D L Rimoin - Concepedia

Author

D L Rimoin

Cedars-Sinai Medical Center

Also Known As

D L Rimoin, D Rimoin, D. L. Rimoin, D. Rimoin, D.L. Rimoin, David L. Rimoin

Publications

2.5K

Citations

H-Index

Concepts

All Affiliations

Cedars-Sinai Medical Center Harbor–UCLA Medical Center University of California, Los Angeles UCLA Medical Center Medical University of Vienna

About

D L Rimoin is an author at Cedars-Sinai Medical Center specializing in medicine, orthopaedics, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	13	15	1.6K
2	Anatomy	3	3	813
3	Education	1	1	57
4	Health Sciences	1	1	183
5	Natural Sciences	1	1	151

D L Rimoin

Publications

2.4K

Citations

H-Index

Page 1

	Year	Citations
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
Atelosteogenesis type II is caused by mutations in the diastrophic dysplasia sulfate-transporter gene (DTDST): evidence for a phenotypic series involving three chondrodysplasias. Johanna Hästbacka, Andrea Superti‐Furga, William R. Wilcox, PubMed	1996	203
Osteogenesis imperfecta type II delineation of the phenotype with reference to genetic heterogeneity David Sillence, K. K. Barlow, Ann Garber, American Journal of Medical Genetics GeneticsOsteogenesisType IiOsteoporosisOrthopaedic Surgery	1984	183
Clinical variability in osteogenesis imperfecta-variable expressivity or genetic heterogeneity. David Sillence, D L Rimoin, D. M. Danks PubMed Bone DiseaseBone RemodelingOrthopaedicsOsteogenesisGenetic Heterogeneity	1979	152
Characterization of novel cathepsin K mutations in the pro and mature polypeptide regions causing pycnodysostosis Wu-Shiun Hou, Dieter Brömme, Yingming Zhao, Journal of Clinical Investigation Protein FunctionSclerostinBiochemistryProtein FoldingNatural Sciences	1999	151
Tandem duplication within a type II collagen gene (COL2A1) exon in an individual with spondyloepiphyseal dysplasia. George E. Tiller, D L Rimoin, Louann W. Murray, Proceedings of the National Academy of Sciences Musculoskeletal ResearchDevelopmental BiologyMendelian DisorderGenetic DisorderGenetics	1990	130
The search for heterogeneity in insulin-dependent diabetes mellitus (IDDM): linkage studies, two-locus models, and genetic heterogeneity. Susan E. Hodge, Carol E. Anderson, Katherine Neiswanger, PubMed	1983	123
Epidemiology of osteochondrodysplasias: Changing trends due to advances in prenatal diagnosis Sonja A. Rasmussen, Frederick R. Bieber, Beryl R. Benacerraf, American Journal of Medical Genetics	1996	118
Human X-autosome translocations: differential inactivation of the X chromosome in a kindred with an X-9 translocation. Jaakko Leisti, Michael M. Kaback, D L Rimoin PubMed	1975	76
A unique association of short stature, dysmorphic features, and speech impairment (Floating-harbor syndrome) Mordechai Shohat, Robin M. Winter, William L. Conte, The Journal of Pediatrics Down SyndromeIntellectual ImpairmentSpeech ImpairmentShort StatureDisability	1988	57

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