|
1
|
Mutations in transforming growth factor-beta receptor type II cause familial thoracic aortic aneurysms and dissections.
|
Circulation
|
2005
|
2.77
|
|
2
|
Mutations in smooth muscle alpha-actin (ACTA2) cause coronary artery disease, stroke, and Moyamoya disease, along with thoracic aortic disease.
|
Am J Hum Genet
|
2009
|
2.50
|
|
3
|
Fatness, physical activity, and television viewing in children during the adiposity rebound period: the Iowa Bone Development Study.
|
Prev Med
|
2002
|
1.97
|
|
4
|
Mapping a locus for familial thoracic aortic aneurysms and dissections (TAAD2) to 3p24-25.
|
Circulation
|
2003
|
1.81
|
|
5
|
Sustained effect of early physical activity on body fat mass in older children.
|
Am J Prev Med
|
2009
|
1.73
|
|
6
|
The microcephaly-capillary malformation syndrome.
|
Am J Med Genet A
|
2011
|
1.50
|
|
7
|
Physical activity augments bone mineral accrual in young children: The Iowa Bone Development study.
|
J Pediatr
|
2006
|
1.28
|
|
8
|
Everyday activity predicts bone geometry in children: the iowa bone development study.
|
Med Sci Sports Exerc
|
2004
|
1.23
|
|
9
|
Early physical activity provides sustained bone health benefits later in childhood.
|
Med Sci Sports Exerc
|
2010
|
1.19
|
|
10
|
Reduced type I collagen utilization: a pathogenic mechanism in COL5A1 haplo-insufficient Ehlers-Danlos syndrome.
|
J Cell Biochem
|
2004
|
0.96
|
|
11
|
Paucity of skeletal manifestations in Hispanic families with FBN1 mutations.
|
Eur J Med Genet
|
2009
|
0.87
|
|
12
|
Rare recessive loss-of-function methionyl-tRNA synthetase mutations presenting as a multi-organ phenotype.
|
BMC Med Genet
|
2013
|
0.86
|
|
13
|
Clinical insights gained from eight new cases and review of reported cases with Jeune syndrome (asphyxiating thoracic dystrophy).
|
Am J Med Genet A
|
2011
|
0.86
|
|
14
|
Effects of enamel matrix genes on dental caries are moderated by fluoride exposures.
|
Hum Genet
|
2014
|
0.81
|
|
15
|
A hip analysis protocol for pediatric bone densitometry: the Iowa Bone Development Study.
|
J Clin Densitom
|
2010
|
0.78
|
|
16
|
Mutations in sphingosine-1-phosphate lyase cause nephrosis with ichthyosis and adrenal insufficiency.
|
J Clin Invest
|
2017
|
0.75
|