Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Sally Yepes"'
Publikováno v:
PLoS ONE, Vol 10, Iss 9, p e0137132 (2015)
Although the identification of inherent structure in chronic lymphocytic leukemia (CLL) gene expression data using class discovery approaches has not been extensively explored, the natural clustering of patient samples can reveal molecular subdivisio
Externí odkaz:
https://doaj.org/article/b31319bd4c25438cad00b0ee35fb1ab5
Autor:
Bing Xia, Kajal Biswas, Tzeh K. Foo, Thiago T. Gomes, Maximilian Riedel‐Topper, Eileen Southon, Zhihua Kang, Yanying Huo, Susan Reid, Stacey Stauffer, Weiyin Zhou, Bin Zhu, Hela Koka, Sally Yepes, Seth A. Brodie, Kristine Jones, Aurelie Vogt, Brian Carter, Neal D. Freedman, Belynda Hicks, Meredith Yeager, Stephen J. Chanock, Fergus Couch, Dilys M. Parry, Alvaro N. Monteiro, Alisa M. Goldstein, Marcelo A. Carvalho, Shyam K. Sharan, Xiaohong R. Yang
Publikováno v:
Human mutation. 43(10)
Chordoma is a rare bone tumor with genetic risk factors largely unknown. We conducted a whole-exome sequencing (WES) analysis of germline DNA from 19 familial chordoma cases in five pedigrees and 137 sporadic chordoma patients and identified 17 rare
Autor:
Sally Yepes, Margaret A. Tucker, Hela Koka, Yanzi Xiao, Tongwu Zhang, Kristine Jones, Aurelie Vogt, Laurie Burdette, Wen Luo, Bin Zhu, Amy Hutchinson, Meredith Yeager, Belynda Hicks, Kevin M. Brown, Neal D. Freedman, Stephen J. Chanock, Alisa M. Goldstein, Xiaohong R. Yang
Publikováno v:
The Journal of investigative dermatology. 142(9)
The application of whole-exome sequencing has led to the identification of high- and moderate-risk variants that contribute to cutaneous melanoma susceptibility. However, confirming disease-causing variants remains challenging. We applied a gene coex
Autor:
Brian D. Carter, Yanzi Xiao, Amy Hutchinson, Xiaohong R. Yang, Mary L. McMaster, Chuzhong Li, Songbai Gui, Laura Beane-Freeman, Jiwei Bai, Alisa M. Goldstein, Nirav N Shah, Sally Yepes, Belynda Hicks, Dilys M. Parry, Mingyi Wang, Hela Koka, Kristine Jones, Neal D. Freedman, Meredith Yeager, Yazhuo Zhang, Aurelie Vogt, Bin Zhu, Stephen J. Chanock
Publikováno v:
Cancers
Volume 13
Issue 11
Cancers, Vol 13, Iss 2704, p 2704 (2021)
Volume 13
Issue 11
Cancers, Vol 13, Iss 2704, p 2704 (2021)
Background: Chordoma is a rare bone cancer with an unknown etiology. TBXT is the only chordoma susceptibility gene identified to date
germline single nucleotide variants and copy number variants in TBXT have been associated with chordoma suscept
germline single nucleotide variants and copy number variants in TBXT have been associated with chordoma suscept
Autor:
Sally Yepes, Bin Zhu, Alisa M. Goldstein, Aurelie Vogt, Yanzi Xiao, Amy Hutchinson, Wen Luo, Neal D. Freedman, Meredith Yeager, Laurie Burdette, Hela Koka, Belynda Hicks, Margaret A. Tucker, Xiaohong R. Yang, Kristine Jones, Stephen J. Chanock
Publikováno v:
Scientific Reports
Scientific Reports, Vol 10, Iss 1, Pp 1-13 (2020)
Scientific Reports, Vol 10, Iss 1, Pp 1-13 (2020)
Although next-generation sequencing has demonstrated great potential for novel gene discovery, confirming disease-causing genes after initial discovery remains challenging. Here, we applied a network analysis approach to prioritize candidate genes id
Autor:
Rafael Andrade, Maria Mercedes Torres, Liliana López-Kleine, Sally Yepes, Rocío López, Paula A Rodriguez-Urrego
Publikováno v:
Genomics. 108:93-101
Co-expression networks may provide insights into the patterns of molecular interactions that underlie cellular processes. To obtain a better understanding of miRNA expression patterns in gastric adenocarcinoma and to provide markers that can be assoc
Autor:
Bin Zhu, Hela Koka, Laurie Burdette, Meredith Yeager, Xiaohong R. Yang, Wen Luo, Aurelie Vogt, Stephen J. Chanock, Sally Yepes, Alisa M. Goldstein, Kristine Jones, Neal D. Freedman, Margaret A. Tucker, Belynda Hicks
Publikováno v:
Cancer Research. 79:1638-1638
Background: Known cutaneous malignant melanoma (CMM) genes account for melanoma risk in less than 40% of melanoma-prone families, suggesting the existence of additional risk genes or other modifiers. Whole exome sequencing (WES) of high-risk families
Autor:
Sally Yepes, Maria Mercedes Torres
Publikováno v:
Journal of Data Mining in Genomics & Proteomics.
Given the heterogeneity in the clinical behavior of cancer patients with identical histopathological diagnosis, the search for unrecognized molecular subtypes, subtype-specific markers and the evaluation of their clinical-biological relevance are a n
Publikováno v:
World Journal of Gastroenterology. 18:685
To assess the significance of chromosome translocation t(11;18)(q21;q21), B-cell lymphoma 10 (BCL-10) protein and Helicobacter pylori (H. pylori) infection in gastric mucosa-associated lymphoid tissue (MALT) lymphoma in Colombia.Fifty cases of gastri
Autor:
Sally, Yepes, Merced, Torres Carvajal Maria de la, Rocio, Lopez Panqueva, Rafael, Andrade, Paula, Rodriguez, Liliana, Lopez Kleine
Publikováno v:
In Annals of Oncology June 2014 25 Supplement 2:ii15-ii15