Example of Journal of Clinical Laboratory Analysis format
Recent searches

Example of Journal of Clinical Laboratory Analysis format Example of Journal of Clinical Laboratory Analysis format Example of Journal of Clinical Laboratory Analysis format Example of Journal of Clinical Laboratory Analysis format Example of Journal of Clinical Laboratory Analysis format Example of Journal of Clinical Laboratory Analysis format Example of Journal of Clinical Laboratory Analysis format Example of Journal of Clinical Laboratory Analysis format Example of Journal of Clinical Laboratory Analysis format Example of Journal of Clinical Laboratory Analysis format Example of Journal of Clinical Laboratory Analysis format
Sample paper formatted on SciSpace - SciSpace
This content is only for preview purposes. The original open access content can be found here.
Look Inside
Example of Journal of Clinical Laboratory Analysis format Example of Journal of Clinical Laboratory Analysis format Example of Journal of Clinical Laboratory Analysis format Example of Journal of Clinical Laboratory Analysis format Example of Journal of Clinical Laboratory Analysis format Example of Journal of Clinical Laboratory Analysis format Example of Journal of Clinical Laboratory Analysis format Example of Journal of Clinical Laboratory Analysis format Example of Journal of Clinical Laboratory Analysis format Example of Journal of Clinical Laboratory Analysis format Example of Journal of Clinical Laboratory Analysis format
Sample paper formatted on SciSpace - SciSpace
This content is only for preview purposes. The original open access content can be found here.
open access Open Access

Journal of Clinical Laboratory Analysis — Template for authors

Publisher: Wiley
Categories Rank Trend in last 3 yrs
Medical Laboratory Technology #12 of 27 -
Public Health, Environmental and Occupational Health #251 of 526 down down by 9 ranks
Microbiology (medical) #68 of 116 up up by 1 rank
Hematology #74 of 123 up up by 4 ranks
Biochemistry (medical) #35 of 54 down down by 3 ranks
Immunology and Allergy #130 of 182 up up by 8 ranks
Clinical Biochemistry #87 of 113 up up by 2 ranks
journal-quality-icon Journal quality:
Good
calendar-icon Last 4 years overview: 1273 Published Papers | 3226 Citations
indexed-in-icon Indexed in: Scopus
last-updated-icon Last updated: 02/07/2020
Related journals
Insights
General info
Top papers
Popular templates
Get started guide
Why choose from SciSpace
FAQ

Related Journals

open access Open Access

Wiley

Quality:  
Good
CiteRatio: 3.4
SJR: 0.705
SNIP: 1.105
open access Open Access
recommended Recommended

American Society for Microbiology

Quality:  
High
CiteRatio: 39.4
SJR: 9.177
SNIP: 10.528
open access Open Access

Springer

Quality:  
High
CiteRatio: 5.0
SJR: 0.649
SNIP: 1.155
open access Open Access

Springer

Quality:  
High
CiteRatio: 7.7
SJR: 1.633
SNIP: 1.452

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.

1.54

11% from 2018

Impact factor for Journal of Clinical Laboratory Analysis from 2016 - 2019
Year Value
2019 1.54
2018 1.728
2017 1.303
2016 1.521
graph view Graph view
table view Table view

2.5

4% from 2019

CiteRatio for Journal of Clinical Laboratory Analysis from 2016 - 2020
Year Value
2020 2.5
2019 2.4
2018 2.1
2017 2.1
2016 2.0
graph view Graph view
table view Table view

insights Insights

  • Impact factor of this journal has decreased by 11% in last year.
  • This journal’s impact factor is in the top 10 percentile category.

insights Insights

  • CiteRatio of this journal has increased by 4% 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.

0.536

21% from 2019

SJR for Journal of Clinical Laboratory Analysis from 2016 - 2020
Year Value
2020 0.536
2019 0.443
2018 0.509
2017 0.448
2016 0.497
graph view Graph view
table view Table view

0.747

24% from 2019

SNIP for Journal of Clinical Laboratory Analysis from 2016 - 2020
Year Value
2020 0.747
2019 0.603
2018 0.66
2017 0.543
2016 0.732
graph view Graph view
table view Table view

insights Insights

  • SJR of this journal has increased by 21% in last years.
  • This journal’s SJR is in the top 10 percentile category.

insights Insights

  • SNIP of this journal has increased by 24% in last years.
  • This journal’s SNIP is in the top 10 percentile category.

