Faculty

Institution

Unit

Venue

Wayne W. Grody

Professor

University of California, Los Angeles

Affiliations

David Geffen School of Medicine

Human Genetics

the College

Society and Genetics

Wayne W. Grody is currently serving as a David Geffen School Of Medicine Professor at University of California, Los Angeles.

Honors

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Experiences

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Education

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Wayne W. Grody

University of California, Los Angeles

Professor

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genetics genomics medical genetics molecular genetics human genetics molecular biology medicine mammalian biology genome biology molecular diagnostics health sciences hematology cystic fibrosis genetic testing membrane biology population genetics bioinformatics medicinal research genetic disorders genome sequencing molecular physiology protein science laboratory medicine cancer genetics dna sequencing applied genetics animal physiology neonatology developmental genetics prenatal diagnosis disease progression next-generation sequencing clinical exome liver physiology variant interpretation knockout mice genetic counseling somatic cell genetics molecular pathology cytogenetics incidental findings acmg recommendations arginase deficiency pharmacogenetic biomarkers molecular cell biology intellectual disability respiratory medicine biochemical sciences oncogenes avian biology bone research genome analysis host genetics mutagenesis global developmental delay tissue physiology cardiomyopathy quality control protein genetics mammalian physiology gene function clinical neurology maternal plasma laboratory standards mouse model mouse tissues technical standards early hearing detection autism spectrum disorder mendelian disorder reporting standard benchmark studies sequence variants joint consensus recommendation rare mendelian disorders genetic identification pathology forensic genetics diagnosis disease gene identification disease susceptibility gene expression

Video Presentations

Notable Scholarly Works

Notable Federal Grants

Collaborators

High-Throughput Genomics Identify Novel Fbn1/2 Variants in Severe Neonatal Marfan Syndrome and Congenital Heart Defects. International Journal of Molecular Sciences (2024)

Gloria ZodanuJohn HwangZubin MehtaCarlos SisniegaAlexander BarsegianXuedong KangReshma BiniwaleMing-Sing SiGary SatouNancy HalnonWayne GrodyGlen Van ArsdellStanley NelsonMarlin Touma

genome analysisgenomicsgenome biologydevelopmental biologymolecular geneticsmolecular biologyhuman geneticshigh-throughput genomicscomputational genomicsmedical geneticsbioinformaticsgenetics

P672: Commercial Cystic Fibrosis Carrier Screening Tests and Coverage of the Acmg 100 Recommended Variants. Genetics in Medicine Open (2024)

Timothy TidwellAnthony GreggWayne GrodyMichael GuoHutton KearneyKristin MonaghanJennifer TaylorCinthya Zepeda MendozaCatherine ZiatsJoshua DeignanKaren Raraigh

cystic fibrosisgenomicsapplied geneticsmedicinemedical geneticsgenetic testinggenetics

A Primer on Gene Editing: What Does It Mean for Pathologists?. Archives of Pathology & Laboratory Medicine (2023)

Allison Cushman-VokounRyan J. SchmidtMatthew Charles HiemenzMark FungBing Melody ZhangGeorganne BradshawManish GandhiJinJuan YaoSophia YoheAmy BeckmanWayne W. GrodyPetros Giannikopoulos

gene editingpathologylaboratory medicine

Large-Scale Whole Genome Sequence Analysis of 22,000 Subjects Provides No Evidence of Fmr1 Premutation Allele Involvement in Autism Spectrum Disorder. Genes (2023)

Alex ChubickEvan WangCora AuWayne W. GrodyRoel A. Ophoff

autism spectrum disordergenome sequencinggenomicsgenetics

Updated Recommendations for Cftr Carrier Screening: A Position Statement of the American College of Medical Genetics and Genomics (Acmg). Genetics in Medicine (2023)

Joshua L. DeignanAnthony R. GreggWayne W. GrodyMichael H. GuoHutton KearneyKristin G. MonaghanKaren S. RaraighJennifer TaylorCinthya J. Zepeda-MendozaCatherine Ziats

updated recommendationscftr carrier screeninggenomicsposition statementmedical geneticsgenetics

