Certificates of Confidentiality and the Personalized Medicine Research Project

द्वारा Foth, Wendy, Waudby, Carol, Brilliant, Murray H.
प्रकाशित 2012

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

द्वारा Epperla, Narendranath, Brilliant, Murray H, Vidaillet, Humberto
प्रकाशित 2014

Personalized Medicine Going Precise: From Genomics to Microbiomics

द्वारा Shukla, Sanjay K., Murali, Narayan S., Brilliant, Murray H.
में प्रकाशित Trends Mol Med (2015)

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

द्वारा Leary, Emili, Brilliant, Murray, Peissig, Peggy, Griesbach, Sara
में प्रकाशित Am J Health Syst Pharm (2019)

Progress in oral personalized medicine: contribution of ‘omics’

द्वारा Glurich, Ingrid, Acharya, Amit, Brilliant, Murray H., Shukla, Sanjay K.
में प्रकाशित J Oral Microbiol (2015)

The Oral-Systemic Personalized Medicine Model at Marshfield Clinic

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

Sox6 regulation of cardiac myocyte development

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

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

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

A PheWAS approach in studying HLA-DRB1*1501

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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