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Terry Jo Bichell
Terry Jo Bichell
Director, COMBINEDBrain
Verified email at bu.edu - Homepage
Title
Cited by
Cited by
Year
A neurodevelopmental survey of Angelman syndrome with genotype-phenotype correlations
JK Gentile, WH Tan, LT Horowitz, CA Bacino, SA Skinner, ...
Journal of Developmental & Behavioral Pediatrics 31 (7), 592-601, 2010
1562010
Microarray based comparative genomic hybridization testing in deletion bearing patients with Angelman syndrome: genotype-phenotype correlations
T Sahoo, SU Peters, NS Madduri, DG Glaze, JR German, LM Bird, ...
Journal of Medical Genetics 43 (6), 512-516, 2006
1402006
Angelman syndrome: Mutations influence features in early childhood
WH Tan, CA Bacino, SA Skinner, I Anselm, R Barbieri‐Welge, ...
American journal of medical genetics Part A 155 (1), 81-90, 2011
1372011
Tissue-specific variation of Ube3a protein expression in rodents and in a mouse model of Angelman syndrome
RM Gustin, TJ Bichell, M Bubser, J Daily, I Filonova, D Mrelashvili, ...
Neurobiology of disease 39 (3), 283-291, 2010
1122010
Sleep in children and adolescents with Angelman syndrome: association with parent sleep and stress
SE Goldman, TJ Bichell, K Surdyka, BA Malow
Journal of Intellectual Disability Research 56 (6), 600-608, 2012
1082012
Ube3a imprinting impairs circadian robustness in Angelman syndrome models
S Shi, TJ Bichell, RA Ihrie, CH Johnson
Current Biology 25 (5), 537-545, 2015
842015
Double‐blind therapeutic trial in Angelman syndrome using betaine and folic acid
SU Peters, LM Bird, V Kimonis, DG Glaze, LM Shinawi, TJ Bichell, ...
American journal of medical genetics Part A 152 (8), 1994-2001, 2010
522010
Allosteric activation of M4 muscarinic receptors improve behavioral and physiological alterations in early symptomatic YAC128 mice
T Pancani, DJ Foster, MS Moehle, TJ Bichell, E Bradley, TM Bridges, ...
Proceedings of the National Academy of Sciences 112 (45), 14078-14083, 2015
462015
Measuring what matters to individuals with Angelman syndrome and their families: development of a patient-centered disease concept model
T Willgoss, D Cassater, S Connor, ML Krishnan, MT Miller, ...
Child Psychiatry & Human Development 52, 654-668, 2021
402021
Reduced bioavailable manganese causes striatal urea cycle pathology in Huntington's disease mouse model
TJV Bichell, M Wegrzynowicz, KG Tipps, EM Bradley, MA Uhouse, ...
Biochimica et Biophysica Acta (BBA)-Molecular Basis of Disease 1863 (6 …, 2017
392017
BDNF and Huntingtin protein modifications by manganese: Implications for striatal medium spiny neuron pathology in manganese neurotoxicity
KH Stansfield, TJ Bichell, AB Bowman, TR Guilarte
Journal of neurochemistry 131 (5), 655-666, 2014
242014
Beyond epilepsy and autism: disruption of GABRB3 causes ocular hypopigmentation
RJ Delahanty, Y Zhang, TJ Bichell, W Shen, K Verdier, RL Macdonald, ...
Cell reports 17 (12), 3115-3124, 2016
212016
Huntington’s disease genotype suppresses global manganese-responsive processes in pre-manifest and manifest YAC128 mice
AC Pfalzer, JM Wilcox, SG Codreanu, M Totten, TJV Bichell, T Halbesma, ...
Metallomics 12 (7), 1118-1130, 2020
202020
Novel BAC mouse model of Huntington's disease with 225 CAG repeats exhibits an early widespread and stable degenerative phenotype
M Wegrzynowicz, TJ Bichell, BD Soares, MK Loth, JL McGlothan, ...
Journal of Huntington's disease 4 (1), 17-36, 2015
162015
Embryonic mutant huntingtin aggregate formation in mouse models of Huntington’s disease
AP Osmand, TJ Bichell, AB Bowman, GP Bates
Journal of Huntington's Disease 5 (4), 343-346, 2016
122016
Are children with Angelman syndrome at high risk for anesthetic complications?
IS Landsman, HM Mitzel, SU Peters, TJ Bichell
Pediatric Anesthesia 22 (3), 263-267, 2012
102012
A disease concept model for STXBP1‐related disorders
KR Sullivan, SM Ruggiero, J Xian, KM Thalwitzer, R Ali, S Stewart, ...
Epilepsia Open 8 (2), 320-333, 2023
82023
A placebo-controlled trial of folic acid and betaine in identical twins with Angelman syndrome
J Han, TJ Bichell, S Golden, I Anselm, S Waisbren, CA Bacino, SU Peters, ...
Orphanet journal of rare diseases 14, 1-8, 2019
72019
A draft conceptual model of SLC6A1 neurodevelopmental disorder
K Goodspeed, LR Mosca, NC Weitzel, K Horning, EW Simon, AC Pfalzer, ...
Frontiers in neuroscience 16, 1026065, 2023
52023
Treatment with THI, an inhibitor of sphingosine-1-phosphate lyase, modulates glycosphingolipid metabolism and results therapeutically effective in experimental models of …
G Pepe, L Capocci, F Marracino, N Realini, P Lenzi, K Martinello, ...
Molecular Therapy 31 (1), 282-299, 2023
52023
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