Constance Smith‐Hicks

2.2k total citations
31 papers, 1.1k citations indexed

About

Constance Smith‐Hicks is a scholar working on Genetics, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, Constance Smith‐Hicks has authored 31 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Genetics, 12 papers in Molecular Biology and 12 papers in Cognitive Neuroscience. Recurrent topics in Constance Smith‐Hicks's work include Genetics and Neurodevelopmental Disorders (19 papers), Autism Spectrum Disorder Research (12 papers) and Family and Disability Support Research (4 papers). Constance Smith‐Hicks is often cited by papers focused on Genetics and Neurodevelopmental Disorders (19 papers), Autism Spectrum Disorder Research (12 papers) and Family and Disability Support Research (4 papers). Constance Smith‐Hicks collaborates with scholars based in United States, United Kingdom and Germany. Constance Smith‐Hicks's co-authors include Paul Worley, Dietmar Kuhl, David J. Linden, Jason D. Shepherd, Richard L. Huganir, Alexey G. Ryazanov, Sangmok Kim, Jin-Ah Kim, Shoaib Chowdhury and Walter E. Kaufmann and has published in prestigious journals such as Neuron, The EMBO Journal and Nature Neuroscience.

In The Last Decade

Constance Smith‐Hicks

29 papers receiving 1.1k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Constance Smith‐Hicks United States	15	555	413	411	275	102	31	1.1k
Won Mah South Korea	12	635 1.1×	428 1.0×	551 1.3×	463 1.7×	67 0.7×	16	1.3k
Giovanni Provenzano Italy	17	381 0.7×	333 0.8×	423 1.0×	518 1.9×	84 0.8×	43	1.1k
Laura Schaevitz United States	17	541 1.0×	258 0.6×	506 1.2×	387 1.4×	205 2.0×	26	1.1k
Ioanna Konidari United States	17	625 1.1×	329 0.8×	618 1.5×	500 1.8×	50 0.5×	26	1.6k
Shane McCarthy United States	9	1.0k 1.8×	324 0.8×	458 1.1×	225 0.8×	155 1.5×	16	1.5k
Josien Levenga United States	15	732 1.3×	338 0.8×	633 1.5×	452 1.6×	137 1.3×	20	1.3k
Vijayendran Chandran United States	11	709 1.3×	169 0.4×	542 1.3×	379 1.4×	75 0.7×	16	1.1k
Holly N. Cukier United States	16	525 0.9×	147 0.4×	518 1.3×	403 1.5×	46 0.5×	26	1.0k
Itaru Kushima Japan	17	456 0.8×	179 0.4×	314 0.8×	229 0.8×	67 0.7×	81	899

Countries citing papers authored by Constance Smith‐Hicks

Since Specialization

Citations

This map shows the geographic impact of Constance Smith‐Hicks's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Constance Smith‐Hicks with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Constance Smith‐Hicks more than expected).

Fields of papers citing papers by Constance Smith‐Hicks

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Constance Smith‐Hicks. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Constance Smith‐Hicks. The network helps show where Constance Smith‐Hicks may publish in the future.

Co-authorship network of co-authors of Constance Smith‐Hicks

This figure shows the co-authorship network connecting the top 25 collaborators of Constance Smith‐Hicks. A scholar is included among the top collaborators of Constance Smith‐Hicks based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Constance Smith‐Hicks. Constance Smith‐Hicks is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Ludwig, Natasha N., et al.. (2024). Cortical Vision Impairment (CVI)-informed assessment and treatment of challenging behavior in a child with SCN2A-related disorder. Journal of Neurodevelopmental Disorders. 16(1). 66–66. 1 indexed citations

Smith‐Hicks, Constance, et al.. (2024). Resolution of severe neurobehavioral difficulties in an individual with Primrose syndrome with sertraline. American Journal of Medical Genetics Part A. 194(8). e63610–e63610.

