Douglas J. Wilkin
National Institutes of Health(US)National Human Genome Research Institute(US)
Publications by Year
Research Areas
Connective tissue disorders research, Cell Adhesion Molecules Research, Osteoarthritis Treatment and Mechanisms, Mitochondrial Function and Pathology, Bone Metabolism and Diseases
Most-Cited Works
- → Thanatophoric dysplasia (types I and II) caused by distinct mutations in fibroblast growth factor receptor 3(1995)605 cited
- → Calcification in atherosclerosis: Bone biology and chronic inflammation at the arterial crossroads(2003)452 cited
- → Heterozygous mutations in the gene encoding noggin affect human joint morphogenesis(1999)346 cited
- → The Molecular and Genetic Basis of Fibroblast Growth Factor Receptor 3 Disorders: The Achondroplasia Family of Skeletal Dysplasias, Muenke Craniosynostosis, and Crouzon Syndrome with Acanthosis Nigricans*(2000)321 cited
- → 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
- → Mutations in Fibroblast Growth-Factor Receptor 3 in Sporadic Cases of Achondroplasia Occur Exclusively on the Paternally Derived Chromosome(1998)227 cited
- → Increased Expression of Membrane Type 3-Matrix Metalloproteinase in Human Atherosclerotic Plaque(2002)175 cited
- → The Xenopus XIHbox 6 homeo protein, a marker of posterior neural induction, is expressed in proliferating neurons(1990)126 cited
- → The Stickler syndrome: Genotype/phenotype correlation in 10 families with Stickler syndrome resulting from seven mutations in the type II collagen gene locus COL2A1(2003)105 cited