Terry Jo Bichell - Concepedia

Author

Terry Jo Bichell

Also Known As

T BICHELL, T. J. Bichell, T.J. Bichell, Terry Bichell, Terry J V Bichell, Terry J. Bichell, Terry Jo Bichell, Terry Jo V. Bichell, Terry Jo. Bichell, Terry Jo Bichell

Publications

Citations

H-Index

Concepts

All Affiliations

Vanderbilt University Vanderbilt University Medical Center John F. Kennedy Center for the Performing Arts University of California San Diego Baylor College of Medicine

About

Terry Jo Bichell is an author at Vanderbilt University specializing in medicine, genetics, and neurodegeneration.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	5	5	237
2	Biochemistry	2	2	35
3	Cell Biology	2	2	119
4	Natural Sciences	1	1	106
5	Social Sciences	1	1	13

Terry Jo Bichell

Publications

981

Citations

H-Index

Page 1

	Year	Citations
A Neurodevelopmental Survey of Angelman Syndrome With Genotype-Phenotype Correlations Jennifer Gentile, Wen‐Hann Tan, Lucia T. Horowitz, Journal of Developmental & Behavioral Pediatrics	2010	165
Angelman syndrome: Mutations influence features in early childhood Wen‐Hann Tan, Carlos A. Bacino, Steven A. Skinner, American Journal of Medical Genetics Part A	2010	129
Sleep in children and adolescents with Angelman syndrome: association with parent sleep and stress Suzanne E. Goldman, Terry Jo Bichell, Kyla Surdyka, Journal of Intellectual Disability Research	2011	112
Tissue-specific variation of Ube3a protein expression in rodents and in a mouse model of Angelman syndrome Richard M. Gustin, Terry Jo Bichell, Michael Bubser, Neurobiology of Disease Developmental BiologyMolecular PhysiologyProtein ExpressionAngelman SyndromeMedicine	2010	106
Ube3a Imprinting Impairs Circadian Robustness in Angelman Syndrome Models Shu-qun Shi, Terry Jo Bichell, Rebecca A. Ihrie, Current Biology SleepAlertnessMedicineGeneticsNeuroscience	2015	83
Measuring What Matters to Individuals with Angelman Syndrome and Their Families: Development of a Patient-Centered Disease Concept Model Tom Willgoss, Daiana Cassater, Siobhan Connor, Child Psychiatry & Human Development	2020	74
Allosteric activation of M <sub>4</sub> muscarinic receptors improve behavioral and physiological alterations in early symptomatic YAC128 mice Tristano Pancani, Daniel J. Foster, Mark S. Moehle, Proceedings of the National Academy of Sciences	2015	49
Double‐blind therapeutic trial in Angelman syndrome using betaine and folic acid Sarika U. Peters, Lynne M. Bird, Virginia Kimonis, American Journal of Medical Genetics Part A	2010	44
Reduced bioavailable manganese causes striatal urea cycle pathology in Huntington's disease mouse model Terry Jo Bichell, Michał Węgrzynowicz, K. Grace Tipps, Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease	2017	43
Huntington’s disease genotype suppresses global manganese-responsive processes in pre-manifest and manifest YAC128 mice Anna C. Pfalzer, Jordyn M. Wilcox, Simona G. Codreanu, Metallomics	2020	24

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