Faculty

Institution

Unit

Venue

Matt Wright

Lecturer CCRMA

Stanford University

Affiliations

School of Humanities and Sciences

Music

Matt Wright is currently serving as a Music Lecturer CCRMA at Stanford University.

Honors

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Experiences

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Education

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Matt Wright

Stanford University

Lecturer CCRMA

You can click a keyword to filter the displayed items

genetics genomics bioinformatics molecular biology genomic medicine medical genetics medicine data science genome biology variant interpretation disease classification personalized medicine metabolism molecular genetics human genetics health informatics machine learning biomedical informatics scientific data cancer care music psychology evidence-based recommendations biomedical data analysis biomedical data science scientific data management biomedical data integration radiation biology cancer genomics cancer biology cytogenetics cancer genetics translational bioinformatics psychophysics auditory science psychoacoustics evidence criteria variant classification platform inborn errors phenylalanine hydroxylase gene sequence variant interpretation clingen data platforms clingen data platform expression profiling accurate prediction irradiation-induced dna damage clinical variant classification altered auditory feedback musical rhythm design musical expression sound design audio interface ethnomusicology music generation computer music graphic interface music music technology (electronic and digital) music information retrieval

Video Presentations

Notable Scholarly Works

Notable Federal Grants

Collaborators

Generating Clinical-Grade Gene–Disease Validity Classifications Through the Clingen Data Platforms. Annual Review of Biomedical Data Science (2024)

Matt W. WrightCourtney L. ThaxtonTristan NelsonMarina T. DiStefanoJuliann M. SavattMatthew H. BrushGloria CheungMark E. MandellBryan WulfTJ WardScott GoehringerTerry O'NeillPhil WellerChristine G. PrestonIngrid M. KeselerJennifer L. GoldsteinNatasha T. StrandeJennifer McGlaughonDanielle R. AzzaritiIneke CordovaHannah DziadzioLawrence BabbKevin RiehleAleksandar MilosavljevicChrista Lese MartinHeidi L. RehmSharon E. PlonJonathan S. BergErin R. RiggsTeri E. Klein

biomedical informaticsscientific databiomedical data analysisgeneticsclingen data platformshealth informaticsbioinformaticsbiomedical data sciencemachine learningscientific data managementdata sciencegenomicsbiomedical data integrationdisease classificationhealth sciences

Performance Monitoring of Improvisation and Score‐Playing in a Turn‐Taking Piano Duet: An Eeg Study Using Altered Auditory Feedback. Psychophysiology (2024)

Kunwoo KimNoah FramBarbara NernessCara TurnbullAditya ChanderElena GeorgievaSebastian JamesMatt WrightTakako Fujioka

improvisationaltered auditory feedbackmusic psychologyperformance studiespsychophysicsauditory sciencepsychologymusicpsychoacoustics

Accessing Clinical-Grade Genomic Classification Data Through the Clingen Data Platform. Biocomputing (2022)

Karen P. DaltonHeidi L. RehmMatt W. WrightMark E. MandellKilannin KrysiakLawrence BabbKevin RiehleTristan NelsonAlex H. Wagner

clingen data platformdata sciencebioinformaticsgenomics

Clingen Variant Curation Interface: A Variant Classification Platform for the Application of Evidence Criteria From Acmg/Amp Guidelines. Genome Medicine (2022)

Christine G. PrestonMatt W. WrightRao MadhavraoSteven M. HarrisonJennifer L. GoldsteinXi LuoHannah WandBryan WulfGloria CheungMark E. MandellHoward TongShaung ChengMichael A. IacoccaArturo Lopez PinedaAlice B. PopejoyKaren DaltonJimmy ZhenSelina S. DwightLawrence BabbMarina DiStefanoJulianne M. O’DanielKristy LeeErin R. RiggsDiane B. ZastrowJessica L. MesterDeborah I. RitterRonak Y. PatelSai Lakshmi SubramanianAleksander MilosavljevicJonathan S. BergHeidi L. RehmSharon E. PlonJ. Michael CherryCarlos D. BustamanteHelio A. Costa

personalized medicinegeneticsmedicinegenomic medicinebioinformaticsevidence criteriamedical geneticsgenomicsvariant classification platformgenome biologymolecular biology

Evaluating the Impact of in Silico Predictors on Clinical Variant Classification. bioRxiv (Cold Spring Harbor Laboratory) (2021)

Emma H. WilcoxMahdi SarmadyBryan WulfMatt W. WrightHeidi L. RehmLeslie G. BieseckerAhmad N. Abou Tayoun

variant interpretationgeneticsgenomic medicineclinical variant classificationbiomolecular engineeringbioinformaticsfunctional genomicsmedical geneticsgenomicsdisease classificationgenetic variationmolecular biologytranslational bioinformatics

Recommendations for Application of the Functional Evidence Ps3/Bs3 Criterion Using the Acmg/Amp Sequence Variant Interpretation Framework. Genome Medicine (2019)

