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

Congenital microcoria deletion in mouse links Sox21 dysregulation to disease and suggests a role for TGFB2 in glaucoma and myopia.

小鼠先天性小角膜缺失将 Sox21 失调与疾病联系起来，并表明 TGFB2 在青光眼和近视中发挥作用

期刊:American Journal of Human Genetics
影响因子:8.1
doi:10.1016/j.ajhg.2024.08.019
Erjavec Elisa, Angée Clémentine, Hadjadj Djihad, Passet Bruno, David Pierre, Kostic Corinne, Dodé Emmanuel, Zanlonghi Xavier, Cagnard Nicolas, Nedelec Brigitte, Crippa Sylvain V, Bole-Feysot Christine, Zarhrate Mohammed, Creuzet Sophie, Castille Johan, Vilotte Jean-Luc, Calvas Patrick, Plaisancié Julie, Chassaing Nicolas, Kaplan Josseline, Rozet Jean-Michel, Fares Taie L
Mouse
SOX2
发表日期：2024
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PupilMetrics: a support system for preprocessing of pupillometric data and extraction of outcome measures

PupilMetrics：一个用于瞳孔测量数据预处理和结果指标提取的支持系统

期刊:Scientific Reports
影响因子:3.9
doi:10.1038/s41598-024-79920-z
Amiot, Victor; Tomasoni, Mattia; Minier, Astrid; Gisselbaek, Sara; Kawasaki, Aki; Kostic, Corinne
发表日期：2024
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Lentiviral Vectors for Ocular Gene Therapy

用于眼部基因治疗的慢病毒载体

期刊:Pharmaceutics
影响因子:5.5
doi:10.3390/pharmaceutics14081605
Arsenijevic, Yvan; Berger, Adeline; Udry, Florian; Kostic, Corinne
微生物学
基因治疗
发表日期：2022
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Enhancer of Zeste Homolog 2 (EZH2) Contributes to Rod Photoreceptor Death Process in Several Forms of Retinal Degeneration and Its Activity Can Serve as a Biomarker for Therapy Efficacy.

Zeste同源物2增强子（EZH2）在多种视网膜变性中促进视杆感光细胞死亡过程，其活性可作为治疗效果的生物标志物

期刊:International Journal of Molecular Sciences
影响因子:4.9
doi:10.3390/ijms22179331
Mbefo Martial, Berger Adeline, Schouwey Karine, Gérard Xavier, Kostic Corinne, Beryozkin Avigail, Sharon Dror, Dolfuss Hélène, Munier Francis, Tran Hoai Viet, van Lohuizen Maarten, Beltran William A, Arsenijevic Yvan
细胞生物学
发表日期：2021
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Quantification of the early pupillary dilation kinetic to assess rod and cone activity

量化早期瞳孔扩张动力学以评估视杆细胞和视锥细胞的活动

期刊:Scientific Reports
影响因子:3.9
doi:10.1038/s41598-021-88915-z
Kostic, Corinne; Crippa, Sylvain V; Leon, Lorette; Hamel, Christian; Meunier, Isabelle; Kawasaki, Aki
细胞生物学
发表日期：2021
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Maturation of the Pupil Light Reflex Occurs Until Adulthood in Mice

小鼠瞳孔对光反射的成熟过程持续到成年期。

期刊:Frontiers in Neurology
影响因子:2.8
doi:10.3389/fneur.2019.00056
Kircher, Noémie; Crippa, Sylvain V; Martin, Catherine; Kawasaki, Aki; Kostic, Corinne
发表日期：2019
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Animal modelling for inherited central vision loss

遗传性中心视力丧失的动物模型

期刊:Journal of Pathology
影响因子:5.2
doi:10.1002/path.4641
Kostic, Corinne; Arsenijevic, Yvan
发表日期：2016
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Determination of Rod and Cone Influence to the Early and Late Dynamic of the Pupillary Light Response

确定视杆细胞和视锥细胞对瞳孔光反应早期和晚期动态的影响

期刊:Investigative Ophthalmology & Visual Science
影响因子:4.7
doi:10.1167/iovs.16-19150
Kostic, Corinne; Crippa, Sylvain V; Martin, Catherine; Kardon, Randy H; Biel, Martin; Arsenijevic, Yvan; Kawasaki, Aki
细胞生物学
发表日期：2016
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Amyloid Precursor-Like Protein 2 deletion-induced retinal synaptopathy related to congenital stationary night blindness: structural, functional and molecular characteristics

淀粉样前体蛋白样蛋白2缺失诱导的视网膜突触病变与先天性静止性夜盲症相关：结构、功能和分子特征

期刊:Molecular Brain
影响因子:2.9
doi:10.1186/s13041-016-0245-z
Dinet, Virginie; Ciccotosto, Giuseppe D; Delaunay, Kimberley; Borras, Céline; Ranchon-Cole, Isabelle; Kostic, Corinne; Savoldelli, Michèle; El Sanharawi, Mohamed; Jonet, Laurent; Pirou, Caroline; An, Na; Abitbol, Marc; Arsenijevic, Yvan; Behar-Cohen, Francine; Cappai, Roberto; Mascarelli, Frédéric
神经科学
发表日期：2016
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Adamts18 deletion results in distinct developmental defects and provides a model for congenital disorders of lens, lung, and female reproductive tract development

Adamts18基因缺失会导致明显的发育缺陷，并为晶状体、肺和女性生殖道发育的先天性疾病提供了一个模型。

期刊:Biology Open
影响因子:1.7
doi:10.1242/bio.019711
Ataca, Dalya; Caikovski, Marian; Piersigilli, Alessandra; Moulin, Alexandre; Benarafa, Charaf; Earp, Sarah E; Guri, Yakir; Kostic, Corinne; Arsenijevic, Yvan; Soininen, Raija; Apte, Suneel S; Brisken, Cathrin
发育与干细胞
发表日期：2016
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