria PattersonFarid UllahLaura BryantDong LiJohn N. GriffinAlpa SidhuSheila SaligananMackenzie BlaileMargarita S. SaenzRosemarie SmithSara EllingwoodDorothy K. GrangeXuyun HuMaimaiti MireguliYanfei LuoYiping ShenMaureen MulhernElaine ZackaiAlyssa RitterKosuke IzumiJulia HoefeleMatias WagnerKorbinian M. RiedhammerBarbara SeitzNathaniel H. RobinDana GoodloeCyril MignotBoris KerenHelen CoxJoanna JarvisMaja HempelCynthia Forster GibsonFrederic Tran Mau-ThemAntonio VitobelloAnge-Line BruelArthur SorlinSarju MehtaF. Lucy RaymondKelly GilmoreBradford C. PowellKaren WeckChumei LiAnneke T. Vulto-van SilfhoutThea GiacominiMaria Margherita MancardiAndrea AccogliVincenzo SalpietroFederico ZaraNeeta L. VoraErica E. DavisRebecca D. BurdineElizabeth Bhoj

congenital anomaliesprotein geneticsgeneticsmammalian biologydevelopmental geneticsscience advancedevelopmental biologyabnormal developmenthuman genetics

Association of Deep Phenotyping With Diagnostic Yield of Prenatal Exome Sequencing for Fetal Brain Abnormalities. Genetics in Medicine (2023)

Kathleen A. DrexlerAsha N. TalatiKelly L. GilmoreRachel V. VeazeyBradford C. PowellKaren E. WeckErica E. DavisNeeta L. Vora

genomicsgenome biologymedicinediagnostic yieldgeneticsgenome analysisgenome sequencingmolecular diagnosticsdevelopmental biologymedical geneticsdeep phenotypingprenatal exomeneonatologyfetal brain abnormalitiesbioinformatics

Cyp3A4 and Cyp3A5 Genotyping Recommendations. Journal of Molecular Diagnostics (2023)

Victoria M. PrattLarisa H. CavallariMakenzie L. FulmerAndrea GaedigkHouda HachadYuan JiLisa V. KalmanReynold C. LyAnn M. MoyerStuart A. ScottRon H.N. van SchaikMichelle Whirl-CarrilloKaren E. Weck

molecular diagnosticsdiagnosismolecular biologypharmacology

Public Interest in Population Genetic Screening for Cancer Risk. Frontiers in Genetics (2022)

Megan C. RobertsKimberly S. FossGail E. HendersonSabrina N. PowellKatherine W. SaylorKaren E. WeckLaura V. Milko

public healthgeneticspublic interestpopulation genetic screeningcancer riskpopulation geneticshealth policy

The Rise of Population Genomic Screening: Characteristics of Current Programs and the Need for Evidence Regarding Optimal Implementation. Journal of Personalized Medicine (2022)

Kimberly FossJulianne O’DanielJonathan BergSabrina PowellRosemary CadiganKristine KuczynskiLaura MilkoKatherine SaylorMegan RobertsKaren WeckGail Henderson

public healthmedicineoptimal implementationpersonalized medicinepopulation genomic screeningcurrent programspopulation genomicshealth sciences

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Karen Weck

Professor

University of North Carolina at Chapel Hill

Affiliations

School of Medicine

Pathology and Laboratory Medicine

Karen Weck is currently serving as a Pathology And Laboratory Medicine Professor at University of North Carolina At Chapel Hill.

Honors

Create free account to unlock more features

Experiences

Create free account to unlock more features

Education

Create free account to unlock more features

Karen Weck

University of North Carolina at Chapel Hill

Professor

You can click a keyword to filter the displayed items

Notable Scholarly Works

Notable Federal Grants

Collaborators

Foss, Kimberly S.O’Daniel, Julianne M.Berg, Jonathan S.Powell, Sabrina N.Cadigan, Rosemary JeanKuczynski, Kristine J.Milko, Laura V.Saylor, Katherine W.Roberts, MeganWeck, KarenHenderson, Gail E.

public healthmedicineoptimal implementationpersonalized medicinepopulation genomic screeningcurrent programshealth sciences

Dpyd Genotyping Recommendations. Journal of Molecular Diagnostics (2024)

Editorial Board. Brachytherapy (2024)

Wdr44 Loss‐of‐Function Promoter Deletion in a Male Newborn With a Ciliopathy Phenotype. American Journal of Medical Genetics Part A (2024)

Tam P. SneddonKelly L. GilmoreMai XiongKaren E. WeckBradford C. PowellNeeta L. Vora

ciliopathy phenotypegeneticsmedical geneticshuman geneticsgenetic disorders

P735: Structural Variant Analysis Unveils Loss-Of-Function Promoter Deletion in Candidate Gene Wdr44. Genetics in Medicine Open (2024)

Tam SneddonMai XiongKelly GilmoreKaren WeckBradford PowellNeeta Vora

genomicsmedicinegeneticsmolecular geneticsepigeneticsmedical geneticshuman genetics

Abrogation of Map4K4 Protein Function Causes Congenital Anomalies in Humans and Zebrafish. Science Advances (2023)

congenital anomaliesprotein geneticsgeneticsmammalian biologydevelopmental geneticsscience advancedevelopmental biologyabnormal developmenthuman genetics

Association of Deep Phenotyping With Diagnostic Yield of Prenatal Exome Sequencing for Fetal Brain Abnormalities. Genetics in Medicine (2023)

Kathleen A. DrexlerAsha N. TalatiKelly L. GilmoreRachel V. VeazeyBradford C. PowellKaren E. WeckErica E. DavisNeeta L. Vora

Cyp3A4 and Cyp3A5 Genotyping Recommendations. Journal of Molecular Diagnostics (2023)

Victoria M. PrattLarisa H. CavallariMakenzie L. FulmerAndrea GaedigkHouda HachadYuan JiLisa V. KalmanReynold C. LyAnn M. MoyerStuart A. ScottRon H.N. van SchaikMichelle Whirl-CarrilloKaren E. Weck

molecular diagnosticsdiagnosismolecular biologypharmacology

Public Interest in Population Genetic Screening for Cancer Risk. Frontiers in Genetics (2022)

Megan C. RobertsKimberly S. FossGail E. HendersonSabrina N. PowellKatherine W. SaylorKaren E. WeckLaura V. Milko

public healthgeneticspublic interestpopulation genetic screeningcancer riskpopulation geneticshealth policy

The Rise of Population Genomic Screening: Characteristics of Current Programs and the Need for Evidence Regarding Optimal Implementation. Journal of Personalized Medicine (2022)

Kimberly FossJulianne O’DanielJonathan BergSabrina PowellRosemary CadiganKristine KuczynskiLaura MilkoKatherine SaylorMegan RobertsKaren WeckGail Henderson

public healthmedicineoptimal implementationpersonalized medicinepopulation genomic screeningcurrent programspopulation genomicshealth sciences

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