Sakkubai Naidu - Concepedia

Author

Sakkubai Naidu

Kennedy Krieger Institute

Also Known As

S Naidu, SAKKUBAI NAIDU, SakkuBai Naidu, SakkuBai R. Naidu, Sakkubai Naidu, Sakkubai R. Naidu

127

Publications

7.2K

Citations

H-Index

123

Concepts

All Affiliations

Kennedy Krieger Institute Johns Hopkins University Johns Hopkins Medicine Amsterdam UMC Location Vrije Universiteit Amsterdam Hospital for Sick Children

About

Sakkubai Naidu is an author at Kennedy Krieger Institute specializing in medicine, pathology, and neuropathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	22	26	2.4K
2	Health Sciences	6	6	187
3	Arts	3	3	62
4	Natural Sciences	1	1	41
5	Public Health	1	1	28

Sakkubai Naidu

Publications

6.4K

Citations

H-Index

Page 1

	Year	Citations
Subunits of the translation initiation factor eIF2B are mutant in leukoencephalopathy with vanishing white matter Peter A. J. Leegwater, Gerre Vermeulen, Andrea A.M. Könst, Nature Genetics Translational BiologyDisease MechanismWhite MatterPathogenesisImmunology	2001	412
Lysosomal glycogen storage disease with normal acid maltase Moris J. Danon, Shin J. Oh, Salvatore DiMauro, Neurology	1981	402
Mutations in each of the five subunits of translation initiation factor eIF2B can cause leukoencephalopathy with vanishing white matter Marjo S. van der Knaap, Peter A. J. Leegwater, Andrea A.M. Könst, Annals of Neurology	2001	380
Plasma very long chain fatty acids in 3,000 peroxisome disease patients and 29,000 controls Ann B. Moser, Nancy A. Kreiter, Lena Bezman, Annals of Neurology	1999	344
Alexander disease: diagnosis with MR imaging. Marjo S. van der Knaap, Sakkubai Naidu, Steven N. Breiter, PubMed	2001	340
Mutations in CTC1, encoding conserved telomere maintenance component 1, cause Coats plus Beverley Anderson, Paul R. Kasher, Joséphine Mayer, Nature Genetics ChromatinGenome InstabilityCause CoatsGenetic DisorderGenetics	2012	285
Glial fibrillary acidic protein mutations in infantile, juvenile, and adult forms of Alexander disease Rong Li, Gajja S. Salomons, James E. Goldman, Annals of Neurology	2005	268
Diagnoses of neuronal ceroid‐lipofuscinosis by immunochemical methods Syed Hosain, Walter E. Kaufmann, Gisela Negrin, American Journal of Medical Genetics	1995	255
Phenotype of patients with peroxisomal disorders subdivided into sixteen complementation groups Ann B. Moser, Magnhild Rasmussen, Sakkubai Naidu, The Journal of Pediatrics Clinical DisordersMendelian DisorderGenetic DisorderMedicineInherited Metabolic Disease	1995	244
Defining and Categorizing Leukoencephalopathies of Unknown Origin: MR Imaging Approach Marjo S. van der Knaap, Steve N. Breiter, Sakkubai Naidu, Radiology	1999	241

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