| Dysfunction in GABA signalling mediates autism-like stereotypies and Rett syndrome phenotypes HT Chao, H Chen, RC Samaco, M Xue, M Chahrour, J Yoo, JL Neul, ... Nature 468 (7321), 263-269, 2010 | 1234 | 2010 |
| Epigenetic overlap in autism-spectrum neurodevelopmental disorders: MECP2 deficiency causes reduced expression of UBE3A and GABRB3 RC Samaco, A Hogart, JM LaSalle Human molecular genetics 14 (4), 483-492, 2005 | 511 | 2005 |
| Adult neural function requires MeCP2 CM McGraw, RC Samaco, HY Zoghbi Science 333 (6039), 186-186, 2011 | 298 | 2011 |
| Deletion of Mecp2 in Sim1-expressing neurons reveals a critical role for MeCP2 in feeding behavior, aggression, and the response to stress SL Fyffe, JL Neul, RC Samaco, HT Chao, S Ben-Shachar, P Moretti, ... Neuron 59 (6), 947-958, 2008 | 279 | 2008 |
| Loss of MeCP2 in aminergic neurons causes cell-autonomous defects in neurotransmitter synthesis and specific behavioral abnormalities RC Samaco, C Mandel-Brehm, HT Chao, CS Ward, SL Fyffe-Maricich, ... Proceedings of the National Academy of Sciences 106 (51), 21966-21971, 2009 | 278 | 2009 |
| miR-19, miR-101 and miR-130 co-regulate ATXN1 levels to potentially modulate SCA1 pathogenesis Y Lee, RC Samaco, JR Gatchel, C Thaller, HT Orr, HY Zoghbi Nature neuroscience 11 (10), 1137-1139, 2008 | 246 | 2008 |
| Multiple pathways regulate MeCP2 expression in normal brain development and exhibit defects in autism-spectrum disorders RC Samaco, RP Nagarajan, D Braunschweig, JM LaSalle Human molecular genetics 13 (6), 629-639, 2004 | 223 | 2004 |
| A partial loss of function allele of Methyl-CpG-binding protein 2 predicts a human neurodevelopmental syndrome RC Samaco, JD Fryer, J Ren, S Fyffe, HT Chao, Y Sun, JJ Greer, ... Human molecular genetics 17 (12), 1718-1727, 2008 | 213 | 2008 |
| Preclinical research in Rett syndrome: setting the foundation for translational success DM Katz, JE Berger-Sweeney, JH Eubanks, MJ Justice, JL Neul, ... Disease models & mechanisms 5 (6), 733-745, 2012 | 200 | 2012 |
| Female Mecp2+/− mice display robust behavioral deficits on two different genetic backgrounds providing a framework for pre-clinical studies RC Samaco, CM McGraw, CS Ward, Y Sun, JL Neul, HY Zoghbi Human molecular genetics 22 (1), 96-109, 2013 | 190 | 2013 |
| Forniceal deep brain stimulation rescues hippocampal memory in Rett syndrome mice S Hao, B Tang, Z Wu, K Ure, Y Sun, H Tao, Y Gao, AJ Patel, DJ Curry, ... Nature 526 (7573), 430-434, 2015 | 181 | 2015 |
| Crh and Oprm1 mediate anxiety-related behavior and social approach in a mouse model of MECP2 duplication syndrome RC Samaco, C Mandel-Brehm, CM McGraw, CA Shaw, BE McGill, ... Nature genetics 44 (2), 206-211, 2012 | 171 | 2012 |
| Complexities of Rett syndrome and MeCP2 RC Samaco, JL Neul Journal of Neuroscience 31 (22), 7951-7959, 2011 | 142 | 2011 |
| X-Chromosome inactivation ratios affect wild-type MeCP2 expression within mosaic Rett syndrome and Mecp2−/+ mouse brain D Braunschweig, T Simcox, RC Samaco, JM LaSalle Human molecular genetics 13 (12), 1275-1286, 2004 | 138 | 2004 |
| Perihepatic packing of major liver injuries: complications and mortality DM Caruso, FD Battistella, JT Owings, SL Lee, RC Samaco Archives of Surgery 134 (9), 958-963, 1999 | 135 | 1999 |
| A framework for the investigation of rare genetic disorders in neuropsychiatry SJ Sanders, M Sahin, J Hostyk, A Thurm, S Jacquemont, P Avillach, ... Nature medicine 25 (10), 1477-1487, 2019 | 118 | 2019 |
| Duplication of Atxn1l suppresses SCA1 neuropathology by decreasing incorporation of polyglutamine-expanded ataxin-1 into native complexes AB Bowman, YC Lam, P Jafar-Nejad, HK Chen, R Richman, RC Samaco, ... Nature genetics 39 (3), 373-379, 2007 | 97 | 2007 |
| MECP2 mutations in Rett syndrome adversely affect lymphocyte growth, but do not affect imprinted gene expression in blood or brain D Balmer, J Arredondo, RC Samaco, JM LaSalle Human genetics 110, 545-552, 2002 | 92 | 2002 |
| Rigor and reproducibility in rodent behavioral research M Gulinello, HA Mitchell, Q Chang, WT O'Brien, Z Zhou, T Abel, L Wang, ... Neurobiology of learning and memory 165, 106780, 2019 | 85 | 2019 |
| Otud7a knockout mice recapitulate many neurological features of 15q13. 3 microdeletion syndrome J Yin, W Chen, ES Chao, S Soriano, L Wang, W Wang, SE Cummock, ... The American Journal of Human Genetics 102 (2), 296-308, 2018 | 71 | 2018 |
Surabi VeeraragavanBaylor College of MedicineVerified email at bcm.edu
