Example of Journal of Molecular Neuroscience format
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Example of Journal of Molecular Neuroscience format Example of Journal of Molecular Neuroscience format Example of Journal of Molecular Neuroscience format Example of Journal of Molecular Neuroscience format Example of Journal of Molecular Neuroscience format Example of Journal of Molecular Neuroscience format Example of Journal of Molecular Neuroscience format Example of Journal of Molecular Neuroscience format Example of Journal of Molecular Neuroscience format Example of Journal of Molecular Neuroscience format Example of Journal of Molecular Neuroscience format Example of Journal of Molecular Neuroscience format Example of Journal of Molecular Neuroscience format Example of Journal of Molecular Neuroscience format Example of Journal of Molecular Neuroscience format Example of Journal of Molecular Neuroscience format Example of Journal of Molecular Neuroscience format Example of Journal of Molecular Neuroscience format
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Example of Journal of Molecular Neuroscience format Example of Journal of Molecular Neuroscience format Example of Journal of Molecular Neuroscience format Example of Journal of Molecular Neuroscience format Example of Journal of Molecular Neuroscience format Example of Journal of Molecular Neuroscience format Example of Journal of Molecular Neuroscience format Example of Journal of Molecular Neuroscience format Example of Journal of Molecular Neuroscience format Example of Journal of Molecular Neuroscience format Example of Journal of Molecular Neuroscience format Example of Journal of Molecular Neuroscience format Example of Journal of Molecular Neuroscience format Example of Journal of Molecular Neuroscience format Example of Journal of Molecular Neuroscience format Example of Journal of Molecular Neuroscience format Example of Journal of Molecular Neuroscience format Example of Journal of Molecular Neuroscience format
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open access Open Access

Journal of Molecular Neuroscience — Template for authors

Publisher: Springer
Categories Rank Trend in last 3 yrs
Cellular and Molecular Neuroscience #61 of 88 down down by 9 ranks
journal-quality-icon Journal quality:
Medium
calendar-icon Last 4 years overview: 718 Published Papers | 3308 Citations
indexed-in-icon Indexed in: Scopus
last-updated-icon Last updated: 11/07/2020
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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.

2.678

4% from 2018

Impact factor for Journal of Molecular Neuroscience from 2016 - 2019
Year Value
2019 2.678
2018 2.577
2017 2.454
2016 2.229
graph view Graph view
table view Table view

4.6

2% from 2019

CiteRatio for Journal of Molecular Neuroscience from 2016 - 2020
Year Value
2020 4.6
2019 4.5
2018 4.6
2017 4.8
2016 4.6
graph view Graph view
table view Table view

insights Insights

  • Impact factor of this journal has increased by 4% 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.

0.936

9% from 2019

SJR for Journal of Molecular Neuroscience from 2016 - 2020
Year Value
2020 0.936
2019 0.861
2018 0.933
2017 0.974
2016 0.951
graph view Graph view
table view Table view

0.755

7% from 2019

SNIP for Journal of Molecular Neuroscience from 2016 - 2020
Year Value
2020 0.755
2019 0.704
2018 0.693
2017 0.672
2016 0.647
graph view Graph view
table view Table view

insights Insights

  • SJR of this journal has increased by 9% in last years.
  • This journal’s SJR is in the top 10 percentile category.

insights Insights

  • SNIP of this journal has increased by 7% in last years.
  • This journal’s SNIP is in the top 10 percentile category.

Journal of Molecular Neuroscience

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Springer

Journal of Molecular Neuroscience

The Journal of Molecular Neuroscience is committed to the rapid publication of original findings that increase our understanding of the molecular structure, function, and development of the nervous system. The criteria for acceptance of manuscripts will be scientific excellenc...... Read More

Medicine

i
Last updated on
11 Jul 2020
i
ISSN
0895-8696
i
Impact Factor
High - 2.229
i
Acceptance Rate
Not provided
i
Frequency
Not provided
i
Open Access
Yes
i
Sherpa RoMEO Archiving Policy
Green faq
i
Plagiarism Check
Available via Turnitin
i
Endnote Style
Download Available
i
Bibliography Name
SPBASIC
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Citation Type
Author Year
(Blonder et al, 1982)
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Bibliography Example
Beenakker CWJ (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

Journal Article DOI: 10.1007/S12031-007-0029-0
Diffusion Tensor Imaging (DTI)-based White Matter Mapping in Brain Research: A Review
Yaniv Assaf1, Ofer Pasternak1

