Marcy C. Speer - Concepedia

Author

Marcy C. Speer

Also Known As

Hirata, Hiromi, Hu-Lince, Diane, M C Speer, M Speer, M. C. SPEER, M. C. Speer, M. SPEER, M. Speer, M.C Speer, M.C. Speer

173

Publications

13.2K

Citations

H-Index

122

Concepts

All Affiliations

Duke Medical Center Duke University Hospital Duke University Center for Human Genetics University of Miami

About

Marcy C. Speer is an author at Duke Medical Center specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	29	48	5.8K
2	Public Health	10	10	569
3	Health Sciences	2	2	105
4	Natural Sciences	2	2	53
5	Engineering	1	1	230

Marcy C. Speer

Publications

11.8K

Citations

H-Index

Page 1

	Year	Citations
Autosomal dominant hypophosphataemic rickets is associated with mutations in FGF23 Kenneth E. White, W. Evans, Jeffery L.H. O'Riordan, Nature Genetics Developmental BiologyMendelian DisorderGenetic DisorderGeneticsInherited Metabolic Disease	2000	1.5K
Chiari I Malformation Redefined: Clinical and Radiographic Findings for 364 Symptomatic Patients Thomas H. Milhorat, Mike W. Chou, Elizabeth M. Trinidad, Neurosurgery	1999	1.3K
A Common <i>MUC5B</i> Promoter Polymorphism and Pulmonary Fibrosis Max A. Seibold, Anastasia L. Wise, Marcy C. Speer, New England Journal of Medicine	2011	1.2K
Mutations in the activin receptor–like kinase 1 gene in hereditary haemorrhagic telangiectasia type 2 David W. Johnson, Jonathan Berg, Melanie A. Baldwin, Nature Genetics Activin Receptor–likeDevelopmental BiologySignal TransductionGenetic DisorderGenetics	1996	1.1K
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, American Journal of Respiratory and Critical Care Medicine	2002	644
Clinical and Pathologic Features of Familial Interstitial Pneumonia Mark P. Steele, Marcy C. Speer, James E. Loyd, American Journal of Respiratory and Critical Care Medicine	2005	423
Mutations in the pleckstrin homology domain of dynamin 2 cause dominant intermediate Charcot-Marie-Tooth disease Stephan Züchner, Maher Noureddine, Marina Kennerson, Nature Genetics Mendelian DisorderGeneticsPathogenesisPleckstrin Homology DomainMolecular Biology	2005	356
Stac3 is a component of the excitation–contraction coupling machinery and mutated in Native American myopathy Eric J. Horstick, Jeremy W. Linsley, James J. Dowling, Nature Communications CytoskeletonPhysiologyMolecular BiologyNative American Myopathy	2013	256
Type VI collagen mutations in Bethlem myopathy, an autosomal dominant myopathy with contractures G. Joost Jöbsis, H Keizers, Jeroen Vreijling, Nature Genetics RheumatologyMendelian DisorderAutoimmune DiseaseGenetic DisorderBethlem Myopathy	1996	249
Review Article: Chiari Type I Malformation with or Without Syringomyelia: Prevalence and Genetics Marcy C. Speer, David S. Enterline, Lorraine Mehltretter, Journal of Genetic Counseling	2003	237

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