ISSN: 1098-3600

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Genetics in Medicine Q1 Unclaimed

Lippincott Williams and Wilkins Ltd. United States

Unfortunately this journal has not been claimed yet. For this reason, some information may be unavailable.

Genetics in Medicine is a journal indexed in SJR in Medicine (miscellaneous) and Genetics (clinical) with an H index of 139. It has a price of 3000 €. It has an SJR impact factor of 2.877 and it has a best quartile of Q1. It is published in English. It has an SJR impact factor of 2.877.

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

Type: Journal

Type of Copyright:

Languages: English

Open Access Policy: Open Choice

Type of publications:

Publication frecuency: -

Categories: Genetics (clinical) (Q1) Medicine (miscellaneous) (Q1)

Price

3000 €

Inmediate OA

NPD

Embargoed OA

0 €

Non OA

Metrics

2.877

SJR Impact factor

139

H Index

323

Total Docs (Last Year)

874

Total Docs (3 years)

9393

Total Refs

5542

Total Cites (3 years)

728

Citable Docs (3 years)

5.91

Cites/Doc (2 years)

29.08

Ref/Doc

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Aims and Scope

Best articles by citations

Introduction

Meetings Calendar

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

Attitudes of African American premedical students toward genetic testing and screening

Clinical validation of genetic tests

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

In Response

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

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

Reflections on the ethics of genetic enhancement

Heterogeneity of late-infantile neuronal ceroid lipofuscinosis

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

SHOW MORE ARTICLES

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

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

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

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

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

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

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

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

Allele frequency determination of publicly available cSNPs in the Korean population

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

Some ethical implications of The Human Genome Project

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