Instructions for Authors
Contents
1. About Submissions
Article Processing Charges (APCs)
Metabolic Medicine does not charge any fees for manuscript submission or publication. All articles accepted for publication are published free of charge. There are no submission fees, editorial processing charges, page charges, or colour figure fees. Editorial decisions are based exclusively on scientific quality, methodological rigor, and relevance to the journal's scope, and are entirely independent of any financial considerations.
Language
Manuscripts should be written in clear, professional English. Authors whose first language is not English are strongly encouraged to have their manuscript reviewed by a fluent English speaker or professional language editing service prior to submission.
How to Submit
Manuscripts should be submitted via e-mail to editorialoffice@rootsinscience.com. Authors are requested to clearly indicate the name of the journal to which the manuscript is being submitted. Roots will soon adopt an online submission system for manuscript submission and editorial communication.
2. Article Types
Metabolic Medicine aims to publish impactful, high-quality articles on all aspects of human metabolism and metabolic diseases, from basic science to translational research and clinical investigation, in order to advance knowledge in the rapidly evolving field of metabolic health.
All submissions are subject to the journal’s double-blind peer review process (see Policies, Licensing and COI). Authors are responsible for selecting the most appropriate article category and ensuring compliance with the journal’s formatting and reporting standards.
Unless otherwise specified, word counts refer to the main text only (excluding title page, abstract, references, tables, figures, and supplementary material).
Brief Communication
Concise reports of preliminary findings, pilot studies, innovative care models, or focused research observations. Submissions must maintain methodological clarity and scientific rigor.
Recommended length:
- Text: approximately 1,000–1,500 words
- Abstract: up to 200 words
- References: up to 20
- Tables/Figures: up to 4
- Keywords: 3–6
Case Reports and Case Series
Reports of clinically significant, rare, or educational cases related to metabolic diseases, metabolic complications, or metabolic manifestations of systemic disorders. Submissions should provide novel insights into diagnosis, pathophysiology, or management. Written informed consent from the patient(s) is required.
Recommended length:
- Text: approximately 1,500–2,000 words
- Structured Abstract: (Background, Case Presentation, Results, Conclusions): 200–250 words
- References: up to 20
- Tables/Figures: up to 5
- Keywords: 3–6
Commentary
Commentaries provide expert perspectives, critical analysis, or discussion of emerging issues in metabolic medicine, including clinical practice, research advances, and public health implications.
Recommended length:
- Text: approximately 1,500–2,500 words
- Abstract: optional (up to 200 words)
- References: up to 15
- Tables/Figures: up to 2
- Keywords: 3–6
Conference Proceeding and Meeting Report
Conference Proceedings may include collections of abstracts. Meeting Reports summarize scientific meetings, symposia, or workshops focused on metabolic research and clinical practice. Authors are advised to contact the Editorial Office prior to submission.
Recommended length (Meeting Reports):
- Text: approximately 1,000–1,500 words
- No abstract required
- References: as appropriate
- Keywords: 3–6
Editorial
Editorials provide authoritative insights into emerging topics, significant publications, or strategic directions in metabolic medicine.
Recommended length:
- Text: approximately 2,000 words
- No abstract required
- References: up to 25
- Tables/Figures: up to 2
- Keywords: 3–6
Letter to the Editor
Letters to the Editor provide scholarly commentary on articles previously published in the journal. Authors of the original article may be invited to submit a Reply for publication alongside the Letter.
Recommended length:
- Text: approximately 350–500 words
- No abstract required
- References: up to 5
- Tables/Figures: 1 (if essential)
- Keywords: 3–6
Narrative Review (including Mini-Review)
Narrative Reviews provide a comprehensive and critical overview of a topic of current interest in metabolic medicine, integrating existing evidence with expert interpretation. Unlike systematic reviews, they do not require a predefined protocol but should present a balanced, structured, and evidence-informed discussion. Topics may include pathophysiology, clinical management, emerging therapies, or conceptual advances in metabolic health and disease. Mini-Reviews offer a more concise and focused synthesis of a specific aspect of a broader topic.
