NATURE REVIEWS NEUROSCIENCE自然综述·神经科学

NATURE REVIEWS NEUROSCIENCE(英文缩写 NAT REV NEUROSCI),ISSN 1471-003X,eISSN 1471-0048,中文译名:自然综述·神经科学 是一本学术期刊。本页汇总该期刊的最新影响因子、分区信息以及最新收录于 PubMed 的文献,帮助您快速了解期刊全貌。

2026 年数据 · 影响因子
29.000
JCR 分区
Q1
CAS 分区
B1
近一年发文量
126
本站 PubMed 收录统计

发文量统计区间:2025-09-27 至 2026-09-27,按本站收录文献的发表日期统计。

ISSN: 1471-003X · eISSN: 1471-0048 · 缩写: NAT REV NEUROSCI ·中文: 自然综述·神经科学

期刊介绍

选择期刊介绍栏目

期刊简介

《自然综述·神经科学》是神经科学领域的高端综述期刊,聚焦分子、细胞、环路与认知神经科学的前沿进展,兼顾神经系统疾病机制。读者主要为神经科学研究者、临床神经科医师及交叉学科人员。文章以权威性、整合性和前瞻性著称,常由领域领军学者撰写,适合希望快速把握重大方向与争议的读者。

研究方向

主要覆盖神经发育、突触可塑性、感觉与运动系统、学习记忆、情绪与动机、神经免疫、神经退行性疾病及精神障碍的生物学基础。论文类型以特邀综述和观点文章为主,兼有短篇评论与展望,强调机制整合与跨尺度讨论。

期刊特色

研究取向偏重概念框架与领域批判性梳理,而非原始数据报告。文章通常图文并茂、引用密集,注重提出新假说和未来方向。适合资深研究者、青年学者及临床医生用于选题定位和教学参考,也适合跨学科读者了解神经科学全局。

投稿难度

投稿难度很高,通常为编辑邀约或预提交提案后邀请,对作者的国际影响力、综述整合能力和写作水平要求严格。建议先以预提交信函说明选题新颖性与必要性,并积累领域内代表性成果;不宜仅凭分区判断录用可能。

历年影响因子趋势

JCR 数据年份影响因子JCR 分区
202138.755Q1
202234.700Q1
202328.700Q1
202426.700Q1
202529.000Q1

NATURE REVIEWS NEUROSCIENCE 最新收录文献

  1. JCR分区: Q1 CAS分区: B1 影响因子: 29
  2. JCR分区: Q1 CAS分区: B1 影响因子: 29
  3. JCR分区: Q1 CAS分区: B1 影响因子: 29
  4. JCR分区: Q1 CAS分区: B1 影响因子: 29
  5. JCR分区: Q1 CAS分区: B1 影响因子: 29

    5. Early life experiences, the neural epigenome and affective disorder risk.

    作者:
    Ashley M Cunningham, Ian Maze
    日期:
    2026-10-01

    Early life stress shapes brain development during sensitive developmental windows through persistent epigenomic changes that influence gene regulation, neural circuit maturation and susceptibility to neuropsychiatric disorders. Evidence from animal models and human studies demonstrates that early adversity remodels DNA methylation, histone post-translational modifications and chromatin organization, leading to lasting alterations in transcriptional programmes. These responses are highly cell-type specific, brain-region specific and developmental-stage specific, with neurons and glia exhibiting distinct molecular adaptations that contribute to behavioural outcomes. Emerging evidence also implicates non-coding RNAs as important regulators of stress-induced gene expression, although their long-term roles remain less well defined than those of other epigenetic mechanisms. Peripheral epigenetic signatures associated with early life stress may provide accessible biomarkers of exposure and disease risk. Integrating epigenomic, transcriptomic, circuit-level and behavioural approaches will be essential for understanding biological embedding and identifying mechanisms that promote resilience and improve therapeutic interventions.

