Alan K. Percy - Concepedia

Author

Alan K. Percy

University of Alabama at Birmingham ORCID

Also Known As

A K Percy, A Percy, A. K. PERCY, A. K. Percy, A. Percy, A.K. Percy, ALAN K. PERCY, ALAN PERCY, Alan K Percy, Alan K. Percy

336

Publications

15.2K

Citations

H-Index

283

Concepts

All Affiliations

University of Alabama at Birmingham Baylor College of Medicine Civitan International Greenwood Genetic Center Vanderbilt University Medical Center

About

Alan K. Percy is an author at University of Alabama at Birmingham specializing in medicine, neurology, and neuropathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	43	79	5.6K
2	Health Sciences	6	6	382
3	Natural Sciences	6	6	274
4	Education	4	4	245
5	Nursing	1	1	123

Alan K. Percy

168

Publications

13.5K

Citations

H-Index

Page 1

	Year	Citations
Rett syndrome: Revised diagnostic criteria and nomenclature Jeffrey L. Neul, Walter E. Kaufmann, Daniel G. Glaze, Annals of Neurology	2010	1.4K
Specific mutations in <i>Methyl-CpG-Binding Protein 2</i> confer different severity in Rett syndrome Jeffrey L. Neul, Ping Fang, James P. Barrish, Neurology	2008	492
An update on clinically applicable diagnostic criteria in Rett syndrome Bengt Hagberg, F. Hanefeld, Alan K. Percy, European Journal of Paediatric Neurology DiagnosisPathologyNeuropathologyMedicineApplicable Diagnostic Criteria	2002	393
Influence of mutation type and X chromosome inactivation on Rett syndrome phenotypes Ruthie E. Amir, Ignatia B. Van den Veyver, Rebecca Schultz, Annals of Neurology Mendelian DisorderGenetic DisorderGeneticsMecp2 MutationsMutation Type	2000	345
<i>Methyl-CpG-binding protein 2</i> (<i>MECP2</i>) mutation type is associated with disease severity in Rett syndrome Vishnu Anand Cuddapah, Rajesh B Pillai, Kiran V Shekar, Journal of Medical Genetics	2014	306
Progressive Hearing Loss in Infants With Asymptomatic Congenital Cytomegalovirus Infection W. Daniel Williamson, Gail J. Demmler, Alan K. Percy, PEDIATRICS	1992	273
Occipital horn syndrome and a mild Menkes phenotype associated with splice site mutations at the MNK locus Stephen G. Kaler, Linda K. Gallo, Virginia K. Proud, Nature Genetics Mild Menkes PhenotypeMendelian DisorderGenetic DisorderGeneticsPathogenesis	1994	260
Dendritic spine pathologies in hippocampal pyramidal neurons from Rett syndrome brain and after expression of Rett-associated MECP2 mutations Christopher A. Chapleau, Gastón Diego Calfa, Meredith C. Lane, Neurobiology of Disease Synaptic PlasticityDendritic Spine PathologiesHippocampal Pyramidal NeuronsNeuroanatomyCortical Remodeling	2009	254
Loss of MeCP2 in aminergic neurons causes cell-autonomous defects in neurotransmitter synthesis and specific behavioral abnormalities Rodney C. Samaco, Caleigh Mandel‐Brehm, Hsiao-Tuan Chao, Proceedings of the National Academy of Sciences	2009	251
Investigating genotype–phenotype relationships in Rett syndrome using an international data set Ami Bebbington, Alison Anderson, David Ravine, Neurology	2008	240

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