E. J. M. Schuurman
Combined Ophthalmic Research Rotterdam(NL)
Publications by Year
Research Areas
Retinal Development and Disorders, melanin and skin pigmentation, Retinal Diseases and Treatments, Photoreceptor and optogenetics research, Glaucoma and retinal disorders
Most-Cited Works
- → Multipoint linkage analysis in X-linked ocular albinism of the Nettleship-Falls type(1991)35 cited
- → Refinement of the Localization of the X-Linked Ocular Albinism Gene(1993)17 cited
- → Additional Evidence for a Gene Locus for Progressive Cone Dystrophy with Late Rod Involvement in Xp21.1-p11.3(1993)16 cited
- → Multipoint linkage analysis and homogeneity tests in 15 Dutch X-linked retinitis pigmentosa families(1995)15 cited
- → Detection of a new submicroscopic Norrie disease deletion interval with a novel DNA probe isolated by differential <i>Alu </i>PCR fingerprint cloning(1993)15 cited
- → Nance-Horan Syndrome: Linkage Analysis in a Family from The Netherlands(1994)14 cited
- → Conclusive evidence for a distinct congenital stationary night blindness locus in Xp21.1.(1996)11 cited
- → Localization of a novel X-linked congenital stationary night blindness locus: close linkage to the RP3 type retinitis pigmentosa gene region(1995)10 cited
- → DNA carrier detection in X‐linked progressive cone dystrophy(1994)4 cited
- Are X-linked congenital stationary night blindness and X-linked retinitis pigmentosa genetically allelic?(1996)