Default: Genetics in Medicine

ISSN: 1098-3600

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Genetics in Medicine Q1 Unclaimed

Elsevier B.V. Netherlands
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Genetics in Medicine is a journal indexed in SJR in Medicine (miscellaneous) and Genetics (clinical) with an H index of 159. It has a price of 3000 €. It has an SJR impact factor of 2,697 and it has a best quartile of Q1. It is published in English. It has an SJR impact factor of 2,697.

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

Type: Journal

Type of Copyright:

Languages: English

Open Access Policy: Open Choice

Type of publications:

Publication frecuency: -


3000 €

Inmediate OA


Embargoed OA

0 €

Non OA


Genetics in Medicine


SJR Impact factor


H Index


Total Docs (Last Year)


Total Docs (3 years)


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Total Cites (3 years)


Citable Docs (3 years)


Cites/Doc (2 years)




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Aims and Scope

clinical, genetic, variants, colorectal, resource, cancer, medical, consent, xy, data, early, enrolled, characteristics, frequent, genes, genesa, genesclinphen, dysgenesis, disease, directly, burden, carrier, counseling, curriculum, cystic, deahbox, development, dhx, diagnosis, diagnosisunderstanding,

Best articles by citations


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

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Attitudes of African American premedical students toward genetic testing and screening

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Clinical validation of genetic tests

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Fostering applications of genetics in primary care: What will it take?

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In Response

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

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Structural brain abnormalities in adult males with clefts of the lip and/or palate

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Reflections on the ethics of genetic enhancement

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Heterogeneity of late-infantile neuronal ceroid lipofuscinosis

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

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Insurance reimbursement for risk-reducing mastectomy and oophorectomy in women with BRCA1 or BRCA2 mutations

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Hereditary hemochromatosis: Perspectives of public health, medical genetics, and primary care

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Extensive sequencing of the cystic fibrosis transmembrane regulator gene: Assay validation and unexpected benefits of developing a comprehensive test

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

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

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The GM2 gangliosidoses datanases: Allelic variation at the HEXA, HEXB, and GMWA gene loci

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Why has the relationship between psychiatry and genetics been so contentious?

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Advocating for genetics at the local level: The Medicare Part B Carrier Advisory Committee

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Allele frequency determination of publicly available cSNPs in the Korean population

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Molecular diagnosis and inborn errors of metabolism: A practitioner's view

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Some ethical implications of The Human Genome Project

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Mapping the human genome: An assessment of media coverage and public reaction

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