  6. JCR分区: Q1 CAS分区: B1 影响因子: 29

    6. Neural circuits for mammalian parental behaviour.

    作者:
    Bradley B Jamieson, Johannes Kohl
    日期:
    2026-10-01

    Most mammalian offspring are born helpless and depend on sustained parental care for survival, making caregiving one of the most conserved and essential behavioural repertoires in mammals. Yet infant-directed behaviours can be remarkably variable, ranging from care to neglect and aggression, even within the same individual. How neural circuits support both the robustness and the flexibility of parental behaviour remains poorly understood. Here we review recent advances in our understanding of the neural mechanisms of mammalian caregiving, placing circuit-level insights from rodent models into the broader context of parental diversity across mammals. Emerging evidence indicates that internal state and social experience dynamically reshape parental circuits across timescales from hours to weeks and that these circuits adapt their function to generate life stage-appropriate behavioural output. Rather than acting as fixed control systems for instinctive actions, parental circuits are highly plastic and context dependent. Parental behaviour therefore provides a powerful model for understanding how neural circuits are reconfigured to meet changing behavioural demands.

  7. JCR分区: Q1 CAS分区: B1 影响因子: 29

    7. Cerebellar rhythms: mechanisms, functions and translational opportunities.

    7. 小脑节律:机制、功能和翻译机会
    作者:
    Danny Adrian Spampinato, Annibale Antonioni, Egidio D'Angelo, Giacomo Koch
    日期:
    2026-10-01

    Cerebellar rhythms provide frequency-specific support for motor, cognitive and affective functions. These oscillations are not epiphenomenal but rather dynamically regulated, spatially organized control signals that contribute to the coordination of prediction, error correction, learning and internal model updating. By synchronizing neuronal activity across cerebellar and distributed brain networks at multiple timescales, cerebellar rhythms enable precise and adaptable behaviour and coordination across neural systems. Accordingly, they offer biologically grounded targets for network-level diagnostics and therapeutic neuromodulation. At the circuit level, cerebellar rhythms within distinct frequency bands, ranging from theta and beta to gamma and very high-frequency oscillations, arise from specific microcircuit mechanisms within the inferior olive, the granular and molecular layers of the cerebellar cortex, and the deep cerebellar nuclei. These rhythms structure spike timing and help shape synaptic plasticity windows, forming a frequency-organized substrate for learning and control. Here we describe a frequency-function-modulation framework that links cerebellar oscillations to their behavioural roles and to neuromodulatory interventions. By integrating evidence from animal studies, computational models and non-invasive stimulation studies, we position cerebellar oscillations as a bridge between cerebellar circuit dynamics and systems-level coordination, thereby providing a mechanistic rationale for precision neuromodulation across motor and cognitive domains in neurological and psychiatric conditions.

  8. JCR分区: Q1 CAS分区: B1 影响因子: 29

    8. Microglial states revisited: from homeostasis to disease.

    8. 重新审视小胶质细胞状态:从稳态到疾病
    作者:
    Bart J L Eggen, Susanne M Kooistra
    日期:
    2026-10-01

    Microglia, the resident macrophages of the CNS parenchyma, are recognized as highly plastic, transcriptionally diverse cells whose phenotypes are moulded by development, region, sex, age, genotype and environment. Advances in single-cell and single-nucleus transcriptomics, chromatin accessibility profiling, and spatial multi-omics have negated binary frameworks of 'resting versus activated' or 'M1 (pro-inflammatory) versus M2 (anti-inflammatory)' and revealed a multidimensional state space that supports brain development, homeostasis and adaptive responses to perturbation. Building on the foundational concepts of the microglial sensome, homeostatic and disease-associated signatures, microglia exhibit transcriptomic state transitions in neurodegeneration, demyelination, infection and systemic inflammation. Moreover, a mechanistic framework for more 'hidden' microglial states has emerged, in which latent programmes that appear homeostatic at baseline are revealed by challenges and are instructed through innate immune training or tolerance. We argue that these covert reprogrammed states, which are shaped by ageing, genotype, sex, location and prior exposures such as sepsis or viral infection, help explain interindividual variability in disease trajectories. We conclude by outlining priorities for unifying state annotation across species and modalities, and for translating state-resolved insights into biomarkers and interventions.

  9. JCR分区: Q1 CAS分区: B1 影响因子: 29

    9. Quantum computing for neuroscience: opportunities beyond classical limits.

    作者:
    Annemarie Wolff, Alexandre Choquette, Georg Northoff, Atsushi Iriki, Guillaume Dumas
    日期:
    2026-09-24

    该文献暂无摘要。

  10. JCR分区: Q1 CAS分区: B1 影响因子: 29

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指标接近的期刊