Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Danielle Pendrick"'
Autor:
Lianna J. Marks, Jennifer A. Oberg, Danielle Pendrick, Anthony N. Sireci, Chana Glasser, Carrie Coval, Rebecca J. Zylber, Wendy K. Chung, Jiuhong Pang, Andrew T. Turk, Susan J. Hsiao, Mahesh M. Mansukhani, Julia L. Glade Bender, Andrew L. Kung, Maria Luisa Sulis
Publikováno v:
Frontiers in Pediatrics, Vol 5 (2017)
BackgroundThe advent of comprehensive genomic profiling has markedly advanced the understanding of the biology of pediatric hematological malignancies, however, its application to clinical care is still unclear. We present our experience integrating
Externí odkaz:
https://doaj.org/article/72d22ad9cdc54209a38fa6c39fc9b294
Autor:
Sheryl M. Strasser, Megan Smith, Danielle Pendrick-Denney, Sarah Boos-Beddington, Ken Chen, Frances McCarty
Publikováno v:
Western Journal of Emergency Medicine, Vol 13, Iss 3, Pp 298-304 (2012)
Intimate Partner Violence (IPV) is a major public health issue occurring in the United States and globally. While little is known in general about IPV, understanding about the prevalence of physical IPV among gay men is even more obscure. There is a
Externí odkaz:
https://doaj.org/article/a374df110c22455bb1b70be6f6df5334
Autor:
Jiuhong Pang, Hongai Xia, Shijun Mi, Wen Zhang, Danielle Pendrick, Christopher Freeman, Helen Fernandes, Mahesh Mansukhani, Susan J Hsiao
Publikováno v:
Journal of Clinical Pathology. 76:276-280
Tumour mutational burden (TMB) is used to predict response to immunotherapies. Although several groups have proposed calculation methods for TMB, a clear consensus has not yet emerged. In this study, we explored TMB calculation approaches with a 586-
Autor:
Susan J. Hsiao, Anthony N. Sireci, Richard D. Carvajal, Brian S. Henick, Mahesh Mansukhani, Helen Fernandes, Danielle Pendrick, Christopher E. Freeman, Jennifer A. Oberg, Gary K. Schwartz, Kevin A. Roth
Publikováno v:
JCO Precision Oncology. :1038-1048
PURPOSE The routine use of large next-generation sequencing (NGS) pan-cancer panels is required to identify the increasing number of, but often uncommon, actionable alterations to guide therapy. Inconsistent coverage and variable payment is hindering
Autor:
George Zanazzi, Danielle Pendrick, Kevin A. Roth, Dominique M. Higgins, Chun Chieh Lin, Susan Hsiao, Jeffrey A Bruce
Publikováno v:
Journal of Neuropathology & Experimental Neurology. 79:929-931
Autor:
Matija Snuderl, Danielle Pendrick, Susan J. Hsiao, Kevin A. Roth, Benjamin Liechty, Olga Krasnozhen-Ratush, Jeffrey C. Allen, James Garvin, George Zanazzi, Mahesh Mansukhani
Publikováno v:
Cold Spring Harbor Molecular Case Studies
We report a case of a slow-growing, diffuse, infiltrating glioma in the right brainstem of a 9-yr-old boy. The tumor was negative by immunohistochemical staining for histone H3 K27M, BRAF V600E, and IDH1 R132H mutations. Fluorescence in situ hybridiz
Autor:
Susan Hsiao, Mahesh Mansukhani, Jennifer A. Oberg, Luca Szalontay, Julia L. Glade Bender, James Garvin, Anthony N. Sireci, Eileen Stark, Danielle Pendrick, Richard C. E. Anderson, Andrew T. Turk, Neil A. Feldstein
INTRODUCTION: Whole exome sequencing (WES) of newly diagnosed pediatric central nervous system (CNS) tumors is quickly becoming part of routine care. Through the Precision in Pediatric Sequencing (PiPseq) program at Columbia University, we have found
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bb140f038069b36b2bfc13fcefd8c496
https://europepmc.org/articles/PMC5475213/
https://europepmc.org/articles/PMC5475213/
Autor:
Christopher E Freeman, Danielle Pendrick, Gary K. Schwartz, Jennifer A. Oberg, Anthony N. Sireci, Susan Jean Hsiao, Richard D. Carvajal, Mahesh M. Mansukhani, Jessica Yang
Publikováno v:
Journal of Clinical Oncology. 37:6593-6593
6593 Background: The routine use of large next generation sequencing (NGS) cancer panels is required to identify the increasing number of, but often uncommon actionable alterations present across multiple tumor histologies to guide therapy. Inconsist
Autor:
Maria Luisa Sulis, Mahesh Mansukhani, Anthony N. Sireci, Wendy K. Chung, Carrie Koval, Jennifer A. Oberg, Chana L. Glasser, Jennifer H. Kuo, Prakash Satwani, Susan J. Hsiao, Julia L. Glade Bender, Danielle Pendrick
Publikováno v:
Cold Spring Harbor Molecular Case Studies
The incorporation of tumor-normal genomic testing into oncology can identify somatic mutations that inform therapeutic measures but also germline variants associated with unsuspected cancer predisposition. We describe a case in which a RET variant wa
Autor:
Danielle Pendrick Denney, Megan O. Smith, Sheryl Strasser, Pamela L Buckmaster, Matt C. Jackson
Publikováno v:
American Journal of Health Education. 44:259-264
Background: Poverty is a pervasive condition linked to a myriad of health conditions and severe health outcomes. Public health professionals are at the forefront of addressing poverty-related issues and require education that enhances their understan