Example of Depression and Anxiety format
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Example of Depression and Anxiety format Example of Depression and Anxiety format Example of Depression and Anxiety format Example of Depression and Anxiety format Example of Depression and Anxiety format Example of Depression and Anxiety format
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Example of Depression and Anxiety format Example of Depression and Anxiety format Example of Depression and Anxiety format Example of Depression and Anxiety format Example of Depression and Anxiety format Example of Depression and Anxiety format
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This content is only for preview purposes. The original open access content can be found here.
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Depression and Anxiety — Template for authors

Publisher: Wiley
Categories Rank Trend in last 3 yrs
Clinical Psychology #8 of 283 down down by 2 ranks
Psychiatry and Mental Health #26 of 502 down down by 5 ranks
journal-quality-icon Journal quality:
High
calendar-icon Last 4 years overview: 434 Published Papers | 3981 Citations
indexed-in-icon Indexed in: Scopus
last-updated-icon Last updated: 11/07/2020
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FAQ

Related Journals

open access Open Access

SAGE

Quality:  
High
CiteRatio: 3.7
SJR: 0.858
SNIP: 1.482
open access Open Access

Cambridge University Press

Quality:  
High
CiteRatio: 4.4
SJR: 1.074
SNIP: 1.257
open access Open Access

Springer

Quality:  
High
CiteRatio: 4.6
SJR: 1.395
SNIP: 1.291
open access Open Access

Springer

Quality:  
High
CiteRatio: 4.3
SJR: 1.568
SNIP: 1.655

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.

4.702

5% from 2018

Impact factor for Depression and Anxiety from 2016 - 2019
Year Value
2019 4.702
2018 4.935
2017 5.043
2016 4.971
graph view Graph view
table view Table view

9.2

2% from 2019

CiteRatio for Depression and Anxiety from 2016 - 2020
Year Value
2020 9.2
2019 9.0
2018 8.9
2017 9.3
2016 9.6
graph view Graph view
table view Table view

insights Insights

  • Impact factor of this journal has decreased by 5% in last year.
  • This journal’s impact factor is in the top 10 percentile category.

insights Insights

  • CiteRatio of this journal has increased by 2% 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.

2.634

4% from 2019

SJR for Depression and Anxiety from 2016 - 2020
Year Value
2020 2.634
2019 2.544
2018 2.76
2017 2.934
2016 2.987
graph view Graph view
table view Table view

2.202

12% from 2019

SNIP for Depression and Anxiety from 2016 - 2020
Year Value
2020 2.202
2019 1.96
2018 1.843
2017 1.708
2016 1.825
graph view Graph view
table view Table view

insights Insights

  • SJR of this journal has increased 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 12% in last years.
  • This journal’s SNIP is in the top 10 percentile category.

Depression and Anxiety

Guideline source: View

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Wiley

Depression and Anxiety

Depression and Anxiety welcomes original research and synthetic review articles covering molecular, genetic, biopsychosocial, neurochemical, neuropsychological, physiological, behavioral, sociological, psychodynamic, psychotherapeutic, cognitive and pharmacotherapeutic aspects...... Read More

Psychology

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Last updated on
10 Jul 2020
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ISSN
1091-4269
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Impact Factor
High - 1.916
i
Open Access
Yes
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Sherpa RoMEO Archiving Policy
Yellow faq
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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: 10.1002/DA.10113
Development of a new resilience scale: The Connor‐Davidson Resilience Scale (CD‐RISC)
Kathryn M. Connor1, Kathryn M. Connor2, Jonathan R.T. Davidson1
01 Sep 2003 - Depression and Anxiety

Abstract:

Resilience may be viewed as a measure of stress coping ability and, as such, could be an important target of treatment in anxiety, depression, and stress reactions. We describe a new rating scale to assess resilience. The Connor-Davidson Resilience scale (CD-RISC) comprises of 25 items, each rated on a 5-point scale (0–4), wi... Resilience may be viewed as a measure of stress coping ability and, as such, could be an important target of treatment in anxiety, depression, and stress reactions. We describe a new rating scale to assess resilience. The Connor-Davidson Resilience scale (CD-RISC) comprises of 25 items, each rated on a 5-point scale (0–4), with higher scores reflecting greater resilience. The scale was administered to subjects in the following groups: community sample, primary care outpatients, general psychiatric outpatients, clinical trial of generalized anxiety disorder, and two clinical trials of PTSD. The reliability, validity, and factor analytic structure of the scale were evaluated, and reference scores for study samples were calculated. Sensitivity to treatment effects was examined in subjects from the PTSD clinical trials. The scale demonstrated good psychometric properties and factor analysis yielded five factors. A repeated measures ANOVA showed that an increase in CD-RISC score was associated with greater improvement during treatment. Improvement in CD-RISC score was noted in proportion to overall clinical global improvement, with greatest increase noted in subjects with the highest global improvement and deterioration in CD-RISC score in those with minimal or no global improvement. The CDRISC has sound psychometric properties and distinguishes between those with greater and lesser resilience. The scale demonstrates that resilience is modifiable and can improve with treatment, with greater improvement corresponding to higher levels of global improvement. Depression and Anxiety 18:76–82, 2003. & 2003 Wiley-Liss, Inc. read more read less

