Example of Neural Development format
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Example of Neural Development format Example of Neural Development format Example of Neural Development format Example of Neural Development format Example of Neural Development format Example of Neural Development format Example of Neural Development format Example of Neural Development format Example of Neural Development format Example of Neural Development format Example of Neural Development format Example of Neural Development format Example of Neural Development format Example of Neural Development format Example of Neural Development format Example of Neural Development format Example of Neural Development format Example of Neural Development format
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Example of Neural Development format Example of Neural Development format Example of Neural Development format Example of Neural Development format Example of Neural Development format Example of Neural Development format Example of Neural Development format Example of Neural Development format Example of Neural Development format Example of Neural Development format Example of Neural Development format Example of Neural Development format Example of Neural Development format Example of Neural Development format Example of Neural Development format Example of Neural Development format Example of Neural Development format Example of Neural Development format
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open access Open Access

Neural Development — Template for authors

Publisher: Springer
Categories Rank Trend in last 3 yrs
Developmental Neuroscience #13 of 35 up up by 4 ranks
journal-quality-icon Journal quality:
Good
calendar-icon Last 4 years overview: 71 Published Papers | 363 Citations
indexed-in-icon Indexed in: Scopus
last-updated-icon Last updated: 01/07/2020
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Related Journals

open access Open Access

Springer

Quality:  
High
CiteRatio: 6.8
SJR: 1.582
SNIP: 1.194
open access Open Access
recommended Recommended

Springer

Quality:  
High
CiteRatio: 9.5
SJR: 2.638
SNIP: 1.916
open access Open Access
recommended Recommended

Elsevier

Quality:  
High
CiteRatio: 8.0
SJR: 1.779
SNIP: 1.181
open access Open Access
recommended Recommended

Wiley

Quality:  
High
CiteRatio: 7.8
SJR: 1.716
SNIP: 0.906

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.

2.63

14% from 2018

Impact factor for Neural Development from 2016 - 2019
Year Value
2019 2.63
2018 2.317
2017 2.13
2016 2.077
graph view Graph view
table view Table view

5.1

16% from 2019

CiteRatio for Neural Development from 2016 - 2020
Year Value
2020 5.1
2019 4.4
2018 3.8
2017 4.1
2016 5.2
graph view Graph view
table view Table view

insights Insights

  • Impact factor of this journal has increased by 14% in last year.
  • This journal’s impact factor is in the top 10 percentile category.

insights Insights

  • CiteRatio of this journal has increased by 16% 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.

1.899

13% from 2019

SJR for Neural Development from 2016 - 2020
Year Value
2020 1.899
2019 1.675
2018 1.819
2017 1.821
2016 1.698
graph view Graph view
table view Table view

0.96

19% from 2019

SNIP for Neural Development from 2016 - 2020
Year Value
2020 0.96
2019 0.807
2018 0.654
2017 0.704
2016 0.743
graph view Graph view
table view Table view

insights Insights

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

insights Insights

  • SNIP of this journal has increased by 19% in last years.
  • This journal’s SNIP is in the top 10 percentile category.

Neural Development

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Springer

Neural Development

Approved by publishing and review experts on SciSpace, this template is built as per for Neural Development formatting guidelines as mentioned in Springer author instructions. The current version was created on and has been used by 644 authors to write and format their manuscripts to this journal.

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Last updated on
01 Jul 2020
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ISSN
1606-8610
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Open Access
Yes
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Sherpa RoMEO Archiving Policy
White faq
i
Plagiarism Check
Available via Turnitin
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Endnote Style
Download Available
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Citation Type
Numbered
[25]
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Bibliography Example
Blonder, G.E., Tinkham, M., Klapwijk, T.M.: Transition from metallic to tunneling regimes in superconducting microconstrictions: Excess current, charge imbalance, and supercurrent conversion. Phys. Rev. B 25(7), 4515–4532 (1982)

Top papers written in this journal

open accessOpen access Journal Article DOI: 10.1186/1749-8104-3-5
Amplification of neural stem cell proliferation by intermediate progenitor cells in Drosophila brain development
Bruno Bello1, Natalya Izergina1, Emmanuel Caussinus1, Heinrich Reichert1
19 Feb 2008 - Neural Development

Abstract:

In the mammalian brain, neural stem cells divide asymmetrically and often amplify the number of progeny they generate via symmetrically dividing intermediate progenitors. Here we investigate whether specific neural stem cell-like neuroblasts in the brain of Drosophila might also amplify neuronal proliferation by generating sy... In the mammalian brain, neural stem cells divide asymmetrically and often amplify the number of progeny they generate via symmetrically dividing intermediate progenitors. Here we investigate whether specific neural stem cell-like neuroblasts in the brain of Drosophila might also amplify neuronal proliferation by generating symmetrically dividing intermediate progenitors. Cell lineage-tracing and genetic marker analysis show that remarkably large neuroblast lineages exist in the dorsomedial larval brain of Drosophila. These lineages are generated by brain neuroblasts that divide asymmetrically to self renew but, unlike other brain neuroblasts, do not segregate the differentiating cell fate determinant Prospero to their smaller daughter cells. These daughter cells continue to express neuroblast-specific molecular markers and divide repeatedly to produce neural progeny, demonstrating that they are proliferating intermediate progenitors. The proliferative divisions of these intermediate progenitors have novel cellular and molecular features; they are morphologically symmetrical, but molecularly asymmetrical in that key differentiating cell fate determinants are segregated into only one of the two daughter cells. Our findings provide cellular and molecular evidence for a new mode of neurogenesis in the larval brain of Drosophila that involves the amplification of neuroblast proliferation through intermediate progenitors. This type of neurogenesis bears remarkable similarities to neurogenesis in the mammalian brain, where neural stem cells as primary progenitors amplify the number of progeny they generate through generation of secondary progenitors. This suggests that key aspects of neural stem cell biology might be conserved in brain development of insects and mammals. read more read less

Topics:

Ganglion mother cell (67%)67% related to the paper, Neuroblast (64%)64% related to the paper, Neurogenesis (60%)60% related to the paper, Neural stem cell (59%)59% related to the paper, Neuroblast proliferation (59%)59% related to the paper
View PDF
348 Citations
open accessOpen access Journal Article DOI: 10.1186/1749-8104-8-3
Neurogenesis in zebrafish – from embryo to adult
Rebecca J. Schmidt1, Uwe Strähle1, Steffen Scholpp1
21 Feb 2013 - Neural Development

Abstract:

Neurogenesis in the developing central nervous system consists of the induction and proliferation of neural progenitor cells and their subsequent differentiation into mature neurons. External as well as internal cues orchestrate neurogenesis in a precise temporal and spatial way. In the last 20 years, the zebrafish has proven... Neurogenesis in the developing central nervous system consists of the induction and proliferation of neural progenitor cells and their subsequent differentiation into mature neurons. External as well as internal cues orchestrate neurogenesis in a precise temporal and spatial way. In the last 20 years, the zebrafish has proven to be an excellent model organism to study neurogenesis in the embryo. Recently, this vertebrate has also become a model for the investigation of adult neurogenesis and neural regeneration. Here, we summarize the contributions of zebrafish in neural development and adult neurogenesis. read more read less

Topics:

Neurogenesis (72%)72% related to the paper, Proneural genes (60%)60% related to the paper, Neural development (57%)57% related to the paper, Neural stem cell (55%)55% related to the paper, Zebrafish (54%)54% related to the paper
View PDF
267 Citations
open accessOpen access Journal Article DOI: 10.1186/1749-8104-1-2
Polarization and orientation of retinal ganglion cells in vivo
Flavio R. Zolessi1, Lucia Poggi1, Christopher J. Wilkinson1, Chi-Bin Chien2, William A. Harris1
13 Oct 2006 - Neural Development

Abstract:

In the absence of external cues, neurons in vitro polarize by using intrinsic mechanisms. For example, cultured hippocampal neurons extend arbitrarily oriented neurites and then one of these, usually the one nearest the centrosome, begins to grow more quickly than the others. This neurite becomes the axon as it accumulates mo... In the absence of external cues, neurons in vitro polarize by using intrinsic mechanisms. For example, cultured hippocampal neurons extend arbitrarily oriented neurites and then one of these, usually the one nearest the centrosome, begins to grow more quickly than the others. This neurite becomes the axon as it accumulates molecular components of the apical junctional complex. All the other neurites become dendrites. It is unclear, however, whether neurons in vivo, which differentiate within a polarized epithelium, break symmetry by using similar intrinsic mechanisms. To investigate this, we use four-dimensional microscopy of developing retinal ganglion cells (RGCs) in live zebrafish embryos. We find that the situation is indeed very different in vivo, where axons emerge directly from uniformly polarized cells in the absence of other neurites. In vivo, moreover, components of the apical complex do not localize to the emerging axon, nor does the centrosome predict the site of axon emergence. Mosaic analysis in four dimensions, using mutants in which neuroepithelial polarity is disrupted, indicates that extrinsic factors such as access to the basal lamina are critical for normal axon emergence from RGCs in vivo. read more read less

Topics:

Retinal ganglion (59%)59% related to the paper, Axon (59%)59% related to the paper, Neurite (56%)56% related to the paper, Apical complex (56%)56% related to the paper, Cell polarity (56%)56% related to the paper
View PDF
231 Citations
open accessOpen access Journal Article DOI: 10.1186/1749-8104-2-1
Regulation of spindle orientation and neural stem cell fate in the Drosophila optic lobe
Boris Egger1, Jason Q. Boone2, Naomi R Stevens1, Andrea H. Brand1, Chris Q. Doe2
05 Jan 2007 - Neural Development

