Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Jessica D. Reynolds"'
Autor:
Catalin Barbacioru, Virginia A. LiVolsi, Jonathan I. Wilde, Lyssa Friedman, P. Sean Walsh, Richard B. Lanman, Edward Y. Tom, Moraima Pagan, Juan Rosai, Giulia C. Kennedy, Richard T. Kloos, Darya Chudova, Mei Wong, Jessica D. Reynolds
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 98:E761-E768
The purpose of this study was to determine the frequency of BRAF mutation in cytologically indeterminate thyroid nodules and to investigate whether adding the BRAF test improves diagnostic accuracy of the Afirma Gene Expression Classifier (GEC).BRAF
Autor:
Lyssa Friedman, Daphne C. Chen, Giulia C. Kennedy, Daniel G. Pankratz, Robert Monroe, Darya Chudova, Mark A. Lupo, Richard B. Lanman, P. Sean Walsh, Mei Wong, Edward Y. Tom, Jonathan I. Wilde, Jessica D. Reynolds, David L. Steward, James G. Veitch, Moraima Pagan
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 97:E2297-E2306
Our objective was to verify the analytical performance of the Afirma gene expression classifier (GEC) in the classification of cytologically indeterminate thyroid nodule fine-needle aspirates (FNAs).Analytical performance studies were designed to cha
Autor:
C. Charles Wang, C. Ted Rigl, Eric T. Wang, Moraima Pagan, Ed Tom, Richard B. Lanman, Juan Rosai, Virginia A. LiVolsi, Jessica D. Reynolds, Jonathan I. Wilde, Hui Wang, Giulia C. Kennedy, Martha A. Zeiger, Lyssa Friedman, Giovanni Fellegara, Electron Kebebew, Nusrat Rabbee, Darya Chudova, Camila M. Egidio
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 95:5296-5304
We set out to develop a molecular test that distinguishes benign and malignant thyroid nodules using fine-needle aspirates (FNA).We used mRNA expression analysis to measure more than 247,186 transcripts in 315 thyroid nodules, comprising multiple sub
Autor:
Moraima Pagan, Jessica D. Reynolds, James C. Diggans, Daniel G. Pankratz, Su Yeon Kim, Giulia C. Kennedy, Ed Tom, Richard B. Lanman, Juan Rosai, P. Sean Walsh, Richard T. Kloos, Zhanzhi Hu, Virginia A. LiVolsi, Mei G. Wong, Robert Monroe
Publikováno v:
Pacific Symposium on Biocomputing
The promise of personalized medicine will require rigorously validated molecular diagnostics developed on minimally invasive, clinically relevant samples. Measurement of DNA mutations is increasingly common in clinical settings but only higher-preval