Recommended length (Narrative Review):
- Main text: approximately 3,000–4,000 words
- Abstract: up to 250 words
- References: up to 50
- Tables/Figures: up to 6
- Keywords: 3–6
Recommended length (Mini-Review):
- Main text: approximately 1,500–2,500 words
- Abstract: up to 200 words
- References: up to 30
- Tables/Figures: up to 4
- Keywords: 3–6
Opinion Article
Opinion Articles provide author-driven, clearly argued positions on controversial, emerging, or underexplored topics in metabolic medicine. These articles should be grounded in current evidence while allowing for informed speculation, conceptual innovation, or debate. Submissions should clearly articulate their relevance to metabolic health, research, clinical practice, or policy.
Recommended length:
- Main text: approximately 1,500–2,500 words
- Abstract: optional (up to 200 words)
- References: up to 20
- Tables/Figures: up to 3
- Keywords: 3–6
Original Article
Original Articles present novel empirical research in metabolic science, including basic, translational, clinical, and population-based studies. Submissions must include a clearly defined research question, appropriate study design, transparent methodology, robust data analysis, and a discussion that contextualizes findings within existing literature. Authors must follow the appropriate reporting guideline according to study design (e.g., CONSORT, STROBE).
Recommended length:
- Text: approximately 4,000–5,000 words
- Structured abstract (Background, Methods, Results, Conclusions): 250–300 words
- References: up to 50
- Tables/Figures: up to 6
- Keywords: 3–6
Perspective Article
Perspective Articles provide scholarly reflection, contextual analysis, or expert interpretation of issues related to metabolic health, disease mechanisms, or therapeutic innovation. Perspectives should be scholarly, balanced, and grounded in current evidence, while highlighting new directions or unresolved questions.
Recommended length:
- Text: approximately 1,500–3,000 words
- Abstract: optional (up to 200 words)
- References: up to 30
- Tables/Figures: up to 4
- Keywords: 3–6
Research Protocols
Research Protocols describe the rationale and methodology of proposed or ongoing studies that have not yet completed participant recruitment at the time of submission. Protocols should include the study objectives, design, eligibility criteria, sample size considerations (where applicable), planned statistical analyses, details of ethical approval, and plans for dissemination of results.
Recommended length:
- Text: approximately 3,000–4,000 words
- Abstract: up to 250 words
- References: up to 50
- Tables/Figures: up to 6
- Keywords: 3–6
Systematic Review and Meta-Analysis
Systematic Reviews critically identify, appraise, and synthesize available evidence addressing a focused research question. Meta-Analysis apply statistical techniques to quantitatively combine results from multiple studies. Manuscripts must adhere to PRISMA guidelines and provide a transparent search strategy, eligibility criteria, risk-of-bias assessment, and detailed methods of analysis.
Recommended length:
- Text: approximately 4,000–5,000 words
- Structured abstract: around 250–300 words
- References: up to 70
- Tables/Figures: up to 6 combined
3. Manuscript Preparation
Authors are responsible for preparing manuscripts in accordance with the journal's scope, ethical standards, and formatting requirements. Submissions that do not comply may be returned prior to peer review.
Unless otherwise specified, word counts refer to the main text only (excluding abstract, references, tables, figures, and supplementary material). For the specific requirements of each article type, please refer to the section Article Types.
General Formatting Requirements
- Submit in an editable format (e.g., Word, no PDF).
- Use a standard readable font (11–12 pt).
- Double or 1.5 line spacing.
- Number pages consecutively.
- Use SI units.
- Define a list of abbreviations at first mention and use consistently.
4. Submission Files
To comply with double-blind peer review, submit the following as separate files:
4.1 Cover Letter
Include:
- Importance and originality of the work.
