|
1
|
TGFB2 mutations cause familial thoracic aortic aneurysms and dissections associated with mild systemic features of Marfan syndrome.
|
Nat Genet
|
2012
|
2.50
|
|
2
|
Recurrent chromosome 16p13.1 duplications are a risk factor for aortic dissections.
|
PLoS Genet
|
2011
|
1.35
|
|
3
|
Copy number gain at Xp22.31 includes complex duplication rearrangements and recurrent triplications.
|
Hum Mol Genet
|
2011
|
1.25
|
|
4
|
Rare, nonsynonymous variant in the smooth muscle-specific isoform of myosin heavy chain, MYH11, R247C, alters force generation in the aorta and phenotype of smooth muscle cells.
|
Circ Res
|
2012
|
1.10
|
|
5
|
Aortic remodeling after transverse aortic constriction in mice is attenuated with AT1 receptor blockade.
|
Arterioscler Thromb Vasc Biol
|
2013
|
0.99
|
|
6
|
Small rare recurrent deletions and reciprocal duplications in 2q21.1, including brain-specific ARHGEF4 and GPR148.
|
Hum Mol Genet
|
2012
|
0.85
|
|
7
|
FOXE3 mutations predispose to thoracic aortic aneurysms and dissections.
|
J Clin Invest
|
2016
|
0.78
|
|
8
|
Top advances in functional genomics and translational biology for 2012.
|
Circ Cardiovasc Genet
|
2013
|
0.75
|