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期刊名称：CIRCULATION-CARDIOVASCULAR IMAGING

ISSN：1941-9651
出版频率：Monthly
出版社：LIPPINCOTT WILLIAMS & WILKINS, TWO COMMERCE SQ, 2001 MARKET ST, PHILADELPHIA, USA, PA, 19103
  出版社网址：http://www.lww.com/
期刊网址：http://www.lww.com/product/?1941-9651
影响因子：7.792
主题范畴：CARDIAC & CARDIOVASCULAR SYSTEMS;    RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING

期刊简介(About the journal)    投稿须知(Instructions to Authors)    编辑部信息(Editorial Board)   


About the journal
Circulation: Cardiovascular Imaging will publish research in and the practice of non-invasive cardiology, including observational studies, clinical trials, and advances in applied (translational) research in echocardiography, cardiac computed tomography, cardiac magnetic resonance imaging and spectroscopy, magnetic resonance angiography, cardiac positron emission tomography, noninvasive vascular imaging, noninvasive assessment of vascular and endothelial function, radionuclide imaging, molecular imaging, and others.
Instructions to Authors
 

How to Prepare a Manuscript:

Circulation: Cardiovascular Imaging publishes several types of manuscripts under the umbrella of full-length articles. A brief description of each type follows:

Original Research Articles

Circulation: Cardiovascular Imaging considers all types of original research articles, including experiments conducted in human subjects, laboratory animals, and in vitro.


Review Series

Please note that the editors invite most review articles. However, unsolicited material will be considered for publication.

  • Advances in Cardiovascular Imaging: will include a wide range of topics that are relevant to research in and practice of noninvasive cardiovascular imaging. This series will include clinically relevant, disease-based perspectives on current applications of imaging. The series will also feature novel imaging technologies and their potential clinical role, reviews on methodological and analytical issues affecting imaging-based research, and others.

  • Clinical Implications of Molecular Imaging Research: This will emphasize translational aspects of molecularly-targeted approaches to imaging.

  • Controversies in Imaging: will feature scientifically-grounded expressions of critical opinions and discussions on controversial topics affecting the practice of noninvasive imaging, including technical aspects of clinical importance and patient-centered approaches to diagnosis and management of cardiovascular disease. Opposite viewpoints will be presented in tandem, with rebuttal responses by both authors included.

Special Sections
  • Book Reviews: Reviews of selected books on cardiovascular imaging, including books that present innovative concepts, books that describe state-of-the-art diagnostic and therapeutic methods or important advances, and textbooks will be reviewed in this section. Unsolicited book reviews will be considered for publication online. In addition, authors or publishers may submit books, as well as a list of suggested reviewers, to the editorial office at the address noted above.

  • Correspondence: Letters to the Editor, which pertain directly to an article published in the journal within the preceding 8 weeks, will be considered for publication online. A letter must not exceed 500 words in length and must be limited to three authors and five references. They should not have tables or figures. Authors of the original article cited in the letter will be invited to reply. Letters to the editor should be submitted via the online manuscript submission process as described below.

  • Cardiovascular Images: Clinical or basic science images (including motion studies) that illustrate either important "classic" or novel findings, provide insight into basic mechanisms responsible for cardiovascular disease, emphasize an abnormality, or highlight a potential new role for noninvasive imaging will be considered for publication in online format. The written portion of the submission should include a title page, descriptive text of no more than two pages with up to 4 references (if appropriate) and a figure legend. Movie clips are encouraged and may be submitted in any of the standard formats (e.g. avi, mov, etc) and codecs.

General Preparation Instructions:

  • Maximum Word Length: 6000 words

  • Including title page, abstract, text, references, tables, and figure legends

  • Maximum Number of References: 50

  • Maximum Number of Figures and Figure Legends: 8

  • Manuscript should be typed double-spaced, including title page, abstract, text, references, figure legends, and tables. Text should only appear on one side of the page. Acceptable formats are Word or WordPerfect.

  • Leave a 1-inch margin on all sides. Do not use justified margins.

  • Cite references, figures, and tables in numeric order. For review, acceptable figure formats are GIF, TIFF, EPS, JPEG, and single slides of Power Point.