- Confirmation the manuscript is not published and not under consideration elsewhere.
- Disclosure of conflicts of interest.
- Funding sources (if applicable).
- Confirmation of ethical approval and informed consent.
- Clinical trial registration details (if applicable).
4.2 Title Page
Must include:
- Full title and running head (short title).
- Full names of all authors.
- Affiliations for each author (Department, Institution, City, State).
- Corresponding author's full address and email.
- ORCID iDs (if available).
- Funding statement.
- Conflict of interest declaration.
- Author contribution statement (if required).
4.3 Manuscript File
For the specific requirements of each article type, please refer to the section Article Types. For most research articles, manuscripts should be structured as reported in the section Manuscript Structure.
5. Manuscript Structure
Title
Clear, concise, and reflective of the study.
Abstract and Keywords
- Structured (Background, Methods, Results, Conclusions) depending on the article (see "Article Types" section).
- 250–300 words unless otherwise specified by article type.
- No references or undefined abbreviations.
- Include 3–6 keywords (preferably MeSH terms where appropriate).
Main Text
Introduction
In the introduction section, the authors should situate the study within a broader scholarly context and clearly explain its relevance in relation to existing literature. They should explicitly state the objectives of the work and clearly articulate the specific hypothesis being tested. It is also essential to clarify whether the observations are grounded in previous research conducted by others or derived from the authors' own pilot study. Additionally, a concise summary of key findings from relevant prior studies should be included to provide a solid background for the research.
In summary, the introduction should clearly present:
- Context and rationale.
- Clear study objectives or research question.
Methods
The Methods section must provide a clear, transparent, and sufficiently detailed description of how and why the study was conducted in a particular manner. The rationale underlying the study design and methodological decisions should be clearly explained to allow readers to understand the scientific approach.
New or innovative procedures, instruments, or protocols must be described in adequate detail to permit replication. Well-established methods may be described more concisely, provided appropriate and up-to-date references are cited.
All methodological descriptions must include sufficient information to enable reproducibility by a knowledgeable reader.
Study Design
The study design must be explicitly stated (e.g., randomized controlled trial, cohort study, case–control study, qualitative study, mixed-methods study). Authors should clearly describe:
- Study setting and timeframe;
- Inclusion and exclusion criteria;
- Recruitment procedures;
- Control or comparison groups, where applicable.
Participant Selection and Description
Authors must provide a detailed explanation of how participants were selected for observational or experimental research. This should include:
- Clear eligibility and exclusion criteria;
- Description of the source population;
- Recruitment methods;
- Sample size determination (if applicable);
- Characteristics of study groups and control groups.
The sex and/or gender of participants must be reported and appropriately considered in the analysis. Any sex- or gender-based analysis should be clearly described. If only one sex or gender is included, this must be scientifically justified.
Control groups must be described with the same level of detail as experimental groups.
Animal Studies
Research involving animals must comply with internationally recognized ethical standards and adhere to the ARRIVE guidelines for reporting experiments involving live animals.
Authors must report:
- Animal species and strain;
- Sex;
- Source (vendor name and location);
- Age range;
- Weight;
- Housing and care conditions (where relevant);
- Any additional relevant biological or environmental variables.
The use of both male and female animals is encouraged. Studies using animals of a single sex must provide scientific justification.
Ethical approval for animal research must be clearly stated, including the name of the approving body and approval reference number.
Materials and Equipment
Descriptions of reagents, instruments, devices, and software must include sufficient detail to allow replication. Manufacturer name, city, and country should be specified where relevant.
Statistical Analysis
All quantitative studies must include a dedicated subsection titled Statistical Analysis. This section must clearly describe:
- Statistical methods applied;
- Assumptions underlying the statistical tests;
- Handling of missing data;
- Adjustments for multiple comparisons (if applicable);
- Significance thresholds;
- Measures of effect size and precision;
- Statistical software used, including version number.
