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Ophthalmic Genetics|April 13, 2005
Novel mutations in MYO7A and USH2A in Usher syndromeCécilia Maubaret, Jean-Michel Griffoin, Bernard Arnaud, et al.DNA and Cell Biology|December 20, 2002
Identification of preferentially expressed mRNAs in retina and cochleaCécilia Maubaret, Cécile Delettre, Sandrine Sola, et al.The Journal of Clinical Endocrinology and Metabolism|May 15, 2014
Plasma estrogen levels, estrogen receptor gene variation, and ischemic arterial disease in postmenopausal women: the three-city prospective cohort studyValérie Scarabin-Carré, Sylvie Brailly-Tabard, Marie-Laure Ancelin, et al.Molecular Vision|March 16, 2012
Functional characterization of a novel c.614-622del rhodopsin mutation in a French pedigree with retinitis pigmentosaCécilia Maubaret, Maria Kosmaoglou, Sancy Low, et al.Plos One|November 14, 2013
Association of HDL-related loci with age-related macular degeneration and plasma lutein and zeaxanthin: the Alienor studyBénédicte M J Merle, Cécilia Maubaret, Jean-François Korobelnik, et al.BMC Public Health|July 31, 2012
Health and aging in elderly farmers: the AMI cohortKarine Pérès, Fanny Matharan, Michèle Allard, et al.Journal of Neurology, Neurosurgery, and Psychiatry|February 15, 2013
The Val158Met COMT polymorphism is a modifier of the age at onset in Parkinson's disease with a sexual dimorphismStephan Klebe, Jean-Louis Golmard, Michael A Nalls, et al.Nature Genetics|September 1, 2014
Genome-wide analysis of multi-ancestry cohorts identifies new loci influencing intraocular pressure and susceptibility to glaucomaPirro G Hysi, Ching-Yu Cheng, Henriët Springelkamp, et al.Pageof 1