Example of Human Genomics format
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Example of Human Genomics format Example of Human Genomics format Example of Human Genomics format Example of Human Genomics format Example of Human Genomics format Example of Human Genomics format Example of Human Genomics format Example of Human Genomics format Example of Human Genomics format Example of Human Genomics format Example of Human Genomics format Example of Human Genomics format Example of Human Genomics format Example of Human Genomics format Example of Human Genomics format Example of Human Genomics format Example of Human Genomics format Example of Human Genomics format
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Example of Human Genomics format Example of Human Genomics format Example of Human Genomics format Example of Human Genomics format Example of Human Genomics format Example of Human Genomics format Example of Human Genomics format Example of Human Genomics format Example of Human Genomics format Example of Human Genomics format Example of Human Genomics format Example of Human Genomics format Example of Human Genomics format Example of Human Genomics format Example of Human Genomics format Example of Human Genomics format Example of Human Genomics format Example of Human Genomics format
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open access Open Access

Human Genomics — Template for authors

Publisher: Springer
Categories Rank Trend in last 3 yrs
Drug Discovery #49 of 145 down down by 9 ranks
Genetics #115 of 325 up up by 1 rank
Molecular Medicine #77 of 167 down down by 5 ranks
Molecular Biology #178 of 382 down down by 14 ranks
journal-quality-icon Journal quality:
Good
calendar-icon Last 4 years overview: 191 Published Papers | 1018 Citations
indexed-in-icon Indexed in: Scopus
last-updated-icon Last updated: 18/06/2020
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Related Journals

open access Open Access

Bentham Science

Quality:  
Good
CiteRatio: 4.7
SJR: 0.704
SNIP: 0.589
open access Open Access
recommended Recommended

Springer

Quality:  
High
CiteRatio: 15.2
SJR: 5.564
SNIP: 2.245
open access Open Access

Taylor and Francis

Quality:  
High
CiteRatio: 8.2
SJR: 1.864
SNIP: 1.641
open access Open Access
recommended Recommended

PLOS

Quality:  
High
CiteRatio: 7.3
SJR: 2.628
SNIP: 1.713

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.

5.3

33% from 2019

CiteRatio for Human Genomics from 2016 - 2020
Year Value
2020 5.3
2019 4.0
2018 5.1
2017 5.1
2016 5.3
graph view Graph view
table view Table view

1.414

11% from 2019

SJR for Human Genomics from 2016 - 2020
Year Value
2020 1.414
2019 1.594
2018 1.632
2017 1.501
2016 1.77
graph view Graph view
table view Table view

1.018

15% from 2019

SNIP for Human Genomics from 2016 - 2020
Year Value
2020 1.018
2019 0.885
2018 0.791
2017 0.816
2016 0.861
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

  • SJR of this journal has decreased by 11% in last years.
  • This journal’s SJR is in the top 10 percentile category.

insights Insights

  • SNIP of this journal has increased by 15% in last years.
  • This journal’s SNIP is in the top 10 percentile category.

Human Genomics

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Springer

Human Genomics

Approved by publishing and review experts on SciSpace, this template is built as per for Human Genomics formatting guidelines as mentioned in Springer author instructions. The current version was created on and has been used by 539 authors to write and format their manuscripts to this journal.

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Last updated on
18 Jun 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: 10.1186/1479-7364-4-1-59
The cytochrome p450 homepage.
David R. Nelson1
01 Oct 2009 - Human Genomics

Abstract:

The Cytochrome P450 Homepage is a universal resource for nomenclature and sequence information on cytochrome P450 (CYP) genes. The site has been in continuous operation since February 1995. Currently, naming information for 11,512 CYPs are available on the web pages. The P450 sequences are manually curated by David Nelson, an... The Cytochrome P450 Homepage is a universal resource for nomenclature and sequence information on cytochrome P450 (CYP) genes. The site has been in continuous operation since February 1995. Currently, naming information for 11,512 CYPs are available on the web pages. The P450 sequences are manually curated by David Nelson, and the nomenclature system conforms to an evolutionary scheme such that members of CYP families and subfamilies share common ancestors. The organisation and content of the Homepage are described. read more read less
View PDF
887 Citations
open accessOpen access Journal Article DOI: 10.1186/1479-7364-3-3-281
Human ATP-binding cassette (ABC) transporter family.
Vasilis Vasiliou1, Konstandinos Vasiliou1, Daniel W. Nebert2
01 Jan 2008 - Human Genomics