Unless explicitly justified, two-tailed significance tests should be used.
Measures of central tendency must be accompanied by measures of variability (e.g., standard deviation, interquartile range, confidence intervals), together with appropriate probability values (e.g., p-values).
Clinical trial reports must include a description of sample size calculation and statistical power.
The level of detail provided must enable a knowledgeable reader to verify the results using the original dataset.
Ethical Approval
All studies involving human participants must include a statement confirming approval by an appropriate ethics committee or institutional review board. The name of the approving body and the approval number must be reported.
Authors must confirm that the research was conducted in accordance with the principles of the Declaration of Helsinki and applicable national regulations.
If ethical approval was not required, a clear justification must be provided.
Use of Artificial Intelligence in Research
If artificial intelligence (AI) tools or generative technologies were used in data analysis, image processing, modeling, or other aspects of the research, this must be clearly described within the Methods section.
Authors must specify:
- The name of the tool or model;
- Version number;
- Purpose of use;
- Relevant parameters or settings.
Descriptions must be sufficiently detailed to allow replication of the analytical approach. Authors retain full responsibility for the integrity, accuracy, and validity of all results generated using AI tools.
In summary, the Methods should clearly present:
- Study design.
- Setting and participants.
- Data collection procedures.
- Statistical analysis (if applicable).
- Ethical approval (including committee name and approval number).
- Trial registration (if applicable).
Results
This section should present all findings obtained during the study and, where applicable, from follow-up analyses. All predefined outcomes and any additional relevant results must be clearly reported and supported by appropriate data. The presentation of results should be objective, concise, and directly aligned with the study objectives and hypotheses outlined in the introduction.
Both primary and secondary outcomes should be described in a logical sequence, ensuring that the data are accurately represented without interpretation or discussion. Quantitative results should include appropriate statistical indicators (e.g., measures of central tendency, variability, confidence intervals, and p-values where relevant), while qualitative findings should be clearly categorized and supported by representative evidence.
Tables and figures should be used to summarize the most important findings effectively, enhancing clarity and readability. They must complement, not duplicate, the text and should highlight key results. Additional technical details, extended datasets, methodological clarifications, or supplementary analyses may be provided as supplementary materials or appendices to maintain the focus and coherence of the main manuscript.
In summary, the Results should present:
- Clear presentation of findings.
- Avoid duplication between text and tables/figures.
Discussion
In the Discussion section, authors should go beyond merely restating the results and instead provide a comprehensive interpretation of the findings. The results should be critically analyzed, explained in depth, and contextualized within the broader scientific framework. Authors are expected to clarify the implications of their findings, anticipate the main conclusions, and emphasize the most significant and novel aspects of the study.
This section should integrate the study outcomes with existing literature, drawing comparisons with previously published research to highlight similarities, discrepancies, or advancements. Appropriate references to relevant studies are strongly recommended to support interpretations and to situate the work within the current state of knowledge.
Finally, a dedicated paragraph addressing the limitations of the study is strongly encouraged. A transparent discussion of methodological constraints, potential biases, and other weaknesses enhances the credibility and scientific rigor of the work, while also suggesting directions for future research.
In summary, the Discussion should present:
- Interpretation of findings.
- Comparison with existing literature.
- Strengths and limitations.
- Clinical or research implications.
Conclusions
In this final section, the authors should clearly summarize the main findings and overall outcomes of the study, emphasizing their scientific and practical significance. The conclusions must be directly supported by the results presented and aligned with the original objectives and research questions.
If the findings are preliminary or limited in scope, the need for further research should be explicitly acknowledged. Authors should outline potential directions for future studies, particularly where unanswered questions remain or additional validation is required.
Where appropriate, practical implications, recommendations, or suggestions for other researchers may be included to enhance the contribution of the work to the scientific community. A well-structured conclusion should provide a clear and meaningful synthesis of the study, reinforcing its relevance and value within the broader field of research.