Topics:

Resilience (network) (54%)54% related to the paper, Rating scale (53%)53% related to the paper, Anxiety (52%)52% related to the paper
View PDF
6,854 Citations
Journal Article DOI: 10.1002/DA.1029
Clinician-administered PTSD scale: A review of the first ten years of research
Frank W. Weathers1, Terence M. Keane2, Jonathan R.T. Davidson3
01 Jan 2001 - Depression and Anxiety

Abstract:

The Clinician-Administered PTSD Scale (CAPS) is a structured interview for assessing posttraumatic stress disorder (PTSD) diagnostic status and symptom severity. In the 10 years since it was developed, the CAPS has become a standard criterion measure in the field of traumatic stress and has now been used in more than 200 stud... The Clinician-Administered PTSD Scale (CAPS) is a structured interview for assessing posttraumatic stress disorder (PTSD) diagnostic status and symptom severity. In the 10 years since it was developed, the CAPS has become a standard criterion measure in the field of traumatic stress and has now been used in more than 200 studies. In this paper, we first trace the history of the CAPS and provide an update on recent developments. Then we review the empirical literature, summarizing and evaluating the findings regarding the psychometric properties of the CAPS. The research evidence indicates that the CAPS has excellent reliability, yielding consistent scores across items, raters, and testing occasions. There is also strong evidence of validity: The CAPS has excellent convergent and discriminant validity, diagnostic utility, and sensitivity to clinical change. Finally, we address several concerns about the CAPS and offer recommendations for optimizing the CAPS for various clinical research applications. read more read less

Topics:

Clinician Administered PTSD Scale (68%)68% related to the paper, Discriminant validity (52%)52% related to the paper, Test validity (52%)52% related to the paper
1,812 Citations
Role of serotonergic and noradrenergic systems in the pathophysiology of depression and anxiety disorders.
Kerry J. Ressler1, Charles B. Nemeroff1
01 Jan 2000 - Depression and Anxiety

Abstract:

There is abundant evidence for abnormalities of the norepinephrine (NE) and serotonin (5HT) neurotransmitter systems in depression and anxiety disorders. The majority of evidence supports underactivation of serotonergic function and complex dysregulation of noradrenergic function, most consistent with overactivation of this s... There is abundant evidence for abnormalities of the norepinephrine (NE) and serotonin (5HT) neurotransmitter systems in depression and anxiety disorders. The majority of evidence supports underactivation of serotonergic function and complex dysregulation of noradrenergic function, most consistent with overactivation of this system. Treatment for these disorders requires perturbation of these systems. Reproducible increases in serotonergic function and decreases in noradrenergic function accompany treatment with antidepressants, and these alterations may be necessary for antidepressant efficacy. Dysregulation of these systems clearly mediates many symptoms of depression and anxiety. The underlying causes of these disorders, however, are less likely to be found within the NE and 5HT systems, per se. Rather their dysfunction is likely due to their role in modulating, and being modulated by, other neurobiologic systems that together mediate the symptoms of affective illness. Clarification of noradrenergic and serotonergic modulation of various brain regions may yield a greater understanding of specific symptomatology, as well as the underlying circuitry involved in euthymic and abnormal mood and anxiety states. Disrupted cortical regulation may mediate impaired concentration and memory, together with uncontrollable worry. Hypothalamic abnormalities likely contribute to altered appetite, libido, and autonomic symptoms. Thalamic and brainstem dysregulation contributes to altered sleep and arousal states. Finally, abnormal modulation of cortical-hippocampal-amygdala pathways may contribute to chronically hypersensitive stress and fear responses, possibly mediating features of anxiety, anhedonia, aggression, and affective dyscontrol. The continued appreciation of the neural circuitry mediating affective states and their modulation by neurotransmitter systems should further the understanding of the pathophysiology of affective and anxiety disorders. Depression and Anxiety, Volume 12, Supplement 1:2–19, 2000. © 2000 Wiley-Liss, Inc. read more read less

Topics:

Anxiety (57%)57% related to the paper, Serotonergic (57%)57% related to the paper, Anhedonia (52%)52% related to the paper, Arousal (51%)51% related to the paper
View PDF
922 Citations
open accessOpen access Journal Article DOI: 10.1002/DA.20837
Synthesis of the psychometric properties of the PTSD checklist (PCL) military, civilian, and specific versions.
C B A Kendall Wilkins1, Ariel J. Lang1, Sonya B. Norman1
01 Jul 2011 - Depression and Anxiety

