Liesbeth M. Bleeker-Wagemakers
Leiden University(NL)Trinity College Dublin(IE)Institute of Human Genetics(PL)Combined Ophthalmic Research Rotterdam(NL)University of Amsterdam(NL)Erasmus University Rotterdam(NL)University of Lübeck(DE)
Publications by Year
Research Areas
Retinal Development and Disorders, Neurological diseases and metabolism, melanin and skin pigmentation, Oral Health Pathology and Treatment, Porphyrin Metabolism and Disorders
Most-Cited Works
- → Gelsolin–derived familial amyloidosis caused by asparagine or tyrosine substitution for aspartic acid at residue 187(1992)176 cited
- → Mutations in the candidate gene for Norrie disease(1992)144 cited
- → Assignment of a Gene for Autosomal Recessive Retinitis Pigmentosa (RP12) to Chromosome 1q31-q32.1 in an Inbred and Genetically Heterogeneous Disease Population(1994)119 cited
- → Submicroscopic interstitial deletion of the X chromosome explains a complex genetic syndrome dominated by Norrie disease(1986)74 cited
- → Nome's disease: close linkage with genetic markers from the proximal short arm of the X chromosome(1985)54 cited
- → Close linkage between Norrie disease, a cloned DNA sequence from the proximal short arm, and the centromere of the X chromosome(1985)52 cited