Reed E. Pyeritz - Concepedia

Author

Reed E. Pyeritz

Also Known As

Bartolomeo Di, Calif, Carla Bann, G McGee, Lori A. Orlando, Pyeritz Reed, Pyeritz, R. E., Pyeritz, Reed, Pyeritz, Reed E., R E Pyeritz

473

Publications

37.2K

Citations

H-Index

257

Concepts

All Affiliations

Johns Hopkins University University of Pennsylvania Johns Hopkins Medicine University of Michigan Massachusetts General Hospital

About

Reed E. Pyeritz is an author at Johns Hopkins University specializing in medicine, cardiology, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	48	102	11.9K
2	Health Sciences	7	7	435
3	Education	1	1	131
4	Engineering	1	1	73
5	Humanities	1	1	26

Reed E. Pyeritz

201

Publications

31.4K

Citations

H-Index

Page 1

	Year	Citations
The revised Ghent nosology for the Marfan syndrome: Table 1 Bart Loeys, Harry C. Dietz, Alan C. Braverman, Journal of Medical Genetics	2010	2.2K
Marfan syndrome caused by a recurrent de novo missense mutation in the fibrillin gene Harry C. Dietz, Carry Cutting, Reed E. Pyeritz, Nature Marfan SyndromeMendelian DisorderGenetic DisorderGeneticsPathogenesis	1991	2K
Transplantability and therapeutic effects of bone marrow-derived mesenchymal cells in children with osteogenesis imperfecta Edwin M. Horwitz, Darwin J. Prockop, Lorraine A. Fitzpatrick, Nature Medicine Tissue EngineeringRegenerative MedicineCell TherapyTransplantationMarrow Transplantation	1999	1.8K
Aneurysm Syndromes Caused by Mutations in the TGF-β Receptor Bart Loeys, Ulrike Schwarze, Tammy M. Holm, New England Journal of Medicine	2006	1.6K
Revised diagnostic criteria for the Marfan syndrome Anne De Paepe, Richard B. Devereux, Harry C. Dietz, American Journal of Medical Genetics	1996	1.6K
The natural history of homocystinuria due to cystathionine beta-synthase deficiency. S. Harvey Mudd, Flemming Skovby, Harvey L. Levy, PubMed	1985	1.3K
Progression of Aortic Dilatation and the Benefit of Long-Term β-Adrenergic Blockade in Marfan's Syndrome Jennifer L. Shores, Kenneth R. Berger, Edmond A. Murphy, New England Journal of Medicine	1994	1.1K
International guidelines for the diagnosis and management of hereditary haemorrhagic telangiectasia Marie E. Faughnan, Valerie A. Palda, Guadalupe García–Tsao, Journal of Medical Genetics	2009	1.1K
International nosology of heritable disorders of connective tissue, Berlin, 1986 Peter Beighton, A. De Paepe, D. M. Danks, American Journal of Medical Genetics Gross AnatomyMendelian DisorderHistopathologyInternational NosologyPathology	1988	729
Clinical responses to bone marrow transplantation in children with severe osteogenesis imperfecta Edwin M. Horwitz, Darwin J. Prockop, Patricia Gordon, Blood	2001	566

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