Muriel I. Kaiser‐Kupfer

Author

Also Known As

M I Kaiser-Kupfer, M Kaiser-Kupfer, M. I. KAISER‐KUPFER, M. I. Kaiser-Kupfer, M. I. Kaiser‐Kupfer, M. Kaiser-Kupfer, M.I. KAISER-KUPFER, MURIEL I. KAISER-KUPFER, MURIEL KAISER–KUPFER, Muriel I Kaiser-Kupfer

132

Publications

7.1K

Citations

H-Index

Concepts

All Affiliations

National Eye Institute National Institutes of Health Howard Hughes Medical Institute Johns Hopkins University Eunice Kennedy Shriver National Institute of Child Health and Human Development

About

Muriel I. Kaiser‐Kupfer is an author at National Eye Institute specializing in medicine, ophthalmology, and glaucoma.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	34	47	3.8K
2	Health Sciences	3	3	226
3	Natural Sciences	2	2	218
4	Public Health	1	1	34
5	Social Sciences	1	1	36

Muriel I. Kaiser‐Kupfer

Publications

6.5K

Citations

H-Index

Page 1

	Year	Citations
Neurofibromatosis 2 (NF2): Clinical characteristics of 63 affected individuals and clinical evidence for heterogeneity Dilys M. Parry, Roswell Eldridge, Muriel I. Kaiser‐Kupfer, American Journal of Medical Genetics Neurological DisorderPathologyBrain LesionNeuromasPathologic Lesion	1994	417
Cogan Syndrome Barton F. Haynes, Muriel I. Kaiser‐Kupfer, Pamela Mason, Medicine RheumatologyTranslational MedicineTypical Cogan SyndromeSystemic CorticosteroidsAutoimmune Disease	1980	384
Genetic Defects and Clinical Characteristics of Patients with a Form of Oculocutaneous Albinism (Hermansky–Pudlak Syndrome) W. A. Gahl, Mark Brantly, Muriel I. Kaiser‐Kupfer, New England Journal of Medicine	1998	305
Bietti Crystalline Corneoretinal Dystrophy Is Caused by Mutations in the Novel Gene CYP4V2 Anren Li, Xiaodong Jiao, Francis L. Munier, The American Journal of Human Genetics Mendelian DisorderOphthalmologyCorneal DystrophyGenetic DisorderGenetics	2004	280
Germ-line mutations in the neurofibromatosis 2 gene: correlations with disease severity and retinal abnormalities. Dilys M. Parry, M. MacCollin, Muriel I. Kaiser‐Kupfer, PubMed	1996	218
Use of nitisinone in patients with alkaptonuria Pim Suwannarat, Kevin O’Brien, Monique B. Perry, Metabolism MedicineUrological ResearchPharmacotherapy	2005	161
Clinical Biochemical and Pathologic Correlations in Bietti's Crystalline Dystrophy Muriel I. Kaiser‐Kupfer, Chi‐Chao Chan, Thomas C. Markello, American Journal of Ophthalmology UrologyClinical BiochemicalHistopathologyDegenerative DiseaseNeuropathology	1994	157
Autosomal dominant zonular cataract with sutural opacities is associated with a splice mutation in the betaA3/A1-crystallin gene. Chitra Kannabiran, Peter K. Rogan, L. Olmos, PubMed	1998	142
Long-term Ocular Manifestations in Nephropathic Cystinosis Muriel I. Kaiser‐Kupfer, Rafael C. Caruso, D Minkler, Archives of Ophthalmology	1986	141
1. Tamoxifen Retinopathy Muriel I. Kaiser‐Kupfer, M. A. B. Rodrigues Ophthalmology	1981	131

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