Hayley Moss
Overview
Explore the profile of Hayley Moss including associated specialties, affiliations and a list of published articles.
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9
Citations
331
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Recent Articles
1.
Source-based morphometry reveals structural brain pattern abnormalities in 22q11.2 deletion syndrome
Ge R, Ching C, Bassett A, Kushan L, Antshel K, van Amelsvoort T, et al.
Hum Brain Mapp
. 2024 Jan;
45(1):e26553.
PMID: 38224541
22q11.2 deletion syndrome (22q11DS) is the most frequently occurring microdeletion in humans. It is associated with a significant impact on brain structure, including prominent reductions in gray matter volume (GMV),...
2.
Chawner S, Doherty J, Anney R, Antshel K, Bearden C, Bernier R, et al.
Am J Psychiatry
. 2021 Jan;
178(1):77-86.
PMID: 33384013
Objective: Certain copy number variants (CNVs) greatly increase the risk of autism. The authors conducted a genetics-first study to investigate whether heterogeneity in the clinical presentation of autism is underpinned...
3.
Ching C, Gutman B, Sun D, Villalon Reina J, Ragothaman A, Isaev D, et al.
Am J Psychiatry
. 2020 Feb;
177(7):589-600.
PMID: 32046535
Objective: 22q11.2 deletion syndrome (22q11DS) is among the strongest known genetic risk factors for schizophrenia. Previous studies have reported variable alterations in subcortical brain structures in 22q11DS. To better characterize...
4.
Cleynen I, Engchuan W, Hestand M, Heung T, Holleman A, Johnston H, et al.
Mol Psychiatry
. 2020 Feb;
26(8):4496-4510.
PMID: 32015465
Schizophrenia occurs in about one in four individuals with 22q11.2 deletion syndrome (22q11.2DS). The aim of this International Brain and Behavior 22q11.2DS Consortium (IBBC) study was to identify genetic factors...
5.
Zhao Y, Diacou A, Johnston H, Musfee F, McDonald-McGinn D, McGinn D, et al.
Am J Hum Genet
. 2019 Dec;
106(1):26-40.
PMID: 31870554
The 22q11.2 deletion syndrome (22q11.2DS) results from non-allelic homologous recombination between low-copy repeats termed LCR22. About 60%-70% of individuals with the typical 3 megabase (Mb) deletion from LCR22A-D have congenital...
6.
Villalon-Reina J, Martinez K, Qu X, Ching C, Nir T, Kothapalli D, et al.
Mol Psychiatry
. 2019 Jul;
25(11):2818-2831.
PMID: 31358905
22q11.2 deletion syndrome (22q11DS)-a neurodevelopmental condition caused by a hemizygous deletion on chromosome 22-is associated with an elevated risk of psychosis and other developmental brain disorders. Prior single-site diffusion magnetic...
7.
Chawner S, Niarchou M, Doherty J, Moss H, Owen M, van den Bree M
J Psychiatr Res
. 2018 Nov;
109:10-17.
PMID: 30458299
Individuals with 22q11.2 Deletion Syndrome (22q11.2DS) are at substantial increased risk of psychosis spectrum outcomes including schizophrenia. We conducted a prospective, longitudinal study of the psychopathological and neurocognitive correlates of...
8.
Sun D, Ching C, Lin A, Forsyth J, Kushan L, Vajdi A, et al.
Mol Psychiatry
. 2018 Jun;
25(8):1822-1834.
PMID: 29895892
The 22q11.2 deletion (22q11DS) is a common chromosomal microdeletion and a potent risk factor for psychotic illness. Prior studies reported widespread cortical changes in 22q11DS, but were generally underpowered to...
9.
Chawner S, Doherty J, Moss H, Niarchou M, Walters J, Owen M, et al.
Br J Psychiatry
. 2017 Sep;
211(4):223-230.
PMID: 28882829
22q11.2 deletion syndrome (22q11.2DS) is associated with a high risk of childhood as well as adult psychiatric disorders, in particular schizophrenia. Childhood cognitive deterioration in 22q11.2DS has previously been reported,...