Hough, David M., Alice R. Mao, Michael G. Aman, et al.. (2023). Randomized clinical trial of low dose suramin intravenous infusions for treatment of autism spectrum disorder. Annals of General Psychiatry. 22(1). 45–45. 4 indexed citations

Frazier, Thomas, Robyn M. Busch, Patricia Klaas, et al.. (2023). Development of informant‐report neurobehavioral survey scales for PTEN hamartoma tumor syndrome and related neurodevelopmental genetic syndromes. American Journal of Medical Genetics Part A. 191(7). 1741–1757. 7 indexed citations

Smith‐Hicks, Constance, et al.. (2023). An exploratory study of sleep quality and quantity in children with causal variants in SYNGAP1, an autism risk gene. Sleep Medicine. 107. 101–107. 5 indexed citations

McGraw, Sarah, et al.. (2023). Meaningful Improvements in Rett Syndrome: A Qualitative Study of Caregivers. Journal of Child Neurology. 38(5). 270–282. 6 indexed citations

Ludwig, Natasha N., et al.. (2023). Severe behavior problems in SYNGAP1-related disorder: A summary of 11 consecutive patients in a tertiary care specialty clinic. Epilepsy & Behavior. 150. 109584–109584. 6 indexed citations

Pinard, Maxime, Constance Smith‐Hicks, Trevor L. Hoffman, et al.. (2021). De novo variants in POLR3B cause ataxia, spasticity, and demyelinating neuropathy. The American Journal of Human Genetics. 108(1). 186–193. 16 indexed citations

Gold, Nina B., Dong Li, Anna Chassevent, et al.. (2020). Heterozygous de novo variants in CSNK1G1 are associated with syndromic developmental delay and autism spectrum disorder. Clinical Genetics. 98(6). 571–576. 10 indexed citations

10.

Nusbaum, Rachel, et al.. (2019). Caregivers' perception of and experience with variants of uncertain significance from whole exome sequencing for children with undiagnosed conditions. Journal of Genetic Counseling. 28(2). 304–312. 14 indexed citations

11.

Ullman, Natalie, Constance Smith‐Hicks, Sonal Desai, & Carl E. Stafstrom. (2018). De Novo HECW2 Mutation Associated With Epilepsy, Developmental Decline, and Intellectual Disability: Case Report and Review of Literature. Pediatric Neurology. 85. 76–78. 15 indexed citations

12.

Smith‐Hicks, Constance, Siddharth Gupta, Joshua B. Ewen, et al.. (2017). Randomized open-label trial of dextromethorphan in Rett syndrome. Neurology. 89(16). 1684–1690. 37 indexed citations

13.

Smith‐Hicks, Constance, Peiling Cai, Alena Savonenko, Roger H. Reeves, & Paul Worley. (2017). Increased Sparsity of Hippocampal CA1 Neuronal Ensembles in a Mouse Model of Down Syndrome Assayed by Arc Expression. Frontiers in Neural Circuits. 11. 6–6. 5 indexed citations

14.

Sun, Lisa R., Thangamadhan Bosemani, & Constance Smith‐Hicks. (2016). Neuroimaging Abnormalities in a Child With Infantile Spasms on High-Dose Vigabatrin. Pediatric Neurology. 67. 109–110. 3 indexed citations

15.

Smith‐Hicks, Constance. (2013). GABAergic dysfunction in pediatric neuro-developmental disorders. Frontiers in Cellular Neuroscience. 7. 269–269. 18 indexed citations

16.

Albéri, Lavinia, Shuxi Liu, Yue Wang, et al.. (2011). Activity-Induced Notch Signaling in Neurons Requires Arc/Arg3.1 and Is Essential for Synaptic Plasticity in Hippocampal Networks. Neuron. 69(3). 437–444. 166 indexed citations

17.

Smith‐Hicks, Constance, Bo Xiao, Yi‐Fei Ji, et al.. (2010). SRF binding to SRE 6.9 in the Arc promoter is essential for LTD in cultured Purkinje cells. Nature Neuroscience. 13(9). 1082–1089. 53 indexed citations

18.

Kadam, Shilpa D., Constance Smith‐Hicks, Dani R. Smith, Paul Worley, & Anne M. Comi. (2010). Functional integration of new neurons into hippocampal networks and poststroke comorbidities following neonatal stroke in mice. Epilepsy & Behavior. 18(4). 344–357. 19 indexed citations

19.

Park, Sung Jin, Joo Min Park, Sangmok Kim, et al.. (2008). Elongation Factor 2 and Fragile X Mental Retardation Protein Control the Dynamic Translation of Arc/Arg3.1 Essential for mGluR-LTD. Neuron. 59(1). 70–83. 427 indexed citations

20.

Smith‐Hicks, Constance, Kurt C. Sizer, James F. Powers, Arthur S. Tischler, & Frank Costantini. (2000). C-cell hyperplasia, pheochromocytoma and sympathoadrenal malformation in a mouse model of multiple endocrine neoplasia type 2B. The EMBO Journal. 19(4). 612–622. 115 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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