Example of Chromosome Research format
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Example of Chromosome Research format Example of Chromosome Research format Example of Chromosome Research format Example of Chromosome Research format Example of Chromosome Research format Example of Chromosome Research format Example of Chromosome Research format Example of Chromosome Research format Example of Chromosome Research format Example of Chromosome Research format Example of Chromosome Research format Example of Chromosome Research format Example of Chromosome Research format Example of Chromosome Research format Example of Chromosome Research format Example of Chromosome Research format Example of Chromosome Research format Example of Chromosome Research format
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Example of Chromosome Research format Example of Chromosome Research format Example of Chromosome Research format Example of Chromosome Research format Example of Chromosome Research format Example of Chromosome Research format Example of Chromosome Research format Example of Chromosome Research format Example of Chromosome Research format Example of Chromosome Research format Example of Chromosome Research format Example of Chromosome Research format Example of Chromosome Research format Example of Chromosome Research format Example of Chromosome Research format Example of Chromosome Research format Example of Chromosome Research format Example of Chromosome Research format
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open access Open Access

Chromosome Research — Template for authors

Publisher: Springer
Categories Rank Trend in last 3 yrs
Genetics #76 of 325 up up by 35 ranks
journal-quality-icon Journal quality:
High
calendar-icon Last 4 years overview: 97 Published Papers | 638 Citations
indexed-in-icon Indexed in: Scopus
last-updated-icon Last updated: 05/06/2020
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CiteRatio: 11.0
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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.

3.413

56% from 2018

Impact factor for Chromosome Research from 2016 - 2019
Year Value
2019 3.413
2018 2.183
2017 2.909
2016 2.385
graph view Graph view
table view Table view

6.6

35% from 2019

CiteRatio for Chromosome Research from 2016 - 2020
Year Value
2020 6.6
2019 4.9
2018 6.0
2017 5.2
2016 4.7
graph view Graph view
table view Table view

insights Insights

  • Impact factor of this journal has increased by 56% in last year.
  • This journal’s impact factor is in the top 10 percentile category.

insights Insights

  • CiteRatio of this journal has increased by 35% 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.

2.08

27% from 2019

SJR for Chromosome Research from 2016 - 2020
Year Value
2020 2.08
2019 1.635
2018 1.666
2017 1.425
2016 1.303
graph view Graph view
table view Table view

1.084

40% from 2019

SNIP for Chromosome Research from 2016 - 2020
Year Value
2020 1.084
2019 0.776
2018 0.634
2017 0.692
2016 0.619
graph view Graph view
table view Table view

insights Insights

  • SJR of this journal has increased by 27% in last years.
  • This journal’s SJR is in the top 10 percentile category.

insights Insights

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

Chromosome Research

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Springer

Chromosome Research

Approved by publishing and review experts on SciSpace, this template is built as per for Chromosome Research formatting guidelines as mentioned in Springer author instructions. The current version was created on and has been used by 497 authors to write and format their manuscripts to this journal.

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Last updated on
05 Jun 2020
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ISSN
1573-6849
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Open Access
Hybrid
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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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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: 10.1023/A:1018445520117
A drying-down technique for the spreading of mammalian meiocytes from the male and female germline.
01 Feb 1997 - Chromosome Research

Abstract:

A.H.F.M. Peters (corresponding author), A.W. Plug, M.J. van Vugt and P. de Boer are at the Department of Genetics, Wageningen Institute of Animal Sciences, Wageningen Agricultural University, Dreijenlaan 2, NL-6703 HA Wageningen, The Netherlands. Tel: (‡ 31) 317 483147; Fax: (‡ 31) 317 483929; Email: Antoine.Peters@alg.vf.wau... A.H.F.M. Peters (corresponding author), A.W. Plug, M.J. van Vugt and P. de Boer are at the Department of Genetics, Wageningen Institute of Animal Sciences, Wageningen Agricultural University, Dreijenlaan 2, NL-6703 HA Wageningen, The Netherlands. Tel: (‡ 31) 317 483147; Fax: (‡ 31) 317 483929; Email: Antoine.Peters@alg.vf.wau.nl. A.W. Plug is now at the Department of Genetics, Yale University School of Medicine, New Haven, CT 06510, USA. read more read less
647 Citations
open accessOpen access Journal Article DOI: 10.1007/S10577-010-9177-0
The fractal globule as a model of chromatin architecture in the cell
Leonid A. Mirny1
28 Jan 2011 - Chromosome Research

Abstract:

The fractal globule is a compact polymer state that emerges during polymer condensation as a result of topological constraints which prevent one region of the chain from passing across another one. This long-lived intermediate state was introduced in 1988 (Grosberg et al. 1988) and has not been observed in experiments or simu... The fractal globule is a compact polymer state that emerges during polymer condensation as a result of topological constraints which prevent one region of the chain from passing across another one. This long-lived intermediate state was introduced in 1988 (Grosberg et al. 1988) and has not been observed in experiments or simulations until recently (Lieberman-Aiden et al. 2009). Recent characterization of human chromatin using a novel chromosome conformational capture technique brought the fractal globule into the spotlight as a structural model of human chromosome on the scale of up to 10 Mb (Lieberman-Aiden et al. 2009). Here, we present the concept of the fractal globule, comparing it to other states of a polymer and focusing on its properties relevant for the biophysics of chromatin. We then discuss properties of the fractal globule that make it an attractive model for chromatin organization inside a cell. Next, we connect the fractal globule to recent studies that emphasize topological constraints as a primary factor driving formation of chromosomal territories. We discuss how theoretical predictions, made on the basis of the fractal globule model, can be tested experimentally. Finally, we discuss whether fractal globule architecture can be relevant for chromatin packing in other organisms such as yeast and bacteria. read more read less