Journal of Clinical Laboratory Analysis

Guideline source: View

All company, product and service names used in this website are for identification purposes only. All product names, trademarks and registered trademarks are property of their respective owners.

Use of these names, trademarks and brands does not imply endorsement or affiliation. Disclaimer Notice

Wiley

Journal of Clinical Laboratory Analysis

Journal of Clinical Laboratory Analysis publishes original articles on newly developing modes of technology and laboratory assays, with emphasis on their application in current and future clinical laboratory testing. This includes reports from the following fields: immunochemi...... Read More

Medical Laboratory Technology

Public Health, Environmental and Occupational Health

Microbiology (medical)

Biochemistry, medical

Hematology

Clinical Biochemistry

Immunology and Allergy

Health Professions

i
Last updated on
02 Jul 2020
i
ISSN
1098-2825
i
Acceptance Rate
Not Provided
i
Frequency
Not Provided
i
Open Access
Not Provided
i
Sherpa RoMEO Archiving Policy
Yellow faq
i
Plagiarism Check
Available via Turnitin
i
Endnote Style
Download Available
i
Bibliography Name
apa
i
Citation Type
Numbered
[25]
i
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)1098-2825(1997)11:5<287::AID-JCLA6>3.0.CO;2-4
Wine as a biological fluid: History, production, and role in disease prevention
George J. Soleas1, Eleftherios P. Diamandis1, David M. Goldberg1

Abstract:

Wine has been part of human culture for 6,000 years, serving dietary and socio-religious functions. Its production takes place on every continent, and its chemical composition is profoundly influenced by enological techniques, the grape cultivar from which it originates, and climatic factors. In addition to ethanol, which in ... Wine has been part of human culture for 6,000 years, serving dietary and socio-religious functions. Its production takes place on every continent, and its chemical composition is profoundly influenced by enological techniques, the grape cultivar from which it originates, and climatic factors. In addition to ethanol, which in moderate consumption can reduce mortality from coronary heart disease by increasing high-density lipoprotein cholesterol and inhibiting platelet aggregation, wine (especially red wine) contains a range of polyphenols that have desirable biological properties. These include the phenolic acids (p-coumaric, cinnamic, caffeic, gentisic, ferulic, and vanillic acids), trihydroxy stilbenes (resveratrol and polydatin), and flavonoids (catechin, epicatechin, and quercetin). They are synthesized by a common pathway from phenylalanine involving polyketide condensation reactions. Metabolic regulation is provided by competition between resveratrol synthase and chalcone synthase for a common precursor pool of acyl-CoA derivatives. Polymeric aggregation gives rise, in turn to the viniferins (potent antifungal agents) and procyanidins (strong antioxidants that also inhibit platelet aggregation). The antioxidant effects of red wine and of its major polyphenols have been demonstrated in many experimental systems spanning the range from in vitro studies (human low-density lipoprotein, liposomes, macrophages, cultured cells) to investigations in healthy human subjects. Several of these compounds (notably catechin, quercetin, and resveratrol) promote nitric oxide production by vascular endothelium; inhibit the synthesis of thromboxane in platelets and leukotriene in neutrophils, modulate the synthesis and secretion of lipoproteins in whole animals and human cell lines, and arrest tumour growth as well as inhibit carcinogenesis in different experimental models. Target mechanisms to account for these effects include inhibition of phospholipase A2 and cyclo-oxygenase, inhibition of phosphodiesterase with increase in cyclic nucleotide concentrations, and inhibition of several protein kinases involved in cell signalling. Although their bioavailability remains to be fully established, red wine provides a more favourable milieu than fruits and vegetables, their other dietary source in humans. read more read less

Topics:

Resveratrol (56%)56% related to the paper, Wine (55%)55% related to the paper, Catechin (51%)51% related to the paper, Quercetin (51%)51% related to the paper, Low-density lipoprotein (51%)51% related to the paper
View PDF
675 Citations
open accessOpen access Journal Article DOI: 10.1002/JCLA.1860050510
Carcinoembryonic antigen gene family: molecular biology and clinical perspectives.
John A. Thompson1, Fritz Grunert1, Wolfgang Zimmermann1

Abstract:

The carcinoembryonic antigen (CEA) gene family belongs to the immunoglobulin supergene family and can be divided into two main subgroups based on sequence comparisons In humans it is clustered on the long arm of chromosome 19 and consists of approximately 20 genes The CEA subgroup genes code for CEA and its classical crossrea... The carcinoembryonic antigen (CEA) gene family belongs to the immunoglobulin supergene family and can be divided into two main subgroups based on sequence comparisons In humans it is clustered on the long arm of chromosome 19 and consists of approximately 20 genes The CEA subgroup genes code for CEA and its classical crossreacting antigens, which are mainly membrane-bound, whereas the other subgroup genes encode the pregnancy-specific glycoproteins (PSG), which are secreted Splice variants of individual genes and differential post-translational modifications of the resulting proteins, eg, by glycosylation, indicate a high complexity in the number of putative CEA-related molecules So far, only a limited number of CEA-related antigens in humans have been unequivocally assigned to a specific gene Rodent CEA-related genes reveal a high sequence divergence and, in part, a completely different domain organization than the human CEA gene family, making it difficult to determine individual gene counterparts However, rodent CEA-related genes can be assigned to human subgroups based on similarity of expression patterns, which is characteristic for the subgroups Various functions have been determined for members of the CEA subgroup in vitro, including cell adhesion, bacterial binding, an accessory role for collagen binding or ecto-ATPases activity Based on all that is known so far on its biology, the clinical outlook for the CEA family has been reassessed read more read less

Topics:

Gene family (58%)58% related to the paper, Carcinoembryonic antigen (53%)53% related to the paper, Gene (52%)52% related to the paper
View PDF
617 Citations
open accessOpen access Journal Article DOI: 10.1002/JCLA.2058
Multiplex polymerase chain reaction: a practical approach.
Panayotis Markoulatos1, Nikolaos Siafakas1, Maurice L. J. Moncany2

Abstract:

Considerable time and effort can be saved by simultaneously amplifying multiple sequences in a single reaction, a process referred to as multiplex polymerase chain reaction (PCR). Multiplex PCR requires that primers lead to amplification of unique regions of DNA, both in individual pairs and in combinations of many primers, u... Considerable time and effort can be saved by simultaneously amplifying multiple sequences in a single reaction, a process referred to as multiplex polymerase chain reaction (PCR). Multiplex PCR requires that primers lead to amplification of unique regions of DNA, both in individual pairs and in combinations of many primers, under a single set of reaction conditions. In addition, methods must be available for the analysis of each individual amplification product from the mixture of all the products. Multiplex PCR is becoming a rapid and convenient screening assay in both the clinical and the research laboratory. The development of an efficient multiplex PCR usually requires strategic planning and multiple attempts to optimize reaction conditions. For a successful multiplex PCR assay, the relative concentration of the primers, concentration of the PCR buffer, balance between the magnesium chloride and deoxynucleotide concentrations, cycling temperatures, and amount of template DNA and Taq DNA polymerase are important. An optimal combination of annealing temperature and buffer concentration is essential in multiplex PCR to obtain highly specific amplification products. Magnesium chloride concentration needs only to be proportional to the amount of dNTP, while adjusting primer concentration for each target sequence is also essential. The list of various factors that can influence the reaction is by no means complete. Optimization of the parameters discussed in the present review should provide a practical approach toward resolving the common problems encountered in multiplex PCR (such as spurious amplification products, uneven or no amplification of some target sequences, and difficulties in reproducing some results). Thorough evaluation and validation of new multiplex PCR procedures is essential. The sensitivity and specificity must be thoroughly evaluated using standardized purified nucleic acids. Where available, full use should be made of external and internal quality controls, which must be rigorously applied. As the number of microbial agents detectable by PCR increases, it will become highly desirable for practical purposes to achieve simultaneous detection of multiple agents that cause similar or identical clinical syndromes and/or share similar epidemiological features. read more read less

Topics:

Applications of PCR (68%)68% related to the paper, Primer dimer (66%)66% related to the paper, Polymerase chain reaction optimization (66%)66% related to the paper, Multiplex polymerase chain reaction (64%)64% related to the paper, Multiple displacement amplification (62%)62% related to the paper
View PDF
608 Citations
open accessOpen access Journal Article DOI: 10.1002/(SICI)1098-2825(1999)13:6<273::AID-JCLA4>3.0.CO;2-X
Reference distributions for the negative acute-phase serum proteins, albumin, transferrin and transthyretin: a practical, simple and clinically relevant approach in a large cohort.

