ISSN: 1868-310X

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Journal of Community Genetics Q2 Unclaimed

Springer Verlag Germany

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Journal of Community Genetics is a journal indexed in SJR in Public Health, Environmental and Occupational Health and Epidemiology with an H index of 36. It has a price of 2690 €. It has an SJR impact factor of 0,643 and it has a best quartile of Q2. It is published in English. It has an SJR impact factor of 0,643.

Type: Journal

Type of Copyright:

Languages: English

Open Access Policy: Open Choice

Type of publications:

Publication frecuency: -

Categories: Public Health, Environmental and Occupational Health (Q2) Epidemiology (Q3) Genetics (clinical) (Q3)

Price

2690 €

Inmediate OA

NPD

Embargoed OA

0 €

Non OA

Metrics

0,643

SJR Impact factor

36

H Index

69

Total Docs (Last Year)

189

Total Docs (3 years)

2886

Total Refs

370

Total Cites (3 years)

177

Citable Docs (3 years)

1.84

Cites/Doc (2 years)

41.83

Ref/Doc

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Aims and Scope

Best articles by citations

Efficacy of an educational intervention on family physicians' risk assessment and management of colorectal cancer

"Awakening to" a new meaning of being at-risk for arrhythmogenic right ventricular cardiomyopathy: a grounded theory study

Using a "genomics tool" to develop disease prevention strategy in a low-income setting: lessons from the podoconiosis research project

Awareness of risks of biobank research may affect public attitudes toward consent

How obedience of marriage rules may counteract genetic drift

Two decades of pre-marital screening for beta-thalassemia in central Iran

Ethics, genetics and public policies in Uruguay: newborn and infant screening as a paradigm

BRCA sequencing and large rearrangement testing in young Black women with breast cancer

Definitions of genetic testing in European legal documents

Upcoming special issues in the Journal of Community Genetics

Gene-environment interactions and health inequalities: views of underserved communities

Power, expertise and the limits of representative democracy: genetics as scientific progress or political legitimation in carcinogenic risk assessment of pharmaceuticals?

SHOW MORE ARTICLES

Evaluation of cortisol and telomere length measurements in ethnically diverse women with breast cancer using culturally sensitive methods

Public attitudes regarding the use of electronic health information and residual clinical tissues for research

Challenges in recruiting Mexican women for cancer genetics research

Frequency distribution of the single-nucleotide -108C/T polymorphism at the promoter region of the PON1 gene in Asian Indians and its relationship with coronary artery disease

Parental information use in the context of newborn bloodspot screening. An exploratory mixed methods study

Are family-oriented interventions in Portuguese genetics services a remote possibility? Professionals' views on a multifamily intervention for cancer susceptibility families

Genetic testing for familial/hereditary breast cancer - comparison of guidelines and recommendations from the UK, France, the Netherlands and Germany

Expanded universal carrier screening and its implementation within a publicly funded healthcare service

Primary prevention of neural tube defects in Brazil: insights into anencephaly

Reasons for participating and genetic information needs among racially and ethnically diverse biobank participants: a focus group study

Population structure and inherited genetic disorders in the Bedouin of the Negev