|
1
|
Association of oestrogen receptor alpha gene polymorphism with the angiographic extent of coronary artery disease.
|
Eur Heart J
|
2004
|
1.14
|
|
2
|
Refractive profile in oculocutaneous albinism and its correlation with final visual outcome.
|
Br J Ophthalmol
|
2011
|
1.06
|
|
3
|
Amelogenin, a major structural protein in mineralizing enamel, is also expressed in soft tissues: brain and cells of the hematopoietic system.
|
Eur J Oral Sci
|
2006
|
1.05
|
|
4
|
Amelogenin in cranio-facial development: the tooth as a model to study the role of amelogenin during embryogenesis.
|
J Exp Zool B Mol Dev Evol
|
2009
|
1.04
|
|
5
|
Homozygosity for a novel ABCA4 founder splicing mutation is associated with progressive and severe Stargardt-like disease.
|
Invest Ophthalmol Vis Sci
|
2007
|
1.00
|
|
6
|
Amelogenin expression in long bone and cartilage cells and in bone marrow progenitor cells.
|
Anat Rec (Hoboken)
|
2007
|
0.97
|
|
7
|
Regeneration of bone and periodontal ligament induced by recombinant amelogenin after periodontitis.
|
J Cell Mol Med
|
2009
|
0.96
|
|
8
|
High yield of biologically active recombinant human amelogenin using the baculovirus expression system.
|
Protein Expr Purif
|
2005
|
0.96
|
|
9
|
Identification of the first non-Jewish mutation in familial Dysautonomia.
|
Am J Med Genet A
|
2003
|
0.91
|
|
10
|
Estrogen receptor alpha gene polymorphisms are associated with the angiographic extent of coronary artery disease.
|
J Clin Endocrinol Metab
|
2005
|
0.88
|
|
11
|
A new genetic isolate with a unique phenotype of syndromic oculocutaneous albinism: clinical, molecular, and cellular characteristics.
|
Hum Mutat
|
2006
|
0.87
|
|
12
|
Localization, quantification, and characterization of tuftelin in soft tissues.
|
Anat Rec (Hoboken)
|
2007
|
0.80
|
|
13
|
Retinitis pigmentosa caused by mutations in the ciliary MAK gene is relatively mild and is not associated with apparent extra-ocular features.
|
Acta Ophthalmol
|
2014
|
0.78
|
|
14
|
A novel de novo PAX6 mutation in an Ashkenazi-Jewish family with aniridia.
|
Mol Vis
|
2008
|
0.78
|
|
15
|
Biphasic influence of hypoxia on tuftelin expression in mouse mesenchymal C3H10T1/2 stem cells.
|
Eur J Oral Sci
|
2011
|
0.77
|
|
16
|
Fetal inherited thrombophilias influence the severity of preeclampsia, IUGR and placental abruption.
|
Eur J Obstet Gynecol Reprod Biol
|
2004
|
0.77
|
|
17
|
The induction of tuftelin expression in PC12 cell line during hypoxia and NGF-induced differentiation.
|
J Cell Physiol
|
2011
|
0.76
|
|
18
|
Prenatal molecular diagnosis of oculocutaneous albinism (OCA) in a large cohort of Israeli families.
|
Prenat Diagn
|
2009
|
0.75
|
|
19
|
Combined Occurrence of Autosomal Dominant Aniridia and Autosomal Recessive Albinism in Several Members of a Family.
|
Ophthalmic Genet
|
2015
|
0.75
|