    Formats NOT supported are as follows: Object Linking and Embedding (OLE), Bitmap (.bmp), PICT (.pict), Excel (.xls), Photoshop (.psd), Canvas (.cnv), CorelDRAW (.cdr), and locked or encrypted PDFs. For publication, see acceptable figure requirements under 揂ccepted Manuscripts? below.

  • Use SI units of measure. A more conventionally used measurement may follow in parentheses. Make all conversions before manuscript submission.

  • Please provide sex-specific and/or racial/ethnic-specific data when appropriate, in describing the outcomes of epidemiologic analyses or clinical trials; or specifically state that no sex-based or racial/ethnic-based differences were present.

  • Consult the American Medical Association Manual of Style, 9th ed, Baltimore, Md, Williams & Wilkins, 1998, for style.

  • Manuscripts must conform to the 揢niform Requirements for Manuscripts Submitted to Biomedical Journals?http://www.icmje.org/.

  • Assemble the manuscript in this order: Title Page, Abstract, Text, Acknowledgments, Funding Sources, Disclosures, References, Figure Legends, Tables, and Figures.

Title Page

The title page (page 1, do not number) should contain these elements:

  • Full title

  • First authoræsurname and short title (not to exceed 50 characters, including spaces)

  • Authorsnames, academic degrees, and affiliations

  • Name and complete address for correspondence (include street name and address as well as post office box, and address for reprints if different from correspondence)

  • Fax number, telephone number and email address

  • The total word count of the manuscript, including the title page, abstract, text, references, tables and figures legends

  • The Journal Subject Codes pertaining to the article. Please refer to the subject code list.

Abstract and Key Words

  • Do not cite references in the abstract

  • Limit use of acronyms and abbreviations. Define at first use acronym or abbreviation in parenthesis.

  • Be concise (250 words maximum)

  • Use the following headings:

  • Background ?rationale for study

  • Methods and Results ?brief presentation of methods and presentation of significant results; please include the sample size

  • Conclusions succinct statement of data interpretation

  • When applicable, include a fourth heading: "Clinical Trial Registration Information". Please list the URL, as well as the unique identifier, for the publicly accessible website on which the trial is registered.

  • Insert three to five Key Words after abstract. Please refer to the key word list.

Text

  • Typical main headings include Methods, Results, and Discussion

  • Number pages

  • Abbreviations must be defined at first mention

  • Methods

    Please note that the print version of the Methods and Results should be able to stand alone and should provide sufficient information for the reader to understand the basic methods of the study and to review the fundamental findings in a mechanistic way.

  • Experimental animals: State the species, strain, number used, and pertinent descriptive characteristics. When describing surgical procedures, identify the preanesthetic and anesthetic agents used and the amounts, concentrations, routes, and frequency of administration of each. Paralytic agents are not considered acceptable substitutes for anesthetics. For other invasive procedures on animals, report the analgesic or tranquilizing drug used. If none were used, provide justification for exclusion.

  • Human studies: Indicate that the study was approved by an institutional review committee and that the subjects gave informed consent.

  • Drugs and Devices: In the Methods, the complete name and location of the manufacturer must be supplied for all reagents, equipment, and devices used. In all other instances, the generic rather than trademark names of all drugs and devices.

  • Independent Data Access and Analysis: The Editors consider it preferable for investigators to have direct access to the primary data in a clinical trial (raw and derived datasets) when reporting results of the trial. Alternatively, an independent party with an academic affiliation who has access to the primary data may serve as the analyst for the investigators. It is recognized that for logistical reasons these options may not be possible in all instances. At a minimum, the authors should have the ability to query any aspect of the data either directly or through an independent analysis. However, the Editors reserve the right to ask for additional information from the corresponding author regarding measures that were taken to minimize bias and verify the integrity of the primary data and any analyses performed.

  • Guidelines for Clinical Trials

    • In accordance with the Clinical Trial Registration Statement from the International Committee of Medical Journal Editors (Circulation. 2005;111:1337) and (http://content.nejm.org/cgi/content/full/NEJMe078110), all clinical trials in Circulation: Cardiovascular Imaging must be registered in a public trials registry at or before the onset of participant enrollment. This requirement applies to all clinical trials that begin enrollment after July 1, 2005.