In summary, the Conclusions should be:
- Concise and supported by results.
6. Statements
Authors must include the following sections immediately after the Conclusions and before the References, in this order:
- Acknowledgements
- Artificial Intelligence (AI) – Assisted Technology Statement (if applicable; otherwise declare no AI use)
- Authors' Contributions
- Clinical Trial Registration (if applicable)
- Conflict of Interest (or: "The authors declare that they have no conflict of interest to disclose.")
- Data Availability Statement
- Ethics Approval (or waiver with justification)
- Funding (or: "No funding was declared for this study.")
- Informed Consent (as applicable; required for case reports where identifiable details/images may appear)
- ORCID ID (recommended)
- Supplementary Material (if applicable)
1. Acknowledgements
This section should include brief acknowledgements of individuals who made genuine contributions to the work but do not meet the criteria for authorship (e.g., technical support, language editing, data collection assistance).
All acknowledged individuals must have provided written consent to be named.
Authors must also confirm that permission has been obtained for the use of any copyrighted material (text, tables, figures, illustrations).
2. Artificial Intelligence (AI) – Assisted Technology Statement
At submission, authors must disclose whether AI-assisted technologies (e.g., Large Language Models, chatbots, image generators) were used.
If AI was used:
- It must be disclosed in both the Cover Letter and this section.
- The purpose of use must be described.
- AI tools must not be listed as authors.
- Authors retain full responsibility for the accuracy and integrity of the content.
Example:
"The authors used [Tool Name, Version] for language editing. All outputs were reviewed and verified by the authors."
If no AI tools were used:
"No AI-assisted technologies were used in the preparation of this manuscript."
3. Authors' Contributions
For manuscripts with more than one author, a clear description of each author's contribution must be provided. Author names must not be abbreviated.
Contributions may include:
- Conceptualization and study design
- Data acquisition
- Data analysis and interpretation
- Drafting of the manuscript
- Critical revision for intellectual content
- Supervision
- Validation
- Final approval of the version to be published
All authors must have approved the final manuscript and agree to be accountable for its content.
4. Clinical Trial Registration
For clinical trials:
"This trial was registered at [Registry Name] (Registration No. XXX)."
5. Conflict of Interest
All authors must disclose any financial or personal relationships that could influence (bias) their work. Examples include:
- Consultancy roles
- Employment
- Stock ownership
- Honoraria
- Paid expert testimony
- Patent applications or ownership
- Grants or other funding
If conflicts exist, they must be fully described.
If no conflicts exist, authors must include the following statement:
"The authors declare that they have no conflict of interest to disclose."
6. Data Availability Statement
All articles containing original data must include a Data Availability Statement placed after the Conflict of Interest section. Acceptable formats include:
- "The datasets generated and/or analyzed during the current study are available in the repository [NAME], [persistent link]."
- "The datasets are available from the corresponding author upon reasonable request."
- "Data are not publicly available due to [ethical/legal reason] but are available upon reasonable request."
- "Data sharing is not applicable to this article as no datasets were generated or analyzed."
- "All data generated or analyzed during this study are included in this published article and/or its supplementary material."
Authors must ensure compliance with data protection regulations.
7. Ethics Approval
All research involving human participants or animals must include a formal ethics statement.
For human studies:
- Name of the approving ethics committee or institutional review board.
- Approval number (if applicable).
- Confirmation of compliance with the Declaration of Helsinki.
Example:
"This study was conducted in accordance with the Declaration of Helsinki and approved by the Institutional Review Board of [Institution Name] (Protocol No. XXX; date of approval)."
If ethical review was waived:
"Ethical review and approval were waived for this study due to [provide justification]."
For animal studies:
- Name of approving authority.
- Confirmation of compliance with relevant national/international guidelines.
- Adherence to ARRIVE guidelines.
