BMC Medical Genetics

Journal

Overview
Identity

Publication Venue For

Genome-wide association study of lung function and clinical implication in heavy smokers. 19. 2018

Analysis of TACI mutations in CVID & RESPI patients who have inherited HLA B*44 or HLA*B8. 10:100. 2009

Genomewide association study for onset age in Parkinson disease. 10:98. 2009

The INSIG2 rs7566605 genetic variant does not play a major role in obesity in a sample of 24,722 individuals from four cohorts. 10. 2009

QTLs of factors of the metabolic syndrome and echocardiographic phenotypes: The hypertension genetic epidemiology network study. 9. 2008

Polymorphisms near EXOC4 and LRGUK on chromosome 7q32 are associated with Type 2 Diabetes and fasting glucose; The NHLBI Family Heart Study. 9. 2008

Failure to replicate an association of SNPs in the oxidized LDL receptor gene (OLR1) with CAD. 9. 2008

Dominant inhibition of Fas ligand-mediated apoptosis due to a heterozygous mutation associated with autoimmune lymphoproliferative syndrome (ALPS) Type Ib. 8. 2007

Genome-wide significance for a modifier of age at neurological onset in Huntington's disease at 6q23-24: The HD MAPS study. 7. 2006

Evidence for a gene influencing heart rate on chromosome 5p13-14 in a meta-analysis of genome-wide scans from the NHLBI Family Blood Pressure Program. 7. 2006

International Standard Serial Number (issn)

1471-2350

Electronic International Standard Serial Number (eissn)

1471-2350