    • Research is considered to be a clinical trial if it involves prospective assignment of human subjects to an intervention or comparison group to study the relation between a health-related intervention and a health outcome. Health-related interventions include any intervention used to modify a biomedical or health-related outcome (for example, drugs, surgical procedures, devices, behavioral treatments, dietary interventions, and process-of-care changes). Health outcomes include any biomedical or health-related measures obtained in patients or participants, including pharmacokinetic measures and adverse events. As previously, purely observational studies (those in which the assignment of the medical intervention is not at the discretion of the investigator) will not require registration. We will start to implement the expanded definition of clinically directive trials for all trials that begin enrollment on or after July 1, 2008. Those who are uncertain whether their trial meets the expanded ICMJE definition should err on the side of registration if they wish to seek publication.

    • The registry must be accessible to the public at no charge, searchable, open to all prospective registrants, and managed by a not-for-profit organization. The registry must include the following information: a unique identifying number, a statement of the intervention(s), study hypothesis, definition of primary and secondary outcome measurements, eligibility criteria, target number of subjects, funding source, contact information for the principal investigator, and key dates (registration date, start date, and completion date). The registry sponsored by the United States National Library of Medicine (http://www.clinicaltrials.gov) meets these requirements and is recommended by the editors.

      Other registries are acceptable if they meet these requirements. In addition to www.clinicaltrials.gov, the following registries are recommended by the ICMJE:
      1) http://isrctn.org
      2) www.umin.ac.jp/ctr/index/htm
      3) www.actr.org.au
      4) www.trialregister.nl

      In accordance with the ICMJE抿recommendation, we will also accept registration of clinical trials in any of the primary registers that participate in the World Health Organization抿International Clinical Trial Registry Platform. Primary registers are WHO selected registers managed by not-for-profit entities that will accept registrations for any interventional trials, delete duplicate entries from their own register, and provide data directly to the WHO. Please note that registration in any WHO partner registers is insufficient.

    • The authors will be requested to provide the exact URL and unique identification number for the trial registration at the time of submission. Since this information will be published, we ask that you include a fourth heading in your abstract: "Clinical Trial Registration Information". Please list the URL, as well as the unique identifier, for the publicly accessible website on which the trial is registered in this section.

    • Clinical trial reports should also comply with the Consolidated Standards of Reporting Trials (CONSORT) and include a flow diagram presenting the enrollment, intervention allocation, follow-up, and data analysis with number of subjects for each (www.consort-statement.org). Please also refer specifically to the CONSORT Checklist of items to include when reporting a randomized clinical trial.

    • Results posted in the same clinical trials registry in which the primary registration resides will not be considered prior publication if they are presented in the form of a brief abstract (<500 words or less) or a table.

  • Guidelines for Meta-Analyses

    See 揗eta-analysis of Observational Studies in Epidemiology: A Proposal for Reporting,?JAMA. 2000; 283: 2008-2012.

  • Guidelines for Studies on Diagnostic Tests

    See 揟he STARD Statement for Reporting Studies of Diagnostic Accuracy: Explanation and Elaboration,?Ann Intern Med. 2003; 138: 40-44.

  • Guidelines for Human Phenotype-Genotype Association or Linkage Studies

    A. Reporting issues.
    1. Report process for selecting genes and SNPs.
    2. Report Hardy-Weinberg statistics or p-values and method of calculating same.
    3. Refer to existing public domain websites for the Human Gene Ontology name and the rs number for SNPs.
    ?http://www.gene.ucl.ac.uk/nomenclature/
    ?http://www.ncbi.nlm.nih.gov/projects/SNP/
    ?http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=Snp
    4. Describe genotyping methods. If numerous primers have been used, please include them in an online supplement.

