Maureen A. McCall - Concepedia

Author

Maureen A. McCall

Also Known As

M A McCall, M McCall, M. A. McCall, M. McCall, M.A. McCALL, M.A. McCall, MA McCall, MAUREEN A. MCCALL, MAUREEN A. McCALL, Maureen A McCall

174

Publications

5.2K

Citations

H-Index

Concepts

All Affiliations

University of Louisville University of Wisconsin–Madison Cleveland Eye Clinic Case Western Reserve University Cleveland Clinic

About

Maureen A. McCall is an author at University of Louisville specializing in medicine, ophthalmology, and neuroscience.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	23	29	2.3K
2	Social Sciences	12	14	941
3	Health Sciences	5	5	400
4	Natural Sciences	3	3	174
5	Public Health	1	1	22

Maureen A. McCall

Publications

4.6K

Citations

H-Index

Page 1

	Year	Citations
Targeted deletion in astrocyte intermediate filament (Gfap) alters neuronal physiology. Maureen A. McCall, Ronald G. Gregg, Richard R. Behringer, Proceedings of the National Academy of Sciences Synaptic TransmissionCellular NeurobiologySocial SciencesExperimental NeuropathologyNeurology	1996	351
Mutations in TRPM1 Are a Common Cause of Complete Congenital Stationary Night Blindness Maria M. van Genderen, Mieke M. C. Bijveld, Y. Claassen, The American Journal of Human Genetics Developmental BiologyOphthalmologyGenetic DisorderGeneticsMedicine	2009	237
The<i>nob2</i>mouse, a null mutation in<i>Cacna1f</i>: Anatomical and functional abnormalities in the outer retina and their consequences on ganglion cell visual responses Bo Chang, John R. Heckenlively, Philippa R. Bayley, Visual Neuroscience	2006	205
Engineering adeno-associated viral vectors to evade innate immune and inflammatory responses Ying Chan, Sean K. Wang, Colin J. Chu, Science Translational Medicine	2021	189
A naturally occurring mouse model of X-linked congenital stationary night blindness. Machelle T. Pardue, Maureen A. McCall, M. M. LaVail, PubMed	1998	162
GPR179 Is Required for Depolarizing Bipolar Cell Function and Is Mutated in Autosomal-Recessive Complete Congenital Stationary Night Blindness Neal S. Peachey, Thomas A. Ray, Ralph Florijn, The American Journal of Human Genetics Is MutatedBipolar Cell FunctionPhotoreceptor CellMolecular NeuroscienceOphthalmology	2012	158
Generation of an Inbred Miniature Pig Model of Retinitis Pigmentosa Jason W. Ross, Juan P. Fernandez de Castro, Jianguo Zhao, Investigative Ophthalmology & Visual Science	2012	154
Failure to Maintain Eye-Specific Segregation in nob, a Mutant with Abnormally Patterned Retinal Activity Jay Demas, Botir T. Sagdullaev, Erick Green, Neuron Ocular DiseaseRetinaMaintain Eye-specific SegregationOphthalmologyGenetics	2006	137
Behavioral and anatomical abnormalities in a sodium iodate-induced model of retinal pigment epithelium degeneration Volker Enzmann, Barry W. Row, Yasuyuki Yamauchi, Experimental Eye Research Ocular DiseasePhotoreceptor CellRetinaOphthalmologyExperimental Ophthalmology	2005	132
Presynaptic Inhibition Modulates Spillover, Creating Distinct Dynamic Response Ranges of Sensory Output Botir T. Sagdullaev, Maureen A. McCall, Peter D. Lukasiewicz Neuron Synaptic PlasticityCognitive ScienceNeural MechanismNeurodynamicsNeurophysiology	2006	130

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