Abstract:

The posttraumatic stress disorder checklist is a commonly used measure, with military (PCL-M), civilian (PCL-C), and specific trauma (PCL-S) versions. This synthesis of the psychometric properties of all three versions found the PCL to be a well-validated measure. The PCL shows good temporal stability, internal consistency, t... The posttraumatic stress disorder checklist is a commonly used measure, with military (PCL-M), civilian (PCL-C), and specific trauma (PCL-S) versions. This synthesis of the psychometric properties of all three versions found the PCL to be a well-validated measure. The PCL shows good temporal stability, internal consistency, test-retest reliability, and convergent validity. The majority of structural validity studies support four factor models. Little is available on discriminant validity and sensitivity to change. Strengths, limitations, and future research directions are discussed. Understanding the PCL's psychometric properties, strengths (e.g., items map on to DSM-IV diagnostic criteria), and limitations (e.g., may overestimate PTSD prevalence) will help clinicians and researchers make educated decisions regarding the appropriate use of this measure in their particular setting. read more read less

Topics:

Convergent validity (58%)58% related to the paper, Discriminant validity (57%)57% related to the paper, Test validity (55%)55% related to the paper
View PDF
842 Citations
Epidemiology of DSM-III-R Major Depression and Minor Depression Among Adolescents and Young Adults in the National Comorbidity Survey
Ronald C. Kessler1, Ellen E. Walters1
01 Jan 1998 - Depression and Anxiety

Abstract:

Data on the prevalences, comorbidities, and cohort effects of DSM-III-R major depression (MD) and minor depression (mD) are reported for the nationally representative sample of n = 1,769 adolescents and young adults who participated in the National Comorbidity Survey. Lifetime prevalences are 15.3% (MD) and 9.9% (mD), while 3... Data on the prevalences, comorbidities, and cohort effects of DSM-III-R major depression (MD) and minor depression (mD) are reported for the nationally representative sample of n = 1,769 adolescents and young adults who participated in the National Comorbidity Survey. Lifetime prevalences are 15.3% (MD) and 9.9% (mD), while 30-day prevalences are 5.8% (MD) and 2.1% (mD). Most cases reported recurrent episodes (73.9% of those with MD and 69.2% with mD) and significant role impairment, including attempted suicide among 21.9% of those with MD. The majority of lifetime cases (76.7% of those with MD and 69.3% with mD) reported other comorbid lifetime NCS/ DSM-III-R disorders. Depression was temporally secondary in the majority of these cases. Number of prior disorders was more important than type of disorders in predicting subsequent depression, raising the possibility that secondary depression is a nonspecific severity marker for earlier disorders. A cohort effect for both MD and mD was documented that persisted even for episodes lasting a year or longer. Increasing prevalences of prior comorbid disorders were found to play an important part in explaining the cohort effect for depression. read more read less

Topics:

Depression (differential diagnoses) (54%)54% related to the paper, National Comorbidity Survey (54%)54% related to the paper, Poison control (50%)50% related to the paper
821 Citations
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Frequently asked questions

1. Can I write Depression and Anxiety in LaTeX?

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

2. Do you follow the Depression and Anxiety guidelines?

Yes, the template is compliant with the Depression and Anxiety 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 Depression and Anxiety?

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 Depression and Anxiety citation style.

4. Can I use the Depression and Anxiety 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 Depression and Anxiety.

5. Can I use a manuscript in Depression and Anxiety 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 Depression and Anxiety that you can download at the end.

6. How long does it usually take you to format my papers in Depression and Anxiety?

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

7. Where can I find the template for the Depression and Anxiety?

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 Depression and Anxiety'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 Depression and Anxiety'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. Depression and Anxiety an online tool or is there a desktop version?

SciSpace's Depression and Anxiety 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 Depression and Anxiety?

Sure. You can request any template and we'll have it setup within a few days. You can find the request box in Journal Gallery on the right side bar under the heading, "Couldn't find the format you were looking for like Depression and Anxiety?”

11. What is the output that I would get after using Depression and Anxiety?

After writing your paper autoformatting in Depression and Anxiety, you can download it in multiple formats, viz., PDF, Docx, and LaTeX.

12. Is Depression and Anxiety'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 Depression and Anxiety?

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 Depression and Anxiety. 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 Depression and Anxiety?

The 5 most common citation types in order of usage for Depression and Anxiety 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 Depression and Anxiety?

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 Depression and Anxiety's guidelines and download the same in Word, PDF and LaTeX formats? Give us a try!.

16. Can I download Depression and Anxiety 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 Depression and Anxiety Endnote style according to Elsevier guidelines.

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