Certificates of Confidentiality and the Personalized Medicine Research Project

Tekijä Foth, Wendy, Waudby, Carol, Brilliant, Murray H.
Julkaistu 2012

Topical timolol for treatment of epistaxis in hereditary haemorrhagic telangiectasia associated with bradycardia: a look at CYP2D6 metabolising variants

Tekijä Epperla, Narendranath, Brilliant, Murray H, Vidaillet, Humberto
Julkaistu 2014

Personalized Medicine Going Precise: From Genomics to Microbiomics

Tekijä Shukla, Sanjay K., Murali, Narayan S., Brilliant, Murray H.
Julkaisussa Trends Mol Med (2015)

Preliminary outcomes of preemptive warfarin pharmacogenetic testing at a large rural healthcare center

Tekijä Leary, Emili, Brilliant, Murray, Peissig, Peggy, Griesbach, Sara
Julkaisussa Am J Health Syst Pharm (2019)

Progress in oral personalized medicine: contribution of ‘omics’

Tekijä Glurich, Ingrid, Acharya, Amit, Brilliant, Murray H., Shukla, Sanjay K.
Julkaisussa J Oral Microbiol (2015)

The Oral-Systemic Personalized Medicine Model at Marshfield Clinic

Tekijä Glurich, Ingrid, Acharya, Amit, Shukla, Sanjay K., Nycz, Greg R, Brilliant, Murray H.
Julkaistu 2012

Sox6 regulation of cardiac myocyte development

Tekijä Cohen-Barak, Orit, Yi, Zanhua, Hagiwara, Nobuko, Monzen, Koshiro, Komuro, Issei, Brilliant, Murray H.
Julkaistu 2003

PS3-2: Informatics Challenges to Implement Pharmacogenetics to Clinical Practice

Tekijä Zhou, Zhiyi, He, Max, Brilliant, Murray, Brautbar, Ariel, Miller, Aaron, Weichelt, Bryan, Lin, Simon
Julkaistu 2013

A PheWAS approach in studying HLA-DRB1*1501

Tekijä Hebbring, Scott J., Schrodi, Steven J., Ye, Zhan, Zhou, Zhiyi, Page, David, Brilliant, Murray H
Julkaistu 2013

Sox6 is a candidate gene for p(100H) myopathy, heart block, and sudden neonatal death

Tekijä Hagiwara, Nobuko, Klewer, Scott E., Samson, Ricardo A., Erickson, Drew T., Lyon, Mary F., Brilliant, Murray H.
Julkaistu 2000

Author Response: Relationship Between Foveal Cone Specialization and Pit Morphology in Albinism

Tekijä Wilk, Melissa A., Dubra, Alfredo, Curcio, Christine A., Brilliant, Murray H., Summers, C. Gail, Carroll, Joseph
Julkaisussa Invest Ophthalmol Vis Sci (2014)

KNOWLEDGE DRIVEN BINNING AND PHEWAS ANALYSIS IN MARSHFIELD PERSONALIZED MEDICINE RESEARCH PROJECT USING BIOBIN()

Tekijä BASILE, ANNA O, WALLACE, JOHN R, PEISSIG, PEGGY, MCCARTY, CATHERINE A, BRILLIANT, MURRAY, RITCHIE, MARYLYN D
Julkaisussa Pac Symp Biocomput (2016)

Differential Lipid Response to Statins is Associated with Variants in the BUD13-APOA5 Gene Region

Tekijä O'Brien, Sarah E, Schrodi, Steven J, Ye, Zhan, Brilliant, Murray H, Virani, Salim S., Brautbar, Ariel
Julkaisussa J Cardiovasc Pharmacol (2015)

Genome wide association study of SNP-, gene-, and pathway-based approaches to identify genes influencing susceptibility to Staphylococcus aureus infections

Tekijä Ye, Zhan, Vasco, Daniel A., Carter, Tonia C., Brilliant, Murray H., Schrodi, Steven J., Shukla, Sanjay K.
Julkaistu 2014

Development of an Integrated Platform Using Multidisciplinary Real‐World Data to Facilitate Biomarker Discovery for Medical Products

Tekijä Dabic, Stefan, Azarbaijani, Yasameen, Karapetyan, Tigran, Loyo‐Berrios, Nilsa, Simonyan, Vahan, Kitchner, Terrie, Brilliant, Murray, Torosyan, Yelizaveta
Julkaisussa Clin Transl Sci (2019)

Posterior staphyloma in oculocutaneous albinism: another possible cause of reduced visual acuity

Tekijä Lee, Susan, Schimmenti, Lisa A., King, Richard A., Brilliant, Murray, Anderson, Jennifer L., Schoonveld, Cheri, Summers, C. Gail
Julkaisussa J AAPOS (2015)

Using Machine Learning to Identify Patterns of Lifetime Health Problems in Decedents with Autism Spectrum Disorder

Tekijä Bishop-Fitzpatrick, Lauren, Movaghar, Arezoo, Greenberg, Jan S., Page, David, DaWalt, Leann S., Brilliant, Murray H., Mailick, Marsha R.
Julkaisussa Autism Res (2018)

Mutations in the Human Orthologue of the Mouse underwhite Gene (uw) Underlie a New Form of Oculocutaneous Albinism, OCA4

Tekijä Newton, J. M., Cohen-Barak, Orit, Hagiwara, Nobuko, Gardner, John M., Davisson, Muriel T., King, Richard A., Brilliant, Murray H.
Julkaistu 2001

Validation of PhenX measures in the personalized medicine research project for use in gene/environment studies

Tekijä McCarty, Catherine A, Berg, Richard, Rottscheit, Carla M, Waudby, Carol J, Kitchner, Terrie, Brilliant, Murray, Ritchie, Marylyn D
Julkaistu 2014

Artificial intelligence–assisted phenotype discovery of fragile X syndrome in a population-based sample

Tekijä Movaghar, Arezoo, Page, David, Scholze, Danielle, Hong, Jinkuk, DaWalt, Leann Smith, Kuusisto, Finn, Stewart, Ron, Brilliant, Murray, Mailick, Marsha
Julkaisussa Genet Med (2021)