Scott C. Wildenberg
University of Minnesota(US)
Publications by Year
Research Areas
melanin and skin pigmentation, Biochemical Analysis and Sensing Techniques, Corneal surgery and disorders, Connective tissue disorders research, RNA and protein synthesis mechanisms
Most-Cited Works
- → Evidence That a Locus for Familial High Myopia Maps to Chromosome 18p(1998)279 cited
- → A Second Locus for Familial High Myopia Maps to Chromosome 12q(1998)266 cited
- Mutation in and lack of expression of tyrosinase-related protein-1 (TRP-1) in melanocytes from an individual with brown oculocutaneous albinism: a new subtype of albinism classified as "OCA3".(1996)
- → New Locus for Autosomal Dominant High Myopia Maps to the Long Arm of Chromosome 17(2003)180 cited
- → The mouse pale ear ( ep ) mutation is the homologue of human Hermansky–Pudlak syndrome(1997)133 cited
- A gene causing Hermansky-Pudlak syndrome in a Puerto Rican population maps to chromosome 10q2.(1995)
- → Evidence for Locus Heterogeneity in Puerto Ricans with Hermansky-Pudlak Syndrome(1997)62 cited
- → Identification of a Novel Transcript Produced by the Gene Responsible for the Hermansky–Pudlak Syndrome in Puerto Rico(1998)14 cited
- → <title>Genetic linkage analysis using pooled DNA and infrared detection of tailed STRP primer patterns</title>(1996)1 cited
- Identification of a mutation in the tyrosinase related protein 1 (TRP1) gene associated with brown oculocutaneous albinism (OCA3)(1994)