Example of Human Mutation format
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Example of Human Mutation format Example of Human Mutation format Example of Human Mutation format Example of Human Mutation format Example of Human Mutation format Example of Human Mutation format Example of Human Mutation format Example of Human Mutation format Example of Human Mutation format Example of Human Mutation format Example of Human Mutation format Example of Human Mutation format Example of Human Mutation format Example of Human Mutation format Example of Human Mutation format Example of Human Mutation format Example of Human Mutation format Example of Human Mutation format Example of Human Mutation format
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Example of Human Mutation format Example of Human Mutation format Example of Human Mutation format Example of Human Mutation format Example of Human Mutation format Example of Human Mutation format Example of Human Mutation format Example of Human Mutation format Example of Human Mutation format Example of Human Mutation format Example of Human Mutation format Example of Human Mutation format Example of Human Mutation format Example of Human Mutation format Example of Human Mutation format Example of Human Mutation format Example of Human Mutation format Example of Human Mutation format Example of Human Mutation format
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This content is only for preview purposes. The original open access content can be found here.
open access Open Access

Human Mutation — Template for authors

Publisher: Wiley
Categories Rank Trend in last 3 yrs
Genetics #66 of 325 down down by 24 ranks
Genetics (clinical) #22 of 87 down down by 10 ranks
journal-quality-icon Journal quality:
High
calendar-icon Last 4 years overview: 750 Published Papers | 5317 Citations
indexed-in-icon Indexed in: Scopus
last-updated-icon Last updated: 09/06/2020
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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.

4.124

7% from 2018

Impact factor for Human Mutation from 2016 - 2019
Year Value
2019 4.124
2018 4.453
2017 5.359
2016 4.601
graph view Graph view
table view Table view

7.1

5% from 2019

CiteRatio for Human Mutation from 2016 - 2020
Year Value
2020 7.1
2019 7.5
2018 8.3
2017 8.7
2016 10.3
graph view Graph view
table view Table view

insights Insights

  • Impact factor of this journal has decreased by 7% in last year.
  • This journal’s impact factor is in the top 10 percentile category.

insights Insights

  • CiteRatio of this journal has decreased by 5% 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.

1.981

18% from 2019

SJR for Human Mutation from 2016 - 2020
Year Value
2020 1.981
2019 2.41
2018 3.088
2017 3.246
2016 3.231
graph view Graph view
table view Table view

1.465

10% from 2019

SNIP for Human Mutation from 2016 - 2020
Year Value
2020 1.465
2019 1.631
2018 1.53
2017 1.563
2016 1.494
graph view Graph view
table view Table view

insights Insights

  • SJR of this journal has decreased by 18% in last years.
  • This journal’s SJR is in the top 10 percentile category.

insights Insights

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

Human Mutation

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Wiley

Human Mutation

Human Mutation is a peer-reviewed journal that offers publication of original Research Articles, Methods, Mutation Updates, Reviews, Database Articles, Mutations in Brief (MIBs), Rapid Communications, and Letters on broad aspects of mutation research in humans. Reports of nove...... Read More

Genetics

Genetics(clinical)

Biochemistry, Genetics and Molecular Biology

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Last updated on
08 Jun 2020
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ISSN
1059-7794
i
Impact Factor
High - 1.732
i
Open Access
Yes
i
Sherpa RoMEO Archiving Policy
Yellow faq
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Plagiarism Check
Available via Turnitin
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Endnote Style
Download Available
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Bibliography Name
apa
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Citation Type
Numbered
[25]
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Bibliography Example
Beenakker, C.W.J. (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

open accessOpen access Journal Article DOI: 10.1002/(SICI)1098-1004(200001)15:1<7::AID-HUMU4>3.0.CO;2-N
Mutation nomenclature extensions and suggestions to describe complex mutations: a discussion.
01 Jan 2000 - Human Mutation

Abstract:

Consistent gene mutation nomenclature is essential for efficient and accurate reporting, testing, and curation of the growing number of disease mutations and useful polymorphisms being discovered in the human genome. While a codified mutation nomenclature system for simple DNA lesions has now been adopted broadly by the medic... Consistent gene mutation nomenclature is essential for efficient and accurate reporting, testing, and curation of the growing number of disease mutations and useful polymorphisms being discovered in the human genome. While a codified mutation nomenclature system for simple DNA lesions has now been adopted broadly by the medical genetics community, it is inherently difficult to represent complex mutations in a unified manner. In this article, suggestions are presented for reporting just such complex mutations. read more read less