Abstract:

Diffusion tensor imaging (DTI) has become one of the most popular MRI techniques in brain research, as well as in clinical practice. The number of brain studies with DTI is growing steadily and, over the last decade, has produced more than 700 publications. Diffusion tensor imaging enables visualization and characterization o... Diffusion tensor imaging (DTI) has become one of the most popular MRI techniques in brain research, as well as in clinical practice. The number of brain studies with DTI is growing steadily and, over the last decade, has produced more than 700 publications. Diffusion tensor imaging enables visualization and characterization of white matter fascicli in two and three dimensions. Since the introduction of this methodology in 1994, it has been used to study the white matter architecture and integrity of the normal and diseased brains (multiple sclerosis, stroke, aging, dementia, schizophrenia, etc.). Although it provided image contrast that was not available with routine MR techniques, unique information on white matter and 3D visualization of neuronal pathways, many questions were raised regarding the origin of the DTI signal. Diffusion tensor imaging is constantly validated, challenged, and developed in terms of acquisition scheme, image processing, analysis, and interpretation. While DTI offers a powerful tool to study and visualize white matter, it suffers from inherent artifacts and limitations. The partial volume effect and the inability of the model to cope with non-Gaussian diffusion are its two main drawbacks. Nevertheless, when combined with functional brain mapping, DTI provides an efficient tool for comprehensive, noninvasive, functional anatomy mapping of the human brain. This review summarizes the development of DTI in the last decade with respect to the specificity and utility of the technique in radiology and anatomy studies. read more read less

Topics:

Diffusion MRI (60%)60% related to the paper, Tractography (59%)59% related to the paper, Neural tract (54%)54% related to the paper
View PDF
1,315 Citations
Patent DOI: 10.1385/JMN:14:3:175
Molecular functionalization of carbon nanotubes and use as substrates for neuronal growth
Mark P. Mattson1, Mark P. Mattson2, Robert C. Haddon2, Apparao M. Rao2

Abstract:

A cell and substrate system and nerve regeneration implant are disclosed including a carbon nanotube and a neuron growing on the carbon nanotube. Both unfunctionalized carbon nanotubes and carbon nanotubes functionalized with a neuronal growth promoting agent may be utilized in the invention. A method is also disclosed for pr... A cell and substrate system and nerve regeneration implant are disclosed including a carbon nanotube and a neuron growing on the carbon nanotube. Both unfunctionalized carbon nanotubes and carbon nanotubes functionalized with a neuronal growth promoting agent may be utilized in the invention. A method is also disclosed for promoting neuronal growth. read more read less

Topics:

Carbon nanotube (58%)58% related to the paper
View PDF
674 Citations
Journal Article DOI: 10.1385/JMN:17:2:101
Pathologic correlates of nondemented aging, mild cognitive impairment, and early-stage Alzheimer's disease.
John C. Morris1, Joseph L. Price1

Abstract:

The results of studies from the Washington University Alzheimer Disease (AD) Research Center and those from other centers and investigators regarding the neuropathologic correlates of normal aging and early-stage AD are reviewed. We conclude that widespread amyloid plaques in the neocortex best distinguishes very early stage ... The results of studies from the Washington University Alzheimer Disease (AD) Research Center and those from other centers and investigators regarding the neuropathologic correlates of normal aging and early-stage AD are reviewed. We conclude that widespread amyloid plaques in the neocortex best distinguishes very early stage AD, including “MCI” stage, and preclinical stages, from healthy brain aging. Other AD lesions, including increased formation of neurofibrillary tangles and neuronal degeneration appear to result from the amyloid-initiated pathologic process, although they may have a more immediate effect on expression and severity of dementia. These data provide strong support for anti-amyloid intervention as a preventive therapy for AD. It is now critical to develop methods to detect preclinical AD during life. read more read less

Topics:

Alzheimer's disease (57%)57% related to the paper, Dementia (56%)56% related to the paper
498 Citations
Journal Article DOI: 10.1385/JMN:28:1:65
Neuroactive steroids: A therapeutic approach to maintain peripheral nerve integrity during neurodegenerative events.

