JAMA DermatologyJAMA皮肤病学

JAMA Dermatology(英文缩写 JAMA DERMATOL),ISSN 2168-6068,eISSN 2168-6084,中文译名:JAMA皮肤病学 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
10.900
JCR 分区
Q1
CAS 分区
B1
近一年发文量
299
本站 PubMed 收录统计

发文量统计区间:2025-10-01 至 2026-09-30,按本站收录文献的发表日期统计。

ISSN: 2168-6068 · eISSN: 2168-6084 · 缩写: JAMA DERMATOL ·中文: JAMA皮肤病学

期刊介绍

选择期刊介绍栏目

期刊简介

JAMA Dermatology 是国际知名的临床皮肤病学期刊,主要发表皮肤病诊断、治疗与预防的高质量原创研究、综述和临床评论。内容覆盖炎症性皮肤病、皮肤肿瘤、感染、美容皮肤科及皮肤外科等领域,读者群为皮肤科医师、临床研究者及相关专科医生。

研究方向

主要方向包括临床与转化研究、随机对照试验、队列研究、诊断准确性研究、系统综述及临床指南。主题涉及银屑病、特应性皮炎、黑色素瘤、非黑色素瘤皮肤癌、皮肤感染、脱发及皮肤外科等,也关注医疗质量与患者结局。

期刊特色

研究取向偏重临床实用性与方法学严谨性,论文强调对诊疗决策的直接影响。常见类型有原创研究、研究快报、综述和观点评论。适合有扎实临床数据或高质量试验设计的皮肤科研究者,也适合关注循证医学的临床医生阅读。

投稿难度

投稿难度较高,对研究设计、样本量、统计分析和临床意义要求严格。建议在投稿前完善试验注册、伦理审批和报告规范,突出创新点与临床转化价值,并针对皮肤科读者清晰阐述实践意义,避免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
202111.816Q1
202210.900Q1
202311.500Q1
202411.000Q1
202510.900Q1

JAMA Dermatology 最新收录文献

  1. JCR分区: Q1 CAS分区: B1 影响因子: 10.9

    1. Pseudofolliculitis Barbae Diagnosis and Treatment in US Veterans.

    作者:
    Courtney A Smith, Olivia Collins, Chiagoziem Ohamadike, Howa Yeung
    日期:
    2026-09-30

    该文献暂无摘要。

  2. JCR分区: Q1 CAS分区: B1 影响因子: 10.9

    2. Longitudinal Growth in Children With Epidermal Differentiation Disorders.

    作者:
    Caroline Echeandia-Francis, Angela J Luo, William Liu, Mitra V Mani, Tiffany X Chen, Emily Sirotich, Riddhi D Patel, Lidia Ossowska, Geliang Gan, Yanhong Deng, Amy S Paller, Keith A Choate
    日期:
    2026-09-30

    Children with epidermal differentiation disorders (EDDs) frequently exhibit impaired growth, yet longitudinal growth trajectories across multiple EDD genotypes have not been systematically evaluated. To characterize longitudinal growth outcomes, including height, weight, and head circumference, in children with EDDs and evaluate genotype-specific associations. This longitudinal cohort study of children with EDDs used registry-based survey data and pediatric growth measurements through age 18 years. Data were collected from June 2022 to June 2025 and analyzed in September 2025. Participants were recruited through the National Registry for Ichthyosis; growth data were analyzed using US Centers for Disease Control and Prevention/World Health Organization pediatric growth standards. A total of 135 individuals aged 30 years or younger from 129 kindreds with confirmed EDDs and 26 unaffected siblings from 20 kindreds were included. Participants were classified into 5 genotype-based groups: autosomal recessive nonsyndromic-EDDs (nEDD), SPINK5-syndromic EDD (sEDD), keratinopathic-nEDDs, FLG-nEDD, and STS-sEDD. The primary exposure was EDD genotype. Secondary exposures included supplemental caloric intake, gastrostomy tube use, preterm birth, and neonatal intensive care unit admission. Primary outcomes were longitudinal height, weight, and head circumference percentiles from birth to age 18 years. Growth trajectories were analyzed using linear mixed-effects models, comparing EDD subtypes with population norms at monthly points within prespecified age intervals (age 0-24, 25-48, and >48 months). Among 135 participants (62 female [45.9%] and 73 male individuals [54.1%]; mean [SD] age, 10.5 [6.8] years; 13 Asian [9.6%], 7 Black [5.2%], 9 Hispanic [6.7%], and 89 White individuals [65.9%]), mean weight and height were less than the 50th percentile during the first 24 months of life (weight, 31.4th percentile; P < .001; height, 39.0th percentile; P = .02), with no significant difference from the population median thereafter. Growth impairment depended on genotype: individuals with SPINK5 variants exhibited persistent deficits at age 25 to 48 months (weight, 17.7th percentile; P = .002; height, 6.8th percentile; P < .001), whereas early deficits associated with ABCA12 and KRT10 variants attenuated over time and were no longer statistically significant. The results of this cohort study suggest that growth impairment in EDDs depends on genotype and is most prominent during the earliest months of life. Routine growth monitoring should be standard of care, particularly for children with high-risk genotypes, such as SPINK5.

