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

Utilizing Pharmacogenetic Results to Optimize Medication Management in Hospice Care: A Pilot Study

利用药物遗传学结果优化临终关怀药物管理:一项试点研究

Dreikorn, Erika N; Maxwell, Carolyn; Rowe, Kayla; Brooks, Brianna; Munro, Christine; Robin Berman, Natasha; Berenbrok, Lucas A; Massart, Mylynda B

Case report: Early use of whole exome sequencing unveils HNRNPU-related neurodevelopmental disorder and answers additional clinical questions through reanalysis

病例报告:早期应用全外显子组测序揭示了HNRNPU相关神经发育障碍,并通过重新分析解答了其他临床问题

Dreikorn, Erika Nicole; Munro, Christine; Robin Berman, Natasha; Kunovac, Amina; Bellissimo, Daniel; Massart, Mylynda B

Documenting Pharmacogenomic Test Results in Electronic Health Records: Practical Considerations for Primary Care Teams

在电子健康记录中记录药物基因组学检测结果:基层医疗团队的实用考量

Gammal, Roseann S; Berenbrok, Lucas A; Empey, Philip E; Massart, Mylynda B

Alternating Hemiplegia of Childhood: Retrospective Genetic Study and Genotype-Phenotype Correlations in 187 Subjects from the US AHCF Registry

儿童交替性偏瘫:美国AHCF登记处187例受试者的回顾性遗传学研究及基因型-表型相关性分析

Viollet, Louis; Glusman, Gustavo; Murphy, Kelley J; Newcomb, Tara M; Reyna, Sandra P; Sweney, Matthew; Nelson, Benjamin; Andermann, Frederick; Andermann, Eva; Acsadi, Gyula; Barbano, Richard L; Brown, Candida; Brunkow, Mary E; Chugani, Harry T; Cheyette, Sarah R; Collins, Abigail; DeBrosse, Suzanne D; Galas, David; Friedman, Jennifer; Hood, Lee; Huff, Chad; Jorde, Lynn B; King, Mary D; LaSalle, Bernie; Leventer, Richard J; Lewelt, Aga J; Massart, Mylynda B; Mérida, Mario R 2nd; Ptáček, Louis J; Roach, Jared C; Rust, Robert S; Renault, Francis; Sanger, Terry D; Sotero de Menezes, Marcio A; Tennyson, Rachel; Uldall, Peter; Zhang, Yue; Zupanc, Mary; Xin, Winnie; Silver, Kenneth; Swoboda, Kathryn J