Abstract:

Inflammation is associated with diverse clinical conditions accompanied by characteristic changes in serum levels of the acute-phase proteins that can be used to stage the inflammatory process and evaluate the impact of treatment. Some acute-phase proteins increase during inflammation, while others, such as albumin, transferr... Inflammation is associated with diverse clinical conditions accompanied by characteristic changes in serum levels of the acute-phase proteins that can be used to stage the inflammatory process and evaluate the impact of treatment. Some acute-phase proteins increase during inflammation, while others, such as albumin, transferrin, and transthyretin, decrease. The current study reports reference ranges for serum levels of albumin, transferrin, and transthyretin based on a cohort of over 124,000 Caucasian individuals from northern New England, tested in our laboratory between 1986 and 1998. Measurements were standardized against CRM 470 (RPPHS) and analyzed using a previously validated statistical approach. Individuals with laboratory evidence of inflammation (C-reactive protein of 10 mg/L or higher) were excluded. The levels of all three analytes varied by age, generally rising until the second or third decade of life and then decreasing thereafter. Albumin and transthyretin levels were higher during midlife among males as compared to females; the maximum being at 25 years for albumin (5%) and 35 years for transthyretin (16%). In contrast, above the age of 10 years, transferrin levels were increasingly higher among females (7% at 20 years). When values were expressed as multiples of the age- and gender-specific median levels, the resulting distributions fitted a log-Gaussian distribution. When patient data are normalized in this manner, the distribution parameters can be used to assign a corresponding centile to an individual's measurement simplifying interpretation. The ultimate interpretation of an individual's measurement relies upon the clinical setting. read more read less

Topics:

Acute-phase protein (58%)58% related to the paper, Transthyretin (57%)57% related to the paper, Reference range (51%)51% related to the paper, Albumin (50%)50% related to the paper
View PDF
260 Citations
open accessOpen access Journal Article DOI: 10.1002/JCLA.23618
Ferritin in the coronavirus disease 2019 (COVID-19): A systematic review and meta-analysis.
Linlin Cheng1, Haolong Li1, Liubing Li1, Chenxi Liu1, Songxin Yan1, Haizhen Chen1, Haizhen Chen2, Yongzhe Li1

Abstract:

OBJECTIVE: The coronavirus disease 2019 (COVID-19) has rapidly developed into a pandemic. Increased levels of ferritin due to cytokine storm and secondary hemophagocytic lymphohistiocytosis were found in severe COVID-19 patients. Therefore, the aim of this study was to determine the role of ferritin in COVID-19. METHODS: Stud... OBJECTIVE: The coronavirus disease 2019 (COVID-19) has rapidly developed into a pandemic. Increased levels of ferritin due to cytokine storm and secondary hemophagocytic lymphohistiocytosis were found in severe COVID-19 patients. Therefore, the aim of this study was to determine the role of ferritin in COVID-19. METHODS: Studies investigating ferritin in COVID-19 were collected from PubMed, EMBASE, CNKI, SinoMed, and WANFANG. A meta-analysis was performed to compare the ferritin level between different patient groups: non-survivors versus survivors; more severe versus less severe; with comorbidity versus without comorbidity; ICU versus non-ICU; with mechanical ventilation versus without mechanical ventilation. RESULTS: A total of 52 records involving 10 614 COVID-19-confirmed patients between December 25, 2019, and June 1, 2020, were included in this meta-analysis, and 18 studies were included in the qualitative synthesis. The ferritin level was significantly increased in severe patients compared with the level in non-severe patients [WMD 397.77 (95% CI 306.51-489.02), P < .001]. Non-survivors had a significantly higher ferritin level compared with the one in survivors [WMD 677.17 (95% CI 391.01-963.33), P < .001]. Patients with one or more comorbidities including diabetes, thrombotic complication, and cancer had significantly higher levels of ferritin than those without (P < .01). Severe acute liver injury was significantly associated with high levels of ferritin, and its level was associated with intensive supportive care, including ICU transfer and mechanical ventilation. CONCLUSIONS: Ferritin was associated with poor prognosis and could predict the worsening of COVID-19 patients. read more read less

Topics:

Ferritin (57%)57% related to the paper
View PDF
223 Citations
Author Pic

SciSpace is a very innovative solution to the formatting problem and existing providers, such as Mendeley or Word did not really evolve in recent years.