    B. False positive and false negative concerns. Given well-described problems with both false positive and false negative associations, phenotype-genotype association studies should meet some or all of the criteria below:
    1. Phenotype is clearly defined, is heritable, and if a quantitative phenotype is reported, reproducibility data are provided.
    2. The sample size is adequate to detect a SNP or haplotype with a modest effect. For genotype-trait associations, provide an estimate of the effect size that could be detected with power 0.80 or higher with the allele frequency and sample size reported.
    3. Since multiple statistical testing methods are frequently used in genotyping-phenotyping studies, please include specifics of the primary model(s) tested. Nonessential secondary models may be published as electronic data supplements. Clinically relevant confounders should be included in multivariable models or residuals.

    C. Review criteria for human linkage studies. Manuscripts should include the following:
    1. Identifying plausible candidate genes under the linkage peak.
    2. Follow-up fine mapping to narrow the region of linkage, &/or genotyping some of the candidate genes under the linkage peak.
    3. Replication data from another sample.

  • Guidelines for Genomic and Proteomic Studies

    • Preparation of Data Submitted: Data should follow the MIAME checklist (for more information see http://www.mged.org/Workgroups/MIAME/miame_checklist.html).

    • Accessibility of Data: Authors of papers that include genomic, proteomic, or other high-throughput data are required to make their data easily accessible for the reviewers and the editors during the review process.

    • You may submit your data to the NCBI gene expression and hybridization array data repository (GEO, http://www.ncbi.nlm.nih.gov/geo/) and provide the GEO accession number; or,

    • You may provide a link to a secure or publicly accessible website which hosts the data. Prior to publication, the data must be submitted and an accession number obtained. Access to the information in the database must be available at the time of publication. GEO has a web-based submission route, suitable for a small number of samples, or a batch submission tool (called SOFT). GEO is accessible from http://www.ncbi.nlm.nih.gov/geo/. The submission FAQ is available at http://www.ncbi.nlm.nih.gov/projects/geo/info/faq.html.

  • Guidelines for Proteins and Nucleic Acid Sequences

    Newly reported nucleotide or protein sequences must be deposited in GenBank or EMBL databases, and an accession number must be obtained. Access to the information in the database must be available at the time of publication. Authors are responsible for arranging release of data at the time of publication. The authors must also provide a statement in the manuscript that this sequence has been scanned against the database and all sequences with significant relatedness to the new sequence identified (and their accession numbers included in the text of the manuscript).

    GenBank

    GenBank Submissions
    National Center for Biotechnology Information
    8600 Rockville Pike, Building 38A
    Room 8N-805
    Bethesda, MD 20894
    Tel: (301) 496-2475
    On the web at: http://www.ncbi.nlm.nih.gov/Genbank/index.html

    EMBL Nucleotide Sequence Submissions

    European Bioinformatics Institute
    Hinxton Hall
    Hinxton, Cambridge CB10 1SD, UK
    Tel.: 44-1223-494401; Fax: 44-1223-494472
    e-mail: support@ebi.ac.uk
    On the web at: http://www.ebi.ac.uk

    DNA Data Bank of Japan

    Center for Information Biology
    National Institute of Genetics
    Mishima, Shizuoka, 411, Japan
    Tel.: 81-559-81-6853; Fax: 81-559-81-6849
    On the web at: http://www.ddbj.nig.ac.jp

    Submission to any data bank is sufficient to ensure entry in all.
Acknowledgments

Authors should obtain written permission from all individuals who are listed in the 揂cknowledgments?section of the manuscript, because readers may infer their endorsement of data and conclusions. The corresponding author must sign the Acknowledgment Section of the Copyright Transfer Agreement, certifying that (1) all persons who have made substantial contributions in the manuscript (eg, data collection, analysis, or writing or editing assistance), but who do not fulfill authorship criteria, are named with their specific contributions in the Acknowledgments section of the manuscript; (2) all persons named in the Acknowledgments section have provided the corresponding author with written permission to be named in the manuscript; and (3) if an Acknowledgments section is not included, no other persons have made substantial contributions to this manuscript.

Funding Sources
  • All sources of support for the research should be listed under this heading.
  • All grant funding agency abbreviations should be completely spelled out, with the exception of the NIH.

