Constance Smith‐Hicks

2.2k citations

31 papers · 1.1k indexed · h-index 15

Impact in

Developmental Neuroscience top 5%
- Neurogenesis and neuroplasticity mechanisms
Cellular and Molecular Neuroscience top 5%
- Neuroscience and Neuropharmacology Research

Papers in ⓘ

Developmental Neuroscience 3
Genetics 20
- Genetics and Neurodevelopmental Disorders 19
- Genomics and Rare Diseases 3
- Genomic variations and chromosomal abnormalities 3

Co-authors: Paul Worley (5 shared papers)Dietmar Kuhl (3 shared papers)Richard L. Huganir (2 shared papers)David J. Linden (2 shared papers)Jason D. Shepherd (2 shared papers)Alexey G. Ryazanov (1 shared paper)Shoaib Chowdhury (1 shared paper)Sangmok Kim (1 shared paper)
Journals: Pediatric Neurology (2 papers)Epilepsy & Behavior (2 papers)Neuron (2 papers)Sleep Medicine (1 paper)Journal of Neurodevelopmental Disorders (1 paper)
Partner nations: United States United Kingdom Germany

In The Last Decade

Constance Smith‐Hicks

29 papers receiving 1.1k citations

Peers

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-authors

The 25 scholars most cited alongside Constance Smith‐Hicks, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Constance Smith‐Hicks Line = papers co-authored together Constance Smith‐Hicks links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 31 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Elongation Factor 2 and Fragile X Mental Retardation Protein Control the Dynamic Translation of Arc/Arg3.1 Essential for mGluR-LTD Neuron ·Sung Jin Park, Joo Min Park, Sangmok Kim, Jin-Ah Kim, Jason D. Shepherd, Constance Smith‐Hicks, Shoaib Chowdhury, Walter E. Kaufmann, Dietmar Kuhl, Alexey G. Ryazanov, Richard L. Huganir, David J. Linden, Paul Worley	2008	427
2	Activity-Induced Notch Signaling in Neurons Requires Arc/Arg3.1 and Is Essential for Synaptic Plasticity in Hippocampal Networks Neuron ·Lavinia Albéri, Shuxi Liu, Yue Wang, Ramy Badie, Constance Smith‐Hicks, Jing Wu, Tarran J. Pierfelice, Bagrat Abazyan, Mark P. Mattson, Dietmar Kuhl, Mikhail V. Pletnikov, Paul Worley, Nicholas Gaiano	2011	166
3	C-cell hyperplasia, pheochromocytoma and sympathoadrenal malformation in a mouse model of multiple endocrine neoplasia type 2B The EMBO Journal ·Constance Smith‐Hicks, Kurt C. Sizer, James F. Powers, Arthur S. Tischler, Frank Costantini	2000	115
4	SRF binding to SRE 6.9 in the Arc promoter is essential for LTD in cultured Purkinje cells Nature Neuroscience ·Constance Smith‐Hicks, Bo Xiao, Rongkang Deng, Yi‐Fei Ji, Xia Zhao, Jason D. Shepherd, Guido Posern, Dietmar Kuhl, Richard L. Huganir, David D. Ginty, Paul Worley, David J. Linden	2010	53
5	A double blind randomized placebo control trial of levetiracetam in tourette syndrome Movement Disorders ·Constance Smith‐Hicks, Dana Bridges, Nina P. Paynter, Harvey S. Singer	2007	53
6	Randomized open-label trial of dextromethorphan in Rett syndrome Neurology ·Constance Smith‐Hicks, Siddharth Gupta, Joshua B. Ewen, Manisha Hong, Lisa E. Kratz, Richard I. Kelley, Elaine Tierney, Rebecca Vaurio, Genila Bibat, Abanti Sanyal, Gayane Yenokyan, Nga Brereton, Michael V. Johnston, Sakkubai Naidu	2017	37
7	Monogenic disorders that mimic the phenotype of Rett syndrome Neurogenetics ·Siddharth Srivastava, Sonal Desai, Julie S. Cohen, Constance Smith‐Hicks, Kristin Barañano, Ali Fatemi, SakkuBai Naidu	2018	37
8	Rett Syndrome and CDKL5 Deficiency Disorder: From Bench to Clinic International Journal of Molecular Sciences ·Shilpa D. Kadam, Brennan J. Sullivan, Archita Goyal, Mary E. Blue, Constance Smith‐Hicks	2019	35
9	Evaluation of QTc in Rett syndrome: Correlation with age, severity, and genotype American Journal of Medical Genetics Part A ·Jane E. Crosson, Siddharth Srivastava, Genila Bibat, Siddharth Gupta, Aditi Kantipuly, Constance Smith‐Hicks, Scott M. Myers, Abanti Sanyal, Gayane Yenokyan, Joel I. Brenner, Sakkubai Naidu	2017	24
10	Sleep Abnormalities in the Synaptopathies—SYNGAP1-Related Intellectual Disability and Phelan–McDermid Syndrome Brain Sciences ·Constance Smith‐Hicks, Damien Wright, Aisling Kenny, Robert C. Stowe, Maria McCormack, Andrew C. Stanfield, J. Lloyd Holder	2021	23
11	The Impact of X-Chromosome Inactivation on Phenotypic Expression of X-Linked Neurodevelopmental Disorders Brain Sciences ·Boudewien Brand, Alyssa Blesson, Constance Smith‐Hicks	2021	21
12	Functional integration of new neurons into hippocampal networks and poststroke comorbidities following neonatal stroke in mice Epilepsy & Behavior ·Shilpa D. Kadam, Constance Smith‐Hicks, Dani R. Smith, Paul Worley, Anne M. Comi	2010	19
13	GABAergic dysfunction in pediatric neuro-developmental disorders Frontiers in Cellular Neuroscience ·Constance Smith‐Hicks	2013	18
14	De novo variants in POLR3B cause ataxia, spasticity, and demyelinating neuropathy The American Journal of Human Genetics ·Djurdja Djordjevic, Maxime Pinard, Marie-Soleil Gauthier, Constance Smith‐Hicks, Trevor L. Hoffman, Nicole I. Wolf, Renske Oegema, Ellen van Binsbergen, Berivan Baskin, Geneviève Bernard, Sébastien Fribourg, Benoit Coulombe, Grace Yoon	2021	16
15	De Novo HECW2 Mutation Associated With Epilepsy, Developmental Decline, and Intellectual Disability: Case Report and Review of Literature Pediatric Neurology ·Natalie Ullman, Constance Smith‐Hicks, Sonal Desai, Carl E. Stafstrom	2018	15
16	Caregivers' perception of and experience with variants of uncertain significance from whole exome sequencing for children with undiagnosed conditions Journal of Genetic Counseling ·Xin Li, Rachel Nusbaum, Constance Smith‐Hicks, Leila Jamal, Shannan Dixon, Sonal Mahida	2019	14
17	APIGHmutation leading to GPI deficiency is associated with developmental delay and autism Human Mutation ·Thi Tuyet Mai Nguyen, Sonal Mahida, Constance Smith‐Hicks, Philippe M. Campeau	2018	12
18	Heterozygous de novo variants in CSNK1G1 are associated with syndromic developmental delay and autism spectrum disorder Clinical Genetics ·Nina B. Gold, Dong Li, Anna Chassevent, Frank J. Kaiser, Ilaria Parenti, Tim M. Strom, Feliciano J. Ramos, Beatriz Puisac, Juan Pié, Kirsty McWalter, María J. Guillen Sacoto, Hong Cui, Reem Saadeh‐Haddad, Constance Smith‐Hicks, Lance H. Rodan, Edward Blair, Elizabeth Bhoj	2020	10
19	Development of informant‐report neurobehavioral survey scales for PTEN hamartoma tumor syndrome and related neurodevelopmental genetic syndromes American Journal of Medical Genetics Part A ·Thomas Frazier, Robyn M. Busch, Patricia Klaas, Katherine Lachlan, Shafali Jeste, Alexander Kolevzon, Eva Loth, Jacqueline K. Harris, Leslie Speer, Thomas Pepper, Kristin Anthony, J. Michael Graglia, Christal G. Delagrammatikas, Sandra Bedrosian‐Sermone, Jenine Beekhuyzen, Constance Smith‐Hicks, Mustafa Şahin, Charis Eng, Antonia Y. Hardan, Mirko Uljarević	2023	7
20	Severe behavior problems in SYNGAP1-related disorder: A summary of 11 consecutive patients in a tertiary care specialty clinic Epilepsy & Behavior ·Benjamin R. Thomas, Natasha N. Ludwig, John Michael Falligant, Patricia F. Kurtz, Constance Smith‐Hicks	2023	6