8. Funding
Authors must clearly state all sources of funding and financial support related to the work. Examples:
- "This study was supported by [Funding Agency], grant number [XXXX]."
- "The writing of this manuscript was funded by [Organization]."
- "Initial data analysis was performed by [Name], employee of [Company], funded by [Organization]."
If no funding was received, authors must state:
"No funding was declared for this study."
Where applicable (e.g., NIH-funded research), grant numbers must be included.
9. Informed Consent
For studies involving human participants, authors must confirm that informed consent was obtained.
Example:
"All participants provided written informed consent prior to inclusion in the study."
For case reports:
"Written informed consent was obtained from the patient (or legal guardian) for publication of this case report and accompanying images."
10. ORCID ID
Authors are encouraged to provide their ORCID identifiers to ensure correct attribution of their work.
Format: Name Surname – ORCID: 0000-0000-0000-0000
11. Supplementary Material
If applicable:
"Supplementary material associated with this article can be found in the online version."
7. Figures, Tables and Supplementary Material
Figures
Figures must be submitted as separate files and must not be embedded in the main manuscript. Each file must include the figure number in the file name (e.g., Figure 1.jpg). Figures must be cited consecutively in the text using Arabic numerals.
Formats: TIFF, EPS, JPG
Minimum resolution at final size:
- Line art: 600 dpi
- Halftone photos (B/W or colour): 300 dpi
- Combination: 600 dpi
Images should be sharp and clear. Blurred or pixelated figures will not be accepted.
Figure Legends
Figure legends must be included in the main manuscript file (after the reference list), not within the figure file. Legends should be concise yet sufficiently detailed and must define all abbreviations used.
Tables
Tables must be included in the main manuscript, immediately after figure legends, and submitted in editable format (preferably Word). Tables must be self-contained, not duplicate the text, and be numbered consecutively.
- Define abbreviations in footnotes.
- Define statistical measures (e.g., SD, SEM) in the table heading.
- Footnote symbols order: †, ‡, §, ¶
- Reserve *, **, *** for p-values only.
Supplementary Material
Supplementary material may be submitted to support and enhance the scientific content of the manuscript. Examples include:
- Extended datasets
- Additional tables or figures
- Detailed methodological descriptions
- Statistical code
- Questionnaires or interview guides
- Multimedia files (e.g., video or audio material)
Submission Requirements
- Supplementary files must be submitted separately from the main manuscript.
- Each file must be clearly labelled (e.g., Supplementary Table 1, Supplementary Figure 2).
- All supplementary material must be cited in the main text.
- Files should be provided in commonly accessible, non-proprietary formats whenever possible.
Accepted supplementary files will be published online alongside the article. Authors are responsible for ensuring accuracy, completeness, and appropriate anonymization of any shared data.
8. Nomenclature, Units and Abbreviations
Authors must ensure clarity, consistency, and accuracy in terminology, units of measurement, and abbreviations throughout the manuscript.
Nomenclature
Scientific terminology should follow internationally recognized standards relevant to the discipline. Authors should:
- Use accepted medical and scientific terminology.
- Prefer generic names over proprietary or brand names for drugs, devices, and equipment (brand names may be included in parentheses at first mention, if necessary).
- Ensure consistency in terminology throughout the manuscript.
- Use internationally accepted anatomical and clinical terminology.
Gene names, species names, and technical classifications must follow established conventions and formatting rules (e.g., italicization where appropriate).
Units of Measurement
All measurements must be reported using the International System of Units (SI).
- Units should be expressed consistently throughout the manuscript.
- A space should separate the numerical value from the unit (e.g., 10 kg, 5 mL).
- Decimal points (not commas) should be used in English-language manuscripts.
- Derived units and concentrations must follow standard scientific notation.
9. References
Authors are responsible for the accuracy and completeness of all references. References must be formatted according to the journal’s reference style and must be cited in the text in numerical order.
Metabolic Medicine follows the Vancouver reference style according to ICMJE recommendations.