      Disclosures

      • All potential conflicts of interest must be stated within the text of the manuscript, under this heading. This pertains to relationships with pharmaceutical companies, biomedical device manufacturers, or other corporations whose products or services are related to the subject matter of the article. Such relationships include, but are not limited to, employment by an industrial concern, ownership of stock, membership on a standing advisory council or committee, being on the board of directors, or being publicly associated with the company or its products. Other areas of real or perceived conflict of interest could include receiving honoraria or consulting fees or receiving grants or funds from such corporations or individuals representing such corporations.

      References

      • Accuracy of reference data is the responsibility of the author

      • Verify all references against original sources

      • List all authors for each reference; do not use 

      • Example of a good reference:
        1. Smith HJ, Allen S, Yu W, Fard S. This is the title. Circulation. 2004; 104:276-308.

        Please note that if you use reference software tools (e.g. EndNote or Reference Manager), they do not always match our style and you may need to manually correct your references..

      • Cite references in numeric order according to first mention in the text. In the text, ensure accuracy of spelling and details of publication, i.e., the text citation should match the reference information.

      • Personal communications, unpublished observations, and submitted manuscripts are not legitimate references. They must be cited in the text only (not in the reference list) as follows: author name, degree(s) held, unpublished data, year.

      • Abstracts may be cited only if they are the sole source and must be identified in the reference as 揂bstract.

      • References must be from a full length publication in a peer reviewed journal.

      • 揑n press?citations must have been accepted for publication and the name of the journal or book publisher must be included.

      Figures

      • Figure parts should be clearly labeled. Letters and locants must be uniform in size and style within each figure, and when possible, between figures. (The font size must be 10 point or higher.)

      • Avoid headings on the figure. Heading information should appear in the figure legend.

      • Line art should not contain hair lines, which are hard to reproduce

      • Supply a scale bar with photomicrographs

      • Provide double-spaced copy for figure legends on a separate page

      • Symbols and abbreviations must be defined in the figure or its legend

      • Limit white space between the panel and panel label

      • Figures should be sized as close as possible to their final print size. Please note that very few figures qualify for a 2-column format.

      Tables

      • Begin each table on a separate page, double-spaced. Please remember that tables prepared with Excel are not accepted unless embedded within your text document.

      • The table number should be Arabic, followed by a period and brief title

      • Use same size type as in text

      • Supply a brief heading for each column

      • Indicate footnotes in this order:

      • Do not use vertical lines between columns. Use horizontal lines above and below the column headings and at the bottom of the table only. Use extra space to delineate sections within the table.

      • Abbreviations used in the table must be defined in a footnote to the table.

      Online Data Supplements

      Online Data Supplements are encouraged as an enhancement to the print Methods section. This optional section provides an opportunity to present supporting materials to the manuscript. Please note that all supplements undergo peer review and must be submitted with the original submission of the manuscript.

      Online Data Supplements can consist of the following:

      • Expanded Methods and Results

      • Additional Figures

      • Additional Tables

      • Video Files

      If citations are made in an Online Data Supplement, the supplement must contain its own Reference Section, with references numbered sequentially beginning with the number 1. Please try to keep the individual file size to 10 MB or less to facilitate easier downloading for readers.

      Online Supplemental Data: A combined PDF of your supplemental data must be provided. The first page of this PDF should include the heading, "SUPPLEMENTAL MATERIAL." Please note that this single PDF would include all of the supplemental material related to your manuscript, except for the Video or Movie files. The supplemental material to be included in this PDF is as follows: Supplemental Methods, Supplemental Tables, Supplemental Figures and Figure Legends, and Supplemental References. Lastly, the legends for the Video files should also be included in this PDF. Please upload this PDF to your author area.

      Supplemental Materials Required for Review

    • A copy of all submitted manuscripts mentioned in the article must be submitted as part of the review process

    • A copy of all manuscripts, either in preparation or submitted, that potentially overlap with your Circulation: Cardiovascular Imaging submission. Please note that failure to include such material is a violation of the journal's Ethical Policy, below.

