Example of Journal of Cutaneous Pathology format
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Example of Journal of Cutaneous Pathology format Example of Journal of Cutaneous Pathology format Example of Journal of Cutaneous Pathology format Example of Journal of Cutaneous Pathology format Example of Journal of Cutaneous Pathology format Example of Journal of Cutaneous Pathology format
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Example of Journal of Cutaneous Pathology format Example of Journal of Cutaneous Pathology format Example of Journal of Cutaneous Pathology format Example of Journal of Cutaneous Pathology format Example of Journal of Cutaneous Pathology format Example of Journal of Cutaneous Pathology format
Sample paper formatted on SciSpace - SciSpace
This content is only for preview purposes. The original open access content can be found here.
open access Open Access

Journal of Cutaneous Pathology — Template for authors

Publisher: Wiley
Categories Rank Trend in last 3 yrs
Dermatology #56 of 117 up up by 10 ranks
Pathology and Forensic Medicine #99 of 191 down down by 3 ranks
Histology #37 of 60 down down by 1 rank
journal-quality-icon Journal quality:
Good
calendar-icon Last 4 years overview: 753 Published Papers | 1663 Citations
indexed-in-icon Indexed in: Scopus
last-updated-icon Last updated: 02/07/2020
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Related Journals

open access Open Access
recommended Recommended

Springer

Quality:  
High
CiteRatio: 7.5
SJR: 1.64
SNIP: 1.281
open access Open Access

Elsevier

Quality:  
High
CiteRatio: 6.8
SJR: 1.329
SNIP: 0.968
open access Open Access
recommended Recommended

Wiley

Quality:  
High
CiteRatio: 11.5
SJR: 2.538
SNIP: 1.696
open access Open Access
recommended Recommended

Wiley

Quality:  
High
CiteRatio: 7.3
SJR: 1.626
SNIP: 1.702

Journal Performance & Insights

Impact Factor

CiteRatio

Determines the importance of a journal by taking a measure of frequency with which the average article in a journal has been cited in a particular year.

A measure of average citations received per peer-reviewed paper published in the journal.

1.373

10% from 2018

Impact factor for Journal of Cutaneous Pathology from 2016 - 2019
Year Value
2019 1.373
2018 1.524
2017 1.532
2016 1.317
graph view Graph view
table view Table view

2.2

12% from 2019

CiteRatio for Journal of Cutaneous Pathology from 2016 - 2020
Year Value
2020 2.2
2019 2.5
2018 2.3
2017 2.2
2016 2.4
graph view Graph view
table view Table view

insights Insights

  • Impact factor of this journal has decreased by 10% in last year.
  • This journal’s impact factor is in the top 10 percentile category.

insights Insights

  • CiteRatio of this journal has decreased by 12% in last years.
  • This journal’s CiteRatio is in the top 10 percentile category.

SCImago Journal Rank (SJR)

Source Normalized Impact per Paper (SNIP)

Measures weighted citations received by the journal. Citation weighting depends on the categories and prestige of the citing journal.

Measures actual citations received relative to citations expected for the journal's category.

0.597

4% from 2019

SJR for Journal of Cutaneous Pathology from 2016 - 2020
Year Value
2020 0.597
2019 0.622
2018 0.745
2017 0.66
2016 0.581
graph view Graph view
table view Table view

0.924

2% from 2019

SNIP for Journal of Cutaneous Pathology from 2016 - 2020
Year Value
2020 0.924
2019 0.907
2018 0.967
2017 1.025
2016 0.915
graph view Graph view
table view Table view

insights Insights

  • SJR of this journal has decreased by 4% in last years.
  • This journal’s SJR is in the top 10 percentile category.

insights Insights

  • SNIP of this journal has increased by 2% in last years.
  • This journal’s SNIP is in the top 10 percentile category.

Journal of Cutaneous Pathology

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Wiley

Journal of Cutaneous Pathology

Journal of Cutaneous Pathology publishes manuscripts relevant to diseases of the skin in a broad sense, with the aims of advancing scientific knowledge regarding dermatopathology and enhancing the communication between clinical practitioners and research scientists. Original s...... Read More

Medicine

i
Last updated on
02 Jul 2020
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ISSN
0303-6987
i
Impact Factor
High - 1.179
i
Open Access
Yes
i
Sherpa RoMEO Archiving Policy
Yellow faq
i
Plagiarism Check
Available via Turnitin
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Endnote Style
Download Available
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Bibliography Name
apa
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Citation Type
Numbered
[25]
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Bibliography Example
Beenakker, C.W.J. (2006) Specular andreev reflection in graphene.Phys. Rev. Lett., 97 (6), 067 007. URL 10.1103/PhysRevLett.97.067007.

