verified SJR 2,683 · Q1 • database Scopus / SJR & Web of Science indexed

Netherlands · Elsevier B.V.

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Genetics in Medicine

Genetics in Medicine is a journal indexed in SJR in Medicine (miscellaneous) and Genetics (clinical) with an H index of 167. It has a price of 3000 €. It has an SJR impact factor of 2,683 and it has a best quartile of Q1. It is published in English. It has an SJR impact factor of 2,683.

Genetics in Medicine focuses its scope in these topics and keywords: genetic, variants, clinical, resource, colorectal, medical, consent, cancer, data, xy, ...

ISSN: 1098-3600

Editorial: Elsevier B.V.

Category: Medicine (miscellaneous)

Indexation: verifiedScopus / SJR verifiedWeb of Science

Unclaimed profile — some fields may be incomplete.

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schedule Datos CoP · solo campos en BD

SJR Impact Factor trending_up

2,683 Q1

H-index 167

Tasa de Aceptación pie_chart

22% Selectiva

Fuente Acceptance_Rate

Tiempo a publicación hourglass_top

NPD

Campo Sin dato

Coste de Publicación (APC) payments

3.000 € Open Access

Ruta Non-OA 0 €

Metrics

Campos Scimago / CoP — sin series inventadas

Scopus / SJR Web of Science

SJR Impact

2,683

H-index

167

Docs (year)

160

Docs 3y

768

Total refs

6038

Cites 3y

4303

Citable 3y

668

Cites/Doc 2y

5.12

Ref/Doc

37.74

Immediate OA

3000 €

Embargoed OA

NPD

Non OA / Submission

0 €

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Best articles by citations

Clinical validation of genetic tests

Will the learners be learned?

End-of-life issues in genetic disorders: Summary of workshop held at the National Institutes of Health on September 26, 2001

Does knowledge about the genetics of breast cancer differ between nongeneticist physicians who do or do not discuss or order BRCA testing?

Do geneticists need Babel fish?

Diffusion of innovations

Diagnostic testing for Prader-Willi syndrome and Angelman syndrome: A cost comparison

Detection of deletions in de novo "balanced" chromosome rearrangements: Further evidence for their role in phenotypic abnormalities

Cystic fibrosis carrier screening: Issues in implementation

CRISPR/Cas9-targeted enrichment and long-read sequencing of the Fuchs endothelial corneal dystrophy-associated TCF4 triplet repeat

Considerations for a multiaxis nomenclature system for medical genetics

Consent for genetic research in a general population: The NHANES experience

SHOW MORE ARTICLES

Clinical-biochemical correlation in molecularly characterized patients with Niemann-Pick type C

Adding another "hatched pink" chromosome

Characterization of mutations in 22 females with X-linked dominant chondrodysplasia punctata (Happle syndrome)

Challenges in communicating genetics: A public health approach

British Society of Human Genetics

Biochemical genetics: From mechanisms to diagnosis and management of genetic disease

Barriers to the provision of genetic services by primary care physicians: A systematic review of the literature

Attitudes of the broader hearing, deaf, and hard-of-hearing community toward genetic testing for deafness

Attitudes of African American premedical students toward genetic testing and screening

Analytic validity of cystic fibrosis testing: A preliminary estimate

American College of Medical Genetics and Genomics guideline for the clinical evaluation and etiologic diagnosis of hearing loss

Allele frequency determination of publicly available cSNPs in the Korean population

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