|
1
|
Early auditory processing in area V5/MT+ of the congenitally blind brain.
|
J Neurosci
|
2013
|
1.58
|
|
2
|
Novel heterozygous OTX2 mutations and whole gene deletions in anophthalmia, microphthalmia and coloboma.
|
Hum Mutat
|
2008
|
1.21
|
|
3
|
How genetically heterogeneous is Kabuki syndrome?: MLL2 testing in 116 patients, review and analyses of mutation and phenotypic spectrum.
|
Eur J Hum Genet
|
2011
|
1.20
|
|
4
|
Imaging studies in congenital anophthalmia reveal preservation of brain architecture in 'visual' cortex.
|
Brain
|
2009
|
1.14
|
|
5
|
ALDH1A3 mutations cause recessive anophthalmia and microphthalmia.
|
Am J Hum Genet
|
2013
|
1.12
|
|
6
|
Recessive and dominant mutations in retinoic acid receptor beta in cases with microphthalmia and diaphragmatic hernia.
|
Am J Hum Genet
|
2013
|
1.04
|
|
7
|
Different mutations in the NF1 gene are associated with Neurofibromatosis-Noonan syndrome (NFNS).
|
Am J Med Genet A
|
2003
|
1.01
|
|
8
|
Language networks in anophthalmia: maintained hierarchy of processing in 'visual' cortex.
|
Brain
|
2012
|
0.93
|
|
9
|
Absence of SIX6 mutations in microphthalmia, anophthalmia, and coloboma.
|
Invest Ophthalmol Vis Sci
|
2004
|
0.89
|
|
10
|
MLGA: a cost-effective approach to the diagnosis of gene deletions in eye development anomalies.
|
Mol Vis
|
2009
|
0.79
|
|
11
|
The fate of the oculomotor system in clinical bilateral anophthalmia.
|
Vis Neurosci
|
2012
|
0.75
|