ISSN: 1662-4246
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Public health genomics Q3 Unclaimed
Public health genomics is a journal indexed in SJR in Public Health, Environmental and Occupational Health and Genetics (clinical) with an H index of 56. It has an SJR impact factor of 0,512 and it has a best quartile of Q3. It has an SJR impact factor of 0,512.
Type: Journal
Type of Copyright:
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Open Access Policy:
Type of publications:
Publication frecuency: -
- €
Inmediate OANPD
Embargoed OA- €
Non OAMetrics
0,512
SJR Impact factor56
H Index25
Total Docs (Last Year)102
Total Docs (3 years)1157
Total Refs206
Total Cites (3 years)100
Citable Docs (3 years)1.72
Cites/Doc (2 years)46.28
Ref/DocOther journals with similar parameters
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Obesity Medicine Q3
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Journal of Health and Pollution Q3
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Aims and Scope
Best articles by citations
Ethical Issues in Molecular Screening for Heterozygous Familial Hypercholesterolemia: The Complexity of Dealing with Genetic Susceptibility to Coronary Artery Disease
View moreUptake and Impact of Carrier Testing for Cystic Fibrosis
View moreA National Dialogue on Genetics and Minority Issues
View moreCommunity Genetics in Eastern Quebec: The Experience of the Corporation for Research and Action on Hereditary Diseases
View morePrivacy and Antidiscrimination Issues: Genetics Legislation in the United States
View moreCommunity Genetics in South Africa
View moreCommunity Genetics in The Netherlands
View moreThe Difficulties of Recruiting Minorities to Studies of Ethics and Values in Genetics
View moreAge at Postnatal Diagnosis of Down Syndrome in the Northern Netherlands for the Period 1981-2000
View moreDetection of Congenital Anomalies by Fetal Ultrasonographic Examination across Europe
View moreNew Developments in Genetics for the New Millennium: The Concept of Clinical Bioinformatics
View moreGenetic Technologies and Courts of Law
View moreRole of Primary Care Providers in the Delivery of Genetics Services
View moreGenetic Testing for Cancer Risk: A Population Survey on Attitudesand Intention
View moreExplorative Study of Costs, Effects and Savings of Screening for Female Fragile X Premutation and Full Mutation Carriers in the General Population
View moreTesting for Hereditary Risk of Breast and Ovarian Cancer
View moreTo Screen or Not to Screen:When Should Screening Be Offered?
View moreGenetic Testing: Can It Predict the Lived Experience of Individuals and Families? A Personal Testimony
View moreFrom Community Genetics to Community Genomics: The Quebec Experience
View moreGenetic Testing: Policy Issues for the New Millennium
View moreThe UK's Policies on Genetic Testing for Late-Onset Disorders
View moreThe UK's Policy on Genetic Testing Services Supplied Direct to the Public -Two Spheres and Two Tiers
View moreThe Hungarian Periconceptional Service as a Model for Community Genetics
View moreGenes and Languages
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