Certificates of Confidentiality and the Personalized Medicine Research Project

door Foth, Wendy, Waudby, Carol, Brilliant, Murray H.
Gepubliceerd in 2012

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

door Epperla, Narendranath, Brilliant, Murray H, Vidaillet, Humberto
Gepubliceerd in 2014

Personalized Medicine Going Precise: From Genomics to Microbiomics

door Shukla, Sanjay K., Murali, Narayan S., Brilliant, Murray H.
Gepubliceerd in Trends Mol Med (2015)

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

door Leary, Emili, Brilliant, Murray, Peissig, Peggy, Griesbach, Sara
Gepubliceerd in Am J Health Syst Pharm (2019)

Progress in oral personalized medicine: contribution of ‘omics’

door Glurich, Ingrid, Acharya, Amit, Brilliant, Murray H., Shukla, Sanjay K.
Gepubliceerd in J Oral Microbiol (2015)

The Oral-Systemic Personalized Medicine Model at Marshfield Clinic

door Glurich, Ingrid, Acharya, Amit, Shukla, Sanjay K., Nycz, Greg R, Brilliant, Murray H.
Gepubliceerd in 2012

Sox6 regulation of cardiac myocyte development

door Cohen-Barak, Orit, Yi, Zanhua, Hagiwara, Nobuko, Monzen, Koshiro, Komuro, Issei, Brilliant, Murray H.
Gepubliceerd in 2003

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

door Zhou, Zhiyi, He, Max, Brilliant, Murray, Brautbar, Ariel, Miller, Aaron, Weichelt, Bryan, Lin, Simon
Gepubliceerd in 2013

A PheWAS approach in studying HLA-DRB1*1501

door Hebbring, Scott J., Schrodi, Steven J., Ye, Zhan, Zhou, Zhiyi, Page, David, Brilliant, Murray H
Gepubliceerd in 2013

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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