Central 22Q11.2 Deletion ( Lcr22 B‐D ) in a Fetus With Severe Fetal Growth Restriction and a Mother With Severe Systemic Lupus Erythematosus: Further Evidence of Crkl Haploinsufficiency in the Pathogenesis of 22Q11.2 Deletion Syndrome. American Journal of Medical Genetics Part A (2021)

Isabella LinYalda AfsharJeffrey GoldsteinJennifer GrossmanWayne W. GrodyFabiola Quintero‐Rivera

deletion syndromematernal-fetal medicineimmunologyfurther evidencehematologyhla typingdevelopmental biologypopulation geneticsmedical geneticsgenetics

Integrated Genomics Analysis Identifies Recessive Ciliopathy Mutations in Primary Endocardial Fibroelastosis: A Rare Neonatal Cardiomyopathy. Research Square (2021)

Yan ZhaoWang Lee-KaiAscia EskinXuedong KangViviana M. FajardoZubin MehtaStacy PinelesRyan J. SchmidtAaron NagielGary SatouMeena GargMyke FedermanLeigh C. ReardonSteven L. LeeReshma BiniwaleWayne W. GrodyNancy HalnonNegar KhanlouFabiola Quintero-RiveraJuan C. AlejosAtsushi NakanoGregory A. FishbeinGlen S. Van ArsdellStanley F. NelsonMarlin Touma

ciliopathy mutationspediatricsprimary endocardial fibroelastosisgenomicshematologydisease gene identificationmolecular geneticscancer geneticsmolecular biologyhuman geneticsgene expressionmedical geneticsgenetics

Recessive Ciliopathy Mutations in Primary Endocardial Fibroelastosis: A Rare Neonatal Cardiomyopathy in a Case of Alstrom Syndrome. Journal of Molecular Medicine (2021)

Yan ZhaoLee-kai WangAscia EskinXuedong KangViviana M. FajardoZubin MehtaStacy PinelesRyan J. SchmidtAaron NagielGary SatouMeena GargMyke FedermanLeigh C. ReardonSteven L. LeeReshma BiniwaleWayne W. GrodyNancy HalnonNegar KhanlouFabiola Quintero-RiveraJuan C. AlejosAtsushi NakanoGregory A. FishbeinGlen S. Van ArsdellStanley F. NelsonMarlin Touma

disease progressionalstrom syndromeneuroscienceprimary endocardial fibroelastosisgeneticscell and molecular biologyrecessive ciliopathy mutationshematologymolecular sciencemolecular biologycerebrovascular diseasecardiomyopathycardiologyearly diagnosistranslational medicinemolecular diagnosticsmolecular medicinemolecular virologymammalian biology

Response to Biesecker Et Al.. The American Journal of Human Genetics (2021)

Ada HamoshJoanna S. AmbergerCarol A. BocchiniJoann BodurthaCarol J. BultChristopher G. ChuteGarry R. CuttingHarry C. DietzHelen V. FirthRichard A. GibbsWayne W. GrodyMelissa A. HaendelJames R. LupskiJennifer E. PoseyPeter N. RobinsonLynn M. SchrimlAlan F. ScottNara L. SobreiraDavid ValleNan WuSonja A. Rasmussen

human geneticsgenetics

A Diagnostic Ceiling for Exome Sequencing in Cerebellar Ataxia and Related Neurological Disorders (2006). Neurology (2020)

Kathie NgoJessica RexachHane LeeLauren PettySusan PerlmanJuliana ValeraJoshua DeignanYuanming MaoMamdouh AkerJennifer PoseyShalini JhangianiZeynep Coban-AkdemirEric BoerwinkleDonna MuznyAlexandra NelsonSharon Hassin-BaerGemma PokeKatherine NeasMichael GeschwindWayne GrodyRichard GibbsDaniel GeschwindJames LupskiJennifer BelowStanley NelsonBrent Fogel

neurologydna sequencinggenomicsneuroscienceexome sequencingmolecular diagnosticsdiagnostic ceilingcerebellar ataxiagenetics

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Wayne W. Grody

Professor

University of California, Los Angeles

Affiliations

David Geffen School of Medicine

Human Genetics

the College

Society and Genetics

Wayne W. Grody is currently serving as a David Geffen School Of Medicine Professor at University of California, Los Angeles.

