Back to Top
Go Back
Journal Photo for BMC Medical Genetics
Peer reviewed only Open Access

BMC Medical Genetics (BMCMG)

Publisher : BioMed Central
Clinical medicine Pathology
Claim Your Journal Get PRC Visit Website
e-ISSN 1471-2350
Issue Frequency Monthly
Impact Factor 4.4
Est. Year 2000
Mobile 4402031922009
Country United Kingdom
Language English
APC YES
Impact Factor Assignee Google Scholar
Email bmcmedicalgenomics@biomedcentral.com

Journal Descriptions

BMC Medical Genomics is an open access journal publishing original peer-reviewed research articles in all aspects of functional genetics and genomics, genome structure, genome-scale population genetics, epigenetics and epigenomics, proteomics, systems analysis, and pharmacogenomics in relation to human health and disease.

BMC Medical Genetics (BMCMG) is :-

  • International, Peer-Reviewed, Open Access, Refereed, Clinical medicine, Pathology , Online , Monthly Journal

  • UGC Approved, ISSN Approved: P-ISSN E-ISSN: 1471-2350, Established: 2000, Impact Factor: 4.4
  • Does Not Provide Crossref DOI

  • Indexed in: DOAJ

  • Not indexed in Scopus, WoS, PubMed, UGC CARE

Indexing

Publications of BMCMG

Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness
Emelia J. Benjamin November, 2007
ackground About one quarter of adults are hypertensive and high blood pressure carries increased risk for heart disease, stroke, kidney disease and death. Increased arterial stiffness is a ...
Framingham Heart Study 100K project: genome-wide associations for cardiovascular disease outcomes
Emelia J. Benjamin September, 2007
Background Cardiovascular disease (CVD) and its most common manifestations – including coronary heart disease (CHD), stroke, heart failure (HF), and atrial fibrillation (AF) – are major...
Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study
Emelia J. Benjamin September, 2007
Background Family studies and heritability estimates provide evidence for a genetic contribution to variation in the human life span. Methods We conducted a genome wide association stud...
The Framingham Heart Study 100K SNP genome-wide association study resource: overview of 17 phenotype working group reports
Emelia J. Benjamin September, 2007
Background The Framingham Heart Study (FHS), founded in 1948 to examine the epidemiology of cardiovascular disease, is among the most comprehensively characterized multi-generational studie...