Molly Bray

Author PubWeight™ 13.96^‹?›

Top papers

Rank	Title	Journal	Year	PubWeight™‹?›
1	A combined analysis of genomewide linkage scans for body mass index from the National Heart, Lung, and Blood Institute Family Blood Pressure Program.	Am J Hum Genet	2002	1.87
2	Mutations in SPATA7 cause Leber congenital amaurosis and juvenile retinitis pigmentosa.	Am J Hum Genet	2009	1.72
3	Genome-wide association study identifies a susceptibility locus for thoracic aortic aneurysms and aortic dissections spanning FBN1 at 15q21.1.	Nat Genet	2011	1.48
4	Altered DNA methylation profile in idiopathic pulmonary fibrosis.	Am J Respir Crit Care Med	2012	1.47
5	Gene expression in the human mammary epithelium during lactation: the milk fat globule transcriptome.	Physiol Genomics	2008	1.28
6	The genetics of colored sequence synesthesia: suggestive evidence of linkage to 16q and genetic heterogeneity for the condition.	Behav Brain Res	2011	1.14
7	Risk of atherosclerosis: interaction of smoking and glutathione S-transferase genes.	Epidemiology	2003	0.94
8	LPL polymorphism predicts stroke risk in men.	Genet Epidemiol	2002	0.92
9	Genomic screening identifies novel linkages and provides further evidence for a role of MYH9 in nonsyndromic cleft lip and palate.	Eur J Hum Genet	2008	0.88
10	MCTP2 is a dosage-sensitive gene required for cardiac outflow tract development.	Hum Mol Genet	2013	0.83
11	Human genome-wide association and mouse knockout approaches identify platelet supervillin as an inhibitor of thrombus formation under shear stress.	Circulation	2012	0.81
12	Large deletions and uniparental disomy detected by SNP arrays in adults with thoracic aortic aneurysms and dissections.	Am J Med Genet A	2010	0.76