Eduard Schmid

Author PubWeight™ 9.03^‹?›

Rank	Title	Journal	Year	PubWeight™‹?›
1	Mutations in RDH12 encoding a photoreceptor cell retinol dehydrogenase cause childhood-onset severe retinal dystrophy.	Nat Genet	2004	2.40
2	CaV1.3 L-type Ca2+ channels modulate depression-like behaviour in mice independent of deaf phenotype.	Int J Neuropsychopharmacol	2009	1.10
3	The phenotype of early-onset retinal degeneration in persons with RDH12 mutations.	Invest Ophthalmol Vis Sci	2007	0.89
4	Peptidergic nerves in the eye, their source and potential pathophysiological relevance.	Brain Res Rev	2006	0.84
5	Joubert-like syndrome unlinked to known candidate loci.	J Pediatr	2004	0.79
6	Secretoneurin in the peripheral ocular innervation.	Invest Ophthalmol Vis Sci	2005	0.79
7	Tolerability of N-chlorotaurine plus ammonium chloride in the rabbit and human eye--a phase 1 clinical study.	Graefes Arch Clin Exp Ophthalmol	2008	0.78
8	Secretoneurin and the tachykinins substance P and neurokinin-A/B in NMDA-induced excitotoxicity in the rat retina.	Regul Pept	2010	0.77
9	N-chlorotaurine and its analogues N,N-dichloro-2,2-dimethyltaurine and N-monochloro-2,2-dimethyltaurine are safe and effective bactericidal agents in ex vivo corneal infection models.	Acta Ophthalmol	2012	0.76
10	Substance P and secretoneurin in vitreous aspirates of patients with various vitreoretinal diseases.	Peptides	2008	0.75
11	VIP, PACAP-38, BDNF and ADNP in NMDA-induced excitotoxicity in the rat retina.	Acta Ophthalmol	2010	0.75
12	PE-11, a peptide derived from chromogranin B, in the rat eye.	Peptides	2011	0.75