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verified SJR 0,491 · Q3 • database Scopus / SJR & Web of Science indexed
Public health genomics
Switzerland · S. Karger AG
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Public health genomics

Public health genomics is a journal indexed in SJR in Public Health, Environmental and Occupational Health and Genetics (clinical) with an H index of 60. It has an SJR impact factor of 0,491 and it has a best quartile of Q3. It has an SJR impact factor of 0,491.

ISSN: 1662-4246
Editorial: S. Karger AG
Category: Public Health, Environmental and Occupational Health
Indexation: verifiedScopus / SJR verifiedWeb of Science

Unclaimed profile — some fields may be incomplete.

open_in_new Portal NPD menu_book Guidelines NPD
schedule Datos CoP · solo campos en BD
SJR Impact Factor trending_up
0,491 Q3
H-index 60
Tasa de Aceptación pie_chart
30% Selectiva
Fuente Acceptance_Rate
Tiempo a publicación hourglass_top
NPD
Campo Sin dato
Coste de Publicación (APC) payments
NPD Subscription
Ruta Non-OA NPD

Metrics

Campos Scimago / CoP — sin series inventadas

Scopus / SJR Web of Science

SJR Impact

0,491

H-index

60

Docs (year)

28

Docs 3y

88

Total refs

1190

Cites 3y

141

Citable 3y

86

Cites/Doc 2y

1.33

Ref/Doc

42.5

Immediate OA

—

Embargoed OA

NPD

Non OA / Submission

—

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Best articles by citations

Banking Biological Collections: Data Warehousing, Data Mining, and Data Dilemmas in Genomics and Global Health Policy

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Uptake and Impact of Carrier Testing for Cystic Fibrosis

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Detection of Congenital Anomalies by Fetal Ultrasonographic Examination across Europe

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Current Challenges to Appropriate Clinical Use of New Genetic Knowledge in Different Countries

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Counselling following the Prenatal Diagnosis of Klinefelter Syndrome: Comparisons between Geneticists and Obstetricians in Five European Countries

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Concerns over Participation in Genetic Research among Malay-Muslims, Chinese and Indians in Singapore: A Focus Group Study

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Community Genetics in The Netherlands

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Community Genetics in South Africa

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Community Genetics in Eastern Quebec: The Experience of the Corporation for Research and Action on Hereditary Diseases

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Community Diagnosis of Maternal Exposure to Risk Factors for Congenital Defects

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Common Language for Measures of Occurrence of Congenital Anomalies and Genetic Diseases: Incidence or Birth Prevalence

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Between Acculturation and Ambivalence: Knowledge of Genetics and Attitudes towards Genetic Testing in a Consanguineous Bedouin Community

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Benefits and Costs of Genetic Screening for Breast Cancer

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A Commentary on the NIH Consensus Development Statement 'Genetic Testing for Cystic Fibrosis'

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Availability of Genetic Services: Implementation and Policy Issues

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Attitudes about Genetics in Underserved, Culturally Diverse Populations

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Assessment of Family Cancer History Collection and Utilization in Patient Care

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Are Practicing and Future Physicians Prepared to Obtain Informed Consent? The Case of Genetic Testing forSusceptibility to Breast Cancer

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Analysis of the Population Structure in Oman

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Alzheimer's Disease: Genes, Pathogenesis and Risk Prediction

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Age at Postnatal Diagnosis of Down Syndrome in the Northern Netherlands for the Period 1981-2000

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Advances in Genetics: Issues for US Racial and Ethnic Minorities: An Asian American and Pacific Islander Perspective

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Achondroplasia in the Northern Province, South Africa: Case Finding through the Genetic Services System

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Access to Genetic Tests: A Legal Perspective

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