Abstract:

There exist four fundamentally different classes of membrane-bound transport proteins: ion channels; transporters; aquaporins; and ATP-powered pumps. ATP-binding cassette (ABC) transporters are an example of ATP-dependent pumps. ABC transporters are ubiquitous membrane-bound proteins, present in all prokaryotes, as well as pl... There exist four fundamentally different classes of membrane-bound transport proteins: ion channels; transporters; aquaporins; and ATP-powered pumps. ATP-binding cassette (ABC) transporters are an example of ATP-dependent pumps. ABC transporters are ubiquitous membrane-bound proteins, present in all prokaryotes, as well as plants, fungi, yeast and animals. These pumps can move substrates in (influx) or out (efflux) of cells. In mammals, ABC transporters are expressed predominantly in the liver, intestine, blood-brain barrier, blood-testis barrier, placenta and kidney. ABC proteins transport a number of endogenous substrates, including inorganic anions, metal ions, peptides, amino acids, sugars and a large number of hydrophobic compounds and metabolites across the plasma membrane, and also across intracellular membranes. The human genome contains 49 ABC genes, arranged in eight subfamilies and named via divergent evolution. That ABC genes are important is underscored by the fact that mutations in at least I I of these genes are already known to cause severe inherited diseases (eg cystic fibrosis and X-linked adrenoleukodystrophy [X-ALD]). ABC transporters also participate in the movement of most drugs and their metabolites across cell surface and cellular organelle membranes; thus, defects in these genes can be important in terms of cancer therapy, pharmacokinetics and innumerable pharmacogenetic disorders. read more read less

Topics:

ATP-binding domain of ABC transporters (77%)77% related to the paper, ATP-binding cassette transporter (65%)65% related to the paper, Efflux (53%)53% related to the paper
View PDF
645 Citations
open accessOpen access Journal Article DOI: 10.1186/1479-7364-2-2-138
Analysis and update of the human aldehyde dehydrogenase (ALDH) gene family
Vasilis Vasiliou1, Daniel W. Nebert2
01 Jun 2005 - Human Genomics

Abstract:

The aldehyde dehydrogenase (ALDH) gene superfamily encodes enzymes that are critical for certain life processes and detoxification via the NAD(P)+-dependent oxidation of numerous endogenous and exogenous aldehyde substrates, including pharmaceuticals and environmental pollutants. Analysis of the ALDH gene superfamily in the l... The aldehyde dehydrogenase (ALDH) gene superfamily encodes enzymes that are critical for certain life processes and detoxification via the NAD(P)+-dependent oxidation of numerous endogenous and exogenous aldehyde substrates, including pharmaceuticals and environmental pollutants. Analysis of the ALDH gene superfamily in the latest databases showed that the human genome contains 19 putatively functional genes and three pseudogenes. A number of ALDH genes are upregulated as a part of the oxidative stress response and inexplicably overexpressed in various tumours, leading to problems during cancer chemotherapy. Mutations in ALDH genes cause inborn errors of metabolism -- such as the Sjogren - Larsson syndrome, type II hyperprolinaemia and γ-hydroxybutyric aciduria -- and are likely to contribute to several complex diseases, including cancer and Alzheimer's disease. The ALDH gene products appear to be multifunctional proteins, possessing both catalytic and non-catalytic properties. read more read less

Topics:

Aldehyde dehydrogenase (60%)60% related to the paper, Gene family (53%)53% related to the paper, Pseudogene (51%)51% related to the paper, Gene (50%)50% related to the paper
View PDF
342 Citations
open accessOpen access Journal Article DOI: 10.1186/1479-7364-5-3-170
The human fatty acid-binding protein family: evolutionary divergences and functions.
Rebecca L. Smathers1, Dennis R. Petersen1
01 Mar 2011 - Human Genomics

Abstract:

Fatty acid-binding proteins (FABPs) are members of the intracellular lipid-binding protein (iLBP) family and are involved in reversibly binding intracellular hydrophobic ligands and trafficking them throughout cellular compartments, including the peroxisomes, mitochondria, endoplasmic reticulum and nucleus. FABPs are small, s... Fatty acid-binding proteins (FABPs) are members of the intracellular lipid-binding protein (iLBP) family and are involved in reversibly binding intracellular hydrophobic ligands and trafficking them throughout cellular compartments, including the peroxisomes, mitochondria, endoplasmic reticulum and nucleus. FABPs are small, structurally conserved cytosolic proteins consisting of a water-filled, interior-binding pocket surrounded by ten anti-parallel beta sheets, forming a beta barrel. At the superior surface, two alpha-helices cap the pocket and are thought to regulate binding. FABPs have broad specificity, including the ability to bind long-chain (C16-C20) fatty acids, eicosanoids, bile salts and peroxisome proliferators. FABPs demonstrate strong evolutionary conservation and are present in a spectrum of species including Drosophila melanogaster, Caenorhabditis elegans, mouse and human. The human genome consists of nine putatively functional protein-coding FABP genes. The most recently identified family member, FABP12, has been less studied. read more read less

Topics:

Fatty acid-binding protein (56%)56% related to the paper, Peroxisome (52%)52% related to the paper, Conserved sequence (51%)51% related to the paper, Protein structure (51%)51% related to the paper, Cellular compartment (51%)51% related to the paper
View PDF
342 Citations
open accessOpen access Journal Article DOI: 10.1186/1479-7364-3-2-195
Analysis and update of the human solute carrier (SLC) gene superfamily
Lei He1, Konstandinos Vasiliou2, Daniel W. Nebert3
01 Jan 2009 - Human Genomics

Abstract:

The solute-carrier gene (SLC) superfamily encodes membrane-bound transporters The SLC superfamily comprises 55 gene families having at least 362 putatively functional protein-coding genes The gene products include passive transporters, symporters and antiporters, located in all cellular and organelle membranes, except, perhap... The solute-carrier gene (SLC) superfamily encodes membrane-bound transporters The SLC superfamily comprises 55 gene families having at least 362 putatively functional protein-coding genes The gene products include passive transporters, symporters and antiporters, located in all cellular and organelle membranes, except, perhaps, the nuclear membrane Transport substrates include amino acids and oligopeptides, glucose and other sugars, inorganic cations and anions (H+, HCO3-, Cl-, Na+, K+, Ca2+, Mg2+, PO43-, HPO42-, H2PO4-, SO42-, C2O42-, OH-,CO32-), bile salts, carboxylate and other organic anions, acetyl coenzyme A, essential metals, biogenic amines, neurotransmitters, vitamins, fatty acids and lipids, nucleosides, ammonium, choline, thyroid hormone and urea Contrary to gene nomenclature commonly assigned on the basis of evolutionary divergence http://wwwgenenamesorg/, the SLC gene superfamily has been named based largely on transporter function by proteins having multiple transmembrane domains Whereas all the transporters exist for endogenous substrates, it is likely that drugs, non-essential metals and many other environmental toxicants are able to 'hitch-hike' on one or another of these transporters, thereby enabling these moieties to enter (or leave) the cell Understanding and characterising the functions of these transporters is relevant to medicine, genetics, developmental biology, pharmacology and cancer chemotherapy read more read less

Topics:

Solute carrier family (61%)61% related to the paper, Gene family (51%)51% related to the paper, Amino acid (51%)51% related to the paper
View PDF
328 Citations
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With SciSpace, you do not need a word template for Human Genomics.

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Frequently asked questions

1. Can I write Human Genomics 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 Genomics guidelines and auto format it.

2. Do you follow the Human Genomics guidelines?

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

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 Genomics citation style.

4. Can I use the Human Genomics 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 Genomics.

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

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

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 Genomics.

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

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 Genomics'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 Genomics'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 Genomics an online tool or is there a desktop version?

SciSpace's Human Genomics 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 Genomics?

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 Genomics?”

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

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

12. Is Human Genomics'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 Genomics?

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 Genomics. 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 Genomics?

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

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

16. Can I download Human Genomics 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 Genomics 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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