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

Correction: Methodology for clinical genotyping of CYP2D6 and CYP2C19

更正:CYP2D6 和 CYP2C19 临床基因分型方法

Henriques, Beatriz Carvalho; Buchner, Avery; Hu, Xiuying; Wang, Yabing; Yavorskyy, Vasyl; Wallace, Keanna; Dong, Rachael; Martens, Kristina; Carr, Michael S; Asl, Bahareh Behroozi; Hague, Joshua; Sivapalan, Sudhakar; Maier, Wolfgang; Dernovsek, Mojca Z; Henigsberg, Neven; Hauser, Joanna; Souery, Daniel; Cattaneo, Annamaria; Mors, Ole; Rietschel, Marcella; Pfeffer, Gerald; Hume, Stacey; Aitchison, Katherine J

Expression of risk genes linked to vitamin D receptor super-enhancer regions and their association with phenotype severity in multiple sclerosis

与维生素D受体超级增强子区域相关的风险基因的表达及其与多发性硬化症表型严重程度的关系

Orton, Sarah M; Sangha, Amarpreet; Gupta, Mehul; Martens, Kristina; Metz, Luanne M; de Koning, A P J; Pfeffer, Gerald

Highly Elevated Prevalence of Spinobulbar Muscular Atrophy in Indigenous Communities in Canada Due to a Founder Effect.

加拿大原住民社区脊髓延髓肌萎缩症患病率极高,这是由于创始人效应所致

Leckie Jamie N, Joel Matthew M, Martens Kristina, King Alexandra, King Malcolm, Korngut Lawrence W, de Koning A P Jason, Pfeffer Gerald, Schellenberg Kerri L

Association Between BDNF Val66Met Polymorphism and Mild Behavioral Impairment in Patients With Parkinson's Disease

BDNF Val66Met多态性与帕金森病患者轻度行为障碍的关联

Ramezani, Mehrafarin; Ruskey, Jennifer A; Martens, Kristina; Kibreab, Mekale; Javer, Zainul; Kathol, Iris; Hammer, Tracy; Cheetham, Jenelle; Leveille, Etienne; Martino, Davide; Sarna, Justyna R; Gan-Or, Ziv; Pfeffer, Gerald; Ismail, Zahinoor; Monchi, Oury

Colchicine Myopathy: A Case Series Including Muscle MRI and ABCB1 Polymorphism Data.

秋水仙碱肌病:包括肌肉 MRI 和 ABCB1 多态性数据的病例系列

Gupta Mehul, Nikolic Ana, Ng Denise, Martens Kristina, Ebadi Hamid, Chhibber Sameer, Pfeffer Gerald

GNE Myopathy With Novel Mutations and Pronounced Paraspinal Muscle Atrophy

伴有新型突变和显著椎旁肌萎缩的GNE肌病

Soule, Tyler; Phan, Cecile; White, Chris; Resch, Lothar; Lacson, Atilano; Martens, Kristina; Pfeffer, Gerald