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

Physiologically Based Pharmacokinetic Modelling of Inhaled Nemiralisib: Mechanistic Components for Pulmonary Absorption, Systemic Distribution, and Oral Absorption

吸入奈米拉利西布的生理药代动力学模型：肺部吸收、全身分布和口服吸收的机制组成部分

期刊:Clinical Pharmacokinetics
影响因子:4
doi:10.1007/s40262-021-01066-2
Miller, Neil A; Graves, Rebecca H; Edwards, Chris D; Amour, Augustin; Taylor, Ed; Robb, Olivia; O'Brien, Brett; Patel, Aarti; Harrell, Andrew W; Hessel, Edith M
发表日期：2022
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Pharmacogene Variation Consortium: A Global Resource and Repository for Pharmacogene Variation

药物基因变异联盟：药物基因变异的全球资源和存储库

期刊:Clinical Pharmacology & Therapeutics
影响因子:5.5
doi:10.1002/cpt.2321
Gaedigk, Andrea; Casey, Scott T; Whirl-Carrillo, Michelle; Miller, Neil A; Klein, Teri E
发表日期：2021
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PharmVar and the Landscape of Pharmacogenetic Resources

PharmVar 和药物遗传资源格局

期刊:Clinical Pharmacology & Therapeutics
影响因子:5.5
doi:10.1002/cpt.1654
Gaedigk, Andrea; Whirl-Carrillo, Michelle; Pratt, Victoria M; Miller, Neil A; Klein, Teri E
发表日期：2020
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Long-Distance Phasing of a Tentative "Enhancer" Single-Nucleotide Polymorphism With CYP2D6 Star Allele Definitions

利用 CYP2D6 星号等位基因定义对疑似“增强子”单核苷酸多态性进行长距离定相

期刊:Frontiers in Pharmacology
影响因子:4.8
doi:10.3389/fphar.2020.00486
Boone, Erin C; Wang, Wendy Y; Gaedigk, Roger; Cherner, Mariana; Bérard, Anick; Leeder, J Steven; Miller, Neil A; Gaedigk, Andrea
发表日期：2020
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Mitochondria-to-nucleus retrograde signaling drives formation of cytoplasmic chromatin and inflammation in senescence

线粒体至细胞核逆行信号传导驱动细胞质染色质的形成和衰老过程中的炎症

期刊:Genes & Development
影响因子:1.9
doi:10.1101/gad.331272.119
Maria Grazia Vizioli, Tianhui Liu #, Karl N Miller #, Neil A Robertson, Kathryn Gilroy, Anthony B Lagnado, Arantxa Perez-Garcia, Christos Kiourtis, Nirmalya Dasgupta, Xue Lei, Patrick J Kruger, Colin Nixon, William Clark, Diana Jurk, Thomas G Bird, João F Passos, Shelley L Berger, Zhixun Dou, Peter
信号转导
细胞生物学
其它细胞
FCM
IF
IHC-P
WB
Immunology/Inflammation
Senescence
JNK
发表日期：2020
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The NSIGHT1-randomized controlled trial: rapid whole-genome sequencing for accelerated etiologic diagnosis in critically ill infants

NSIGHT1随机对照试验：快速全基因组测序加速危重婴儿病因诊断

期刊:npj Genomic Medicine
影响因子:4.8
doi:10.1038/s41525-018-0045-8
Petrikin, Josh E; Cakici, Julie A; Clark, Michelle M; Willig, Laurel K; Sweeney, Nathaly M; Farrow, Emily G; Saunders, Carol J; Thiffault, Isabelle; Miller, Neil A; Zellmer, Lee; Herd, Suzanne M; Holmes, Anne M; Batalov, Serge; Veeraraghavan, Narayanan; Smith, Laurie D; Dimmock, David P; Leeder, J Steven; Kingsmore, Stephen F
发表日期：2018
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Whole exome sequencing reveals HSPA1L as a genetic risk factor for spontaneous preterm birth.

全外显子组测序揭示 HSPA1L 是自发性早产的遗传风险因素

期刊:PLoS Genetics
影响因子:3.7
doi:10.1371/journal.pgen.1007394
Huusko Johanna M, Karjalainen Minna K, Graham Britney E, Zhang Ge, Farrow Emily G, Miller Neil A, Jacobsson Bo, Eidem Haley R, Murray Jeffrey C, Bedell Bruce, Breheny Patrick, Brown Noah W, Bødker Frans L, Litterman Nadia K, Jiang Pan-Pan, Russell Laura, Hinds David A, Hu Youna, Rokas Antonis, Teramo Kari, Christensen Kaare, Williams Scott M, Rämet Mika, Kingsmore Stephen F, Ryckman Kelli K, Hallman Mikko, Muglia Louis J
其它
发表日期：2018
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Erratum: Constellation: a tool for rapid, automated phenotype assignment of a highly polymorphic pharmacogene, CYP2D6, from whole-genome sequences

勘误：Constellation：一种利用全基因组序列快速、自动地对高度多态性药理基因CYP2D6进行表型分配的工具

期刊:npj Genomic Medicine
影响因子:4.8
doi:10.1038/npjgenmed.2016.39
Twist, Greyson P; Gaedigk, Andrea; Miller, Neil A; Farrow, Emily G; Willig, Laurel K; Dinwiddie, Darrell L; Petrikin, Josh E; Soden, Sarah E; Herd, Suzanne; Gibson, Margaret; Cakici, Julie A; Riffel, Amanda K; Leeder, J Steven; Dinakarpandian, Deendayal; Kingsmore, Stephen F
发表日期：2017
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Constellation: a tool for rapid, automated phenotype assignment of a highly polymorphic pharmacogene, CYP2D6, from whole-genome sequences

Constellation：一种利用全基因组序列快速、自动地对高度多态性药理基因CYP2D6进行表型分配的工具

期刊:npj Genomic Medicine
影响因子:4.8
doi:10.1038/npjgenmed.2015.7
Twist, Greyson P; Gaedigk, Andrea; Miller, Neil A; Farrow, Emily G; Willig, Laurel K; Dinwiddie, Darrell L; Petrikin, Josh E; Soden, Sarah E; Herd, Suzanne; Gibson, Margaret; Cakici, Julie A; Riffel, Amanda K; Leeder, J Steven; Dinakarpandian, Deendayal; Kingsmore, Stephen F
发表日期：2016
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Whole-genome sequencing for identification of Mendelian disorders in critically ill infants: a retrospective analysis of diagnostic and clinical findings

利用全基因组测序鉴定危重婴儿孟德尔遗传病：诊断和临床结果的回顾性分析

期刊:Lancet Respiratory Medicine
影响因子:32.8
doi:10.1016/S2213-2600(15)00139-3
Willig, Laurel K; Petrikin, Josh E; Smith, Laurie D; Saunders, Carol J; Thiffault, Isabelle; Miller, Neil A; Soden, Sarah E; Cakici, Julie A; Herd, Suzanne M; Twist, Greyson; Noll, Aaron; Creed, Mitchell; Alba, Patria M; Carpenter, Shannon L; Clements, Mark A; Fischer, Ryan T; Hays, J Allyson; Kilbride, Howard; McDonough, Ryan J; Rosterman, Jamie L; Tsai, Sarah L; Zellmer, Lee; Farrow, Emily G; Kingsmore, Stephen F
发表日期：2015
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