Douglas J. Wilkin

Thanatophoric dysplasia (types I and II) caused by distinct mutations in fibroblast growth factor receptor 3

Patricia L. Tavormina, Rita Shiang, Leslie M. Thompson et al. · Nature Genetics · 1995 · 605 citations

Thanatophoric Dysplasia, Fibrosis, Mendelian Disorder +8

Calcification in atherosclerosis: Bone biology and chronic inflammation at the arterial crossroads

Terence M. Doherty, Kamlesh Asotra, Lorraine A. Fitzpatrick et al. · Proceedings of the National Academy of Sciences · 2003 · 449 citations · Full text

Engineering, Biomedical Engineering, Orthopaedic Surgery +20

Heterozygous mutations in the gene encoding noggin affect human joint morphogenesis

Yaoqin Gong, Deborah Krakow, José Roberto Marcelino et al. · Nature Genetics · 1999 · 346 citations

Developmental Biology, Genetic Disorder, Developmental Genetics +7

Evidence That a Locus for Familial High Myopia Maps to Chromosome 18p

Terri L. Young, Shawn M. Ronan, Leslie A. Drahozal et al. · The American Journal of Human Genetics · 1998 · 279 citations · Full text

Developmental Biology, Cytogenetics, Genetic Disorder +3

A Second Locus for Familial High Myopia Maps to Chromosome 12q

Terri L. Young, Shawn M. Ronan, Alison B. Alvear et al. · The American Journal of Human Genetics · 1998 · 266 citations · Full text

Ophthalmology, Cytogenetics, Genetic Disorder +5