    • A copy of all in press articles cited in the Reference section must be supplied for review by the editors and the reviewers

      • Ethical Policy

      Manuscripts are considered on the understanding that they contain original material, that the manuscript and material within the manuscript have not been published and are not being considered for publication elsewhere in whole or in part in any language, including publicly accessible web sites or e-print servers, except as an abstract. The authors also certify that any and all other work in preparation, submitted, in press, or published that is potentially overlapping either in the actual data presented or in the conceptual approach is enclosed along with the original submission. Any material within the manuscript that has appeared elsewhere must be cross-referenced and permission to use or adapt the material must be received, in writing from the copyright holder.

      Abstracts and Webcasts

      If some or all of the work in the manuscript has been published or submitted in abstract form, and/or overlapping data exists, the following rules apply:

      • The published or submitted abstract must accompany the submitted manuscript.

      • The abstract cannot itself have been referenced in MEDLINE or PubMed.

      • The potentially overlapping work and a separate explanation of the nature of any possible overlap with the submitted manuscript must accompany the submitted manuscript.

      These restrictions generally do not apply to presentations or press reports published in connection with scientific meetings, or to poster presentations at scientific meetings that are videotaped, provided that the material has not been widely circulated, copyrighted or sold. Posting an audio recording, video recording, or short summary of a presentation made at a professional meeting on the Internet would be considered as a meeting presentation by the American Heart Association and would not compromise consideration of a submission. Direct release of information through press releases or media briefings may preclude publication.

      Embargo Policy

      All content information of an accepted paper is strictly confidential and cannot appear in the media (in print or electronic form) before its embargo date and time. Authors/researchers, their respective public relations representatives and funding sponsors may not distribute or promote their work to the media prior to embargo.

      In the event that the American Heart Association/American Stroke Association selects the manuscript for promotion in a news release, news conference, video news release or podcast, AHA/ASA staff will contact the author/researcher to inform him/her of the pending news materials and to notify him/her that he/she may give reporters pre-embargo interviews based upon the media requests generated by the AHA/ASA news materials. Authors/researchers must ensure that the reporter understands and will adhere to the embargo time.

      If an embargo break is the result of any action by an author/researcher, he/she risks withdrawal of publication of his/her manuscript. Violations of the embargo policy may also jeopardize future acceptance of manuscripts to be published in AHA/ASA scientific journals.

      Generally, embargoes on journal articles lift the day and the time the article is published, either on-line or in print (whichever comes first) by the American Heart Association/American Stroke Association.

      Questions about media embargoes should be directed to Cathy Lewis, Senior Manager, Corporate & Media Communications, AHA National Center, 7272 Greenville Avenue, Dallas, TX 75231-4596; Tel: 214-706-1324; Email: cathy.lewis@heart.org .

      Although the Editorial Office will endeavor to notify authors of the anticipated publication date/time, neither the Editorial Office nor the AHA/ASA will be responsible for any consequences of early online posting with regard to the intellectual property rights. To safeguard their intellectual property, authors should ensure that appropriate reports of invention and patent applications have been filed before the manuscript is accepted.


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      How to Submit a Manuscript:

      All manuscripts must be submitted electronically. Before proceeding to the online submission site, please prepare your manuscript according to the instructions listed above under the heading, 揌ow to Prepare a Manuscript.?When your manuscript is ready for submission, please follow the instructions below.

      Revised Manuscripts:

      • All revisions must be received within 90 days of the original decision date. If your revision is not received within that specified time limit, the manuscript will be considered de novo.

      • Please remember that your manuscript text, including title page, abstract, references, figure legends, and tables, should not exceed 6,000 words. Manuscripts exceeding this limit will be returned to authors for further revision, prior to review. Word count is calculated by the Editorial Office using the Microsoft Word tool.

      • Please label each page of your revision using your manuscript number followed by /R1, /R2, /R3, etc.

      • In your written response to the reviewers' comments, give the exact page number(s), paragraphs(s) and line number(s) where each revision was made.

      • A marked up version of the revision, with the changes to the manuscript highlighted or tracked, should be uploaded as a Supplemental File.

      • Enter Conflict of Interest Disclosures. You will need to describe conflicts regarding this manuscript for all authors. Please refer to the Online Conflict Reference Form prior to submission.

      • Original manuscript files should be submitted electronically to the Editorial Office, so as not to delay publication if and when the paper is accepted.



