| Elongation factor 2 and fragile X mental retardation protein control the dynamic translation of Arc/Arg3. 1 essential for mGluR-LTD S Park, JM Park, S Kim, JA Kim, JD Shepherd, CL Smith-Hicks, ... Neuron 59 (1), 70-83, 2008 | 600 | 2008 |
| Activity-induced Notch signaling in neurons requires Arc/Arg3. 1 and is essential for synaptic plasticity in hippocampal networks L Alberi, S Liu, Y Wang, R Badie, C Smith-Hicks, J Wu, TJ Pierfelice, ... Neuron 69 (3), 437-444, 2011 | 229 | 2011 |
| C‐cell hyperplasia, pheochromocytoma and sympathoadrenal malformation in a mouse model of multiple endocrine neoplasia type 2B CL Smith‐Hicks, KC Sizer, JF Powers, AS Tischler, F Costantini The EMBO journal, 2000 | 188 | 2000 |
| Neurologic phenotypes associated with COL4A1/2 mutations: Expanding the spectrum of disease S Zagaglia, C Selch, JR Nisevic, D Mei, Z Michalak, ... Neurology 91 (22), e2078-e2088, 2018 | 110 | 2018 |
| A double blind randomized placebo control trial of levetiracetam in Tourette syndrome CL Smith‐Hicks, DD Bridges, NP Paynter, HS Singer Movement disorders: official journal of the Movement Disorder Society 22 (12 …, 2007 | 85 | 2007 |
| SRF binding to SRE 6.9 in the Arc promoter is essential for LTD in cultured Purkinje cells C Smith-Hicks, B Xiao, R Deng, Y Ji, X Zhao, JD Shepherd, G Posern, ... Nature neuroscience 13 (9), 1082-1089, 2010 | 77 | 2010 |
| Natural history and genotype‐phenotype correlations in 72 individuals with SATB2‐associated syndrome YA Zarate, CL Smith‐Hicks, C Greene, MA Abbott, VM Siu, ... American Journal of Medical Genetics Part A 176 (4), 925-935, 2018 | 57 | 2018 |
| De novo variants in MAPK8IP3 cause intellectual disability with variable brain anomalies K Platzer, H Sticht, SL Edwards, W Allen, KM Angione, MT Bonati, ... The American Journal of Human Genetics 104 (2), 203-212, 2019 | 52 | 2019 |
| Monogenic disorders that mimic the phenotype of Rett syndrome S Srivastava, S Desai, J Cohen, C Smith-Hicks, K Barañano, A Fatemi, ... Neurogenetics 19, 41-47, 2018 | 50 | 2018 |
| Randomized open-label trial of dextromethorphan in Rett syndrome CL Smith-Hicks, S Gupta, JB Ewen, M Hong, L Kratz, R Kelley, E Tierney, ... Neurology 89 (16), 1684-1690, 2017 | 44 | 2017 |
| Rett syndrome and CDKL5 deficiency disorder: from bench to clinic SD Kadam, BJ Sullivan, A Goyal, ME Blue, C Smith-Hicks International journal of molecular sciences 20 (20), 5098, 2019 | 41 | 2019 |
| NFIB haploinsufficiency is associated with intellectual disability and macrocephaly I Schanze, J Bunt, JWC Lim, D Schanze, RJ Dean, M Alders, P Blanchet, ... The American Journal of Human Genetics 103 (5), 752-768, 2018 | 40 | 2018 |
| De novo missense variants in FBXW11 cause diverse developmental phenotypes including brain, eye, and digit anomalies RJ Holt, RM Young, B Crespo, F Ceroni, CJ Curry, E Bellacchio, DA Bax, ... The American Journal of Human Genetics 105 (3), 640-657, 2019 | 34 | 2019 |
| The broad phenotypic spectrum of PPP2R1A-related neurodevelopmental disorders correlates with the degree of biochemical dysfunction L Lenaerts, S Reynhout, I Verbinnen, F Laumonnier, A Toutain, ... Genetics in Medicine 23 (2), 352-362, 2021 | 31 | 2021 |
| De novo and inherited variants in ZNF292 underlie a neurodevelopmental disorder with features of autism spectrum disorder GM Mirzaa, JX Chong, A Piton, B Popp, K Foss, H Guo, R Harripaul, K Xia, ... Genetics in Medicine 22 (3), 538-546, 2020 | 31 | 2020 |
| Evaluation of QTc in Rett syndrome: correlation with age, severity, and genotype J Crosson, S Srivastava, GM Bibat, S Gupta, A Kantipuly, C Smith‐Hicks, ... American Journal of Medical Genetics Part A 173 (6), 1495-1501, 2017 | 28 | 2017 |
| De novo variants in POLR3B cause ataxia, spasticity, and demyelinating neuropathy D Djordjevic, M Pinard, MS Gauthier, C Smith-Hicks, TL Hoffman, NI Wolf, ... The American Journal of Human Genetics 108 (1), 186-193, 2021 | 27 | 2021 |
| Sleep Abnormalities in the Synaptopathies—SYNGAP1-Related Intellectual Disability and Phelan–McDermid Syndrome C Smith-Hicks, D Wright, A Kenny, RC Stowe, M McCormack, ... Brain Sciences 11 (9), 1229, 2021 | 26 | 2021 |
| Functional integration of new neurons into hippocampal networks and poststroke comorbidities following neonatal stroke in mice SD Kadam, CL Smith-Hicks, DR Smith, PF Worley, AM Comi Epilepsy & Behavior 18 (4), 344-357, 2010 | 25 | 2010 |
| GABAergic dysfunction in pediatric neuro-developmental disorders CL Smith-Hicks Frontiers in cellular neuroscience 7, 269, 2013 | 23 | 2013 |
Paul WorleyJohns Hopkins School of MedicineVerified email at jhmi.edu
