Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Mark Bellafante"'
Autor:
Susan K. Delaney, Ruth Brenner, Tara J. Schmidlen, Michael P. Dempsey, Kim E. London, Erynn S. Gordon, Mark Bellafante, Ashley Nasuti, Laura B. Scheinfeldt, Kaveri D. Rajula, Leo Jose, Joseph P. Jarvis, Norman P. Gerry, Michael F. Christman
Publikováno v:
npj Genomic Medicine, Vol 2, Iss 1, Pp 1-5 (2017)
Abstract Following several years enrolling disease-specific and otherwise healthy cohorts into the Coriell Personalized Medicine Collaborative, a prospective study aimed at evaluating the clinical utility of personal genomic information for common co
Externí odkaz:
https://doaj.org/article/1fbcf28497574158bb0e60cdda521aa4
Autor:
Kandamurugu Manickam, Mark Bellafante, Tara J. Schmidlen, Wolfgang Sadee, J. Felipe Garcia-Espana, Amanda E. Toland, Ray E. Hershberger, Catharine B Stack, Kevin Sweet, Peter J. Embi, Michael F. Christman, Margaret A. Keller, Amy C. Sturm, Philip F. Binkley, Erynn S. Gordon, Neeraj Tayal, Clay B. Marsh
Publikováno v:
Journal of Personalized Medicine; Volume 4; Issue 1; Pages: 1-19
Journal of Personalized Medicine, Vol 4, Iss 1, Pp 1-19 (2014)
Journal of Personalized Medicine
Journal of Personalized Medicine, Vol 4, Iss 1, Pp 1-19 (2014)
Journal of Personalized Medicine
We describe the development and implementation of a randomized controlled trial to investigate the impact of genomic counseling on a cohort of patients with heart failure (HF) or hypertension (HTN), managed at a large academic medical center, the Ohi
Autor:
Tara J. Schmidlen, Kim E. London, Ashley Nasuti, Norman P. Gerry, Michael F. Christman, Susan K. Delaney, Erynn S. Gordon, Ruth Brenner, Michael P. Dempsey, Laura B. Scheinfeldt, Mark Bellafante, Kaveri D. Rajula, Joseph P. Jarvis, Leo Jose
Publikováno v:
NPJ Genomic Medicine
npj Genomic Medicine, Vol 2, Iss 1, Pp 1-5 (2017)
npj Genomic Medicine, Vol 2, Iss 1, Pp 1-5 (2017)
Following several years enrolling disease-specific and otherwise healthy cohorts into the Coriell Personalized Medicine Collaborative, a prospective study aimed at evaluating the clinical utility of personal genomic information for common complex dis