Topics:

Gene mutation (59%)59% related to the paper, Mutation (genetic algorithm) (51%)51% related to the paper
View PDF
1,744 Citations
open accessOpen access Journal Article DOI: 10.1002/HUMU.10212
Human Gene Mutation Database (HGMD): 2003 update.
01 Jun 2003 - Human Mutation

Abstract:

The Human Gene Mutation Database (HGMD) constitutes a comprehensive core collection of data on germ-line mutations in nuclear genes underlying or associated with human inherited disease (www.hgmd.org). Data catalogued includes: single base-pair substitutions in coding, regulatory and splicing-relevant regions; micro-deletions... The Human Gene Mutation Database (HGMD) constitutes a comprehensive core collection of data on germ-line mutations in nuclear genes underlying or associated with human inherited disease (www.hgmd.org). Data catalogued includes: single base-pair substitutions in coding, regulatory and splicing-relevant regions; micro-deletions and micro-insertions; indels; triplet repeat expansions as well as gross deletions; insertions; duplications; and complex rearrangements. Each mutation is entered into HGMD only once in order to avoid confusion between recurrent and identical-by-descent lesions. By March 2003, the database contained in excess of 39,415 different lesions detected in 1,516 different nuclear genes, with new entries currently accumulating at a rate exceeding 5,000 per annum. Since its inception, HGMD has been expanded to include cDNA reference sequences for more than 87% of listed genes, splice junction sequences, disease-associated and functional polymorphisms, as well as links to data present in publicly available online locus-specific mutation databases. Although HGMD has recently entered into a licensing agreement with Celera Genomics (Rockville, MD), mutation data will continue to be made freely available via the Internet. read more read less

Topics:

Gene mutation (59%)59% related to the paper, Mutation (genetic algorithm) (51%)51% related to the paper
View PDF
1,644 Citations
open accessOpen access Journal Article DOI: 10.1002/HUMU.20921
Updated Comprehensive Phylogenetic Tree of Global Human Mitochondrial DNA Variation
Mannis van Oven1, Manfred Kayser1
01 Feb 2009 - Human Mutation

Abstract:

Human mitochondrial DNA is widely used as tool in many fields including evolutionary anthropology and population history, medical genetics, genetic genealogy, and forensic science. Many applications require detailed knowledge about the phylogenetic relationship of mtDNA variants. Although the phylogenetic resolution of global... Human mitochondrial DNA is widely used as tool in many fields including evolutionary anthropology and population history, medical genetics, genetic genealogy, and forensic science. Many applications require detailed knowledge about the phylogenetic relationship of mtDNA variants. Although the phylogenetic resolution of global human mtDNA diversity has greatly improved as a result of increasing sequencing efforts of complete mtDNA genomes, an updated overall mtDNA tree is currently not available. In order to facilitate a better use of known mtDNA variation, we have constructed an updated comprehensive phylogeny of global human mtDNA variation, based on both coding- and control region mutations. This complete mtDNA tree includes previously published as well as newly identified haplogroups, is easily navigable, will be continuously and regularly updated in the future, and is online available at http://www.phylotree.org. © 2008 Wiley-Liss, Inc. read more read less

Topics:

Human evolutionary genetics (57%)57% related to the paper, Genealogical DNA test (55%)55% related to the paper, Phylogenetic tree (54%)54% related to the paper, Human mitochondrial genetics (53%)53% related to the paper, Population (52%)52% related to the paper
View PDF
1,628 Citations
open accessOpen access Journal Article DOI: 10.1002/HUMU.20495
Impact of mutant p53 functional properties on TP53 mutation patterns and tumor phenotype: lessons from recent developments in the IARC TP53 database.
01 Jun 2007 - Human Mutation

Abstract:

