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BMC Medical Genetics


👁  36948 View(s)

 3 Review(s)  

 Open Access      SCIE      Official Website     Submission Website
 

*Average Peer Review
Average 12 Month(s)
*Competitiveness
About 75%
CiteScore
2.3
CiteScore Rank
Subject Area Rank Percentile
Category: Medicine
Subcategory: Genetics (clinical)		 70 / 90
Category: Medicine
Subcategory: Genetics		 232 / 324
Link to PubMed Central (PMC)
https://www.ncbi.nlm.nih.gov/nlmcatalog?term=1471-2350%5BISSN%5D

Indexing (SCI collection)
Directory of Open Access Journals (DOAJ)

Country/Area of Publication
ENGLAND
Publication Frequency
Irregular
Publisher
BioMed Central

ISSN
1471-2350
E-ISSN
1471-2350
Year Publication Started
2000

Self-citation (2025-2026)
N/A
Annual Article Volume
0
Gold OA Percentage
99.08%

Open Access Info
APC APC Waiver Other Charges
Yes: Check details
( GBP1790; )		Yes: Check detailsNo
Journal Aim & Scope
BMC Medical Genetics is an open access journal publishing original peer-reviewed research articles in the effects of genetic variation in individuals, families and among populations in relation to human health and disease.

Note: BMC Medical Genetics is now closed. This journal has merged with BMC Medical Genomics, a broad-scope, open access community journal for all medical genetics and genomics research.

Web of Science Quartiles
N/A
*Crowdsourced data
  • Journals In The Same Subject Area
  • CiteScore Trends
  • Self Citation Trends
  • Annual Article Volume Trends
  • Journal Title h-index CiteScore
    NATURE REVIEWS GENETICS32074.80
    NATURE GENETICS52738.60
    TRENDS IN GENETICS20825.10
    Annual Review of Genetics17112.20
    Annual Review of Genomics and Human Genetics10415.10
    AMERICAN JOURNAL OF HUMAN GENETICS28012.50
    GENETICS2238.70
    GENETICS IN MEDICINE11111.20
    CURRENT GENE THERAPY656.70
    FUNCTIONAL & INTEGRATIVE GENOMICS665.90
  • BMC Medical Genetics BMC Medical Genetics
    Predict CiteScore Trend：
    Steady Increase No Change Gradual Decline　 Refresh
 
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    ☰  Review(s)        
 
 
 

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    Journals In The Same Field
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