2.1(top 8%)
Impact Factor
2.3(top 8%)
extended IF
72(top 5%)
H-Index
3.6K
authors
2.3K
papers
41.4K
citations
4.1K
citing journals
38.1K
citing authors

Most Cited Articles of BMC Medical Genetics

TitleYearCitations
A genome-wide association study for blood lipid phenotypes in the Framingham Heart Study2007257
An open access database of genome-wide association results2009228
Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness2007216
Association of HLA class I with severe acute respiratory syndrome coronavirus infection2003204
Genome-wide association with bone mass and geometry in the Framingham Heart Study2007200
Impact of nine common type 2 diabetes risk polymorphisms in Asian Indian Sikhs: PPARG2 (Pro12Ala), IGF2BP2, TCF7L2 and FTO variants confer a significant risk2008199
Theories of schizophrenia: a genetic-inflammatory-vascular synthesis2005190
Genome-wide association of sleep and circadian phenotypes2007183
Association between TCF7L2 gene polymorphisms and susceptibility to type 2 diabetes mellitus: a large Human Genome Epidemiology (HuGE) review and meta-analysis2009173
Generation Scotland: the Scottish Family Health Study; a new resource for researching genes and heritability2006164
Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study2007156
Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study2007156
The Framingham Heart Study 100K SNP genome-wide association study resource: overview of 17 phenotype working group reports2007152
Cytogenetic abnormalities and fragile-X syndrome in Autism Spectrum Disorder2005152
The SDH mutation database: an online resource for succinate dehydrogenase sequence variants involved in pheochromocytoma, paraganglioma and mitochondrial complex II deficiency2005142
Association of HLA-B*5801 allele and allopurinol-induced Stevens Johnson syndrome and toxic epidermal necrolysis: a systematic review and meta-analysis2011139
Framingham Heart Study 100K project: genome-wide associations for cardiovascular disease outcomes2007139
Genome-wide association to body mass index and waist circumference: the Framingham Heart Study 100K project2007128
Genome-wide association study identifies candidate genes for Parkinson's disease in an Ashkenazi Jewish population2011126
118 SNPs of folate-related genes and risks of spina bifida and conotruncal heart defects2009124
The FH mutation database: an online database of fumarate hydratase mutations involved in the MCUL (HLRCC) tumor syndrome and congenital fumarase deficiency2008115
New adipokines vaspin and omentin. Circulating levels and gene expression in adipose tissue from morbidly obese women2011113
Association of the rs738409 polymorphism in PNPLA3 with liver damage and the development of nonalcoholic fatty liver disease2010110
Genome-wide association study for subclinical atherosclerosis in major arterial territories in the NHLBI's Framingham Heart Study2007110
Genome-wide and Ordered-Subset linkage analyses provide support for autism loci on 17q and 19p with evidence of phenotypic and interlocus genetic correlates2005110