Abstract:

The choice of a stem cell to divide symmetrically or asymmetrically has profound consequences for development and disease. Unregulated symmetric division promotes tumor formation, whereas inappropriate asymmetric division affects organ morphogenesis. Despite its importance, little is known about how spindle positioning is reg... The choice of a stem cell to divide symmetrically or asymmetrically has profound consequences for development and disease. Unregulated symmetric division promotes tumor formation, whereas inappropriate asymmetric division affects organ morphogenesis. Despite its importance, little is known about how spindle positioning is regulated. In some tissues cell fate appears to dictate the type of cell division, whereas in other tissues it is thought that stochastic variation in spindle position dictates subsequent sibling cell fate. Here we investigate the relationship between neural progenitor identity and spindle positioning in the Drosophila optic lobe. We use molecular markers and live imaging to show that there are two populations of progenitors in the optic lobe: symmetrically dividing neuroepithelial cells and asymmetrically dividing neuroblasts. We use genetically marked single cell clones to show that neuroepithelial cells give rise to neuroblasts. To determine if a change in spindle orientation can trigger a neuroepithelial to neuroblast transition, we force neuroepithelial cells to divide along their apical/basal axis by misexpressing Inscuteable. We find that this does not induce neuroblasts, nor does it promote premature neuronal differentiation. We show that symmetrically dividing neuroepithelial cells give rise to asymmetrically dividing neuroblasts in the optic lobe, and that regulation of spindle orientation and division symmetry is a consequence of cell type specification, rather than a mechanism for generating cell type diversity. read more read less

Topics:

Neuroblast (60%)60% related to the paper, Neuroepithelial cell (59%)59% related to the paper, Cell fate determination (53%)53% related to the paper, Cell division (52%)52% related to the paper, Neural stem cell (51%)51% related to the paper
View PDF
225 Citations
open accessOpen access Journal Article DOI: 10.1186/S13064-018-0104-Y
Astrocytes, neurons, synapses: a tripartite view on cortical circuit development.
Isabella Farhy-Tselnicker1, Nicola J. Allen1
01 May 2018 - Neural Development

Abstract:

In the mammalian cerebral cortex neurons are arranged in specific layers and form connections both within the cortex and with other brain regions, thus forming a complex mesh of specialized synaptic connections comprising distinct circuits. The correct establishment of these connections during development is crucial for the p... In the mammalian cerebral cortex neurons are arranged in specific layers and form connections both within the cortex and with other brain regions, thus forming a complex mesh of specialized synaptic connections comprising distinct circuits. The correct establishment of these connections during development is crucial for the proper function of the brain. Astrocytes, a major type of glial cell, are important regulators of synapse formation and function during development. While neurogenesis precedes astrogenesis in the cortex, neuronal synapses only begin to form after astrocytes have been generated, concurrent with neuronal branching and process elaboration. Here we provide a combined overview of the developmental processes of synapse and circuit formation in the rodent cortex, emphasizing the timeline of both neuronal and astrocytic development and maturation. We further discuss the role of astrocytes at the synapse, focusing on astrocyte-synapse contact and the role of synapse-related proteins in promoting formation of distinct cortical circuits. read more read less

Topics:

Synapse (55%)55% related to the paper, Cortex (anatomy) (55%)55% related to the paper, Neuron (53%)53% related to the paper, Cerebral cortex (52%)52% related to the paper, Neurogenesis (51%)51% related to the paper
View PDF
222 Citations
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Frequently asked questions

1. Can I write Neural Development in LaTeX?

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

2. Do you follow the Neural Development guidelines?

Yes, the template is compliant with the Neural Development 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 Neural Development?

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 Neural Development citation style.

4. Can I use the Neural Development 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 Neural Development.

5. Can I use a manuscript in Neural Development 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 Neural Development that you can download at the end.

6. How long does it usually take you to format my papers in Neural Development?

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

7. Where can I find the template for the Neural Development?

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 Neural Development'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 Neural Development'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. Neural Development an online tool or is there a desktop version?

SciSpace's Neural Development 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 Neural Development?

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 Neural Development?”

11. What is the output that I would get after using Neural Development?

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

12. Is Neural Development'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 Neural Development?

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 Neural Development. 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 Neural Development?

The 5 most common citation types in order of usage for Neural Development 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 Neural Development?

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

16. Can I download Neural Development 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 Neural Development Endnote style according to Elsevier guidelines.

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I spent hours with MS word for reformatting. It was frustrating - plain and simple. With SciSpace, I can draft my manuscripts and once it is finished I can just submit. In case, I have to submit to another journal it is really just a button click instead of an afternoon of reformatting.

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