Top papers written in this journal

open accessOpen access Journal Article DOI: 10.1034/J.1600-0560.2001.028003113.X
Acute generalized exanthematous pustulosis (AGEP)--a clinical reaction pattern.
Alexis Sidoroff1, Sima Halevy2, Jan Nico Bouwes Bavinck3, Loïc Vaillant4, Jean-Claude Roujeau

Abstract:

Background: A wide range of diseases or reactions can cause pustular eruptions of the skin. In this spectrum there seems to be a subgroup with characteristic clinical features and a typical course which is mostly caused by drugs for which the term acute generalized exanthematous pustulosis (AGEP) has been established. Obje... Background: A wide range of diseases or reactions can cause pustular eruptions of the skin. In this spectrum there seems to be a subgroup with characteristic clinical features and a typical course which is mostly caused by drugs for which the term acute generalized exanthematous pustulosis (AGEP) has been established. Objective: To describe the clinical features of AGEP. Methods: The authors’ experience from a multinational epidemiological study on severe cutaneous adverse reactions and a comprehensive review of the literature were used to provide an overview of the disease and it’s possible causes. An algorithm for validating cases which was established for this study is also presented. Results: AGEP typically presents with at least dozens of non follicular sterile pustules occurring on a diffuse, edematous erythema predominalty in the folds and/or on the face. Fever and elevated blood neutrophils are common. Histopathology typically shows spongiform subcorneal and/or intraepidermal pustules, a marked edema of the papillary dermis, and eventually vasculitis, eosinophils and/or focal necrosis of keratinocytes. Onset is acute, most often following drug intake, but viral infections can also trigger the disease. Pustules resolve spontaneously in less than 15 days. Conclusion: The diagnosis AGEP should be considered in cases of acute pustular rashes and detection of the causative drug should be strived for. Knowledge of the clinical features and usual course of this disease can often prevent unnecessary therapeutical measures. read more read less

Topics:

Acute generalized exanthematous pustulosis (62%)62% related to the paper, Pustulosis (60%)60% related to the paper, Pustular Eruption (54%)54% related to the paper, Papillary dermis (54%)54% related to the paper
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687 Citations
Journal Article DOI: 10.1111/J.1600-0560.2007.00891.X
Immunohistochemical characteristics of melanoma.
Steven J. Ohsie1, G. Peter Sarantopoulos1, Alistair J. Cochran1, Scott W. Binder1

Abstract:

Melanoma has a wide spectrum of histologic features which mimic epithelial, hematologic, mesenchymal, and neural tumors. Immunohistochemistry has been the primary tool to distinguish melanomas from these other tumors; it has also been studied for use as an adjunct to distinguish benign and malignant melanocytic tumors and to ... Melanoma has a wide spectrum of histologic features which mimic epithelial, hematologic, mesenchymal, and neural tumors. Immunohistochemistry has been the primary tool to distinguish melanomas from these other tumors; it has also been studied for use as an adjunct to distinguish benign and malignant melanocytic tumors and to elucidate prognosis. Furthermore, there has been extensive effort to find a suitable marker to differentiate spindle cell and desmoplastic melanoma from other tumors. We have reviewed the literature investigating melanocytic differentiation markers, proliferation markers, immunomodulatory markers, signaling molecules, and nerve growth factors and receptors. Despite the proliferation of immunohistochemical markers, S-100 remains the most sensitive marker for melanocytic lesions, while markers such as HMB-45, MART-1/Melan-A, tyrosinase, and MITF demonstrate relatively good specificity but not as good sensitivity as S-100. No marker has proven useful in distinguishing spindle cell and desmoplastic melanomas from other tumors. Ki67 remains the most useful adjunct in distinguishing benign from malignant melanocytic tumors. None of the markers reviewed has been shown conclusively to have prognostic value for melanocytic neoplasms. read more read less

Topics:

HMB-45 (67%)67% related to the paper, Desmoplastic melanoma (63%)63% related to the paper, Melanoma (51%)51% related to the paper
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485 Citations
Journal Article DOI: 10.1111/J.1600-0560.2009.01370.X
Merkel cell carcinoma demographics, morphology, and survival based on 3870 cases: A population based study

Abstract:

