日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Minimal Residual Disease using a Plasma-Only Circulating Tumor DNA Assay to Predict Recurrence of Metastatic Colorectal Cancer Following Curative Intent Treatment

利用仅检测血浆中循环肿瘤DNA的检测方法来预测根治性治疗后转移性结直肠癌的复发,从而评估微小残留病灶。

Parikh, Aparna R; Chee, Bryant H; Tsai, Jill; Rich, Thereasa A; Price, Kristin S; Patel, Sonia A; Zhang, Li; Ibrahim, Faaiz; Esquivel, Mikaela; Van Seventer, Emily E; Jarnagin, Joy X; Raymond, Victoria M; Corvera, Carlos U; Hirose, Kenzo; Nakakura, Eric K; Corcoran, Ryan B; Van Loon, Katherine; Atreya, Chloe E

Duration of Targeted Therapy in Patients With Advanced Non-small-cell Lung Cancer Identified by Circulating Tumor DNA Analysis

通过循环肿瘤DNA分析确定晚期非小细胞肺癌患者靶向治疗的持续时间

Reckamp, Karen L; Patil, Tejas; Kirtane, Kedar; Rich, Thereasa A; Espenschied, Carin R; Weipert, Caroline M; Raymond, Victoria M; Santana-Davila, Rafael; Doebele, Robert C; Baik, Christina S

Identification of Actionable Fusions as an Anti-EGFR Resistance Mechanism Using a Circulating Tumor DNA Assay

利用循环肿瘤DNA检测鉴定可作为抗EGFR耐药机制的可靶向融合基因

Clifton, Katherine; Rich, Thereasa A; Parseghian, Christine; Raymond, Victoria M; Dasari, Arvind; Pereira, Allan Andresson Lima; Willis, Jason; Loree, Jonathan M; Bauer, Todd M; Chae, Young Kwang; Sherrill, Gary; Fanta, Paul; Grothey, Axel; Hendifar, Andrew; Henry, David; Mahadevan, Daruka; Nezami, Mohammad Amin; Tan, Benjamin; Wainberg, Zev A; Lanman, Richard; Kopetz, Scott; Morris, Van

Recontacting Patients with Updated Genetic Testing Recommendations for Medullary Thyroid Carcinoma and Pheochromocytoma or Paraganglioma

针对甲状腺髓样癌、嗜铬细胞瘤或副神经节瘤,向患者提供更新的基因检测建议。

Romero Arenas, Minerva A; Rich, Thereasa A; Hyde, Samuel M; Busaidy, Naifa L; Cote, Gilbert J; Hu, Mimi I; Gagel, Robert F; Gidley, Paul W; Jimenez, Camilo; Kupferman, Michael E; Peterson, Susan K; Sherman, Steven I; Ying, Anita; Bassett, Roland L Jr; Waguespack, Steven G; Perrier, Nancy D; Grubbs, Elizabeth G

Prevalence by age and predictors of medullary thyroid cancer in patients with lower risk germline RET proto-oncogene mutations

按年龄划分的甲状腺髓样癌患病率及低风险生殖系RET原癌基因突变患者的预测因素

Rich, Thereasa A; Feng, Lei; Busaidy, Naifa; Cote, Gilbert J; Gagel, Robert F; Hu, Mimi; Jimenez, Camilo; Lee, Jeffrey E; Perrier, Nancy; Sherman, Steven I; Waguespack, Steven G; Ying, Anita; Grubbs, Elizabeth

Preliminary whole-exome sequencing reveals mutations that imply common tumorigenicity pathways in multiple endocrine neoplasia type 1 patients

初步全外显子组测序揭示了多发性内分泌肿瘤1型患者中存在提示常见致瘤通路的突变

Romero Arenas, Minerva Angélica; Fowler, Richard G; San Lucas, F Anthony; Shen, Jie; Rich, Thereasa A; Grubbs, Elizabeth G; Lee, Jeffrey E; Scheet, Paul; Perrier, Nancy D; Zhao, Hua

Comparison of attitudes regarding preimplantation genetic diagnosis among patients with hereditary cancer syndromes

比较遗传性癌症综合征患者对胚胎植入前遗传学诊断的态度

Rich, Thereasa A; Liu, Mei; Etzel, Carol J; Bannon, Sarah A; Mork, Maureen E; Ready, Kaylene; Saraiya, Devki S; Grubbs, Elizabeth G; Perrier, Nancy D; Lu, Karen H; Arun, Banu K; Woodard, Terri L; Schover, Leslie R; Litton, Jennifer K

Ultrasonography should not guide the timing of thyroidectomy in pediatric patients diagnosed with multiple endocrine neoplasia syndrome 2A through genetic screening

对于通过基因筛查确诊为多发性内分泌肿瘤综合征2A型的儿科患者,不应以超声检查作为甲状腺切除术时机的指导。

Morris, Lilah F; Waguespack, Steven G; Edeiken-Monroe, Beth S; Lee, Jeff E; Rich, Thereasa A; Ying, Anita K; Warneke, Carla L; Evans, Douglas B; Perrier, Nancy D; Grubbs, Elizabeth G

Multiple endocrine neoplasia type 2B with a RET proto-oncogene A883F mutation displays a more indolent form of medullary thyroid carcinoma compared with a RET M918T mutation

与RET M918T突变相比,携带RET原癌基因A883F突变的多发性内分泌肿瘤2B型表现出更为惰性的甲状腺髓样癌。

Jasim, Sina; Ying, Anita K; Waguespack, Steven G; Rich, Thereasa A; Grubbs, Elizabeth G; Jimenez, Camilo; Hu, Mimi I; Cote, Gilbert; Habra, Mouhammed Amir

A novel SDHB mutation associated with hereditary head and neck paraganglioma

一种与遗传性头颈部副神经节瘤相关的新型SDHB基因突变

Peck, Brandon W; Rich, Thereasa A; Jimenez, Camilo; Kupferman, Michael E