Honors

Create free account to unlock more features

Experiences

Create free account to unlock more features

Education

Create free account to unlock more features

Wayne W. Grody

University of California, Los Angeles

Professor

You can click a keyword to filter the displayed items

Video Presentations

Notable Scholarly Works

Notable Federal Grants

Collaborators

High-Throughput Genomics Identify Novel Fbn1/2 Variants in Severe Neonatal Marfan Syndrome and Congenital Heart Defects. International Journal of Molecular Sciences (2024)

Gloria ZodanuJohn HwangZubin MehtaCarlos SisniegaAlexander BarsegianXuedong KangReshma BiniwaleMing-Sing SiGary SatouNancy HalnonWayne GrodyGlen Van ArsdellStanley NelsonMarlin Touma

genome analysisgenomicsgenome biologydevelopmental biologymolecular geneticsmolecular biologyhuman geneticshigh-throughput genomicscomputational genomicsmedical geneticsbioinformaticsgenetics

P672: Commercial Cystic Fibrosis Carrier Screening Tests and Coverage of the Acmg 100 Recommended Variants. Genetics in Medicine Open (2024)

Timothy TidwellAnthony GreggWayne GrodyMichael GuoHutton KearneyKristin MonaghanJennifer TaylorCinthya Zepeda MendozaCatherine ZiatsJoshua DeignanKaren Raraigh

cystic fibrosisgenomicsapplied geneticsmedicinemedical geneticsgenetic testinggenetics

A Primer on Gene Editing: What Does It Mean for Pathologists?. Archives of Pathology & Laboratory Medicine (2023)

Allison Cushman-VokounRyan J. SchmidtMatthew Charles HiemenzMark FungBing Melody ZhangGeorganne BradshawManish GandhiJinJuan YaoSophia YoheAmy BeckmanWayne W. GrodyPetros Giannikopoulos

gene editingpathologylaboratory medicine

Large-Scale Whole Genome Sequence Analysis of 22,000 Subjects Provides No Evidence of Fmr1 Premutation Allele Involvement in Autism Spectrum Disorder. Genes (2023)

Alex ChubickEvan WangCora AuWayne W. GrodyRoel A. Ophoff

autism spectrum disordergenome sequencinggenomicsgenetics

Updated Recommendations for Cftr Carrier Screening: A Position Statement of the American College of Medical Genetics and Genomics (Acmg). Genetics in Medicine (2023)

Joshua L. DeignanAnthony R. GreggWayne W. GrodyMichael H. GuoHutton KearneyKristin G. MonaghanKaren S. RaraighJennifer TaylorCinthya J. Zepeda-MendozaCatherine Ziats

updated recommendationscftr carrier screeninggenomicsposition statementmedical geneticsgenetics

Isabella LinYalda AfsharJeffrey GoldsteinJennifer GrossmanWayne W. GrodyFabiola Quintero‐Rivera

deletion syndromematernal-fetal medicineimmunologyfurther evidencehematologyhla typingdevelopmental biologypopulation geneticsmedical geneticsgenetics

Integrated Genomics Analysis Identifies Recessive Ciliopathy Mutations in Primary Endocardial Fibroelastosis: A Rare Neonatal Cardiomyopathy. Research Square (2021)

Recessive Ciliopathy Mutations in Primary Endocardial Fibroelastosis: A Rare Neonatal Cardiomyopathy in a Case of Alstrom Syndrome. Journal of Molecular Medicine (2021)

Response to Biesecker Et Al.. The American Journal of Human Genetics (2021)

human geneticsgenetics

A Diagnostic Ceiling for Exome Sequencing in Cerebellar Ataxia and Related Neurological Disorders (2006). Neurology (2020)

neurologydna sequencinggenomicsneuroscienceexome sequencingmolecular diagnosticsdiagnostic ceilingcerebellar ataxiagenetics

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