Background: Merkel cell carcinoma (MCC) is a rare and aggressive neuroendocrine tumor arising predominantly on sun-exposed skin of older and usually immunosuppressed individuals. Methods: Using data from NCI's SEER (Surveillance, Epidemiology, and End Results) Program from 1973 to 2006, we analyzed the demographics and sur... Background: Merkel cell carcinoma (MCC) is a rare and aggressive neuroendocrine tumor arising predominantly on sun-exposed skin of older and usually immunosuppressed individuals. Methods: Using data from NCI's SEER (Surveillance, Epidemiology, and End Results) Program from 1973 to 2006, we analyzed the demographics and survival of MCC. Results: SEER had recorded 3870 cases of MCC. The incidence was higher in men (2380 cases, 61.5%) than in women (1490 cases, 38.5%). Most patients were White (94.9%) between 60 and 85 years of age. MCC was rare in Blacks. The most common location was the head and neck. The salivary glands, nasal cavity, lip, lymph nodes, vulva, vagina and esophagus were the most common extracutaneous sites. The 10-year relative survival rate was higher in women than men (64.8% vs. 50.5%, p < 0.001). Patients 50–69 years had the highest 10-year relative survival rate (59.6%). Stage of disease was the best predictor of survival. Conclusions: MCC arises predominantly in the skin of head and neck in White men above 70 years of age. Cases also occurred in extracutaneous sites. Age did not predict survival, yet gender, site and tumor size revealed clear differences. The most significant predictor of survival was tumor stage. read more read less

Topics:

Survival rate (59%)59% related to the paper, Merkel cell carcinoma (56%)56% related to the paper, Merkel cell polyomavirus (54%)54% related to the paper
482 Citations
Journal Article DOI: 10.1111/J.1600-0560.1997.TB01318.X
Infection by Borrelia burgdorferi and cutaneous B-cell lymphoma.
Lorenzo Cerroni1, Natalie Zöchling1, Barbara Pütz1, Helmut Kerl1

Abstract:

In past years, association of primary cutaneous B-cell lymphoma (CBCL) with infection by Borrelia burgdorferi has been reported in a few patients. The evidence for a pathogenetic role was based on clinical grounds or raised titre of antibodies in serum. Both methods, however, do not prove the association between the micro-org... In past years, association of primary cutaneous B-cell lymphoma (CBCL) with infection by Borrelia burgdorferi has been reported in a few patients. The evidence for a pathogenetic role was based on clinical grounds or raised titre of antibodies in serum. Both methods, however, do not prove the association between the micro-organism and the CBCL, especially in countries where infection by Borrelia burgdorferi is endemic. Moreover, the exact percentage of Borrelia burgdorferi-positive CBCL is not known. We retrieved from our files 50 cases of CBCL to perform PCR analysis of Borrelia burgdorferi DNA on paraffin-embedded tissue sections. Only patients with primary CBCL were selected. In all cases, monoclonality of the infiltrate was confirmed by immunohistological pattern of immunoglobulin light chains or molecular analysis of J H gene rearrangement, or both. Specific DNA sequences of Borrelia burgdorferi were identified in cutaneous lesions from 9 patients (follicle center lymphoma: 3/20; immunocytoma: 3/4; marginal zone B-cell lymphoma: 2/20; diffuse large B-cell lymphoma: 1/6). Specificity was confirmed by Southern blot hybridisation in all positive cases. We could show that Borrelia burgdorferi DNA is present in skin lesions from a small proportion of patients (18%) with various types of CBCL. Our results may have therapeutic implications. In analogy to Helicobacter pylori-associated MALT-lymphomas, which in some cases can be cured by eradication of Helicobacter pylori infection, a proportion of CBCL may be cured with antibiotic therapy against Borrelia burgdorferi. Although yet speculative, adequate antibiotic treatment for patients with primary CBCL should be considered before more aggressive therapeutic options are applied, particularly in countries where infection by Borrelia burgdorferi is endemic. PCR analysis of Borrelia burgdorferi DNA is a fast test that should be performed in all patients with CBCL to identify those who more likely could benefit from an early antibiotic treatment. read more read less

Topics:

Borrelia burgdorferi (67%)67% related to the paper, Borrelia (55%)55% related to the paper, Cutaneous B-cell lymphoma (52%)52% related to the paper, Primary cutaneous marginal zone lymphoma (51%)51% related to the paper
391 Citations
open accessOpen access Journal Article DOI: 10.1111/J.0303-6987.2005.00495.X
WHO/EORTC classification of cutaneous lymphomas 2005: histological and molecular aspects.

Abstract:

The new WHO/EORTC classification for cutaneous lymphomas comprises mature T-cell and natural killer (NK)-cell neoplasms, mature B-cell neoplasms, and immature hematopoietic malignancies. It reflects the unique features of lymphoproliferative diseases of the skin, and at the same time it is as compatible as possible with the c... The new WHO/EORTC classification for cutaneous lymphomas comprises mature T-cell and natural killer (NK)-cell neoplasms, mature B-cell neoplasms, and immature hematopoietic malignancies. It reflects the unique features of lymphoproliferative diseases of the skin, and at the same time it is as compatible as possible with the concepts underlying the WHO classification for nodal lymphomas and the EORTC classification of cutaneous lymphomas. This article reviews the histological, phenotypical, and molecular genetic features of the various nosological entities included in this new classification. These findings always have to be interpreted in the context of the clinical features and biologic behavior read more read less
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333 Citations
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Journal of Cutaneous Pathology format uses apa citation style.

