| Rank |
Title |
Journal |
Year |
PubWeight™‹?› |
|
1
|
Fox's in development and disease.
|
Trends Genet
|
2003
|
2.80
|
|
2
|
A review of anterior segment dysgeneses.
|
Surv Ophthalmol
|
2006
|
1.99
|
|
3
|
Repair of the degenerate retina by photoreceptor transplantation.
|
Proc Natl Acad Sci U S A
|
2012
|
1.79
|
|
4
|
Defining the integration capacity of embryonic stem cell-derived photoreceptor precursors.
|
Stem Cells
|
2012
|
1.52
|
|
5
|
Long-term survival of photoreceptors transplanted into the adult murine neural retina requires immune modulation.
|
Stem Cells
|
2010
|
1.42
|
|
6
|
Proper patterning of the optic fissure requires the sequential activity of BMP7 and SHH.
|
Development
|
2006
|
1.28
|
|
7
|
The level of BMP4 signaling is critical for the regulation of distinct T-box gene expression domains and growth along the dorso-ventral axis of the optic cup.
|
BMC Dev Biol
|
2006
|
1.19
|
|
8
|
Anophthalmos, microphthalmos, and typical coloboma in the United Kingdom: a prospective study of incidence and risk.
|
Invest Ophthalmol Vis Sci
|
2011
|
1.19
|
|
9
|
Comparative analysis of progenitor cells isolated from the iris, pars plana, and ciliary body of the adult porcine eye.
|
Stem Cells
|
2007
|
1.17
|
|
10
|
Adult ciliary epithelial cells, previously identified as retinal stem cells with potential for retinal repair, fail to differentiate into new rod photoreceptors.
|
Stem Cells
|
2010
|
1.13
|
|
11
|
Brief report: self-organizing neuroepithelium from human pluripotent stem cells facilitates derivation of photoreceptors.
|
Stem Cells
|
2013
|
1.11
|
|
12
|
A novel mechanistic spectrum underlies glaucoma-associated chromosome 6p25 copy number variation.
|
Hum Mol Genet
|
2008
|
1.09
|
|
13
|
Digenic inheritance of mutations in FOXC1 and PITX2 : correlating transcription factor function and Axenfeld-Rieger disease severity.
|
Hum Mutat
|
2011
|
1.08
|
|
14
|
Ocular developmental abnormalities and glaucoma associated with interstitial 6p25 duplications and deletions.
|
Invest Ophthalmol Vis Sci
|
2002
|
1.05
|
|
15
|
A novel homeobox mutation in the PITX2 gene in a family with Axenfeld-Rieger syndrome associated with brain, ocular, and dental phenotypes.
|
Am J Med Genet B Neuropsychiatr Genet
|
2006
|
0.99
|
|
16
|
Migration, integration and maturation of photoreceptor precursors following transplantation in the mouse retina.
|
Stem Cells Dev
|
2014
|
0.96
|
|
17
|
Absence of chx10 causes neural progenitors to persist in the adult retina.
|
Invest Ophthalmol Vis Sci
|
2006
|
0.93
|
|
18
|
Delayed expression of the Crx gene and photoreceptor development in the Chx10-deficient retina.
|
Invest Ophthalmol Vis Sci
|
2004
|
0.92
|
|
19
|
Anophthalmos, microphthalmos, and Coloboma in the United kingdom: clinical features, results of investigations, and early management.
|
Ophthalmology
|
2011
|
0.92
|
|
20
|
ATOH7 mutations cause autosomal recessive persistent hyperplasia of the primary vitreous.
|
Hum Mol Genet
|
2012
|
0.90
|
|
21
|
Induced pluripotent stem cell technology for generating photoreceptors.
|
Regen Med
|
2011
|
0.89
|
|
22
|
Regenerative medicine: DIY eye.
|
Nature
|
2011
|
0.89
|
|
23
|
Loss of Tbx2 delays optic vesicle invagination leading to small optic cups.
|
Dev Biol
|
2009
|
0.89
|
|
24
|
X-linked megalocornea caused by mutations in CHRDL1 identifies an essential role for ventroptin in anterior segment development.
|
Am J Hum Genet
|
2012
|
0.85
|
|
25
|
Foveal cavitation as an optical coherence tomography finding in central cone dysfunction.
|
Retina
|
2012
|
0.85
|
|
26
|
ARNT2 mutation causes hypopituitarism, post-natal microcephaly, visual and renal anomalies.
|
Brain
|
2013
|
0.84
|
|
27
|
Genetic risk for primary open-angle glaucoma determined by LMX1B haplotypes.
|
Invest Ophthalmol Vis Sci
|
2008
|
0.83
|
|
28
|
Derepression of HMGA2 gene expression in retinoblastoma is associated with cell proliferation.
|
Mol Med
|
2003
|
0.83
|
|
29
|
Neuronal function of Tbx20 conserved from nematodes to vertebrates.
|
Dev Biol
|
2008
|
0.82
|
|
30
|
Comparative analysis of the retinal potential of embryonic stem cells and amniotic fluid-derived stem cells.
|
Stem Cells Dev
|
2010
|
0.81
|
|
31
|
Mutation of SALL2 causes recessive ocular coloboma in humans and mice.
|
Hum Mol Genet
|
2014
|
0.81
|
|
32
|
CYP1B1-related anterior segment developmental anomalies novel mutations for infantile glaucoma and von Hippel's ulcer revisited.
|
Ophthalmology
|
2011
|
0.80
|
|
33
|
Atypical Peters plus syndrome with new associations.
|
J AAPOS
|
2010
|
0.79
|
|
34
|
Functional analysis of FOXE3 mutations causing dominant and recessive ocular anterior segment disease.
|
Hum Mutat
|
2015
|
0.79
|
|
35
|
Von Hippel-Lindau protein in the RPE is essential for normal ocular growth and vascular development.
|
Development
|
2012
|
0.79
|
|
36
|
Common TGFβ2, BMP4, and FOXC1 variants are not associated with primary open-angle glaucoma.
|
Mol Vis
|
2012
|
0.75
|
|
37
|
Isolation and culture of adult ciliary epithelial cells, previously identified as retinal stem cells, and retinal progenitor cells.
|
Curr Protoc Stem Cell Biol
|
2011
|
0.75
|