Example of Frontline Gastroenterology format
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Example of Frontline Gastroenterology format Example of Frontline Gastroenterology format Example of Frontline Gastroenterology format Example of Frontline Gastroenterology format Example of Frontline Gastroenterology format Example of Frontline Gastroenterology format Example of Frontline Gastroenterology format Example of Frontline Gastroenterology format Example of Frontline Gastroenterology format
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Example of Frontline Gastroenterology format Example of Frontline Gastroenterology format Example of Frontline Gastroenterology format Example of Frontline Gastroenterology format Example of Frontline Gastroenterology format Example of Frontline Gastroenterology format Example of Frontline Gastroenterology format Example of Frontline Gastroenterology format Example of Frontline Gastroenterology format
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open access Open Access

Frontline Gastroenterology — Template for authors

Categories Rank Trend in last 3 yrs
Gastroenterology #76 of 136 up up by 11 ranks
Hepatology #40 of 62 up up by 3 ranks
journal-quality-icon Journal quality:
Medium
calendar-icon Last 4 years overview: 180 Published Papers | 573 Citations
indexed-in-icon Indexed in: Scopus
last-updated-icon Last updated: 22/07/2020
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Related Journals

open access Open Access
recommended Recommended

Elsevier

Quality:  
High
CiteRatio: 9.9
SJR: 2.634
SNIP: 2.121
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Hindawi

Quality:  
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CiteRatio: 3.0
SJR: 0.622
SNIP: 0.823
open access Open Access

SAGE

Quality:  
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CiteRatio: 6.2
SJR: 1.667
SNIP: 1.516
open access Open Access

Springer

Quality:  
High
CiteRatio: 6.1
SJR: 1.203
SNIP: 1.387

Journal Performance & Insights

CiteRatio

SCImago Journal Rank (SJR)

Source Normalized Impact per Paper (SNIP)

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

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.

3.2

23% from 2019

CiteRatio for Frontline Gastroenterology from 2016 - 2020
Year Value
2020 3.2
2019 2.6
2018 2.0
2017 1.7
2016 3.8
graph view Graph view
table view Table view

0.919

40% from 2019

SJR for Frontline Gastroenterology from 2016 - 2020
Year Value
2020 0.919
2019 0.655
2018 0.507
2017 0.39
2016 0.803
graph view Graph view
table view Table view

0.798

13% from 2019

SNIP for Frontline Gastroenterology from 2016 - 2020
Year Value
2020 0.798
2019 0.707
2018 0.426
2017 0.316
2016 0.858
graph view Graph view
table view Table view

insights Insights

  • CiteRatio of this journal has increased by 23% in last years.
  • This journal’s CiteRatio is in the top 10 percentile category.

insights Insights

  • SJR of this journal has increased by 40% in last years.
  • This journal’s SJR is in the top 10 percentile category.

insights Insights

  • SNIP of this journal has increased by 13% in last years.
  • This journal’s SNIP is in the top 10 percentile category.
Frontline Gastroenterology

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BMJ Publishing Group

Frontline Gastroenterology

Frontline Gastroenterology aims to accelerate the adoption of best practice in the fields of gastroenterology and hepatology. It is multidisciplinary and focuses on the needs of patients and the professionals caring for them. The principal criterion for publication is potentia...... Read More

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Last updated on
21 Jul 2020
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ISSN
2041-4137
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Acceptance Rate
55%
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Open Access
Yes
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Sherpa RoMEO Archiving Policy
Green faq
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Plagiarism Check
Available via Turnitin
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Endnote Style
Download Available
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Bibliography Name
unsrt
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Citation Type
Numbered
[25]
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Bibliography Example
C. W. J. Beenakker. Specular andreev reflection in graphene. Phys. Rev. Lett., 97(6):067007, 2006.

Top papers written in this journal

open accessOpen access Journal Article DOI: 10.1136/FLGASTRO-2013-100329
The molecular genetics of colorectal cancer
Iain Ewing1, Joanna J Hurley2, Eleni Josephides3, Andrew Millar1

Abstract:

Colorectal cancer is a common but heterogeneous disease, which arises through the accumulation of genetic mutations Knowledge of the molecular basis of colorectal cancer has advanced at a rapid pace in recent years, reflecting progress made in the field of genomic medicine Targeted therapies have come into mainstream use, and... Colorectal cancer is a common but heterogeneous disease, which arises through the accumulation of genetic mutations Knowledge of the molecular basis of colorectal cancer has advanced at a rapid pace in recent years, reflecting progress made in the field of genomic medicine Targeted therapies have come into mainstream use, and the exciting prospect of treatment regimens tailored to the mutation profile of individual tumours is beginning to emerge In order to understand the development and application of the next generation of colorectal cancer treatments, it is important that gastroenterologists have a working knowledge of the pathological mechanisms that drive the disease This review examines our current understanding of the molecular genetics of colorectal carcinogenesis read more read less
View PDF
708 Citations
open accessOpen access Journal Article DOI: 10.1136/FLGASTRO-2013-100403
Non-alcoholic fatty liver disease: a practical approach to diagnosis and staging
Jessica K Dyson1, Quentin M. Anstee1, Stuart McPherson1

