Example of Journal of Community Genetics format
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Example of Journal of Community Genetics format Example of Journal of Community Genetics format Example of Journal of Community Genetics format Example of Journal of Community Genetics format Example of Journal of Community Genetics format Example of Journal of Community Genetics format Example of Journal of Community Genetics format Example of Journal of Community Genetics format Example of Journal of Community Genetics format Example of Journal of Community Genetics format Example of Journal of Community Genetics format Example of Journal of Community Genetics format Example of Journal of Community Genetics format Example of Journal of Community Genetics format Example of Journal of Community Genetics format Example of Journal of Community Genetics format Example of Journal of Community Genetics format Example of Journal of Community Genetics format
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Example of Journal of Community Genetics format Example of Journal of Community Genetics format Example of Journal of Community Genetics format Example of Journal of Community Genetics format Example of Journal of Community Genetics format Example of Journal of Community Genetics format Example of Journal of Community Genetics format Example of Journal of Community Genetics format Example of Journal of Community Genetics format Example of Journal of Community Genetics format Example of Journal of Community Genetics format Example of Journal of Community Genetics format Example of Journal of Community Genetics format Example of Journal of Community Genetics format Example of Journal of Community Genetics format Example of Journal of Community Genetics format Example of Journal of Community Genetics format Example of Journal of Community Genetics format
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open access Open Access

Journal of Community Genetics — Template for authors

Publisher: Springer
Categories Rank Trend in last 3 yrs
Public Health, Environmental and Occupational Health #172 of 526 up up by 12 ranks
Epidemiology #57 of 99 up up by 4 ranks
Genetics (clinical) #60 of 87 up up by 9 ranks
journal-quality-icon Journal quality:
Good
calendar-icon Last 4 years overview: 179 Published Papers | 629 Citations
indexed-in-icon Indexed in: Scopus
last-updated-icon Last updated: 21/07/2020
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Related Journals

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Quality:  
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CiteRatio: 8.4
SJR: 1.718
SNIP: 1.845
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Quality:  
High
CiteRatio: 3.8
SJR: 1.0
SNIP: 1.155

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.

3.5

13% from 2019

CiteRatio for Journal of Community Genetics from 2016 - 2020
Year Value
2020 3.5
2019 3.1
2018 2.6
2017 2.7
2016 3.5
graph view Graph view
table view Table view

0.774

16% from 2019

SJR for Journal of Community Genetics from 2016 - 2020
Year Value
2020 0.774
2019 0.669
2018 0.782
2017 0.687
2016 0.723
graph view Graph view
table view Table view

1.015

22% from 2019

SNIP for Journal of Community Genetics from 2016 - 2020
Year Value
2020 1.015
2019 0.833
2018 0.669
2017 0.901
2016 0.83
graph view Graph view
table view Table view

insights Insights

  • CiteRatio of this journal has increased by 13% in last years.
  • This journal’s CiteRatio is in the top 10 percentile category.

insights Insights

  • SJR of this journal has increased by 16% in last years.
  • This journal’s SJR is in the top 10 percentile category.

insights Insights

  • SNIP of this journal has increased by 22% in last years.
  • This journal’s SNIP is in the top 10 percentile category.

Journal of Community Genetics

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Springer

Journal of Community Genetics

The Journal of Community Genetics is an international forum for research in the ever-expanding field of community genetics, the art and science of applying medical genetics to human communities for the benefit of their individuals. Community genetics comprises all activities w...... Read More

Public Health, Environmental and Occupational Health

Epidemiology

Genetics(clinical)

Medicine

i
Last updated on
20 Jul 2020
i
ISSN
1868-310X
i
Impact Factor
High - 1.068
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
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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

open accessOpen access Journal Article DOI: 10.1007/S12687-011-0072-Y
Consanguineous marriages: Preconception consultation in primary health care settings
Hanan Hamamy1

Abstract:

Consanguinity is a deeply rooted social trend among one-fifth of the world population mostly residing in the Middle East, West Asia and North Africa, as well as among emigrants from these communities now residing in North America, Europe and Australia. The mounting public awareness on prevention of congenital and genetic diso... Consanguinity is a deeply rooted social trend among one-fifth of the world population mostly residing in the Middle East, West Asia and North Africa, as well as among emigrants from these communities now residing in North America, Europe and Australia. The mounting public awareness on prevention of congenital and genetic disorders in offspring is driving an increasing number of couples contemplating marriage and reproduction in highly consanguineous communities to seek counseling on consanguinity. Primary health care providers are faced with consanguineous couples demanding answers to their questions on the anticipated health risks to their offspring. Preconception and premarital counseling on consanguinity should be part of the training of health care providers particularly in highly consanguineous populations. read more read less

