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

Improving women's healthcare providers' knowledge about fragile X-associated primary ovarian insufficiency through a novel educational tool

通过一种新型教育工具提高女性医疗保健提供者对脆性X染色体相关原发性卵巢功能不全的认识

期刊:Journal of Assisted Reproduction and Genetics
影响因子:2.7
doi:10.1007/s10815-025-03734-9
Peery, Emily; Singleton, Alexandra L; Merkison, Jamie; Brockman, Deanna; Hipp, Heather; Ali, Nadia; Lichten, Lauren; Allen, Emily G
发表日期：2026
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The effect of sample type on genetic testing completion in pediatric congenital hearing loss patients

样本类型对儿童先天性听力损失患者基因检测完成率的影响

期刊:Journal of Community Genetics
影响因子:1.8
doi:10.1007/s12687-025-00834-y
Adams, Brittany; Lichten, Lauren; Heyward, Aaliyah; Govil, Nandini
发表日期：2026
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Exploring Motivation and Emotional Experience in Observational Research for Individuals at Risk of ALS/FTD Spectrum Disorders

探索ALS/FTD谱系障碍高危人群的动机和情感体验：一项观察性研究

期刊:Neurology-Clinical Practice
影响因子:3.2
doi:10.1212/CPJ.0000000000200538
Jadeja, Niharika; Ali, Nadia; Dratch, Laynie; Stanislaw, Christine; Barvin, Daniel; Fournier, Christina N; Lichten, Lauren
ALS
发表日期：2025
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Reflections on my international genetic counseling rotations: Contrasts in practice between India and the United States

关于我的国际遗传咨询轮岗经历的反思：印度和美国实践的差异

期刊:Genetics in Medicine Open
影响因子:
doi:10.1016/j.gimo.2024.101871
Jadeja, Niharika; Rajakumar, Nivedita; Reddy, Neeraja; Ali, Nadia; Lichten, Lauren
发表日期：2024
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Incorporating Genetic Testing Into the Care of Patients With Amyotrophic Lateral Sclerosis/Frontotemporal Degeneration Spectrum Disorders

将基因检测纳入肌萎缩侧索硬化症/额颞叶变性谱系障碍患者的护理中

期刊:Neurology-Clinical Practice
影响因子:3.2
doi:10.1212/CPJ.0000000000200201
Chambers, Chelsea; Lichten, Lauren; Crook, Ashley; Uhlmann, Wendy R; Dratch, Laynie
发表日期：2023
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The qualitative experiences of otolaryngologists with genetic services in pediatric hearing loss evaluation

耳鼻喉科医生在儿科听力损失评估中使用遗传服务的定性经验

期刊:Journal of Community Genetics
影响因子:1.8
doi:10.1007/s12687-023-00649-9
Heyward, Aaliyah; Hagerty, Kelsi; Lichten, Lauren; Howell, Julie; Tey, Ching Siong; Dedhia, Kavita; Kavalieratos, Dio; Govil, Nandini
发表日期：2023
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Turning coldspots into hotspots: targeted recruitment of axis protein Hop1 stimulates meiotic recombination in Saccharomyces cerevisiae

将冷点转变为热点：轴蛋白 Hop1 的靶向募集刺激酿酒酵母的减数分裂重组

期刊:Genetics
影响因子:3.3
doi:10.1093/genetics/iyac106
Anura Shodhan, Martin Xaver, David Wheeler, Michael Lichten
微生物学
发表日期：2022
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Developmental trauma: Conceptual framework, associated risks and comorbidities, and evaluation and treatment

发展性创伤：概念框架、相关风险和合并症、评估和治疗

期刊:Frontiers in Psychiatry
影响因子:3.2
doi:10.3389/fpsyt.2022.800687
Cruz, Daniel; Lichten, Matthew; Berg, Kevin; George, Preethi
发表日期：2022
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Rad51-mediated interhomolog recombination during budding yeast meiosis is promoted by the meiotic recombination checkpoint and the conserved Pif1 helicase

芽殖酵母减数分裂过程中 Rad51 介导的同源物间重组由减数分裂重组检查点和保守的 Pif1 解旋酶促进

期刊:PLoS Genetics
影响因子:
doi:10.1371/journal.pgen.1010407
Andrew Ziesel, Qixuan Weng, Jasvinder S Ahuja, Abhishek Bhattacharya, Raunak Dutta, Evan Cheng, G Valentin Börner, Michael Lichten, Nancy M Hollingsworth
信号转导
Checkpoint
Donkey
IgG
发表日期：2022
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Repeated strand invasion and extensive branch migration are hallmarks of meiotic recombination.

反复的链入侵和广泛的分支迁移是减数分裂重组的标志

期刊:Molecular Cell
影响因子:16.6
doi:10.1016/j.molcel.2021.08.003
Ahuja Jasvinder S, Harvey Catherine S, Wheeler David L, Lichten Michael
发表日期：2021
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