| The tail suspension test A Can, DT Dao, CE Terrillion, SC Piantadosi, S Bhat, TD Gould JoVE (Journal of Visualized Experiments), e3769, 2012 | 664 | 2012 |
| 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 | 320 | 2012 |
| Mutations in UPF3B, a member of the nonsense-mediated mRNA decay complex, cause syndromic and nonsyndromic mental retardation PS Tarpey, F Lucy Raymond, LS Nguyen, J Rodriguez, A Hackett, ... Nature genetics 39 (9), 1127-1133, 2007 | 296 | 2007 |
| 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 | 66 | 2018 |
| 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 | 61 | 2008 |
| 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), e77906, 2013 | 48 | 2013 |
| 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 | 31 | 2015 |
| 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 | 30 | 2008 |
| 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, 2005 | 29 | 2005 |
| 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 | 20 | 2010 |
| 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. Part A 138 (1), 70-72, 2005 | 19 | 2005 |
| SIRT3, a metabolic target linked to ataxia-telangiectasia mutated (ATM) gene deficiency in diffuse large B-cell lymphoma K Bhalla, S Jaber, K Reagan, A Hamburg, KF Underwood, A Jhajharia, ... Scientific Reports 10 (1), 21159, 2020 | 11 | 2020 |
| 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 |
Charles SchwartzDirector of Research, Greenwood Genetic CenterVerified email at ggc.org
