Certificates of Confidentiality and the Personalized Medicine Research Project

Bằng Foth, Wendy, Waudby, Carol, Brilliant, Murray H.
Được phát hành 2012

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

Bằng Epperla, Narendranath, Brilliant, Murray H, Vidaillet, Humberto
Được phát hành 2014

Personalized Medicine Going Precise: From Genomics to Microbiomics

Bằng Shukla, Sanjay K., Murali, Narayan S., Brilliant, Murray H.
Xuất bản năm Trends Mol Med (2015)

Progress in oral personalized medicine: contribution of ‘omics’

Bằng Glurich, Ingrid, Acharya, Amit, Brilliant, Murray H., Shukla, Sanjay K.
Xuất bản năm J Oral Microbiol (2015)

The Oral-Systemic Personalized Medicine Model at Marshfield Clinic

Bằng Glurich, Ingrid, Acharya, Amit, Shukla, Sanjay K., Nycz, Greg R, Brilliant, Murray H.
Được phát hành 2012

Sox6 regulation of cardiac myocyte development

Bằng Cohen-Barak, Orit, Yi, Zanhua, Hagiwara, Nobuko, Monzen, Koshiro, Komuro, Issei, Brilliant, Murray H.
Được phát hành 2003

A PheWAS approach in studying HLA-DRB1*1501

Bằng Hebbring, Scott J., Schrodi, Steven J., Ye, Zhan, Zhou, Zhiyi, Page, David, Brilliant, Murray H
Được phát hành 2013

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

Bằng Hagiwara, Nobuko, Klewer, Scott E., Samson, Ricardo A., Erickson, Drew T., Lyon, Mary F., Brilliant, Murray H.
Được phát hành 2000

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

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

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

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

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

Bằng Ye, Zhan, Vasco, Daniel A., Carter, Tonia C., Brilliant, Murray H., Schrodi, Steven J., Shukla, Sanjay K.
Được phát hành 2014

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

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

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

Bằng Newton, J. M., Cohen-Barak, Orit, Hagiwara, Nobuko, Gardner, John M., Davisson, Muriel T., King, Richard A., Brilliant, Murray H.
Được phát hành 2001

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

Bằng Summers, C Gail, Connett, John E, Holleschau, Ann M, Anderson, Jennifer L, De Becker, Inge, McKay, Brian S, Brilliant, Murray H
Được phát hành 2014

Phenome-wide association studies (PheWASs) for functional variants

Bằng Ye, Zhan, Mayer, John, Ivacic, Lynn, Zhou, Zhiyi, He, Min, Schrodi, Steven J, Page, David, Brilliant, Murray H, Hebbring, Scott J
Xuất bản năm Eur J Hum Genet (2015)

A 122.5-Kilobase Deletion of the P Gene Underlies the High Prevalence of Oculocutaneous Albinism Type 2 in the Navajo Population

Bằng Yi, Zanhua, Garrison, Nanibaa’, Cohen-Barak, Orit, Karafet, Tatiana M., King, Richard A., Erickson, Robert P., Hammer, Michael F., Brilliant, Murray H.
Được phát hành 2003

Applying family analyses to electronic health records to facilitate genetic research

Bằng Huang, Xiayuan, Elston, Robert C, Rosa, Guilherme J, Mayer, John, Ye, Zhan, Kitchner, Terrie, Brilliant, Murray H, Page, David, Hebbring, Scott J
Xuất bản năm Bioinformatics (2018)

FMR1 Low Zone CGG Repeats: Phenotypic Associations in the Context of Parenting Stress

Bằng Mailick, Marsha R., Hong, Jinkuk, DaWalt, Leann Smith, Greenberg, Jan S., Movaghar, Arezoo, Baker, Mei Wang, Rathouz, Paul J., Brilliant, Murray H.
Xuất bản năm Front Pediatr (2020)

Sox6 Directly Silences Epsilon Globin Expression in Definitive Erythropoiesis

Bằng Yi, Zanhua, Cohen-Barak, Orit, Hagiwara, Nobuko, Kingsley, Paul D, Fuchs, Deborah A, Erickson, Drew T, Epner, Elliot M, Palis, James, Brilliant, Murray H
Được phát hành 2006

FMR1 CGG Expansions: Prevalence and Sex Ratios

Bằng Maenner, Matthew J., Baker, Mei W., Broman, Karl W., Tian, Jianan, Barnes, Janel K., Atkins, Anne, McPherson, Elizabeth, Hong, Jinkuk, Brilliant, Murray H., Mailick, Marsha R.
Được phát hành 2013