      Compliance With NIH and Other Research Funding Agency Accessibility Requirements

      Several research funding agencies now require or request authors to submit the post-print (the article after peer review and acceptance but not the final published article) to a repository that is accessible online by all without charge. Within medical research, 3 funding agencies in particular have announced such policies:

      • The US National Institutes of Health (NIH) requires authors to deposit post-prints of articles, which have received NIH funding, in its repository PubMed Central (PMC). This deposit should be done within the 12 months after publication of the final article in the journal.

      • The Howard Hughes Medical Institute (HHMI) requires, as a condition of research grants, deposit in PMC, but within 6 months after publication of the final article.

      • The Wellcome Trust requires, as a condition of research grants, deposit in UK PMC within 6 months after publication of the final article.

      As a service to authors, the Publisher (Wolters Kluwer Health/Lippincott Williams & Wilkins) of the AHA journals will identify to PMC articles that require depositing. The Copyright Transfer Agreement provides the primary mechanism for identifying such articles. The AHA also requests that, during the submission process in Bench>Press, funding is indicated in the first page of the submission process.

      WKH/LWW will transmit the post-print of an article, which is based on research funded in whole or in part by 1 or more of these 3 agencies, to PMC.

      On NIH request, it remains the legal responsibility of the author(s) to confirm with the NIH the provenance of their manuscript for purposes of deposit.

      • Author(s) will not deposit their articles themselves.

      • Author(s) will not alter the post-print already transmitted to NIH.

      • Author(s) will not authorize the display of the post-print prior to:
      1. 12 months after publication of the final article, in the case of NIH,
      2. 6 months after publication of the final article, in the case of HHMI and the Wellcome Trust

        For more information about authors?rights and responsibilities, please visit the AHA Authorship Responsibility and Copyright Transfer Agreement.

        For more information on PMC, please visit http://nihms.nih.gov.

        A Permissions and Rights Question and Answer is also available; please visit http://www.ahajournals.org/rights.

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        Accepted Manuscripts:

        The following are required for publication:

        • Original source files for the manuscript text, tables and figures.

        • PDF of the final version of each figure or 1 glossy print of each figure.

        • Original source files for each online data supplement or a combined PDF of the online data supplement. If figure or movie files are included, please be sure to include figure and/or movie legends.

          For detailed information about submitting print publication-quality digital art, please visit http://circ.ahajournals.org/misc/ifora.pdf. Note that:

        • Only TIFF (tagged image file format), EPS (encapsulated postscript) and PPT (Microsoft PowerPoint) files are acceptable for publication.

        • Color files must be saved as CMYK (Cyan-Magenta-Yellow-Black) not RGB (Red-Green-Blue).

        • Line art must be saved at resolution of at least 1200 dpi; photographs, CT scans, radiographs, etc, should be saved at a resolution of at least 300 dpi. Images saved at 72 dpi are not acceptable for printed publications.

        • PowerPoint files can be acceptable, although PowerPoint is not a recommended application for image preparation. Color figures submitted as PowerPoint may experience a shift in hue. PowerPoint files must contain only supported fonts (Arial, Helvetica, Times Roman, and Symbol). If other fonts are used in the PowerPoint file or in EPS files embedded in a PowerPoint document, there is a significant chance of formatting errors or character substitutions. Images must be embedded in PowerPoint files, rather than 搇inked?

        • Each panel of the figure should be saved in a separate file.

          •

        • Prior to publication, the Copyright Transfer Agreement form must be completed by each author and faxed to the editorial office. To ensure proper handling, it is suggested that the corresponding author collect the completed forms from each author and fax them, simultaneously, to the Editorial Office. Please note the American Heart Association's new Authorship Responsibility and Copyright Transfer Agreement form, a link to which can be found at the top of this page.

        • Written permission from all persons acknowledged by name

        • Online Supplemental Data: A combined PDF of your supplemental data must be provided. The first page of this PDF should include the heading, "SUPPLEMENTAL MATERIAL." Please note that this single PDF would include all of the supplemental material related to your manuscript, except for the Video or Movie files. The supplemental material to be included in this PDF is as follows: Supplemental Methods, Supplemental Tables, Supplemental Figures and Figure Legends, and Supplemental References. Lastly, the legends for the Video files should also be included in this PDF. Please upload this PDF to your author area.