About Constance Smith‐Hicks

Constance Smith‐Hicks is a scholar working on Developmental Neuroscience, Genetics, Cognitive Neuroscience, Psychiatry and Mental health and Cell Biology, having authored 31 papers that have together received 1.1k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (19 papers), Autism Spectrum Disorder Research (12 papers), Family and Disability Support Research (4 papers), Genomics and Rare Diseases (3 papers), Neuroscience and Neuropharmacology Research (3 papers), Mitochondrial Function and Pathology (3 papers), Genomic variations and chromosomal abnormalities (3 papers) and Behavioral and Psychological Studies (2 papers). The work is most often cited by research in Developmental Neuroscience (102 citations), Cellular and Molecular Neuroscience (413 citations), Genetics (411 citations), Cognitive Neuroscience (275 citations) and Biological Psychiatry (25 citations). Constance Smith‐Hicks has collaborated with scholars based in United States, United Kingdom and Germany. Frequent co-authors include Paul Worley, Dietmar Kuhl, Richard L. Huganir, David J. Linden, Jason D. Shepherd, Alexey G. Ryazanov, Shoaib Chowdhury, Sangmok Kim, Walter E. Kaufmann and Joo Min Park. Their work appears in journals such as Pediatric Neurology, Epilepsy & Behavior, Neuron, Sleep Medicine and Journal of Neurodevelopmental Disorders.

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