Abstract:

It is now well known that peripheral nerves are a target for the action of neuroactive steroids. This review summarizes observations obtained so far, indicating that through the interaction with classical and nonclassical steroid receptors, neuroactive steroids (e.g., progesterone, testosterone and their derivatives, estrogen... It is now well known that peripheral nerves are a target for the action of neuroactive steroids. This review summarizes observations obtained so far, indicating that through the interaction with classical and nonclassical steroid receptors, neuroactive steroids (e.g., progesterone, testosterone and their derivatives, estrogens, etc.) are able to influence several parameters of the peripheral nervous system, particularly its glial compartment (i.e., Schwann cells). Interestingly, some of these neuroactive steroids might be considered as promising neuroprotective agents. They are able to counteract neurodegenerative events of rat peripheral nerves occurring after experimental physical trauma, during the aging process, or in hereditary demyelinating diseases. On this basis, the hypothesis that neuroactive steroids might represent a new therapeutic strategy for peripheral neuropathy is proposed. read more read less

Topics:

Neuroactive steroid (61%)61% related to the paper
466 Citations
Journal Article DOI: 10.1385/JMN:18:1-2:07
Interactions of glucagon-like peptide-1 (GLP-1) with the blood-brain barrier.
Abba J. Kastin1, Victoria Akerstrom2, Weihong Pan2

Abstract:

Glucagon-like peptide-1 (GLP-1) reduces insulin requirement in diabetes mellitus and promotes satiety. GLP-1 in the periphery (outside the CNS) has been shown to act on the brain to reduce food ingestion. As GLP-1 is readily degraded in blood, we focused on the interactions of [Ser 8 ]GLP-1, an analog with similar biological ... Glucagon-like peptide-1 (GLP-1) reduces insulin requirement in diabetes mellitus and promotes satiety. GLP-1 in the periphery (outside the CNS) has been shown to act on the brain to reduce food ingestion. As GLP-1 is readily degraded in blood, we focused on the interactions of [Ser 8 ]GLP-1, an analog with similar biological effects and greater stability, with the blood-brain barrier (BBB). The influx of radiolabeled [Ser 8 ]GLP-1 into brain has several distinctive characteristics: 1. A rapid influx rate of 8.867 ± 0.798 × 10 4 mL/g-min as measured by multiple-time regression analysis after iv injection in mice. 2. Lack of self-inhibition by excess doses of the unlabeled [Ser 8 ]GLP-1 either iv or by in situ brain perfusion, indicating the absence of a saturable transport system at the BBB. 3. Lack of modulation by short-term fasting and some other ingestive peptides that may interact with GLP-1, including leptin, glucagon, insulin, neuropeptide Y, and melanin-concentrating hormone. 4. No inhibition of influx by the selective GLP-1 receptor antagonist exendin(9–39), suggesting that the GLP-1 receptor is not involved in the rapid entry into brain. Similarly, there was no efflux system for [Ser 8 ]GLP-1 to exit the brain other than following the reabsorption of cerebrospinal fluid (CSF). The fast influx was not associated with high lipid solubility. Upon reaching the brain compartment, substantial amounts of [Ser 8 ]GLP-1 entered the brain parenchyma, but a large proportion was loosely associated with the vasculature at the BBB. Finally, the influx rate of [Ser 8 ]GLP-1 was compared with that of GLP-1 in a blood-free brain perfusion system; radiolabeled GLP-1 had a more rapid influx than its analog and neither peptide showed the self-inhibition indicative of a saturable transport system. Therefore, we conclude that [Ser 8 ]GLP-1 and the endogenous peptide GLP-1 can gain access to the brain from the periphery by simple diffusion and thus contribute to the regulation of feeding. read more read less

Topics:

Glucagon (55%)55% related to the paper, Blood–brain barrier (53%)53% related to the paper, Glucagon-like peptide-1 (51%)51% related to the paper
440 Citations
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Journal of Molecular Neuroscience format uses SPBASIC citation style.

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Frequently asked questions

1. Can I write Journal of Molecular Neuroscience in LaTeX?

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

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

3. Can I cite my article in multiple styles in Journal of Molecular Neuroscience?

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

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

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

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

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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.

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SciSpace's Journal of Molecular Neuroscience 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.

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

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

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

13. What is Sherpa RoMEO Archiving Policy for Journal of Molecular Neuroscience?

SHERPA/RoMEO Database

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

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

14. What are the most common citation types In Journal of Molecular Neuroscience?

The 5 most common citation types in order of usage for Journal of Molecular Neuroscience are:.

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

15. How do I submit my article to the Journal of Molecular Neuroscience?

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

16. Can I download Journal of Molecular Neuroscience in Endnote format?

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

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