V. R. Miller

发表

Significance of Patient Registries for Dermatological Disorders

M. Souza, V. R. Miller, 2012 .

Creating a global rare disease patient registry linked to a rare diseases biorepository database: Rare Disease-HUB (RD-HUB).

Helen M. Moore, Jim Vaught, Yaffa R Rubinstein, 2010, Contemporary clinical trials.

Targeted comparative genomic hybridization array for the detection of single- and multiexon gene deletions and duplications

Lora J. H. Bean, M. Hegde, M. Tayeh, 2009, Genetics in Medicine.

The RD-Connect Registry & Biobank Finder: a tool for sharing aggregated data and metadata among rare disease researchers

Marco Roos, Domenica Taruscio, Hanns Lochmüller, 2018, European Journal of Human Genetics.

Quality assurance for Duchenne and Becker muscular dystrophy genetic testing: development of a genomic DNA reference material panel.

Tengyu Ma, N. Gerry, J. Gastier-Foster, 2011, The Journal of molecular diagnostics : JMD.

ClinGen's GenomeConnect registry enables patient‐centered data sharing

Danielle R Azzariti, D. Ledbetter, H. Rehm, 2018, Human mutation.

GenomeConnect: Matchmaking Between Patients, Clinical Laboratories, and Researchers to Improve Genomic Knowledge

Erin Rooney Riggs, Danielle R Azzariti, Heidi Rehm, 2015, Human mutation.

The RD-Connect Registry & Biobank Finder: a tool for sharing aggregated data and metadata among rare disease researchers

Robert Reihs, D. Taruscio, M. Roos, 2018, European Journal of Human Genetics.

Systemic Mastocytosis Patient Experience from Mast Cell Connect, the First Patient-Reported Registry for Mastocytosis

S. Verstovsek, A. Boral, T. George, 2016 .

Informed consent process for patient participation in rare disease registries linked to biorepositories.

Yaffa R Rubinstein, Vanessa Rangel Miller, Jack Schwartz, 2012, Contemporary clinical trials.