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Frequently asked questions

1. Can I write Journal of Cutaneous Pathology in LaTeX?

Absolutely not! Our tool has been designed to help you focus on writing. You can write your entire paper as per the Journal of Cutaneous Pathology guidelines and auto format it.

2. Do you follow the Journal of Cutaneous Pathology guidelines?

Yes, the template is compliant with the Journal of Cutaneous Pathology guidelines. Our experts at SciSpace ensure that. If there are any changes to the journal's guidelines, we'll change our algorithm accordingly.

3. Can I cite my article in multiple styles in Journal of Cutaneous Pathology?

Of course! We support all the top citation styles, such as APA style, MLA style, Vancouver style, Harvard style, and Chicago style. For example, when you write your paper and hit autoformat, our system will automatically update your article as per the Journal of Cutaneous Pathology citation style.

4. Can I use the Journal of Cutaneous Pathology templates for free?

Sign up for our free trial, and you'll be able to use all our features for seven days. You'll see how helpful they are and how inexpensive they are compared to other options, Especially for Journal of Cutaneous Pathology.

5. Can I use a manuscript in Journal of Cutaneous Pathology that I have written in MS Word?

Yes. You can choose the right template, copy-paste the contents from the word document, and click on auto-format. Once you're done, you'll have a publish-ready paper Journal of Cutaneous Pathology that you can download at the end.

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It only takes a matter of seconds to edit your manuscript. Besides that, our intuitive editor saves you from writing and formatting it in Journal of Cutaneous Pathology.

7. Where can I find the template for the Journal of Cutaneous Pathology?

It is possible to find the Word template for any journal on Google. However, why use a template when you can write your entire manuscript on SciSpace , auto format it as per Journal of Cutaneous Pathology's guidelines and download the same in Word, PDF and LaTeX formats? Give us a try!.

8. Can I reformat my paper to fit the Journal of Cutaneous Pathology's guidelines?

Of course! You can do this using our intuitive editor. It's very easy. If you need help, our support team is always ready to assist you.

9. Journal of Cutaneous Pathology an online tool or is there a desktop version?

SciSpace's Journal of Cutaneous Pathology is currently available as an online tool. We're developing a desktop version, too. You can request (or upvote) any features that you think would be helpful for you and other researchers in the "feature request" section of your account once you've signed up with us.

10. I cannot find my template in your gallery. Can you create it for me like Journal of Cutaneous Pathology?

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11. What is the output that I would get after using Journal of Cutaneous Pathology?

After writing your paper autoformatting in Journal of Cutaneous Pathology, you can download it in multiple formats, viz., PDF, Docx, and LaTeX.

12. Is Journal of Cutaneous Pathology's impact factor high enough that I should try publishing my article there?

To be honest, the answer is no. The impact factor is one of the many elements that determine the quality of a journal. Few of these factors include review board, rejection rates, frequency of inclusion in indexes, and Eigenfactor. You need to assess all these factors before you make your final call.

13. What is Sherpa RoMEO Archiving Policy for Journal of Cutaneous Pathology?

SHERPA/RoMEO Database

We extracted this data from Sherpa Romeo to help researchers understand the access level of this journal in accordance with the Sherpa Romeo Archiving Policy for Journal of Cutaneous Pathology. The table below indicates the level of access a journal has as per Sherpa Romeo's archiving policy.

RoMEO Colour Archiving policy
Green Can archive pre-print and post-print or publisher's version/PDF
Blue Can archive post-print (ie final draft post-refereeing) or publisher's version/PDF
Yellow Can archive pre-print (ie pre-refereeing)
White Archiving not formally supported
FYI:
  1. Pre-prints as being the version of the paper before peer review and
  2. Post-prints as being the version of the paper after peer-review, with revisions having been made.

14. What are the most common citation types In Journal of Cutaneous Pathology?

The 5 most common citation types in order of usage for Journal of Cutaneous Pathology are:.

S. No. Citation Style Type
1. Author Year
2. Numbered
3. Numbered (Superscripted)
4. Author Year (Cited Pages)
5. Footnote

15. How do I submit my article to the Journal of Cutaneous Pathology?

It is possible to find the Word template for any journal on Google. However, why use a template when you can write your entire manuscript on SciSpace , auto format it as per Journal of Cutaneous Pathology's guidelines and download the same in Word, PDF and LaTeX formats? Give us a try!.

16. Can I download Journal of Cutaneous Pathology in Endnote format?

Yes, SciSpace provides this functionality. After signing up, you would need to import your existing references from Word or Bib file to SciSpace. Then SciSpace would allow you to download your references in Journal of Cutaneous Pathology Endnote style according to Elsevier guidelines.

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