Topics:

Health care (54%)54% related to the paper, Consanguinity (52%)52% related to the paper
View PDF
318 Citations
open accessOpen access Journal Article DOI: 10.1007/S12687-017-0316-6
Diversity and inclusion in genomic research: why the uneven progress?
Amy R. Bentley1, Shawneequa L. Callier2, Shawneequa L. Callier1, Charles N. Rotimi1

Abstract:

Conducting genomic research in diverse populations has led to numerous advances in our understanding of human history, biology, and health disparities, in addition to discoveries of vital clinical significance. Conducting genomic research in diverse populations is also important in ensuring that the genomic revolution does no... Conducting genomic research in diverse populations has led to numerous advances in our understanding of human history, biology, and health disparities, in addition to discoveries of vital clinical significance. Conducting genomic research in diverse populations is also important in ensuring that the genomic revolution does not exacerbate health disparities by facilitating discoveries that will disproportionately benefit well-represented populations. Despite the general agreement on the need for genomic research in diverse populations in terms of equity and scientific progress, genomic research remains largely focused on populations of European descent. In this article, we describe the rationale for conducting genomic research in diverse populations by reviewing examples of advances facilitated by their inclusion. We also explore some of the factors that perpetuate the disproportionate attention on well-represented populations. Finally, we discuss ongoing efforts to ameliorate this continuing bias. Collaborative and intensive efforts at all levels of research, from the funding of studies to the publication of their findings, will be necessary to ensure that genomic research does not conserve historical inequalities or curtail the contribution that genomics could make to the health of all humanity. read more read less
View PDF
201 Citations
open accessOpen access Journal Article DOI: 10.1007/S12687-012-0114-0
Prevalence of β-thalassemia and other haemoglobinopathies in six cities in India: a multicentre study

Abstract:

The population of India is extremely diverse comprising of more than 3,000 ethnic groups who still follow endogamy. Haemoglobinopathies are the commonest hereditary disorders in India and pose a major health problem. The data on the prevalence of β-thalassemias and other haemoglobinopathies in different caste/ethnic groups of... The population of India is extremely diverse comprising of more than 3,000 ethnic groups who still follow endogamy. Haemoglobinopathies are the commonest hereditary disorders in India and pose a major health problem. The data on the prevalence of β-thalassemias and other haemoglobinopathies in different caste/ethnic groups of India is scarce. Therefore the present multicentre study was undertaken in six cities of six states of India (Maharashtra, Gujarat, West Bengal, Assam, Karnataka and Punjab) to determine the prevalence of haemoglobinopathies in different caste/ethnic groups using uniform methodology. Fifty-six thousand seven hundred eighty individuals (college students and pregnant women) from different caste/ethnic groups were screened. RBC indices were measured on an automated haematology counter while the percentage of HbA2, HbF and other abnormal Hb variants were estimated by HPLC on the Variant Hemoglobin Testing System. The overall prevalence of β-thalassemia trait was 2.78 % and varied from 1.48 to 3.64 % in different states, while the prevalence of β-thalassemia trait in 59 ethnic groups varied from 0 to 9.3 %. HbE trait was mainly seen in Dibrugarh in Assam (23.9 %) and Kolkata in West Bengal (3.92 %). In six ethnic groups from Assam, the prevalence of HbE trait varied from 41.1 to 66.7 %. Few subjects with δβ-thalassemia, HPFH, HbS trait, HbD trait, HbE homozygous and HbE β-thalassemia as well as HbS homozygous and HbS-β-thalassemia (<1 %) were also identified. This is the first large multicentre study covering cities from different regions of the country for screening for β-thalassemia carriers and other haemoglobinopathies where uniform protocols and methodology was followed and quality control ensured by the co-ordinating centre. This study also shows that establishment of centres for screening for β-thalassemia and other haemoglobinopathies is possible in medical colleges. Creating awareness, screening and counselling can be done at these centres. This experience will help to formulate a national thalassemia control programme in India. read more read less

Topics:

Population (51%)51% related to the paper
164 Citations
open accessOpen access Journal Article DOI: 10.1007/S12687-010-0023-Z
Where are you going, where have you been: a recent history of the direct-to-consumer genetic testing market
Pascal Borry1, Martina C. Cornel2, Heidi Carmen Howard1

Abstract:

In recent years, various private companies have been marketing and offering genetic tests directly to consumers. This article reviews the recent history of this commercial phenomenon. In particular, we discuss and describe the following subjects: (1) the factors that allowed for the creation of the direct-to-consumer (DTC) ge... In recent years, various private companies have been marketing and offering genetic tests directly to consumers. This article reviews the recent history of this commercial phenomenon. In particular, we discuss and describe the following subjects: (1) the factors that allowed for the creation of the direct-to-consumer (DTC) genetic testing (GT) market; (2) information regarding the size and potential success or failure of the DTC GT market; (3) recent changes in the DTC GT market; and (4) the recent events that may have an impact on the regulatory oversight of DTC genetic testing and the future evolution of this market. This review of factors suggests that despite the possibility of a change of business model as well as increased regulation, the commercialization of genetic testing is here to stay. As such it is important to pay close attention not only to the science underlying these tests but also to the ethical, legal, and social issues. read more read less

Topics:

Genetic testing (51%)51% related to the paper
View PDF
102 Citations
open accessOpen access Journal Article DOI: 10.1007/S12687-012-0127-8
Epidemiological profile of common haemoglobinopathies in Arab countries.
Hanan Hamamy1, Nasir A. S. Al-Allawi2

Abstract:

Haemoglobinopathies including the thalassemias and sickle cell disease are known to be prevalent inherited disorders in most Arab countries with varying prevalence rates and molecular characterisation. β-thalassemia is encountered in polymorphic frequencies in almost all Arab countries with carrier rates of 1–11 % and a varyi... Haemoglobinopathies including the thalassemias and sickle cell disease are known to be prevalent inherited disorders in most Arab countries with varying prevalence rates and molecular characterisation. β-thalassemia is encountered in polymorphic frequencies in almost all Arab countries with carrier rates of 1–11 % and a varying number of mutations. The most widespread mutation in Lebanon, Egypt, Syria, Jordan, Tunisia and Algeria is the IVS-I-110 (G>A). In the Eastern Arabian Peninsula, the Asian Indian mutations (IVS-I-5 (G>C), codons 8/9 (+G) and IVS-I (−25 bp del)) are more common. The α-thalassemias are encountered in the majority of Arab countries in frequencies ranging from 1 to 58 % with the highest frequencies reported from Gulf countries. The (−α3.7) mutation is the most frequent followed by the non-deletional α2 polyadenylation signal mutation (AATAAA>AATAAG) and the α2 IVS1 5-bp deletion. The rates of sickle cell trait in Arab countries range from 0.3 to 30 %, with the Benin, the Arab-Indian and the Bantu haplotypes constituting the bulk of the haplotypes, leading to two major phenotypes; a mild one associated with the Arab-Indian and a severe one with the Benin and Bantu haplotypes. Public health approaches targeting prevention of haemoglobinopathies in Arab countries include newborn screening for sickle cell disease, and premarital screening for carriers of β-thalassemia and sickle cell disease. These services are still patchy and inadequate in many Arab countries recommending the upgrade of these services with strengthening of the education and training of health care providers and raising public awareness on the feasibility of prevention and care for haemoglobinopathies. read more read less
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95 Citations
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Frequently asked questions

1. Can I write Journal of Community Genetics 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 Community Genetics guidelines and auto format it.

2. Do you follow the Journal of Community Genetics guidelines?

Yes, the template is compliant with the Journal of Community Genetics 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 Community Genetics?

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 Community Genetics citation style.

4. Can I use the Journal of Community Genetics 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 Community Genetics.

5. Can I use a manuscript in Journal of Community Genetics 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 Community Genetics that you can download at the end.

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7. Where can I find the template for the Journal of Community Genetics?

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8. Can I reformat my paper to fit the Journal of Community Genetics'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.

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SciSpace's Journal of Community Genetics 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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11. What is the output that I would get after using Journal of Community Genetics?

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

12. Is Journal of Community Genetics'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 Community Genetics?

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 Community Genetics. 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 Community Genetics?

The 5 most common citation types in order of usage for Journal of Community Genetics 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 Community Genetics?

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

16. Can I download Journal of Community Genetics 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 Community Genetics Endnote style according to Elsevier guidelines.

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