Jules G. Leroy

Mutations in the Transmembrane Natriuretic Peptide Receptor NPR-B Impair Skeletal Growth and Cause Acromesomelic Dysplasia, Type Maroteaux

Cynthia F. Bartels, Hülya Bükülmez, Pius S. Padayatti et al. · The American Journal of Human Genetics · 2004 · 363 citations · Full text

Sclerostin, Signal Transduction, Molecular Physiology +8

Mutant Enzymatic and Cytological Phenotypes in Cultured Human Fibroblasts

Jules G. Leroy, Robert DeMars · Science · 1967 · 244 citations

Fibrosis, Ocular Disease, Acid Phosphatase +15

Mutations in PIEZO2 Cause Gordon Syndrome, Marden-Walker Syndrome, and Distal Arthrogryposis Type 5

Margaret J. McMillin, Anita E. Beck, Jessica X. Chong et al. · The American Journal of Human Genetics · 2014 · 214 citations · Full text

Mendelian Disorder, Genetic Disorder, Genetics +4

I-Cell Disease: Biochemical Studies

Jules G. Leroy, Mae Wan Ho, Monica C. MacBrinn et al. · Pediatric Research · 1972 · 213 citations · Full text

Autoimmune Disease, Disease Mechanism, Pathogenesis +6

Mutations in different components of FGF signaling in LADD syndrome

Edyta Rohmann, Han G. Brunner, Hülya Kayserili et al. · Nature Genetics · 2006 · 207 citations

Developmental Biology, Mendelian Disorder, Human Growth +7