        Timely publication of a manuscript will depend upon all of the above.

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        Cost to Authors

        • Page Charges: $70 per typeset page to defray publication costs
          Authors of papers exceeding our 6,000 word limit will be charged for the overage. Minimum fee for papers exceeding this maximum will be $425. In addition, authors will be charged an additional $425 for each additional 1,000 words over 6,000. The usual $70 page charge will also apply. Word count will be calculated by the editorial office, using the Microsoft Word tool. Title page, abstract, references, tables and figures legends are included in the total word count.

        • Color Figure Reproduction: Publisher will provide an estimate for author抿approval before publication

        • Reprint expenses: Price lists are sent with author抿proofs.

        • Excessive author alterations to typeset page: $50 per page.

        • Correction (erratum): $100 per page if error results from an author抿oversight.


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        Permissions

        • Requests for permission to reproduce figures, tables, or portions of articles originally published in Circulation: Cardiovascular Imaging can be obtained via Rightslink (a service of the Copyright Clearance Center), not the Editorial Office. All permission requests are now processed via the Rightslink online system. Steps for obtaining permission include:
          1. On Circulation: Cardiovascular Imaging's home page, either search for the article using the Search feature or locate a copy of the article in the online archives for which you are requesting permission.
          2. Next, select the Full Text or PDF version of the article.
          3. Then, locate the "Request Permissions" link in the menu on the right side of the Web page (under "Services"). A new Web browser will open, which is Rightslink.
          4. Follow the step-by-step instructions in Rightslink for requesting permission by:
          • selecting the way the content will be used.
          • creating an account, if one does not exist already.
          • accepting the terms and conditions for reuse.
          • determining method of payment.

        Conflict of Interest Policy for Editors

        Original manuscripts authored or coauthored by the Editor-in-Chief, the Editor, and the Senior Associate Editor are handled by a Consulting Editor, who makes all the decisions about the manuscript (including choice of referees and ultimate acceptance or rejection). The entire process is handled confidentially. All manuscripts submitted from the Editor抿home institution are also handled entirely by a Consulting Editor. The Editor (in Chief) may additionally, from time to time, refer a manuscript to a Consulting Editor to avoid a real or reasonably perceived conflict of interest.

        Disclaimer

        Statements, opinions, and results of studies published in Circulation: Cardiovascular Imaging are those of the authors and do not reflect the policy or position of the American Heart Association, and the American Heart Association provides no warranty as to their accuracy or reliability.


        1. Editorial Board
        Editor
        Marcelo F. Di Carli
         
        Senior Associate Editor
        Ravin Davidoff

        Section Editor
        Sharmila Dorbala         		Associate Editors
        Linda D. Gillam
        Udo Hoffmann
        Subha V. Raman
        		 Senior Guest Editors
        Donna K. Arnett
        Judith Hochman
        Elizabth Murphy         		Statistical Consultants
        Nancy R. Cook
        Roger B. Davis
        Kimberlee Gauvreau
        Martin G. Larson
        Kathryn Lunetta
         
        Editorial Board
        Stephan Achenbach
        Jeroen J. Bax
        Rob S. Beanlands
        Frank M. Bengel
        Daniel S. Berman
        Vasken Dilsizian
        Noyan Gokce
        Robert Gropler
        Rory Hachamovitch
        Vincent B. Ho
        		 William G. Hundley
        Michael Jerosch-Herold
        Raymond J. Kim
        Juhani Knuuti
        Raymond Y. Kwong
        Roberto M. Lang
        Joao A. Lima
        Jonathan R. Lindner
        Warren G. Manning
        Thomas H. Marwick
        		 Matthias Nahrendorf
        Jae K. Oh
        Frederick L. Ruberg
        Markus Schwaiger
        Leslee J. Shaw
        Albert J. Sinusas
        Allen J. Taylor
        James D. Thomas
        Flordeliza S. Villanueva
        Joseph C. Wu
         
        Staff
        Managing Editor: Karen Barry
        Assistant Managing Editor: Kristina Sine


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