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

Clinical Pharmacogenetics Implementation Consortium (CPIC) Guideline for Thiopurine Dosing Based on TPMT and NUDT15 Genotypes: 2025 Update

基于TPMT和NUDT15基因型的硫嘌呤类药物剂量临床药物遗传学实施联盟(CPIC)指南:2025年更新版

Maillard, Maud; Schwab, Matthias; Whirl-Carrillo, Michelle; Moyer, Ann M; Suarez-Kurtz, Guilherme; Pui, Ching-Hon; Stein, C Michael; Klein, Teri E; Spahn, Claire; Kwon, Sooyeon; Hartono, Juanda Leo; de Boer, Nanne K; Ahmad, Tariq; Antillon-Klussmann, Federico Guillermo; Caudle, Kelly E; Kato, Motohiro; Yeoh, Allen E J; Schmiegelow, Kjeld; Yang, Jun J

Autosomal-Recessive LMNA Dilated Cardiomyopathy

常染色体隐性遗传性LMNA扩张型心肌病

Sterner, Rosalie M; Coon, Lea M; Black, John L; Moyer, Ann M; Maleszewski, Joseph J; Baudhuin, Linnea M

Clinical Outcomes and Treatment Strategies of Adult Transplant-Associated Thrombotic Microangiopathy: External Validation of Harmonizing Definitions and High-Risk Criteria

成人移植相关血栓性微血管病的临床结果和治疗策略:统一定义和高危标准的外部验证

Acosta-Medina, Aldo A; Sridharan, Meera; Go, Ronald S; Moyer, Ann M; Leung, Nelson; Willrich, Maria Alice V; Wolf, Robert; Kassis, Rabee; Manasrah, Almothana; Kohorst, Mira A; Durani, Urshila; Matin, Aasiya; Hefazi, Mehrdad; Kenderian, Saad J; Mangaonkar, Abhishek A; Shah, Mithun V; Litzow, Mark R; Hogan, William J; Dingli, David; Alkhateeb, Hassan B

An Ambiguous NUDT15 Signal in a Child with B-cell Acute Lymphoblastic Leukemia

B细胞急性淋巴细胞白血病患儿中NUDT15信号不明确

Sterner, Rosalie M; Sherani, Farha; DiGuardo, Margaret A; Greipp, Patricia T; Moyer, Ann M

Integrating Pharmacogenomics into the Broader Construct of Genomic Medicine: Efforts by the ClinGen Pharmacogenomics Working Group (PGxWG)

将药物基因组学整合到更广泛的基因组医学框架中:ClinGen 药物基因组学工作组 (PGxWG) 的努力

Gong, Li; Klein, Clarissa J; Caudle, Kelly E; Moyer, Ann M; Scott, Stuart A; Whirl-Carrillo, Michelle; Klein, Teri E

Complement-mediated HUS revisited: evolving insights into pathophysiology, diagnosis, and treatment

补体介导的溶血性尿毒综合征再探:病理生理学、诊断和治疗的最新进展

Alyamany, Ruah; Moyer, Ann M; Willrich, Maria Alice V; Sridharan, Meera

Feasibility of DNA-Based Diagnosis of Fibrinogen A Alpha-Chain Amyloidosis From Paraffin-Embedded Kidney Tissue

基于DNA的石蜡包埋肾组织纤维蛋白原Aα链淀粉样变性诊断的可行性

Buglioni, Alessia; Dasari, Surendra; Bu, Lihong; Sethi, Sanjeev; Moyer, Ann M; Baudhuin, Linnea M; Hasadsri, Linda; Leung, Nelson; McPhail, Ellen D; Nasr, Samih H

Progress in Pharmacogenomics Implementation in the United States: Barrier Erosion and Remaining Challenges

美国药物基因组学实施进展:障碍消除与剩余挑战

Smith, D Max; Douglas, Michael P; Aquilante, Christina L; Deverka, Patricia A; Devine, Beth; Dunnenberger, Henry M; Empey, Philip E; Hertz, Daniel L; Monte, Andrew A; Moyer, Ann M; Patel, Jai N; Pratt, Victoria M; Saulsberry, Loren; Scott, Stuart A; Voora, Deepak; Woodahl, Erica L; Whirl-Carrillo, Michelle; Oni-Orisan, Akinyemi

Pharmacogenomic Testing in the Clinical Laboratory: Historical Progress and Future Opportunities

临床实验室中的药物基因组学检测:历史进展与未来机遇

Moyer, Ann M; Black, John L

New Resources to Identify Characterized DNA Reference Materials for Pharmacogenetic (PGx) and Human Leukocyte Antigen (HLA) Testing: The Genetic Testing Reference Material (GeT-RM) Program PGx Search Tool and GeT-RM Consolidated PGx and HLA Table

用于药物遗传学 (PGx) 和人类白细胞抗原 (HLA) 检测的特征性 DNA 参考物质的新资源:基因检测参考物质 (GeT-RM) 项目 PGx 搜索工具和 GeT-RM PGx 和 HLA 综合表

Scheinfeldt, Laura; Kusic, Dara; Gaedigk, Andrea; Turner, Amy J; Moyer, Ann M; Pratt, Victoria M; Kalman, Lisa V