Citation in the Text
- References must be cited using Arabic numerals in square brackets, in the order in which they first appear in the text (e.g., [1], [2]).
- Multiple references should be separated by commas (e.g., [3,4,7]).
- Consecutive references should be indicated using a hyphen (e.g., [5–8]).
- References cited in tables or figure legends must follow the numbering sequence of their first mention in the text.
Reference List
The reference list must:
- Be arranged in numerical order corresponding to in-text citations.
- Include only references cited in the manuscript.
- Contain complete and accurate bibliographic details.
- Include DOI numbers whenever available.
Authors are encouraged to limit references to relevant and recent literature.
How to cite Journal Articles
Author(s). Title of article. Journal Title. Year;Volume(Issue):Page range. doi
Example: Infante M, Silvestri F, Padilla N, Pacifici F, Pastore D, Maia Pinheiro M, et al. Unveiling the Therapeutic Potential of the Second-Generation Incretin Analogs Semaglutide and Tirzepatide in Type 1 Diabetes and Latent Autoimmune Diabetes in Adults. J Clin Med. 2025;14(4):1303. doi:10.3390/jcm14041303
If there are more than six authors, list the first six followed by “et al.”
How to cite Books
Author(s). Title of Book. Edition (if not first). Place of publication: Publisher; Year.
Example: Ricordi C, Strom TB. Transplantation and Cellular Therapy in Metabolic Diseases. 2nd ed. New York: Springer; 2020.
How to cite Book Chapters
Author(s) of chapter. Title of chapter. In: Editor(s), editor(s). Title of Book. Place of publication: Publisher; Year. p. page range.
Example: Infante M, Ricordi C. Role of oxidative stress in metabolic disorders. In: Moller DE, Flier JS, editors. Metabolic Diseases: Pathophysiology and Clinical Management. New York: McGraw-Hill; 2021. p. 245–262.
How to cite Online Resources
Online material should be used cautiously and only when from authoritative sources.
Author(s) or Organization. Title of document. Website name. Published year. Available at: URL. Accessed [Month Year].
Example: International Diabetes Federation. IDF Diabetes Atlas (10th edition). International Diabetes Federation website. 2021. Available at: https://diabetesatlas.org. Accessed March 2026.
Where available, a DOI should be used instead of a URL.
Data Citation
Publicly available datasets must be cited in the reference list and include:
- Author(s);
- Year;
- Dataset title;
- Repository name;
- DOI or persistent link.
Unpublished Material
Personal communications, unpublished data, or manuscripts under review should not appear in the reference list. Such information may be cited in the text only, with written permission from the source.
Reference Accuracy
Authors must:
- Verify all references against original sources.
- Ensure consistency between in-text citations and reference list.
- Confirm correct spelling of author names, journal titles, volume numbers, and page ranges.
Incorrect or incomplete references may result in delays during production.
Please note:
- Ensure all references cited in the text are included in the reference list and vice versa.
- Follow the journal’s prescribed reference style consistently.
- Avoid excessive citation.
- Clearly identify preprints where applicable.
- Authors are responsible for reference accuracy.
10. Submission Checklist
Manuscript Files
- Cover Letter included
- Title Page submitted separately
- Blinded manuscript file uploaded
- Tables and figures prepared as required
- Supplementary material (if applicable)
Content and Structure
- Abstract within limits and correctly structured
- 3–6 keywords provided
- Word count within limits for article type
- Tables/figures cited in text
- References formatted correctly
Ethical and Legal Requirements
- Ethics approval statement included
- Informed consent statement included (if applicable)
- Trial registration details provided (if applicable)
- Conflict of interest statement included
- Funding statement included
- AI statement included (as applicable)
Double-Blind Compliance
- No identifying information in the manuscript file
Final Verification
- Manuscript proofread for language and clarity
- All required sections complete
- Corresponding author details accurate