Shambhu Bhat
Shambhu Bhat
Research Scientist
Verified email at psych.umaryland.edu
TitleCited byYear
Mutations in UPF3B, a member of the nonsense-mediated mRNA decay complex, cause syndromic and nonsyndromic mental retardation
PS Tarpey, FL Raymond, LS Nguyen, J Rodriguez, A Hackett, ...
Nature genetics 39 (9), 1127-1133, 2007
2052007
CACNA1C (Cav1. 2) in the pathophysiology of psychiatric disease
S Bhat, DT Dao, CE Terrillion, M Arad, RJ Smith, NM Soldatov, TD Gould
Progress in neurobiology 99 (1), 1-14, 2012
2012012
The tail suspension test
A Can, DT Dao, CE Terrillion, SC Piantadosi, S Bhat, TD Gould
JoVE (Journal of Visualized Experiments), e3769, 2012
1852012
Capturing CO2 in flue gas from fossil fuel-fired power plants using dry regenerable alkali metal-based sorbent
C Zhao, X Chen, EJ Anthony, X Jiang, L Duan, Y Wu, W Dong, C Zhao
Progress in energy and combustion science 39 (6), 515-534, 2013
1222013
Disruption of the IL1RAPL1 gene associated with a pericentromeric inversion of the X chromosome in a patient with mental retardation and autism
SS Bhat, S Ladd, F Grass, JE Spence, CK Brasington, RJ Simensen, ...
Clinical genetics 73 (1), 94-96, 2008
472008
Defining the contribution of CNTNAP2 to autism susceptibility
S Sampath, S Bhat, S Gupta, A O’Connor, AB West, DE Arking, ...
PloS one 8 (10), 2013
292013
Evidence that SIZN1 is a candidate X‐linked mental retardation gene
G Cho, SS Bhat, J Gao, JS Collins, RC Rogers, RJ Simensen, ...
American Journal of Medical Genetics Part A 146 (20), 2644-2650, 2008
242008
Sex‐dependent modulation of age‐related cognitive decline by the L‐type calcium channel gene Cacna1c (Cav1.2)
P Zanos, S Bhat, CE Terrillion, RJ Smith, LH Tonelli, TD Gould
European Journal of Neuroscience 42 (8), 2499-2507, 2015
152015
Disruption of DMD and deletion of ACSL4 causing developmental delay, hypotonia, and multiple congenital anomalies
SS Bhat, KR Schmidt, S Ladd, KC Kim, CE Schwartz, RJ Simensen, ...
Cytogenetic and genome research 112 (1-2), 170-175, 2006
152006
A novel in-frame deletion in ARX is associated with lissencephaly with absent corpus callosum and hypoplastic genitalia
SS Bhat, RC Rogers, KR Holden, AK Srivastava
American journal of medical genetics 138 (1), 70-72, 2005
142005
Dopamine and stress system modulation of sex differences in decision making
P Georgiou, P Zanos, S Bhat, JK Tracy, IJ Merchenthaler, MM McCarthy, ...
Neuropsychopharmacology 43 (2), 313-324, 2018
132018
Intellectual disability, midface hypoplasia, facial hypotonia, and Alport syndrome are associated with a deletion in Xq22. 3
JD Rodriguez, SS Bhat, I Meloni, S Ladd, ND Leslie, EO Doyne, A Renieri, ...
American Journal of Medical Genetics Part A 152 (3), 713-717, 2010
102010
Sex-Dependent Modulation of Decision-Making in the Rat Gambling Task: Involvement of Brain Dopaminergic and Stress Systems
P Georgiou, P Zanos, S Bhat, M McCarthy, I Merchenthaler, K Tracy, ...
NEUROPSYCHOPHARMACOLOGY 41, S485-S485, 2016
2016
Reduced Function of L-type Calcium Channels Rescues Reproductive Depression in Female Mice
M Arad, S Bhat, RJ Smith, MM McCarthy, TD Gould
BIOLOGICAL PSYCHIATRY 75 (9), 315S-315S, 2014
2014
尾懸垂テスト
A Can, DT Dao, CE Terrillion, SC Piantadosi, S Bhat, TD Gould
2012
La coda di test Sospensione
A Can, DT Dao, CE Terrillion, SC Piantadosi, S Bhat, TD Gould
2012
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Articles 1–16