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Analysis of institutional authors

Mascaro JAuthorHernández-Rodríguez JAuthor

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November 15, 2019
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Dermatologic and dermatopathologic features of monogenic autoinflammatory diseases

Publicated to: Frontiers in Immunology. 10 (OCT): 2448- - 2019-10-29 10(OCT), DOI: 10.3389/fimmu.2019.02448

Authors:

Figueras-Nart, Ignasi; Mascaro, Jose M, Jr; Solanich, Xavier; Hernandez-Rodriguez, Jose
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Affiliations

Traslational Medicine. Cardiovascular, Respiratory and Systemic Diseases and cellular aging Program. Systemic Diseases and Ageing - Author
Univ Barcelona, Bellvitge Hosp, Dept Dermatol, Barcelona, Spain - Author
Univ Barcelona, Bellvitge Hosp, Dept Internal Med, Barcelona, Spain - Author
Univ Barcelona, Clin Unit, Autoinflammatory Dis & Vasculitis Res Unit, Dept Autoimmune Dis,Hosp Clin,IDIBAPS, Barcelona, Spain - Author
Univ Barcelona, IDIBAPS, Hosp Clin, Dept Dermatol, Barcelona, Spain - Author
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Abstract

© 2019 Figueras-Nart, Mascaró, Solanich and Hernández-Rodríguez. Autoinflammatory diseases include disorders with a monogenic cause and also complex conditions associated to polygenic or multifactorial factors. An increased number of both monogenic and polygenic autoinflammatory conditions have been identified during the last years. Although skin manifestations are often predominant in monogenic autoinflammatory diseases, clinical and histopathological information regarding their dermatological involvement is still scarce. Monogenic autoinflammatory diseases with cutaneous expression can be classified based on the predominant lesion: (1) maculopapular rashes or inflammatory plaques; (2) urticarial rashes; (3) pustular, pyogenic or neutrophilic dermatosis-like rashes; (4) panniculitis or subcutaneous nodules; (5) vasculitis or vasculopathy; (6) hyperkeratotic lesions; (7) hyperpigmented lesions; (8) bullous lesions; and (9) aphthous lesions. By using this classification, this review intends to provide clinical and histopathological knowledge about cutaneous involvement in monogenic autoinflammatory diseases.
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Keywords

Acute febrile neutrophilic dermatosisAdalimumabAicardi goutieres syndromeAphthous stomatitisAutoimmune diseasesAutoimmunityAutoinflammation and plc gamma 2 associated antibody deficiency and immune dysregulationAutoinflammatory diseaseAutoinflammatory diseasesAutoinflammatory periodic fever, immunodeficiency,and thrombocytopeniaAutosomal dominant disorderBiomarkersBiopsyBlau syndromeC/ebp epsilon associated autoinflammation and immune impairment of neutrophilsCanakinumabCard 14 mediated psoriasisChronic atypical neutrophilic dermatitis with lipodystrophy and elevated temperature syndromeCinca syndromeClassificationClinical dermatologyDeficiency of adenosine deaminase 2Deficiency of il 1 receptor antagonistDeficiency of il 36 receptor antagonistDermatitisDermatologíaDermatologyDermatopathologyDiagnosis, differentialErysipeloidEtanerceptFamilial chilblain lupusFamilial mediterranean feverGene mutationGenetic association studiesGenetic predisposition to diseaseGlucocorticoidH syndromeHistopathologyHumanHuman tissueHumansHyperimmunoglobulinemia d and periodic fever syndromeHyperkeratosisImmune dysregulationImmunoglobulin enhancer binding proteinInflamacióInflammationInfliximabInterleukin 1 receptor blocking agentMaculopapular rashMajeed syndromeMonogenic autoinflammatory diseasesNfkb1 associated autoinflammatory diseaseNlrc4 associated autoinflammatory diseaseNlrp 1 associated diseaseNlrp12 associated autoinflammatory diseaseOtulipeniaPanniculitisPapa syndromePhenotypePhospholipase c gamma2Protein expressionPustulePyrin associated autoinflammation with neutrophilic dermatosisRela haploinsufficiencyReviewSingleton merten syndromeSkinSkin diseaseSkin manifestationSpondyloenchondrodysplasia with immune dysregulationSting associated vasculopathy with onset in infancySymptom assessmentTocilizumabTumor necrosis factor receptorTumor necrosis factor receptor associated periodic syndromeUrticariaUrticarial rashVesicular rashVibratory urticaria

Quality index

Bibliometric impact. Analysis of the contribution and dissemination channel

The work has been published in the journal Frontiers in Immunology due to its progression and the good impact it has achieved in recent years, according to the agency WoS (JCR), it has become a reference in its field. In the year of publication of the work, 2019, it was in position 39/159, thus managing to position itself as a Q1 (Primer Cuartil), in the category Immunology.

Independientemente del impacto esperado determinado por el canal de difusión, es importante destacar el impacto real observado de la propia aportación.

Según las diferentes agencias de indexación, el número de citas acumuladas por esta publicación hasta la fecha 2026-04-06:

  • WoS: 24
  • Scopus: 27
  • Europe PMC: 7
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Impact and social visibility

From the perspective of influence or social adoption, and based on metrics associated with mentions and interactions provided by agencies specializing in calculating the so-called "Alternative or Social Metrics," we can highlight as of 2026-04-06:

  • The use, from an academic perspective evidenced by the Altmetric agency indicator referring to aggregations made by the personal bibliographic manager Mendeley, gives us a total of: 67.
  • The use of this contribution in bookmarks, code forks, additions to favorite lists for recurrent reading, as well as general views, indicates that someone is using the publication as a basis for their current work. This may be a notable indicator of future more formal and academic citations. This claim is supported by the result of the "Capture" indicator, which yields a total of: 67 (PlumX).

With a more dissemination-oriented intent and targeting more general audiences, we can observe other more global scores such as:

  • The Total Score from Altmetric: 5.
  • The number of mentions on the social network Facebook: 2 (Altmetric).
  • The number of mentions on the social network X (formerly Twitter): 9 (Altmetric).

It is essential to present evidence supporting full alignment with institutional principles and guidelines on Open Science and the Conservation and Dissemination of Intellectual Heritage. A clear example of this is:

  • The work has been submitted to a journal whose editorial policy allows open Open Access publication.
  • Assignment of a Handle/URN as an identifier within the deposit in the Institutional Repository: http://hdl.handle.net/2445/176848
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Leadership analysis of institutional authors

There is a significant leadership presence as some of the institution’s authors appear as the first or last signer, detailed as follows: Last Author (Hernández Rodríguez, José).

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