- Andreas Frutiger, Researcher, ETH Zurich, Institute for Biomedical Engineering

Get MS-Word and LaTeX output to any Journal within seconds
1
Choose a template
Select a template from a library of 40,000+ templates
2
Import a MS-Word file or start fresh
It takes only few seconds to import
3
View and edit your final output
SciSpace will automatically format your output to meet journal guidelines
4
Submit directly or Download
Submit to journal directly or Download in PDF, MS Word or LaTeX

(Before submission check for plagiarism via Turnitin)

clock Less than 3 minutes

What to expect from SciSpace?

Speed and accuracy over MS Word

''

With SciSpace, you do not need a word template for Journal of Clinical Laboratory Analysis.

It automatically formats your research paper to Wiley formatting guidelines and citation style.

You can download a submission ready research paper in pdf, LaTeX and docx formats.

Time comparison

Time taken to format a paper and Compliance with guidelines

Plagiarism Reports via Turnitin

SciSpace has partnered with Turnitin, the leading provider of Plagiarism Check software.

Using this service, researchers can compare submissions against more than 170 million scholarly articles, a database of 70+ billion current and archived web pages. How Turnitin Integration works?

Turnitin Stats
Publisher Logos

Freedom from formatting guidelines

One editor, 100K journal formats – world's largest collection of journal templates

With such a huge verified library, what you need is already there.

publisher-logos

Easy support from all your favorite tools

Journal of Clinical Laboratory Analysis format uses apa citation style.

Automatically format and order your citations and bibliography in a click.

SciSpace allows imports from all reference managers like Mendeley, Zotero, Endnote, Google Scholar etc.

Frequently asked questions

1. Can I write Journal of Clinical Laboratory Analysis in LaTeX?

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

2. Do you follow the Journal of Clinical Laboratory Analysis guidelines?

Yes, the template is compliant with the Journal of Clinical Laboratory Analysis 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 Journal of Clinical Laboratory Analysis?

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 Journal of Clinical Laboratory Analysis citation style.

4. Can I use the Journal of Clinical Laboratory Analysis 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 Journal of Clinical Laboratory Analysis.

5. Can I use a manuscript in Journal of Clinical Laboratory Analysis 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 Journal of Clinical Laboratory Analysis that you can download at the end.

6. How long does it usually take you to format my papers in Journal of Clinical Laboratory Analysis?

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

7. Where can I find the template for the Journal of Clinical Laboratory Analysis?

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 Journal of Clinical Laboratory Analysis'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 Journal of Clinical Laboratory Analysis'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. Journal of Clinical Laboratory Analysis an online tool or is there a desktop version?

SciSpace's Journal of Clinical Laboratory Analysis 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 Journal of Clinical Laboratory Analysis?

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 Journal of Clinical Laboratory Analysis?”

11. What is the output that I would get after using Journal of Clinical Laboratory Analysis?

After writing your paper autoformatting in Journal of Clinical Laboratory Analysis, you can download it in multiple formats, viz., PDF, Docx, and LaTeX.

12. Is Journal of Clinical Laboratory Analysis'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 Journal of Clinical Laboratory Analysis?

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 Journal of Clinical Laboratory Analysis. 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 Journal of Clinical Laboratory Analysis?

The 5 most common citation types in order of usage for Journal of Clinical Laboratory Analysis 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 Journal of Clinical Laboratory Analysis?

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 Journal of Clinical Laboratory Analysis's guidelines and download the same in Word, PDF and LaTeX formats? Give us a try!.

16. Can I download Journal of Clinical Laboratory Analysis 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 Journal of Clinical Laboratory Analysis Endnote style according to Elsevier guidelines.

Fast and reliable,
built for complaince.

Instant formatting to 100% publisher guidelines on - SciSpace.

Available only on desktops 🖥

No word template required

Typset automatically formats your research paper to Journal of Clinical Laboratory Analysis formatting guidelines and citation style.

Verifed journal formats

One editor, 100K journal formats.
With the largest collection of verified journal formats, what you need is already there.

Trusted by academicians

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.

Andreas Frutiger
Researcher & Ex MS Word user
Use this template