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Anthony R. Soltis

uniformed services university of the health sciences
H指数:18
被引数:1,750

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The Development of Tools to Investigate Potential Sources of Sample Misidentification Within a Biorepository: Case Studies

生物样本库内样本误识别潜在来源调查工具的开发:案例研究

2026-05-010
PRE
Proteogenomic characterization of invasive breast tumors in young women

青年女性侵袭性乳腺癌的蛋白质组学表征

2025-08-180
OAAI
Multiomic analysis of uterine leiomyomas in self-described Black and White women: molecular insights into health disparities

自我描述的黑人和白人妇女的子宫平滑肌瘤的多组学分析: 对健康差异的分子见解

2024-09-011
PRE
Proteogenomic analysis of enriched HGSOC tumor epithelium identifies prognostic signatures and therapeutic vulnerabilities (vol 8, 68, 2024)

富集HGSOC肿瘤上皮的蛋白质基因组分析确定预后特征和治疗弱点 (vol 8,68,2024)

2024-05-060
OAAI
Proteogenomic characterization of primary invasive breast tumors from young women compared to matched tumors from older women
2024-05-020
PRE
Proteogenomic analysis of enriched HGSOC tumor epithelium identifies prognostic signatures and therapeutic vulnerabilities

富集HGSOC肿瘤上皮的蛋白质基因组分析确定预后特征和治疗脆弱性

2024-03-132
OAAI
Proteogenomic analysis of enriched tumor epithelium identifies prognostic signatures and an increased dependency of homologous recombination proficient cells on bmi1 in high grade serous ovarian cancer
2024-03-040
PRE
Association of cardiovascular disease management drugs with Lewy body dementia: a case-control study

心血管疾病管理药物与路易体痴呆的关系: 一项病例对照研究

2023-12-183
OA
Proteogenomic analysis of lung adenocarcinoma reveals tumor heterogeneity, survival determinants, and therapeutically relevant pathways

肺腺癌的蛋白质基因组分析揭示了肿瘤异质性,生存决定因素和治疗相关途径

2022-11-0127
OAAI
Rare variant association study of veteran twin whole-genomes links severe depression with a nonsynonymous change in the neuronal gene BHLHE22

资深双胞胎全基因组的罕见变异关联研究将严重抑郁症与神经元基因BHLHE22的非同义变化联系起来

2021-11-292
OAAI
Personalized Single-Cell Proteogenomics to Distinguish Acute Myeloid Leukemia from nonmalignant Clonal Hematopoiesis

个性化单细胞蛋白质组学区分急性髓系白血病与非恶性克隆造血

2021-05-2525
OA
Proteogenomic landscape of uterine leiomyomas from hereditary leiomyomatosis and renal cell cancer patients

遗传性平滑肌瘤病和肾细胞癌患者子宫平滑肌瘤的蛋白质基因组景观

2021-04-309
OAAI
Large-scale pathway specific polygenic risk and transcriptomic community network analysis identifies novel functional pathways in Parkinson disease
2020-06-2963
OAAI