Example of Neuroscience and Behavioral Physiology format
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Example of Neuroscience and Behavioral Physiology format Example of Neuroscience and Behavioral Physiology format Example of Neuroscience and Behavioral Physiology format Example of Neuroscience and Behavioral Physiology format Example of Neuroscience and Behavioral Physiology format Example of Neuroscience and Behavioral Physiology format Example of Neuroscience and Behavioral Physiology format Example of Neuroscience and Behavioral Physiology format Example of Neuroscience and Behavioral Physiology format Example of Neuroscience and Behavioral Physiology format Example of Neuroscience and Behavioral Physiology format Example of Neuroscience and Behavioral Physiology format Example of Neuroscience and Behavioral Physiology format Example of Neuroscience and Behavioral Physiology format Example of Neuroscience and Behavioral Physiology format Example of Neuroscience and Behavioral Physiology format Example of Neuroscience and Behavioral Physiology format Example of Neuroscience and Behavioral Physiology format
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open access Open Access

Neuroscience and Behavioral Physiology — Template for authors

Publisher: Springer
Categories Rank Trend in last 3 yrs
Neuroscience (all) #108 of 110 down down by 1 rank
journal-quality-icon Journal quality:
Low
calendar-icon Last 4 years overview: 669 Published Papers | 236 Citations
indexed-in-icon Indexed in: Scopus
last-updated-icon Last updated: 20/06/2020
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Related Journals

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SJR: 1.187
SNIP: 1.192
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SJR: 0.866
SNIP: 1.035
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CiteRatio: 11.0
SJR: 4.127
SNIP: 2.005

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.

0.4

33% from 2019

CiteRatio for Neuroscience and Behavioral Physiology from 2016 - 2020
Year Value
2020 0.4
2019 0.3
2018 0.3
2017 0.3
2016 0.2
graph view Graph view
table view Table view

0.137

SJR for Neuroscience and Behavioral Physiology from 2016 - 2020
Year Value
2020 0.137
2019 0.137
2018 0.139
2017 0.133
2016 0.122
graph view Graph view
table view Table view

0.134

1% from 2019

SNIP for Neuroscience and Behavioral Physiology from 2016 - 2020
Year Value
2020 0.134
2019 0.135
2018 0.152
2017 0.14
2016 0.13
graph view Graph view
table view Table view

insights Insights

  • CiteRatio of this journal has increased by 33% in last years.
  • This journal’s CiteRatio is in the top 10 percentile category.

insights Insights

  • This journal’s SJR is in the top 10 percentile category.

insights Insights

  • SNIP of this journal has decreased by 1% in last years.
  • This journal’s SNIP is in the top 10 percentile category.

Neuroscience and Behavioral Physiology

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Springer

Neuroscience and Behavioral Physiology

Neuroscience and Behavioral Physiology contains translations of papers selected from top Russian journals describing significant results of studies on the nervous system. Priority is given to new experimental findings.Neuroscience and Behavioral Physiology publishes contributi...... Read More

Neuroscience

i
Last updated on
20 Jun 2020
i
ISSN
0097-0549
i
Impact Factor
Low - 0.123
i
Open Access
No
i
Sherpa RoMEO Archiving Policy
Green faq
i
Plagiarism Check
Available via Turnitin
i
Endnote Style
Download Available
i
Bibliography Name
SPBASIC
i
Citation Type
Author Year
(Blonder et al, 1982)
i
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: 10.1023/A:1021171129766
Influence of postweaning social isolation in the rat on brain development, conditioned behavior, and neurotransmission.
Maria Danet S. Lapiz1, A. Fulford2, S. Muchimapura1, Robert Mason1, T.L. Parker1, Charles A. Marsden1

Abstract:

There is substantial evidence that early life events influence brain development and subsequent adult behavior and play an important role in the causation of certain psychiatric disorders including schizophrenia and depression. The underlying mechanism of the effects of these early environmental factors is still not understoo... There is substantial evidence that early life events influence brain development and subsequent adult behavior and play an important role in the causation of certain psychiatric disorders including schizophrenia and depression. The underlying mechanism of the effects of these early environmental factors is still not understood. It is a challenge to attempt to model early environmental factors in animals to gain understanding of the basic mechanisms that underlie the long-term effects. This paper reviews the effects of rearing rats from weaning in social isolation and reports some recent results indicating hippocampal dysfunction. Isolation rearing in rats from weaning produces a range of persistent behavioral changes in the young adult, including hyperactivity in response to novelty and amphetamine and altered responses to conditioning. These are associated with alterations in the central aminergic neurotransmitter functions in the mesolimbic areas and other brain regions. Isolation-reared rats have enhanced presynaptic dopamine (DA) and 5-HT function in the nucleus accumbens (NAC) associated with decreased presynaptic 5-HT function in the frontal cortex and hippocampus. Isolation-reared rats have reduced presynaptic noradrenergic function in the hippocampus, but have enhanced presynaptic DA function in the amygdala. These neurochemical imbalances may contribute to the exaggerated response of the isolated rat to a novel stimulus or to stimuli predictive of danger, and isolation-induced behavioral changes. These changes have neuroanatomical correlates, changes which seem to parallel to a certain degree those seen in human schizophrenia. A greater understanding of the processes that underlie these changes should improve our knowledge of how environmental events may alter brain development and function, and play a role in the development of neuropsychiatric disorders. read more read less