Abstract:

Non-alcoholic fatty liver disease (NAFLD) is now the commonest cause of abnormal liver function tests (LFTs) in the UK with approximately a third of the population being affected. The exact prevalence is not known, but population studies from the USA and China using magnetic resonance spectroscopy estimate that approximately ... Non-alcoholic fatty liver disease (NAFLD) is now the commonest cause of abnormal liver function tests (LFTs) in the UK with approximately a third of the population being affected. The exact prevalence is not known, but population studies from the USA and China using magnetic resonance spectroscopy estimate that approximately 30% of the general population have steatosis. It is a spectrum of disease ranging from simple steatosis, to non-alcoholic steatohepatitis (NASH), through to advanced fibrosis and cirrhosis. The majority have simple steatosis, but approximately 10–30% develop NASH and the development of NASH cirrhosis is associated with a poor long-term prognosis. Patients with NASH have increased liver-related and cardiovascular mortality. Many patients with NAFLD remain undiagnosed, and recognising those at risk is the first step. Clinicians overly rely on abnormal liver enzymes to identify patients with NAFLD, so patients with significant liver disease can be overlooked, potentially missing opportunities for intervention. Although liver biopsy is the gold standard method for diagnosing and staging NAFLD, the majority of patients can be effectively diagnosed non-invasively with tests that are routinely available in the clinic today. This review discusses a pragmatic approach to diagnosis and staging of NAFLD so that patients at the highest risk of liver-related complications can be identified. read more read less

Topics:

Fatty liver (61%)61% related to the paper, Steatohepatitis (60%)60% related to the paper, Liver disease (59%)59% related to the paper, Liver biopsy (56%)56% related to the paper, Abnormal Liver Function Test (55%)55% related to the paper
View PDF
255 Citations
open accessOpen access Journal Article DOI: 10.1136/FLGASTRO-2013-100361
Hepatitis B in pregnancy

Abstract:

Objective Vertical transmission of the hepatitis B virus (HBV) is the commonest mode of infection and can be prevented with immunoprophylaxis of the infant and antiviral therapy in the mother. Our aim was to review a cohort of subjects with HBV in pregnancy to determine the prevalence of active disease or high HBV-DNA levels ... Objective Vertical transmission of the hepatitis B virus (HBV) is the commonest mode of infection and can be prevented with immunoprophylaxis of the infant and antiviral therapy in the mother. Our aim was to review a cohort of subjects with HBV in pregnancy to determine the prevalence of active disease or high HBV-DNA levels that required treatment to prevent transmission, and to review the management of mothers and infants. Methods A retrospective case-note review was conducted of all the HBV-infected pregnant women and their infants who attended the Newcastle obstetric services from 2007 to 2011. Results There were 113 pregnancies in 81 women (median age 28 years; 15% hepatitis B e antigen (HBeAg) positive) during 2007–11. 71% of mothers were first diagnosed with HBV during pregnancy. The mothers were born in 28 different countries. 69% of mothers had an HBV-DNA level less than 2000 IU/mL and 13% had HBV-DNA levels greater than 1.0×10 7 IU/mL so would be eligible for antiviral therapy to prevent transmission to the infant. 9% had active eAg-positive HBV and 3% had active eAg-negative HBV requiring treatment. All infants born to HBeAg-positive mothers received hepatitis B immunoglobulin (HBIG) appropriately and 76% of infants received a full HBV vaccination course. One infant born to an HBeAg-negative mother was hepatitis B surface antigen positive 1 year post-delivery. Conclusions One in six women had active HBV requiring treatment or high HBV-DNA levels that would benefit from antiviral treatment to reduce the transmission risk. HBIG was administered appropriately but completion of the vaccination course was suboptimal. read more read less

Topics:

Hepatitis B virus (60%)60% related to the paper, Hepatitis B (57%)57% related to the paper, HBeAg (55%)55% related to the paper, Pregnancy (50%)50% related to the paper
View PDF
114 Citations
open accessOpen access Journal Article DOI: 10.1136/FLGASTRO-2013-100404
Non-alcoholic fatty liver disease: a practical approach to treatment
Jessica K Dyson1, Quentin M. Anstee1, Stuart McPherson1

Abstract:

Non-alcoholic fatty liver disease (NAFLD) affects up to a third of the population in many developed countries. Between 10% and 30% of patients with NAFLD have non-alcoholic steatohepatitis (NASH) that can progress to cirrhosis. There are metabolic risk factors common to both NAFLD and cardiovascular disease, so patients with ... Non-alcoholic fatty liver disease (NAFLD) affects up to a third of the population in many developed countries. Between 10% and 30% of patients with NAFLD have non-alcoholic steatohepatitis (NASH) that can progress to cirrhosis. There are metabolic risk factors common to both NAFLD and cardiovascular disease, so patients with NASH have an increased risk of liver-related and cardiovascular death. Management of patients with NAFLD depends largely on the stage of disease, emphasising the importance of careful risk stratification. There are four main areas to focus on when thinking about management strategies in NAFLD: lifestyle modification, targeting the components of the metabolic syndrome, liver-directed pharmacotherapy for high risk patients and managing the complications of cirrhosis. read more read less

Topics:

Steatohepatitis (58%)58% related to the paper, Fatty liver (55%)55% related to the paper, Chronic liver disease (54%)54% related to the paper, Metabolic syndrome (52%)52% related to the paper, Population (51%)51% related to the paper
View PDF
91 Citations
open accessOpen access Journal Article DOI: 10.1136/FLGASTRO-2014-100432
Non-alcoholic fatty liver disease is associated with higher levels of objectively measured sedentary behaviour and lower levels of physical activity than matched healthy controls

Abstract:

Background and aims Physical activity is a key determinant of metabolic control and is recommended for people with non-alcoholic fatty liver disease (NAFLD), usually alongside weight loss and dietary change. To date, no studies have reported the relationship between objectively measured sedentary behaviour and physical activi... Background and aims Physical activity is a key determinant of metabolic control and is recommended for people with non-alcoholic fatty liver disease (NAFLD), usually alongside weight loss and dietary change. To date, no studies have reported the relationship between objectively measured sedentary behaviour and physical activity, liver fat and metabolic control in people with NAFLD, limiting the potential to target sedentary behaviour in clinical practice. This study determined the level of sedentary behaviour and physical activity in people with NAFLD, and investigated links between physical activity, liver fat and glucose control. Methods Sedentary behaviour, physical activity and energy expenditure were assessed in 37 adults with NAFLD using a validated multisensor array over 7 days. Liver fat and glucose control were assessed, respectively, by 1 H-MRS and fasting blood samples. Patterns of sedentary behaviour were assessed by power law analyses of the lengths of sedentary bouts fitted from raw sedentary data. An age and sex-matched healthy control group wore the activity monitor for the same time period. Results People with NAFLD spent approximately half an hour extra a day being sedentary (1318±68 vs1289±60 mins/day; p<0.05) and walked 18% fewer steps (8483±2926 vs 10377±3529 steps/ day; p<0.01). As a consequence, active energy expenditure was reduced by 40% (432±258 vs 732±345 kcal/day; p<0.01) and total energy expenditure was lower in NAFLD (2690±440 vs 2901±511 kcal/day; p<0.01). Power law analyses of the lengths of sedentary bouts demonstrated that patients with NAFLD also have a lower number of transitions from being sedentary to active compared with controls (13±0.03 vs15 ±0.03%; p<0.05). Conclusions People with NAFLD spend more time sedentary and undertake less physical activity on a daily basis than healthy controls. High levels of sedentary behaviour and low levels of physical activity represent a therapeutic target that may prevent progression of metabolic conditions and weight gain in people with NAFLD and should be considered in clinical care. read more read less

Topics:

Weight gain (51%)51% related to the paper
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88 Citations
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Frontline Gastroenterology format uses unsrt citation style.

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Frequently asked questions

1. Can I write Frontline Gastroenterology in LaTeX?

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

2. Do you follow the Frontline Gastroenterology guidelines?

Yes, the template is compliant with the Frontline Gastroenterology 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 Frontline Gastroenterology?

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 Frontline Gastroenterology citation style.

4. Can I use the Frontline Gastroenterology 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 Frontline Gastroenterology.

5. Can I use a manuscript in Frontline Gastroenterology 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 Frontline Gastroenterology that you can download at the end.

6. How long does it usually take you to format my papers in Frontline Gastroenterology?

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

7. Where can I find the template for the Frontline Gastroenterology?

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 Frontline Gastroenterology'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 Frontline Gastroenterology'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. Frontline Gastroenterology an online tool or is there a desktop version?

SciSpace's Frontline Gastroenterology 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 Frontline Gastroenterology?

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 Frontline Gastroenterology?”

11. What is the output that I would get after using Frontline Gastroenterology?

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

12. Is Frontline Gastroenterology'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 Frontline Gastroenterology?

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 Frontline Gastroenterology. 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 Frontline Gastroenterology?

The 5 most common citation types in order of usage for Frontline Gastroenterology 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 Frontline Gastroenterology?

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

16. Can I download Frontline Gastroenterology 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 Frontline Gastroenterology Endnote style according to Elsevier guidelines.

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