Raju K. Pullarkat - Concepedia

Author

Raju K. Pullarkat

New York State Office for People With Developmental Disabilities

Also Known As

R K Pullarkat, R PULLARKAT, R Pullarkat, R. K. Pullarkat, R. Pullarkat, R.K. Pullarkat, RAJU K. PULLARKAT, Raju K Pullarkat, Raju K. PULLARKAT, Raju K. Pullarkat

Publications

3.4K

Citations

H-Index

134

Concepts

All Affiliations

New York State Office for People With Developmental Disabilities Indiana University – Purdue University Indianapolis New York State Department of State University of Helsinki Indiana University School of Medicine

About

Raju K. Pullarkat is an author at New York State Office for People With Developmental Disabilities specializing in medicine, pathology, and neurology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	24	39	2.3K
2	Health Sciences	6	6	220
3	Natural Sciences	5	5	154
4	Engineering	2	2	47
5	Public Health	1	1	47

Raju K. Pullarkat

Publications

3.2K

Citations

H-Index

Page 1

	Year	Citations
Association of Mutations in a Lysosomal Protein with Classical Late-Infantile Neuronal Ceroid Lipofuscinosis David E. Sleat, Robert Donnelly, Henry Lackland, Science Lysosomal ProteinPathologyDefective GeneLincl PatientsMendelian Disorder	1997	579
Targeted Disruption of the Cln3 Gene Provides a Mouse Model for Batten Disease Hannah M. Mitchison, David J. Bernard, Nicholas D. E. Greene, Neurobiology of Disease Knockout MouseGenome InstabilityBatten DiseaseCln3 Gene ProvidesGenetics	1999	205
Mutational Analysis of the Defective Protease in Classic Late-Infantile Neuronal Ceroid Lipofuscinosis, a Neurodegenerative Lysosomal Storage Disorder David E. Sleat, Rosalie M. Gin, István Sohár, The American Journal of Human Genetics Neurodegenerative DiseasesDefective ProteaseMutational AnalysisPathologyDegenerative Disease	1999	174
Batten disease: Past, present, and future J. Alfred Rider, Dean L. Rider, John M. Opitz, American Journal of Medical Genetics	1988	158
Proteomic studies identified a single nucleotide polymorphism in glyoxalase I as autism susceptibility factor Mohammed Junaid, Dagmar Kowal, Madhabi Barua, American Journal of Medical Genetics Part A NeurogenomicsSingle Nucleotide PolymorphismBrain DevelopmentGeneticsHuman Polymorphism	2004	153
Hypothesis: Prenatal Ethanol‐Induced Birth Defects and Retinoic Acid Raju K. Pullarkat Alcoholism Clinical and Experimental Research Didehydroretinoic AcidDevelopmental BiologyBrain DevelopmentDevelopmental ToxicologyPhysiology	1991	113
Accumulation of dolichols in brains of elderly. Raju K. Pullarkat, Henry Reha Journal of Biological Chemistry Neurodegenerative DiseasesNeuropsychologyAgingBrain DevelopmentMedicine	1982	110
Clinical classification of neuronal ceroid-lipofuscinosis subtypes Rose‐Mary Boustany, Joseph Alroy, Edwin H. Kolodny, American Journal of Medical Genetics	1988	90
Clinico-pathological variability in the childhood neuronal ceroid-lipofuscinoses and new observations on glycoprotein abnormalities K. E. Wisniewski, I. Rapin, Joy Heaney-Kieras, American Journal of Medical Genetics Developmental AnomalyNeuro-oncologyJuvenile NclPediatric Brain TumorsPediatric Neurosurgery	1988	80
Reconsideration of the classification of the neuronal ceroid-lipofuscinoses Paul Dyken, John M. Opitz, James F. Reynolds, American Journal of Medical Genetics	1988	77

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