Topics:

Neurochemical (52%)52% related to the paper, Amygdala (51%)51% related to the paper, Nucleus accumbens (51%)51% related to the paper, Amphetamine (50%)50% related to the paper
292 Citations
Journal Article DOI: 10.1023/B:NEAB.0000038139.39812.EB
Analysis of evoked EEG synchronization and desynchronization in conditions of emotional activation in humans: temporal and topographic characteristics.
L.I. Aftanas1, N.V. Reva, A. A. Varlamov, S.V. Pavlov, V P Makhnev

Abstract:

Studies in 20 healthy right-handed subjects analyzed evoked EEG synchronization and desynchronization in the delta, theta1, theta2, alpha1, alpha2, beta1, beta2, beta3, and gamma ranges in response to sequential presentation of stimuli from the International Affective Picture System (IAPS) with low, medium, and high emotional... Studies in 20 healthy right-handed subjects analyzed evoked EEG synchronization and desynchronization in the delta, theta1, theta2, alpha1, alpha2, beta1, beta2, beta3, and gamma ranges in response to sequential presentation of stimuli from the International Affective Picture System (IAPS) with low, medium, and high emotional activation impact Each signal presentation was accompanied by subjective scaling of the extent of its emotional impact EEG traces were recorded in 62 channels as signals were presented These experiments showed that the degree of emotional impact of the signal was significantly associated with increases in evoked synchronization in the delta, theta1, theta2, beta1, beta3, and gamma ranges and with the effects of combined changes in evoked synchronization and desynchronization in the alpha2 frequency range The interhemisphere distribution of evoked changes in power provided evidence that not only the posterior areas of the right hemisphere were involved in analyzing the emotional significance of images, as indicated by changes in evoked theta1 and theta2 synchronization and alpha2 desynchronization, but also the anterior areas of the left hemisphere, as indicated by changes in evoked theta2 synchronization From the standpoint of affective chronometry, the earliest discrimination of the emotional content of stimuli, regardless of the sign of the emotion, occurred in the lower theta range and was seen at 0-600 msec after the start of stimulus presentation This process was delayed 600-1000 msec in the theta2, alpha2, and gamma ranges read more read less

Topics:

International Affective Picture System (51%)51% related to the paper, Electroencephalography (51%)51% related to the paper
204 Citations
Journal Article DOI: 10.1007/S11055-008-0025-Z
Nestin in central nervous system cells.
A. V. Gilyarov1

Abstract:

This literature review reflects current knowledge on the intermediate filament protein nestin, which most authors regard as a marker of "neural stem/progenitor cells." The structural-functional characteristics of nestin and its presence in various central nervous system cells at different stages of ontogenesis in normal and p... This literature review reflects current knowledge on the intermediate filament protein nestin, which most authors regard as a marker of "neural stem/progenitor cells." The structural-functional characteristics of nestin and its presence in various central nervous system cells at different stages of ontogenesis in normal and pathological conditions are discussed. read more read less

Topics:

Nestin (72%)72% related to the paper, Neurosphere (59%)59% related to the paper, Progenitor cell (52%)52% related to the paper
189 Citations
Journal Article DOI: 10.1007/BF01182672
Absolute number of neurons and thickness of the cerebral cortex during aging, senile and vascular dementia, and Pick's and Alzheimer's diseases.
Shefer Vf1

Abstract:

The absolute number of neurons and thickness of the cortex were studied in areas 6, 10, 18, 21, 21/38 and 40 and in the subiculum of mentally healthy persons of different ages and in patients with senile and vascular dementia or with Pick's or Alzheimer's disease. In old age the mean absolute number of neurons in mentally hea... The absolute number of neurons and thickness of the cortex were studied in areas 6, 10, 18, 21, 21/38 and 40 and in the subiculum of mentally healthy persons of different ages and in patients with senile and vascular dementia or with Pick's or Alzheimer's disease. In old age the mean absolute number of neurons in mentally healthy persons is reduced by 20%, while the thickness of the cortex on the free surface of the gyri remains unchanged. In persons with senile and vascular dementia the number of nerve cells is reduced by 35–38%, but there is no decrease in the thickness of the cortex on its free surface. In Alzheimer's disease the number of nerve cells is reduced by half and the thickness of the cortex by 6%. Pick's disease is characterized by mass death of nerve cells in the affected areas, leading to a reduction of 14–30 in their number, and to a decrease in thickness of the cortex by half. The subicular cortex thickness in old age is reduced by 28% and in diseases leading to dementia by 47–71%. read more read less

Topics:

Cortex (anatomy) (59%)59% related to the paper, Vascular dementia (54%)54% related to the paper, Cerebral cortex (54%)54% related to the paper, Dementia (52%)52% related to the paper, Subiculum (52%)52% related to the paper
124 Citations
Journal Article DOI: 10.1007/S11055-008-9077-3
Efficacy and safety of galantamine (reminyl) for dementia in patients with Parkinson's disease (an open controlled trial).
I. V. Litvinenko1, Odinak Mm1, V. I. Mogil’naya1, A. Yu. Emelin1

Abstract:

An open controlled trial of the use of galantamine at a maximum dose of 16 mg/day included 41 patients with Parkinson's disease with dementia randomized to a galantamine treatment group (21 patients) and a control group (20 patients). Cognitive, neuropsychiatric, and motor symptoms were assessed clinically before the trial an... An open controlled trial of the use of galantamine at a maximum dose of 16 mg/day included 41 patients with Parkinson's disease with dementia randomized to a galantamine treatment group (21 patients) and a control group (20 patients). Cognitive, neuropsychiatric, and motor symptoms were assessed clinically before the trial and at 4, 12, and 24 weeks, using the Mini Mental State Examination (MMSE), the cognitive Alzheimer's Disease Assessment Scale (ADAS-cog), the clock drawing test, the Frontal Assessment Battery (FAB), and the Neuropsychiatric Inventory (NPI) with assessment of distress in relatives. Patients treated with galantamine had better scores on the MMSE (p < 0.05),ADAS-cog (p < 0.05), the clock drawing test (p < 0.05), and the FAB (p < 0.01) at the end of the study period as compared with the control group. Changes in total point scores on the NPI-12 at the ends of weeks 12 and 24, as compared with the beginning of the trial, were in favor of the group treated with galantamine, with significant changes in the hallucinations (p = 0.0002), anxiety (p = 0.04), sleep disturbance (p = 0.04), and apathy (p = 0.006) sections. Galantamine treatment was accompanied by decreases in the level of distress in patients' relatives (p = 0.007) and improvements in daily activity (p = 0.003). Improvements in gait and decreases in freezing and falls were seen in the galantamine treatment group. However, two patients of this group showed minor increases in tremor. Side effects (drooling, postural hypotension, nausea, dysuria) occurred in seven patients (30%). read more read less

Topics:

Galantamine (56%)56% related to the paper, Mini–Mental State Examination (50%)50% related to the paper
117 Citations
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Neuroscience and Behavioral Physiology format uses SPBASIC citation style.

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Frequently asked questions

1. Can I write Neuroscience and Behavioral Physiology in LaTeX?

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

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Yes, the template is compliant with the Neuroscience and Behavioral Physiology 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 Neuroscience and Behavioral Physiology?

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 Neuroscience and Behavioral Physiology citation style.

4. Can I use the Neuroscience and Behavioral Physiology 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 Neuroscience and Behavioral Physiology.

5. Can I use a manuscript in Neuroscience and Behavioral Physiology 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 Neuroscience and Behavioral Physiology that you can download at the end.

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

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

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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 Neuroscience and Behavioral Physiology 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 Neuroscience and Behavioral Physiology, you can download it in multiple formats, viz., PDF, Docx, and LaTeX.

12. Is Neuroscience and Behavioral Physiology'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 Neuroscience and Behavioral Physiology?

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 Neuroscience and Behavioral Physiology. 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 Neuroscience and Behavioral Physiology?

The 5 most common citation types in order of usage for Neuroscience and Behavioral Physiology 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 Neuroscience and Behavioral Physiology?

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16. Can I download Neuroscience and Behavioral Physiology 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 Neuroscience and Behavioral Physiology Endnote style according to Elsevier guidelines.

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