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

SLC6A3 coding variant Ala559Val found in two autism probands alters dopamine transporter function and trafficking.

在两名自闭症先证者中发现的 SLC6A3 编码变异 Ala559Val 会改变多巴胺转运体的功能和运输

Bowton E, Saunders C, Reddy I A, Campbell N G, Hamilton P J, Henry L K, Coon H, Sakrikar D, Veenstra-VanderWeele J M, Blakely R D, Sutcliffe J, Matthies H J G, Erreger K, Galli A

Inclusion of pediatric samples in an opt-out biorepository linking DNA to de-identified medical records: pediatric BioVU

将儿科样本纳入选择退出式生物样本库,并将DNA与去标识化的医疗记录关联起来:儿科BioVU

McGregor, T L; Van Driest, S L; Brothers, K B; Bowton, E A; Muglia, L J; Roden, D M

Operational implementation of prospective genotyping for personalized medicine: the design of the Vanderbilt PREDICT project

前瞻性基因分型在个性化医疗中的应用:范德比尔特PREDICT项目的设计

Pulley, J M; Denny, J C; Peterson, J F; Bernard, G R; Vnencak-Jones, C L; Ramirez, A H; Delaney, J T; Bowton, E; Brothers, K; Johnson, K; Crawford, D C; Schildcrout, J; Masys, D R; Dilks, H H; Wilke, R A; Clayton, E W; Shultz, E; Laposata, M; McPherson, J; Jirjis, J N; Roden, D M

Predicting clopidogrel response using DNA samples linked to an electronic health record

利用与电子健康记录关联的DNA样本预测氯吡格雷疗效

Delaney, J T; Ramirez, A H; Bowton, E; Pulley, J M; Basford, M A; Schildcrout, J S; Shi, Y; Zink, R; Oetjens, M; Xu, H; Cleator, J H; Jahangir, E; Ritchie, M D; Masys, D R; Roden, D M; Crawford, D C; Denny, J C