Researchclopedia

Research Researchers Institutions Topics Submit About

Command Palette

Search for a command to run...

Researchclopedia

Research Researchers Institutions About

© 2026 Researchclopedia. Powered by OpenAlex under CC0 license.

Clair A. Francomano | Researchclopedia

Back to researchers

Clair A. Francomano

Indiana University Health ORCID

238

Works

17,711

Citations

61

h-index

142

i10-index

Research Topics

Connective tissue disorders research Dermatological and Skeletal Disorders Dupuytren's Contracture and Treatments

Affiliations

Rutgers, The State University of New Jersey1984–1984

University of Insubria1998–1998

University of Maryland, Baltimore1984–1984

Hospital for Special Surgery2002–2002

Cedars-Sinai Medical Center1992–1993

Top Works

Marfan syndrome caused by a recurrent de novo missense mutation in the fibrillin gene

Harry C. Dietz,Carry Cutting,et al.

19912,054 citations

Cell Adhesion Molecules Research

Craniofacial Disorders and Treatments

The 2017 international classification of the Ehlers–Danlos syndromes

Fransiska Malfait,Clair A. Francomano,et al.

20171,822 citations

Identification of a mutation in the gene encoding the alpha subunit of the stimulatory G protein of adenylyl cyclase in McCune-Albright syndrome.

William F. Schwindinger,Clair A. Francomano,et al.

1992497 citations

Achondroplasia is defined by recurrent G380R mutations of FGFR3.

Gary A. Bellus,Timothy Hefferon,et al.

1995483 citations

A recurrent mutation in the tyrosine kinase domain of fibroblast growth factor receptor 3 causes hypochondroplasia

Gary A. Bellus,Iain McIntosh,et al.

1995476 citations

The Skipping of Constitutive Exons in Vivo Induced by Nonsense Mutations

Harry C. Dietz,David Valle,et al.

1993432 citations

Mutations in exon 17B of cartilage oligomeric matrix protein (COMP) cause pseudoachondroplasia

Jacqueline T. Hecht,Laura D. Nelson,et al.

1995400 citations

A unique point mutation in the fibroblast growth factor receptor 3 gene (FGFR3) defines a new craniosynostosis syndrome.

Maximilian Muenke,Karen W. Gripp,et al.

1997394 citations

Mutations in a new gene in Ellis-van Creveld syndrome and Weyers acrodental dysostosis

Víctor L. Ruiz‐Pérez,Susan Ide,et al.

2000353 citations