ORAL DISEASES口腔疾病

ORAL DISEASES(英文缩写 ORAL DIS),ISSN 1354-523X,eISSN 1601-0825,中文译名:口腔疾病 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
3.100
JCR 分区
Q1
CAS 分区
B3
近一年发文量
482
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: 1354-523X · eISSN: 1601-0825 · 缩写: ORAL DIS ·中文: 口腔疾病

期刊介绍

选择期刊介绍栏目

期刊简介

《Oral Diseases》是一本聚焦口腔医学基础与临床研究的国际期刊,涵盖口腔黏膜病、牙周病、口腔癌、唾液腺疾病及口腔微生物学等领域。其读者群包括口腔医学研究者、临床医生及基础医学科学家,尤其关注口腔疾病与全身健康的关联。该刊强调多学科交叉,发表原创研究、综述及临床报告,致力于推动口腔疾病机制、诊断与治疗的前沿进展。

研究方向

主要研究方向包括口腔黏膜病变、牙周炎、口腔癌及癌前病变、唾液腺功能障碍、口腔微生物组、免疫与炎症机制、口腔与全身疾病关联等。论文类型涵盖原创研究、系统综述、临床报告及短篇通讯,鼓励转化医学和跨学科研究。

期刊特色

研究取向兼顾基础实验与临床观察,注重机制探索和临床意义。论文特点为数据扎实、方法严谨,常涉及分子生物学、免疫学及流行病学手段。适合口腔医学研究者、临床医师及关注口腔-全身健康关联的科研人员阅读和投稿。

投稿难度

投稿难度中等偏上,对研究的创新性和临床相关性要求较高。建议准备充分的前期数据、清晰的机制阐述及严谨的统计分析,并注重与口腔疾病临床问题的结合。语言表达需符合国际期刊规范,避免仅凭分区判断录用可能性。

历年影响因子趋势

JCR 数据年份影响因子JCR 分区
20214.068Q1
20223.800Q1
20232.900Q1
20242.900Q1
20253.100Q1

ORAL DISEASES 最新收录文献

  1. JCR分区: Q1 CAS分区: B3 影响因子: 3.1
  2. JCR分区: Q1 CAS分区: B3 影响因子: 3.1

    2. Authors' Reply "Increased Genetic Instability in Exfoliated Oral Cells in Patients With Epidermolysis Bullosa".

    作者:
    Ana Carolina Sias Franco Franzosi, Rebeca Ferreira Badaró, Lucas Fernandes Leal, Rosalie Matuk Fuentes Torrelio, Willian Grassi Bautz, Leticia Nogueira da Gama-de-Souza
    日期:
    2026-09-22

    该文献暂无摘要。

  3. JCR分区: Q1 CAS分区: B3 影响因子: 3.1
  4. JCR分区: Q1 CAS分区: B3 影响因子: 3.1
  5. JCR分区: Q1 CAS分区: B3 影响因子: 3.1
  6. JCR分区: Q1 CAS分区: B3 影响因子: 3.1
  7. JCR分区: Q1 CAS分区: B3 影响因子: 3.1

    7. Point-of-Care aMMP-8 Testing as an Objective Trigger for Dental Referral in Diabetes Care.

    作者:
    Pietro Leone, Ismo T Räisänen, Julie Toby Thomas, Timo Sorsa
    日期:
    2026-09-21

    该文献暂无摘要。

  8. JCR分区: Q1 CAS分区: B3 影响因子: 3.1

    8. Family Impact of Burning Mouth Syndrome: A Cross-Sectional Study Using FROM-16.

    作者:
    Mona Jullie Hajj, Nicholas Sotak, Alessandro Villa, Alan Roger Santos-Silva, Lloyd Mancl, Thaís Cristina Esteves-Pereira, Milda Chmieliauskaite
    日期:
    2026-09-21

    Burning mouth syndrome (BMS) is a chronic oral pain condition associated with psychological distress and reduced quality of life. Although BMS' impact on patients is documented, family member impact remains poorly understood. This study evaluated family impact using Family Reported Outcome Measure (FROM-16), explored family burden associations, assessed FROM-16 domains, and identified unmet support needs. This cross-sectional study included 26 patient-family member dyads from an oral medicine clinic. Family burden was assessed using FROM-16. Open-ended responses were analyzed thematically to characterize family experiences and support needs. Associations between family burden and demographic/clinical variables were explored using nonparametric analyses. Median total FROM-16 score was 5.5. Emotional burden exceeded personal/social burden, with worry, sadness, and frustration most common. Disruptions in family activities, eating habits, and family expenses were main social concerns. Lower household income was associated with higher burden scores. Qualitative findings confirmed emotional strain, altered social behaviors, and financial stress. Knowledgeable healthcare providers were the primary support source, although unmet healthcare, mental health, social, and treatment needs persisted. BMS affects families through emotional distress, disrupted eating habits, and social activities. These preliminary findings support evaluation of family-centered multidisciplinary approaches to improve support for patients and families.

  9. JCR分区: Q1 CAS分区: B3 影响因子: 3.1

    9. Assessment of Salivary Flow Patterns in Sjögren's Disease.

    作者:
    Mouna Alsunni, Matthew D Finkelman, Mabi Singh, Athena Papas, Vidya Sankar
    日期:
    2026-09-21

    Salivary flow may follow a circadian rhythm regulated by clock genes and aquaporins. Because aquaporin 5 dysregulation may contribute to Sjögren's disease, we investigated whether daily unstimulated and stimulated salivary flow patterns differed between participants with Sjögren's disease and healthy controls. Thirteen participants were recruited (80% power). Participants with Sjögren's disease met the 2016 American College of Rheumatology/European Alliance of Associations for Rheumatology classification criteria; healthy controls were not taking xerogenic medications. Saliva was collected at home (5:00 AM, 10:00 AM) and in the clinic (3:00 PM) for 5 min (unstimulated) and 2 min (stimulated). Differences were analysed using Friedman's test, the Mann-Whitney U test, and mixed-effects models (α = 0.05). We analysed 13 healthy controls (mean age 48.9 ± 10.7 years) and 13 participants with Sjögren's disease (mean age 65.3 ± 8.4 years). In the Sjögren's disease group, unstimulated flow did not vary over time (p = 0.463), but stimulated flow varied significantly across time points (p = 0.037). Neither measure varied significantly over time in controls (both p = 0.527). Neither group showed clear evidence of a circadian salivary flow pattern, and temporal patterns did not differ significantly between groups.

  10. JCR分区: Q1 CAS分区: B3 影响因子: 3.1

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指标接近的期刊