Sarah E. BrnichAhmad N. Abou TayounFergus J. CouchGarry R. CuttingMarc S. GreenblattChristopher D. HeinenDona M. KanavyXi LuoShannon M. McNultyLea M. StaritaSean V. TavtigianMatt W. WrightSteven M. HarrisonLeslie G. BieseckerJonathan S. Berg

variant interpretationgeneticsmedicinegenomic medicinebioinformaticsmedical geneticsgenomicsevidence-based recommendationsmolecular biology

Unique Aspects of Sequence Variant Interpretation for Inborn Errors of Metabolism (Iem): The Clingen Iem Working Group and the Phenylalanine Hydroxylase Gene. Human Mutation (2018)

Diane B. ZastrowHeather BaudetWei ShenAmanda ThomasYue SiMeredith A. WeaverAngela M. LagerJixia LiuRachel MangelsSelina S. DwightMatt W. WrightSteven F. DobrowolskiKaren EilbeckGregory M. EnnsAnnette FeigenbaumUta Lichter‐KoneckiElaine LyonMarzia PasqualiMichael WatsonNenad BlauRobert D. SteinerWilliam J. CraigenRong Mao

geneticsmetabolismmolecular geneticshuman geneticsinborn errorsgenomicsmolecular biologyphenylalanine hydroxylase genesequence variant interpretation

Accurate Prediction of Brca1 and Brca2 Heterozygous Genotypes Using Expression Profiling of Lymphocytes After Irradiation-Induced Dna Damage. Breast Cancer Research (2008)

Z Kote-JaraiS JugurnauthL MatthewsI GiddingsE BancroftR WilliamsM GirolamiC CampbellRA Eeles

radiation biologycancer genomicsexpression profilinggeneticsoncologyradiation oncologycancer researchcancer biologyaccurate predictioncytogeneticsirradiation-induced dna damagecancer careimmunologycancer geneticsdna repairgene expressionbreast cancergenome biology

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Matt Wright

Lecturer CCRMA

Stanford University

Affiliations

School of Humanities and Sciences

Music

Matt Wright is currently serving as a Music Lecturer CCRMA at Stanford 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

Matt Wright

Stanford University

Lecturer CCRMA

You can click a keyword to filter the displayed items

Video Presentations

Notable Scholarly Works

Notable Federal Grants

Collaborators

Generating Clinical-Grade Gene–Disease Validity Classifications Through the Clingen Data Platforms. Annual Review of Biomedical Data Science (2024)

Performance Monitoring of Improvisation and Score‐Playing in a Turn‐Taking Piano Duet: An Eeg Study Using Altered Auditory Feedback. Psychophysiology (2024)

Kunwoo KimNoah FramBarbara NernessCara TurnbullAditya ChanderElena GeorgievaSebastian JamesMatt WrightTakako Fujioka

improvisationaltered auditory feedbackmusic psychologyperformance studiespsychophysicsauditory sciencepsychologymusicpsychoacoustics

Accessing Clinical-Grade Genomic Classification Data Through the Clingen Data Platform. Biocomputing (2022)

Karen P. DaltonHeidi L. RehmMatt W. WrightMark E. MandellKilannin KrysiakLawrence BabbKevin RiehleTristan NelsonAlex H. Wagner

clingen data platformdata sciencebioinformaticsgenomics

Clingen Variant Curation Interface: A Variant Classification Platform for the Application of Evidence Criteria From Acmg/Amp Guidelines. Genome Medicine (2022)

personalized medicinegeneticsmedicinegenomic medicinebioinformaticsevidence criteriamedical geneticsgenomicsvariant classification platformgenome biologymolecular biology

Evaluating the Impact of in Silico Predictors on Clinical Variant Classification. bioRxiv (Cold Spring Harbor Laboratory) (2021)

Emma H. WilcoxMahdi SarmadyBryan WulfMatt W. WrightHeidi L. RehmLeslie G. BieseckerAhmad N. Abou Tayoun

Recommendations for Application of the Functional Evidence Ps3/Bs3 Criterion Using the Acmg/Amp Sequence Variant Interpretation Framework. Genome Medicine (2019)

variant interpretationgeneticsmedicinegenomic medicinebioinformaticsmedical geneticsgenomicsevidence-based recommendationsmolecular biology

Unique Aspects of Sequence Variant Interpretation for Inborn Errors of Metabolism (Iem): The Clingen Iem Working Group and the Phenylalanine Hydroxylase Gene. Human Mutation (2018)

geneticsmetabolismmolecular geneticshuman geneticsinborn errorsgenomicsmolecular biologyphenylalanine hydroxylase genesequence variant interpretation

Accurate Prediction of Brca1 and Brca2 Heterozygous Genotypes Using Expression Profiling of Lymphocytes After Irradiation-Induced Dna Damage. Breast Cancer Research (2008)

Z Kote-JaraiS JugurnauthL MatthewsI GiddingsE BancroftR WilliamsM GirolamiC CampbellRA Eeles

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