Certificates of Confidentiality and the Personalized Medicine Research Project

Por Foth, Wendy, Waudby, Carol, Brilliant, Murray H.
Publicado em 2012

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

Por Epperla, Narendranath, Brilliant, Murray H, Vidaillet, Humberto
Publicado em 2014

Personalized Medicine Going Precise: From Genomics to Microbiomics

Por Shukla, Sanjay K., Murali, Narayan S., Brilliant, Murray H.
Publicado no Trends Mol Med (2015)

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

Por Leary, Emili, Brilliant, Murray, Peissig, Peggy, Griesbach, Sara
Publicado no Am J Health Syst Pharm (2019)

Progress in oral personalized medicine: contribution of ‘omics’

Por Glurich, Ingrid, Acharya, Amit, Brilliant, Murray H., Shukla, Sanjay K.
Publicado no J Oral Microbiol (2015)

The Oral-Systemic Personalized Medicine Model at Marshfield Clinic

Por Glurich, Ingrid, Acharya, Amit, Shukla, Sanjay K., Nycz, Greg R, Brilliant, Murray H.
Publicado em 2012

Sox6 regulation of cardiac myocyte development

Por Cohen-Barak, Orit, Yi, Zanhua, Hagiwara, Nobuko, Monzen, Koshiro, Komuro, Issei, Brilliant, Murray H.
Publicado em 2003

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

Por Zhou, Zhiyi, He, Max, Brilliant, Murray, Brautbar, Ariel, Miller, Aaron, Weichelt, Bryan, Lin, Simon
Publicado em 2013

A PheWAS approach in studying HLA-DRB1*1501

Por Hebbring, Scott J., Schrodi, Steven J., Ye, Zhan, Zhou, Zhiyi, Page, David, Brilliant, Murray H
Publicado em 2013

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

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

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

Por Wilk, Melissa A., Dubra, Alfredo, Curcio, Christine A., Brilliant, Murray H., Summers, C. Gail, Carroll, Joseph
Publicado no Invest Ophthalmol Vis Sci (2014)

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

Por BASILE, ANNA O, WALLACE, JOHN R, PEISSIG, PEGGY, MCCARTY, CATHERINE A, BRILLIANT, MURRAY, RITCHIE, MARYLYN D
Publicado no Pac Symp Biocomput (2016)

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

Por O'Brien, Sarah E, Schrodi, Steven J, Ye, Zhan, Brilliant, Murray H, Virani, Salim S., Brautbar, Ariel
Publicado no J Cardiovasc Pharmacol (2015)

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

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

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

Por Dabic, Stefan, Azarbaijani, Yasameen, Karapetyan, Tigran, Loyo‐Berrios, Nilsa, Simonyan, Vahan, Kitchner, Terrie, Brilliant, Murray, Torosyan, Yelizaveta
Publicado no Clin Transl Sci (2019)

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

Por Lee, Susan, Schimmenti, Lisa A., King, Richard A., Brilliant, Murray, Anderson, Jennifer L., Schoonveld, Cheri, Summers, C. Gail
Publicado no J AAPOS (2015)

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

Por Bishop-Fitzpatrick, Lauren, Movaghar, Arezoo, Greenberg, Jan S., Page, David, DaWalt, Leann S., Brilliant, Murray H., Mailick, Marsha R.
Publicado no Autism Res (2018)

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

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

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

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

Does levodopa improve vision in albinism? Results of a randomized, controlled clinical trial

Por Summers, C Gail, Connett, John E, Holleschau, Ann M, Anderson, Jennifer L, De Becker, Inge, McKay, Brian S, Brilliant, Murray H
Publicado em 2014