Certificates of Confidentiality and the Personalized Medicine Research Project

av Foth, Wendy, Waudby, Carol, Brilliant, Murray H.
Publicerad 2012

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

av Epperla, Narendranath, Brilliant, Murray H, Vidaillet, Humberto
Publicerad 2014

Personalized Medicine Going Precise: From Genomics to Microbiomics

av Shukla, Sanjay K., Murali, Narayan S., Brilliant, Murray H.
I publikationen Trends Mol Med (2015)

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

av Leary, Emili, Brilliant, Murray, Peissig, Peggy, Griesbach, Sara
I publikationen Am J Health Syst Pharm (2019)

Progress in oral personalized medicine: contribution of ‘omics’

av Glurich, Ingrid, Acharya, Amit, Brilliant, Murray H., Shukla, Sanjay K.
I publikationen J Oral Microbiol (2015)

The Oral-Systemic Personalized Medicine Model at Marshfield Clinic

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

Sox6 regulation of cardiac myocyte development

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

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

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

A PheWAS approach in studying HLA-DRB1*1501

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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