Marcy C. Speer

Autosomal dominant hypophosphataemic rickets is associated with mutations in FGF23

Kenneth E. White, W. Evans, Jeffery L.H. O'Riordan et al. · Nature Genetics · 2000 · 1.5K citations

Developmental Biology, Mendelian Disorder, Genetic Disorder +8

Chiari I Malformation Redefined: Clinical and Radiographic Findings for 364 Symptomatic Patients

Thomas H. Milhorat, Mike W. Chou, Elizabeth M. Trinidad et al. · Neurosurgery · 1999 · 1.3K citations

A Common <i>MUC5B</i> Promoter Polymorphism and Pulmonary Fibrosis

Max A. Seibold, Anastasia L. Wise, Marcy C. Speer et al. · New England Journal of Medicine · 2011 · 1.2K citations · Full text

Mutations in the activin receptor–like kinase 1 gene in hereditary haemorrhagic telangiectasia type 2

David W. Johnson, Jonathan Berg, Melanie A. Baldwin et al. · Nature Genetics · 1996 · 1.1K citations

Activin Receptor–like, Developmental Biology, Signal Transduction +7

Heterozygosity for a Surfactant Protein C Gene Mutation Associated with Usual Interstitial Pneumonitis and Cellular Nonspecific Interstitial Pneumonitis in One Kindred

Alan Q. Thomas, Kirk B. Lane, John A. Phillips et al. · American Journal of Respiratory and Critical Care Medicine · 2002 · 644 citations