Constance L Smith-Hicks
Overview
Explore the profile of Constance L Smith-Hicks including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
13
Citations
472
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Gracia-Diaz C, Zhou Y, Yang Q, Maroofian R, Espana-Bonilla P, Lee C, et al.
Nat Commun
. 2023 Jul;
14(1):4109.
PMID: 37433783
Genetic variants in chromatin regulators are frequently found in neurodevelopmental disorders, but their effect in disease etiology is rarely determined. Here, we uncover and functionally define pathogenic variants in the...
2.
Paasch V, Doucoure A, Bifano M, Smith-Hicks C
Sleep Med
. 2023 May;
107:101-107.
PMID: 37146502
Study Objectives: Sleep disturbances are reported in 62% of children with SYNGAP1-Intellectual Disability (SYNGAP1-ID), a rare neurodevelopmental disorder characterized by intellectual disability, epilepsy, autism spectrum disorder (ASD), sensory and behavioral...
3.
Vedmurthy P, Murray C, Chen B, Asiedu A, Baranano K, Bay M, et al.
Front Rehabil Sci
. 2022 Oct;
3:934558.
PMID: 36275920
Background: The COVID-19 pandemic uniquely affects patients with neurologic and developmental disabilities at the Kennedy Krieger Institute. These patients are at increased risk of co-morbidities, increasing their risk of contracting...
4.
Brand B, Blesson A, Smith-Hicks C
Brain Sci
. 2021 Aug;
11(7).
PMID: 34356138
Nearly 20% of genes located on the X chromosome are associated with neurodevelopmental disorders (NDD) due to their expression and role in brain functioning. Given their location, several of these...
5.
Zagaglia S, Selch C, Radic Nisevic J, Mei D, Michalak Z, Hernandez-Hernandez L, et al.
Neurology
. 2018 Nov;
91(22):e2078-e2088.
PMID: 30413629
Objective: To characterize the neurologic phenotypes associated with mutations and to seek genotype-phenotype correlation. Methods: We analyzed clinical, EEG, and neuroimaging data of 44 new and 55 previously reported patients...
6.
Ullman N, Smith-Hicks C, Desai S, Stafstrom C
Pediatr Neurol
. 2018 May;
85:76-78.
PMID: 29807643
No abstract available.
7.
Natural history and genotype-phenotype correlations in 72 individuals with SATB2-associated syndrome
Zarate Y, Smith-Hicks C, Greene C, Abbott M, Siu V, Calhoun A, et al.
Am J Med Genet A
. 2018 Feb;
176(4):925-935.
PMID: 29436146
SATB2-associated syndrome (SAS) is an autosomal dominant disorder characterized by significant neurodevelopmental disabilities with limited to absent speech, behavioral issues, and craniofacial anomalies. Previous studies have largely been restricted to...
8.
Smith-Hicks C, Gupta S, Ewen J, Hong M, Kratz L, Kelley R, et al.
Neurology
. 2017 Sep;
89(16):1684-1690.
PMID: 28931647
Objective: To determine safety and perform a preliminary assessment of dose-dependent efficacy of dextromethorphan in normalizing electrographic spikes, clinical seizures, and behavioral and cognitive functions in girls with Rett syndrome....
9.
Smith-Hicks C, Cai P, Savonenko A, Reeves R, Worley P
Front Neural Circuits
. 2017 Feb;
11:6.
PMID: 28217086
Down syndrome (DS) is the leading chromosomal cause of intellectual disability, yet the neural substrates of learning and memory deficits remain poorly understood. Here, we interrogate neural networks linked to...
10.
Sun L, Bosemani T, Smith-Hicks C
Pediatr Neurol
. 2016 Dec;
67:109-110.
PMID: 27908655
No abstract available.