Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Ed Tom"'
Publikováno v:
Model Assisted Statistics and Applications. 12:265-273
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0ae8711924904ef18f6b085fda23af43
https://doi.org/10.3233/mas-170401
https://doi.org/10.3233/mas-170401
Autor:
Joshua Barbiarz, Gregory W. Randolph, Peter M. Sadow, Jing Huang, Giulia C. Kennedy, Ed Tom, Michael W. Yeh, Huimin Jiang, Gilbert H. Daniels, Quan-Yang Duh, Richard T. Kloos, Yangyang Hao, Su Yeon Kim
Publikováno v:
Endocrine Practice. 24:319-320
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b423d313865725a350492ed002425d43
https://doi.org/10.1016/s1530-891x(20)47519-6
https://doi.org/10.1016/s1530-891x(20)47519-6
Autor:
Jing Huang, Richard T. Kloos, P. Sean Walsh, Giulia C. Kennedy, Su Yeon Kim, Ed Tom, Kevin Travers, Andrew C. Stewart, Moraima Pagan, Mei G. Wong, Chu-Fang Lin, Robert Monroe, Hajime Matsuzaki
Publikováno v:
BMC Bioinformatics
Background Thyroid carcinomas are known to harbor oncogenic driver mutations and advances in sequencing technology now allow the detection of these in fine needle aspiration biopsies (FNA). Recent work by The Cancer Genome Atlas (TCGA) Research Netwo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa59ce8b2db1a96ebe60ac381f471dce
https://pubmed.ncbi.nlm.nih.gov/26818556
https://pubmed.ncbi.nlm.nih.gov/26818556
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::15cbabc16045f6a3033356f36b6dc45e
https://doi.org/10.1210/jc.2010-1087
https://doi.org/10.1210/jc.2010-1087
Abstract #1192: Detection of Malignancy in Thyroid Carcinoma Samples Through Targeted DNA Sequencing
Autor:
Virginia A. LiVolsi, Manqiu Cao, Susan M. Mockus, Grazyna Fedorowicz, Ed Tom, Giulia C. Kennedy, Jing Huang, Mei Wong, Daniel G. Pankratz, Guru Ananda, Richard T. Kloos, Ed Liu, Kevin Travers, Su Yeon Kim, P. Sean Walsh
Publikováno v:
Endocrine Practice. 22:299-300
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::16ac18a0d65104809fd367abc24ef41b
https://doi.org/10.1016/s1530-891x(20)44841-4
https://doi.org/10.1016/s1530-891x(20)44841-4
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c262583f36e0cdd10108f248525c70e0
https://doi.org/10.1142/9789814644730_0036
https://doi.org/10.1142/9789814644730_0036
Autor:
Jing Huang, Bamboo Lin, Bryan R. Haugen, Moraima Pagan, Giulia C. Kennedy, James C. Diggans, Steven I. Sherman, R. Michael Tuttle, Ed Tom
Publikováno v:
Journal of Clinical Oncology. 33:6044-6044
6044 Background: In addition to improving survival, a risk adapted approach to thyroid cancer therapy should minimize risk of recurrence. Currently, patients are classified post-operatively as high...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::851f2b79173b195ba605572306126fc0
https://doi.org/10.1200/jco.2015.33.15_suppl.6044
https://doi.org/10.1200/jco.2015.33.15_suppl.6044
Autor:
Dave Kowbel, Richard Glynne, Colin Collins, Joe W. Gray, David R. Mack, Russ Baldocchi, Ed Tom
Publikováno v:
Nature Genetics. 27:41-41
Array-based comparative genomic hybridization (CGH) provides a higher-resolution and more quantitative alternative to chromosome CGH for the assessment of abnormalities in genomic copy number. In array-based CGH analyses published to date, array elem
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::171e49dbf95eaeec75a18d34ab8bef32
https://doi.org/10.1038/86992
https://doi.org/10.1038/86992