Topics:

Fractal (53%)53% related to the paper
View PDF
515 Citations
Journal Article DOI: 10.1007/S10577-005-1024-3
Role of linker histone in chromatin structure and function: H1 stoichiometry and nucleosome repeat length
Christopher L. Woodcock1, Arthur I. Skoultchi2, Yuhong Fan2
03 Mar 2006 - Chromosome Research

Abstract:

Despite a great deal of attention over many years, the structural and functional roles of the linker histone H1 remain enigmatic. The earlier concepts of H1 as a general transcriptional inhibitor have had to be reconsidered in the light of experiments demonstrating a minor effect of H1 deletion in unicellular organisms. More ... Despite a great deal of attention over many years, the structural and functional roles of the linker histone H1 remain enigmatic. The earlier concepts of H1 as a general transcriptional inhibitor have had to be reconsidered in the light of experiments demonstrating a minor effect of H1 deletion in unicellular organisms. More recent work analysing the results of depleting H1 in mammals through genetic knockouts of selected H1 subtypes in the mouse has shown that cells and tissues can tolerate a surprisingly low H1 content. One common feature of H1-depleted nuclei is a reduction in nucleosome repeat length (NRL). Moreover, there is a robust linear relationship between H1 stoichiometry and NRL, suggesting an inherent homeostatic mechanism that maintains intranuclear electrostatic balance. It is also clear that the 1 H1 per nucleosome paradigm for higher eukaryotes is the exception rather than the rule. This, together with the high mobility of H1 within the nucleus, prompts a reappraisal of the role of linker histone as an obligatory chromatin architectural protein. read more read less

Topics:

Linker DNA (70%)70% related to the paper, Chromatosome (64%)64% related to the paper, Histone code (63%)63% related to the paper, Histone H1 (62%)62% related to the paper, Nucleosome (62%)62% related to the paper
434 Citations
Journal Article DOI: 10.1023/A:1012495201697
Non-random radial higher-order chromatin arrangements in nuclei of diploid human cells.
01 Jan 2001 - Chromosome Research

Abstract:

A quantitative comparison of higher-order chromatin arrangements was performed in human cell types with three-dimensionally (3D) preserved, differently shaped nuclei. These cell types included flat-ellipsoid nuclei of diploid amniotic fluid cells and fibroblasts and spherical nuclei of B and T lymphocytes from peripheral huma... A quantitative comparison of higher-order chromatin arrangements was performed in human cell types with three-dimensionally (3D) preserved, differently shaped nuclei. These cell types included flat-ellipsoid nuclei of diploid amniotic fluid cells and fibroblasts and spherical nuclei of B and T lymphocytes from peripheral human blood. Fluorescence in-situ hybridization (FISH) was performed with chromosome paint probes for large (#1–5) and small (#17–20) autosomes, and for the two sex chromosomes. Other probes delineated heterochromatin blocks of numerous larger and smaller human chromosomes. Shape differences correlated with distinct differences in higher order chromatin arrangements: in the spherically shaped lymphocyte nuclei we noted the preferential positioning of the small, gene dense #17, 19 and 20 chromosome territories (CTs) in the 3D nuclear interior – typically without any apparent connection to the nuclear envelope. In contrast, CTs of the gene-poor small chromosomes #18 and Y were apparently attached at the nuclear envelope. CTs of large chromosomes were also preferentially located towards the nuclear periphery. In the ellipsoid nuclei of amniotic fluid cells and fibroblasts, all tested CTs showed attachments to the upper and/or lower part of the nuclear envelope: CTs of small chromosomes, including #18 and Y, were located towards the centre of the nuclear projection (CNP), while the large chromosomes were positioned towards the 2D nuclear rim. In contrast to these highly reproducible radial arrangements, 2D distances measured between heterochromatin blocks of homologous and heterologous CTs were strikingly variable. These results as well as CT painting let us conclude that nuclear functions in the studied cell types may not require reproducible side-by-side arrangements of specific homologous or non-homologous CTs. 3D-modelling of statistical arrangements of 46 human CTs in spherical nuclei was performed under the assumption of a linear correlation between DNA content of each chromosome and its CT volume. In a set of modelled nuclei, we noted the preferential localization of smaller CTs towards the 3D periphery and of larger CTs towards the 3D centre. This distribution is in clear contrast to the experimentally observed distribution in lymphocyte nuclei. We conclude that presently unknown factors (other than topological constraints) may play a decisive role to enforce the different radial arrangements of large and small CTs observed in ellipsoid and spherical human cell nuclei. read more read less

Topics:

Chromosome Territory (51%)51% related to the paper, Cell nucleus (50%)50% related to the paper
391 Citations
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Frequently asked questions

1. Can I write Chromosome Research in LaTeX?

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

2. Do you follow the Chromosome Research guidelines?

Yes, the template is compliant with the Chromosome Research 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 Chromosome Research?

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 Chromosome Research citation style.

4. Can I use the Chromosome Research 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 Chromosome Research.

5. Can I use a manuscript in Chromosome Research 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 Chromosome Research that you can download at the end.

6. How long does it usually take you to format my papers in Chromosome Research?

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

7. Where can I find the template for the Chromosome Research?

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 Chromosome Research'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 Chromosome Research'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. Chromosome Research an online tool or is there a desktop version?

SciSpace's Chromosome Research 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 Chromosome Research?

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 Chromosome Research?”

11. What is the output that I would get after using Chromosome Research?

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

12. Is Chromosome Research'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 Chromosome Research?

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 Chromosome Research. 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 Chromosome Research?

The 5 most common citation types in order of usage for Chromosome Research 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 Chromosome Research?

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

16. Can I download Chromosome Research 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 Chromosome Research Endnote style according to Elsevier guidelines.

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