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

Impaired retinoic acid receptor-γ signaling underlies a heritable form of urothelial keratinizing squamous metaplasia

视黄酸受体γ信号传导受损是遗传性尿路上皮角化鳞状化生症的根本原因。

期刊:HGG Advances
影响因子:3.6
doi:10.1016/j.xhgg.2026.100590
Fukushima, Kaya; Avery, Nicole; Desjardins, Jade; Halliday, Benjamin J; Jenkins, Zandra A; Porteous, Robert; Morgan, Tim; Parthasarathy, Padmini; Lau, Michael; Vincent, Michael W; Liu, Karen J; Twigg, Stephen R F; Robertson, Stephen P
信号转导
发表日期：2026
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How Do Optometrists Approach Directed Questioning on Smoking Status in a Centrally Co-Ordinated, Publicly-Funded National Primary Care Eye Health Service?

在由中央协调、公共资助的国家初级保健眼健康服务体系中，验光师如何进行有关吸烟状况的定向询问？

期刊:Clinical Optometry
影响因子:1.8
doi:10.2147/OPTO.S580909
John, Rebecca; George, Michael R; Williams, Gwyn Samuel; Morgan, Tim
发表日期：2026
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The unmet need for certification of vision impairment for people accessing a national primary care-based low vision rehabilitation service

接受国家基层医疗低视力康复服务的人群对视力障碍认证的需求尚未得到满足

期刊:Ophthalmic and Physiological Optics
影响因子:2.4
doi:10.1111/opo.13413
John, Rebecca; Williams, Gwyn; Morgan, Tim; George, Michael R; Reynolds, Rhianon; Acton, Jennifer H
发表日期：2025
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De novo design of modular peptide-binding proteins by superhelical matching

通过超螺旋匹配进行模块化肽结合蛋白的从头设计

期刊:Nature
影响因子:50.5
doi:10.1038/s41586-023-05909-9
Kejia Wu #, Hua Bai #, Ya-Ting Chang, Rachel Redler, Kerrie E McNally, William Sheffler, T J Brunette, Derrick R Hicks, Tomos E Morgan, Tim J Stevens, Adam Broerman, Inna Goreshnik, Michelle DeWitt, Cameron M Chow, Yihang Shen, Lance Stewart, Emmanuel Derivery, Daniel Adriano Silva, Gira Bhabha, Dam
信号转导
FCM
IF
IHC-P
WB
TOM20
发表日期：2023
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FLNA-filaminopathy skeletal phenotypes are not due to an osteoblast autonomous loss-of-function

FLNA丝状蛋白病引起的骨骼表型并非由成骨细胞自主功能丧失所致。

期刊:Bone Reports
影响因子:2.6
doi:10.1016/j.bonr.2023.101668
Wade, Emma M; Goodin, Elizabeth A; Wang, Yongqiang; Morgan, Tim; Callon, Karen E; Watson, Maureen; Daniel, Philip B; Cornish, Jillian; McCulloch, Christopher A; Robertson, Stephen P
细胞生物学
FLNA
发表日期：2023
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Deletion of the last two exons of FGF10 in a family with LADD syndrome and pulmonary acinar hypoplasia

在患有LADD综合征和肺泡发育不全的家族中，FGF10基因最后两个外显子缺失

期刊:European Journal of Human Genetics
影响因子:4.6
doi:10.1038/s41431-021-00902-0
Wade, Emma M; Parthasarathy, Padmini; Mi, Jingyi; Morgan, Tim; Wollnik, Bernd; Robertson, Stephen P; Cundy, Tim
发育与干细胞
FGF1
FGF10
发表日期：2022
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Droplet digital PCR-based detection of circulating tumor DNA from pediatric high grade and diffuse midline glioma patients

基于液滴数字PCR的循环肿瘤DNA检测方法，用于检测儿童高级别和弥漫性中线胶质瘤患者的肿瘤DNA

期刊:NeuroOncology Advances
影响因子:3.7
doi:10.1093/noajnl/vdab013
Elisa Izquierdo ,Paula Proszek ,Giulia Pericoli ,Sara Temelso ,Matthew Clarke ,Diana M Carvalho ,Alan Mackay ,Lynley V Marshall ,Fernando Carceller ,Darren Hargrave ,Birgitta Lannering ,Zdenek Pavelka ,Simon Bailey ,Natacha Entz-Werle ,Jacques Grill ,Gilles Vassal ,Daniel Rodriguez ,Paul S Morgan ,Tim Jaspan ,Angela Mastronuzzi ,Mara Vinci ,Michael Hubank ,Chris Jones
肿瘤免疫
胶质瘤
肿瘤
发表日期：2021
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Effect of Intensive Blood Pressure Reduction on Left Ventricular Mass, Structure, Function, and Fibrosis in the SPRINT-HEART

SPRINT-HEART研究中强化降压对左心室质量、结构、功能和纤维化的影响

期刊:Hypertension
影响因子:8.2
doi:10.1161/HYPERTENSIONAHA.119.13073
Upadhya, Bharathi; Rocco, Michael V; Pajewski, Nicholas M; Morgan, Tim; Blackshear, Joseph; Hundley, William Greg; Oparil, Suzanne; Soliman, Elsayed Z; Cohen, Debbie L; Hamilton, Craig A; Cho, Monique E; Kostis, William J; Papademetriou, Vasilios; Rodriguez, Carlos J; Raj, Dominic S; Townsend, Ray; Vasu, Sujethra; Zamanian, Sara; Kitzman, Dalane W
发表日期：2019
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Biofeedback-Assisted Resilience Training for Traumatic and Operational Stress: Preliminary Analysis of a Self-Delivered Digital Health Methodology

生物反馈辅助的创伤和作战压力适应力训练：一种自主式数字健康方法的初步分析

期刊:Jmir Mhealth and Uhealth
影响因子:6.2
doi:10.2196/12590
Kizakevich, Paul N; Eckhoff, Randall P; Lewis, Gregory F; Davila, Maria I; Hourani, Laurel L; Watkins, Rebecca; Weimer, Belinda; Wills, Tracy; Morgan, Jessica K; Morgan, Tim; Meleth, Sreelatha; Lewis, Amanda; Krzyzanowski, Michelle C; Ramirez, Derek; Boyce, Matthew; Litavecz, Stephen D; Lane, Marian E; Strange, Laura B
发表日期：2019
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Quantification of transmission risk in a male patient with a FLNB mosaic mutation causing Larsen syndrome: Implications for genetic counseling in postzygotic mosaicism cases

对一名携带FLNB嵌合突变导致拉森综合征的男性患者的遗传风险进行量化：对合子后嵌合病例遗传咨询的启示

期刊:Human Mutation
影响因子:3.7
doi:10.1002/humu.23281
Bernkopf, Marie; Hunt, David; Koelling, Nils; Morgan, Tim; Collins, Amanda L; Fairhurst, Joanna; Robertson, Stephen P; Douglas, Andrew G L; Goriely, Anne
FLNB
发表日期：2017
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