Emeline F Nandrot

Author PubWeight™ 10.10^‹?›

Rank	Title	Journal	Year	PubWeight™‹?›
1	TRPM1 is mutated in patients with autosomal-recessive complete congenital stationary night blindness.	Am J Hum Genet	2009	1.93
2	EYS is a major gene for rod-cone dystrophies in France.	Hum Mutat	2010	1.39
3	MerTK activation during RPE phagocytosis in vivo requires alphaVbeta5 integrin.	Adv Exp Med Biol	2006	1.05
4	Three gene-targeted mouse models of RNA splicing factor RP show late-onset RPE and retinal degeneration.	Invest Ophthalmol Vis Sci	2011	0.94
5	Disease-causing mutations in BEST1 gene are associated with altered sorting of bestrophin-1 protein.	Int J Mol Sci	2013	0.94
6	Dietary antioxidants prevent age-related retinal pigment epithelium actin damage and blindness in mice lacking αvβ5 integrin.	Free Radic Biol Med	2011	0.89
7	Human induced pluripotent stem cells as a tool to model a form of Leber congenital amaurosis.	Cell Reprogram	2013	0.86
8	In vitro differentiation of retinal pigment epithelium from adult retinal stem cells.	Pigment Cell Melanoma Res	2010	0.80
9	The Signalling Role of the avβ5-Integrin Can Impact the Efficacy of AAV in Retinal Gene Therapy.	Pharmaceuticals (Basel)	2012	0.77
10	On your marks…get bound…internalize!	Adv Exp Med Biol	2012	0.77
11	Collectin-11 Is an Important Modulator of Retinal Pigment Epithelial Cell Phagocytosis and Cytokine Production.	J Innate Immun	2017	0.75