The tumor suppressor gene TP53 is frequently mutated in human cancers More than 75% of all mutations are missense substitutions that have been extensively analyzed in various yeast and human cell assays The International Agency for Research on Cancer (IARC) TP53 database (www-p53iarcfr) compiles all genetic variations that ha... The tumor suppressor gene TP53 is frequently mutated in human cancers More than 75% of all mutations are missense substitutions that have been extensively analyzed in various yeast and human cell assays The International Agency for Research on Cancer (IARC) TP53 database (www-p53iarcfr) compiles all genetic variations that have been reported in TP53 Here, we present recent database developments that include new annotations on the functional properties of mutant proteins, and we perform a systematic analysis of the database to determine the functional properties that contribute to the occurrence of mutational "hotspots" in different cancer types and to the phenotype of tumors This analysis showed that loss of transactivation capacity is a key factor for the selection of missense mutations, and that difference in mutation frequencies is closely related to nucleotide substitution rates along TP53 coding sequence An interesting new finding is that in patients with an inherited missense mutation, the age at onset of tumors was related to the functional severity of the mutation, mutations with total loss of transactivation activity being associated with earlier cancer onset compared to mutations that retain partial transactivation capacity Furthermore, 80% of the most common mutants show a capacity to exert dominant-negative effect (DNE) over wild-type p53, compared to only 45% of the less frequent mutants studied, suggesting that DNE may play a role in shaping mutation patterns These results provide new insights into the factors that shape mutation patterns and influence mutation phenotype, which may have clinical interest read more read less

Topics:

Mutation rate (62%)62% related to the paper, Missense mutation (61%)61% related to the paper, Germline mutation (61%)61% related to the paper, Suppressor mutation (60%)60% related to the paper, Mutation (genetic algorithm) (57%)57% related to the paper
View PDF
1,589 Citations
open accessOpen access Journal Article DOI: 10.1002/(SICI)1098-1004(200001)15:1<57::AID-HUMU12>3.0.CO;2-G
Online Mendelian Inheritance in Man (OMIM).
Ada Hamosh1, Alan F. Scott1, Joanna S. Amberger1, David Valle1, Victor A. McKusick1
01 Jan 2000 - Human Mutation

Abstract:

Online Mendelian Inheritance In Man (OMIM) is a public database of bibliographic information about human genes and genetic disorders. Begun by Dr. Victor McKusick as the authoritative reference Mendelian Inheritance in Man, it is now distributed electronically by the National Center for Biotechnology Information (NCBI). Mater... Online Mendelian Inheritance In Man (OMIM) is a public database of bibliographic information about human genes and genetic disorders. Begun by Dr. Victor McKusick as the authoritative reference Mendelian Inheritance in Man, it is now distributed electronically by the National Center for Biotechnology Information (NCBI). Material in OMIM is derived from the biomedical literature and is written by Dr. McKusick and his colleagues at Johns Hopkins University and elsewhere. Each OMIM entry has a full text summary of a genetic phenotype and/or gene and has copious links to other genetic resources such as DNA and protein sequence, PubMed references, mutation databases, approved gene nomenclature, and more. In addition, NCBI's neighboring feature allows users to identify related articles from PubMed selected on the basis of key words in the OMIM entry. Through its many features, OMIM is increasingly becoming a major gateway for clinicians, students, and basic researchers to the ever-growing literature and resources of human genetics. read more read less

Topics:

OMIM : Online Mendelian Inheritance in Man (72%)72% related to the paper
View PDF
1,396 Citations
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Human Mutation format uses apa citation style.

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Frequently asked questions

1. Can I write Human Mutation in LaTeX?

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

2. Do you follow the Human Mutation guidelines?

Yes, the template is compliant with the Human Mutation 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 Human Mutation?

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 Human Mutation citation style.

4. Can I use the Human Mutation 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 Human Mutation.

5. Can I use a manuscript in Human Mutation 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 Human Mutation that you can download at the end.

6. How long does it usually take you to format my papers in Human Mutation?

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

7. Where can I find the template for the Human Mutation?

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 Human Mutation'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 Human Mutation'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. Human Mutation an online tool or is there a desktop version?

SciSpace's Human Mutation 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 Human Mutation?

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 Human Mutation?”

11. What is the output that I would get after using Human Mutation?

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

12. Is Human Mutation'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 Human Mutation?

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 Human Mutation. 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 Human Mutation?

The 5 most common citation types in order of usage for Human Mutation 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 Human Mutation?

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

16. Can I download Human Mutation 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 Human Mutation 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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