  3. JCR分区: Q1 CAS分区: B1 影响因子: 10.9

    3. Best Practices for Managing Pseudofolliculitis Barbae: An Expert Consensus Delphi Study.

    作者:
    Simona A Alomary, Nicole J Baker, Grace Ugwueke, Haya Alkiswani, Prince Adotama, Olabola Awosika, Cheryl Burgess, Valerie Callender, Sunghun Cho, Jeanine Downie, Omar Ibrahimi, Joanna Ludzik, Tiffany Mayo, Hope Mitchell, Temitayo Ogunleye, Simon Ritchie, JiaDe Yu, Willis H Lyford, Nada Elbuluk, Susan C Taylor
    日期:
    2026-09-23

    Pseudofolliculitis barbae (PFB) is a chronic inflammatory disease caused by penetration of a shaved, curved hair shaft into the skin. Standardized recommendations for diagnosing and managing PFB are needed. To establish expert consensus recommendations outlining best practices for diagnosing and managing PFB. A 3-round Delphi consensus study was conducted using a panel of board-certified US dermatologists with expertise in PFB. Consensus statements addressing diagnostic criteria, behavioral modification, topical and systemic therapies, procedural interventions, and occupational considerations were developed and evaluated using a 9-point Likert scale. Consensus was predefined as greater than or equal to 75% agreement. Forty statements associated with diagnostic criteria, medical and procedural management, and occupational considerations reached consensus. Behavioral modification of hair removal practices as first-line therapy, use of targeted topical and systemic treatments, and procedural interventions, such as laser hair removal, were supported. No agreement was reached regarding a standardized grading scale, the use of oral isotretinoin for refractory disease, superficial chemical peels, or the use of multiblade razors. Using a Delphi consensus study approach, expert consensus guidelines were established for diagnosing and managing PFB. These recommendations provide an evidence-informed framework to support clinical decision-making, guide future research efforts, and help inform policy considerations associated with PFB management.

  4. JCR分区: Q1 CAS分区: B1 影响因子: 10.9

    4. Robustness of Network Meta-Analysis in Chronic Plaque Psoriasis.

    作者:
    Emilie Sbidian, Sivem Afach, Laurence Le Cleach
    日期:
    2026-09-23

    该文献暂无摘要。

  5. JCR分区: Q1 CAS分区: B1 影响因子: 10.9

    5. Robustness of Network Meta-Analysis in Chronic Plaque Psoriasis-Reply.

    作者:
    April W Armstrong, Yvonne Nong, Joseph F Merola
    日期:
    2026-09-23

    该文献暂无摘要。

  6. JCR分区: Q1 CAS分区: B1 影响因子: 10.9

    6. Lived Experience of Hirsutism in Transfeminine Individuals.

    作者:
    Sarah Gold, Marta Taye, Andrew Murdock, Francisco Delgado, Rebecca Goldberg, Meron Siira, Ketki Joshi, Vin Tangpricha, J Sonya Haw, Jason S Schneider, Michael Goodman, Cam Escoffery, Ashli Owen-Smith, Suephy C Chen, Howa Yeung
    日期:
    2026-09-23

