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

Evaluating the Utility of RNAseq in Prenatal Diagnostics: Expression Profiles of Cultured Chorionic Villus and Amniotic Fluid Samples

评估RNA测序在产前诊断中的应用：培养绒毛膜绒毛和羊水样本的表达谱

期刊:Prenatal Diagnosis
影响因子:2.7
doi:10.1002/pd.70123
Vladoiu, Maria C; Zhao, Sen; Zemet, Roni; Parobek, Christian M; Sinson, Jefferson Cruz; Tankersley, Stacy; Van den Veyver, Ignatia B; Liu, Pengfei
发表日期：2026
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Clinical validation of RNA sequencing for Mendelian disorder diagnostics

RNA测序在孟德尔遗传病诊断中的临床验证

期刊:American Journal of Human Genetics
影响因子:8.1
doi:10.1016/j.ajhg.2025.02.006
Zhao, Sen; Macakova, Kristina; Sinson, Jefferson C; Dai, Hongzheng; Rosenfeld, Jill; Zapata, Gladys E; Li, Shenglan; Ward, Patricia A; Wang, Christiana; Qu, Chunjing; Maywald, Becky; Lee, Brendan; Eng, Christine; Liu, Pengfei
发表日期：2025
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The utility of ultra-deep RNA sequencing in Mendelian disorder diagnostics

超深度RNA测序在孟德尔遗传病诊断中的应用

期刊:American Journal of Human Genetics
影响因子:8.1
doi:10.1016/j.ajhg.2025.09.013
Zhao, Sen; Sinson, Jefferson C; Li, Shenglan; Rosenfeld, Jill A; Zapata, Gladys; Macakova, Kristina; Pena, Mezthly; Maywald, Becky; Worley, Kim C; Burrage, Lindsay C; Weisz-Hubshman, Monika; Ketkar, Shamika; Craigen, William; Emrick, Lisa; Clark, Tyson; Lithwick, Gila Yanai; Shipony, Zohar; Eng, Christine; Lee, Brendan; Liu, Pengfei
发表日期：2025
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The Utility of Ultra-Deep RNA sequencing in Mendelian Disorder Diagnostics

超深度RNA测序在孟德尔遗传病诊断中的应用

期刊:
影响因子:
doi:10.1101/2025.01.28.25321295
Zhao, Sen; Sinson, Jefferson C; Li, Shenglan; Rosenfeld, Jill A; Zapata, Gladys; Macakova, Kristina; Pena, Mezthly; Maywald, Becky; Worley, Kim C; Burrage, Lindsay; Hubshman, Monika Weisz; Ketkar, Shamika; Craigen, William; Emrick, Lisa; Clark, Tyson; Lithwick, Gila Yanai; Shipony, Zohar; Eng, Christine; Lee, Brendan; Liu, Pengfei
发表日期：2025
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High peripheral T cell diversity is associated with lower risk of toxicity and superior response to dual immune checkpoint inhibitor therapy in patients with metastatic NSCLC

外周T细胞多样性高与转移性非小细胞肺癌患者毒性风险降低和对双重免疫检查点抑制剂治疗的疗效更佳相关。

期刊:Journal for ImmunoTherapy of Cancer
影响因子:10.6
doi:10.1136/jitc-2024-008950
Altan, Mehmet; Li, Ruoxing; Li, Ziyi; Chen, Runzhe; Sheshadri, Ajay; Tran, Hai T; Little, Latasha; Baguley, Joshua; Sinson, Jefferson; Vokes, Natalie; Gandhi, Saumil; Antonoff, Mara B; Swisher, Stephen G; Lizee, Greg; Reuben, Alexandre; Heymach, John V; Zhang, Jianjun
肺癌
肿瘤
T细胞
肿瘤免疫
T细胞
细胞生物学
毒理研究
免疫/内分泌
发表日期：2024
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The clinical utility and diagnostic implementation of human subject cell transdifferentiation followed by RNA sequencing

人源细胞转分化结合RNA测序的临床应用及诊断实施

期刊:American Journal of Human Genetics
影响因子:8.1
doi:10.1016/j.ajhg.2024.03.007
Shenglan Li,Sen Zhao,Jefferson C Sinson,Aleksandar Bajic,Jill A Rosenfeld,Matthew B Neeley,Mezthly Pena,Kim C Worley,Lindsay C Burrage,Monika Weisz-Hubshman,Shamika Ketkar,William J Craigen,Gary D Clark,Seema Lalani,Carlos A Bacino,Keren Machol,Hsiao-Tuan Chao,Lorraine Potocki,Lisa Emrick,Jennifer Sheppard,My T T Nguyen,Anahita Khoramnia,Paula Patricia Hernandez,Sandesh Cs Nagamani,Zhandong Liu
Human
细胞生物学
发表日期：2024
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Improving Quality Metrics in Neurosurgery: A Spinal Surgery 3-Year Case Review

提升神经外科质量指标：脊柱外科三年病例回顾

期刊:Neurosurgery Practice
影响因子:0.6
doi:10.1227/neuprac.0000000000000071
Feller, Christina Nicoll; Bodenbach, Erin M; Kolinski, Julie M; Sinson, Grant P
发表日期：2024
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The M2 macrophages infiltration of sebaceous tumors is linked to the aggressiveness of tumors but not to the mismatch repair pathway.

M2巨噬细胞浸润皮脂腺肿瘤与肿瘤的侵袭性有关，但与错配修复途径无关

期刊:Journal of Cancer Research and Clinical Oncology
影响因子:2.8
doi:10.1007/s00432-023-04629-x
Frouin Eric, Alleyrat Camille, Godet Julie, Karayan-Tapon Lucie, Sinson Hélinie, Morel Franck, Lecron Jean-Claude, Favot Laure
肿瘤
发表日期：2023
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Characterization of Cancer Evolution Landscape Based on Accurate Detection of Somatic Mutations in Single Tumor Cells

基于对单个肿瘤细胞中体细胞突变的精确检测来表征癌症演化图谱

期刊:
影响因子:
doi:10.1101/2023.10.09.561356
Niu, Muchun; Zhang, Yang; Luo, Jiayi; Sinson, Jefferson C; Thompson, Alastair M; Zong, Chenghang
肿瘤细胞
细胞生物学
肿瘤
肿瘤免疫
发表日期：2023
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Sequencing individual genomes with recurrent genomic disorder deletions: an approach to characterize genes for autosomal recessive rare disease traits

对具有复发性基因组疾病缺失的个体基因组进行测序：一种表征常染色体隐性罕见病性状基因的方法

期刊:Genome Medicine
影响因子:10.4
doi:10.1186/s13073-022-01113-y.
Bo Yuan ,Katharina V Schulze ,Nurit Assia Batzir ,Jefferson Sinson ,Hongzheng Dai ,Wenmiao Zhu ,Francia Bocanegra ,Chin-To Fong ,Jimmy Holder ,Joanne Nguyen ,Christian P Schaaf ,Yaping Yang ,Weimin Bi ,Christine Eng ,Chad Shaw ,James R Lupski ,Pengfei Liu
发表日期：2022
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