    Hirsutism is commonly associated with gender dysphoria in transgender and gender-diverse individuals, with many seeking permanent hair removal. Little research has examined how hirsutism impacts life and stigma in gender minority groups. To examine lived experiences of hirsutism and hirsutism treatment in transgender and gender-diverse participants. This qualitative study included semistructured interviews with transgender women and nonbinary adults assigned male at birth across 3 clinical settings in Atlanta, Georgia, from February 7 to June 26, 2023. Self-reported hirsutism. Interviews exploring experiences of hirsutism and hirsutism treatment were analyzed via thematic analysis. Among 18 participants who completed the study, 17 were transgender women and 1 was a nonbinary individual assigned male at birth (mean [range] participant age, 38 [22-68] years). Fourteen participants self-rated clinically significant hirsutism levels, and only 1 reported having a diagnosis of hirsutism from a clinician. Participants described experiences of discrimination and rejection related to hirsutism and admitted avoiding social and romantic interactions in anticipation. Hirsutism was also reported to interfere with feminine gender expression and resulted in gender dysphoria. Many individuals went to great lengths to conceal visible hair in public, keeping razors or tweezers readily available for facial hair removal. Barriers to permanent hair removal included appointment burden, clinician attitude, lack of transgender-inclusive hair removal services, cost, and lack of insurance coverage. In this qualitative study, transgender women and nonbinary adults assigned male at birth described experiencing hirsutism-related stigma and facing barriers to permanent hair removal. Multilevel changes aimed to reduce stigma, educate clinicians on hair-removal options, expand transgender-inclusive hair-removal services, and advocate for insurance coverage for permanent hair removal are required to reduce barriers to access medically necessary permanent hair removal for gender dysphoria.

  7. JCR分区: Q1 CAS分区: B1 影响因子: 10.9

    7. Efficacy and Safety of Ruxolitinib Cream in Patients With Cutaneous Lichen Planus: A Randomized Clinical Trial.

    作者:
    Aaron R Mangold, Benjamin Lockshin, Zhihong Lai, Rong Rong, Haq Nawaz, Benjamin D Ehst
    日期:
    2026-09-23

    Lichen planus is a chronic, highly pruritic, inflammatory disease that affects the skin and other tissues. To evaluate the efficacy and safety of ruxolitinib, 1.5%, cream in patients with cutaneous lichen planus. This phase 2, 16-week, randomized, double-blind, vehicle-controlled trial with a 16-week open-label extension was conducted from November 2022 to February 2024. Patients were enrolled from 19 sites in the US and Canada. The trial included adults with predominantly cutaneous lichen planus, an Investigator's Global Assessment (IGA) score of 3 or 4, an Itch Numerical Rating Scale score of 4 or greater, and an affected body surface area of 20% or less were enrolled. Data were analyzed from February to August 2024. Patients were randomized 1:1 to ruxolitinib, 1.5%, twice daily cream or vehicle cream for 16 weeks, after which eligible patients applied ruxolitinib cream twice daily as needed in a 16-week, open-label extension. The primary end point was IGA treatment success (IGA score of 0 or 1 [clear/almost clear skin] with a ≥2-grade improvement from baseline) at week 16. Among 64 randomized patients, 46 (72%) were female, 18 (28%) were male, 18 (28%) were African American/Black, 4 (6%) were Asian, 40 (63%) were White, and the median (range) age was 57.0 (18-78) years. Significantly more patients who applied ruxolitinib, 1.5%, cream vs vehicle achieved IGA treatment success (50.0% [95% CI, 31.9%-68.1%] vs 21.9% [95% CI, 9.3%-40.0%], respectively; response rate difference, 29.4% [95% CI, 7.6%-51.3%]; P = .01; primary end point) at week 16, with further improvement to week 32. Similar results were observed in the proportion of patients who achieved a 4 or greater-point improvement from baseline in Itch Numerical Rating Scale score (week 16, 48.4% [95% CI, 30.2%-66.9%] vs 16.1% [95% CI, 5.5%-33.7%]; response rate difference, 33.5%; 95% CI, 12.2%-54.9%; P = .004; secondary end point). No serious treatment-emergent adverse events or discontinuations due to an adverse event were observed with ruxolitinib cream. The results of this randomized clinical trial suggest that ruxolitinib cream significantly reduced lesions and itch in patients with lichen planus. Therefore, ruxolitinib cream represents a potential treatment option for patients with cutaneous lichen planus. ClinicalTrials.gov Identifier: NCT05593432.

  8. JCR分区: Q1 CAS分区: B1 影响因子: 10.9
  9. JCR分区: Q1 CAS分区: B1 影响因子: 10.9

    9. Elephantiasic Pretibial Myxedema.

    作者:
    Anqi Xie, Tao Wang
    日期:
    2026-09-23

    该文献暂无摘要。

  10. JCR分区: Q1 CAS分区: B1 影响因子: 10.9

    10. Perifollicular Repigmentation After Hair Transplant in Stable Discoid Lupus Erythematosus.

    作者:
    Jorge Larrondo, Marianne Gosch, Raúl Cabrera, Iván Guaya, Alex Castro, Amy J McMichael
    日期:
    2026-09-16

    该文献暂无摘要。

在 JAMA Dermatology 中搜索更多文献

支持中英文检索 · 智能翻译 · 影响因子 · PDF 下载 · AI 文献阅读

指标接近的期刊